YANA - YOU ARE NOT ALONE NOW

PROSTATE CANCER SUPPORT SITE

 

 

BRONZE

John H and Ann live in Alabama USA. He was 48 when he was diagnosed in January 2009. His initial PSA was 2.9 ng/ml, his Gleason Score was 3+3 and although he does not state his staging, it seems likely he was staged T1c. His choice of treatment was robotic surgery. Here is his story.


I am young compared to many of the people I have met with prostate cancer. I am scheduled for surgery with Dr. Scott Tully on April 2, 2009. My urologist tells me that I am young, my PSA (2.9) and Gleason scores (3+3) are low and that I have a bread and butter, easy case.

Unlike many urologists, mine has told me point blank that the best treatment choice is robotic surgery and Scott Tully is one of the best on the United States. With all of that said, I have still spent some time researching other alternative treatment options, but never seriously pursued any of them. I hope the "experts" are correct, because I am less than two weeks from my surgery date.

Is there any advice the survivors of this surgery can tell me so I can best be prepared for the next 6 months??

Regards,

John

 

UPDATED

May 2009

 

 

My robotic surgery went well as far as the cancer was concerned. All of the cancer was contained within the prostate and the margins were clean.

The post surgery was rougher than I expected, but I survived it fine. I am 5 weeks out from the surgery and I am moving in a good direction.

My biggest issue is my incontinence. It has not really improved much since they removed the cath. I had my first follow up with the surgeon yesterday and he was a little concerned about the lack of improvement in my incontinence. He said my surgery was tougher because the prostate was way up behind the pelvis and difficult to get to. He suggested I continue on the same path I am on and call him in a month to give him an update. Everything else seems to be working well!!

I am very grateful to God that I had prostate cancer that was highly curable as opposed to another more difficult cancer.

 

UPDATED

July 2009

 

 

I am now 3 months out. For some reason, the doctor's office forgot to schedule my 3 month follow up and PSA test. My doctor is very busy, so I am now scheduled to see him in mid-August.

As of today, my incontinence has not improved very much since the catheter was pulled. I continue to do the Kegel exercises on a semi-regular basis, but have no real change as a result. I am confident and hopeful this will improve with time.

I still feel blessed that I had prostate vs. some other more difficult cancer.

 

UPDATED

December 2009

 

 

I am now 8 months out. My PSA level is .01, which is exciting. Cancer is gone.

I am however still experiencing incontinence. During the work week I go through approximately 2 Depends in a 24 hour period. On weekends when I am more active, I go through approx. 4 Depends in a 24 hour period. While I am sleeping and sitting I am continent.

Both my GP doctor and my Urologist believe it will not get better and I need to look at installing a sling. I met with the sling "expert" (Dr. Brian Christine)in my Urologist's practice. He has performed approx. 175 slings and claims he is one of the top in the nation on doing these? He did a couple of tests, including filling up my bladder with water. He also believes I am a candidate for a sling.

I am not real excited about more surgery, so I am trying to determine if there are any better alternatives. I have heard in Europe the use a stimulation therapy approach to incontinence. [This is in use in the US too - see Electrical Stimulation - and enter these words in the Site Search engine to see the stories of men who have used this]

Any thoughts on what my next path should be to solve this problem?

John's e-mail address is : johnhardin1@gmail.com

 

 

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