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I had PC (prostate cancer radical prostatectomy) surgery operation nine years ago at age 60. We assume that the
cancer was all removed and has not, to this time, metastasized for surviving cancer. My PSA readings have
all been 0.0. That was all good. Was surgery the correct treatment choice? Would I have better
choices today? As A post-op cancer survivor I don't know. Would I use the same surgeon? Probably not. I would
choose a recent graduate of med school, not an old school URO.
I previously had a 6" to 6.25" erection. After PC surgery my genital erection was at least .5" shorter. Of course I didn't know because of the erectile nerve damage. I used various pills and injections (for penis erections). Erections were not satisfactory. I was now incontinent, and that was a huge problem, even with pads. I could not keep my genital from nesting in urine, and that caused very painful raw places under my foreskin and on the head of my genital. Consistent use of zinc oxide was necessary.
I had, first, an artificial urethral sphincter. That was somewhat successful, still left me with a leaky genital. The only way I have eliminated the urine leak is to use MUSE 500. The MUSE makes my genital larger than the penile implant (AMS 700) and is the only thing that will really fill out the head of my genital. The MUSE completely eliminates my incontinence for 1 to 1 1/2 hours. Insurance pays for six MUSE per month. Being continent is necessary for any sexual activity, because a small amount of urine acts like sandpaper on my genital. I use MUSE so as not to contaminate the home pool.
There are cancer surviving support groups such as USTOO.com that help in (prostate cancer surgery) decision making.
Questions are welcomed.
Jed
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