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#1
Quote from: Lostand Looking24 on February 06, 2024, 03:19:02 AMAlso, the curving when semi erect feels more like the result of the base filling up faster, and so because the right hand side of the top half of the shaft hasnt filled up, it 'falls over' to the right if that makes sense. The semi erect curve is much more severe than when fully erect. I would say 3x as much or even more degree of curvature than when fully erect.

Having the exact same symptoms at the moment. I saw on your posts that you've been using traction therapy, has it had any effect for you so far?
#2
Derfman:

Welcome aboard PDS!

You need to give us more details. At your age, there are many factors that contribute to ED. You need to have a full physical assessment to get a clear picture of what conditions may be contributing to your weak erections. From there, after you check for hypertension, cholesterol, diabetes, heart disease, etc, you choose which treatment is better for you.

Doctors always start by recommending pills. From there on they may talk about vacuum erection devices or injections. But if you want a definitive solution at your stage in life then you have to look into Penile implants.
#3
Fully agree with you, LostandLooking24.
#4
Introduce Yourself / Re: new member
Last post by Pfract - Today at 11:57:56 AM
Welcome Saishu!

How exactly is your condition?
#5
Hello all-
I had a series of verapamil injections over the last 8 months. I originally had a 20 degree downward curve when I first seeked treatment. The doctor was treating plaque on the top of penis, no sure why I had downward curve.

After a few injections, the downward curve corrected, but I had lost length.
I wish I had stopped receiving injections at this point ( around 6 injections), but the doctor told me my plaque was smaller, softer, etc.

Over the course of the next few months, and 4 more injections, I developed a significant upward curve. I told the doctor this, and he said he was targeting the plaque that was causing this. The curve stayed the same, or may have worsened.

I have discontinued the Verapamil injections. Since I received them during the early stages of disease, it's impossible to blame the verapamil for my curvature, but I am confident it did not help. Very reputable doctor as well, I got the feeling he would carry on injecting me indefinitely ($) regardless of outcome.

It is hard to find much positive feedback on Verapamil injections out there.
I have purchased a Restorex device a couple weeks ago and am really hoping for some positive results.
#6
Introduce Yourself / Re: new member
Last post by Stabler - Today at 08:08:57 AM
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
#7
Last year in June another user on this site ''Vett''also sent an email to the researcher Feghali-Bostwick.
He got the response that they hoped it would be avaiable in the next 2 years.

https://www.peyroniesforum.net/index.php/topic,19415.0.html

There's also a screenshot of her message.

 
#8
Walking is an excellent form of physical fitness and it does bring blood into all parts of your body. I walk about 15 to 20 miles a week and it helps out every part of my body.
#9
Introduce Yourself / new member
Last post by Saishu - Today at 03:24:41 AM
I'm glad to have stumbled across this forum while researching Peyronies Disease. I'm a 46 year old that started with this problem about a year ago.
#10
Over 35 years with my penis and I just realized that my flacid blood flow is much better when I did walk a lot the day before. May a lot I mean at least an hour or more.
Maybe this is not for everyone and maybe many of you already know, but for me it is great news. If I walk everyday I can control the blood flow to my penis in a healthy way. No need to take Tadalafil or pentox, which does not help as much or has side effects like flushing.
Maybe walking or not walking even is connected to peyronies, because anytime the symptomes got worse, i was in a phase of staying at home, being sick for a long time, working on my home desk, sitting on the couch a lot, and I didn't walk much! Blood flow was really bad at that time. Anyone else notice this?