Reported experience, not a ranking
The illnesses people named as the most painful thing they have had — and what they said the pain was like
What people named, and what they said it was like
Kidney stones (273 records) and gallbladder attacks (250) are the two answers this thread returns to most, with shingles (244), endometriosis and adenomyosis (154) and depression (151) close behind — and the commenters who have had two of them contradict each other flatly about which was worse. Everything below is one person's account of their own illness, grouped by condition: what they said they had, what they said it felt like, and what they said happened when they asked for help — not a severity ranking, not a diagnosis, and not advice.
- Kidney stones — 273 records, the thread's largest group
- Gallbladder attacks — 250 records, and the commenters who rank them against childbirth
- Shingles — 244 records, and the nerve pain writers say it left behind
- Endometriosis and adenomyosis — 154 records, and the years before a diagnosis
- Depression — 151 records, the answer that argues with the question
- The 36 records about not being believed
- Why none of this is a ranking, a diagnosis or medical advice
Stones, and the organs that make themThe thread's two largest answers by a wide margin, and the organ inflammation that repeatedly follows one of them. 604 records.
Kidney stonesThe largest group of classified records in the thread, and the one commenters most often measure everything else against.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Kidney stones
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Kidney stones
Appears when: Kidney stones
What the pattern means: The largest group in the corpus and the most internally consistent. The pain arrives without warning, frequently out of sleep; no position relieves it; and vomiting recurs as the thing that convinced people this was not a stomach ache. A detail these records keep correcting is which part hurts — several writers expected the stone leaving the body to be the worst of it and report it was painless after days or weeks of colic beforehand. The group is also the thread's reference point: commenters filed under other conditions reach for it to explain their own, in both directions.
What commenters described: Here I was thinking when hearing about kidney stones all my life that the painfull part of kidney stones is when you pee them out - like when the stone is bigger than your urethra. Little did know that the most painfull part is when the little fella starts moving out of the kidney. I woke up at 1am with an upset intestine, thought I ate something wrong and went to the toilet. Shortly after the pain started at the left side of my back and continued for the whole night - didn't know how to move or lie down to make it stop simply nothing seemed to help. Drove to the ER in the morning and they quickly said that's a kidney stone but because they did not have an urologist at hand they send me home with antibiotics and pain meds. During the next night the pain was so bad that I had to call an ambulance and the pain meds they gave me in the ER did not work initially - they kept proceeding to stronger and stronger ones and it wasn't until they pushed piritramide for the third time that my pain finally stopped - which I learned came from a renal colic... got to stay at the hospital for a few days which basically consisted of sleeping during the day and calling for pain meds the whole night. then they did eswl shock wave therapy and send me home again. Had to come back twice I think into the ER so they could give me stronger pain meds than they send me home with. All in all a pretty exhausting and painfull experience. Pissing the stone out itself in the end after 1+ week of pain did not hurt at all but fuck kidney stones
Limit: Stone size, whether anything was blocked and whether an infection followed vary enormously inside this group, and so do the outcomes — some passed a stone unaided, some needed surgery, several report becoming septic. These are individual accounts of what people say happened to them, not a way to recognise a kidney stone or to decide what to do about one.
What replies pushed back on5
Be careful. I took omeprazole for 20 years and now am missing several teeth, due to side effects I was totally unaware of.
Ditto. Had four babies, three without pain meds or epidurals, and kidney stone pain was way worse. Worse than when my colon perforated too.
I thought I had a very high pain tolerance, broken bones etc in the past - until I had my first kidney stone. Was vomiting and curled up on the ground for hours from the pain, is absolutely the worst.
I had a very large stone, too big to pass and I ended up with 3 surgeries to rid me of it. The first Lithotripsy only broke it up, and all the small pieces got stuck and I had to back in to the ER and have another surgery to have them removed AND then, there was still a large piece stuck and so I had to go back in and have that one removed! That was a nasty stone. I had stones several times before that as well over the years! Thanks Dad, I inherited it from you...LOL! He had them too. I remember as a child the ambulance taking him away in the middle of the night, back in the 1960s. He had kidney stones! The other most painful condition I had was a kidney infection, no stones....holey moley...that hurt really bad too! 😱😱
Kidney stones. I’ve broken my back twice and the kidney stones still win. Especially since those tickets wouldn’t pass on their own and required intervention under anesthesia.
Where commenters report limits
I had a kidney stone at 32 weeks pregnant. I would honestly take childbirth over kidney stones again. Unfortunately for me I have two more hanging out in my right kidney and nothing I can do about it until I give birth except hope they don’t decide to pass before then
Yes Kidney Stones I'm 49 and they started at the age of 12 years old, it's been like 5 years since I've had an episode..but the pain can be so crucial that it will literally take yr breath away!!! And no unfortunately my middle daughter started getting them a few years ago but I pray neither of my other two girls get them!!
Source-record spotlights
This should be higher on the list. Extremely painful! I’ve had several.
I have given birth by being induced without pain meds, had a gallbladder attack (and removal) and had kidney stones. Ill take anything over kidney stones.
Kidney stones! Much worse pain than being induced.
Related evidence elsewhere in the index
What the counts show
Across 273 source records, the most common observable tactic structure is “Attach it to an existing routine” (3 records). This is a wording pattern, not a measured outcome.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Observable tactic structures
Counts show source records whose wording matches the tactic structure; biological explanations remain commenter claims unless separately checked below.
Browse the original comments273 preserved records · 273 of 273 source records accounted for
Archive: 273 index entries preserve 273 distinct source records · Every displayed synthesis count resolves to source-record IDs
Gallbladder attacks and gallstonesThe second largest, and the answer whose writers most often say they believed they were having a heart attack.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Gallbladder attacks and gallstones
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Gallbladder attacks and gallstones
Appears when: Gallbladder attacks and gallstones
What the pattern means: The thread's second-largest group, and the one with the most distinctive shared vocabulary: writers repeatedly describe a sense of impending doom, believe they are having a heart attack, and end up on a bathroom floor. Two structural things recur. The first is delay — a large share of this group describes months or years of attacks written off as heartburn, reflux, stress or anxiety before a scan was ordered. The second is the comparison with the operation: writer after writer says the surgery was easier than the attacks that led to it, several of them adding that they felt better the following day.
What commenters described: When I had my gallbladder attack, all I can describe it as is pain that feels like impending doom. Like I really thought I was going to die that night. It was also during Covid quarantine and ain’t no way I was going to the ER so I just curled up in the fetal position on the cold tile of my bathroom floor and made peace with my so thought fate. On top of that were other symptoms like my whole digestive system felt like it was cramping in synchrony, indigestion pressure that felt like an elephant was sitting on top of me, throwing up straight bile, and sweating uncontrollably.
Limit: How long each writer waited for a diagnosis shapes these accounts as much as the condition does, and the group contains its own dissent — at least one commenter declines to rank the pain highly at all. Drugs, diets and operations named here are what individual people say was done in their case; none of it identifies a gallbladder attack or tells anyone else what to do about one.
What replies pushed back on5
You're a woman! Have you tried not being so hysterical? Maybe finally try losing that baby weight?? Meditation??? I was the opposite, sitting in the lobby with two broken arms, calm but dirty after a fall. The male doctor told me I'd *possibly* sprained them because obviously I wasn't screaming in pain. Hey guess what? Two broken arms! I'm just super calm in an emergency but somehow react like I'm being hunted for sport if I have to make a phone call.
I had it a few months ago and having it out was waaaay better than risking another attack. And the recovery was not bad at all. My hernia surgery a few weeks ago was way worse. But still ok.
I had both gallbladder stones and kidney stones (not at the same time). Kidney stones are worse. Even worse than an exploded gallbladder.
When I had mine, I was on vacation in another state and I thought I had food poisoning. The pain was not typical Upper right quadrant . My whole abdomen was in knots. I put it off for three days, the couldn’t stand it any more and went to the ED. It was about an hour from the time I walked into the ED till I was in the operating room. It was gangrenous and fell apart when they tried to remove it. Needless to say, I had to stay in the hospital longer than I wanted. W Moral of the story, don’t ignore the pain.
A broken gallbladder. Before that, I would have said a burst ovarian cyst, but no - a gallbladder that was actually broken, literally non-functioning, was the absolute worst. I remember being doubled over in my kitchen, wishing to just pass out, hoping to not throw up... recovery sucked horribly, but only half as horribly as the Broken Organ sucked. Oof. Childbirth labor and a c-section do not even compare!
Where commenters report limits
i had mine removed one month after i had my first kid too! i was actually having gallbladder attacks while i was pregnant but i thought it was heart burn because i never had heart burn a day in my life. they told me i needed surgery the next day but declined because i had finals and didn’t want to miss them, that didn’t work lol i missed my finals
Mine was bad but (unfortunately) not the worst for me
Source-record spotlights
Gallbladder attack
I’ve delivered 4 babies, one without meds. None of them compared, even remotely, to the pain of a gallbladder attack.
Gallbladder attack was followed in severity closely by a burst appendix. Both attacks were so painful that I almost passed out.
Related evidence elsewhere in the index
What the counts show
Across 250 source records, the most common observable tactic structure is “Attach it to an existing routine” (21 records). This is a wording pattern, not a measured outcome.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Observable tactic structures
Counts show source records whose wording matches the tactic structure; biological explanations remain commenter claims unless separately checked below.
Browse the original comments250 preserved records · 250 of 250 source records accounted for
Archive: 250 index entries preserve 250 distinct source records · Every displayed synthesis count resolves to source-record IDs
PancreatitisNamed both as the thing that followed a gallstone and, on its own, as the worst pain the writer could put into words.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Pancreatitis
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Pancreatitis
Appears when: Pancreatitis
What the pattern means: Two distinct routes into the same group. In one, pancreatitis follows a gallstone and is described as the sequel that turned out worse than the original. In the other it arrives alone and overnight. The accounts converge on duration rather than peak: writers describe days in hospital, nil by mouth, and pain that opioids reduced without removing. Several note in passing that they were asked repeatedly about alcohol.
What commenters described: Pancreatitis. I tried to describe the pain to my husband—I had been throwing up all night and told him it was like there was a heavy, hot, very sharp rock embedded in the left side of my body. He asked if I needed to go to the hospital. I almost said, “no” Was in hospital for five days—painkillers and fluids. They wouldn’t release me because I kept getting a fever. I had a cyst on my pancreas and ended up having surgery to remove the cyst a few months later.
Limit: Causes differ across these records — gallstones, medication, alcohol, a procedure, and several writers who say no cause was ever found — so the accounts are not describing one uniform illness. Nothing here identifies pancreatitis or indicates what should be done about it.
What the replies added1
Pancreatitis!! It started out like a stomach ache and some diarrhea and vomiting. Then it progressively got worse as the night went on. I couldn’t keep anything in my body including water. I began to get a fever and started to think I just had a stomach flu. Then the vomiting and dry heaves were incredibly painful and so hard on my body. I started to throw up what looked like rubber bands and eventually coffee grounds. I begged someone to get me to emergency so my good friend picked me up to take me. She said “did you use self tanner?” Because I was yellow. My skin was yellow and I had jaundice. I don’t recall a lot after getting to emergency because they rushed me in right away and had me hooked up to some IV bags and some pain killers for the pain. They suspected my appendix at first but after bloodwork it seemed more serious. I vomitted once more at the hospital and it was again coffee grounds and a little bit of blood from my esophagus. They knocked me out to do the ultrasound because I was screaming in pain. I woke up hours later with my friend and my mom there and didn’t remember getting to the hospital. They said it was probably my gallbladder at first, according to the bloodwork, but after running tests and ultrasound they said it was my pancreas which was swollen and angry. They gave me some anti-inflammatory medication and some Zofran to stop the nausea and sent me home after 6 bags of saline and a stay overnight to get my hydration back to normal. Luckily I didn’t need any surgery. For days I had horrible muscle pain in my back and stomach from all the heaving and my throat and esophagus was sore and tender so I could only eat soft food and warm water. After a couple of days my skin went back to pink and I was okay but I’ve never had anything like this before. I have had babies without epidurals, I’ve had back injuries, I’ve had a broken foot and I’ve had other stomach issues but nothing like this ever in my life. I truly feel like I could have died (or came really close) if I didn’t get to the hospital that day.
Where commenters report limits
Pancreatitis!! It started out like a stomach ache and some diarrhea and vomiting. Then it progressively got worse as the night went on. I couldn’t keep anything in my body including water. I began to get a fever and started to think I just had a stomach flu. Then the vomiting and dry heaves were incredibly painful and so hard on my body. I started to throw up what looked like rubber bands and eventually coffee grounds. I begged someone to get me to emergency so my good friend picked me up to take me. She said “did you use self tanner?” Because I was yellow. My skin was yellow and I had jaundice. I don’t recall a lot after getting to emergency because they rushed me in right away and had me hooked up to some IV bags and some pain killers for the pain. They suspected my appendix at first but after bloodwork it seemed more serious. I vomitted once more at the hospital and it was again coffee grounds and a little bit of blood from my esophagus. They knocked me out to do the ultrasound because I was screaming in pain. I woke up hours later with my friend and my mom there and didn’t remember getting to the hospital. They said it was probably my gallbladder at first, according to the bloodwork, but after running tests and ultrasound they said it was my pancreas which was swollen and angry. They gave me some anti-inflammatory medication and some Zofran to stop the nausea and sent me home after 6 bags of saline and a stay overnight to get my hydration back to normal. Luckily I didn’t need any surgery. For days I had horrible muscle pain in my back and stomach from all the heaving and my throat and esophagus was sore and tender so I could only eat soft food and warm water. After a couple of days my skin went back to pink and I was okay but I’ve never had anything like this before. I have had babies without epidurals, I’ve had back injuries, I’ve had a broken foot and I’ve had other stomach issues but nothing like this ever in my life. I truly feel like I could have died (or came really close) if I didn’t get to the hospital that day.
Source-record spotlights
Pancreatitis that went necrotic because my ex made me wait hours before he believed that I needed to go to the ER. He said I was “just being dramatic”. In retrospect, I should have called for an ambulance, but I was in too much pain to think with any clarity. I couldn’t even see straight.
Severe Panreatitis.. Had an ERCP done to place a stent in my bile ductand was risk of severe pancreatitis was under 2%. Two hours after the procedure and the abdoninal pain was so bad I was screaming the ward down. I;d describe the pain as "You know that scene in Alien?". Spen two and a half months in hospital reovering from the range of infections that it caused and now have permanent, escessive scar tissue surronding my pancreas.
Pancreatitus felt like a hot knife was being stabbed into me very very slowly. Check your alcohol consumption kids
Related evidence elsewhere in the index
What the counts show
Across 81 source records, the most common observable tactic structure is “Use a sensory reset” (2 records). This is a wording pattern, not a measured outcome.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Observable tactic structures
Counts show source records whose wording matches the tactic structure; biological explanations remain commenter claims unless separately checked below.
Browse the original comments81 preserved records · 81 of 81 source records accounted for
Archive: 81 index entries preserve 81 distinct source records · Every displayed synthesis count resolves to source-record IDs
The gutAnswers from the abdomen: the organ that bursts, the ones that inflame, and the ones that block. 398 records.
AppendicitisThe organ that gives a few hours' notice, from people who reached surgery in time and people who did not.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Appendicitis
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Appendicitis
Appears when: Appendicitis
What the pattern means: The clearest before-and-after in the corpus: a short, escalating window that ends in an operating theatre. What separates these accounts from each other is timing. Writers who reached surgery describe hours of constant, stabbing pain that they could not stand upright through; writers who did not describe rupture, peritonitis, drains and weeks in hospital. A recurring sub-theme is being sent home first — for period cramps, for constipation, for a urinary infection.
What commenters described: Appendicitis. I have a high pain threshold, childbirth without meds for example, but this doubled me over (don't get me wrong, childbirth is no walk in the park). The instant, stabbing pain, the inability to stand straight, takes your breath away.
Limit: These records are written after the fact by people who know how their story ended, which is not the position anybody is in at the time. Nothing here is a way to tell appendicitis from anything else, and the delays described are reported experiences, not a claim about how often that happens.
What the replies added1
Same here (the appendicitis part, being a bloke I won’t experience the childbirth comparison firsthand). Ruined a family holiday age 12 with it. Absolute agony until they gave me the morphine in A&E. Felt a bit better again later, turns out that was probably when my appendix exploded before they could get me to surgery.
Where commenters report limits
1. When my appendix almost burst; 2. Close second was my c-section incision—something wasn’t right and I was in a lot of pain. The surgeon couldn’t figure out what was wrong and said I went off the painkillers too soon. Was discharged, went home, and my incision exploded. Happily, that relieved the pressure and the pain was gone. Unfortunately, my incision became infected and I needed a referral to wound care.
Source-record spotlights
I said shingles (in my eye), until I got gangrene appendicitis.
Interesting. My appendicitis turned out to be chronic and recurrent for years. The last flare made me feel bad for weeks. Doc dismissed me. Carried on for a week. Then the ER sent me home the first time I went, and had me take a laxative cocktail that almost ended me. Second time in the ER they discovered the ruptured appendix and kept me a week after emergency surgery. Still, not the worst/most intense pain I've been in. I'd say that was what the doctors called lumbago. One wrong move and I couldn't sit, stand, lie or walk, could hardly breathe and had to manage crying and vomiting. It took like 12 hours, painkiller pills, injections and several IVs to get back to normal.
appendicitis. it felt as though i was getting punched in the stomach several times over for hours on end
Related evidence elsewhere in the index
What the counts show
Across 82 source records, the most common observable tactic structure is “Attach it to an existing routine” (3 records). This is a wording pattern, not a measured outcome.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Observable tactic structures
Counts show source records whose wording matches the tactic structure; biological explanations remain commenter claims unless separately checked below.
Browse the original comments82 preserved records · 82 of 82 source records accounted for
Archive: 82 index entries preserve 82 distinct source records · Every displayed synthesis count resolves to source-record IDs
Crohn's disease and ulcerative colitisA lifelong condition described by its flares rather than as a single event, and often by what it cost outside the pain.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Crohn's disease and ulcerative colitis
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Crohn's disease and ulcerative colitis
Appears when: Crohn's disease and ulcerative colitis
What the pattern means: Unlike most of this page, these records do not describe an event. They describe a condition measured in years, and the writers reach for what it removed rather than for a pain scale: food, work, a first year with a baby, a colon. Several rank it against acute conditions they have also had — one commenter with colon cancer says the Crohn's was worse — and several describe the humiliation of the symptoms as harder than the pain.
What commenters described: Ulcerative colitis. By the time I was diagnosed I was .05 above the line for a required blood transfusion. Another week and I would have died. Every time I ate it felt like someone twisting and knifing the back of my belly button. I no longer feel organic hunger from the pain associated with my early illness. Spent most of my sons first year in a bathroom because every time he cried I would have a spasm and have to rush to the bathroom. That would drive me down to 100lbs and finally I would be approved for a last resort treatment. I’m 12 years in remission now. I’ll never forget the pain.
Limit: Severity in this group ranges from managed remission to emergency surgery and cancer, so no single account represents the condition. Treatments, diets and surgical outcomes named here are individual reports and are not guidance for anyone else.
What the replies added2
Yep. 18 years here. They've GOT to come up with a cure 😭
Omigosh, I'm sorry to hear that. My best wishes go out to you. You're braver than I would be, I think. 💜
Where commenters report limits
I'm very grateful I've only ever had the one. I hope it stays that way. As for the kidney stones, I unfortunately have Crohn's disease, which increases my risk of getting kidney stones, and I have hyperparathyroidism, which means my calcium levels are super high and it makes calcium accumulate in my kidneys, causing stones. I get stones a lot. Womp womp I guess lol
IBD flare that *everyone* (including myself, because I didn't know I had IBD at the time) thought was gallstones and kidney stones at the same time. Alongside the pain, I wasn't keeping anything in either end, so I was also severely dehydrated, and I've postulated that I actually had a partial bowel obstruction. I am, unfortunately, still in the same flare (with one more episode of hospital worthy symptoms), I get my type confirmation colonoscopy next month (my doctor and I are swaying towards Crohns due to other symptoms) and hopefully this will never happen again 🙃 Most painful experience I've ever had. Got admitted to the Surgical ward because of it. You can bet everyone was as equally confused as they were certain prior when the US showed no such stones. In fact showed nothing remarkable at all, everything intact, and just showed that my pancreas was obscured by excess bowel gas. The pain was so severe I couldn't even sit comfortably in my own wheelchair. The manual abdominal exam was dreadful and I nearly threw up on both doctors that did them. I almost passed out waiting for the CT scan (that never ended up happening), I looked so sick I had to have medical escort from the CT waiting room back to the ward 'just in case'. There was a very serious conversation about removing my gallbladder. Going on a liver shrinkage diet for 2 weeks then yanking that bitch out. To top it off, every time I get even a little stressed, my pancreas joins in. Yeah, my amylase is elevated, almost at 300 now. But this is a consistent upward track, not acute, so that one is just being a dick for the sake of it. It does worry me, though, that I may have gallstones or kidney stones in the future and chalk it up to my very angry-at-life gut.
Source-record spotlights
Colitis with severe sepsis.
Simultaneous c diff colitis with diverticulitis...while recovering from abdominal surgery. It was so bad they discharged me with my own morphine.
Ulcerative colitis flares and whenever I pass a decidual cast.
Related evidence elsewhere in the index
What the counts show
Across 54 source records, the most common observable tactic structure is “Attach it to an existing routine” (4 records). This is a wording pattern, not a measured outcome.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Observable tactic structures
Counts show source records whose wording matches the tactic structure; biological explanations remain commenter claims unless separately checked below.
Browse the original comments54 preserved records · 54 of 54 source records accounted for
Archive: 54 index entries preserve 54 distinct source records · Every displayed synthesis count resolves to source-record IDs
DiverticulitisRepeatedly described as arriving without warning in writers who say they had never heard of it.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Diverticulitis
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Diverticulitis
Appears when: Diverticulitis
What the pattern means: The recurring shape here is surprise: writers say they had not heard of the condition, several were told they were too young for it, and most describe waiting a day before going in because they assumed it was a normal flare-up. What follows is a localised stabbing pain, usually low on the left, that several say outranked a perforated appendix or a hernia they had also had. A number describe perforation, abscess, sepsis and, eventually, the loss of part of the colon.
What commenters described: Most painful to date was diverticulitis. It felt like someone was stabbing me with a thin knife in the lower left part of my abdomen. It would stop and then come back full-force. I was panicked because I thought it was actually appendicitis at first, but thank god it was something I didn't have to have surgery for.
Limit: This group skews towards the writers whose diverticulitis became severe enough to be worth posting about, which is not the whole range of the condition. Nothing here identifies diverticulitis or indicates when to seek care.
What the replies added2
Had to scroll a bit before seeing this! I've been in a lot of pain before and live with chronic pain, but diverticulitis took the cake and then some. I was 23 and my ER doc said I was too young for it at first. I pushed for imaging and I'm glad I did, I came close to needing surgery.
Agreed. I had diverticulitis with a perforation. The pain was the worst I had experienced. 7cm abscess was found, was septic when I went to hospital. Was hospitalized off and on for 6 months, and finally had my colon out 10 months after diagnosis, and 6 months after I had an ileostomy put in. Couple that with my first ever bout of depression which started in the hospital and then medical anxiety which began after a surgeon decided to dig in my side to get my abscess to drain better without pain meds on board. I was a mess for 7 months. An experience I never, ever want to repeat. Scares the hell out of me to think what I endured.
Where commenters report limits
I also waited a day! Maybe a little more, I have bad gastro problems in general and figured I was having some kind of flare at first and my pain tolerance is very high. But in the morning it was so incredibly bad, I was on call with my best friend and it just kept getting worse and they pushed me to get checked out. Called my roommate, they came to take me to the ER and it rapidly got worse. I could barely even talk to the nurse with all the pain, was just screaming and throwing up. I've had cluster headaches, severe suspected endometriosis complicated by being intersex, and an infected tooth among other things. Nothing compares.
Source-record spotlights
Diverticulitis is pretty shitty.
Severe diverticulitis.
Diverticulitis infection that went septic
Related evidence elsewhere in the index
What the counts show
Across 43 source records, the most common observable tactic structure is “Attach it to an existing routine” (2 records). This is a wording pattern, not a measured outcome.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Observable tactic structures
Counts show source records whose wording matches the tactic structure; biological explanations remain commenter claims unless separately checked below.
Browse the original comments43 preserved records · 43 of 43 source records accounted for
Archive: 43 index entries preserve 43 distinct source records · Every displayed synthesis count resolves to source-record IDs
Bowel obstruction, twisting and perforationAnswers where the gut stopped, twisted or tore, most of them ending in emergency surgery.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Bowel obstruction, twisting and perforation
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Bowel obstruction, twisting and perforation
Appears when: Bowel obstruction, twisting and perforation
What the pattern means: The most mechanical answers in the corpus. Writers describe the gut stopping, telescoping into itself or twisting until the blood supply is cut off, and they reach for tearing and evisceration to describe it rather than for cramping. Morphine is mentioned repeatedly as having taken the edge off and no more. Almost every account ends in emergency surgery, several with a length of intestine removed; a number of writers report the obstructions recurring afterwards because of adhesions.
What commenters described: Small bowel obstructions. It feels like I'm being evicerated. Searing pain that doesn't pause or stop. Just keeps up with a ripping and tearing sensation. I just had my 7th obstruction on July 1st. I can expect my next in 19 months. That seems like the frequency. Going to talk with my PCP, oncologist and ER surgeon if I can have a standing order for IV pain meds in my chart for the "next one". Good fun./s
Limit: Several writers here describe being disbelieved or delayed and attribute gangrene to the wait; that is their account of their own case. Nothing in this group distinguishes an obstruction from anything else or says what should be done about one.
What replies pushed back on2
I agree.. I’ve had shingles and the bowel obstruction was way worse.
Aww yes! There is nothing more painful. I think I'd rather be stabbed with a dull knife over and over. I've had over a dozen small bowel obstructions due to Crohn's disease. 0/10 - would not recommend
Source-record spotlights
Bowel obstruction from Crohn’s disease.
