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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

This darn UC

Author Image Gpalma1
Joined December 2022

Hi all, I was dignosed with UC in 2017. Since then my life has completely changed and I am changed too. After 6 years... read more

Twin boys

Author Image Crazedmum
Joined December 2022

My twin sons were diagnosed over years ago with Crohn's, presenting very differently. Ben was severely malnourished,... read more

Newly diagnosed

Author Image Pat
Joined December 2022

I started with abdominal pain, constipation, no appetite,weight lose. Thought I had another diverticulitis attack. Had o... read more

Community Forum

Crohns
Author Image gameofcrohns42
Joined Mar 20, 2023

Social security is a process they gaslighted you normally if you pay on a bill or make payments arrangements they can make you an appointment I recomm....

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any aminosalicylate type ...
Author Image gameofcrohns42
Joined Mar 20, 2023

Keep a good journal write down your triggers meaning foods that aggressive to your stomach or may cause you to flare or inflammation since you can'....

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any aminosalicylate type ...
Author Image Heidi2020
Joined Mar 26, 2023

Newly Diagnosed with Ulcerative Colitis.  I have quite a few allergies, which makes treating this more difficult.  I am wondering if anyone ....

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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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