We're so glad you're here. Scroll down to find some of the Crohn's conversations happening in our community. The more, the merrier—jump in anytime!
Curious to hear how your #UlcerativeColitis or #CrohnsDisease has affected how often you engage in self-care activities.
#InflammatoryBowelDiseaseIBD #ChronicIllness #ChronicPain #Anxiety #DistractMe #CheckInWithMe #MentalHealth
1. It’s full of other people with connections to IBD.
2. It’s a safe forum to ask any and all IBD questions.
3. It’s a way to connect with others on the Mighty community.
4. I’m one of the group leaders (living with #UlcerativeColitis ), and I’m pretty cool.
5. We want to normalize talking about poop.
6. We do Q&As with partners like Girls with Guts.
7. It’s a small but “Mighty” community that we want to grow.
8. It’s supportive.
9. Why not?
10. Do it today!
You can search the groups to join. #CrohnsDisease #InflammatoryBowelDiseaseIBD #ChronicIllness #IrritableBowelSyndromeIBS
What is something you wish people knew about living with Crohn's?
Your response may be used in an article or video on The Mighty.
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Has anyone done camp America with Crohn's disease or any other condition? I'd like to do it but after speaking with some camps I'm now a bit nervous because of how accommodating they can be. So anyone who has done it what insurance did you use? Roughly how much was insurance? How did it work with medications? How did you manage symptoms if any? And how supportive are camps and is it possible to get through it if having bad days with fatigue or other symptoms? #ChronicFatigue #CrohnsDisease #InflammatoryBowelDiseaseIBD