Guest guest Posted September 30, 2010 Report Share Posted September 30, 2010 As we are into 7 1/2 months after my husbands prostate surgery,all I can say is, boy were we nieve to believe our urologist when he said that my husbands case would be quite routine and easy. Since my husband was 56, excellant health, and PSA under 3, and only 2 cores showing cancer, he felt my husband would be fishing in 3 weeks, and back to work as a dentist in 4 weeks. Well, here we are...husband still unable to sit, can't work, and is in so much pain that he still takes vicodin daily. Thank goodness he had disability. We wonder what went wrong! Cnacer gone, not incontinence, and yes some impotence...but this vs. his not being able to sit, work or do anylifting at all, or fishing, or any of his other hobbies...is truly a hardship we NEVER even thought of. Come to find out, there ARE others out there with Pudendal Nerve problems/pain from this type of surgery. More women than men have it (most likely child birthing post op problems) but come on Urologist...don't hide these people, or not put them in your statistics! I am so frustrated that NO doctor in our area will acknowledge this is " failure " from surgery. People are in our world with this problem, and we have met many, but cannot understand why the Dr.'s or reports on Prostate Cancer outcomes, NEVER mention this can happen. What is the deal? If you know anyone who has this, please go to the Pudendal Nerve web site, or this site, and let people know! No one has hind site...but believe me, my husband would rather have his prostate cancer back than be this disabled! Quote Link to comment Share on other sites More sharing options...
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