Health Organization for Pudendal Education

Hi Molly, Thank you so much for your reply, I have been incredibly low with this of late and daring to come onto this site was a huge step. I would really value a link to the Winchester site/name of the physio as that is within a reasonable journey time from where I live. I'll start searching on Win...

Thank you so much for the responses so far. The thought of getting progressively worse is terrifying, and I have seen some evidence of this...for example I forgot to mention that I have developed little feeling in the head of my penis, and a loss of sensation in that area generally. In terms of an e...

I'm nervous about writing as I have never resorted to such before...A sign of desperation I guess. I am a male, mid 40s, and have been diagnoses with Pudendal Neuralgia after 2.5 years of constant pain, prior to which I had experienced misdiagnosis after misdiagnosis from my teens, having experience...