Bauchfell Entzündung als Kind
Small bowel obstruction. I legitimately thought I was dying. I had emergency surgery to fix it. I wouldn’t wish that pain on anyone…
Related evidence elsewhere in the index
What the counts show
The exact phrase “thought i was dying” recurs across 2 of the 49 source records in Bowel obstruction, twisting and perforation; the complete archive stays available below.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Browse the original comments49 preserved records · 49 of 49 source records accounted for
Archive: 49 index entries preserve 49 distinct source records · Every displayed synthesis count resolves to source-record IDs
Stomach ulcers, gastritis and refluxBurning described from the inside, including the ulcers that perforated.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Stomach ulcers, gastritis and reflux
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Stomach ulcers, gastritis and reflux
Appears when: Stomach ulcers, gastritis and reflux
What the pattern means: Burning is the common thread, but the group splits by how it ended. The gastritis accounts describe weeks of vomiting everything, with writers noticing knock-on effects — potassium, weight, teeth — as much as the pain itself. The ulcer accounts describe something abrupt: a perforation, acid in the abdomen, and an emergency. Several writers mention H. pylori and the months it took to get to that answer.
What commenters described: Gastritis is one of the worst things you can experience for weeks. Its inflammation of the lining of your stomach and intestine. It can last upto a couple weeks of just throwing up everything. The one time I had it, my potassium got so low it felt like if I threw up one more time my heart was going to stop.
Limit: These accounts run from an unpleasant fortnight to a life-threatening perforation under the same headings, so the group is not describing one severity. Nothing here identifies an ulcer or gastritis, and the medications named are what individual writers were given.
What the replies added1
I've had it once. I was vomiting for 16 days straight
Where commenters report limits
Gastritis attack- they thought it was pancreatitis. The pain was so horrifically intense that I went to the emergency room because I was literally yelling in pain and crying. They ended up doing a bunch of tests and my lipase level came back three times normal. So they assumed all of that that it was pancreatitis, but it actually was gastritis because the pain subsided significantly with a G.I. cocktail and a IV of Protonix and Pepcid. I think it was possibly. It was so odd though because I swear I had so many staff members coming in because they couldn’t believe that I didn’t drink at the time we believed it was pancreatitis, so they kept saying are you sure you don’t drink alcohol? I’m like yeah I’m pretty sure that I don’t drink lol. That pain was horrible though. One of the worst pain I’ve ever remember was having an abscessed tooth though. I used to get them a lot when I was a child, unfortunately genetics in my family is notorious for having dental issues. I remember the horrible pain of that as a child though.
Source-record spotlights
Perforated ulcer
I have Fibromyalgia, hypermobility, ankylosing spondylitis. I suffer migraines, have had gallbladder done and even a spontaneous pneumotheoax. I also had kidney issues when younger as I Have two tubes from each kidney and it would back flow. I've also given birth with no meds. That was easy. The worst pain I've ever had and still do when it flares up is an excavated ulcer in my small intestine. Which has kick started off Inflammatory Bowel Disease. It's the most encompassing unrelenting pain I've ever experienced Wish it would fuck off
Severe gastritis. I have GERD and recently ate chili too late at night. Woke up to 24 hours of the worst pain I've ever had in my life, worse than the runner-up of endometriosis on my bowel.
Related evidence elsewhere in the index
What the counts show
Across 30 source records, the most common observable tactic structure is “Change the sentence” (2 records). This is a wording pattern, not a measured outcome.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Observable tactic structures
Counts show source records whose wording matches the tactic structure; biological explanations remain commenter claims unless separately checked below.
Browse the original comments30 preserved records · 30 of 30 source records accounted for
Archive: 30 index entries preserve 30 distinct source records · Every displayed synthesis count resolves to source-record IDs
Norovirus, food poisoning and stomach bugsThe short, violent illnesses writers apologise for nominating and then nominate anyway.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Norovirus, food poisoning and stomach bugs
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Norovirus, food poisoning and stomach bugs
Appears when: Norovirus, food poisoning and stomach bugs
What the pattern means: The group with the most self-deprecation attached to it: writers apologise for nominating something so ordinary, then describe cramping severe enough to make them consider an emergency department, hours on a bathroom floor, and abdominal muscles that stayed sore for weeks afterwards. Two things recur — the total loss of dignity, described almost cheerfully, and the fear that they were actually dying, which several attribute to how fast dehydration arrived.
What commenters described: Agree. The pain was up there with childbirth. I had such bad cramps with food poisoning that I thought I was going to pass out from the pain. When it was over, my abdominal muscles were sore for weeks from all the cramping.
Limit: These are short illnesses recalled at a distance and, in several cases, never diagnosed — writers use norovirus, food poisoning and stomach flu interchangeably. Nothing here identifies which infection anybody had or when a stomach bug needs medical attention.
What the replies added1
Was gonna comment this. Had it almost a month ago. Ruined my holiday. Stomach was in agony, couldn’t eat literally anything, barely kept water down. Never again
Where commenters report limits
3 years ago I got food poisoning. Not that shit people say they have hen they get a little upset tummy and call out of work. I'm talking full blown side saddle on the toilet with my head in the bath tub. For 3 days non stop. Water was in and back out. Nothing was coming out of be beside stomach acid, which burned like hell. Stomach felt like it was turning into stone, any pipes leading to and from it were on the verge of melting. My teeth were so sensitive that room temp water hurt. It was like a light switch, pissed before going to bed, got in bed and exorcist vomited all over the room with zero warning.
Source-record spotlights
Mine seems mild compared to everyone else, but food poisoning. Felt like my whole body was on fire the next day, the chills I had and aches in my legs made me seriously consider a&e
No, I get that 100%! So I ended up with a stomach virus, which I thought would be like you know one or two days kind of feeling like crap and then I’d get better. It ended up lasting over seven days and I was so sick. I was like on the bed just couldn’t eat kept going to the bathroom. I turned out. It was like actually an infection like a bacterial infection and I had to go to the emergency room and get put on antibiotics and it did work. Food poisoning can be deadly too especially depend depending on the type of bacteria that’s introduced so it doesn’t surprise me that you literally felt like you were probably gonna freaking fall over. I’m sorry you had to deal with that.
Blasting vomiting and diarrhea+ very bad fewer (39.5°C). And the feeling after circumcision (removing stitches at home was very NOT fun experience), when I was 10. Last one though... I was awake and have seen everything what doctor done. Surprisingly, I wasn't scared at all. Just curious. But couple hours after...
Related evidence elsewhere in the index
What the counts show
Across 81 source records, the most common observable tactic structure is “Attach it to an existing routine” (4 records). This is a wording pattern, not a measured outcome.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Observable tactic structures
Counts show source records whose wording matches the tactic structure; biological explanations remain commenter claims unless separately checked below.
Browse the original comments81 preserved records · 81 of 81 source records accounted for
Archive: 81 index entries preserve 81 distinct source records · Every displayed synthesis count resolves to source-record IDs
Gastroparesis, cyclic vomiting and guts nobody could nameRecurring vomiting and gut pain without a clean diagnosis attached to it.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Gastroparesis, cyclic vomiting and guts nobody could name
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Gastroparesis, cyclic vomiting and guts nobody could name
Appears when: Gastroparesis, cyclic vomiting and guts nobody could name
What the pattern means: What holds this group together is the absence of a clean diagnosis. Writers describe cycles rather than episodes — days of retching with nothing to bring up, dehydration, and the anticipation of the next bout — and several describe years of tests that found nothing. A recurring complication is that the coping strategy makes it worse: drinking to have something to vomit, or a medication that turned out to be the cause.
What commenters described: I have cyclic vomiting syndrome. I vomit for 4-5 days at a time even if nothing is coming out, the heaving still happens. I get so dehydrated because of it and for some reason, it’s a common action of people with CVS to try and chug water or something to at least give something to vomit up but it only hinders you further. The exasperated pains I normally have, throbbing migraine from dehydration & severe muscle pain from all of the retching IS the worst thing I’ve ever dealt with.
Limit: Several conditions with different causes are grouped here because their writers describe them the same way; that is an editorial grouping, not a medical one. Nothing here identifies any of them or indicates a treatment.
What the replies added2
I commented above, thinking I might have been having a gallbladder attack. The way people were commenting, I knew my pain wasn’t what they were experiencing. Their stories sounded terrible, nightmarish. But I didn’t know what was happening. It was Vasovagal syncope. You just described everything I was experiencing. Sorry you have that, I have had it too. Luckily it isn’t gallbladder attack, but still sucks to get
Gastritis? Crohn’s disease? Is there a particular trigger food? I finally realized my gastrointestinal issues are due to a food intolerance to alliums- onion, garlic, leeks, chives, scallions/green onions, shallots, etc. I’ve drastically reduced consumption, with the sole exception of garlic- I just don’t use a lot and it has to be well cooked. I’m feeling a lot better now.
Source-record spotlights
So sometimes when my insomnia flares up and I don't get enough sleep, my gut gets very angry and I get sudden, intense diarrhea with cramps that trigger vasovagal syncope. Basically I pass out from the pain while breaking out in a cold sweat on the toilet. It's miserable.
Unironically... lactose intolerance
Bile acid malabsorption
Related evidence elsewhere in the index
What the counts show
Across 27 source records, the most common observable tactic structure is “Use a sensory reset” (2 records). This is a wording pattern, not a measured outcome.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Observable tactic structures
Counts show source records whose wording matches the tactic structure; biological explanations remain commenter claims unless separately checked below.
Browse the original comments27 preserved records · 27 of 27 source records accounted for
Archive: 27 index entries preserve 27 distinct source records · Every displayed synthesis count resolves to source-record IDs
C. difficile, and what the antibiotics left behindAn infection several writers say arrived after a course of antibiotics taken for something else.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: C. difficile, and what the antibiotics left behind
Source-backed answers are shown before diagnostics; the complete source archive remains below.
C. difficile, and what the antibiotics left behind
Appears when: C. difficile, and what the antibiotics left behind
What the pattern means: A group defined by its cause rather than its site: writers took antibiotics for something minor — a sinus infection, an ear infection, a wound — and describe what followed as worse than what they were treating. The C. difficile accounts describe stabbing gut pain, months of recurrence, isolation rooms and, in several cases, near-death. Alongside them sit writers who attribute lasting damage to a specific drug class.
What commenters described: C diff. Felt like someone was stabbing me over and over in the gut and twisting the knife. Dilaudid didn’t fully get rid of the pain but it did knock my ass out and give me nasty withdrawals for a month after I left the hospital. Before that though, c diff almost killed me.
Limit: These are individual accounts of adverse outcomes, and they say nothing about how common such outcomes are or whether the drugs were the cause. This is not a reason to stop or avoid a prescribed medicine, and nothing here identifies C. difficile.
What the replies added2
Horrific isn't it, took me best part of a year, all thanks to 3 days of augmentin for a dumb sinus infection.. It was 23 yrs ago and I've had antibiotics twice since then, other than prophylactic before surgery a few times. Only when absolutely vital, luckily where I live now they check bloods for bacterial vs viral every time.
Three times is crazy, I’m sorry! I only just finished my steroid course (had this end of April). It’s awful!
Source-record spotlights
C diff. Felt like someone was stabbing me over and over in the gut and twisting the knife. Dilaudid didn’t fully get rid of the pain but it did knock my ass out and give me nasty withdrawals for a month after I left the hospital. Before that though, c diff almost killed me.
Fluoroquinolones toxicity. Devastating and painful disease caused by a rare reaction to an antibiotic. Caused full-body Tendinopathy, tendon rupture, neuropathy, dysautonomia, chronic fatigue and about 20-30 other symptoms for me. 12 months so far.
C. difficile. Also chickenpox as an adult, never had it before and didn’t realize it can kill an adult without medication, you can’t just ride it out like you did when you were a kid lol, but the pain from the C Difficile was brutal as well
Related evidence elsewhere in the index
What the counts show
Across 26 source records, the most common observable tactic structure is “Attach it to an existing routine” (2 records). This is a wording pattern, not a measured outcome.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Observable tactic structures
Counts show source records whose wording matches the tactic structure; biological explanations remain commenter claims unless separately checked below.
Browse the original comments26 preserved records · 26 of 26 source records accounted for
Archive: 26 index entries preserve 26 distinct source records · Every displayed synthesis count resolves to source-record IDs
HerniasA small group, mostly concerned with the wait for the operation.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Hernias
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Hernias
Appears when: Hernias
What the pattern means: Six records, and the subject of most of them is the wait rather than the hernia. Writers describe living with it for months while queued for repair, and one ranks a hernia beginning to incarcerate above a gallbladder attack and pancreatitis he had also had.
What commenters described: Inguinal hernia, hurt like hell and had to wait a year for surgery
Limit: Six records is a thin base, and most state the condition without describing the sensation, so little can be read into the group. Nothing here identifies a hernia or indicates urgency.
Source-record spotlights
Double groin hernia
Gallbladder attack/pancreatitis was horrible, but I think my hernia that was starting to incarcerate may have been worse. The gallbladder was a long time ago though, so maybe the hernia is just fresher on my memory.
Incarcerated umbilical hernia. Thought I was gonna die
What the counts show
This report keeps all 6 source records for Hernias together and surfaces traceable examples without converting anecdotes into proof.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Browse the original comments6 preserved records · 6 of 6 source records accounted for
Archive: 6 index entries preserve 6 distinct source records · Every displayed synthesis count resolves to source-record IDs
The head, the face and the mouthPain inside the skull, and the teeth, ears and nerves that feed it. 361 records.
Cluster headachesDescribed through the specific things writers say they did to their own heads to make it stop.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Cluster headaches
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Cluster headaches
Appears when: Cluster headaches
What the pattern means: The most physically specific answers in the corpus. Writers do not reach for a scale; they describe what they did to their own heads — pressing into the eye socket hard enough to bruise, trying to open the skull, a mother restraining a twelve-year-old. The nickname commenters attach to the condition appears repeatedly and unprompted. The other recurring subject is the cycle: writers describe attacks arriving nightly, seasonally, or every few years, and orient their lives around the calendar rather than the attack.
What commenters described: Cluster headaches. It feels like someone is driving a railway spike through your head with a sledgehammer and no anaesthetic.
Limit: Records here name oxygen, injections, supplements and psychedelics as things writers tried; those are personal reports, not evidence that anything worked, and this page is not a route to any of them. Nothing here distinguishes a cluster headache from another headache.
What the replies added2
Oh man, I've only had one, but it was insane. I was 12, my mom had to restrain me because I tried stabbing myself in the temple with a pen, I was convinced I needed to open up my skull to relieve the pressure or I was gonna die. I thought that was the worst pain I could ever feel until I had a kidney stone last year that required emergency surgery. Somehow that topped the cluster headache, I seriously didn't think anything could be worse than that. I was so, so wrong.
The nickname "suicide headaches" is accurate. The only thing that helps me is intense pressure into my eye socket, which cannot be good. It often gives me black eyes.
Where commenters report limits
God that suuuucks! I have random migraines and cluster headaches too. Makes you want to ram your head into a wall. I also unfortunately get Ice Pick Headaches. I'll just be doing whatever and BAM! like someone put a nail gun straight to my brain. Then just like that gone. When it happens, I basically look like I'm stroking out because I make a face like I'm winking and screaming for my life but there's no sound. And then I have a panic attack because my biggest fear is an aneurysm.
cluster headaches, every year unfortunately.
Source-record spotlights
Cluster headaches. It feels like someone is driving a railway spike through your head with a sledgehammer and no anaesthetic.
Thankfully maybe 2-4 times a year but that was the only time it was that bad. 💜 I wouldn’t wish it on my worst enemy.
Cluster Headaches, COVID-19, Kicked In The Balls, GERD, Pleurisy Pains, Cavity With Exposed Nerve Endings, 2nd Degree Burns From Coil In Oven And Glue Gun, Ear Infection, Once Had A PlayStation Fall Onto My Head As A Baby And Sprayed Blood Everywhere Like A Saw Movie, Stubbing My Pinkie Toe, Dropping A Heavy Glass Lid Onto My Big Toe, And The Nail Turning Black/Purple, Migraine, UTI, And that's just a few of them.
What the counts show
The exact phrase “to relieve the pressure or” recurs across 2 of the 47 source records in Cluster headaches; the complete archive stays available below.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Browse the original comments47 preserved records · 47 of 47 source records accounted for
Archive: 47 index entries preserve 47 distinct source records · Every displayed synthesis count resolves to source-record IDs
Migraines and headaches that would not endMigraine answers, including the ones measured in weeks and months rather than hours.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Migraines and headaches that would not end
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Migraines and headaches that would not end
Appears when: Migraines and headaches that would not end
What the pattern means: The distinguishing claim in this group is duration, not intensity. Writers describe migraines measured in days, weeks, six months and, in one account, twenty years of near-daily attacks, and several say explicitly that they would take worse acute pain over pain that does not stop. The vestibular and ocular variants recur, described by what they take away — vision, balance, speech — rather than by how much they hurt. A persistent complaint is being told it is 'just a headache'.
What commenters described: Chronic intractable migraines. It's not the worst accute pain, it's that it goes on and on and on. And migraine isn't a headache, it's a neurological disorder, so there is other pain (e.g. nerve pain) plus multiple other symptoms. Currently considering getting 32-34 Botox injections in my head, despite the 50-70% likelihood of a reduction in symptoms. At this point, I'd have a microchip implanted in my brain if it was an available treatment option. I'd rather more severe acute pain than bad chronic pain because at least the acute pain ends.
Limit: Writers here use migraine for several different diagnoses and, in a few cases, for headaches that were never diagnosed at all. Medications named are what individual people were prescribed; nothing here is a treatment recommendation or a way to tell one headache from another.
What the replies added1
I still have no idea what happened, but I got the worst migraine I've ever had when I was 12. We were at an agricultural show of some kind (common where I live) and it kept getting worse, so I went to the truck to lay down. I don't really remember it because I was asleep and also in a lot of pain, but I remember at some point it felt like a bucket of lava had been dumped on my head and said lava was slowly cascading down my head and face and burning me. I also felt the same sensation in my hands and fingers, but I was more focused on my head. Fast forward to the next day, and I have blisters on my face. I looked like I'd broken out, but I hadn't hit puberty yet, and they were like the blister you get when you burn yourself. I also ended up shedding my fingernails from the cuticle upward. My nails separated from the nailbed at my cuticles and gradually lifted as the new nail grew in. It took about a month for my fingers to be back to normal, and I had to wear bandaids on my fingers pretty much constantly. Still the strangest thing that's ever happened to my body. Nearly 10 years later and I have no explanation.
Source-record spotlights
Vestibular migraines, truly debilitating.
Migraine pain in migraine with aura. After aura.
Oh, my god, I'm so sorry to hear that. I've applied for disability because of my constant migraines, and honestly, I would rather be able to work. But it's hard to predict when the headaches come. I feel for you; I'm so sorry you are going through this. My heart goes out to you. 💜
Related evidence elsewhere in the index
What the counts show
Across 77 source records, the most common observable tactic structure is “Attach it to an existing routine” (4 records). This is a wording pattern, not a measured outcome.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Observable tactic structures
Counts show source records whose wording matches the tactic structure; biological explanations remain commenter claims unless separately checked below.
Browse the original comments77 preserved records · 77 of 77 source records accounted for
Archive: 77 index entries preserve 77 distinct source records · Every displayed synthesis count resolves to source-record IDs
Trigeminal neuralgiaThe condition most often accompanied in this thread by the nickname commenters attach to it.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Trigeminal neuralgia
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Trigeminal neuralgia
Appears when: Trigeminal neuralgia
What the pattern means: A small group with unusually uniform language: electric shocks, a face hit with a bat, a breeze that feels like razor blades. Two things recur that do not recur elsewhere. The first is unpredictability — writers describe never knowing when a flare starts, and organising their lives around that rather than around the pain. The second is the nickname, which appears in a majority of these records and which several writers say they found validating rather than frightening.
What commenters described: I had that before and it was awful. The intensity and the fact that it just would not stop was insane. It felt like someone hit me in the face with a baseball bat and then set it on fire. The slightest breeze felt like razorblades.
Limit: Several of these records describe suicidal thinking; they are one person's account of their own condition and are not a statement about what the condition does to anyone else. Surgeries and drugs named here are individual reports, not options being recommended. If you are struggling, contact a local crisis line or emergency service.
What the replies added2
I had that before and it was awful. The intensity and the fact that it just would not stop was insane. It felt like someone hit me in the face with a baseball bat and then set it on fire. The slightest breeze felt like razorblades.
Me too. Pretty well medicated at present but one never knows when it will raise its ugly head and have you crying on the floor.
Where commenters report limits
Trigeminal Neuralgia - aka the suicide disease (others also share this name). It started with constant, heat and pressure pain over my right maxillary sinus. It felt like a large c-clamp was heated in a 500 degree oven, then tightened with one end on the outside of my cheek and the other on the roof of my mouth. I had multiple sinus surgeries. Root canals on every tooth on the right side of my head and most on the left. I was misdiagnosed with everything from a chronic bone infection in my skull, to chronic migraine. Then the electrical shocks started. That felt like a 10” chef’s knife was attached to a 240 volt live line and I was stabbed with it over, and over, and over again. Shocking episodes would last from 1 minute to 10 and I was having as many as 100 per day. I had to stop driving after I had several back to back episodes while driving on 495 - the beltway around DC. It was one of those days it was moving at 80 MPH, but bumper to bumper. I slammed on the brakes in the middle lane, let go of the steering wheel and screamed while my husband was freaking out from the semi locking his brakes up behind us. I eventually had brain surgery (MVD), which saved my life but unfortunately the surgery (and likely the years of misdiagnosis) led to CRPS (yay, two suicide diseases for me) and I picked up a chronic, hospital-acquired, multi-drug resistant infection that I still carry 8 years later and it has hospitalized me 23 times, having been septic six of those times. The surgery saved my life, but transformed it forever. In 21, my now ex husband told me he could no longer handle all my medical issues. In 22 I spent 87 days in patient and realized I could no longer work.
Source-record spotlights
Trigeminal neuralgia
Having a trigeminal neuralgia flare in the middle of getting an MRI for my MS. Head was in the cage and everything 😔
I have had trigeminal neuralgia, no remission for 19 years.
Related evidence elsewhere in the index
What the counts show
Across 49 source records, the most common observable tactic structure is “Attach it to an existing routine” (2 records). This is a wording pattern, not a measured outcome.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Observable tactic structures
Counts show source records whose wording matches the tactic structure; biological explanations remain commenter claims unless separately checked below.
Browse the original comments49 preserved records · 49 of 49 source records accounted for
Archive: 49 index entries preserve 49 distinct source records · Every displayed synthesis count resolves to source-record IDs
Ears and sinusesEar and sinus pain, and the eardrums that burst — usually followed in the same sentence by relief.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Ears and sinuses
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Ears and sinuses
Appears when: Ears and sinuses
What the pattern means: The only group in the corpus with a shared happy ending, and it is a disturbing one: writers describe pressure building to the point of screaming, the eardrum bursting, and immediate relief. Several describe the warmth of the discharge as soothing. Where the drum does not burst, the accounts are of sleeplessness and painkillers that did nothing; several writers who have had children rank an adult ear infection above the birth.
What commenters described: I had an ear infection on a flight from Austin to Denver. Shortly before landing in Denver my ear was pounding with pain so bad, it made me nauseous. Right when we landed my ear drum burst and I went from the worst pain I’ve ever experienced to soothing bliss. The pain was gone and the blood from the burst ear drum felt warm and soothing. I can’t describe the relief I experienced but it was so unexpected. 10/10 for worst pain ever. I would not wish this kind of pain on my worst enemies.
Limit: The relief these writers describe follows a perforation, and one commenter in the group points out what that means for the ear. Nothing here should be read as a reason to wait for one, and nothing here identifies an ear or sinus infection.
What the replies added2
Had kidney stones 5 children naturally Numerous broken bones Fibromyalgia Hip labrum tears Covid 3 times and NOTHING brought to me knees like an out of control ear infection. I was laying on the flooring bawling and could not raise my head off the floor due to pain. Husband called our physician (who we knew both personally and professionally) who heard me screaming and crying in the background and he ordered ATBs and pain medication sight unseen. God bless that man!
I had an ear infection that developed over months and got so bad my ear canal was too swollen for fluid to get out and the pressure eventually built up so much it ruptured my eustachian tube and broke the bone at the top of my jaw too. My jaw is still off centre to this day. The earache, broken jaw, ruptured tube combo was not an experience I’d ever recommend.
Where commenters report limits
Had this happen in my 30's. The pain was so intense I screamed for my mom at one point and right when I did that the eardrum burst and the relief was incredible. Unfortunately, the hole never healed (I'm in my 40's now) and need to have surgery to repair it.
Source-record spotlights
I had an ear infection on a flight from Austin to Denver. Shortly before landing in Denver my ear was pounding with pain so bad, it made me nauseous. Right when we landed my ear drum burst and I went from the worst pain I’ve ever experienced to soothing bliss. The pain was gone and the blood from the burst ear drum felt warm and soothing. I can’t describe the relief I experienced but it was so unexpected. 10/10 for worst pain ever. I would not wish this kind of pain on my worst enemies.
I had an ear drum rupture once because of an infection, lord the relief!
I had an ear infection that developed over months and got so bad my ear canal was too swollen for fluid to get out and the pressure eventually built up so much it ruptured my eustachian tube and broke the bone at the top of my jaw too. My jaw is still off centre to this day. The earache, broken jaw, ruptured tube combo was not an experience I’d ever recommend.
Related evidence elsewhere in the index
What the counts show
Across 55 source records, the most common observable tactic structure is “Attach it to an existing routine” (3 records). This is a wording pattern, not a measured outcome.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Observable tactic structures
Counts show source records whose wording matches the tactic structure; biological explanations remain commenter claims unless separately checked below.
Browse the original comments55 preserved records · 55 of 55 source records accounted for
Archive: 55 index entries preserve 55 distinct source records · Every displayed synthesis count resolves to source-record IDs
Teeth, jaws and mouthsThe answer people most often apologise for giving before they give it.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Teeth, jaws and mouths
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Teeth, jaws and mouths
Appears when: Teeth, jaws and mouths
What the pattern means: The answer people apologise for before giving it, and then describe in terms nothing else on this page uses: pain that reaches the brain, that makes vision unreliable, that cannot be escaped by any position or distraction. Two structural features recur. Painkillers are described as useless — writers list ibuprofen, paracetamol, codeine and tramadol failing in sequence. And delay is nearly always self-imposed: fear of the dentist, no money, no appointment, in accounts running from days to ten months.
