If you are a young person living with Crohn’s disease or ulcerative colitis, or a parent/caregiver supporting one, you know that the reality is that managing a chronic health condition is complex. On any given day, you might be juggling appointments, managing symptoms, remembering medications, and finding the right tools to stay on track.

Have you ever wondered if the apps, resources, and community support you use actually make a measurable difference in your ability to manage your health? The CLARE Study (Community Learning About Results of Engagement) is on a mission to find out—and we need your voice to do it.

Autonomy means being in control of your own decisions. For pediatric patients living with IBD, there comes a time when you get to start making decisions about your health and care more on your own. Join me (Hannah), Leela, Kera, Fizza and Ryleigh for a chat about patient autonomy in IBD care.

Hi! My name is Fizza, and I am 17 years old. I was diagnosed in March 2021 with Crohn’s disease. One interesting thing people don’t know about me is that I love to do makeup. It’s like therapy to me.