It's been at least 8 months it's been like that, a pink ring around my ostomy. I went to see a stomo-nurse but he said it's probably nothing, but he did say that I was too ''tight'' because he couldnot insert the tip of his little finger inside (yes he had glove and it's normal to do that).
Here a picture if you want http://i.imgur.com/cu9O6HG.jpg
So im guessing it's probably due to blood who isn't pumped enough there?
Also Im pretty skinny and lately, because of depression I haven't been eating well and enough for the past 2 years.
I can't see my doctor because it's been more than 5 years I haven't seen her and I need to submit a new appointment since im in a new city and it's been months I have asked for it. The only way to see someone fast is to go to emergency but I don't want to stay 8 hours there just to see someone.
Anyway, if you saw or heard of something like mine, just tell me!
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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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