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I'm trying to decide next steps and have these questions for anyone who has actually been diagnosed with mucosal prolapse:

1) How long after surgery to connect the j-pouch were you diagnosed?

2) With what examinations or tests were you diagnosed?  And if you know, what degree of occlusion did the condition cause?

3) What were your symptoms? Difficulty evacuating? Leaking? Frequency? Spasm? Other?

4) What medical and/or surgical treatments have you tried and - what worked?

Thanks!

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