Received some counselling from FORCE, a local cancer charity, but if you have a specialist prostate cancer group in your area (which I don't), I think it might help to talk to other people that have had the same treatment
The main cause of worry for me is that even after 6 years, I am still on 3 monthly PSA tests. My hospital uses an alert level of 0.1 and I have never been below the level of 0.01 which I believe some hospitals use. I have reached the alert level 3 times but my PSA levels then went down again. My consultant thinks that they left a small piece of benign prostate behind on doing nerve sparing but as she says she cannot guarantee this. Obviously, this is a constant source of worry to me. I will always wonder if the nerve sparing was worthwhile.
Yes
It seemed right for me at the time - might have not gone for nerve sparing. With what I know from other people, I might have considered Brachytherapy had it been offered to me.
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