What commenters described: A tooth infection that rocked my skull for 3 days. Never did I think pain could feel that bad. I've injured myself in so many dumb ways, but that kind of pain tore into my brain. Ibuprofen nor acetaminophen didn't touch the pain on their own or combined Eating hurt, breathing hurt, sleeping was impossible, getting work done was impossible since it affected my vision. Day 3 I finally got in to my dentist who confirmed what I already knew and gave me an antibiotic. In a last ditch effort I took 4 extra strength Tylenol and at that dose, it dulled the pain enough to let me fall asleep while the antibiotic kick in. About 6 hours after I took the antibiotic, the pain had subsided to a very manageable point. After three-ish days, chewing food didn't hurt with every bite. But yeah, that was probably the worst physical pain I've ever felt Though not an illness and not my pain, one of my best friends used to get period cramps so bad they put her out of work for the first two days. She would just lay on the floor or her bed and cry. I forget what the condition she had was called. She was 28 at the time and said that the pain like this started around the age of 19. She was not internet savvy, nor did she have money to see a doctor, so I spent hours digging online to try and find anything to help her and there was one specific brand of birth control that seemed like it could and after another year of the pain, she finally decided to give it a shot and according to her "it was like magic." The first month was more tolerable and it just dropped off after that. I think about that whenever I get a pain. Yeah, I might be in pain now, but at least it's not a recurring, near lifetime issue. That takes some real strength to deal with
Limit: Several records here describe taking more than the labelled dose of over-the-counter painkillers, and the thread's own replies dispute that; reported here, recommended nowhere. Nothing in this group identifies a dental infection or indicates how to treat one.
What the replies added3
Those are fucking horrible, I lived with a broken tooth for 2 years (NHS dentists were in shortage because Covid related violence had made a lot of Chinese dentists go back to China, and my area had lots of Chinese dentists)
My dentist thought I had a tooth infection and prescribed antibiotics and Tylenol 2 or whatever the Tylenol with codeine is. Told me to go the office after the antibiotics did their thing to have a root canal done. Turns out that Tylenol makes me puke violently. The utter amount of pain that radiated from my jaw all the way up to my brain behind my eye made me want to shoot myself. I couldn’t even think straight. It was feeling like a red hot dagger was shoved up under my jaw all the way to my brain. Absolutely the worst physical pain I have ever felt and I’ve broke 8 bones, torn ligaments, and numerous other stupid injuries. Turns out my tooth wasn’t infected. It was shattered below the gum line and my nerve was completely exposed. And that’s how I learned I grind and clench my teeth in my sleep!
Had a horribly infected wisdom tooth they wouldn't pull. Put me on antibiotics which didn't work. I went septic. I went in the Monday after Thanksgiving. It was pulled January 3rd. It was a month of no sleep agonizing pain and thoughts of suicide. It was when opioids were easier to get and I went through an astronomical amount, which barely touched the pain. And I'm not exaggerating I nearly killed myself the pain was so brutal. I've passed a kidney stone, popped a few discs in my lower back, had a contusion to my spinal cord, broken bones, and nothing was even half of that damn wisdom tooth.
Where commenters report limits
Had a horribly infected wisdom tooth they wouldn't pull. Put me on antibiotics which didn't work. I went septic. I went in the Monday after Thanksgiving. It was pulled January 3rd. It was a month of no sleep agonizing pain and thoughts of suicide. It was when opioids were easier to get and I went through an astronomical amount, which barely touched the pain. And I'm not exaggerating I nearly killed myself the pain was so brutal. I've passed a kidney stone, popped a few discs in my lower back, had a contusion to my spinal cord, broken bones, and nothing was even half of that damn wisdom tooth.
I have had 3 children where the epidural didn’t work but still the worst pain I ever had was when I was 11 weeks pregnant and got an abscess in my top back right tooth that also needed a root canal. The pain was like nothing I have experienced in my life. It was like pain in my jaw, cheek and brain. It’s hard to explain. I hope to never experience it ever again.
Source-record spotlights
In order: 1. Tooth abcess - when it was happening I was too afraid of the dentist to go. I let it go on for 8 months until the pain was so bad i was throwing up over it. Went in. Found an **amazing** dentist. My teeth are perfect now. 2. Idiopathic anaphylaxis - this one hurts in a way that is so much more than physical. I have no triggers - which means no way to stay safe. I have to constantly think about what my plan in if I start going into anaphylaxis. It means never traveling solo, because I may die.
Hard tie between dry socket that turned into a jawbone infection or the year of c diff that came after the antibiotics I had to take for the infection.
Dry socket was unbelievably painful. Inflamed bowel following a bad reaction to medication, than god for morphine.
Related evidence elsewhere in the index
What the counts show
Across 106 source records, the most common observable tactic structure is “Swap instead of subtract” (4 records). This is a wording pattern, not a measured outcome.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Observable tactic structures
Counts show source records whose wording matches the tactic structure; biological explanations remain commenter claims unless separately checked below.
Browse the original comments106 preserved records · 106 of 106 source records accounted for
Archive: 106 index entries preserve 106 distinct source records · Every displayed synthesis count resolves to source-record IDs
EyesCorneas, retinas and eye infections, from people who did not know an eye could hurt like that.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Eyes
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Eyes
Appears when: Eyes
What the pattern means: A small group whose writers share one reaction: surprise that an eye could produce pain on this scale. The specifics differ — a scratched cornea, an ulcer, an amoeba, iritis, a retina — but the descriptions converge on the impossibility of blinking, light as an active source of pain, and, in the chronic accounts, the relentlessness of something that recurs every morning on waking.
What commenters described: Dry eye disease. Imagine having a searing hot needle piercing your cornea, every day, for ten years. Or the feeling of a fresh papercut opening up on the surface of your eye, every ten seconds. That's dry eye disease.
Limit: Most of these conditions appear once or twice, so the group is a collection of individual cases rather than a pattern. Nothing here identifies an eye condition, and eye symptoms are not something this page can help anyone assess.
What the replies added1
I had corneal abrasions in both eyes at the same time. It is not something I ever want to experience again.
Where commenters report limits
Iritis. Attacked typically in the spring, with no warning and with no obvious known causes. That until I discovered that I do have the HLA-B27 marker, which explained everything. Luckily, I dont have those month-plus long episodes anymore that were so cripling.
Source-record spotlights
Ocular rosacea: imagine being not only allergic to sunlight, but basically getting sunburn on your eyes that takes weeks to recover from after only being out without protective sunglasses for like five minutes.
Reoccurring corneal abrasion. Your eyelid sticks to a scar on your eyeball and as you wake up and open your eye you rip open the wound. Your tears then feel like acid.
Acanthamoeba keratitis. There's a reason why that eye pain is rated worse than childbirth.
Related evidence elsewhere in the index
What the counts show
Across 27 source records, the most common observable tactic structure is “Change the sentence” (2 records). This is a wording pattern, not a measured outcome.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Observable tactic structures
Counts show source records whose wording matches the tactic structure; biological explanations remain commenter claims unless separately checked below.
Browse the original comments27 preserved records · 27 of 27 source records accounted for
Archive: 27 index entries preserve 27 distinct source records · Every displayed synthesis count resolves to source-record IDs
Nerves, the spine and the backThe thread's third-largest answer and the nerve conditions filed beside it. 486 records.
Shingles, and the nerve pain it leaves behindThe third-largest group, and the one whose writers most often bring up their age and the vaccine unprompted.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Shingles, and the nerve pain it leaves behind
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Shingles, and the nerve pain it leaves behind
Appears when: Shingles, and the nerve pain it leaves behind
What the pattern means: The third-largest group, and the one where the writers' age is part of almost every account: commenters in their twenties and thirties report being told they were too young, and several say that cost them the window for antiviral treatment. The pain is described as nerve pain rather than skin pain — burning, electrocution, a hand under the ribcage — and touch is the recurring trigger, with clothing, a bra strap, a seatbelt and moving air all named. The group's distinctive feature is what happens afterwards: writers describe postherpetic pain lasting months or years, and a specific dread of any twinge in the same place.
What commenters described: Came here to say this! Neuralgic pain from shingles feels like someone running you through with a red hot sword, then electrocuting you and kicking you in the back, all at the same time.
Limit: This group is a self-selected set of severe cases, and it contains its own counter-examples — several writers report mild episodes. Vaccination is raised constantly by commenters, both for and against, and none of that is verified or endorsed here; eligibility and advice are matters for a clinician, not a comment thread.
What replies pushed back on6
Shingles on my fucking face 😭 left scars too because I thought it was acne when it first popped up and put treatments on that made it way worse. Awful experience, just awful.
I describe my 33 year old shingles bout as if someone jammed an ice pick into my skull and then lit my head on fire. No sleep 72 hours straight, sheer pain, and a male doctor who didn’t believe me and did nothing for me. I have Adenomyosis, and issues with that monthly but jeebus the shingles pain was the worst non-relenting pain and ibuprofen/naproxen didn’t scratch the surface.
Nope. From experience: Kidney stones.
Shingles is pretty high on the list.. I also got to discover that the deeply painful sores can hurt BEFORE the rash shows up. I had what felt like a very deep tissue, large bruise for like a week before the first hint of a rash. There was nothing there so I kept assuming I was sitting wrong or somehow hurting it in my sleep or something. The first bits of rash showed up exactly where the pain was. Went to the urgent care and got anti-viral medication at the first suspicion of shingles and that painful shit still lasted a month. Was right where my bra sits too so it was constantly being irritated.
I had it when I was 4 and 46. I've nerve pain in both sites. Extremely painful. Tops broken bones, gallstones, endometriosis, strep throat, root canal. It is brutal.
I've had kidney infections and stones, had an embolism in my lung due to covid 19, gave birth, broke my pelvis, has stitches without anesthetic, had a burn that required a skin graft - shingles, hands down, is the worst thing I have ever experienced. I thought I was going to die and I was ready to if it ment the pain would stop.
Where commenters report limits
I describe my 33 year old shingles bout as if someone jammed an ice pick into my skull and then lit my head on fire. No sleep 72 hours straight, sheer pain, and a male doctor who didn’t believe me and did nothing for me. I have Adenomyosis, and issues with that monthly but jeebus the shingles pain was the worst non-relenting pain and ibuprofen/naproxen didn’t scratch the surface.
I was right on the cusp timewise my first infection. I'm 'too young' to have shingles, so the first 3 health professionals I spoke to about the pain (shooting out my ear), then rash (was told irritation due to heat/oils etc I was trying in my sore ear) dismissed any concerns. It was the headache that wouldn't quit. I saw the doctor, and before I'd even say down he told me it was shingles. The second time, I was in a foreign country. I woke up with a rash, and that pain - no advanced warning (though - I guess I had been favouring my face the week prior), and sought emergency treatment on day 1. This was when I asked for a treatment to keep on hand for if it happened again The third time, no blisters appeared, but that same zinger of pain plus prolonged headache. The headache stopped the second day of my antivirals, and I restocked my to have on hand supply. I have definitely thought about asking for an ongoing daily dose. I'd wondered if that would help. I'd rather try that than to increase my gabapentin and/or amitriptyline (I take both to combat the shingle tingle that's been left behind) again. I'll have to make sure I ask for some.
Source-record spotlights
I had a shingles lesion near my clit. I woke up one morning and it fucking hurt. I can’t even express how much it hurt and I’ve had kidney stones and given birth unmedicated. I went to the walk in clinic and I had shingles and a UTI. Happy 30th birthday to me.
Shingles made me pass out from the pain, but then I also had a tear in my sciatic nerve and when the nerve began to heal and the pathways reconnected to my spine I scream so loud for hours and hours it was agony and I sure passed out
Same on all accounts. It's like a million needles that are on fire being stabbed into your back. 🥴 I was in high school and I still recoil at the thought of it. Luckily I got the vaccine so hopefully I'm good now.
Related evidence elsewhere in the index
What the counts show
Across 244 source records, the most common observable tactic structure is “Attach it to an existing routine” (9 records). This is a wording pattern, not a measured outcome.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Observable tactic structures
Counts show source records whose wording matches the tactic structure; biological explanations remain commenter claims unless separately checked below.
Browse the original comments244 preserved records · 244 of 244 source records accounted for
Archive: 244 index entries preserve 244 distinct source records · Every displayed synthesis count resolves to source-record IDs
Sciatica, discs and the spineBack and nerve pain described mainly through the absence of any position that helped.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Sciatica, discs and the spine
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Sciatica, discs and the spine
Appears when: Sciatica, discs and the spine
What the pattern means: Defined less by intensity than by the absence of relief: writers repeatedly say there was no position, sitting, standing or lying, that helped, and several describe sleeplessness rather than pain as the thing that broke them. The comparisons are unusually specific — one commenter who has had both shingles and sciatica ranks them by whether he could finish a sentence on the telephone. Timescales are long: months, sometimes years, and several writers describe surgery as the point where it stopped.
What commenters described: Was shingles, until new record set by second onset of sciatica. Added: I just realized the scale after pondering this question. I could talk on the phone with shingles, barely, while I couldn't talk with sciatica, couldn't finish a sentence without groaning. Sciatica further onsets may be worse, I've learned.
Limit: Sciatica here covers several different underlying causes, and one commenter in the group warns that persistent sciatic pain can turn out to be something else entirely. That is one person's account of a relative's case, not a diagnostic rule, and nothing here indicates what any individual's back pain is.
What the replies added3
Herniated lumbar disc. Never felt such a severe, instantaneous pain. It’s the only pain I’ve had that made me nearly unable to walk. I actually had to use a walker on the first day it happened because I could barely weight bear. And I’ve had kidney stones, two unmedicated IUD insertions AND attempted expulsions via literal uterine contractions, a broken ankle, a concussion, a torn rotator cuff, torn meniscus, multiple ankle and wrist sprains, damn near chronic migraines for several years, a herniated thoracic disc, and all sorts of other random injuries throughout my life. Herniated lumbar disc fucked me up for weeks and still occasionally causes me issues but is mostly better now 🙏 it’s the only injury I’ve ever had that immediately immobilized me. Normally I can walk and talk through pain but not for that.
Back injury (L4/L5). I have had countless dislocations, I've broken bones, gotten 3rd degree burns, recovered from abdominal surgery and nothing has even been so defeating and painful as my back injury. I got better though :)
Back pain for me. I’ve had back pain since I was 16 but a few years ago it cranked up. Full seizing and locking up. It was 3 months or so before I had any relief. I was living on the couch because we didn’t have a bathroom upstairs and I couldn’t physically make it downstairs to pee if I had to. I remember crumpling in a ball at the top and bottom of the stairs crying in pain at 3am trying to get to the bathroom. Had relief for a month then it came back for another stint. Then it kicked up to 11 with sciatic pain and piriformis syndrome. Nerve pain was no joke. I was on opiates, nerve meds, and relaxants and nothing touched it. I couldn’t stand for more than 2 minutes without crumpling to the ground. I was using a cane at age 34. 4 months of some of the most intense pain between January and April before it finally let up. Total was about 9 months of some of the worst pain. Still going to physio years later because I don’t want to go through that again. It mentally broke me
Source-record spotlights
Was shingles, until new record set by second onset of sciatica. Added: I just realized the scale after pondering this question. I could talk on the phone with shingles, barely, while I couldn't talk with sciatica, couldn't finish a sentence without groaning. Sciatica further onsets may be worse, I've learned.
Back injury with a screw left on a nerve during surgery has been worse than endometriosis for me.
Hi, thanks for the information, I appreciate it. It has definitely been longer than 6 weeks - currently going on 4.5 months but I have had an MRI done and two disc bulges is the cause of this. Pain has definitely gotten better but it's very up and down and my main issue is sitting as of now.
Related evidence elsewhere in the index
What the counts show
Across 129 source records, the most common observable tactic structure is “Attach it to an existing routine” (8 records). This is a wording pattern, not a measured outcome.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Observable tactic structures
Counts show source records whose wording matches the tactic structure; biological explanations remain commenter claims unless separately checked below.
Browse the original comments129 preserved records · 129 of 129 source records accounted for
Archive: 129 index entries preserve 129 distinct source records · Every displayed synthesis count resolves to source-record IDs
Complex regional pain syndromeA small group whose members describe the condition as permanent rather than as an episode.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Complex regional pain syndrome
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Complex regional pain syndrome
Appears when: Complex regional pain syndrome
What the pattern means: The distinguishing claim in this small group is permanence. Writers explicitly separate their condition from the acute answers around it — a kidney stone ends, this does not — and several describe it starting from an unremarkable injury years earlier. The recurring detail is that the affected limb cannot be touched at all. Several writers use the condition's nickname and one adds a statistic to it.
What commenters described: Complex regional pain syndrome It really Fing sucks. There is a reason it’s nicknamed the $ucide syndrome. I’ve had kidney stones and gallstones, both are horrible please let me pass out pain but it ends. CRPS never ends 😖
Limit: The figure one commenter attaches to the condition's nickname is that commenter's own assertion and is not checked or endorsed here. These records describe suicidal thinking; they are personal accounts, not a statement about what the condition does to anyone else. If you are struggling, contact a local crisis line or emergency service.
What the replies added4
My husband had this. And other painful conditions so all together it was just about unbearable able for him. I swear the painful conditions are the reason he died at 65 of a massive heart attack. The stress it puts in you body will take years off your life. His “pain management” doctor did nothing to help him all.
My best friend has this. She broke her foot 8 years ago and still uses a knee scooter to get around. Her entire foot is black now and she can’t have anything touch it. She’s so positive about everything, but I know it must be hard. We need to bring more awareness to this condition as it’s definitely becoming more common (at least from what I’ve noticed).
Complex Regional Pain Syndrome AKA Suicide Diease (because something like 80% of those diagnosed kill themselves after 11 years. I imagine they hit the 10 year anniversary of the injury and cant go on. I'm on year 8 and I fucking get it.) OR Emdometriosis Trigeminal neuralgia Back spasm following a spinal tap Cluster head aches Migraines Broken teeth (from clenching through the pain. )
Chronic regional pain syndrome crps from 11-17. Ruined my life and because of it happening at such a vital developmental age I have trouble fitting in as an adult now despite having a decade of counseling sessions
Where commenters report limits
My husband had this. And other painful conditions so all together it was just about unbearable able for him. I swear the painful conditions are the reason he died at 65 of a massive heart attack. The stress it puts in you body will take years off your life. His “pain management” doctor did nothing to help him all.
Source-record spotlights
Complex regional pain syndrome It really Fing sucks. There is a reason it’s nicknamed the $ucide syndrome. I’ve had kidney stones and gallstones, both are horrible please let me pass out pain but it ends. CRPS never ends 😖
Complex regional pain syndrome is definitely up there or when there was CSF leak and I had to lay completely flat as possible until they could fix it. That headache man. A couple open fractures. waking up from my hip replacement. Dude I cannot pick one.
Ladies and gentlemen, read in depth about CRPS. I’ve had it for 12 years. Most days you don’t want to live. Other than that, I’m hanging in there with various meds.
Related evidence elsewhere in the index
What the counts show
The exact phrase “the suicide disease” recurs across 2 of the 25 source records in Complex regional pain syndrome; the complete archive stays available below.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Browse the original comments25 preserved records · 25 of 25 source records accounted for
Archive: 25 index entries preserve 25 distinct source records · Every displayed synthesis count resolves to source-record IDs
Pinched nerves and neuropathyNerve pain without a disc or a diagnosis named alongside it.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Pinched nerves and neuropathy
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Pinched nerves and neuropathy
Appears when: Pinched nerves and neuropathy
What the pattern means: Nerve pain without a disc, a diagnosis or an event attached to it. The descriptions are electrical and positional — no posture helps, movement is what triggers it — and several writers report losing the use of an arm or a leg alongside the pain. What separates this group from the spine group is that its members often cannot say where it came from: an old workout injury, a night's sleep, nothing at all.
What commenters described: I am currently dealing with a pinched nerve between cervical and thoracic spine and it is absolutely the worst agony I have ever experienced. There is literally no position I can be in that offers any relief. After a month it’s just starting to ease… right in time for the epidural steroid injection. Not recommended.
Limit: These records collect several different nerve conditions whose only common feature is how their writers describe them. Nothing here identifies a pinched nerve or neuropathy, or indicates what should be done about one.
What the replies added2
Not sure if this technically counts as an illness, but *really badly* pinching a nerve in my neck. It started as some pain down my side to my kidney, and down my arm. Then it got worse, and worse, and worse, and worse until I had to wake up my wife and tell her I needed to go to the ER. Once there the doctor, he looks at my x-rays and goes "Oh yeah, yeah, I know this one. Yeah, lets get you some *really* good pain meds". I've cut my finger off, been hit by a car, broken my foot, split open my head, had tooth infections, ear infections, I once infected my knee so badly I couldn't stand, had sciatica, damaged by hamstrings, damaged my rotator cuff, nothing was like this. This was literally the pain center of my nervous system going "3 ALARM FIRE". Fortunately it started getting better that day, and was all better within a week.
1: pudendal neuralgia flare while also having a severe untreated UTI At the same time 2: pudendal neuralgia flare (nerve pain in layman’s terms but that is oversimplifying the condition) 3: dry socket while also having severe infection after tooth extraction These are in order of severity, I am unfortunately a woman and I only say that because of the gaslighting i received over 1 and 2 as it’s a rare enough condition and I overheard a nurse accuse me of drug seeing behaviour and being overly dramatic. The man beside me who broke his finger (this is a less painful thing I have also experienced) was given morphine while I was told to stop crying and given ineffective paracetamol lV. Sigh. I have great doctors and stable treatment and pain relief now which I’m so grateful for. We women really go through a lot when it comes to being listened to and believed with healthcare. I have faced so much contempt.
Where commenters report limits
Not sure if this technically counts as an illness, but *really badly* pinching a nerve in my neck. It started as some pain down my side to my kidney, and down my arm. Then it got worse, and worse, and worse, and worse until I had to wake up my wife and tell her I needed to go to the ER. Once there the doctor, he looks at my x-rays and goes "Oh yeah, yeah, I know this one. Yeah, lets get you some *really* good pain meds". I've cut my finger off, been hit by a car, broken my foot, split open my head, had tooth infections, ear infections, I once infected my knee so badly I couldn't stand, had sciatica, damaged by hamstrings, damaged my rotator cuff, nothing was like this. This was literally the pain center of my nervous system going "3 ALARM FIRE". Fortunately it started getting better that day, and was all better within a week.
1: pudendal neuralgia flare while also having a severe untreated UTI At the same time 2: pudendal neuralgia flare (nerve pain in layman’s terms but that is oversimplifying the condition) 3: dry socket while also having severe infection after tooth extraction These are in order of severity, I am unfortunately a woman and I only say that because of the gaslighting i received over 1 and 2 as it’s a rare enough condition and I overheard a nurse accuse me of drug seeing behaviour and being overly dramatic. The man beside me who broke his finger (this is a less painful thing I have also experienced) was given morphine while I was told to stop crying and given ineffective paracetamol lV. Sigh. I have great doctors and stable treatment and pain relief now which I’m so grateful for. We women really go through a lot when it comes to being listened to and believed with healthcare. I have faced so much contempt.
Source-record spotlights
Erythromelalgia. During a flare up it feels like the affected body part is on fire. A newspaper reporter dubbed it "Man on Fire Syndrome ". Imagine the pain of walking barefoot across a hot pool deck but affecting more than just the soles of your feet and you start to fet the idea. I have flare ups every day.
Thoracic outlet syndrome
Pinched nerve in my neck which caused me to lose function of my arm. Hurt every single day, every second. It felt like someone was trying to rip my nerves out of the back of my neck, pulling on them as hard as they could.
Related evidence elsewhere in the index
What the counts show
Across 26 source records, the most common observable tactic structure is “Attach it to an existing routine” (3 records). This is a wording pattern, not a measured outcome.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Observable tactic structures
Counts show source records whose wording matches the tactic structure; biological explanations remain commenter claims unless separately checked below.
Browse the original comments26 preserved records · 26 of 26 source records accounted for
Archive: 26 index entries preserve 26 distinct source records · Every displayed synthesis count resolves to source-record IDs
Epilepsy, MS, strokes and palsiesNeurological conditions offered as the most painful thing the writer has had.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Epilepsy, MS, strokes and palsies
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Epilepsy, MS, strokes and palsies
Appears when: Epilepsy, MS, strokes and palsies
What the pattern means: Neurological conditions offered as the most painful thing the writer has had, and the group where the answer is least often about a sensation. Writers describe what the condition removed — driving, working, memory, the ability to bathe their own child — and several say the psychological component outweighed the physical one. Where pain is described it is usually pressure inside the skull or the aftermath of a seizure rather than the condition itself.
What commenters described: Idiopathic intracranial hypertension - aka "we don't know why inside your skull there's too much pressure" Imagine the worst headache you've ever had, only it never goes away (*...and you have constant tinnitus, dizziness and sometimes nausea, but the doctor thinks it's just stress / tension, but then your vision starts getting distorted like there's wavy lines where there should be straight lines so you go to see the eye doctor and suddenly everything is a lot more serious and it's not "just stress" and you have to have an MRI scan and a lumbar puncture and luckily there's no brain tumour, but instead of your opening pressure on your spinal fluid being around 18 it's 43, and there's no cure*)
Limit: This group holds a wide range of unrelated diagnoses whose writers reached for the same framing, so it describes a way of answering rather than a family of illnesses. Nothing here identifies any of them.
What the replies added3
Eithet broken neck or stroke. But o recovered from both
Cerebellar ectopia. The base of my brain has slipped into the hole at the bottom of my skull. It tends to not cause too many issues, however, I can get headaches out of the blue that feels like my brain is going to burst like a balloon. I've even passed out from the pain. Kidney stones, and the recovery after operation is a close second. I was in so much pain the morphine I was given didn't work in the slightest, the nurse kept coming into my room stroking my hand, trying to comfort me. I felt like an old man, having a nurse ten years my junior being so concerned for me
I have intracranial hypertension, occipital neuralgia, trigeminal neuralgia, and have had low CSF headaches. I also have lichens schlerosis, and persistent genital arousal syndrome. And graves disease. And I've had upper pallet expansion surgery. I've have a tooth pushed into an nerve, and a ruptured ovarian cyst. A gallstone. And an IUD implanted and removed. My dad died. My DOG died. Broken bones. Glass shattered into my hand. Idk. Stuff.
