I’m looking to see if anyone else on here is an ostomy brother or sister? I’d enjoy hearing your stories and will share mine as well! Stoma buddies have to stick together!
Stoma buddies
- Thread starter Cathy B. (1224212482)
- Start date
I’m not familiar with a J pouch. I have Interstitial Cystitis, and can’t use my native bladder anymore. 14 years ago I got a Continent urinary diversion, it ended up leaking about 3 years ago, we tried everything even surgery last Oct to make it work again but it didn’t. So on March 20th I converted to a full time ostomy.
I had an ex with UC I know how terribly frustrating it is!
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