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Reply to "Spasmodic Pouch?"

I think Jan can better answer this question and hopefully she will jump on the post

I am not sure cuffitis applies if you have never had UC or a history of chronic inflammation. Perhaps you are still adjusting to your pouch expanding. I do recall experiencing more of what you are describing earlier on in my recovery. I am two years out now and still have that sensation at times but I also have chronic cuffitis. Truthfully that sensation is what often wakes me at night to empty my pouch and I never have nighttime leakage or accidents so in my case I have just kind of gotten accustomed to it. It is definitely a different feeling when you need to empty your pouch than it was when you had a colon. Not sure if that helps it not. Possibly trying the anti spasmodics will help.
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