Here's a brief history of my PC. 2/29/2000 diagnosed with PC (Age 50). Stage T3a gleason 4+3=7 Initial PSA was 6.7. Had RRP on 5/15/2000. No other treatment at that time. I had a Sural Nerve Graft which was considered experimental at the time. Did not work. I am completly non functional since then but lucky to be in relativly good health at this time.
PSA went up to .3 in 2003. From 1/19/2004 to 3/15/2004 underwent external beam rad.
PSA okay until 2005, then it went up to .2 then .3.
I am now on Lupron (1 every 4 mos.) and so far my PSA has been < .1.
What I'd like to know is, does anyone know about the positive effects of pomegrante juice? I have been taking it on the advise of a friend but when I ask the doctor about it he just says that it, "Can't hurt.", but that's all.
I know that no one can predict what my lifespan will be, but is there anyone out there that has a similar history like mine, and how are you doing?
Thanks for listening.