Crohn's & Colitis Foundation

Our Mission: To cure Crohn's disease and ulcerative colitis, and to improve the quality of life of children and adults affected by these diseases.

[Crohn's & Colitis Foundation @CrohnsColitisFn]

Living with Crohn’s disease or ulcerative colitis? You don’t have to navigate it alone.
The Power of Two connects people with IBD to trained volunteer mentors for goal-focused conversations. Whether you're learning to manage your care as a young adult, looking to improve your eating habits, or considering ostomy surgery, mentors share their lived experience to provide real-world guidance and help you build confidence.

Applications are open for mentors and mentees—see if the new Power of Two is right for you: https://t.co/3w96s6T4ds

[Crohn's & Colitis Foundation @CrohnsColitisFn]

You can’t always see IBD—but it’s always there.

Sara Levitt is a content creator and model living with Crohn’s disease and a permanent ostomy—sharing what life really looks like beyond the highlight reel.

She’s opening the door to conversations most people avoid.

Watch her story and visit https://t.co/p5eguD5Il3 for more stories from people living with IBD and resources.

[Crohn's & Colitis Foundation @CrohnsColitisFn]

The 2026 Team Challenge jerseys are here! 🚴💜

On July 25, our team of 20 will take on the Spellbound Century in New Jersey, already having raised more than $55,000 to support those affected by IBD.

[Crohn's & Colitis Foundation @CrohnsColitisFn]

Get to know our tools designed to support you at every stage of life with IBD—from prepping for an endoscopy to aging with IBD. Explore our trusted app list for symptom, diet, and mental health support, plus expanded MyIBD Connections programs for diverse communities. Read more about these powerful new resources and tap the link to start building your IBD toolkit today. https://t.co/STnbCrcN9M

[Crohn's & Colitis Foundation @CrohnsColitisFn]

Happy Independence Day!

Whether you're firing up the grill or gathering with family and friends, delicious food should be part of the celebration. Explore Gut Friendly Recipes, our free recipe finder featuring 500+ dietitian-approved dishes designed for people with IBD. https://t.co/Op4nUQeLMz

[Crohn's & Colitis Foundation @CrohnsColitisFn]

Need a sweet way to cool down this summer?

These Apple, Peach & Strawberry Popsicles are made with just a handful of ingredients and are a refreshing frozen treat for warm days. Plus, they're easy to make and naturally packed with fruity flavor.

Head to the link for the full step-by-step recipe, and don't forget to explore Gut Friendly Recipes, the Foundation's free recipe finder featuring 500+ easy, dietitian-approved recipes for every meal, snack, and season

https://t.co/9tttCPRdDG

[Crohn's & Colitis Foundation @CrohnsColitisFn]

“Everyone here just gets it.”

That’s the power of Camp Oasis—our camp for kids and teens with IBD. New data from the Foundation show Camp Oasis campers are nearly 50% less likely to feel embarrassed about their IBD after attending, underscoring the camp’s impact.

Read more about how our Camp Oasis experience is creating confidence, connection, and belonging for kids with IBD. https://t.co/uAoOkUAZYi

[Crohn's & Colitis Foundation @CrohnsColitisFn]

Taco night just got a summer upgrade.

These fish tacos are packed with fresh flavor—flaky cod, pineapple salsa, and a creamy cashew crema—and come together in just 35 minutes.

Head to the link for the full step-by-step recipe, then explore Gut Friendly Recipes, the Foundation’s free recipe finder with 500+ dietitian-approved dishes to help make mealtime easier:
https://t.co/Op4nUQeLMz

[Crohn's & Colitis Foundation @CrohnsColitisFn]

What exactly is a "Barbie butt," and what is it like living with one?

Sara Levitt—Foundation social media ambassador, model, and content creator living with Crohn's disease—is answering your questions from our Let's Go There: Ask Me Anything poll. From life with an ostomy to surgery, body image, and everything in between, she's getting real about her experience.

Watch the video to hear Sara's answers. 💜 #LetsGoThere

[Crohn's & Colitis Foundation @CrohnsColitisFn]

Got questions about Crohn's disease or ulcerative colitis?

Alan Moss, MD, Chief Scientific Officer at the Crohn's & Colitis Foundation, is launching a new series, Crohn's & Colitis Mythbusting, to separate fact from fiction.

What questions do you want answered? Comment 👇

[Crohn's & Colitis Foundation @CrohnsColitisFn]

You can’t always see IBD—but for Rob Nunnery, it’s part of every day.

A professional pickleball player living with Crohn’s disease and a permanent ostomy, Rob is redefining what strength looks like while opening up about the realities of life with an invisible illness.

His story is just one of many featured in the Crohn’s & Colitis Foundation’s “Spill Your Guts” PSA.

Watch his story and visit https://t.co/p5eguD5Il3 for more stories from people living with IBD and resources.

[Crohn's & Colitis Foundation @CrohnsColitisFn]

New data from a Crohn’s & Colitis Foundation survey reveals young adults with IBD face growing barriers to care, including step therapy requirements. Nearly 1 in 5 report taking on extra work to afford care, highlighting the financial strain during this life stage. Learn how these challenges are shaping access to care—and what needs to change. https://t.co/VRNaKvgc6J

[Crohn's & Colitis Foundation @CrohnsColitisFn]

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://t.co/HNVLrRrGFA #sponsored

[Crohn's & Colitis Foundation @CrohnsColitisFn]

Today, we commemorate Juneteenth. Click the link in our bio for resources on IBD in the Black/African American community.

https://t.co/9YoD75B49n

[Crohn's & Colitis Foundation @CrohnsColitisFn]

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 & life hacks & ask questions about anything. Learn more & find your community of support at https://t.co/oPIV2Qjvw0

[Crohn's & Colitis Foundation @CrohnsColitisFn]

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://t.co/p5eguD5Il3 for more stories from people living with IBD and resources.

[Crohn's & Colitis Foundation @CrohnsColitisFn]

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://t.co/wO4MUD10fk

[Crohn's & Colitis Foundation @CrohnsColitisFn]

If you are an adult with moderate to severe ulcerative colitis (UC) who has failed at least one other therapy, you may be eligible for the KWAN study evaluating the efficacy and safety of using a combination of the study drug LY4268989 and mirikizumab compared to mirikizumab alone in treating UC.

Click here to learn more: https://t.co/fAmbfQIZKP

#clinicalresearch #sponsored #UlcerativeColitis

[Crohn's & Colitis Foundation @CrohnsColitisFn]

Experiencing frequent cramping, urgency, constipation, loss of appetite, or other disruptive digestive symptoms? You are not alone.

Join us for a special community webinar to hear experts and advocates review the importance of gut health for your overall well-being, what your symptoms may mean, when you should contact a physician.

Understanding Your Gu
📅 DATE: Tuesday, June 23
⌚TIME: 7–8 p.m. ET

Don’t miss the Q&A with our presenters! Come get the answers you need and hear about resources to help improve your quality of life--register today: https://t.co/AjFm5NO28t

[Crohn's & Colitis Foundation @CrohnsColitisFn]

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://t.co/jyOJUiKnKy