Hi
Following a visiting to my GP for a check up on my bladder frequency habit in December (I am 65 so so didn't really expect this as being unusual )and a blood test such revealed a PSA of 24.5 I subsequentally had numerous tests culminating in a CT scan.
I was given the news on the 16/2/2017 that I had a Gleason score of 4+5 and that the PC had spread to my right pelvic hip and left seventh rib.
To say this was upsetting does not really describe mine and our family's feeling as all on here know.
I was prescribed Cyoroterone Acetate and an appointment was made with an oncologist I subsequently had a prostap injection which is to be repeated 3 monthly.
Within a fortnight I had to attend urgent care as I was unable to pass water and a catheter was fitted which obviously added to the concerns
I saw my oncologist on the 6/3 and she explained that this was an aggressive PC and booked me in for 6X doxetaxol chemo sessions commencing on the 16/3.
On the 5/4 I had my best day to date when I had the trial without catheter and it was subsequently removed and I was given my blood test results which showed a PSA of 5.4 as at 6/3!
The next day I had my second chemo and my PSA was 2.2 as at 6/4. By my 3rd chemo the PSA had dropped to 1.1 so I hope that so far so good?
Throughout the process I have been pleasantly surprised that the NHS is treating me promptly despite the horror stories circulated......
My chemo has not been as drastic as I expected and other then hair loss and the odd ache I have arrived at chemo session 4 due tomorrow fairly unscathed. I am well aware this can change daily and have to say that PC certainly refocused our priorities. We walk between 3-5 miles daily and have generally managed to continue with this exercise.
Our thoughts are turning inevitably to what happens when the chemo finishes and no doubt my oncologist will update me in due course.