Crohn's and Ulcerative Colitis

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This is a support group for people with Crohn's Disease and Ulcerative Colitis, and their familes.

Rules:

Be Kind
This is a safe space. Hate has no home here.
If you are unsure, see Rule 1 and 2

founded 1 year ago

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MorganCS

Hi, fellow IBDers! Hope this community gets going 🙂 (self.crohnsandcolitis)

submitted 1 year ago by BackOnMyBS to c/crohnsandcolitis

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Hi all,

I've had ulcerative colitis for 20 years now and mostly stay in remission with only 4 hospitalizations total. Still, I deal with UC difficulties on a regular basis, but don't know anyone in my daily life that has IBD, so I hope this community takes off to have a community of other IBDers to provide and receive support. I'll do my part to try to stay active here.

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[–] BackOnMyBS 1 points 1 year ago

Hi! Yes, the therapist that first pointed out my autistic traits to me said that the GI system has lots of nerve cells, so I think there might be something to out brain styles and IBD. Interestingly, my flares are all associated with prolonged, highly stressful experiences.

I used to do the thighs before. It's a different deeper pain since it's in the muscle. I haven't injected there in years, but I remember preferring the lighted shallow pain in the abs. I could try the thigh again at my next dose just to check. Thanks for the suggestion 🙂

I'll definitely make a post if I go on Remicade 👍