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Share Your Peyronie's Experience

The purpose of this website, and me sharing my Peyronie's experience, is to raise the awareness of Peyronie's disease and encourage men to seek treatment as soon as possible.

As part of my Peyronie’s awareness effort, I’m looking for other Peyronie’s sufferers to share their experience of the disease.

Men share their Peyronie's experience

Why Share Your Peyronie's Story?

I have received nothing but positive response from sharing my personal experience so I know how much it really means for other men with the disease.

There are number of reasons why reading real life Peyronie's stories are helpful for men battling Peyronie's disease. Firstly, they can help them realize that they are not alone going through what they are going through.

As importantly, real life stories can give them hope and much needed motivation while undergoing their Peyronie's treatment. They can also help them to put their disease into perspective, i.e. to realize it could be worse and that there is still life very much worth living despite having Peyronie's disease.

So why not help me inspire other men in their battle with the Peyronie’s disease. It is after all, always good to talk, or in this case, write.

Who Can Tell Their Peyronie's Experience?

Any man that has Peyronie's disease can share his story. You don't have to have completed your treatment to be able to share your experience. However if you have, I would very much like to hear all about it.

It would also be great to get progress stories. So why not tell us about what you have done to date and update your progress as you continue your Peyronie's treatment.

I would also really like to hear from Peyronie's partners. So if you are a partner of Peyronie's sufferer, why not share your experience with us. Share your thoughts and emotions and how you support your partner in his fight against the disease.

The same applies about other people supporting men with Peyronie's disease, e.g. parents or friends. Why not share your experience and offer your advice to others playing similar role.

Read existing Peyronie's Stories.

How To Share Your Peyronie's Experience

The process is simple. Just use the form below to write your story. Only few simple rules before you start:

  1. Your story needs to be at least 300 words in length but there is no upper limit
  2. You do not have to use your real name but it would be useful to know your age and approximate democratic location, e.g. country
  3. If you got pictures you want to share, then that is no problem, just upload them (max 4 though)

And that's it, couldn't be easier.

I suggest you write your story using Microsoft Word or other word processing software, just to ensure spelling and grammar is good (makes better reading) and then copy it into the form. Safe your work regularly so if there is a technical glitch you will not have to rewrite it.

If the form below does not work for some technical reason, then just e-mail your Peyronie's experience to me at yourstory@mypeyronies.com.

The readers of My Peyronie's will be able to comment on your Peyronie's story and they might even ask you some questions. In order to follow up on any comments, make sure you tick the three notify me when tick boxes that become available once you click the Send Me Your Story button.

This means you will need to provide a valid e-mail address. Your e-mail address is private and confidential and will not be shared with anyone (see the Privacy Policy). It will only be used to advice you about time of publishing and new comments.

Once you have sent me your story, I will review it as soon as possible and publish it on My Peyronie's. Once it has been published, you will be notified via e-mail (i.e. if you choose to be notified).

I really hope you will share your Peyronie's experience with us. By doing so, you could make a big difference for some fellow Peyronie's sufferers.

Thank you.

Birgir



Share Your Experience With Us

Your story can inspire others to seek professional advice in their battle with Peyronie's disease.

We would like to hear everything about your experience – When did you first notice something was wrong, how did it manifest itself, did you seek medical advice immediately, your experience with medical team, how did PD affect you physically and emotionally, did you involve your partner (if you got one), has it impacted on your relationship, what treatment did you get (or are getting), progress to date, how did you research the subject, was it easy to find experienced doctor, and so forth.

IMPORTANT! – Start writing your story and save a copy using a word processing software, so that if there is a technical glitch, you won’t have to rewrite it.

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Hello, I'm Birgir

This website is based on my experience of Peyronie's disease