Really good thread here. After I was diagnosed in Jan 2016, I had to wait a week for the bone scan and ct scan. This was very stressful. Kept thinking about
my younger brother.
Little brother had a high PSA around 2002 but a clear biopsy. He thought he was fine. He never went back to the urologist after he lost his job and health insurance. Several years later, he took a free PSA test at a music street fair. Stage 4 with bone mestases diagnosed in 2006 or 2007, with multiple lymph node infiltration. When he called me with the news, I had no idea that he had any issues with his prostate.
He was treated at Fox Chase primarily with HDT therapy but he died in 2012 at 57.
Back to my diagnosis in 2016, I kept thinking that I was late. Gleason 8 - I was sure that Every small ache or pain was caused by spreading PCa
After I received the first Lupron shot, I started listening to my urologist.
I just needed to know that treatment started.
When you watch someone die from PCa, you want treatment to start immediately.
Post Edited (Manfred) : 3/7/2016 9:19:05 PM (GMT-7)