Chronic Abdominal Pain
I have had acute abdominal pain since April 2011 and it has escalated over the months.. The pain begins early morning, remains unrelenting and escalates throughout the day. It is sharp at times and gnawing most of the time. It radiates down from my sternum and to the lower left of my abdomen. My family doctor nor GI specialists cannot find the cause. I have had CT scans, ultrasound, video capsule endoscopy, colonoscopy, blood tests, push endoscope, H pylori tests, ova stool test for parasites and MRI, to name a few. EVERY test result has been returned as "unremarkable"--no cause found. I am currently taking Paxil 25mg, Nexium and Oxycodein for the pain. Nothing has helped me determine the source of this pain. I am reaching out to this community to see is anyone has a similar experience.
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Hello. I feel so compelled to reply to you as I believe I am reading about myself--minus the weight loss. I am 1.5 years into what must be a maddening debilitating brain-gut disorder causing extreme daily bloat, gas buildup, etc. I have given up on all G.I. docs--out of 6, I have seen 2 who thought "out-of-the-box" to attempt to help me. I have also had every type of CT, MRI, gastro test x2 out there. Normal except slow motility. All Rx's, and even non-Rx's do not help me. My reject box of meds has grown (thank you,
Amazon!). I do a considerable amount of reading and attempt modalities on my own. I referred myself to the Cleveland Clinic G.I. team and their doc told my last G.I. doc what further tests I needed. However, after those results didn't yield anything besides slow motility, she basically threw up her hands.
I had spine surgery 14 months ago and got COVID. Both of those undoubtedly play into my condition. IBS-C is definitely what I have. I have seen a pelvic floor P/T who has helped me more than any doc. But still I suffer. Best of luck to you.
Thank you, I know I have IBS-C, I have had it for a long time. The new thing is the abdominal pain when I eat or drink. Do you know what tests they ordered? I would be interested to see what they looked at. I am considering Mayo Clinic or Cleveland Clinic but am hesitant since I have been to Hopkins years ago and UPenn both which were supposed to be leading edge programs. The thought of starting over again... is just overwhelming as well as the travel that would be needed. Thanks for your insights and if you are comfortable please let me know what additional tests they ordered.
The tests that the C.C doc ordered were: 1. Sitz marker test; and 2. Colonic motility test. The Sitz marker test can be done at most radiology/imaging centers. The colonic test I had to go to the University of Washington medical center for it. Just an fyi.
Thanks, I have had the site marker test and 10 of the 12 markers were still in the colon 6 days after the test. I have not had a colonic motility test.
I am so sorry to know this. I experienced something similar when none of the doctors in Germany or India could find anything wrong with my body despite me telling them of the unimaginable pain I feel in my lower abdomen and when all the results came back normal they asked me to consult with a psychiatrist. I did not listen to this because I knew the pain I felt was something wrong with my body and not mind. DO NOT stop listening to your body even when the doctors ask you to. I was diagnosed with a tumor and a genetic disorder after I ended up in the ER with blood coming out of my stools. That is when they finally took me seriously. I believe I have IBS-C too, and what greatly helps me is this medicine called Bullrich Healing Clay tablets. Also, staying hydrated is what I found out to be extremely helpful. Doctors have not been of much help.
Thank you for sharing your story—I'm so sorry you had to go through such a difficult and painful experience just to be taken seriously. It's incredibly frustrating how often people, especially women, are told their symptoms are psychological when they know something is truly wrong in their body.
If you're comfortable sharing more, I’d be interested to know: what kind of tumor were you eventually diagnosed with, and what was the genetic disorder they discovered? Also, how long have you been taking the Bullrich Healing Clay tablets, and have they made a noticeable difference for you?
I really appreciate your openness—your story is a powerful reminder to trust ourselves and keep pushing for answers.
likely is mesenteric panniculitis