I have had my ileostomy since 1986 due to UC. I had a great stoma therapist prior to and after surgery, and I know that has made a HUGE impact on my recovery, acceptance, or whatever you want to call it. Because of her, I am pretty much an open book and have always been willing to help other ileostomates when questions and concerns arise. Which brings me to this posting.
Once again, I have been approached by a person who is suffering from “bag blowouts.” Their confidence is so low they often don't want you to leave the house because of this fear.
Why the problem is the most often asked question. Sadly, I don't have a post-surgery answer for most of them, as I very, very seldom have this problem except when it gets really hot (sweating) or if I push “just one more day” and I'll change it “tomorrow.”
What I see as the most common problem these folks have is where the surgeon has placed the stoma. Seems they do not pay attention to where the belt line is and place it too high so the belt/waist line rides on the stoma, just underneath the stoma, or cuts the pouch. All three of those situations can cause BM waste to build up and pop the wafer. Why can't the surgeons take some time to educate themselves as to where a stoma should be located to ease this problem?
My ostomy therapist spent quite a while judging where my stoma should be located. She made note of my belt line and waist, where my tummy bulged when I bent over, then marked with a pen exactly where my stomach should protrude and be located. The night/day before surgery, the doctor, she, and I met, and she showed him my placement mark. I estimate it to be 3.5 inches lower than my belly button and maybe 3 inches to the right. (Estimation key word)
I know that not all situations allow this step due to some being emergency surgeries (vehicle accident, etc.), but if time allowed, this knowledge that surgeons should know could benefit many ostomy patients.
Just sayin.