I have an Oncologist who I see regularly. I don't have a Urologist. My Oncologist consults the Urologist at his hospital when necessary. Do you folks have both or just an Oncologist like me? (I'm Stage 4, PSA-5, Taking Lupron and Xgeva, just completed Provenge treatment, completed chemo last winter, diagnosed 1.5 years ago)
Do you have a Urologist and an Oncolo... - Advanced Prostate...
Do you have a Urologist and an Oncologist?
I have stage 4 with extensive mets so don't see the need for a Urologist. My PCa is not confined to prostate or surrounding area so not having surgery at this point. I feel you need an Oncologist once you have stage 4.
I have both. My urologist performed my prostate biopsy and also prescribes my medication for urinary frequency (Myrbetriq) and ED medication (Stendra). I see him 2-times per year.
I also use my visits to see if he had heard of any new treatments i should be aware of.
Hope this helps.
James
Thanks. That makes sense. Now I just need to find a good Urologist near me. My last one was awful.
If your insurance will cover your visits with an Urologist, it wouldn't hurt to have one on your team, just in case.
I fired my urologist. Said I only had 5 years expected survival. Asked him if he would suggest M.D. Anderson or Sloan Kettering. He said I should go to New York. Better food and plays. Just find a doctor that you like keep up your research. My oncologist can do all I need for my stage 4 care so no urologist right now. Always remember that no one will work harder than yourself to keep you alive.
I have both but I see the oncologist for cancer care and the urologist for urinary issues. I have been dealing with prostate cancer for 18 years.
Medical oncologist and radiation oncologist
Same. Dropped my Surgeon Uro soon after RRP in 1996. Pompous ass. When I agonized about ED at age 49, he responded “Be glad you’re alive. Wait a few years to see what comes back.” Nothing ever did. Now, MO keeping tabs on the cancer; RO just zapped two abdominal Mets with SBRT.
I trust Urologists as far as I can toss a cement truck.
My urologist retired form general practice. I have two oncologists, one at a NCI, and the other in my local area.
Rich
I have a urologist where I get injections and a local and distant Radiation Oncologist who treats only PCa and is excellent. . No MO yet as my stage 4 is under control with ADT3 and xgeva.
I was diagnosed with a rare form of cancer (Ductal)that had spread to the pelvic area. At first I went to an urologist for the surgery, then a radiologist for (of course) radiation. Finally my primary doctor now is a medical oncologist (for Lupron and Zytiga). As I am getting man boobs, I think a trip back to the Radiologist is in order.
With each doctor I saw I had to inform and argue with them on what Ductal cancer is and the best way to treat it. Some of these discussions lasted for months. As a result I will have to say that a fourth doctor I see is myself.
Walt (a chemist not a MD)
I have both... in fact I just saw my Urologist Dr. Lee a few hours ago... I gave him a paper weight inscribed " TROUBLE WITH YOUR PEE? SEE DR. LEE"...
j -o-h-n Monday (Cyber) 11/27/2017 6:00 PM EST
I have both and use the urologist as a second opinion when I get a recommendation from the oncologist. My urologist diagnosed my cancer 11 years ago and directed me to my oncologist. Recently I have a kidney stone in both kidneys and a small amount of blood in the urine. So he is a great doctor who really cares and works with my oncologist. Best of luck and each of us have different reasons for our choices.
My uro interned at Moffitt Cancer Center here in FL and has a lot of PCa experience. I get my 6 month Lupron there. I see my onc monthly as I get Zometa infusions. Currently am on Zytiga with Prednisone. PSA is creeping back down. Man boobs are growing. Working full time. Life is good!! Merry Christmas all. 🎄