For over two years now my wife (now 34) has been having “attacks” of massive upper abdominal pain. We’ve seen so many doctors and had so many tests, but none have found the source of the pain. The pain is all around the front just under the ribcage and radiates around the back. It’s like an inch or two wide ring of pain. The pain comes and goes, but she usually has at least a minor attack every day. The attacks last from a few minutes to 17 hours. She describes the pain as “vice-like”, meaning it’s someone is tightening a vice around one of her
organsOrgan-1 nr. Every few months the pain gets just terrible and we make a trip to the ER. She has given birth to our 3 children without any painkillers and says this pain gets way worse than childbirth. The strange part about hers, which seems to differ from lots of posts I have read, is that there are no other symptoms and no triggers that we can identify. The ONLY symptom is massive pain. There is no diarrhea or nausea most of the time (only
twiceTwice-a-day ever, probably a coincidence). The attacks seem totally random as far as we can tell. They don’t appear to be caused by diet (hers is low fat anyway) or anything else we can identify. The only pattern is that the attacks seem to occur most frequently around 4am. She has had tons of tests and they haven’t revealed the source of the pain.
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The pain started while she was pregnant with our 3rd child and they thought it was just heartburn. A few weeks after delivery she had her first real bad attack and we took her to the ER (first of many trips). They said they saw gallstones, and that sure seemed like a likely cause for her symptoms so they took out her gall bladder. Well as you guessed, that didn’t make any difference. Nothing seems to relieve the pain, however balling up in a fetal position with her knees down and her back up feels a little better than laying on her back or side when she is having pain. Also when they give her morphine in the ER, it seems to make the pain worse, not better. Since then we have had the following tests:
1) 2 ERCPs, one with a Sphincter Of Odimenometry. Both gave her massive pancreatitus (pancreatitis) and the pain felt exactly the same (however other times she has attacks the blood tests don’t show pancreatitus (pancreatitis)). Sphinter Of Odimenometry came back showing no problems, but the DR couldn’t get everywhere he needed to to test the pressures so this is still a small possibility, but they said we should never do that again because it caused the severe pancreatitis
2) 2 upper and lower GI cat scans
3) MRI
4) Endoscopy
5) Colonoscopy
6) Abdominal ultrasound
7) Kidney ultrasound (showed a slight calcification, but DR didn’t think it’s the cause of the pain)
8) IVP
9) EKG
10) Blood tests (showed she was slightly anemic)
11) Urinalysis
12) Stool sample
13) 2 chest x-rays
14) Allergy testing
15) Anti-Nuclear Antibody (ANA) test with results of 1/640, which is abnormally high. We are seeing a Rhumatologist now to see if it could be a connective tissue disorder like Lupus, but he said pain this severe is not usually associated with those type of diseases.
Here is a list of medications and other things we’ve tried:
1) Demerol (does nothing for the pain)
2) Percoset
3) Antacids
4) Zantac / acid inhibitor
5) GI cocktails (pain got better one time after taking one, but other times it didn’t help)
6) Levsin
7) Carafate
8) Papaya Enzyme
9) Celebrex
10) Zoloft
11) Allegra
12) Neurontin
13) Some medicine for a spastic colon
14) Sleeping upright
15) Waking up to urinate before bladder fills to much
16) Morphine (we think it may make the pain worse)
17) Vioxx
18) Ativan (last time in the ER about 20 minutes after she took this, the pain got much better. She had also just taken a GI cocktail. We don’t know of either of these helped or it was a coincidence. We’ll try again next time in the ER.
Does anyone have any clues what this could be? Any suggestions on tests to ask for? Any suggestions on anything to try to relieve the pain?
Thanks very much for your help,
Guy Kendall (guy.***@****)
I had the same attacks you discribe for a number of years. My first one was when I was 16 (I'm 36)they came on and off every 3 months or so for many years. Then one day they just kept coming and didn't end until last week. In my case I always got them at night. At first it felt like alot of gas pressure. I'd get up walk around they would go away. The pain has been it's worst just these past 2 years. They'd start sometime during the night and sometimes wouldn't go away until lunch time. The pain was always in the same spot right under the sturmun and radiate to the back - sometimes the back pain was just as bad.
I just recently found a Dr after several - who knew when I walked in what was wrong. The opening to my bile duct didn't open enough to let the bile out, so for years it backed up into my gallbladder. Then my gallbladder failed and had to go. When the gallbladder wasn't there to take the back up my liver started showing signs of problems then my pancreas. I was in so much pain and not one of the Drs would even concider the bile duct. They all just threw their hands up and said no can't be that. Well it was and last week I had the surgery to fix it and haven't had pain since. I really feel like a new person.
