My husband has had a colostomy stoma for 3 months now, and the most recent problem is that his bag keeps being being pushed off by the output, with resultant messes!! We think he needs to find a better bag. We are in touch with the stoma nurses, but wondered if anyone here has any ideas?
Hi NannyAnny
Sounds like a different product might help. I also have a permanent colostomy, and changed to a different bag which is much better. for the same reason as your husband. It will depend on different factors, like his body shape, and rolls and dips/folds in the skin etc. This is where the stoma nurse can be a good source of advice and recommendation and can provide different bags to try.
Additional products can also be helpful-I use extra adhesive applicators for my urostomy, and also flange extenders, which both give a much better feeling of security as the bag is much more secure.
Sarah xx
Hi there.
The stoma nurses will be able to help with this. I had a wobbly start but they changed my products and gave me the confidence to carry on.
we are all individual but there’s lots here with convex pouches. Mine can also have a a strap attached for extra security
whrn I am away I invest in some brava extra elastic strips that stick around the plate giving me even more confidence though they can be tough to get off so I only use them when sleeping away or special events.
I hope that your stoma nurses help soon i
Ann
The brava ones are the ones I use Ann. Do you not use an adhesive remover spray or wipes to get them off? They stick very well!
Sarah xx
So glad you had a successful trip Ann-that’s brilliant! I am a big advocate of Brava strips! So glad you have got the confidence for more trips.
Sarah xx
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