Crohn’s and Colitis Are Invisible, But We Are Not

By Editorial Team

November 30, 2020

person with the word pain written on them

This month we'll be focusing on sharing personal stories from our community members and patient advocates, as well as sharing resources to help those of you living with Crohn's disease or ulcerative colitis.

We'd love to hear from you as well – here are a few ways to get involved:

Ask your questions:

Receive answers or advice from our team and community. No judgments here! Have a question? ANYTHING at all?

Ask your questions here

person with the word fatigue written on them

Help spread awareness by sharing your own story:

What do you wish people knew about your journey with IBD? What has impacted you the most while living with this invisible illness?

Click here to share your story

person with the word anxiety written on them

Connect socially:

Stay up to date on all things Crohn's and colitis by following us on Twitter, liking us on Facebook (Crohn's Disease / Ulcerative Colitis) or following us on Instagram (Crohn's Disease / Ulcerative Colitis).

Enter our Squatty Potty Giveaway:

We asked, and you answered! During a recent poll survey, many of you provided feedback that you'd be happy to win a Squatty Potty, or you have one and you LOVE it. Keep it for yourself or gift it to a friend.

Our giveaway runs from December 1, 2020 through December 15, 2020. Click here to enter!