TOPIC: When the Pouch Swells Up Like a Balloon
I've had a radical ileostomy with complete removal of the large intestine and rectum. It was non-reversible surgery. I've been
living with it since October 1992. The topic I want to discuss now is when your ileostomy pouch swells up like a balloon. The most
inconvenient time this usually happens is in the middle of the night when you're sleeping. There are some appliances which have
a kind of gas release valve at the top. But I've never had much luck with those appliances.
A month or two after surgery, I attended a class at Bethesda North Hospital where a nurse talked about living with a permanent
ostomy with an appliance. Everyone in the classroom was an ostomate. One bald-headed middle-aged man kept complaining to the
nurse about how his pouch swelled up like a balloon at night, so tight it could easily burst. The nurse didn't have too much advice
on how to handle such a problem.
In my case, I've learned to live with it. A number of times during the night when I come out of a deep sleep and am in that
hypnagogic state when I'm half-asleep and half-awake, I look down and see the pouch swelled up like a balloon ready to burst.
Sometimes I force myself to get up, go to the bathroom, and release it. Other times I'm just too tired to get up and go
through all this bs and just lie lightly on my side until the alarm clock rings.
As I mentioned in a comment elsewhere, the best way to stop this is by not eating any full meal after 7 p.m. and not doing any
heavy snacking after that time either. I've had about four accidents over the many years, and there's not a whole lot I can
do about this damn situation except what I previously mentioned.
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Hi gang,
I was thinking what a great resource this site has been for me since I found it. It would have been really helpful, but maybe a bit scary, to have found it before my ostomy, but that's water under the bridge. But I got thinking about it, and now I'm questioning why doctors and hospitals don't provide this site's contact info to any patient even considering an ostomy today. And how can we change that so potential ostomates can learn about the road ahead for them by getting on here and asking questions before the docs go chop-chop. How exactly do you get all hospitals to provide their patients specific information, like this website?
I just happened to find this site something like 4 years after my ostomy when I Googled "ostomy forum" or something like that. But I never found it during previous searches.....so I found this site pretty much by pure luck. We need to find a way to make this site available to new or soon-to-be ostomates......as that's when we really need to commiserate with fellow ostomates. Anybody have any thoughts on how we do this?
Thanks,
Bob
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