Ricky, you're onto something there. I finally got my 'new' urologist to review my surgical notes and discuss why I am still suffering ED 2 1/2 years after the initial
open surgery. My path report stated a gland size of 110gms. I have speculated for sometime that even though I had nerve sparing, that the extra work needed to remove this huge organ did do more than the usual amount of damage to the nerves, in addition to them having been stretched both before and during surgery, just from the sheer size of the organ. Makes sense, as I had begun to experience some ED a year before PCa detection, hadn't gone to the pills yet though. He agreed with my speculation that this could be the root cause of my continuing failure. As to hopes for the future recovery of function, if this new theory is correct, then I/we don't expect any big improvement to magically occur. Maybe in 5 years, probably not..