Guy
If you live in Georgia (I do) I really would suggest the Borland Groover Clinic in Jacksonville. Even if SOD isn't what you have. I'm sure would be able to help you. Look them up at borland-groover.com I have military insurance and they were able to work with me. They'd jump over hoops to help.
I have severe upper abdominal pain that comes and goes but when i have it it radiates to my back. I went in emergency last week they just did blood tests gave me dilaudid and sent me home. It is back and i get alot of gas bubbling in my stomach at night all night long and it burns when i have to go potty.
I did wake up last week in the middle of the night with acid in my throat but i have no burning in my esophagus.
I dont have medical insurance but have to go back to get tests done. Does anyone have these symptoms. Upper stomach sore to the touch, hurts alot, i have diahrea with any fatty foods i eat immediately and it burns. All bowel movements burn like there is acid in them. I have severe pain in my upper tummy like somone punched me, it hurts to breathe.
Is this my gallbladder? what kind of tests do i need. I am so scared now cause this is getting worse.
The pain is so severe i cannot stand it. I am taking maalox and tagamet but it does not good.
Doctors at the hospital said blood tests were normal and sent me home but i am in severe pain and can hardly eat anything that doesent make me have diahrea.
Please any suggestions, i need help with this one. I am scared
My pain is still there under my ribs but not servere. I do not eat anything after 8 o'clock at night and only sip on water if thirsty..That way my digestive tract gets a rest and hopefully there will be no more early morning attacks......I'll keep posting and let you know how I'm doing...........Aniee
e.....yeah, right!
I am a 23 year old female. One and a half years ago I ended up in the emergency room after an evening of extreme pain. I had gall stones (hereditary) and had emergency surgery that evening to remove my gall bladder. 4 or 5 days later I had my first attack of the pain. The pain is located directly under the zyphoid process, or point where the ribs meet at the bottom. It feels like a giant knot, or someone squeezing, and it is unbearable. There are times when I feel a mild burning sensation, but not always. I cannot function in any capacity until it is gone. I usually stand up, leaning over a table or desk until the pain has passed. During the first attack I got extremely hot, but that doesn't happen all the time. Sometimes I feel a little nauseous, but not always. Sometimes it is immediately followed by a bowel movement, but not always. I've found no link to diet or menstrual cycle. An attack lasts no more than 5-10 minutes. Attacks occur anytime of day or night (and at night they are so painful they wake me up and I am unable to fall asleep until they pass). The attacks can happen once every 3 months, once every week, and once I even had 2 in a row. Recently a dull version of the pain has become more constant. I have also found that since my gall bladder was removed, feeling hungry has become uncomfortable and slightly painful. There is only one way I've found that I can trigger an attack, drinking alcohol (not just one drink, but going out to a bar kind of drinking). That works most of the time, not all the time.
I have had bloodwork, x-rays of my abdomen, ultrasound, an endoscopy, an IVP, and a CAT-scan. Visiting a doctor or the emergency room is a waste, as the pain is so brief that it has passed before I can be seen. I've been put on Zantac, Prilosec, GI cocktails, etc., but the pain is so random and short in length that it is impossible to tell if anything has helped. The surgeon that removed my gall bladder thinks the next step is exploratory surgery, and I would be more than willing to do that if it would give me an answer. I will do whatever it takes to not have to live with this condition any longer. (Unfortunately I am currently without health insurance, so I have no choice but to deal with the pain for a few more months.)
I will continue to check back to find out if anyone has any definitive answers.
I can tell you during the year and a half that I suffered with the biliary pain. There were times on and off that I would get the strangest stomach aches. Felt like I had food poisoning or something. It wasn't until I had pancreatitis that I figured out that I was having pancreatitis like attacks all along. My Dr told me months before that Chronic pancreatitis is very hard to diagnose ,because it can go on without changes in your blood work. Like me the signs came and went before I had a chance to see a Dr. Since my sphincterotomy I have had no biliary pain, and only minor gas pain in the area of the pancreas which I'm told will go away once everything is healed. I feel for me the risk involved with the ERCP with menometry was completely worth it. I have now been pain free for 3 weeks.
The only thing I know about the pancreas is if it is Chronic pancreatitis this will cure it in most cases. (this is what I was told) Look up borland-groover.com and research sphincter of oddi dysfunction. Good luck I hope this helps you. So many people on this forum are not willing to take the risk of this test, and seem to stick with probotics or other natural rememedies. To me I'd rather get rid of the pain for good.