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lefthook

Hi my name is Guy and I live in Ottawa, Ontario, Canada.

I'm 60 years old and started noticing pain in my penis on erections about 4-5 years ago. The pain subsided with time but I was left with about a 45 degree left wards angle starting at the base of the penis and some shortening.

I was able to manage to continue to have sexual relations with my wife until just recently. It was already kind of discouraging as I'm still interested in sex but her libido has been waning over the last few years. Now this.

Initially when I mentioned my problem to my urologist he guessed it might be peyronies but he was not knowledgeable in that area so he referred me to a Dr Bella whom he highly recommended. I think I waited a year to get an appointment with him but it never happened. I've heard he has his own health issues as well as a lot of existing patients. So finally I got referred to a Dr. Maciejewski who I saw in Nov of 2019. The basic impression I got from him was there was little to offer except potentially some expensive and painful injections with the potential for serious side-effects. He suggested that if I'm still able to function sexually to take a 'wait and see' approach.

Well, now I'm at the point things don't work anymore sexually so I'm looking for solutions. Looking online I see maybe traction is an option.

I was glad to find this forum because, man this is a lonely disease!

Guy in Ottawa
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nemo

Welcome Guy, and you are certainly right, this is a lonely disease!

The best thing we can recommend for you up-front is to read the Survival Guide on the main listing of forums. It has a comprehensive overview of treatments, and from there, you can decide what sort of questions you have for us. It talks about traction, VED, supplements, injections, surgery - an overview of just about everything.

Take a read through that page, then hit us up with whatever questions you might have.

No need to be lonely here - we're all in this thing together.

Regards,
Nemo
51 yrs. old, multiple auto-immune conditions. First episode of Peyronies Disease in 2002. Recurred a couple times since. Over the years I have tried Topical Verapamil, Iontophoresis, all the supps and Cialis + Pentoxifylline. Still functional, always worried.

Interstellar50

Hello, I'm a newbie too. I hope the two of us can share our knowledge.  
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LWillisjr

lefthook,
Link to survival guide.

https://www.peyroniesforum.net/index.php/topic,3180.0.html


Interstellar50,
You might consider making you own post in the introductory board and provide information about yourself regarding symptoms, diagnosis, etc.
Developed peyronies 2007 - 70 degree dorsal curve
Traction/MEDs/Injections/Surgery 2008 16 years Peyronies free now
My History