Are you running any specific PE schedule, or just doing whatever seems best for the day?I don’t want to sound like I’m nagging at you for updates, but a lot of guys are scared shitless when they find out they have prostate cancer, and have heard way too many tales of incontinence and impotence from the old-school medical procedures. You’re doing them a great service by sharing your experience.
My routine mostly consists of using my auto extender at night with heat, its not an all night thing, and generally comes off in an hour or so. In the AM I generally manually stretch all directions for 10-15 minutes. My weekend routine, since I have more time, is to do the same but get in some extra extender time and/or hang time attempting an extra 30 minutes each day.
When I was diagnosed, I knew I had a limited amount of time to do PE as I was worried about coming out of surgery with less length than I had going in. That said, I was pretty aggressive using the auto extender, as much as I could, manual stretching every day, pumping and hanging on the weekends. Starting at about 4.8" BPEL, reaching my first goal of 6" BPEL in a few months.
Incontinence issues: mostly leaking after urination, or when attempting to pass gas. This is mostly resolved and I stopped using the pads a few months back. I occasionally still leak after urination.
Impotence Issues: I am never again going to be able to impregnate or produce semen. The penis has the ability to produce a tiny bit of fluid, but not much. I am only able to obtain about a 85% erection. But this getting better as time passes. I am able to reach orgasm, sometimes intense, sometimes not so much. To my surprise, at the point of orgasm, the pulsating generally associated with ejaculation is still happens. I thought that this was part of the prostate gland, but is is not. Things (visual, oral, or touching) that used cause an erection no longer do. It takes a lot of stimulation to get an 85%, at that point, I am really close to orgasm. So this is a work in progress,
