← Return to Testosterone Replacement Therapy after RALP

Discussion

Testosterone Replacement Therapy after RALP

Prostate Cancer | Last Active: Mar 18 4:54pm | Replies (40)

Comment receiving replies
@someotherguy

Thank you, @heavyphil, and all of you guys. You are being really helpful.

Today, I've delayed the surgery for the time being. They will pay me back. I'm worried that this delay might worsen things if I eventually end up taking the surgery route, but I think I need to compile all the relevant information to make the most informed decision, such as a genomic test. I would also like to know my father's Gleason at the time of the procedure when he underwent open surgery in 2007. I believe those are key pieces of data I should know before I make the most solid decision. It may end up being the same decision, but at least, if something goes wrong, I will know I did my homework.

I would also like to gather as many of my surgeon's stats and reputation indicators as possible, given that his skill is so important in the outcome. I think @tuckerp suggested that Mayo helped him gather information about the surgeon who operated on him (only after surgery)? I would love to know that about the surgeon of my choice. I've tried, believe me, but it's no easy task. At least, here in Spain. @tuckerp, do you know if Mayo provides such information from surgeons abroad?

Also, @heavyphil, the doctor who was going to operate on me said he was prone to discard focal therapy, given the fact that two cores out of the lesion came back positive, which suggests a multifocal tumor.

Thank you, guys. I hope I didn't f*** it up by canceling next week's surgery.

Jump to this post


Replies to "Thank you, @heavyphil, and all of you guys. You are being really helpful. Today, I've delayed..."

No. I am such a babe in the woods compared to the guys on this site. I would not be much help. I answered your comments because we are very similar except for your age. I wanted you to know there are risks. My second opinion at Mayo revealed that the Mayo surgeon would not have done my surgery although he could not find any issues. Good Luck.

Well, your doctor is doing what he knows best - not what’s best for you.
Look up TulsaPro, which is usually used in focal therapy; a poster just this morning had his ENTIRE gland ablated - no surgery, no pain, nada!!
Catheter for 2 weeks but that’s to be expected. If you have some $$ see if you can pay privately for a consult - or fly to another EU country that does focal/non-removal procedures. It’s well worth it!