Where commenters report limits
Cerebellar ectopia. The base of my brain has slipped into the hole at the bottom of my skull. It tends to not cause too many issues, however, I can get headaches out of the blue that feels like my brain is going to burst like a balloon. I've even passed out from the pain. Kidney stones, and the recovery after operation is a close second. I was in so much pain the morphine I was given didn't work in the slightest, the nurse kept coming into my room stroking my hand, trying to comfort me. I felt like an old man, having a nurse ten years my junior being so concerned for me
Source-record spotlights
post concussion syndrome
Guillain-Barré syndrome
PPPD and nervous system dysfunction/ FND (not painful, but very much symptomatic and emotionally painful)
Related evidence elsewhere in the index
What the counts show
Across 62 source records, the most common observable tactic structure is “Change the sentence” (4 records). This is a wording pattern, not a measured outcome.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Observable tactic structures
Counts show source records whose wording matches the tactic structure; biological explanations remain commenter claims unless separately checked below.
Browse the original comments62 preserved records · 62 of 62 source records accounted for
Archive: 62 index entries preserve 62 distinct source records · Every displayed synthesis count resolves to source-record IDs
The reproductive and urinary tractThe answers that come round on a cycle, and the ones that arrive once and put somebody in an ambulance. 509 records.
Endometriosis and adenomyosisThe largest answer from the reproductive tract, and one of the most repeated in the whole thread.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Endometriosis and adenomyosis
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Endometriosis and adenomyosis
Appears when: Endometriosis and adenomyosis
What the pattern means: The largest answer from the reproductive tract and one of the most consistent in the corpus. Three things recur in nearly every account. The first is that the pain recalibrated the writer's whole scale — commenters describe rating a kidney stone or sepsis lower afterwards, and one says her personal scale now runs to twelve. The second is the delay: writers repeatedly report years, and in several cases two decades, between the first episode and a diagnosis. The third is what happens after surgery, which splits — some describe learning to live without pain for the first time, others say the hysterectomy did not fix it.
What commenters described: THIS! My personal pain scale used to be 1-10 like everyone else, but now goes 1-12 because 10 just wasnt enough to express the true, consuming agony of endo cramps and hemorrhaging.
Limit: The outcomes described after surgery contradict each other inside this group, and several writers say explicitly that a hysterectomy did not help them; treat neither outcome as the expected one. Nothing here identifies endometriosis or indicates what any individual should do about pelvic pain.
What replies pushed back on5
Came here to say the same! Specifically endo when I had an IUD. Made my symptoms way worse.
I had mid-stage labor level contractions because of my endo. It happened during a road trip and my ex and I had to pull over and she helped me the rest of the night in a motel room like the classic spouse in the hospital room (bringing me ice and pain meds, rubbing my back, all sorts). We looked up labor positions and I figured out which ones helped the pain the most. For whatever reason squatting while hanging onto the back of a chair was the best. I was sobbing and screaming in the car and realized how bad (unmedicated) birth must be because imagine it gets even worse than that and you're actually giving birth to a baby and dealing with everything else on top of the pain alone. (Plus I downed homemade weed butter straight out of a ramekin for the pain and got high out of my mind, which you definitely can't do during birth.) The next day (and for several days after) I could feel soreness deep inside of my body, like I swear I could feel my uterus/surrounding muscles being super sore like a leg or arm muscle after a workout. Fully get why the human brain makes people forget how bad it is.
Yep, Stage 4 endo here. I’ve broken bones, had appendicitis that would have ruptured if I hadn’t gotten to ER when I did, and have had horrific gallbladder attacks. Endo is the worst of it all, especially when my endo caused ovarian torsion. :D I had surgery for it and lost an ovary and my fertility—one ovary crushed by the grapefruit sized cyst, the other so damaged by the adhesions that it’s useless except for hormones. And everyone always talks about the sheer AGONY of it, but there’s so many other batshit symptoms that go with it—my chronic UTIs were cured by surgery. For the months leading up to my surgery, I also had horrific constipation because the endo was all around my bowels and adhering my rectum to my uterus. Instantly cured after surgery. Not to mention the chronic fatigue, the horrific anxiety and depression and having to pee all the time. I’m not cured, it does grow back, but it’s like night and fucking day. It was surreal learning how to live without pain.
100% this At one point I couldn't walk. I now have monthly injections which have put me in the menopause aged 37 and on the waiting list for a hysterectomy. I wouldn't be going through all of that if it wasn't awful. I've given birth twice, I've broken bones, I've slipped a disc. Endometriosis beats it all.
I’m so glad the IUD helped! I have stage IV and the IUD made it worse 😂🙄 can’t win
Where commenters report limits
I’m so glad the IUD helped! I have stage IV and the IUD made it worse 😂🙄 can’t win
This. Unfortunately, my endometriosis is in my diaphragm so it mimics gallbladder attacks. I only know this because after the first real one I had that sombitch removed, three years later during a flare up another "attack" hit. The og attack had me projectile vomiting so hard I wet myself and ended up in tears writhing on the floor. Sis thought I was dying, so did I.
Source-record spotlights
Yes! I had endo and adeno and after my hysterectomy it literally took me months to get used to living without pain because I had been dealing with it so long I didn’t know what it felt like to be pain free.
This. Unfortunately, my endometriosis is in my diaphragm so it mimics gallbladder attacks. I only know this because after the first real one I had that sombitch removed, three years later during a flare up another "attack" hit. The og attack had me projectile vomiting so hard I wet myself and ended up in tears writhing on the floor. Sis thought I was dying, so did I.
Adenomyosis. Did you know sometimes your uterus can just decide to not stop bleeding for months?
Related evidence elsewhere in the index
What the counts show
Across 154 source records, the most common observable tactic structure is “Attach it to an existing routine” (8 records). This is a wording pattern, not a measured outcome.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Observable tactic structures
Counts show source records whose wording matches the tactic structure; biological explanations remain commenter claims unless separately checked below.
Browse the original comments154 preserved records · 154 of 154 source records accounted for
Archive: 154 index entries preserve 154 distinct source records · Every displayed synthesis count resolves to source-record IDs
Ovarian cysts, torsion and fibroidsCysts that burst and ovaries that twisted, several of them initially treated as a suspected appendix.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Ovarian cysts, torsion and fibroids
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Ovarian cysts, torsion and fibroids
Appears when: Ovarian cysts, torsion and fibroids
What the pattern means: Almost every account here is sudden. Writers describe collapsing where they stood, vision going black, and being unable to make a sound — and a striking number describe being assessed for appendicitis first, because that is what it looked like. The torsion accounts are the most severe and the most time-critical: several end with the ovary lost. Two recurring details are unexpected: pain referred to the collarbone from internal bleeding, and the number of writers who were sent home to rest.
What commenters described: Oh my god I wouldn’t wish a ruptured ovarian cyst on my worst enemy. 10/10 pain. I was walking home at night when it happened to me and had to fight my body into staying conscious. My vision completely blacked out, it was like my brain went “yeah we don’t need to see right now, just go to sleep”. I had to find my way home completely blind. The second I got through the front door I collapsed and screamed bloody murder. My parents called an ambulance and I was admitted to the ER immediately because they suspected appendicitis. Thankfully didn’t need surgery but I was hospitalized for 3 days. I started high school a week after I got out and still felt so sore. At least I got a pretty early PCOS diagnosis.
Limit: Ruptures, torsions and fibroids are grouped together here because their writers describe them together; they are not the same event. Nothing in these records distinguishes one from appendicitis or from each other.
What the replies added3
I had a cyst the broke and led to inner bleeding (not the correct translation but you get the point). Gallbladder attack was a walk in the park in comparison to that day. 😳
Cyste wrapped around my ovary. Happened 8/10 times over a few years, extremely painfill. Eventually the cyst exploded or something and I have never been in so much pain. Thank god a neighbour heard me screaming, broke into the house and called an ambulance 🙏
I’ve had all the things: gall stones, kidney stones, shingles outbreaks, tuberculosis, pneumonia, pleurisy, bone spurs in both hips, spina bifida, etc. etc. The most painful thing I’ve ever experienced is a torsed ovary. I had a very large (9lb) ovarian tumor that surrounded my left ovary and then, while I was playing with my dog, it twisted (torsed). I’ve never in my life felt pain like that. I couldn’t stand up straight and I couldn’t stop vomiting. I was on daily doses of vicodin at the time and they gave me another dose at the hospital. It did nothing. It was after the ER doc took films and brought in a Dilaudid pain pump that I started to think maybe it wasn’t food poisoning. Worst. Pain. Ever.
Where commenters report limits
Usually it’s from a cyst on your ovary causing it to become lopsided and twist. It is the worst pain I have experienced by far. My entire abdominal wall involuntarily seized up and was rock hard. I threw up from how much it hurt. Unfortunately my mom didn’t believe me and kept me at home for like 13 hours before taking me to the hospital (was a minor at the time). Ended up losing that ovary.
it's a tie between a burst ovarian cyst and a lipschültz ulcer (these can be pretty brutal to look at, also genital warning for if you look up pics)
Source-record spotlights
An ovarian cyst. My mom thought it was appendicitis and took me to the ER and they sent me home with no pain killers and told me to bed rest. Flat on my back for 3 days.
Ruptured ovarian cyst
Ovarian "torsion". That's in inverted commas because I actually pulled my own ovary off through a combination of an inability to fold collagen properly (EDS), an already attached blood supply, a blood-filled cyst, an abdominal adhesion, and getting up awkwardly from wrapping Xmas presents.
Related evidence elsewhere in the index
What the counts show
Across 105 source records, the most common observable tactic structure is “Attach it to an existing routine” (4 records). This is a wording pattern, not a measured outcome.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Observable tactic structures
Counts show source records whose wording matches the tactic structure; biological explanations remain commenter claims unless separately checked below.
Browse the original comments105 preserved records · 105 of 105 source records accounted for
Archive: 105 index entries preserve 105 distinct source records · Every displayed synthesis count resolves to source-record IDs
Periods, cramps and PMDDPeriod pain nominated on its own, with no diagnosis attached to it.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Periods, cramps and PMDD
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Periods, cramps and PMDD
Appears when: Periods, cramps and PMDD
What the pattern means: Period pain nominated on its own, with no diagnosis attached — and the group where the thread most visibly argues with itself. Writers describe passing out, vomiting and losing days every month; replies underneath insist that this is not normal and press for investigation, while other writers say they assumed for years that everyone felt this. Hormonal treatment is the most common turning point named, and PMDD records describe losing half of every month rather than a peak of pain.
What commenters described: Period cramps that were so bad, they made me unconscious.
Limit: By definition these writers have no diagnosis, so the group cannot say what any of them actually had — several replies inside it suspect endometriosis or adenomyosis. Contraceptives and devices named here are individual reports, not recommendations, and nothing here tells anyone whether their own period pain is normal.
What replies pushed back on2
I’m so glad the IUD helped! I have stage IV and the IUD made it worse 😂🙄 can’t win
Yep. Took me forever to realize what it actually was. Any "remedy" I try either doesn't work at all, or will work for a while before the symptoms creep back in. Getting an IUD has been the longest source of relief so far, but symptoms still came back after about a year.
Where commenters report limits
Yep. Took me forever to realize what it actually was. Any "remedy" I try either doesn't work at all, or will work for a while before the symptoms creep back in. Getting an IUD has been the longest source of relief so far, but symptoms still came back after about a year.
Cramps. Rarely It’s all consuming, withering in pain kind, delirious but apparently not enough to pass out, unfortunately. I beg my mom to hit me in the head with a baseball bat to knock me out to no avail. Gotta suffer while I wait for the two types of extra strength pain meds to kick in. This or extremely sharp gut pains from lactose intolerance- always happens like a day later after I eat dairy. So strange.
Source-record spotlights
Period cramps that were so bad, they made me unconscious.
PMDD - not fun wanting to unalive yourself every month.
It's a tie between horrible periods (I have fibroids, have had two surgeries already), migraines, and long covid. Long Covid made me "allergic" to heat, the sun, movement, etc. it was truly torture until I found meds that help.
What the counts show
The exact phrase “period cramps that” recurs across 2 of the 25 source records in Periods, cramps and PMDD; the complete archive stays available below.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Browse the original comments25 preserved records · 25 of 25 source records accounted for
Archive: 25 index entries preserve 25 distinct source records · Every displayed synthesis count resolves to source-record IDs
Childbirth, caesareans and what came afterGiven as an answer by writers who mostly note in the same breath that it is not an illness.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Childbirth, caesareans and what came after
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Childbirth, caesareans and what came after
Appears when: Childbirth, caesareans and what came after
What the pattern means: Given as an answer by writers who mostly note in the same breath that it is not an illness, and the reference point the rest of the thread keeps reaching for. The accounts themselves are less about the peak than about the conditions: a failed epidural, an induction, hours without food, a cord prolapse. The group also holds what came afterwards — mastitis, described with unusual specificity, blood clots, HELLP syndrome and infected incisions — and several writers rank those above the birth.
What commenters described: These women are brave. I did it, got to eight cm before I was begging for the epidural. It fucking *hurts* Like "yes please shove a needle into my spine if it'll stop this agony" hurts. And I didn't have a hard birth. Thought I had a high pain tolerance, can sit and be tattooed for hours, lived with endo my whole adult life, hockey goalkeeper who happily gets brutalized every week... But no. Childbirth humbled the fuck out of me. Gimme all the drugs.
Limit: Roughly a third of this group is about complications rather than labour, so it is not a description of childbirth in general. Procedures and remedies described here are what individual people say was done or advised in their case, and nothing here is antenatal guidance.
What the replies added3
Eating watermelon? They allowed you to eat? That’s honestly mindblowing 🤯. For my labor/delivery… I checked into the hospital for my routine normal run-of-the-mill induction on a Monday morning at 6am. I was immediately listed as NPO except for water and that restriction was held from the moment I got there, checked in, and was given the first pill of misoprostol in my cheek until I had the baby 42 hours later 😭. Apparently it’s so that if anything goes wrong and you need a c-section or emergency surgery where you’ll have to be under anesthesia, you won’t aspirate from having food in your stomach when they intubate you. But my labor was totally normal and low-risk so I was at the lowest possible risk of needing any type of c-section or interventional care (I’d had two previous totally normal pregnancies and labor/deliveries and this pregnancy had been entirely normal and boring as well lol). Around hour 38, shit was getting really really real and I still hadn’t gotten my epidural yet and I’d been having regular contractions on and off (depending on how high they had the pitocin flow- genuinely FUCK pitocin and the unnaturally horrific contractions it causes 😭) but I hadn’t eaten in 50hrs by that point. I had been told I couldn’t eat anything starting 12hrs before my check in time… so I checked in at 6am on Monday morning and had had to stop eating or drinking anything but water at 6pm the night before… so by the time I was 38hrs into my labor and things were getting really bad, it had been 50hrs since I’d eaten ANYTHING 😩. I was so drained. I hadn’t slept since we (my husband and I) woke up Monday morning… so I’d been awake for 38hrs straight, was in immense pain from hours and hours and hours of those evil pitocin contractions, hadn’t been allowed to eat the entire time, and was legitimately feeling so weak and tapped out. I was so exhausted, drained, pretty much useless physically. And I still had to do the hardest part of the whole process (which didn’t happen for another 4 hours) with my gas tank on E… running on literal fumes 😩. It was 8pm on a Tuesday night and things were pretty quiet outside of the room. By that point I was so exhausted, cranky, and honestly just completely and utterly fed up. And the reason wasn’t even really because of the pain or the miserable labor process in general- it was mostly because of the fact that I was just absolutely RAVENOUS, and had been throughout the entire 38hrs that I’d been in labor so far. I was so damn hungry and weak that I essentially broke, and begged my husband to find me some food. Literally ANY food. I would have eaten a half eaten cheeseburger out of the garbage at that point- I’m so serious too 😅. He snuck out to the sandwich cart and stole me 4 grape uncrustables and two apple juices because that’s all that was left on the cart. When he came back in to the room and pulled the loot out of his pockets I legit ugly cried from happiness and relief lol. Then I wolfed all four uncrustables down in like 2 minutes flat, washed them down with both apple juices, and within about 30 minutes I felt WORLDS better. Like… that food- albeit not the healthiest meal in the world- was probably the most instrumental thing in getting me through to the end, aside from the epidural I eventually finally got. That gave me the energy I needed to finally push our son into this world four more hours later. I understand I technically took a “risk”, but tbh… for low risk pregnancies, we should be allowed to fucking eat at least a little bit. Literally STARVING a woman in labor for DAYS is straight up cruelty and it makes the incredibly physically grueling process her body is going through a zillion times harder on her than it needs to be. Honest question- was your care team actually okay with you eating the watermelon/eating in general, or did you have to sneak it behind their backs? If they were cool with it- how did you manage to get them on board with you not having the NPO restriction? Regardless, I’m happy you were able to nourish your body during your labor/delivery. ♥️
Mastitis. Infection of the milk duct. The fever is intense. I hit 41⁰c. Your legs cramp so bad you can hardly walk. The pain starts at your lower back, goes down your thighs then hits your calves. The headache is even worse. Then there's the breast. You can literally see a bright red triangle. Feed the baby from that side first, they tell you. Every time. The agony is indescribeable. Like its mouth is made of broken glass. And if you don't work the clots out, it doesn't heal. How do you work the clots out? You get in the shower. Get a hair comb. Run the comb through a bar of soap. And comb your literal flesh, from chest to nipple. Five times a day. The hottest water you can manage to help the milk flow. I got mastitis four times total
My personal rating of pain: 1#- birth of my first child--- 26 hours of labour until I caved and had an epidural. 2#- a gout attack in my wrist. Holy smokes! Huge gap in pain here 3#- unmedicated labour and birth of my second kiddo 4#- Gallbladder attack 5#- migraine 6#- broken ankle
Where commenters report limits
Migraines, before I got pregnant. After that, it was the sudden onset of HELLP syndrome. 8 hours of debilitating mid-section pain, never going away only getting worse. Everything between ribs and hips, excluding the uterus thankfully, felt as if it was packed with stones. I couldn't take a single deep breath in order to get some sort of "muscle reset", some sort of break. Nothing. Too many doses of morphine with little to no effect. Hooked on blood pressure medication. People say they dislike the magnesium you get, but to me it was such a nice muscle relief for 5 minutes, albeit did nothing for the pain. Couldn't stay still, couldn't move, couldn't find a single position that felt ok. Didn't even mind getting the catheter. All good at the morning tests, ready to be discharged, then liver failure by lunch. But yeah, let's instead fund more "studies" to find out if women with endometriosis are more attractive or not 🙃.
Source-record spotlights
These women are brave. I did it, got to eight cm before I was begging for the epidural. It fucking *hurts* Like "yes please shove a needle into my spine if it'll stop this agony" hurts. And I didn't have a hard birth. Thought I had a high pain tolerance, can sit and be tattooed for hours, lived with endo my whole adult life, hockey goalkeeper who happily gets brutalized every week... But no. Childbirth humbled the fuck out of me. Gimme all the drugs.
Children. And birthing those children.
Pregnancy - besides the childbirth there was gas pains, round ligament pain, constant heartburn, back pain, nausea, etc.
Related evidence elsewhere in the index
What the counts show
Across 48 source records, the most common observable tactic structure is “Attach it to an existing routine” (6 records). This is a wording pattern, not a measured outcome.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Observable tactic structures
Counts show source records whose wording matches the tactic structure; biological explanations remain commenter claims unless separately checked below.
Browse the original comments48 preserved records · 48 of 48 source records accounted for
Archive: 48 index entries preserve 48 distinct source records · Every displayed synthesis count resolves to source-record IDs
Miscarriage, ectopic pregnancy and abortionAnswers about pregnancy loss, several describing internal bleeding the writer did not recognise at the time.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Miscarriage, ectopic pregnancy and abortion
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Miscarriage, ectopic pregnancy and abortion
Appears when: Miscarriage, ectopic pregnancy and abortion
What the pattern means: Short, consistent and frightening. The ectopic accounts share a structure: the pain does not present where the writer expects it, several describe shoulder pain as the symptom that sent them in, and the phrase that recurs is nearly bleeding to death without knowing it. Several writers say they almost did not go to hospital because the pain eased.
What commenters described: Ruptured tube / ectopic pregnancy. No stomach pain , only went to hospital because I had this horrendous pain in my shoulder. Every breath felt like a struggle that resulted in me being stabbed in the shoulder. Never experienced anything like it and hope to never again.
Limit: This is a small group describing emergencies, written by the people who survived them, so it is not a picture of how such pregnancies usually present. Nothing here identifies an ectopic pregnancy or a miscarriage.
What the replies added2
In-clinic Abortion. Never again.
Ruptured tube / ectopic pregnancy. No stomach pain , only went to hospital because I had this horrendous pain in my shoulder. Every breath felt like a struggle that resulted in me being stabbed in the shoulder. Never experienced anything like it and hope to never again.
Source-record spotlights
Not illness but ectopic pregnancy, almost died on my 21st birthday
miscarriage oh my gosh. type 1 diabetes is pretty painful emotionally though
I had an ectopic pregnancy throwing up from the pain
What the counts show
This report keeps all 21 source records for Miscarriage, ectopic pregnancy and abortion together and surfaces traceable examples without converting anecdotes into proof.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Browse the original comments21 preserved records · 21 of 21 source records accounted for
Archive: 21 index entries preserve 21 distinct source records · Every displayed synthesis count resolves to source-record IDs
Gynaecological procedures, infections and everything elseInsertions, biopsies, sweeps and infections — the answers where a procedure, not a disease, is what the writer is describing.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Gynaecological procedures, infections and everything else
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Gynaecological procedures, infections and everything else
Appears when: Gynaecological procedures, infections and everything else
What the pattern means: The group where the subject is the procedure, not the disease, and it is the angriest set of records in the corpus. Writers describe IUD insertions, biopsies, membrane sweeps and cervical procedures done with no anaesthesia and, in several accounts, no warning or consent, after being told to take an over-the-counter painkiller beforehand. The recurring detail is not the pain but the framing around it: being told it would be a pinch, and being moved out of the room for the next patient. Alongside the procedures sit Bartholin cysts and other infections, described in similar terms.
What commenters described: not an illness but as a tatted, pierced, high pain tolerance person: an IUD is the worst pain I've felt. You ever have so much pain that all air is sucked out of your lungs and can't catch a breathe to make any noise? And they told you to 'just take Tylenol beforehand'? Then after the procedure, youre faint because you weren't breathing and you were too young to know what to do with so much pain and a nurse comes in to ask you "are you ready to leave yet? We have another patient waiting for theirs"? Then when you tell anyone they dismiss the pain as not that bad but when you tell anyone who has also had the procedure and they validate you, tell you to watch what it is, only to see your CERVIX GETS PIERCED? Then you try to be an activist for IUD anesthesia or numbing because you never want another AFAB, ESPECIALLY minor, to feel such frightening pain but hear absurd bullshit as to why not? I still have it in & im so so so scared to have it removed because I'm scared of the pain/being dismissed ;;
Limit: These are the accounts of people motivated to write about a bad experience, and other commenters in the same group report insertions that barely hurt; both are here. Nothing on this page indicates what pain relief is available for any procedure — that is a conversation with a clinician.
What the replies added2
That’s why I didn’t go that route. Too much pain that could easily be avoided if women’s pain was taken seriously! It’s 2026, why has this issue not been resolved?
"Without your consent" and "medical procedure" should never be in the same sentence :(( makes me so happy to read they put you under where you are, FINALLY
Where commenters report limits
Endometritrus and endometriosis is not the same thing, just as a warning. I've had both shingles and Endometritrus, and I think the endo was worse but the shingles lasted so much longer (once I got the right antibiotics). Endometritrus is an infection in the living of your uterus, I got mine after an emergency c-section.
Source-record spotlights
That’s why I didn’t go that route. Too much pain that could easily be avoided if women’s pain was taken seriously! It’s 2026, why has this issue not been resolved?
Bartholin’s gland infections and abscesses: chronic migraine; trigeminal neuralgia; and psychotic depression are all pretty much neck neck and neck for me.
Not an illness but: a doc doing a careless IUD insertion. I've previously had appendicitis that burst and needed immediate surgery, but that was nothing in comparison.
Related evidence elsewhere in the index
What the counts show
Across 62 source records, the most common observable tactic structure is “Attach it to an existing routine” (7 records). This is a wording pattern, not a measured outcome.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Observable tactic structures
Counts show source records whose wording matches the tactic structure; biological explanations remain commenter claims unless separately checked below.
Browse the original comments62 preserved records · 62 of 62 source records accounted for
Archive: 62 index entries preserve 62 distinct source records · Every displayed synthesis count resolves to source-record IDs
Bladder, kidney infections and the prostateUrinary answers, including the chronic bladder condition several writers rank above kidney stones.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Bladder, kidney infections and the prostate
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Bladder, kidney infections and the prostate
Appears when: Bladder, kidney infections and the prostate
What the pattern means: Two very different sets of records under one heading. The infection accounts are acute and escalate fast — several writers describe a urinary infection reaching the kidneys and then the bloodstream within a day or two. The chronic accounts are the ones that redefine the group: writers with interstitial cystitis and chronic prostatitis describe pain that has no infection behind it, no end point, and no treatment that has worked, and several rank it above kidney stones.
What commenters described: Interstitial cystitis, when in a bad flare every time I have to urinate it feels like I’m being stabbed in the guts with knives accompanied by intense burning pain. This is accompanied by constantly feeling like I need to urinate really bad, but every time I go the sensation just gets worse instead of better. These flares can last hours to days.
Limit: Acute infections and chronic pain conditions are grouped together here because they involve the same organs, not because they are alike. Several records describe long-term opioid use and suicidal thinking; those are personal accounts, not guidance. If you are struggling, contact a local crisis line or emergency service.
