Peyronies Disease - Vitamin E Effectiveness

S Mark

New Member

Joined : Nov 2008

Posts : 12

Posted 1/22/2010 2:50 AM (GMT 0)

It has been 2 1/2 years since my RRP but I am still unable to achieve a usable erection. Have tried Cialis, VED and Trimix. Unfortunately, what I did obtain is Peyronies Disease. Has anyone had success taking Vitamin E to reverse the effects of the desease? My Uro has suggested 800 Internation units per day.

Thanks for any help with this and any other thoughts regarding the pursuit of a erection.

Age 58 - 6'2" 190lbs

Overall Heath Condition - Good

PSA - July 2006 & Jan 2007 -> 14.3

Biopsy - 03/04/07 -> Gleason 6

05/03/07 - RRP

Catheter 5 weeks

(Both nerve bundles supposedly saved)

Post RRP PSA's <0.1

Swimom

Veteran Member

Joined : Apr 2006

Posts : 1732

Posted 1/23/2010 3:01 AM (GMT 0)

Try this site. You should be able to find some useful information. Vitamin E is first line treatment but after 2 years? Not sure.

http://www.peyroniesforum.net/index.php

S Mark

New Member

Joined : Nov 2008

Posts : 12

Posted 1/27/2010 8:40 PM (GMT 0)

Thanks Swimom

hb2006

Regular Member

Joined : Nov 2008

Posts : 299

Posted 1/28/2010 1:56 PM (GMT 0)

Hi

You might also see if your Urologist will prescribe Trental 400. Which is also known as "Pentox". I'm on both web sites, the other one has much more info about Peyronies. There are also a number of "quackery" web sites in regards to PD. Don't fall for any of the quick healing stories.

The ultimate solution might be a penile implant. There are guys on both web sites that have had a lot of success with an implant.

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