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Hi, I'm 47 years old and recently diagnosed with Peyronies after increasing difficulty and discomfort having intercourse with my wife over the last year. As a newcomer to the board, I'm particularly interested in exploring non-invasive self-help treatments and will be reading through them for recommendations on VED and traction devices.
Thanks for adding me. I'm sure I'll find the forum helpful and informative.
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Hello and welcome to the forum. Please take a couple minutes to fill in your signature under your profile settings. This will help keep you from having to repeat why your here in the forum when you post.

I have sent a PM explaining how and giving you some guidelines for the forum. We are happy you are here and look forward to helping

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.


Welcome Slid to the forum. Here you will find a great community of men who share what you are going through as we have all been there. Read the survival guide per Stabler's recommendation and you will get a better understanding about peyronies.

One thing to first get control over is any anxiety and worrying regarding this as that will do more damage than peyronies sometimes. I would look into VED and traction therapy and heat therapy if you are in pain. Doing nothing will solve nothing and things could get worse. Remember to adopt the mindset that this is a marathon and not a sprint. Also please fill in your signature line.  :)

Lump 4/2020, age 63 , Dr Levine 6-26-20, Dors Curve 11/2020, Peyronies
Vit E400mg, COQ10, Heat Therapy, Penimaster, Pentox, Cialis, Restorex
SNHL 7/2020 - Stopped all Meds because ototoxicity  Heat/traction/VED are working. CPPS Diagnosis - Stable :)


Welcome aboard Slid!