Just found out about this site as I am a lifetime member as of 3-30-09.
Had UC in '93, wore the bag for 11 months. Now I've turned 40 and for my milestone birthday, I was blessed with Crohn's and the bag! Just wanted to get on here and chitchat with you folks who are walking in the same shoes I am. Talk shop, you know, all the things we ostomates deal with on a daily basis. Anyone out there, I'd love to talk. I am in Cleveland, Ohio, had my surgery at the Cleveland Clinic. Actually, right now I'm still on the mend. The doctors put a suprapubic tube (for urine) in me as well, so there is no activity out the back or front. Go back on 9-18 to get opened up again to remove my "J"-pouch from '93, make sure the healing is complete, take the "P" tube out, staple me back up, and only have to deal with the ostomy bag.
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First off, this is a pretty cool site with 37,000 members who truly understand you.
It's not all about ostomy. We talk about everything.
Many come here for advice or to give advice, others have found good friends, and some have even found love. Most importantly, people here are honest and genuinely care.
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Create an account and you will be amazed by the warmth of this community.
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Hollister
Urinary tract infections can still occur after urostomy surgery.
Learn about some basic diet and ostomy pouch routines that can help prevent them.
Learn about some basic diet and ostomy pouch routines that can help prevent them.