Just got back from the London Cancer Centre. Afraid the news was not good. I am back on the dug trial but the iconologist doesn't think the drug is effective any more. PSA is climbing fast and the last bone scan was not good. They showed me a copy of it and I looked like a fookin Christmas tree! The cancer has now spread all the way up the spine and other parts of the body. As they believe the study drug is no longer effective, I will likely be on chimo before the new year. As it is, I will be getting a bone drug, intravenously, every three weeks, at Owen Sound, start right away. If and when I start chimo it will also be done every 3 weeks at Owen Sound. I now have a CAT scan scheduled for Nov 22 and that may show more info.
Helen and I are taking this information in our stride and remain optimistic for the future, whatever transpires.