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New app for Peyronies self assessment - Details here



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beauharlan

Hello, I'm beau, 38 years old. Was diagnosed with peyronies a year ago. It was by chance that I found this forum while searching for information.

Hope to gather a lot of experience during the treatment process and share and confide with everyone.
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Stabler

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

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.

Mikel7

Welcome Beauharian to the forum and as Stabler has asked please fill in your signature line. Also download and study our survival guide -->Survival Guide. This will give you a better understanding of peyronies and it's different treatments.

So are you currently in pain and any deformities? How are your erections? Do you have a Dr that is experienced in peyronies? Have you taken and preliminary measurements of your penis for future reference?

Read up on the survival guide and educate yourself on traction therapy and VED therapy. Also look into using Cialis or like minded drugs to help with erections and healing. You will be doing yourself a favor to gain knowledge regarding this terrible disease that afflicts a lot of men everyday. Urologists are usually not t=very educated or experienced in up to date peyronies treatments.      :)

Mikel7  
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 :)

Pfract