I was going to start a new thread, but perhaps it is best to keep it here. I don't really know how this site works. I'm really grateful for all of your responses. They have greatly benefitted me.
In brief, I met with a radiology oncologist two days ago, as had been planned. I really thought that I was going to set up an appointment for my 5-time MR-LINAC treatment. Instead, the doctor said I should start with 6 months of HT, using Bicalutamide and Leuplin (Lupron).
I was honestly taken aback and ended up stuttering through the rest of my session because HT was the last thing on my mind, and all my research indicated that the side effects were unpleasant (that's being kind) and long-lasting.
I said couldn't we move past the HT and start with the MR-LINAC radiation treatments. He said it was possible, but I would first have to have a (rectal) spacer inserted. This was also news to me and threw me off again.
The doctor, I will say, was quite fantastic, and spent nearly two hours with me (and my partner) explaining everything about the HT, the spacer, and the MR-LINAC treatment.
He said, if I understood him correctly (remember, I was basically in shock) that the chance of reoccurrence without doing the HT first was higher.
Obviously, I do not want any chance of any reoccurrence.
I'm saying all this to let you know that the drugs mentioned were Bicalutamide (daily) and Leuplin (Lupron) (injectable, 1x every 3 months).
He said 80-90% of the patients he treated agreed to it.
I am wondering if any of you gentleman had this combination of drugs for HT? Also, did you need to do HT for six months prior to receiving EBR (which is essentially what the MR-LINAC machine offers, if I understand correctly)?
I have been extremely fortunate for 72 years. I do have high blood pressure, for which I've been taking medication for at least 10 years. So, the idea of these two drugs with multiple-side effects has been causing me untold anxiety (although I've been keeping it to myself, hence turning to this community).
Some of you have been very kind to respond to my posts. As I have not actually received treatment yet, I cannot offer words of wisdom to anyone, but I promise that, assuming I get through this in one piece, I will share my experiences in the hope they may benefit someone.
In the meanwhile, I want to know specifically how long your HT was for, which drugs you were told to take, and what kind of an effect they had (or have had) on your life.
Thank you in advance.
(NOTE: As I finished writing this, I see a message from CeePee which brilliantly sums up what I may need to know. Nonetheless, all responses are welcome!)