JPouch Surgery and other Ostomies Community Group
A place where anyone considering, waiting for, recovering from, living with a j-pouch or other ostomy can ask for insight and share their experiences.
A place where anyone considering, waiting for, recovering from, living with a j-pouch or other ostomy can ask for insight and share their experiences.
I just joined this site today, and ran across your post, which resonates greatly with me. I see that you wrote it back in July, but thought I'd respond anyway, in the event that you would get notified. I'm 42, have had UC/Crohn's (undifferentiated) since early adolescence, many surgeries including J Pouch. I also struggle with adhesion issues and a lot of depression issues, the latter of which I strongly suspect is related to my medical history and the "ongoing challenges that are part of life with j-pouch", as you so eloquently stated. My life is certainly better in most ways than when I had active disease, but I don't feel "cured". It's still really hard. I, too, find myself isolating a lot and sometimes wondering "what's wrong with me".
I think there are some long lasting effects of the emotional & physical trauma experienced by people (like us) who undergo long illnesses and multiple invasive medical procedures... like it does something to our wiring. And I've also been reading lately about the brain-gut connection, theories suggesting that our mood is regulated in part by our digestive tracts.
If you're still around, I'd love to continue this conversation. I hope you're feeling better than when you first posted this.
Best, O&F (aka Laura)