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irritated bladder?


Wed, February 25, 2009 11:30 PM

It feels like I have to urnate all the time.  I have tested for a UTI and the last time I was okay- the time before I had an infection.  I cannot tell.  Does anyone have this?  I can deal with this - at night it is a bit annoying because it wakes me up.  I mean it is better than running to the bathroom for the other but it still I just wonder if it is part of the UC or part of the side effects of the steroids or asacol?

FPO asohn
Joined Dec 22, 2008

Mon, March 09, 2009 10:49 PM

 Reply posted for breezy.

I have uc and interstitial cystitis.  Interesting timing, they both presented at the same time.  When I am on Prednisone for the uc, if I am on more than 20 mg. per day, I have no bladder pain, but as soon as I taper lower, the bladder pain is impossible.  Diet helps but meds are critical.  Elmiron is first in importance, and Atarax and Elavil help as well.  The inflammation actually shrinks your bladder capacity, so frequency is a problem, but the pain without an infection distinguishes it from other urinary problems.  It is an inflammatory response so there must be a connection with the IBD but my urologist didn't have any other patients with both of these problems.  Comforting to know others have this same connection.  Also, my ic tends to flare in the spring and my dr. says this is common.  Not sure why but it has something to do with a histamine release that worsens the bladder condition.  Any others with both IBD and IC?

FPO darlene
Joined May 19, 2008

Sat, March 07, 2009 2:36 PM

 Reply posted for asohn.

I'm not sure if it is a side effect to the medication.  I wish I could answer that.

I have Interstitial Cystitis along with Crohn's, IBS and a Hiatus Hernia.  Cystitis is a chronic inflammation of the bladder.  I was have up to 4 UTI's a month.  I was miserable.  So I put my foot down, went to the doctor and said I want a referral to a urologist to find out what the problem is.  The urologist scoped my bladder (wasn't painful at all) and said I had the Cystitis.  The only way to allievate the chronic flare ups - diet.  And it is a drastic one.  And if I eat or drink something I am not suppose to, bam, the pain is excruciating. 

I didn't have this problem until I developed Crohn's.

FPO aca11
Joined Mar 3, 2009

Thu, February 26, 2009 1:00 AM

 Reply posted for asohn.

I have noticed that recently also! I have UC and take Asacol. I would normally wake up during the night because I had diarrhea but now that is becoming more controlled but I'm waking up to urinate. I have tried to not drink anything before going to bed, but it doesn't matter!

FPO aimee
Joined Feb 16, 2009

Thu, February 26, 2009 1:00 AM

 Reply posted for asohn.

I think it is the steroids.  Everytime I change dosage, I spend ALOT of my day in the potty.  My gastro doc says it is not that but I think it is. The urgency to urinate is sometimes so bad that I have leaked.  It takes a few days and it starts to "calm" down. 

Breezy

FPO breezy
Joined Jan 5, 2009

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