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.
The Mighty is a safe, supportive community for people living with disabilities and the people who care for them.
Hi!
I'm Lissa, I' new to the Mighty👋
I was diagnosed with Crohn’s Disease 5 years ago and it has been a whirlwind since. From food flares to actual flares and medication swaps to learning my colon had almost swollen shut, it's safe to say, this isn't for the weak hahaha
I'm blessed to still be able to do so much I used to do before I got any symptoms, but I struggle with my body not keeping up with me and harshly pulling on the emergency brake sometimes.
I made a deal with myself at the start of the year to really show up for myself. So I started going to the gym and I'm now really focusing (even more) on food and finding friends who are in the same boat. So, hi!
I love cooking, reading and so much more. I can't wait to see what this platform has to offer💜