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I Have Peyronie's Disease


Peyronie's Disease anonymous support group with information on diagnosis, treatment, symptoms, along with personal stories and experiences with Peyronie's Disease. You're not alone.

Share My Story

3 Stories

Recently Diagnosed With Peyronie's Disease

I was officially diagnosed with Peyronie's Disease about a week ago. The symptoms started with pain during erection. After a few weeks, my...

Written In Hopes Of Helping Others

Ok so I came across this group and I see it hasn't any posts. I guess I will finally post something here. I was diagnosed with peyronies...

Lived With Peyronie's For Almost A Decade. At The Breaking Point (no Pun Intended). Looking For Real Help

I was with a woman who didn't want to have sex. We sublimated the tension by doing things with our clothes on. It began to irritate my...
No forum posts yet. Be a star and start a topic. The shy ones will thank you.
This Experience at a Glance
Story highlights
These snippets show some of the most common themes mentioned in this experience's stories:
  • "I have pain in my entire abdomen when I try to go and have given up sex because I would immediately get thorny pains and feel like I was kicked in the stomach..."
  • "I called a respected Urology practice in my area, and had to go through the embarrassment of describing my symptoms to a female receptionist and then talk to a female nurse about it..."
  • "I put it off for a while, scared it was too invasive for my already easily scarred parts, but broke down in the guise of knowledge..."
And the Story Awards Go to...
Statistics:

29% of people who have this experience are in their fifties, 21% are in their sixties, and 21% are in their forties. 100% of people who have this experience are men.

You may cite any I Have Peyronie's Disease statistics, provided you link back to this page
Check out this group's What Is It Like To Have Peyronies Disease guide, where people with this experience share their tips and hints.
Members said this page is also related to: Do You Have Peyronie's Disease? , What is it like to Have Peyronie's Disease? ,Have Peyronie's Disease personal stories, Have Peyronie's Disease personal experiences

Other experience groups that have been combined into this group include: None yet.
This is an experience group where everyone says: I Have Peyronie's Disease. It features support, personal stories and experiences, advice, chat, talk, forums, videos, pictures and resources from real people, just like you. It's free to join, and the people in this group would love to meet you! If you've had this experience, or plan on having it in the future, simply click 'Me Too' or 'Plan To' and add it to your experiences. As you add more experiences, we're better able to recommend interesting people to you that share many of your personal experiences.

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