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Crohn’s & Colitis Community

Get the support you need in managing your Crohn's disease or ulcerative colitis. Participate in discussion boards, hear personal stories, ask questions to our panel of experts and much more.

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Our Stories

Long stressful story

Author Image LisaC00
Joined April 2024

I had been sick all of last year to this year I've been in and out of doctors appointments and hospital all told me ... read more

Freedom from fistula

Author Image Julia529
Joined March 2024

My healing journey started when I was diagnosed with Ulcerative Colitits when I was 23 years old. I was a Flight Attenda... read more

How Ulcerative Colitis ch...

Author Image leondeful
Joined February 2024

How Ulcerative Colitis changed my life By Leon C. DeFulgentis           ... read more

Community Forum

Gluten or not gluten that...
Author Image WinchesterWag
Joined May 16, 2024

I understand the pain. I was told to try gluten free (I had been lacto free since middle school) now the clinic wants me back on normal foods complete....

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Peer Advice please Foods ...
Author Image WinchesterWag
Joined May 16, 2024

Before anyone asks I can not change doctors or specialists as they are mile away in the next province and you don't get the option otherwise I wou....

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Breast augmentation and U...
Author Image bodagel6
Joined May 16, 2024

Limited study has been done expressly on how breast augmentation surgery affects symptoms of UC or IBD duck life. Any significant operation,....

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Expert Q&A

Treatment

Q. I was diagnosed with UC a few months ago. I was put on Uceris then Stelara. I have been in remission since I started the Uceris and am tapering off. I have also been recently diagnosed with inappropriate sinus tachycardia (fast resting heart rate), which seemed to start with the UC symptoms. The cardiologist is not worried about it, but cannot explain why it is happening. I have seen that UC can cause a fast heart rate. Is this true? Should it get better if the UC gets better?

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Special Populations

Q. · My son was diagnosed with a Crohn's flare. He started Remicade and methotrexate & having his 3rd infusion next week. More prednisone was also prescribed since his symptoms haven't improved (his doctor said the symptoms might also be side effects of the Remicade). He sleeps all the time, can't work, and is depressed. My son believes the Remicade isn't working and should try Humira. Do you have any recommendations for him?

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Special Populations

Q. I am wondering if there are ways to help reduce my stress levels related to having a chronic illness in the workplace. Should I tell my supervisor that I have IBD? I feel overwhelmed at times at work and feel like I am not able to complete the task needed on time. I am unsure how to cope.

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