Hi. I had a bad accident in July 2023, and ended up with a colostomy. Things went well for 4 plus months, and then they didn't. My pouch leaks almost daily! My stoma is round and protrudes about an inch. I use a Coloplast 1-piece, cut-to-fit, drainable pouch with a flat barrier and a moldable barrier ring. Currently, I use "adhesive removal" wipes because when I remove the leaking pouch, part of the ring is still adhered to my skin. But I follow that by thoroughly rinsing the skin with water and drying it. (In the past, I have used stoma powder and/or skin prep wipes before I understood their purpose.) I am on the "thin side." My peristomal skin is pretty flat, with no creases or folds, and generally pretty healthy (i.e., not irritated). I warm up the barriers prior to applying. I am very careful to get the pouch on properly. I take my time. I also empty the pouch frequently during the day and night to avoid it overfilling. The pouch has leaked during the day but leaks mostly at night. I am desperate. [I don't know what, if anything, changed when I started having problems. It might be linked to my switching from Hollister to Coloplast because I much prefer the filter and closure on the Coloplast pouches, but I am not certain.] I have been told conflicting things by well-meaning WOC nurses but have yet to figure out what I am doing wrong. Does anyone have any insight or advice? Thanks.
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This site is a godsend. As a newbie (colostomy on Nov 8, '21), I look at it every day for a number of reasons. Reading what people are going through makes me grateful that my elective surgery because of a severe case of IBS-C is nothing compared to what they have been through and are still living with.
I don't have to go to the hospital for anything related to my ostomy. I feel sorry for those who do and am in awe of those who can use humor to describe their ordeal. I identify with those who express their fears. I especially identify with those who are depressed because I am clinically depressed and have general anxiety disorder. How ironic that having a colostomy eliminated some of the depression and anxiety that the IBS created. I've been widowed twice and I'm on match.com.
I immediately included my operation in my profile and am pleased to say it doesn't seem to make a difference.
And there is much humor on this site and it's one of the reasons I enjoy it so much.
I could name numerous things I've learned from reading people's comments/questions/answers.
After months following on a daily basis, my only negative comment is I don't like listing the most popular members.
It's not that I don't like these people; I do. It's that I think it elicits some "Facebook"-like banter or comments that are gratuitous.
I don't do any social media and think that its merits are overshadowed by too much negativity.
Meetanostomate is in no way negative. I just think the gallery of "popularity" detracts from what is an excellent website that deals with a serious issue that causes a myriad of emotions.
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