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Dave240

I was wondering if there was a site for men with Peyronies....and seems I found one.  I was diagnosed with the disease 5 years ago (age 59).  I tried some medication to help blood flow, some said take vitamin E.  I dont feel I need surgery, I would like to try other things.  Ive read a bit about Shockwave therapy....does anyone know more on this?
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Stabler

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Stabler
Moderator since 2015- Missouri- I work in the medical field and have strong knowledge of insurance and how to obtain coverage for medication and other treatments. Being a woman I do not have Peyronies but you can ask me anything. I am happy to help.