Recently, due to being able to become a little bit more active, as new herbal medication is masking a lot of the symptoms of my illness, I have discovered that my stoma is no longer sitting in such a deep crater as it once was, as my skin seems to be tightening up. My weight loss had made my abdomen very floppy and loose.
So, I started experimenting under the direction of my stomal therapy nurse, and I discarded the Hollister / Adapt CeraRing, which was making my stoma sit far too low.
I am still using the protective sheets with my moldable ring, which I adhere to my wafer's cut hole, but I am still getting a little leakage underneath where the ring sits. When I last changed my bag, my skin had eroded around my stoma and looked bright red. It's not bothering me, but I'd like to get my skin to grow back around my stoma. Sorry, next time I will take a photo!
Should I try not using the protective sheet so that my moldable ring is flush against my own skin rather than against the protective sheet?
Suggestions would be greatly appreciated.
Thanks,
Gracie
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Geekyjen,
Thanks for the reply. I will be seeing my doctor on Friday and mention Entyvio. I did not remain paralyzed for more than 2 days, but it was terrible and I was so scared. The doctors just used alot of xanax and other drugs like that to UN paralyze my joints that were being attacked by the remicade. Turns out I have been diagnosed with LUPUS. It is attacking my nervous system. I had ulcerative colitis in 1996 and they had to remove my colon. Had a J pouch for 10 years, until it started failing. I then got a permanent iliosomy, and I suffer from severe chronic diareha, and I dehydrate frequently. I recently had a proctectomy, and that is when the new autoimmune disorder, Lupus, appeared. I have had two hospital stays now because of the blisters and the paralyzing incident. I will be dealing with this forever now. I have just been working on acceptance.
I love this website because of wonderful people like you!
Betty
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