What the replies added2
second worse—unmedicated root canals a few months before on my two front teeth because I faceplanted and broke them in half. Dentist said he wasn’t comfortable using pain killer while I was pregnant (which now I know is a total lie and he totally could of it he cared to look it up)
Sudden onset kidney infection with concurrent stones in my appendix. Morphine barely touched the pain. Thought it was appendicitis, I was throwing up from the pain and nausea. Turns out, my appendix just had stones in it and was a liiiittle bit inflamed. My kidneys however, were inflamed too and I had a serious kidney infection. Turns out, I have kinked ureters, and get zero lower uti symptoms, just random kidney infections. Had to get IV antibiotics overnight and an IM injection of more antibiotics before discharge along with oral antibiotics to take home. They did nothing about the appendix because the inflammation was minor. But I still have to get ultrasounds every so often to keep an eye on the stones in case they become a problem 🙃
Where commenters report limits
Sudden onset kidney infection with concurrent stones in my appendix. Morphine barely touched the pain. Thought it was appendicitis, I was throwing up from the pain and nausea. Turns out, my appendix just had stones in it and was a liiiittle bit inflamed. My kidneys however, were inflamed too and I had a serious kidney infection. Turns out, I have kinked ureters, and get zero lower uti symptoms, just random kidney infections. Had to get IV antibiotics overnight and an IM injection of more antibiotics before discharge along with oral antibiotics to take home. They did nothing about the appendix because the inflammation was minor. But I still have to get ultrasounds every so often to keep an eye on the stones in case they become a problem 🙃
Source-record spotlights
UTI (as a guy) felt like peeing acid, and the urethra is on fire. It's a weird burning sensation that hurts and makes you dread urinating. The pain doesn't go away once you finish peeing because your tip of your dick still has agitated skin inside. It's really bad and I was thinking it would be worth paying 2000 to just make it magically disappear, and not experience the pain any longer. I would constantly soak myself in a bathtub filled with warm water to try to relieve the pain, but it was temporary, and I would end up constantly walking back and forth between the bathtub and my toilet, even when I was dead tired and just wanted to sleep. Also, my pee was a reddish orange color. I went to the ER because I was seriously worried I would have some disease, got some pills (idk if they had any effect), and was okay the next couple days after.
Not to mention how awful it becomes to go anywhere. What if there’s not an easily accessible bathroom when I feel like I have to pee every 15 minutes? Movies, concerts, working, everything becomes stressful. And it can feel embarrassing! Thankfully I’m in remission too, but that was hell.
It’s a toss up between kidney infection and ulcer. The ulcer ended me up in hospital as I was doubled over in pain. I can remember sitting in reception then the next thing I was taken through as I’d collapsed unconscious in reception with the pain.
Related evidence elsewhere in the index
What the counts show
Across 74 source records, the most common observable tactic structure is “Change the sentence” (6 records). This is a wording pattern, not a measured outcome.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Observable tactic structures
Counts show source records whose wording matches the tactic structure; biological explanations remain commenter claims unless separately checked below.
Browse the original comments74 preserved records · 74 of 74 source records accounted for
Archive: 74 index entries preserve 74 distinct source records · Every displayed synthesis count resolves to source-record IDs
Testicular torsion and groin injuryA short and unusually consistent set of answers.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Testicular torsion and groin injury
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Testicular torsion and groin injury
Appears when: Testicular torsion and groin injury
What the pattern means: A short and unusually uniform group. The pain is described as travelling — up into the abdomen, into the spine — rather than staying where it started, and several writers say the examination and the ultrasound were worse than the injury. Most of these accounts are from childhood or adolescence, and several end in surgery the same day or the next.
What commenters described: I had testicle torsion in 7th grade from a football. All I can say is I felt the pain literally running up my stomach to my spine.
Limit: Twenty records, several of them a few words long, and most describe an injury rather than an illness. Nothing here identifies testicular torsion or indicates how quickly anyone should act.
Source-record spotlights
Testicular Torsion
It's a toss-up between testicular torsion that doctors thought I made up but ended up needing surgery that split my little guy in two from tip to sack, and an inflamed appendix that, again, doctors thought was clearly just constipation - saw 3 doctors before one called an ambulance and I had it removed literally while it was bursting in the OR.
Testicular torsion. Only time a threw up from pain
What the counts show
Within 20 source records, 1 ask a question and 0 explicitly say they intend to try the idea; neither signal is treated as an outcome.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Browse the original comments20 preserved records · 20 of 20 source records accounted for
Archive: 20 index entries preserve 20 distinct source records · Every displayed synthesis count resolves to source-record IDs
Bones, joints and musclesAnswers about the frame rather than the organs, including the injuries commenters flagged as not being illnesses. 221 records.
Arthritis, lupus and autoimmune diseaseJoint disease described as constant rather than acute, and often as invisible to everyone else.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Arthritis, lupus and autoimmune disease
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Arthritis, lupus and autoimmune disease
Appears when: Arthritis, lupus and autoimmune disease
What the pattern means: These writers do not describe an episode; they describe a baseline. Lupus, rheumatoid arthritis and ankylosing spondylitis accounts converge on the same three things: pain every day rather than in attacks, exhaustion described as physically painful in its own right, and invisibility — the recurring line is that they look fine. A number describe years of being tested for the wrong thing, and several describe the anticipation of the next flare as its own burden.
What commenters described: Lupus. It’s caused severe arthritis throughout my whole body, constant severe muscle tension, debilitating headaches, painful skin issues, gastric difficulties, and multiple organ failure on 3 separate occasions. Plus feeling so tired that it’s physically painful. Been in active disease (basically a nonstop long term flare) for 2 years. Wouldn’t wish this awful disease on anyone.
Limit: Several unrelated autoimmune diagnoses are grouped here because their writers describe them the same way. Drug names, remission and treatment outcomes in these records are individual reports; nothing here identifies an autoimmune condition or indicates a treatment.
What the replies added2
Costochondritis as an onset affect of lupus. My health had been going downhill, and I kept getting this strange sensation that my shirt was too tight in one spot, even if I wasn't wearing a shirt and nothing was touching that spot. Every morning, I woke up stiff and feeling hungover. I tried stretching every day and one day something felt like it shifted in my ribcage and I thought I broke a rib but it was costochondritis. At it's worst, it felt like my rib bones were made of sharp coral, scraping against the inside of my skin. After costochondritis, I started getting all sorts of other shit happening and within 3 years I was diagnosed with lupus and sjogrens. My mom, Grandma who lived to 96, and an uncle all also have lupus.
Rheumatoid arthritis. Bar none. I broke my finger a few weeks ago and was more annoyed than anything, no tears. Monday evening I began an RA flare-up and was wracked with sobs for a couple of hours, which clearly didn’t help anything. It did make it where I couldn’t breathe well though which did make everything just that much worse.
Where commenters report limits
Lupus. It is with me Every. Single. Day. Pain relievers are of little help, and I am allergic to the “good drugs” that are prescribed for many lupus patients. My joints are in constant pain, I haven’t slept well in decades. There are no cures yet for lupus, and the current administration cut research funding for so many diseases, including lupus. I have an entire constellation of other symptoms in addition to my joint pain. I also have Ehlers-Danlos which adds a whole new level of complications. I wouldn’t wish these conditions on anyone. Unfortunately, I wasn’t diagnosed with either lupus or Ehlers-Danlos until after I had my son. Long story short, my son began transitioning when he turned 18; the hormone therapy exacerbated the underlying genetic anomalies, and now she has debilitating Ehlers-Danlos symptoms. I occasionally wear joint stabilizing devices and sometimes must use a cane, but she has to use them every day. I feel immense guilt for bringing a child into the world, not only for the current environmental state of things but for the disease punishment I inflicted upon her.
Source-record spotlights
Lupus. It’s caused severe arthritis throughout my whole body, constant severe muscle tension, debilitating headaches, painful skin issues, gastric difficulties, and multiple organ failure on 3 separate occasions. Plus feeling so tired that it’s physically painful. Been in active disease (basically a nonstop long term flare) for 2 years. Wouldn’t wish this awful disease on anyone.
reactive arthritis & gastritis! i found out that i had reactive arthritis in april, i was completely unable to walk and had to take 2 ibuprofen every morning and night just to be able to function, i couldnt get down the stairs, to the bathroom, or even stand up, this lasted about 3 weeks and then gradually started improving, the worst part is that i know if i come down with another illness, it can set it off again. leading from the reactive arthritis, the amount of ibuprofen i took during those few weeks caused me to get gastritis from nsaid overuse, now i cant eat anything. i know it isnt as bad as the people in the comments too, but im only 17 and this all happened within the span of 2 months💔
Lupus. Not just the overall constant level 4-5 pain level, but the anticipation of a flare is torture. I never feel safe in my body.
Related evidence elsewhere in the index
What the counts show
Across 72 source records, the most common observable tactic structure is “Attach it to an existing routine” (8 records). This is a wording pattern, not a measured outcome.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Observable tactic structures
Counts show source records whose wording matches the tactic structure; biological explanations remain commenter claims unless separately checked below.
Browse the original comments72 preserved records · 72 of 72 source records accounted for
Archive: 72 index entries preserve 72 distinct source records · Every displayed synthesis count resolves to source-record IDs
GoutThe answer most often explained through the weight of a bedsheet or a moving current of air.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Gout
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Gout
Appears when: Gout
What the pattern means: The group with the most distinctive single image in the corpus: writers do not describe pressure or movement but the weight of a bedsheet, a ceiling fan and moving air, and several say that is what made them cry. The joint is almost always the big toe, the onset is overnight, and crawling between rooms recurs. A second, quieter pattern is misrecognition — several writers spent weeks or months treating it as a sprain or a break before anyone named it.
What commenters described: Soooo bad, especially if you don't catch it right away and it goes full-fledged. I've never cried from air touching my skin before.
Limit: Medications, diet changes and injections are named constantly in this group; every one of them is what an individual writer says they were given or tried, and none of it is a recommendation. Nothing here identifies gout or indicates how to manage it.
What replies pushed back on5
This, I spent most of yesterday in the hospital getting x-ray and blood tests, Dr's thought it was septic arthritis due to the size my ankle had swollen to and how much pain I was in. Nope it was a severe attack of gout. If someone had offered to chop my foot off with a blunted rusty axe with no pain relief I would have thanked them.
Agree. 0/10 would not recommend.
Dude same! Got my first flare last Christmas, thought I broke something so I threw that shit in a boot called it a day. Some of the worst two months of my life Just had my second flare last month and was diagnosed. Took meds for a week and cut my recovery in half Not even 30 yet wtf. Not unhealthy either, just bad genes ig
Yeah. Had a kidney stone once, broke my hand once, broke my ankle once. Nothing compares to a bad gout attack.
Gout. Once or twice a year I get flare ups and it’s always just in the knuckles of the big toe. It hurts, I limp around, try and hydrate as much as possible and take some tart cherry pills and it goes away after a few days. This spring I got a flare up that just kept spreading until it got to my ankle. I couldn’t move my foot let alone put any weight on it. Any little movement or pressure felt like my foot was being crushed. I’ve broken my hip, had a strep infection in the skin of my scrotum that almost killed me, and had a tooth pulled where the Novocain didn’t take and this was by far the most painful thing. I went to urgent care as soon as they opened and had to be wheeled in. The PA examined my foot and said he didn’t know what was wrong and listed all the things it could be. I told him I really thought it was bad gout and I’ve had gout before. He sent me to the hospital and 1 ultrasound, lots of morphine, some blood tests, and my insurance buying a walker 10 hours later I was sent home after being treated for gout. Thankfully by the end of the night the pain had gone down enough I could walk. The next day I felt as good as new. All it took was one tiny pill for gout. I never did use the walker and ended up donating it.
Source-record spotlights
This, I spent most of yesterday in the hospital getting x-ray and blood tests, Dr's thought it was septic arthritis due to the size my ankle had swollen to and how much pain I was in. Nope it was a severe attack of gout. If someone had offered to chop my foot off with a blunted rusty axe with no pain relief I would have thanked them.
Fucking gout is painful and so uncomfortable…
Gout. I didn't know air moving over skin could be that painful
Related evidence elsewhere in the index
What the counts show
Across 50 source records, the most common observable tactic structure is “Attach it to an existing routine” (2 records). This is a wording pattern, not a measured outcome.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Observable tactic structures
Counts show source records whose wording matches the tactic structure; biological explanations remain commenter claims unless separately checked below.
Browse the original comments50 preserved records · 50 of 50 source records accounted for
Archive: 50 index entries preserve 50 distinct source records · Every displayed synthesis count resolves to source-record IDs
Broken bones and crush injuriesFractures offered with an explicit note that they are injuries rather than illnesses.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Broken bones and crush injuries
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Broken bones and crush injuries
Appears when: Broken bones and crush injuries
What the pattern means: Offered with an explicit caveat — writers say up front that these are injuries, not illnesses — and interesting mainly for what surprised them. The small bones outrank the large ones in these accounts: a wrist bone beating a broken hip, a tailbone beating everything. The other recurring moment is not the break but the nerve block wearing off afterwards.
What commenters described: Broken wrist bone. Not one of the arm bones NEAR the wrist, but one of the little bones in the wrist itself (scaphoid in my case). I've been through a major car accident in which I almost died, multiple surgeries for various things, broken hip in a biking accident. Nothing and I mean NOTHING came close to pain from the broken wrist bone.
Limit: The writers themselves flag that these are injuries rather than illnesses, and most of the group states the injury without describing the pain. Nothing here is a guide to any fracture or its treatment.
What the replies added3
Physically? Broken bone. Emotionally/Mentally? Grief.
Does a broken femur count?
Broken tailbone taught me how terrible nerve pain is
Where commenters report limits
I had to get my gallbladder removed and I agree with everyone on this post. However, after breaking my ankle and having to get reconstructive surgery I would have to say the worst pain would be when the nerve block wore off. The pain meds they gave me didn’t you touch that pain at all! My mom was with me when it wore off… she was worried! She called emt and they came to check me out. They unfortunately couldn’t administer anything for the pain since I had already took my pain meds lol they said they would give me a ride to the emergency room where the hospital could give me more pain meds and watch me. Btw, during all of this I’m screaming and begging for god or whoever to just kill me. Once I got to the emergency room they put pain meds in me and that helped but what a horrible experience I’ll never forget
Source-record spotlights
Dislocated shoulder with torn rotator cuff and detached labrum. Getting tobogganed down a mountain with said injuries.
I had to get my gallbladder removed and I agree with everyone on this post. However, after breaking my ankle and having to get reconstructive surgery I would have to say the worst pain would be when the nerve block wore off. The pain meds they gave me didn’t you touch that pain at all! My mom was with me when it wore off… she was worried! She called emt and they came to check me out. They unfortunately couldn’t administer anything for the pain since I had already took my pain meds lol they said they would give me a ride to the emergency room where the hospital could give me more pain meds and watch me. Btw, during all of this I’m screaming and begging for god or whoever to just kill me. Once I got to the emergency room they put pain meds in me and that helped but what a horrible experience I’ll never forget
Broken hip and a fractured hip. Had a hip replacement on the left side and had to get the right hip pinned with 4 bolts or whatever they are. Thankfully, both sides heal great and I have full mobility.
Related evidence elsewhere in the index
What the counts show
The exact phrase “when it wore off” recurs across 2 of the 30 source records in Broken bones and crush injuries; the complete archive stays available below.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Browse the original comments30 preserved records · 30 of 30 source records accounted for
Archive: 30 index entries preserve 30 distinct source records · Every displayed synthesis count resolves to source-record IDs
FibromyalgiaWidespread pain described as permanent and, repeatedly, as disbelieved.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Fibromyalgia
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Fibromyalgia
Appears when: Fibromyalgia
What the pattern means: The recurring subject is not the pain but the relationship with medicine around it. Writers describe having run out of treatment options, being told the condition is imaginary, and having stopped going to doctors at all. The pain itself is described as everywhere and as amplifying other things — several writers say fibromyalgia makes every other illness they have hurt more, and one says it has made her stop investigating new symptoms.
What commenters described: I have fibromyalgia, have had for many years and am at a point where I don't have any medication to help with relief of it anymore. Most of the pains I can cope with as I have a high pain threshold but when the bone ache kicks in it completely takes over, the intense pain, like the worst toothache but in the bones, makes me feel sick, and I have no choice to cope until it stops which can be a few hours or days, it will start out of nowhere and leave the same. I hate it but I have no choice because it won't ever stop happening and that's alongside all the rest of the pains I deal with, also it makes breathing hurt some days too.
Limit: Fibromyalgia appears alongside other diagnoses in most of these records, so which condition any writer is describing is not always separable. Medications and supplements named here are personal reports; nothing in this group identifies fibromyalgia or indicates a treatment.
What the replies added2
Fibromyalgia is very painful. Believe it or not, there is starting to be some research into Glp1 medicine working to lower inflammation and lessen fibromyalgia pain. I only found this out because I started a glp1 for my PCOS and within 3 days after my very first dose, I woke up with a large reduction in my pain. Yes, you would lose some weight. No, it doesn't have to be a lot. It's possible to keep a low dose and get relief. I got relief starting at 2.5 mgs. I increased my dose because I also have insulin resistance and PCOS. So I'm on a higher dose. But, I been able to maintain that dose for multiple months now and stabilize my weight. I know that can be a concern for some people because the people that they know are on Glp1s are those that take it too far and become anorexic/unhealthy.
In a flare for the last few months. Living the dreeeaaaammm
Where commenters report limits
I have Fibromyalgia and EDS, unfortunately they play off each other so…both?
Fibromyalgia… it makes all the other pains/illnesses hurt more than they should. Unfortunately it also means that I end up thinking I’m having a heart attack when it’s just gas… or I think one of my organs is going to split open when I just ate something that didn’t agree with me. Now I assume every severe pain is just nothing, so I don’t bother to get it checked out.
Source-record spotlights
In a flare for the last few months. Living the dreeeaaaammm
Fibromyalgia… it makes all the other pains/illnesses hurt more than they should. Unfortunately it also means that I end up thinking I’m having a heart attack when it’s just gas… or I think one of my organs is going to split open when I just ate something that didn’t agree with me. Now I assume every severe pain is just nothing, so I don’t bother to get it checked out.
Fibromyalgia. Diagnosed at 21. It’s a life sentence
Related evidence elsewhere in the index
What the counts show
Across 29 source records, the most common observable tactic structure is “Attach it to an existing routine” (2 records). This is a wording pattern, not a measured outcome.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Observable tactic structures
Counts show source records whose wording matches the tactic structure; biological explanations remain commenter claims unless separately checked below.
Browse the original comments29 preserved records · 29 of 29 source records accounted for
Archive: 29 index entries preserve 29 distinct source records · Every displayed synthesis count resolves to source-record IDs
Tendons, joints and the bones that gave wayFrozen shoulders, torn tendons, bursitis and bone that lost its blood supply.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Tendons, joints and the bones that gave way
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Tendons, joints and the bones that gave way
Appears when: Tendons, joints and the bones that gave way
What the pattern means: The frozen-shoulder accounts dominate and share a single complaint: not intensity but length, measured in years, with sleep as the thing lost. Around them sit bursitis, tenosynovitis, torn tendons and bone that lost its blood supply. Two details recur across the group — a cortisone injection described as more painful than the condition, and writers who have given birth ranking a shoulder above it.
What commenters described: Frozen shoulder syndrome. Worse than labor and dental pain combined and lasted months.
Limit: Recovery in this group is described over years and with contradictory results from the same treatments, so no outcome here is the expected one. Injections, physiotherapy and hormone therapy are named as what individual writers tried, not as options being recommended.
What the replies added1
I don’t know if this classifies as illness but frozen shoulder. And the scariest part once you have had it you are more likely to have it again. I have had 4 kids gall bladder attack broken ankle nothing will ever compare to this pain.
Source-record spotlights
Bursitis in my hip & femur bones. Couldn't sleep, could barely walk to go to the bathroom.
I remeber Synovitis (fluid under kneecap) was excruciating. I couldnt walk or hardly move. Definatley couldnt sleep cuz every time i tried to roll over it made me scream out from pain.
Frozen shoulder syndrome. Worse than labor and dental pain combined and lasted months.
Related evidence elsewhere in the index
What the counts show
Across 40 source records, the most common observable tactic structure is “Attach it to an existing routine” (5 records). This is a wording pattern, not a measured outcome.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Observable tactic structures
Counts show source records whose wording matches the tactic structure; biological explanations remain commenter claims unless separately checked below.
Browse the original comments40 preserved records · 40 of 40 source records accounted for
Archive: 40 index entries preserve 40 distinct source records · Every displayed synthesis count resolves to source-record IDs
InfectionsIllnesses that came from outside — a childhood virus caught in adulthood, a tick bite that took years to name, a fever abroad. 481 records.
Meningitis and encephalitisThe headache a number of writers place above everything else they have ever had.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Meningitis and encephalitis
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Meningitis and encephalitis
Appears when: Meningitis and encephalitis
What the pattern means: The group most willing to rank itself first outright. Writers who have also had childbirth, kidney stones and a ruptured gallbladder put meningitis above all of them, and the description is unusually consistent: a headache that made standing upright impossible, a neck that could not be moved, and opioids that did nothing. Several describe wanting to die and saying so. The recurring aftermath is the lumbar puncture — repeated, sometimes botched, and in several accounts worse than the illness.
What commenters described: Meningitis, no contest. Worst pain I have ever felt in my entire life, and I've given birth and had my gallbladder erupt. Get the vaccine if offered. You can die from it, but even if you don't, you want to.
Limit: Bacterial, viral and recurrent cases are grouped together here although they differ in cause and outcome, and several writers say they were never formally diagnosed. Vaccination is raised repeatedly by commenters and is not endorsed or assessed here. Nothing in this group identifies meningitis.
What the replies added1
Was going to say meningitis, but couldn't decide between that and when I broke my back. Needless to say, both sucked really badly.
Source-record spotlights
Meningitis, spent 3 months in a hospital with the worst fever and headaches I've ever had. Kept relapsing, weekly spinal taps were horrible
Meningitis. I still remember screaming when my chin dipped even the most miniscule amount.
Meningitis, shingles, migraine, kidney stones. In that order.
Related evidence elsewhere in the index
What the counts show
Across 43 source records, the most common observable tactic structure is “Attach it to an existing routine” (2 records). This is a wording pattern, not a measured outcome.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Observable tactic structures
Counts show source records whose wording matches the tactic structure; biological explanations remain commenter claims unless separately checked below.
Browse the original comments43 preserved records · 43 of 43 source records accounted for
Archive: 43 index entries preserve 43 distinct source records · Every displayed synthesis count resolves to source-record IDs
Sepsis and septic shockAnswers where the illness turned systemic, often after something else on this page.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Sepsis and septic shock
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Sepsis and septic shock
Appears when: Sepsis and septic shock
What the pattern means: Rarely the first illness in these accounts — sepsis is what happened next, after a kidney stone, a wound, a tooth, a gallbladder. The descriptions are whole-body rather than local: every joint, every muscle, and an inability to find any position. The recurring theme is how long the recovery took, with several writers describing relearning to walk, and how close they say they came without realising it.
What commenters described: Sepsis. Ain’t nothing like it. I had to learn how to walk again while spending 15 days in the hospital. At 39 in good-ish shape, running 20-ish miles a week. Sepsis destroyed me. I was a few hours away from organ failure according to the docs, because I was too stubborn to go in to the ER. I’ve had gallbladder removal, pneumonia, broken bones, torn knee ligaments, dislocated hip, and sepsis was gnarly.
Limit: These are the accounts of people who survived, written afterwards, and several say they did not know what was happening at the time. Nothing here is a way to recognise sepsis, and delay is described rather than advised against on any authority but the writers' own.
What the replies added3
Hahahahaha It’s so funny looking down the comments for this topic because apparently I’m a collector. I’ve had: Gallbladder attack Kidney stone Shingles Not quite a cluster headache, but a really bad one (Don’t know what caused it, it only happened once, but I was sobbing for hours through the night unable to last more than a couple seconds at a time without sobbing because it hurt so much. I almost went to the ER but after 7 hours it reduced in pain enough for me to sleep) Sciatica Tooth infection Bowel blockage from Crohn’s Depression CPTSD Interestingly, I would judge my most painful as not any of those, though don’t get me wrong, all can hurt BRUTALLY in different ways. For me it’s weird but…sepsis? One of the times I was in the hospital with sepsis due to surgery going poorly, I had various drains in me and apparently one of them slipped or something. Whatever happened, I lost the ability to speak or act it was so painful. The doctors all rushed in and I got to experience going from a patient who is informed and part of the process to a broken object they are trying to figure out what’s going on and fix before my vitals crash further. Ended up going into one of the weirdest surgeries I can remember, where they basically had me in some sort of imaging machine and were taking constant updated images trying to figure out what was going on while also cutting me open a little to manipulate stuff, and I was given conscious sedation so I could feel everything plus or minus the massive amount of pain killers on board. Despite not experiencing the full pain of that surgery, it was still very unpleasant for me. It was as “simple” as finding which drain got dislodged and re-placing it? I think? My memories of that time are very hazy as you might imagine, and I never got an external perspective because my family wasn’t really paying much attention to me in the hospital.
Sepsis. Ain’t nothing like it. I had to learn how to walk again while spending 15 days in the hospital. At 39 in good-ish shape, running 20-ish miles a week. Sepsis destroyed me. I was a few hours away from organ failure according to the docs, because I was too stubborn to go in to the ER. I’ve had gallbladder removal, pneumonia, broken bones, torn knee ligaments, dislocated hip, and sepsis was gnarly.
Sepsis. Septic shock to be exact. No words. Ruined me permanently. I was 18. I lost my life to it. Fuck sexual abuse.
Where commenters report limits
1. Severe sepsis-whole body was in so much pain I couldn't even move for 3 weeks. It had attacked my whole central nervous system, heart, lungs, everything. I had to learn how to walk again. Was in the hospital for a total of 5 weeks but was many months before I was back to normal, however, I am a former heroin addict who was actually off of the heroin when I got sepsis, but because the hospital put me on a button of Dilaudid that I could push every 4 hours for 5 weeks straight, no weening before they discharged me. I was dope sick when I left the hospital and immediately went to get heroin as soon as I got to my car, not totally blaming it on the hospital cuz I was grown but they were told I had this problem, I feel like I was kinda set up to relapse, which I did, big time. Which leads me to my next painful illness... 2. Opiate withdrawal-even if it is self inflicted it doesn't mean it wasn't some of the worst hell I've ever been thru in life.... unfortunately on multiple occasions. I could share details but u would rather not know them. Glad, not proud, but glad to say that I haven't touched them in nearly 6 years now. If I had to go thru withdrawals again, I don't think I would live thru it. People like to say you can't die from opiate withdrawals....bullshit. absolute bullshit. When u can't keep one sip of water or even a lick of s Popsicle down for 6-7 days, and are throwing up stuff from ur body u didn't eat or know existed, turns out ur kidneys start to shutdown. I found out the hard way. And when kidneys shut down, ur done. 3. DRY SOCKET-DONT GET UR WISDOM TEETH EXTRACTED IN POCATELLO, IDAHO. I CAME OUT THE SURGERY WITH DRY SOCKET AND IT WAS LIKE SOMEONE WAS STABBING ME THROUGH MY HEAD AND TOOK MONTHS TO HEAL THE HOLE IN MOUTH THST I HAD TO CONSTANTLY CLEAN SO IT WOULDN'T HEAL UP WITH FOOD INSIDE IT. 4. Cracked Ribs, boyfriend chopped off finger tip when he slammed the front door on it, gout, getting my biceps cut open and half removed due to infection and the doctor giving me literally nothing for pain due to my drug history-6 inch incisions each, crazy ear infections.... What doesn't kill u makes u stronger is what they say but if that was the case, I would have changed genders and tried out for strongman competitions I think lol
Source-record spotlights
I was a day away from developing sepsis that's the most painful illness I've had
Sepsis - felt like every joint in my body was going to explode. Followed closely by kidney stones. At least kidney stones were just pain, and not feeling like I was going to d!e while also being in pain lol
Sepsis. Felt like I was dying. Spoiler: I was dying. Once they stopped me from actively dying, I got all the fentanyl I wanted. The pain was so unbearable that I ended up with a significant amount of fentanyl until I put myself to sleep/unconscious.
