Crohn's & Colitis Foundation

Crohn's & Colitis Foundation Please report any posts that you believe violate our community guidelines. Repeated offenses may result in being muted or banned.
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The mission of the Crohn's & Colitis Foundation is to cure Crohn's disease and ulcerative colitis, and to improve the quality of life of children and adults affected by these diseases. Community Guidelines:

1) Overview: The Crohn’s & Colitis Foundation reserves the right to remove comments, images, or other content that violate our Community Guidelines. Personal attacks or hateful or objectionabl

e comments will be deleted. This includes language abusive, vulgar, obscene, racist, threatening, or harassing comments, libel, slander, and the use of offensive terms that target specific individuals or groups. Posts, images, and/or videos using such language will be removed.

2) Privacy: We welcome posting photos & videos of personal experiences. However, please do not post overly graphic photos. Do not post personal details or share personal information about others. Conversations that occur outside of this page are the responsibility of the individuals concerned.

3) Links: Do not post anything that advertises or sells products and/or services. Do not post links to research that hasn’t been published by a peer-reviewed research journal. Spam posts will be removed.

4) Fundraising: We know many individuals participate in fundraising activities – either personal or through the Foundation or other organizations. However, no posts promoting an individual or team of fundraisers may be shared on this page.

5) Consult a Doctor: We are not medical professionals and cannot offer medical advice. The information shared on this page is meant to be for educational purposes only and should not replace the care of your physician.

6) Contact: This page is managed by Foundation staff members. If you need to contact an administrator, please send us a direct message or email [email protected]

Your support can create a lasting impact for generations to come.By including the Crohn’s & Colitis Foundation in your p...
06/18/2026

Your support can create a lasting impact for generations to come.

By including the Crohn’s & Colitis Foundation in your planned giving, you can help advance research, improve patient care, and support the IBD community for years ahead.

Learn more about ways to leave your legacy and make a difference for the future of IBD care: https://bit.ly/43ILLG1

It can be challenging to manage IBD as a teenager, but a community of support and understanding makes a difference. IBD ...
06/17/2026

It can be challenging to manage IBD as a teenager, but a community of support and understanding makes a difference. IBD Teen Virtual Support Group is a welcoming space for teens living with Crohn’s disease or ulcerative colitis to connect with friends, share experiences and life hacks, and ask questions about anything.

IBD Teen meets twice each month—to learn more and join the group visit https://bit.ly/4evzVoY

06/17/2026

You can’t always see IBD—but it impacts everything.

Victoria Tyler is an influencer and patient advocate living with ulcerative colitis and a permanent ostomy—and she’s using her platform to speak openly about what life with IBD really looks like.

She’s turning her experience into something others can see, understand, and talk about.

Watch her story and visit https://bit.ly/4gkGbkH for more stories from people living with IBD and resources.

06/16/2026

IBD doesn’t stop at borders—and now, research won’t either. Through the Global IBD Registry (GLIDE), the Foundation is uniting data from diverse patients and health systems worldwide to drive smarter care for Crohn’s disease and ulcerative colitis. Read more about how this Foundation-supported registry is unlocking powerful new insights for people living with IBD. https://bit.ly/4uxjiyj

Every IBD journey is unique—especially for those who’ve faced cancer. The SAPPHIRE Registry is studying how past cancer ...
06/11/2026

Every IBD journey is unique—especially for those who’ve faced cancer. The SAPPHIRE Registry is studying how past cancer experiences connect with IBD care and outcomes. By taking part, you’ll help shape future research and support better care for the IBD community.

Learn more and see if you’re eligible: https://bit.ly/40TJOFA

For some people with ulcerative colitis, surgery isn't giving up on treatment — it's the treatment that finally works.In...
06/11/2026

For some people with ulcerative colitis, surgery isn't giving up on treatment — it's the treatment that finally works.

In this Everyday Health Expert Access video, Alan Moss, MD, breaks down the two main surgical options for UC, what the recovery process really involves, and how quality of life can change after the procedure.

Watch now to learn more about J-pouch surgery, ileostomy, and what to expect on the other side. https://bit.ly/4u4PDw3

06/10/2026

You can’t always see IBD.

Today, the Crohn’s & Colitis Foundation released a powerful new “Spill Your Guts” PSA—bringing real stories of life with Crohn’s disease and ulcerative colitis into the spotlight and challenging the stigma that keeps too many people silent.

Rob Nunnery, Sara Levitt, Saxl Rose, and Victoria Tyler share what living with an invisible illness really looks like—and why no one should have to face it alone.

Watch the video and visit our landing page for more stories from people living with IBD and resources: https://www.crohnscolitisfoundation.org/spillyourguts?utm_campaign=SpillYourGutsPSA&utm_source=social&utm_medium=Facebook&utm_content=SpillYourGutsPSA

06/09/2026

IBD prevention is no longer a distant idea—it’s a core focus of our research. With nearly 1 in 100 people living with IBD, Foundation-supported scientists are uncovering early signals in the gut, immune system, and environment to predict risk and inform earlier action. Read more about how the Foundation is helping shape a future where IBD can be detected sooner, stopped from progressing, and ultimately prevented. https://bit.ly/3R6Uv5N

06/09/2026

Something big is coming tomorrow.

Four real people. Four honest stories about life with Crohn's disease and ulcerative colitis — and why it’s time to stop suffering in silence.

The symptoms you can't see. The mental toll. The days you push through anyway.
IBD is hard to talk about. But not as hard as living with it every day.

Check back tomorrow. 👀

Join us on Tuesday, June 16 at 7 p.m. ET for a special MyIBD Connections webinar ‘We Know Better, We Do Better: Reimagin...
06/08/2026

Join us on Tuesday, June 16 at 7 p.m. ET for a special MyIBD Connections webinar ‘We Know Better, We Do Better: Reimagining IBD Care in the Black Community’.

Experts and advocates will review strategies that can and should shape the future of IBD management for Black/African Americans living with Crohn’s or colitis — including improved access to diagnosis and care, equitable treatment options, and better health outcomes. Get the answers you need during our open Q&A.

Explore our exciting agenda and register today: https://www.crohnscolitisfoundation.org/events/myibd-connections-webinar-the-black/aa-community

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