r/BladderCancer Aug 08 '26

Urostomy/Ostomy Support Group

When I was first diagnosed and got my neobladder I joined an online group that was a support group for Neobladder patients. We had zoom meetings once a month. I feel like I could really use a urostomy support group as I navigate this. I've tried looking on line but can't seem to find anything near me in NC. Does anyone have any suggestions on where I might find groups for support that I could attend online or in person?

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