Support and Community For Peyronies Disease from beatpeyronies.com
This website spin-off of www.beatpeyronies.com which offers support and more for men and their parnters impacted by PD. Includling: Our private facebook group - Beat PD. 100% private, the name and description of the group gives nothing away so your friends won't see...
Alternate Peyronies – Penile Curvature Treatment
Hi if you have navigated to this page looking for details on the above subject, then all you need to do is navigate back to the "Home Page" and scroll down. All the details of the Phallosan Forte are on the home page. If you are having any problems viewing the...
Treatment Update : My Peyronies Disease After Two Years
It's been a while since I gave on an update on my Peyronies Disease progress. It's now nearly two years since I first discovered my Peyronies Disease during which time I have spent over £1000 on traction devices, had 2 rounds of XIAFLEX and been consumed, like most of...
Integrity, Principles and Morales Guaranteed
As many of you have noticed, I do go on about the Phallosan Forte quite a lot! There is only one sole reason for this, because it worked for me and really helped me. I was asked a couple of weeks ago if I am linked to Swiss AG the company that produces the Phallosan...
Sense Of Humour – Mine Used To Be This Straight!
It 100% sucks having Peyronies Disease and I have up and down days, today I am feeling ok and I keep being reminded it could be worse. As it's the weekend and I'm smiling today, I thought I'd share this with you 🙂 Remember, we...
Just Setting Up My Blog On Peyronies Disease
Hi I'm Mark Gellar, founder of beatpeyronies.com, I'm just setting up this blog to share my journey of PD and the use of the PF along with tips and advice etc. Feel free to get in touch x