I've been told that I have had fuctional dyspepsia, then IBS, then I was told I have a large chance that I have Crohn's. This is kinda freaking me out! I'm a mess and almost everything I've try does not help. I need someone that knows a lot about crohn's and abdominal pain so I can ask questions! Please. I'm scared.
For the last year I've been treated with ibs and functional dyspepsia meds. I have been going down hill so fast in the last two months that my docs just want to start over. I'm being taken off all my meds. The Only ones I can take now are Zofran, for my extreme nausea, and valium for my really bad flare ups that cripple me! I've gone throw 5 really bad ones in the last three weeks(I was on all normal meds for the first two, then added some new ones, then my last one was with very little meds) at first I thought I was having a really bad reaction to some naproxen, but I stoped and ruled that out. I do notice that any NSAIDs I take really mess with my pain though.
I know that's not a lot of info but I just need some questions answered! My docs are starting to go down the abdominal migraine and abdominal epilepsy path, and I don't think its that because they have done little endoscopy info. I DO NOT want to even think I have some form of epilesy. Plus its rare and I highly dought that its that.
Sorry about the limited info but I really just want to get questions asked and answered. My docs have pushed away many choice because of their inablity to think out side of the box till now. I've been suffering for a year now, I'm only 15 , so the faster I can get
diagnosed, the faster my life can crawl out of a hole in hell.
My life has changed so much that I can't do it any more. I need help. PLEASE! Ask if u have any questions. Message me anytime Please I'm very desperate and frustrated at this point. I'm probably giving myself more ulcers as we speak.