What the counts show
The exact phrase “sepsis felt like” recurs across 3 of the 31 source records in Sepsis and septic shock; the complete archive stays available below.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Browse the original comments31 preserved records · 31 of 31 source records accounted for
Archive: 31 index entries preserve 31 distinct source records · Every displayed synthesis count resolves to source-record IDs
Flu, COVID and high feversInfluenza and COVID, including the long tails writers say both left behind.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Flu, COVID and high fevers
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Flu, COVID and high fevers
Appears when: Flu, COVID and high fevers
What the pattern means: The largest infection group, and the one whose writers most often begin by apologising for the answer. Two descriptions recur that do not appear elsewhere: pain in the skin, so that clothing and washing become intolerable, and pain in the muscles described as being pulled off the bone. The influenza accounts add hallucinations and delirium; the COVID accounts add duration, with several writers describing symptoms that never fully resolved. A number who have had both rank them against each other, and they do not agree.
What commenters described: Don’t laugh…COVID. In addition to the generic feeling like crap, my skin hurt. All of it…like it was raw and burning…clothing was so uncomfortable and bathing or cleaning myself after voiding was torture. Even eating and drinking hurt. I would sit very still holding myself so no part of me touched me and as little of me touched anything else as could be managed. If you’ve ever experienced the joy of hand, foot, and mouth disease, the pain was much like that, but everywhere, all the time…for almost 17 days. To make this story more fun, I caught COVID right after we moved to a brand new house in another state…so we had no furniture, no ability to clean clothing or bedding… and you recall, I mentioned that wearing clothing was extremely painful? Well, we also had no window coverings. So I sat in the very center of my house with no direct windows and did my best to touch as little as possible. It was awful.
Limit: Different strains, different years and, in several cases, no test at all sit under the same heading here, and severity ranges from a bad week to intensive care. Vaccines are argued about throughout this group; none of that is checked or endorsed here.
What the replies added3
I had a really bad flu! Turned into pneumonia and broke a rib coughing! I seriously thought I was going to die! I had a toddler I was trying to take care of and couldn’t walk from the couch to the kitchen in our tiny apartment 😢 that was about 35 years ago and I get a flu shot every year. I’ve only had a couple mild cases since 😀
Yep, I just wanted it to end. I did get vaccines after they came out and then got covid again in 2023 and it wasn't as bad but the first thing I noticed was muscle & joint aches. That time I took paxlovid and I think it really helped. Let's hope never again!!
I broke my leg in 17 places, my gallbladder burst, I burned my groin & thigh with boiling water, and have regular migraines. However, the worst 2 years ago when I had Covid, first-time shingles, first-time facial eczema, and first-time seizures. It was awful.
Where commenters report limits
Flu A in december, it ended up turning into bronchitis, and I ended up going to the ER twice. The first time they did nothing fr, no anti virals as it was too late. I went home tried to recover, they gave me a cough suppressant (which I was confused about because I needed to get the mucus out my chest, and you do that by coughing) but went back because I was struggling to breathe again and it was getting worse. My oxygen levels were reduced and I ended up on an IV drip and a breathing treatment. It ended up giving me asthma. So now I need an inhaler for the foreseeable future . All because someone came to my in laws house while sick with the flu. The nurse basically told me that if i didn’t come in, I could have asphyxiated in my sleep bc my oxygen was dropping, and I could have went into respiratory distress.
Source-record spotlights
Flu so bad I was hallucinating most of the time. It’s hard to sleep when your brain is convinced there’s a man standing slightly behind the closet.
You have no idea. My mom was mad cause I wouldn’t sleep but I was convinced that guy behind the closet would come and attack me the moment I closed my eyes. I had to literally pass out from exhaustion in order to sleep.
H1N1, had me destroyed. The physical pain of everything was fucking horrible.
Related evidence elsewhere in the index
What the counts show
Across 116 source records, the most common observable tactic structure is “Use a sensory reset” (5 records). This is a wording pattern, not a measured outcome.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Observable tactic structures
Counts show source records whose wording matches the tactic structure; biological explanations remain commenter claims unless separately checked below.
Browse the original comments116 preserved records · 116 of 116 source records accounted for
Archive: 116 index entries preserve 116 distinct source records · Every displayed synthesis count resolves to source-record IDs
Throats: strep, tonsillitis and abscessesSwallowing, described again and again through the same handful of images.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Throats: strep, tonsillitis and abscesses
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Throats: strep, tonsillitis and abscesses
Appears when: Throats: strep, tonsillitis and abscesses
What the pattern means: Almost every record here reaches for the same two images — glass and razor blades — and then for the same detail: how many times a day a person swallows. The abscess accounts escalate from there into not swallowing at all, drooling into a cup, and drainage described as the worst part. Tonsillectomy recovery in adults appears repeatedly as a separate, equally bad answer, with several writers who have given birth ranking it above the birth.
What commenters described: Tonsillitis. I was almost in tears swallowing my spit. Think about how many times a day you swallow spit.
Limit: This group mixes ordinary sore throats with airway-threatening abscesses under one heading because its writers described them together. Nothing here distinguishes between them or indicates when a sore throat needs urgent care.
What the replies added2
Kidney stones and tonsillitis. Tonsillitis was so bad my tonsils were blocking my airway and my lips started to turn blue. When they swabbed my throat that was hands down some of the worst pain I’ve ever had I sobbed and screamed. I’ve broken bones, had cancer…none of that was as bad as those events!
Tonsillitis followed by a throat abscess, couldn’t eat or drink. Had to be put on fluids and liquid pain killers. I’ve broken my wrist and this was worse!
Where commenters report limits
I got admitted and they mercifully gave me a suction thing that I just kept in my mouth so I wasn't drooling everywhere 24/7. Unfortunately nobody warned me that if you don't swallow anything including your own saliva for 2 weeks straight, your esophagus can start to ulcerate from drying out. So when I finally started trying to gently eat and swallow things, it was EXCRUCIATING. Everything stung and burned so bad, all I could do was just sit there with white knuckles sweating until it subsided. It took months before I could swallow anything without significant pain.
Source-record spotlights
Peritonsillar Abscess. I dont wish it on my enemies. Very rarely does one go to the hospital and rhe doctor actually does seem to feel very, very sympathetic for you when you have something non fatal. Holy goddamn hell on earth for days.
Oh my God one time I had strep throat and my fever was so high, I think I was in grade school or high school I don’t remember. But I remember I was fever dreaming I used to love the show scrubs on TV and I dreamt that I was at their hospital getting checked out because I was so sick. And then I kind of came too and I went to my mom and I said I need to go to the hospital something wrong and I’d like the highest Fever.
Strep throat for me. Happened shortly after being hospitalized with a kidney infection. I didn’t take the pain meds they gave me at the hospital for the infection, but caved and took them just to be able to sleep when I had strep!
Related evidence elsewhere in the index
What the counts show
Across 61 source records, the most common observable tactic structure is “Attach it to an existing routine” (7 records). This is a wording pattern, not a measured outcome.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Observable tactic structures
Counts show source records whose wording matches the tactic structure; biological explanations remain commenter claims unless separately checked below.
Browse the original comments61 preserved records · 61 of 61 source records accounted for
Archive: 61 index entries preserve 61 distinct source records · Every displayed synthesis count resolves to source-record IDs
Cellulitis, abscesses and bone infectionsSkin, tissue and bone infections, and the drainage that followed them.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Cellulitis, abscesses and bone infections
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Cellulitis, abscesses and bone infections
Appears when: Cellulitis, abscesses and bone infections
What the pattern means: The recurring shape is underestimation. Writers describe an ingrown hair, a bite, a spot, a sprain — and then a fever, a limb they cannot use, and a hospital. MRSA appears repeatedly, in the hand, the face, the leg. The descriptions are mechanical rather than sharp: a nail being twisted, pressure with nowhere to go. Several accounts end with drainage described as the relief, and several with how close the writer says it came to costing them a limb.
What commenters described: I had a MRSA infection in an ingrown hair on my hand. It felt like, at all times, someone was twisting a rusted nail into my hand. It was swollen and left a hell of a scar after I finally got on the appropriate antibiotics.
Limit: These writers are describing the cases that became serious; most skin infections do not. Nothing here identifies an infection or indicates when one needs attention, and the delays described are reported, not endorsed.
What the replies added3
Mystery bump> boil> neurotic sore that ended up being a broken recluse bite.
Staph infection/abscess. Or an infected cracked tooth. Or maybe that cough I had for several months that made it feel like I broke a few ribs. Those are definitely the top 3. They were each their own specific flavor of horrible.
Cervical osteomyelitis. I was asking for pain meds right on the 4hr mark every single time. Morphine did nothing for the pain. The only thing that worked in the beginning was Dilaudid. I’m actually still recovering and am in my 4th week of IV antibiotics.
Where commenters report limits
Cervical osteomyelitis. I was asking for pain meds right on the 4hr mark every single time. Morphine did nothing for the pain. The only thing that worked in the beginning was Dilaudid. I’m actually still recovering and am in my 4th week of IV antibiotics.
Source-record spotlights
I had a MRSA infection in an ingrown hair on my hand. It felt like, at all times, someone was twisting a rusted nail into my hand. It was swollen and left a hell of a scar after I finally got on the appropriate antibiotics.
Cellulitis & Osteomyelitis in my jaw. 20/10 for nerve pain. Would rather natural childbirth. Told my husband if he could guarantee a knockout I’d let him.
Inflammation of a hair follicle in my armpit, ouch. Luckily it's something that clears within a day or so
Related evidence elsewhere in the index
What the counts show
Across 52 source records, the most common observable tactic structure is “Attach it to an existing routine” (3 records). This is a wording pattern, not a measured outcome.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Observable tactic structures
Counts show source records whose wording matches the tactic structure; biological explanations remain commenter claims unless separately checked below.
Browse the original comments52 preserved records · 52 of 52 source records accounted for
Archive: 52 index entries preserve 52 distinct source records · Every displayed synthesis count resolves to source-record IDs
Dengue, chikungunya, malaria and typhoidMosquito- and water-borne fevers, named by writers who caught them abroad and at home.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Dengue, chikungunya, malaria and typhoid
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Dengue, chikungunya, malaria and typhoid
Appears when: Dengue, chikungunya, malaria and typhoid
What the pattern means: The most specific vocabulary in the corpus, and it is about bone. Writers use the disease's own colloquial name, describe being beaten with golf clubs, and single out pain behind the eyes as the symptom they remember. The chikungunya accounts add a long tail — joint pain and fatigue continuing for a year or more afterwards. Several writers report being treated in countries where the disease is unfamiliar and say they were not believed.
What commenters described: dengue fever. Standing, sitting down and laying down brought me pain deep into my bones, headache so bad I couldn't open my eyes for a week, retroorbital pain had me wishing I could just take my eyes out with a spoon. Luckily its limited and in 10 days I was completely fine
Limit: Where these infections were caught, and how they were treated, varies enormously across the group. Nothing here identifies a tropical infection or constitutes travel-health advice.
What the replies added2
I’ve had it twice. It’s really painful but I’ve had migraines that hurt more. Also, dengue felt less painful than when I got CoViD.
Currently recovering from it.. most intense pain I’ve felt in my life.
Source-record spotlights
I’ve never had it myself, but dengue fever is colloquially called “break bone fever” because of how painful it is
Dengue fever. They call it break bone fever for a reason. Putting on the tourniquet to draw blood literally made me cry, as did every needle prick to draw blood (which they did every 4 hours because I was in the ICU.) And while I was in the hospital getting blood transfusions with a near hepatic liver the doctors just gave me Ativan because they didn’t believe me that I was in pain. I’m in the US btw. I got dengue abroad and because it’s not endemic in the US the doctors had never treated a case of it.
Toss up between dengue fever, which I healed from, and chronic akathisia, which I have not. Dengue was 105 fever, 220 heart rate, weeks in the hospital, agonizing pain in every square inch of my body, including deep inside my ears and eyes. Akathisia is never being able to sit still. Not to eat, not to sleep, not to watch TV, not in a car, not ever. Painful restlessness 24/7.
Related evidence elsewhere in the index
What the counts show
Across 27 source records, the most common observable tactic structure is “Attach it to an existing routine” (3 records). This is a wording pattern, not a measured outcome.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Observable tactic structures
Counts show source records whose wording matches the tactic structure; biological explanations remain commenter claims unless separately checked below.
Browse the original comments27 preserved records · 27 of 27 source records accounted for
Archive: 27 index entries preserve 27 distinct source records · Every displayed synthesis count resolves to source-record IDs
Mono and glandular feverGlandular fever, described by its length rather than by its peak.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Mono and glandular fever
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Mono and glandular fever
Appears when: Mono and glandular fever
What the pattern means: Ranked here by length rather than by peak. Writers describe a month or more of not being able to swallow their own saliva, an enlarged spleen or liver, and sleeping through most of it. Several report fatigue that continued for years afterwards. The other recurring element is disbelief — writers describe being suspected of malingering by parents and schools while acutely ill.
What commenters described: Got Mononucleosis when I was seventeen. My throat was incredibly sore and I couldn't swallow without horrible pain, so I could also barely sleep (despite being extremely weak and exhausted) because swallowing my own spit was too painful. It happened over Thanksgiving and all I could eat was mashed potatoes and jellied cranberry sauce, and even then it hurt so badly to swallow that I could barely taste. Just days of lying on the couch, hoping my fever didn't go over 106 (because that meant hospital), my mom dragging me to doctors, and bracing my whole body (which was also sore as hell) whenever I had to swallow my own spit. Then I had a reaction to the drugs they put me on and I broke out in a horrifying rash all over my body that didn't fully go away for weeks. Pretty sure the mono was courtesy of an ex-boyfriend who had cheated on me with his ex-girlfriend, so that was just the cherry on top. I've had Covid twice and it wasn't as bad as that mono.
Limit: Most of these accounts are of adolescents recalling an illness years later, and several were never formally tested. Nothing here identifies glandular fever or indicates what to do about it.
What the replies added2
Got Mononucleosis when I was seventeen. My throat was incredibly sore and I couldn't swallow without horrible pain, so I could also barely sleep (despite being extremely weak and exhausted) because swallowing my own spit was too painful. It happened over Thanksgiving and all I could eat was mashed potatoes and jellied cranberry sauce, and even then it hurt so badly to swallow that I could barely taste. Just days of lying on the couch, hoping my fever didn't go over 106 (because that meant hospital), my mom dragging me to doctors, and bracing my whole body (which was also sore as hell) whenever I had to swallow my own spit. Then I had a reaction to the drugs they put me on and I broke out in a horrifying rash all over my body that didn't fully go away for weeks. Pretty sure the mono was courtesy of an ex-boyfriend who had cheated on me with his ex-girlfriend, so that was just the cherry on top. I've had Covid twice and it wasn't as bad as that mono.
Mono for me was insane. I was out of school for a month straight. Did nothing but sleep for a consecutive 30 days, didnt eat, lost weight and muscle. I swear half the time i was hallucinating i was so sick! I have a chronic illness called HS (Hidradenitis Suppurativa) and that is not for the faint of heart. Currently experiencing a flare up now and have been in and out of the doctor for about a week getting poked, proded, injected, drained, stitched back up, shit sucks so much. Currently wheeling around in a wheelchair bc i cant even walk the flare up is so bad on my groin. Not much of a cure for it either.
Where commenters report limits
Mono for me was insane. I was out of school for a month straight. Did nothing but sleep for a consecutive 30 days, didnt eat, lost weight and muscle. I swear half the time i was hallucinating i was so sick! I have a chronic illness called HS (Hidradenitis Suppurativa) and that is not for the faint of heart. Currently experiencing a flare up now and have been in and out of the doctor for about a week getting poked, proded, injected, drained, stitched back up, shit sucks so much. Currently wheeling around in a wheelchair bc i cant even walk the flare up is so bad on my groin. Not much of a cure for it either.
Source-record spotlights
Glandular fever , made the gout seem like a Christmas present and was left with a codeine addiction. Did loose over two stone and missed half a year of school tho! Whooo
Mono. My spleen was so enlarged and my tonsils were so swollen I couldn’t eat anything but milkshakes for 2 months. Otherwise, fracturing my spine hurt really bad but idk if that’s considered an illness I had my tonsils removed 2 years ago which absolutely sucked it was horrible. But the pain only last 2 weeks where as with mono my tonsils were swollen for months, and I couldn’t eat anything solid for 2 of those months. My tonsils never stopped being swollen in the 10 years after which is why I had them removed. Mono made me sleep 20 hours a day, I couldn’t barely move for a few weeks because of how bad my spleen hurt, and my god having a non-function food pipe is horrible. I’d rank mono symptoms 3rd on my list, with spinal fracture being #1 and contractions being #2.
Mononucleosis. Probably not as bad as others in the thread but I'm a relatively healthy person overall and this shit was vile. I was 14, it started as a normal sore throat, then escalated to a month in the hospital. Fevers of 39°C, total inability to eat solid food, every swallowing a challenge. As I was laying there I once went to make me some tea, I only had a thick walled glass to get hot water. It exploded in my hands and I got burns all over my stomack and fingers. What a fun summer it was.
Related evidence elsewhere in the index
What the counts show
Across 44 source records, the most common observable tactic structure is “Use a sensory reset” (3 records). This is a wording pattern, not a measured outcome.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Observable tactic structures
Counts show source records whose wording matches the tactic structure; biological explanations remain commenter claims unless separately checked below.
Browse the original comments44 preserved records · 44 of 44 source records accounted for
Archive: 44 index entries preserve 44 distinct source records · Every displayed synthesis count resolves to source-record IDs
The childhood illnesses, caught lateChickenpox, mumps, measles, scarlet fever and whooping cough — mostly from writers who caught them as adults.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: The childhood illnesses, caught late
Source-backed answers are shown before diagnostics; the complete source archive remains below.
The childhood illnesses, caught late
Appears when: The childhood illnesses, caught late
What the pattern means: The group's organising fact is age. Chickenpox, mumps, measles, scarlet fever, fifth disease and whooping cough are described almost entirely by adults who caught them late, and the recurring claim is that the adult version bears no relation to what they expected — blisters in the throat and eyes, joints too swollen to bend, ribs broken by coughing. Vaccination is raised unprompted in a large share of these records, usually by writers urging it on other people's children.
What commenters described: Whooping cough. Imagine coughing enough to bruise or break ribs, then coughing more with a bruised or broken rib. You can’t hold it in, you can’t stop it, only coughing. For MONTHS.
Limit: These accounts come from people who had a bad version of a common illness and chose to write about it; most cases are not like this. The vaccination views expressed throughout are commenters' own and are neither checked nor endorsed here.
What the replies added2
Whooping cough. Imagine coughing enough to bruise or break ribs, then coughing more with a bruised or broken rib. You can’t hold it in, you can’t stop it, only coughing. For MONTHS.
Whooping cough. I coughed so hard I broke ribs. Then I coughed with broken ribs. I thought I was going to die.
Source-record spotlights
My baby brother had chicken pox when he was still in diapers and I remember him screaming as mom changed him and I saw his little scrotum just covered in redness and sores. I also had the chicken pox but could hardly complain while he was that miserable. Kids today are lucky to have a vaccine for it.
Mumps... back when kids got mumps before there was a vaccine for it.
Chicken pox (this was before the vaccine was available)
Related evidence elsewhere in the index
What the counts show
Across 63 source records, the most common observable tactic structure is “Attach it to an existing routine” (3 records). This is a wording pattern, not a measured outcome.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Observable tactic structures
Counts show source records whose wording matches the tactic structure; biological explanations remain commenter claims unless separately checked below.
Browse the original comments63 preserved records · 63 of 63 source records accounted for
Archive: 63 index entries preserve 63 distinct source records · Every displayed synthesis count resolves to source-record IDs
Lyme disease and the infections that took years to nameInfections several writers say went undiagnosed for years.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Lyme disease and the infections that took years to name
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Lyme disease and the infections that took years to name
Appears when: Lyme disease and the infections that took years to name
What the pattern means: What binds this group is diagnostic delay rather than a shared organism. Writers describe years of symptoms and a series of doctors before anyone named it, and several say the dismissal was worse than the illness. The pain is described as everywhere rather than anywhere — whole-body aches, joints that feel pulled apart, and, distinctively, pain in the eyeballs, which two separate writers raise independently.
What commenters described: Lyme Disease, hands down. It felt like my skin was being scraped off with a wire brush if anything touched it, especially if that something was cold. There was only one blanket I could use “comfortably,” but it was too hot and made my fever worse which led to shivering. I was shivering and hard that I pulled some muscles, and threw up a few times too which didn’t help. My joints felt bruised and like they were being dislocated / pulled apart at the same time as someone smashing them with a hammer. I had blood drawn after finishing my two weeks of doxycycline and tested positive, but I get rechecked in a week to see if it was a false positive. Fingers crossed that it was, and that I never flare again.
Limit: Chronic Lyme in particular is contested medical ground and this page takes no position on it; what is recorded is what these commenters say they experienced and were told. Nothing here identifies a tick-borne infection.
What the replies added1
Lyme Disease, hands down. It felt like my skin was being scraped off with a wire brush if anything touched it, especially if that something was cold. There was only one blanket I could use “comfortably,” but it was too hot and made my fever worse which led to shivering. I was shivering and hard that I pulled some muscles, and threw up a few times too which didn’t help. My joints felt bruised and like they were being dislocated / pulled apart at the same time as someone smashing them with a hammer. I had blood drawn after finishing my two weeks of doxycycline and tested positive, but I get rechecked in a week to see if it was a false positive. Fingers crossed that it was, and that I never flare again.
Where commenters report limits
I had “tick fever” in South Africa, which is a close relative of Lyme disease. That eyeball pain was bizarre! The symptom I remember most is that my right leg just didn’t work right…I’d try to walk but I ended up half-dragging my leg for a few days.
Source-record spotlights
Yeah the eyeball pain was weird lol. I would get numbness in my left leg that felt like it was asleep.
I had “tick fever” in South Africa, which is a close relative of Lyme disease. That eyeball pain was bizarre! The symptom I remember most is that my right leg just didn’t work right…I’d try to walk but I ended up half-dragging my leg for a few days.
LGV("tropical chlamydia ") in my rectum, open ulcers inside me and everytime I was shitting it felt like passing blades .
What the counts show
The exact phrase “eyeball pain was” recurs across 2 of the 31 source records in Lyme disease and the infections that took years to name; the complete archive stays available below.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Browse the original comments31 preserved records · 31 of 31 source records accounted for
Archive: 31 index entries preserve 31 distinct source records · Every displayed synthesis count resolves to source-record IDs
Herpes, cold sores and mouth ulcersOutbreaks described mainly through what the writer could not do while they lasted.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Herpes, cold sores and mouth ulcers
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Herpes, cold sores and mouth ulcers
Appears when: Herpes, cold sores and mouth ulcers
What the pattern means: Almost every record here is about a first outbreak, and the writers describe it as unrecognisably worse than what they had been led to expect of a common infection. The specifics are practical: not being able to urinate, sit or walk, and in one account using hiking poles to cross a flat. Several writers say the illness that followed the outbreak — fever, weight loss, weeks in bed — was as bad as the sores.
What commenters described: I can't believe this is barely upvoted. My first genital herpes outbreak was the worst illness-related pain I've ever had, and only the second worst pain I've ever felt - first was labor contractions. It was worse than an infected pilonidal cyst or a broken bone. Peeing was agony, plus it was itchy.
Limit: First outbreaks are the most severe and are not representative of the condition afterwards; several writers here say theirs is now controlled. One record in the group repeats a claim about transmission that another commenter disputes, and nothing here should be read as information about how the virus spreads.
What the replies added1
I can't believe this is barely upvoted. My first genital herpes outbreak was the worst illness-related pain I've ever had, and only the second worst pain I've ever felt - first was labor contractions. It was worse than an infected pilonidal cyst or a broken bone. Peeing was agony, plus it was itchy.
Source-record spotlights
Genital herpes outbreak! So common but I sure wish I had been without symptoms like most folks. Ouchy!
Very common. I had a gf who got herpes from a tractor seat. This should be talked about more.
herpes - first breakout was during the pandemic after getting vaccinated. Didn’t know until happened. Had to go to the ER, couldn’t walk, sit or go potty. One of the worst pain i ever experienced as a women
Related evidence elsewhere in the index
What the counts show
Across 13 source records, the most common observable tactic structure is “Attach it to an existing routine” (3 records). This is a wording pattern, not a measured outcome.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Observable tactic structures
Counts show source records whose wording matches the tactic structure; biological explanations remain commenter claims unless separately checked below.
Browse the original comments13 preserved records · 13 of 13 source records accounted for
Archive: 13 index entries preserve 13 distinct source records · Every displayed synthesis count resolves to source-record IDs
The chest, the lungs and the heartThe answers where breathing is what triggers the pain. 127 records.
Lungs, pleura and clotsPleurisy, pneumonia, collapsed lungs and clots — the answers where every breath is the trigger.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Lungs, pleura and clots
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Lungs, pleura and clots
Appears when: Lungs, pleura and clots
What the pattern means: The one group where the trigger is involuntary. Writers describe breathing, coughing, sneezing and laughing as the things that hurt, and several say the fear of the next breath was worse than the breath. The pleurisy accounts reach for sandpaper and stabbing; the pneumonia accounts are about the damage the coughing itself does, with cracked ribs and torn muscles recurring. The clot accounts add a different quality — sudden, and in several cases mistaken for something in the abdomen.
What commenters described: Pleurisy. Every breath was like being stabbed in the chest.
