I thought I would just share a bit for anyone who is just starting out on the PCa 'Journey' (i'm kinda tired of hearing that, but it is accurate)
Six months after being diagnosed I am still a bit unsettled about treatment. Aside from learning about the different treatments, I learned something else about this process. Your feelings about various treatment options change over time. I feel like I had settled on an approach 3 different times, only to get additional information on the treatment that made me rethink. This includes acceptance into a clinical trial. So while I have spent the last 6 months trying to come up with a great way to avoid having this surgery, I am now looking seriously at the surgery option. I am not against the other options, they just may not be right for my circumstances, so I pass no judgements.
I am meeting with Dr. Scardino at MSKCC next week to discuss open RP. I know the recovery time is much greater, but since he is only doing open, I'd like to hear the reasons why. Sometimes a doctor will look at a patient and decide they have physical characterstics that supports one approach better than the other.
After this I plan to meet perhaps with Dr. Eastham or one of the other surgeons at MSKCC to discuss laproscopic/DaVinci.
I haven't had a PSA test in a while as I've also been on the Kidney Stone 'Journey' for several months, which disqualifies you from getting an accurate PSA. Jeez... That journey totally sucked. Hope to see what's going on in that deparment next month.
My MRI a few months ago showed a very tiny tumor completely contained, so while I have time, I still feel like gettin the show on the road.
I wish you all well!