(Sorry, this will be a long post).
Have read all this with interest. My DH had blood in his urine over two years ago and immediately went to our GP. A blood test showed a fairly high PSA count but DH was reluctant to be referred to the hospital as he dreaded a biopsy. Eventually, after more blood tests with up and down PSA counts, he did go for a biopsy, which he found extremely painful. We then had days of waiting for the result which was, thank god, negative.
Since that time, DH has had regular appointments with our GP who is concerned because his blood pressure is high. In fact, the GP has told DH that he (the GP) is 'forgetting about' his high PSA counts until he has his blood pressure lowered and stabilised. This, of course, suited DH although I was secretly concerned about it.
However, the blood pressure medication is causing all sorts of side effects such as itching, swollen ankles and tiredness. The GP keeps trying out different ones but none of them are very successful. This week the side effects of the latest medication became so bad that DH went to the surgery yesterday. This time he saw a different GP who told him that a) his current tablets are not some that he would recommend, b) the itchy spot on his leg is not caused by the medication but is a benign skin condition, and c) the PSA tests must be recommenced.
Poor DH came home in a very depressed state as now the constant PSA test/wait for results/go for biopsy/wait for results syndrome will start all over again, his blood pressure is still high and he is being referred to the hospital for his skin condition.
So, I am in two minds about the benefits of PSA testing and medical opinion seems to be equally divided. On balance, I think I am glad DH is to have another one but I know that he would prefer not.
Well, I feel better for having got that off my chest even if nobody replies! Thanks for reading.