Limit: Pleurisy, pneumonia, collapsed lungs and clots are collected here because their writers describe the same trigger, not because they are related. Nothing here distinguishes chest pain of one kind from another, and chest pain is not something a comment thread can help anyone assess.
What the replies added2
Oh wow. Yeah I had it back when I was in the 3rd grade i was out of school for most of the year, what made it worse was where I live alot of people catch Valley Feaver ( which is a fungus infection) so I had pneumonia and valley fever, I live in the central valley here in California and that shit is ALWAYS in the ground. 🙄
Bronchitis almost pneumonia. My muscles in my neck were so tight I couldn't lay down, sit, talk, turn or anything. My boyfriend forced me to go to the er and they told me if I waited ang longer I would've had pneumonia. Or bulemia. My heart is fucked now and I have heart palpitations. As well as digestive issues. Depended on laxatives just to get thru my days. Never again. 3 months clean though💪
Where commenters report limits
Oh wow. Yeah I had it back when I was in the 3rd grade i was out of school for most of the year, what made it worse was where I live alot of people catch Valley Feaver ( which is a fungus infection) so I had pneumonia and valley fever, I live in the central valley here in California and that shit is ALWAYS in the ground. 🙄
I too have given birth. Unfortunately for me I have post thrombotic syndrome in my leg, which was linked to my PE, and that is a fun thing to manage too 😜. Though an ovarian cyst bursting sounds horrific.
Source-record spotlights
Pulmonary embolism
Bacterial pneumonia. The coughing alone does major harm to the muscles and tendons in the chest, shoulders and back. Add a cracked rib and coughing makes you cry
Fucking severe bronchitis. Felt like every rib and muscle and inner organ was cracking and breaking apart and air moving through my lungs hurt so bad. Steroids are a lifesaver.
Related evidence elsewhere in the index
What the counts show
Across 117 source records, the most common observable tactic structure is “Use a sensory reset” (15 records). This is a wording pattern, not a measured outcome.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Observable tactic structures
Counts show source records whose wording matches the tactic structure; biological explanations remain commenter claims unless separately checked below.
Browse the original comments117 preserved records · 117 of 117 source records accounted for
Archive: 117 index entries preserve 117 distinct source records · Every displayed synthesis count resolves to source-record IDs
Heart attacks and heart diseaseCardiac answers, several of them from writers who say they were sent home first.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Heart attacks and heart disease
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Heart attacks and heart disease
Appears when: Heart attacks and heart disease
What the pattern means: Ten records, and the striking thing is how defensive several of them are: writers pre-empt the objection that a heart attack is not an illness. The descriptions are of pressure rather than sharpness, all-consuming and constant. Elsewhere in the corpus the same sensation appears as a misdiagnosis — the gallbladder and pleurisy groups are full of people who thought this was what they were having.
What commenters described: The Widowmaker heart attack. And don't tell me it's not an illness because I was incredibly ill for a few days and am lucky that I survived.
Limit: Ten records is a very thin base and most name the event without describing it. Nothing here distinguishes cardiac pain from anything else, and chest pain needs emergency assessment rather than a comment thread.
Source-record spotlights
Heart attack from extreme SVT. Followed by endometriosis and ovarian cysts bursting.
Heart pain from a stenotic aortic valve.
Heart Disease... Had Triple Bypass a little over 3 weeks ago
What the counts show
This report keeps all 10 source records for Heart attacks and heart disease together and surfaces traceable examples without converting anecdotes into proof.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Browse the original comments10 preserved records · 10 of 10 source records accounted for
Archive: 10 index entries preserve 10 distinct source records · Every displayed synthesis count resolves to source-record IDs
Cancer, and its treatmentAnswers that separate the disease from what was done about it — and often rank the treatment higher. 72 records.
CancerThe disease itself, from the people who had it and the families who watched.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Cancer
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Cancer
Appears when: Cancer
What the pattern means: Two kinds of record sit here. The first-person accounts are usually about where the cancer had spread rather than the tumour itself — a spine, a bone, a nerve — and several writers note that the disease was painless until it was not. The second kind is written by families, describing somebody else's constant pain and their own helplessness. The recurring structural complaint is the years of dismissal before diagnosis, particularly from writers who were young when the pain started.
What commenters described: I was gonna say bone cancer—not leukemia, but the kind that causes tumors to grow on the bone. Mine was particularly bad around one knee. What made it especially awful was that it went largely ignored for the better part of a decade. Because I was young, I was repeatedly treated like a drug seeker/addict, and insurance made getting something as basic as an MRI an uphill battle. Eventually the pain became so debilitating that I couldn’t reliably work because I never knew when I’d suddenly collapse from it. I had to fight tooth and nail just to get doctors to take the pain seriously enough to figure out what was actually happening and even with a good job and insurance, years to pay for it.
Limit: This group mixes people who had cancer with people who watched somebody else have it, and the diagnoses inside it have almost nothing in common. Nothing here is a way to recognise cancer or to interpret any symptom.
What the replies added1
Lymphoma. It broke my sternum.
Source-record spotlights
I hope you are doing well. My family member had this and I remember vividly how much pain he was in...constantly. Sweating profusely due to the pain. My genuine hugs to you.
Love that you survived that, but seeing that it was the most painful hurts my heart. My dad passed from pancreatic cancer and before we knew that’s what it was, he had been complaining about the pain. I knew it had to be bad because my dad never went to the doctor for anything and never complained about pain, he just always worked through it.
Right frontal lobe brain cancer. Felt like someone was inflating a balloon inside your skull and you feel the pressure on the back of your eyes. Oh also constant agonizing pain.
Related evidence elsewhere in the index
What the counts show
Across 54 source records, the most common observable tactic structure is “Use a sensory reset” (2 records). This is a wording pattern, not a measured outcome.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Observable tactic structures
Counts show source records whose wording matches the tactic structure; biological explanations remain commenter claims unless separately checked below.
Browse the original comments54 preserved records · 54 of 54 source records accounted for
Archive: 54 index entries preserve 54 distinct source records · Every displayed synthesis count resolves to source-record IDs
What the cancer treatment felt likeThe answers that separate the treatment from the cancer and put the treatment first.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: What the cancer treatment felt like
Source-backed answers are shown before diagnostics; the complete source archive remains below.
What the cancer treatment felt like
Appears when: What the cancer treatment felt like
What the pattern means: A group that exists because its writers insist on the distinction: the cancer was not the painful part. What they name instead is specific — bone pain from chemotherapy, mouth sores, radiation burns to skin that has to be sat on, drains, a bone-marrow needle felt at every depth, lymph-node tubes removed without anaesthesia. One writer's summary is that the disease was painless and the cure nearly killed him.
What commenters described: Kidney cancer — except the tumor never hurt at all, they found it by accident after a kidney stone. What hurt was everything after: surgery complications, internal bleeding, transfusions, a stent, 19 days in the hospital. The disease was painless. The cure nearly killed me.
Limit: These are individual experiences of particular regimens, some of them from many years ago, and treatment has changed; nothing here predicts what any treatment will feel like for anyone else, and nothing here is a reason to decline one.
What the replies added1
Not the illness, but the treatment. In 2009 I had leukemia. First the bone marrow test. It's done in a series of needles, each one going a little deeper with meds to numb you. I painfully felt each one. Then the first chemo I was on (for nearly 3 months) was in pill form (several each day). My body did not react nicely too it. Muscle spasms so severe morphine didn't touch the pain. Follow by a bowel blockage. I have had surgery and broken bones before that and since with needing little to no pain meds. But those muscles spasms were torture. At least they found a med to control the spasms that gave me relief.
Source-record spotlights
Getting rectal cancer spots cut out. Crying in the bathroom while trying to poop for a week straight the first 2 times. Was all clear the third though!
Throat cancer, the cancer didn't hurt, but the surgery where they gutted my throat and slit my neck to remove 39 lymph nodes was absolutely brutal. And the recovery was horrible
Testicular cancer, getting my nut taken out and then my lymph nodes sucked. Sucked even more when they raw dogged taking out the tubes going to the points where my lymph nodes where. I’ve never cursed in front of old nurses out as much as I did when that happened. They had like 4 people holding me down by both arms (2 and 2) fuck that shit. 7 years good since then ❤️
What the counts show
The exact phrase “the cancer that caused” recurs across 2 of the 18 source records in What the cancer treatment felt like; the complete archive stays available below.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Browse the original comments18 preserved records · 18 of 18 source records accounted for
Archive: 18 index entries preserve 18 distinct source records · Every displayed synthesis count resolves to source-record IDs
Skin and soft tissueThe surface, and the places on it people were least willing to name. 104 records.
Fissures, abscesses and haemorrhoidsThe answers most often prefaced with an apology for naming them.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Fissures, abscesses and haemorrhoids
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Fissures, abscesses and haemorrhoids
Appears when: Fissures, abscesses and haemorrhoids
What the pattern means: The group most often prefaced with an apology, and the one whose writers are most insistent that it should not be. The fissure accounts describe a specific and unusual dynamic: the pain arrives with a routine bodily function, which produces dread of the bathroom, which several writers say was the worst part. The abscess and pilonidal accounts are about the aftermath rather than the event — months of wound packing, drainage done with anaesthetic that did not work, and repeat surgeries.
What commenters described: Anal fissure. Feels like shitting knives and the only thing to heal it is time. The anxiety that bubbles up when you need to go to the bathroom...I hope it never happens again.
Limit: These records describe severe and often repeatedly operated cases, which is not the usual course. Nothing here identifies any of these conditions or indicates a treatment, and several accounts describe delaying care out of embarrassment rather than recommending it.
What the replies added3
I’ve also had a handful of surgeries and broken bones and they don’t even come close to the fissure I’m currently dealing with. I’m doubled over in pain for hours every day fighting the urge to pass out or vomit each time.
This might get a little gross. I had testicular torsion as a kid which was SO much worse than this issue, but this issue is a little more interesting so I'll mention it. Pilonidal Cyst for physical pain at least. Basically a cyst that forms in a sinus that you have from the top of your buttcrack up the small of your back that lies under your skin. The cyst forms when there is a blockage and buildup of stuff in the pilonidal sinus that then gets irritated, swells up, and turns into a Pilonidal Cyst. On the first day it was a little bit of pressure and wasn't concerning. Day 2 was more pressure and extremely slight discomfort. Day 3 was unbearable pain that was so bad that I was going into shock and having flashes of white in my vision. I had issues with Sciatica as well and this cyst felt like it was RIGHT on top of my sciatic nerve so that's probably where a lot of the pain was coming from. I almost crashed my car driving to the urgent care clinic. The doc sliced it open and pushed down so hard on my lower back/upper but that it almost broke the medical table and an ungodly amount of wet concrete looking stuff came followed by yellow pus and finally blood. It was miserable afterward but it was much better after that pressure got released. I had an open wound in my ass for two months that I had to treat, clean, and repack with gauze every three hours like clockwork. Eventually it healed just fine and I haven't had any issues since. Unfortunately sometimes without actual surgery to remove the pilonidal sinus entirely, pilonidal cysts can be a recurring issue. I haven't had any issues with it for three or four years so hopefully it stays that way.
Pilonoidal sinus. I didn't get it seen to, because I was depressed and had body image issues. So it grew to be the biggest the surgeon had seen. I was in pain walking, sitting, and lying on my back. Only lying on my front had no pain. It was a constant sharp pain that, looking back, I'm surprised never became a massive infection issue. Once it was cut out, the wound took over a year to fill up, and is just a mass of scar tissue now. Part of the healing process involved chemically burning the wound area to try and cauterise the new skin. Never again. Although the absolute relief I felt when I finally realised I could exist without pain almost made me cry.
Where commenters report limits
Not for me, but I *did* have a pileonidal cyst that erupted about 4 years prior. Being me is really fun sometimes /s
This might get a little gross. I had testicular torsion as a kid which was SO much worse than this issue, but this issue is a little more interesting so I'll mention it. Pilonidal Cyst for physical pain at least. Basically a cyst that forms in a sinus that you have from the top of your buttcrack up the small of your back that lies under your skin. The cyst forms when there is a blockage and buildup of stuff in the pilonidal sinus that then gets irritated, swells up, and turns into a Pilonidal Cyst. On the first day it was a little bit of pressure and wasn't concerning. Day 2 was more pressure and extremely slight discomfort. Day 3 was unbearable pain that was so bad that I was going into shock and having flashes of white in my vision. I had issues with Sciatica as well and this cyst felt like it was RIGHT on top of my sciatic nerve so that's probably where a lot of the pain was coming from. I almost crashed my car driving to the urgent care clinic. The doc sliced it open and pushed down so hard on my lower back/upper but that it almost broke the medical table and an ungodly amount of wet concrete looking stuff came followed by yellow pus and finally blood. It was miserable afterward but it was much better after that pressure got released. I had an open wound in my ass for two months that I had to treat, clean, and repack with gauze every three hours like clockwork. Eventually it healed just fine and I haven't had any issues since. Unfortunately sometimes without actual surgery to remove the pilonidal sinus entirely, pilonidal cysts can be a recurring issue. I haven't had any issues with it for three or four years so hopefully it stays that way.
Source-record spotlights
Ongoing: endometriosis Shorter term: perianal abscess w/fistula that required 4 surgeries and a year of wound care
Prolapsed piles of
Haemorrhoids - a pain in the but (literally) Way worse than giving birth (without painkillers or anaesthesia). At least when you give birth the pain (mostly) stop after, but after haemorrhoid surgery the pain was still there for 3 weeks.
Related evidence elsewhere in the index
What the counts show
Across 53 source records, the most common observable tactic structure is “Attach it to an existing routine” (2 records). This is a wording pattern, not a measured outcome.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Observable tactic structures
Counts show source records whose wording matches the tactic structure; biological explanations remain commenter claims unless separately checked below.
Browse the original comments53 preserved records · 53 of 53 source records accounted for
Archive: 53 index entries preserve 53 distinct source records · Every displayed synthesis count resolves to source-record IDs
Hidradenitis suppurativaA chronic skin condition whose sufferers found each other in the thread.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Hidradenitis suppurativa
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Hidradenitis suppurativa
Appears when: Hidradenitis suppurativa
What the pattern means: Thirteen records, and what is notable is that they found each other: several are replies to one another rather than separate answers. The condition is described as a baseline plus an event — a constant sunburn-like soreness wherever skin meets skin, punctuated by lesions and drainage. Writers name weight and biologic treatment as things they have tried, with contradictory results.
What commenters described: hidradentis suppertativa - or however the hell its spelled lol. it causes a LOT of different symptoms, but in short my doc described it as "being allergic to your acne and ingrown hairs". my immune system overeacts to any foreign object under my skin and causes giant painful boils and deep tunneling scars once it heals. on a good day i feel like i have mild sunburn in every area of my body that rubs together (armpits, bikini line, behind my knees, etc), and on bad days i can't get out of bed from the pain. that's not even the worst of it though. the worst part is when its an ingrown hair and the hair follicule ruptures. #1 worst pain i ever felt was when my dermatologist lanced one of those ruptured follicles... i blacked out and kicked the poor guy 😭
Limit: Thirteen records from a self-identified group, several of them a single line, is a narrow base. The treatments named worked for some of these writers and not others; none of it is guidance, and nothing here identifies the condition.
What the replies added2
Oof I feel this, hasn't been as bad since I've lost weight but it's still there nagging me from time to time
also 2k comments nd you nd are the only survivors so far!! ive had our pain since i was 9yrs old nd i believe in you!!
Source-record spotlights
Oof I feel this, hasn't been as bad since I've lost weight but it's still there nagging me from time to time
Hidradenitis suppurativa
I’m currently in the process of losing weight and hoping it helps, I also take Humira on a weekly basis but it has done nothing
What the counts show
This report keeps all 13 source records for Hidradenitis suppurativa together and surfaces traceable examples without converting anecdotes into proof.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Browse the original comments13 preserved records · 13 of 13 source records accounted for
Archive: 13 index entries preserve 13 distinct source records · Every displayed synthesis count resolves to source-record IDs
Skin, hives and the itchHives, psoriasis, burns and the itch several writers rank above any pain they have had.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Skin, hives and the itch
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Skin, hives and the itch
Appears when: Skin, hives and the itch
What the pattern means: The group that argues itch belongs on a pain page, and makes the case through swelling, fever and skin that sloughs off. The urticaria accounts describe a whole body covered, clothing becoming unbearable, and standing outside in the snow for relief; several writers never learned what caused it. Alongside them sit anaphylaxis with no identifiable trigger, Stevens-Johnson syndrome, frostbite and severe sunburn — conditions with nothing in common except that the skin is where they happen.
What commenters described: toss-up but I would have to say hives. these things were the most painful things I've ever dealt with. it caused my hands, feet and knees to swell. my feet would be so swollen . the bottom i couldn't walk. I had fevers, vomiting, diarrhea like it's the craziest shit. after a year a specialist put me on meds that work like a charm, but of course insurance denied it & I have to go thru more drug trials before they'll review.
Limit: Several unrelated conditions are grouped by site rather than by cause, and many of these writers say their own was never explained. Nothing here identifies a skin condition or an allergy, and anaphylaxis in particular is an emergency rather than something to research in a thread.
What the replies added2
Im a paramedic so I read this and was like..holy shit. What a debilitating fucking illness. How often are you having these episodes?
WELL THAT FUCKING SUCKS. wth?!?! How scary & I'm sorry you have to deal with that.
Source-record spotlights
I'm seeing a specialist now, who has figured out that these episodes get worse during my period. So she has me on "maintenance meds" the week before and the week of my cycle. With this, I haven't gone into anaphylactic shock since January. But I still get hives often with throat closing, that happens every month. Sometimes twice a month. But it's slowly getting better. Last month I only got hives. The month before that, it was hives and facial swelling.
Pyroderma gangrenosum. An insanely painful skin condition
Poison ivy that went systemic.
Related evidence elsewhere in the index
What the counts show
Across 38 source records, the most common observable tactic structure is “Turn it into a game” (3 records). This is a wording pattern, not a measured outcome.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Observable tactic structures
Counts show source records whose wording matches the tactic structure; biological explanations remain commenter claims unless separately checked below.
Browse the original comments38 preserved records · 38 of 38 source records accounted for
Archive: 38 index entries preserve 38 distinct source records · Every displayed synthesis count resolves to source-record IDs
Surgery, procedures and recoveryAnswers where the operation or the procedure, rather than the illness, is the thing being described. 66 records.
Surgery, and what came afterOperations and recoveries, including the drains, the gas and the ones that went wrong.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Surgery, and what came after
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Surgery, and what came after
Appears when: Surgery, and what came after
What the pattern means: The most matter-of-fact group in the corpus, and the one that most often reports pain being lower than expected — a run of writers say recovery was easier than the illness that led to it. The pain that does surprise them is incidental: the gas pumped in during laparoscopy travelling to the shoulders, drains being pulled out without anaesthesia, a nerve block wearing off at home. The other half of the group is complications — a clipped bile duct, a stent set crooked, a wound infection.
What commenters described: I wouldn’t say it’s a breeze, it’s still major surgery. However, compared to the pain of a gallbladder attack it is MUCH more preferable! I think I was most unprepared for the pain from the gas they pump you with during the surgery, it traveled into my upper shoulders and freaked me out until my surgeon clarified what was happening. It’s been 2 years since I had mine out and life is great without a gallbladder. Good luck with your surgery!
Limit: These records describe individual operations, techniques and eras, including several from decades ago. Nothing here predicts what any operation will feel like, and the recovery advice commenters exchange in this group is theirs, not this page's.
What the replies added1
3. Broken (kneecap) patella the second time; 2. Broken patella the first time; and 1. Recovery from open heart surgery for 3 way bypass. Breathing hurt, coughing was terribly painful, the healing with wires holding my sawed breastbone together was indescribable. I don’t suggest it. But if you need it, it’s worth it.
Where commenters report limits
Not an illness, but I had a multi level fusion and they took bone for grafts from the crowns of my hips. It was anterior/ posterior surgery, so I was fileted like a trout front and back, and the only pain I remember was from my hips. I was in tears and begging for them to give me stronger medication. It turned out that I'm one of the 10% that morphine has no effect. Luckily they changed it to dilaudid.
Source-record spotlights
It wasn’t great for sure but I also appreciated that the surgery happened so fast and the whole team worked so hard to make sure I could keep breastfeeding my daughter. At one point a different nurse let me sleep through meds and when my pain was uncontrollable later the surgeon came in to check on me several times.
Recovery from a lobectomy (removed sections of my lower left lung) due to lung cancer. I honestly wanted to die to just get the pain to stop. I was so dramatic thinking I was going to be like that forever and that was my life from that point on so there's no point in living. 3 months later I was much better and I'm so glad that I didn't do anything rash.
Post embolization syndrome paired with endometritis following uterine artery embolization for a fibroid. Had no idea it could happen, fever, chills, shits, pain worse than labour (had a home birth, unmedicated).
Related evidence elsewhere in the index
What the counts show
Across 49 source records, the most common observable tactic structure is “Turn it into a game” (2 records). This is a wording pattern, not a measured outcome.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Observable tactic structures
Counts show source records whose wording matches the tactic structure; biological explanations remain commenter claims unless separately checked below.
Browse the original comments49 preserved records · 49 of 49 source records accounted for
Archive: 49 index entries preserve 49 distinct source records · Every displayed synthesis count resolves to source-record IDs
Spinal taps, epidurals and spinal-fluid leaksThe procedure, and the headache that follows when it leaks.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Spinal taps, epidurals and spinal-fluid leaks
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Spinal taps, epidurals and spinal-fluid leaks
Appears when: Spinal taps, epidurals and spinal-fluid leaks
What the pattern means: A group about a procedure and its sequel. The distinctive feature is positional: writers describe a headache that is unbearable upright and vanishes the moment they lie flat, which several found more disturbing than the pain. Durations run from days to, in two accounts, years spent horizontal. The treatment described — an autologous blood patch — is itself named by several writers as the most painful part.
What commenters described: Spinal fluid leak headache after a spinal tap, then the subsequent blood patch. So in a 72 hour period, having a needle injected into my spine, 10/10 headache every time I stood up (That went away the moment I laid down. Trippy experience.), then having more needles injected into my spine to push my own blood over the hole to seal it. 0/10 would not recommend.
Limit: Seventeen records covering deliberate procedures, complications and spontaneous leaks together. These are individual outcomes, not the usual one, and nothing here should discourage anybody from a procedure a clinician has recommended.
What the replies added2
Probably the spinal fluid leak. Had a severe headache every day for like 5 months, then got a blood patch which was probably the most painful experience of my life. Wouldn’t wish it on my worst enemy. I’m past it now but I’ve had nightmares about it coming back, and having to redo the blood patch. Every time I get a headache in the back of my head I get freaked out bc I’m scared it’s leaking again. I’ve broken bones, sprained just about everything, dislocated things, and nothing left me as desperate for relief as the leak.
Post-dural Puncture Headache I had a cerebrospinal fluid leak from a misplaced epidural. For 10 days. Couldn't be upright or even sitting without excrutiating pain. Tylenol and advil didnt work. Wikipedia says it feels like searing hot metal. Unfortunately, pretty accurate... the pain was at the base of my skull and between my eyes. I always say it felt like my head was in a panini press. Add photophobia, severe nausea, a crying newborn, and establishing breastfeeding... and a trip to the hospital to get a second epidural where they inject blood into it to try to clot the hole... that failing... I was not ok. Luckily I have an incredible husband who was basically taking care of me and our newborn infant the whole time.
Where commenters report limits
Post-dural Puncture Headache I had a cerebrospinal fluid leak from a misplaced epidural. For 10 days. Couldn't be upright or even sitting without excrutiating pain. Tylenol and advil didnt work. Wikipedia says it feels like searing hot metal. Unfortunately, pretty accurate... the pain was at the base of my skull and between my eyes. I always say it felt like my head was in a panini press. Add photophobia, severe nausea, a crying newborn, and establishing breastfeeding... and a trip to the hospital to get a second epidural where they inject blood into it to try to clot the hole... that failing... I was not ok. Luckily I have an incredible husband who was basically taking care of me and our newborn infant the whole time.
Source-record spotlights
Not technically an illness, but the aftermath of a lumbar puncture/spinal tap. The doctors doing it were quite dismissive of me, so made me get up and walk back to my bed immediately after. After a few hours, worst headache I ever had in my life. Threw up overnight and was left covered in sick for a while. Nurses wouldn't give me pain relief because they thought I was faking the reason for being there in the first place. (Being a woman is great). Got my mum to take me home the next day. Could not sit up for two weeks without excruciating pain in my head, but was terrified to go back to the hospital and be dismissed again. It eventually resolved on its own, but every time I get a headache now I get a little tinge of fear.
Blood patch a year ago. I was very very careful not to mess it up when I finally got treatment after years.
Poorly done spinal tap resulting in a CSF leak. Also adenomyosis. Also lupus/fibromyalgia.
Related evidence elsewhere in the index
What the counts show
Across 17 source records, the most common observable tactic structure is “Use a sensory reset” (4 records). This is a wording pattern, not a measured outcome.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Observable tactic structures
Counts show source records whose wording matches the tactic structure; biological explanations remain commenter claims unless separately checked below.
Browse the original comments17 preserved records · 17 of 17 source records accounted for
Archive: 17 index entries preserve 17 distinct source records · Every displayed synthesis count resolves to source-record IDs
The body's chemistry, its scaffolding, and the long tailMetabolic and connective-tissue answers, plus the conditions only one or two people in the whole thread named. 64 records.
Diabetes, hormones and organ failureMetabolic answers — sugar, thyroid, electrolytes, and organs that stopped.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Diabetes, hormones and organ failure
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Diabetes, hormones and organ failure
Appears when: Diabetes, hormones and organ failure
What the pattern means: The answers where the body's chemistry, rather than a site, is the subject. Electrolytes recur — potassium in particular, described by several writers as producing pain and paralysis they had no framework for. The diabetes accounts are mostly about mismanagement rather than the diagnosis, and several writers describe intravenous replacement as worse than the deficiency. The organ-failure records are the longest here, and describe cascades rather than events.
What commenters described: I suppose not the disease itself, but everything that comes along with it's mismanagement - Type 1 Diabetes. It's a difficult disease to begin with, moreso if you already struggle with mental health. I could barely look after myself for simple everyday tasks, so managing it was incredibly difficult for me at one point. The muscle pain, the feeling of a thousand hot knives stabbing my legs, the weakness, chest pain, headaches, dehydration, the toothaches from the excess sugars rotting my teeth, and then there's the hospital treatment. Low potassium is no joke, and I will tell anyone who will listen that IV potassium could genuinely be used as a form of torture.
