Due to increasing PSA level allied to my dear Dad having advanced prostate cancer (unfortunately ultimately diagnosed after repeatedly going to GP and being told he was having recurring UTI’s) I’ve been visiting a Urologist relatively regularly.
Nothing to suggest I have Prostate cancer but PSA has increased from 1.3 in November 2019 to 2.0 in June 2023. MRI scan in October 2020 indicated no issues.
My most recent visit was last September where physical check plus PSA blood sample taken.
Following that I received a copy of letter sent to my GP which guided that if PSA had increased then another MRI would be organised or if no change to PSA levels, then PSA test to be repeated every 3 months.
Since then I have had no direct contact from hospital or GP but a cycling friend popped past on Sunday to guide he was undergoing treatment for Prostate cancer – which made me reflect on things with a “I’ve heard nothing…).
Yesterday I emailed the Urologist secretary who guided that the Urologist is on long term absence and they would pass details onto another Urologist for action.
It’s one of those where I’ll give it about a week and if no response will re-engage but at the same time contact private healthcare provider to ask for appt with Urologist.
I guess it just shows how much a squeeze there is on the NHS…