Hello
I have been on this site for a couple of years - always interested in where men are on their journeys and what they are doing for treatments.
Diagnosed Feb 2017 - PSA 340 with mets Immediately started Lupron and bicalutamide . Oncologist - who I trust sent me to an Urologist who I did not like. After a year of having the feeling - in office visits - that I just wanted to slap the arrogant little prick, and experiencing a 12 core sample that was one of the most painful procedures I have ever had - just UGLY, I asked for a referral for a second opinion. Got one to an Oncologist at UofChicago - teacher - researcher - and had an immediate liking - just the style and approach I was used to - the listening - all good. He was more than willing to share his note with my primary care Dr as well as any and all care givers - and interested in what they were saying about my care. The Urologist refused to share his note and was not interested in other - even though he worked in the same Medical group. I switched to the Oncologist full time. He dismissed the bicalutamide, and has administered the Lupron every 3 months. I did go through a course in Oct 2018 of Provenge - an immunotherapy - which he believed helped. I have had
.005 and lower PSA for over the 2 years .
So my question: by using just an Oncologist - with excellent results - am I missing something by not going to a Urologist ? I don't think so but ... thinking.
Second
In January 2019, I presented with Congestive Heart Failure. There was no vascular or valve indications of why, and ended up with a pacemaker in May 2019.
Question: Did the Lupron cause this side effect? I have tried to find some writing/info on this issue and have come up pretty short.
Any thoughts or experiences that anyone might want to share would be appreciated.
P