Limit: These are rare and serious presentations described by the people who survived them; nothing here is typical of any of the conditions named. Nothing in this group identifies a metabolic problem or indicates a treatment.
What the replies added2
Same happened to my mom... Nobody took her seriously, even when her eyes started twitching...
If you have clinically significant and symptomatic low potassium, no amount of bananas will save you. You have to eat hundreds of bananas to get you back. That's a body equilibrium problem. Also, fun fact: per average serving, watermelon and potatoes both contain more potassium than bananas
Where commenters report limits
Diabetic ketoacidosis. At first it wasn’t that bad, then as it got worse my body flooded with endorphins which was great…then the endorphins wore off
Source-record spotlights
Undiagnosed diabetes. Drank 8 liters of water a day and urinated 10 liters a day; went to the bathroom every 45 minutes. Knew I had it once symptoms started, but took 2-3 weeks for doctor appointment to go through.
Hypophosphatemia from iron infusion. I was gaslit by doctors and told it was anxiety, but infact I almost died from undetectable phosphate. I was on supps for 9 months.
Diabetic (type 1) Ketoacidosis. Shingles is a close second. Frozen shoulder is up there too.
Related evidence elsewhere in the index
What the counts show
Across 25 source records, the most common observable tactic structure is “Turn it into a game” (2 records). This is a wording pattern, not a measured outcome.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Observable tactic structures
Counts show source records whose wording matches the tactic structure; biological explanations remain commenter claims unless separately checked below.
Browse the original comments25 preserved records · 25 of 25 source records accounted for
Archive: 25 index entries preserve 25 distinct source records · Every displayed synthesis count resolves to source-record IDs
Ehlers-Danlos and hypermobilityConnective-tissue disorders described through repeated dislocations rather than one event.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Ehlers-Danlos and hypermobility
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Ehlers-Danlos and hypermobility
Appears when: Ehlers-Danlos and hypermobility
What the pattern means: Described through repetition rather than an episode: joints that dislocate or sublux routinely, a body that feels unstable, and pain distributed across most of it. Writers give a baseline number rather than a peak, and several list the conditions that travel with it. The recurring frustration is that the individual events are unremarkable — a stretch on waking, getting out of a chair — while the accumulation is not.
What commenters described: I have hEDS (Hypermobile Ehlers-Danlos Syndrome) A simple explanation is that my body doesn’t make connective tissue very well. This can affect my skin, digestive system, heart and more. I get a lot of dislocations and subluxations, especially in my ribs, fingers, shoulders, and hips. 90% of my joints hurt all the time, I constantly feel like my body is unstable. My head and neck feel like a bobble-head. The fatigue is crushing. I feel like I’m walking through rough waves most of the time. I live at a 6-8 on the pain scale. Pain management is a joke. Add on the ADHD, MCAS, and POTS and it’s been a real fun 50 years dealing with this. 😒 but I’m still here.
Limit: Fourteen records, several from writers who say they are still trying to be taken seriously or formally diagnosed, so some of these are suspected rather than confirmed. Nothing here identifies a connective-tissue disorder or indicates how to manage one.
Source-record spotlights
My Ehlers-Danlos Syndrome Type hEDS, and all the extra Diagnoses caused by it.
Hypermobile Ehlers-Danlos syndrome.
Ehlers Danlos syndrome and its comorbidities.
Related evidence elsewhere in the index
What the counts show
Across 14 source records, the most common observable tactic structure is “Attach it to an existing routine” (2 records). This is a wording pattern, not a measured outcome.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Observable tactic structures
Counts show source records whose wording matches the tactic structure; biological explanations remain commenter claims unless separately checked below.
Browse the original comments14 preserved records · 14 of 14 source records accounted for
Archive: 14 index entries preserve 14 distinct source records · Every displayed synthesis count resolves to source-record IDs
The one-off answersConditions only one or two people in the entire thread named.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: The one-off answers
Source-backed answers are shown before diagnostics; the complete source archive remains below.
The one-off answers
Appears when: The one-off answers
What the pattern means: Conditions named by only one or two people in the entire thread: sickle cell, ME/CFS, haemophilia, carbon monoxide poisoning, compartment syndrome, a terminal diagnosis, and several illnesses whose writers say no doctor ever named them. The group is kept intact deliberately — the long tail is where the thread stops being a list of famous painful conditions and becomes a record of what individual people actually live with.
What commenters described: Physical pain, Hemophilia. Once you’ve had a good old fashioned joint bleed, you’ll never forget it. Emotionally draining kind of pain , idiopathic pulmonary fibrosis. It’s a hoot, my lungs are turning to stone and I’m slowly suffocating. I’m working on getting a gently used pair of lungs, but that’s a whole process in and of itself
Limit: Each of these appears once or twice, so nothing can be generalised from any of them, and several writers say they are still undiagnosed. Nothing here identifies any condition.
What the replies added1
Ooof I heard that one is a beast, hope you're doing good
Source-record spotlights
Sickle Cell Anemia.
The terminal illness I am dying from
Lymphadema it is a forever thing, legs hurt all the time
What the counts show
This report keeps all 25 source records for The one-off answers together and surfaces traceable examples without converting anecdotes into proof.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Browse the original comments25 preserved records · 25 of 25 source records accounted for
Archive: 25 index entries preserve 25 distinct source records · Every displayed synthesis count resolves to source-record IDs
The answers that were not a physical illness at allRecords that answered the question with something other than a body part, and argued for it. 204 records.
Depression and mental illnessThe second-largest single answer in the thread, and the one that argues most directly with the word “painful”.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Depression and mental illness
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Depression and mental illness
Appears when: Depression and mental illness
What the pattern means: The second-largest single answer in the thread, and the one that argues most directly with the question. Writers do not claim depression hurts like a kidney stone; they make a different case — that the physical answers end and this does not. One commenter puts it as the difference between self-limiting and not. The accounts describe physical pain as a genuine symptom rather than a metaphor, and a large sub-thread beneath the top answer is not about pain at all but about how to stay in contact with somebody who has withdrawn.
What commenters described: This was my first thought also. I've experienced many of the other things in this thread and I would trade major depressive disorder for most of them. At least kidney stones, gallbladder attacks, and shingles, are self-limiting. Depression is the gift that keeps on giving
Limit: These are people describing their own mental illness, not clinicians describing a condition, and medications, therapies and side effects named here are individual experiences with contradictory outcomes. Nothing on this page is a substitute for care. If you are struggling, contact a local crisis line or emergency service.
What the replies added3
This, layered with the heartbreak and betrayal from an avoidant ex discarding me. Completely lost myself. Oh, and broken ribs is up there too
Depression has made it so when I’ve actually gotten hurt be it broken bone, laceration etc, I feel more alive than on a normal day. The mental pain is different. Sometimes when I get a migraine and it goes away I miss it as well.
If I were to put physical pain it would be my crohns and all the surgeries I had to deal with before they discovered whats wrong. However my undiagnosed adhd and severe daily suicidal ideation were worse. My whole life I was told I was lazy, to emotional and stupid, I believed everyone cause thats how i felt and then when I was 28 I went to my dr and broke down crying cause I just couldn't do basic things without all this resistance. So she gets me an appointment to talk to someone, we go through all these questions and at the end I'm told I have adhd and my "laziness" was just because I had a severe problem with executive functioning. The amount of anger and grief I felt at learning that is something I can't even describe. Finally at 37 we found a medication that helps with my suicidal thoughts and I'm on adhd meds and life is still hard but it's far better then the hell hole that was my 20's.
Source-record spotlights
a friend of mine, when I was going through the darkest of days, would come by and force me to go to shows with him. He'd drive, get tickets, beers... I really appreciate what he did.
Sadly it's up to that person, they also have to be willing to do so. I was forcing myself to eat, I was supported, I used my savings to get a therapist ASAP and got meds And still there it took me a year to get a good handle on it, but every day was slightly easier, even if sometimes there were lows. It's been a decade since I felt that low, I still get some lows but I also have the tools to push through, I have my meds to help regulate me, my view on life has become very, I'll deal with the issues of right now, and what comes later I will work through that then. I did some sort of meditative yoga at the time too and it was nice, a thing the teacher said stuck with me well. View your body like a guest house, all sorts of people (feelings) will come through, stay, be on their way, some will be good, some will be bad, but it's passing through.
Anxiety and panic attack, when it was really bad I have it 24/7 I wasn't feeling save even for take a shower and I will feel dizziness if I was outside my home
Related evidence elsewhere in the index
What the counts show
Across 151 source records, the most common observable tactic structure is “Change the sentence” (4 records). This is a wording pattern, not a measured outcome.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Observable tactic structures
Counts show source records whose wording matches the tactic structure; biological explanations remain commenter claims unless separately checked below.
Browse the original comments151 preserved records · 151 of 151 source records accounted for
Archive: 151 index entries preserve 151 distinct source records · Every displayed synthesis count resolves to source-record IDs
Addiction and withdrawalAddiction and withdrawal, usually offered with the writer's own caveat about whether they count.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Addiction and withdrawal
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Addiction and withdrawal
Appears when: Addiction and withdrawal
What the pattern means: Almost every record here opens with a caveat about whether it counts, and then describes something with a shape none of the physical groups have: an illness the writer attributes to their own actions, and a pain with a known cure they are refusing. Withdrawal is described in flu terms plus something the writers say has no physical equivalent. Several accounts include a recovery date, offered as the point of the comment.
What commenters described: Opioid withdrawal. It's a hell I never want to go through again.
Limit: These are personal accounts of addiction and withdrawal, including one writer's assertion about what withdrawal can do medically; none of it is verified here. Withdrawal from alcohol and some other drugs can be dangerous, and nothing on this page is a reason to attempt it without medical support.
What the replies added1
i came here to say addiction but you beat me to it! Congrats on your recovery! i just hit 20 months yesterday. feels like just yesterday i went to rehab.
Source-record spotlights
Mental pain: borderline personality disorder Physical pain: drug addiction (IV user). I've been in recovery since 2019 though 💪🏻
Alcohol withdrawal. Symptoms of the flu plus mental hell on earth. But it doesn’t stop there because it also affects your close family.
i came here to say addiction but you beat me to it! Congrats on your recovery! i just hit 20 months yesterday. feels like just yesterday i went to rehab.
What the counts show
This report keeps all 21 source records for Addiction and withdrawal together and surfaces traceable examples without converting anecdotes into proof.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Browse the original comments21 preserved records · 21 of 21 source records accounted for
Archive: 21 index entries preserve 21 distinct source records · Every displayed synthesis count resolves to source-record IDs
Grief and heartbreakBereavement and heartbreak, described by their writers in physical terms.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Grief and heartbreak
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Grief and heartbreak
Appears when: Grief and heartbreak
What the pattern means: Records that answer a question about illness with bereavement, and defend the answer physically rather than emotionally. Writers describe chest pain at a vet's table, a heart rate matching post-surgical recovery, months of panic attacks, and getting physically sick. The recurring structure is the sudden episode — several writers describe something that arrives out of nowhere in the middle of an ordinary evening and lasts twenty minutes, and reply to each other looking for a name for it.
What commenters described: My mom died a couple weeks ago and I keep having these... I don't know what to call them. They're like micro panic attacks that come on suddenly but don't last super long? It feels like I'm dying for 20 minutes, seemingly out of nowhere because I'm in the middle of reading or eating dinner or even having conversation where nothing really reminds me of her.
Limit: This is a thread of strangers describing grief to each other, not bereavement support, and the reassurance commenters offer one another is theirs. If grief is affecting your health, that is worth taking to a clinician rather than to a comment section.
What the replies added2
Not as painful as a broken knee or ankle though.
If a broken heart could kill I would be long dead.
Source-record spotlights
My mom died a couple weeks ago and I keep having these... I don't know what to call them. They're like micro panic attacks that come on suddenly but don't last super long? It feels like I'm dying for 20 minutes, seemingly out of nowhere because I'm in the middle of reading or eating dinner or even having conversation where nothing really reminds me of her.
My uncle passed away from brain cancer earlier this year. He was in his 60s. He ignored his migraines for so long, turns out it was a tumor. I miss him so much. It doesn't feel real. Not to mention that I have so many stressful things going on in my life, I feel like I haven't had time to grieve at all
it's so hard to heal when your life is still burning around you. i was getting better with therapy and medication, genuinely better, and then my grandmother passed last year. i haven't been okay since and had to estrange myself from both parents for my own health. and then last weekend my father was diagnosed with pancreatic cancer. he refused treatment. i hate him a little for being so content with the wasteland he's leaving behind. when i cut him off, all i wanted was peace of mind until he could do some reflection. maybe one day he could finally be the father i needed. now he has weeks at best and i have to make a decision. it's eating me alive. every door to closure slammed shut in an instant. he doesn't deserve forgiveness, but could i forgive myself if i didn't give him one last chance? fuck cancer.
What the counts show
The exact phrase “a broken heart” recurs across 4 of the 32 source records in Grief and heartbreak; the complete archive stays available below.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Browse the original comments32 preserved records · 32 of 32 source records accounted for
Archive: 32 index entries preserve 32 distinct source records · Every displayed synthesis count resolves to source-record IDs
What the pain did, and what happened when they asked for helpAnswers about duration rather than intensity, and answers whose subject is the encounter with a clinician. 55 records.
Chronic pain, and the illnesses nobody could nameAnswers about duration rather than intensity, including illnesses that were never given a name.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Chronic pain, and the illnesses nobody could name
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Chronic pain, and the illnesses nobody could name
Appears when: Chronic pain, and the illnesses nobody could name
What the pattern means: The answers that decline the premise: the question asks for the most painful, and these writers answer with the longest. Several say explicitly that their pain is not excruciating and that this is the point. The second half of the group is about diagnosis rather than duration — writers on their twelfth doctor, told it is their existing condition, told it is nothing, describing the absence of an answer as the worst part.
What commenters described: i have chronic pain. its not quite excruciating but the fact its 25/7/365 days a year. injurywise iys either ear infection or whem i scraped up my lung/inner chest well while coughing during covid.
Limit: By definition many of these writers do not know what they have, so this group cannot describe any condition. Nothing here identifies a cause of chronic pain or indicates what anybody should do next.
What the replies added2
Ugh! I can’t even count the number of times people say, “Well, you look great!” It’s SOOOO frustrating. If my outer appearance matched how I felt on the inside, people would probably weep with sadness at seeing me 💔 And the comments about parking in a handicapped spot WITH appropriate parking permits…so many Karens have complaints about that. I said I wouldn’t wish lupus on anyone, but maybe if they could feel what it’s like for a day? Heck, even a few hours.
Couldn’t agree more and I’m so sorry that you’re experiencing this too. Lots of love 🫶🏼
Where commenters report limits
What ever I have that doctors 12 different ones can’t tell me what I have and everything they say to do does nothing
Source-record spotlights
Yeah it’s really shown me how the world at large feels about invisible disabilities. “Well you don’t look sick!” Thanks Karen, and you don’t look like a nosy bitch but here we are
I understand completely. Chronic pain starts to affect you mentally. Years untreated changed my personality and made me a more negative person. But don’t give up hope! It took a long time to find what works for me but I did and I got my life back. I wish the best for you.
Living 3 years with an undiagnosed chronic autoimmune disease, fatigue and brain fog like none other
Related evidence elsewhere in the index
What the counts show
Across 19 source records, the most common observable tactic structure is “Attach it to an existing routine” (2 records). This is a wording pattern, not a measured outcome.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Observable tactic structures
Counts show source records whose wording matches the tactic structure; biological explanations remain commenter claims unless separately checked below.
Browse the original comments19 preserved records · 19 of 19 source records accounted for
Archive: 19 index entries preserve 19 distinct source records · Every displayed synthesis count resolves to source-record IDs
Not being believedRecords whose subject is the encounter rather than the sensation: being sent home, being told it was anxiety, being read as a drug seeker.
Condition card naming the illness, what commenters reported the pain was like, and the limits on reading it as anything more: Not being believed
Source-backed answers are shown before diagnostics; the complete source archive remains below.
Not being believed
Appears when: Not being believed
What the pattern means: The only group here whose subject is not a sensation. These records are about the encounter: being told it was anxiety, heartburn, stress or period pain; being read as a drug seeker; being called too young for the condition that was eventually found. Two mechanisms come up repeatedly. Writers who cope quietly say composure was used as evidence against them — the recurring phrase is being too cheerful to be in that much pain. And women in particular describe their pain being reframed as emotional, in accounts that end in gangrene, sepsis and emergency surgery.
What commenters described: It's a pretty common issue that people who deal with chronic pain get really good at blocking it out, then create confusion in the ER when it turns out they have an internal issue that *should* have them on the ground screeching but they're just used to it. The triage team is left guessing and then take the blame when the quiet one finally goes back and their appendix bursts. This happened to BOTH of my parents who are very "suck it up, buttercup" types and I've learned that when I walk into the hospital I am to turn into an absolute pussy without shame. The nurses don't know who's a crybaby and who's a monk, you have to meet them in the middle.
Limit: Every record here is one side of an interaction, told afterwards by the person who was dismissed; no clinician's account is available and none of these cases has been verified. It is a record of how these commenters experienced their care, not a finding about medicine.
What the replies added3
You're a woman! Have you tried not being so hysterical? Maybe finally try losing that baby weight?? Meditation??? I was the opposite, sitting in the lobby with two broken arms, calm but dirty after a fall. The male doctor told me I'd *possibly* sprained them because obviously I wasn't screaming in pain. Hey guess what? Two broken arms! I'm just super calm in an emergency but somehow react like I'm being hunted for sport if I have to make a phone call.
I recently learned that my ability to not scream while in insane amounts of pain is the WORST superpower when it comes to being in an ER. I have now had two instances of things happen to me where I was just sent home and told to take Advil. The first was a gallbladder attack and the second was a ruptured ovarian cyst. Both were more painful than when I broke my leg, but I was told “you’re too cheerful to be in THAT much pain!” Ahahahaah. It sucked a lot for the gallbladder thing because I had to go back, and finally they did a scan and were like ohhh oops, you need surgery right now because this is super bad. Why didn’t you say anything? 🙃🙃🙃
You said "two broken arms" and no one made a joke? Reddit is losing the classics.
Source-record spotlights
You're a woman! Have you tried not being so hysterical? Maybe finally try losing that baby weight?? Meditation??? I was the opposite, sitting in the lobby with two broken arms, calm but dirty after a fall. The male doctor told me I'd *possibly* sprained them because obviously I wasn't screaming in pain. Hey guess what? Two broken arms! I'm just super calm in an emergency but somehow react like I'm being hunted for sport if I have to make a phone call.
"Just take more Tylenol and Ibuprofen." From three different GYNs when complaining of new onset of pelvic pain. As if I'm not living on the max clinical dosage around the clock, eating them gel caps like m&ms as is. I didn't want pain relief recommendations, I wanted an answer for what was wrong. Known history of stage IV endo, and when they actually looked at my remaining ovary, it now consists of five endometriomas and zero normal tissue. I should probably just lose some weight and practice mindfulness.
I was 22. Everyone kept telling me I was too young to get shingles until I finally found a doctor that believed me and gave me medication. I was in so much pain.
Related evidence elsewhere in the index
What the counts show
Across 36 source records, the most common observable tactic structure is “Attach it to an existing routine” (5 records). This is a wording pattern, not a measured outcome.
What commenters explicitly report
These buckets are a deterministic partition based on explicit phrasing in the source text; they are not sentiment scores or effectiveness findings.
Observable tactic structures
Counts show source records whose wording matches the tactic structure; biological explanations remain commenter claims unless separately checked below.
Browse the original comments36 preserved records · 36 of 36 source records accounted for
Archive: 36 index entries preserve 36 distinct source records · Every displayed synthesis count resolves to source-record IDs
How this catalog was built
Source: Reddit comments — 1 thread, 4,423 comments (2,862 top-level, 1,561 replies)
Selected comments from the discussion
This export carries real like counts and timestamps. The first 18 are the most resonant on-topic top-level comment from each stage of the discussion, ranked by resonance within their arrival-time cohort so later arrivals are not penalised for having had less time to accumulate likes. The last 6 received no likes at all and were chosen for the specificity of what they describe.
How the discussion breaks down
Relative volume of distinct source-backed records across every reviewed category in this corpus.
Stones, and the organs that make them
604 distinct coded comment records3 normalized answers
The reproductive and urinary tract
509 distinct coded comment records8 normalized answers
Nerves, the spine and the back
486 distinct coded comment records5 normalized answers
Infections
481 distinct coded comment records10 normalized answers
The gut
398 distinct coded comment records9 normalized answers
The head, the face and the mouth
361 distinct coded comment records6 normalized answers
Bones, joints and muscles
221 distinct coded comment records5 normalized answers
The answers that were not a physical illness at all
204 distinct coded comment records3 normalized answers
The chest, the lungs and the heart
127 distinct coded comment records2 normalized answers
Skin and soft tissue
104 distinct coded comment records3 normalized answers
Cancer, and its treatment
72 distinct coded comment records2 normalized answers
Surgery, procedures and recovery
66 distinct coded comment records2 normalized answers
The body's chemistry, its scaffolding, and the long tail
64 distinct coded comment records3 normalized answers
What the pain did, and what happened when they asked for help
55 distinct coded comment records2 normalized answers
What the thread argues about, in its own words
This thread does not agree with itself, and the disagreement is the most useful thing in it. Two answers dominate the count — kidney stones (273 records) and gallbladder attacks (250) — and the people who have had both do not settle which is worse. One is unequivocal: “I've had both and gallbladder was astonishingly, blindingly so much worse than my kidney stones.” Another, in the same thread, has it the other way round: “I’ve had both gallbladder attacks and kidney stones. Both were incredibly painful but kidney stones slightly more. It actually made me vomit and I couldn’t walk. Gallbladder was removed so I don’t have to worry about that anymore but I’m keeping my fingers crossed kidney stones never find me again.”
The comparison the thread keeps reaching for is childbirth. The most-liked record under kidney stones makes it directly: “I have had an unmedicated c section (had to happen fast, couldn’t get me to numb), and my kidney stones are still 10x more painful than the birth of my child.” One reply explains what the writer thinks the difference actually is: “I passed it on my own - it was 6-7mm. I think the biggest difference is that labour pain comes in waves, and you can generally find some sort of relief by changing positions/walking around (I’m currently 39 weeks pregnant with baby #3). With kidney stones, there was NOTHING I could do to get any kind of relief whatsoever. Every position I tried to move into came with the same level of pain, if not more, and it’s completely relentless until your body randomly decides to pass it. I laboured up to 9cm with my first before any sort of pain relief and I was still joking through contractions. With the kidney stones, I had full body shivering and vomiting just from the pain.”
And the comparison is disputed inside the thread too. A commenter under the gallbladder answer declines to rank it high at all: “Interesting. I wouldn't rank my pain from the gallbladder situation very high compared to other things I've dealt with. They kept offering me drugs and I turned them down most of the time. By then my pain tolerance had increased greatly from prior experiences. Like it was crampy for sure but I've had menstrual cramps worse.” Another rejects the ranking exercise outright: “I don't have to imagine. I've had viral meningitis and two ruptured lumbar discs. Pain is pain is pain. Whatever your experience is, the worst is the worst.”
The other recurring subject is not a disease. 36 records are about the encounter rather than the sensation — being sent home, being told it was anxiety, being read as a drug seeker. The most-liked of them is sarcastic: “You're a woman! Have you tried not being so hysterical? Maybe finally try losing that baby weight?? Meditation??? I was the opposite, sitting in the lobby with two broken arms, calm but dirty after a fall. The male doctor told me I'd *possibly* sprained them because obviously I wasn't screaming in pain. Hey guess what? Two broken arms! I'm just super calm in an emergency but somehow react like I'm being hunted for sport if I have to make a phone call.” Another reports what a doctor said to her: “Prescribed laxatives when I had a bowel blockage on my cecum. I thought I was going to die naked on my floor. And I’ve had kidney stones. This didn’t compare. The ER doctor had the audacity to accuse me of seeking pain meds because “women don’t get 10/10 pain worse than childbirth”. It was later found out I had a blockage after I bled for 2 weeks straight.”
None of that is settled here, and this page does not settle it. What follows is a record of what people said they had and what they said it was like — grouped by condition, with every claim attached to the comment that made it. It is not a severity ranking, it is not diagnostic, and it is not advice.
Browse the original comments4,423 audited comments and replies
Dataset, coverage, and methodology
How this was counted
The working unit is a comment record, not a person and not a distinct condition. All 4,423 canonical comments from this one thread (2,862 top-level, 1,561 replies) were read in eighteen passes in thread order — depth-first from each root comment, so every reply was read beneath the comment it answers — and each was assigned to exactly one condition group or one exclusion bucket.
3,752 records name a painful illness, injury or condition, and all 3,752 appear in the complete index above. The other 671 break down as reactions to somebody else's account (127), bare agreements and one-line endorsements (99), records about a drug, dose or vaccine rather than an illness (91), sympathy and well-wishes (89), questions put to another commenter (82), jokes and one-line gags (74), advice offered to another commenter (61), off-topic tangents (16), comments about how patients in general are treated, naming no illness of the writer's own (11), commentary about the thread itself (10), fragments and unreadable text (7), and records about insurance and hospital logistics (4).
A condition named with no description still counts: the name is the answer. A record that names several conditions is filed under the one its writer calls their own worst; where no ranking is given it is filed under the condition it describes most substantively, and its full text is preserved on that row, so a record counted under one condition may also mention two others.
3,752 counts classified comment records, not distinct conditions and not people. Repeats were deliberately kept: 273 records name kidney stones and 154 name endometriosis, and each stays its own row rather than being merged into one.
Group size is not severity. A large group means many people had that condition and chose to write about it; it says nothing about how much it hurts relative to anything else. The thread itself contains repeated, unresolved arguments about which pain is worst, and about whether pain can be ranked at all.
Heart counts are the raw numbers as captured. The first hour of this thread holds 57.1% of all its hearts, so a ranking by raw hearts would mostly rank arrival time; the themes and groups are ordered by how many records they hold, not by popularity.
Nothing here is verified beyond what people typed. Every condition, symptom, duration and outcome is the commenter's own report, unchecked against any medical record. Drugs, doses, procedures, diets and home remedies named in these records are reported as what that person says was done in their case; none of it is a recommendation, and none of it should be used to identify or treat anything. Read this as a record of what a crowd said it had been through.
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