I've had recurrent pouchitis that I can get remitted by Flagyl but after I go off of the antibiotic I'm back at in the same boat within a few days or weeks after. Ive tried Endocort, I was good while on it bad again when off of it. Dr thinks I have Crohns because of location of inflammation in my pouch even tho biopsies say pouchitis.
What's the next step for treatment that everyone graduates to from here? I that no dr wants to use Remicade or 6mp...not sure if he really knows what to do with me. I feel like I know more than my doctor sometimes. I'm so frustrated and depressed living in pain constantly. I've been trying to eliminate gluten, fodmaps, taking leaky gut supplements and collagen. Is this going to do any good?
I have always thought if I couldn't take it anymore I could go with a ostomy, but with the dr thinking that I have Crohns doesn't that mean I might still be at risk for inflammation elsewhere?