So...it seems like most of us don't have prostatitis

But pundendal neuropathy instead like the Italian study confirmed? Have anyone recovered from this? All the symptoms we are getting that we thought where from prostatitis or from cronic pelvic pain (umbrella term) have been documented to be nerves. Myself I have a burning sensation on my scrotum and pain around anus/tailbone also the feeling of being “tight” down there. Anyone been treated for pundendal damage? I really don’t like this road at all…

No1 got any better? well…that is pretty depressing…

I have low left abdomen pain that runs to the left testicle, and my erections have gotten much worse through the years. I think many of us that are in a similar state will eventually have to get a penile implant sooner or later.

do you have varicocele?
Do you have penile numbness?
i am also experiencing left testicular pain and lower left abdominal pain, i am 9 month off fin and things are not getting better. only improvement is a Little less hard flaccid, initial months, my penis was always retracted and hard in flaccid state its is a bit better.

I don’t have those. I have shrinkage, the first 5 years it was fine, I could have sex with PDE5I, I haven’t been able to since 5 years now. I reach 10 years of PFS this year. I’ve been considering implant for a while now, maybe once the Bylor study gets released next year.

Holy hell, 10 years. My god, I am so sorry for you. This is giving me a lot of anxiety because this stupid drug has RUINED everything. Not to be depressing, but I see why suicidal thoughts is a side effect. It’s looking like it’s over for me.