Help Please

[woodsignman]

I've had peyronies for about 4 years. Started with penile discomfort when getting erect like something was trying to push thru. After a couple of months the pain went away but my penis lost about an inch in length and is now bent and tapers to the glans. The glans is not real firm anymore either or near as large when engorged. It doesn't interfer with intercourse or erections or orgasms. I'm 64, almost 65 and I'd like my old penis back. I realize from reading several posts that many of you are much worse off than I am. My sympathies to you. It's been some time since I looked online to see if there was anything new in the way of treatment and that's how I came across this site. I tried one of those penis stretcher torture devices for a few months but noticed no change and was glad to throw it away. I'm curious about any side effect to the pentox (is that the correct name?) I read that it helped someone with tinnitus a bit also which I have quite severely. So I'd be interested in hearing any result type messages.
Thanks

[james1947]

Woodsignman

Welcome to the forum. I "split" you post to have your own topic and to get more attention to your own problems.
I am in the same situation as you, 4 years Peyronies, Christmas will be 65. Maybe worst situation than yours as I have lost 2" from the length and 1/2 of the girth. Also no erection without Viagra 100mg.
How your doctor diagnosed you and what treatment he have subscribed you?
Pentox it is maybe the most important component of any treatment but have other medications/supplements to take also.

As you can see from my daily treatment bellow I have started to do something very late and is very BAD:
2*400mg Pentox – morning/evening, started at January 2012 now on 3*400mg
4mg Cialis (cutting the 20mg in 5pcs) – evening, started at April 2012 replacing Viagra that started at November 2011.
2*500mg Acetyl L-Carnitine – morning/evening, started at September 2012
2*1000mg L-Arginine – evening, stared at June 2012
2*100mg Ubiquinol – morning/evening, started at June 2012
VED, 20 minutes (30 minutes in the last month), started at October 2011
With his treatment (like all the others except surgery) you can expect improvements after six months or more, some people have faster improvement. Consistency is the key of this treatment.

I will advise you also to read the forum to understand what and how the above medications/supplements are helping with Peyronies.

James

[woodsignman]

Thanks James.
My condition is such that I won't do anything as far as meds or supplements if there is a reasonable chance of side effects.
Interesting that my Dad got this in his late 60's. My parents we not real discriptive of the condition but my Mom did mention it once. She didn't know what it was called back then and I didn't think much about it.
I'm still learning your site, but will continue to look around. The fact that the Pentox might help with my tinnitus is a big plus for trying it.
As far as doctor, I kind of self diagnosed and asked him about it and he felt my penis for the obstruction but did really didn't find anything. I left it at that with him. I have my medicare card so I might see a urologist some time.
Thanks again.

[james1947]

As you can see from my post bellow, I am also very cautious with medications/supplements because I have a lot of allergies.
I begin with 1*400mg Pentox, increased to 2*400mg after a week, I had bad side effects from start and very bad with 3*400mg.
Just recently increased to 3*400mg daily, 10 months from start and no problems.
In my opinion, Peyronies have a huge genetic factor. My father get it at 61 (I know that from my mother) I get it at 61, I will prepare my son to be ready
I am still saying you need to be diagnosed. Myself done it also late, treated late, disastrous results.

James