Hi - its been a while for me to post but just about to have a significant meeting I think! 6 months after my first DRE I have had 2 M mpMRIs, a CT scan and a cytoscopy (that was fun). As I am still having prostatitis-like symptoms my Urologist suggested either waiting another 6 months or have a fusion biopsy. I chose the biopsy as it is pretty uncomfortable and I wanted to know either way!
mpMRI was PI RADS 3 first time
mpMRI was PI RADS 2 approximately 3 months later.
Abdomen CT scan (with dye) clear
PSA 0.75 and Cystoscopy showed nothing.
Had the fusion biopsy two weeks ago and get to see the Prof tomorrow afternoon - now the panic is starting to set in!
As I have discomfort in my pelvis, reduced flow etc the Prof thinks chronic non-bacterial prostatitis but he is looking for malignancy.
Not sure why I am posting other than I am very nervous about the results, would like to think he would have contacted me sooner if serious (the results were back a week ago), but the 3am devil is gnawing away at me...
Words of wisdom appreciated of course!
Cheers