New to the forum looking for dvice

[LiamNW]

Hello.
I first noticed the symptoms about 3 years ago. I thought it was penile cancer so I'm actually ok with the fact that it's peyrones. I am now 41, I have a partner and 2 boys (one since I was diagnosed. I realise things could be worse. The curvature isnt so bad and I can get an erection. The problem is I've lost atleast an inch in length and from about a third of the way up from the base it goes really thin. Also it doesn't get as hard as it should and despite still being able to use it, it has been bought to my attention (during an arguement) that it isn't quite doing it for the wife. She has urged me to look into to it, so, here I am

[Jonbinspain]

First stop is your GP. You need an appointment with a competent, Peyronies aware Urologist. Knowing the NHS, you may have to consider a private Appt, if you can stretch to it.

In the meantime read all you can here - know your enemy. Any questions, ask. Somebody here should have a sensible answer for you.  

[LWillisjr]

This might help.


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