I have become very skeptical of what oncologists have to say. It is O.K. for Drs' to say "we just don't know" They should do this more often, My local support group has been WAY more accurate as to treatment results and their original diagnosis as well. As PC sufferers we not only have to deal with our horrible state but the loads of false info as well. "Side effects from Lupron are rare" which is total B.S. That is a quote from a local oncologist WTF! It is really difficult to live my "fullest life" feeling like a bad case of the flu with the worst head cold ever. All the time.We are still eons away from getting publicity out about PC and how common and life ruining it is. High school health class would be a good place to start, ya think?
SW