Welcome to the
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.


Our Stories


Author Image Leapyearink
Joined May 2024

Five years ago my "gut blew up". My body, which was always prone to constipation, saw me on the toilet and a s... read more

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

Community Forum

Exploring Nutrition Throu...
Author Image jacklogon
Joined Jul 23, 2024

Explore nutrition like never before with our engaging 3D animated videos. Dive into insightful content about diet and health, presented in vivid detai....

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Study Abroad and Access t...
Author Image gsdw22
Joined Jun 27, 2024

VoIP facilitates enhanced collaboration through features such as video conferencing, screen sharing, and instant messaging. These tools enable real-ti....

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Skyrizi weight loss and o...
Author Image jdrdrd3
Joined Jul 21, 2024

The brand's dedication to innovation is evident in their development of cutting-edge skincare technologies and trends. They frequently introduce n....

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Expert Q&A


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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