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With the small amount of colon we have left, is it still possible to get microscopic colitis and know about it?

I’ve been having symptoms that might point that way, but I’ve also been taking medications (not connected to j-pouch) that could be causing the symptoms as side effects.

Don’t you love it when medications have a list of side effects as long as your arm so it’s almost impossible to know what is the medication and what is an actual medical problem that you might need to get investigated?

The wait to see anyone GI about this would be loooong so I just thought I’d check with you guys before going down that road. It would be a lot easier to get permission from my autonomic specialist to stop the medications for a few weeks to see whether things improve so I’ll probably try that option first.

Update: I was able to stop both medications (with doctor approval), and the symptoms have reduced a lot. Phew!

Last edited by Kushami
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Hello,

having been diagnosed with cuffitis last October, I can relate to exactly your experience. I restarted a medication after the pouchoscopy unrelated to my pouch.

I had a month of absolute hell with cramps, diarrhea and horrible butt burn.

when I stopped that medication my awful symptoms alleviated. When I restarted it one month later, symptoms returned, so I discontinued that drug permanently.

I (and am assuming we) have to be very careful introducing new drugs and be on the lookout for side affects that can mimic cuffitis, pouchitis, etc.

my new plumbing is very picky when it comes to new drugs and new foods. It can get very upset with me when I change my routine😫

@New577 posted:

Hello,

having been diagnosed with cuffitis last October, I can relate to exactly your experience. I restarted a medication after the pouchoscopy unrelated to my pouch.

I had a month of absolute hell with cramps, diarrhea and horrible butt burn.

when I stopped that medication my awful symptoms alleviated. When I restarted it one month later, symptoms returned, so I discontinued that drug permanently.

I (and am assuming we) have to be very careful introducing new drugs and be on the lookout for side affects that can mimic cuffitis, pouchitis, etc.

my new plumbing is very picky when it comes to new drugs and new foods. It can get very upset with me when I change my routine😫

Hmm, that is very interesting to hear. I am sorry you had such a hard time but am glad you were able to work out what was causing the problem and stop taking the medication.

Just heard back from my specialist and got the okay to stop one of the two possible culprit medications. It has definitely been giving me nightmares and exhausting stress dreams, so I needed to stop it anyway. Will see if my diarrhea and cramps go away as well.

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