Living with metastic prostate cancer: Any positive stories to share?
Diagnosed with metastic prostrate cancer Nov17,2022, the cancer had already spread to my pelvic bone, lymph nodes , thoracic spine and throughout my bones fracturing 11 ribs, and to top it off 3 tumors in my head 1 of them behind my right eye causing vision problems. I started chemo Nov 28 ish , I’m on casodex and get the Lupron injection! My symptoms were back pain and I had seen multiple doctors through middle summer/fall! These doctors had me on physical therapy , accupuncture, 2 specialist stated I needed surgery on my back, they filled me with pain meds..not one doctor did series of blood test! Only test was an X-ray! My wife took me to mercy hospital Nov 11 in Buffalo because I was in so much pain and could barely walk. Within 4 hours in the ER the doctor told us they were quite sure I had cancer and would need to admit me run a lot of tests along with getting me healthy enough to go home.Sure shit I was admitted for 13 days,, then the day after my first chemo I ended up back in the hospital for 7 more days, I have had so many blood transfusion due to my counts being so low, a Foley catheter was put in me as well because I couldn’t urinate! I still have my catheter in and am doing my chemo! Does anyone have anything positive they can share with similarity!!! I am having my wife write this due to my vision
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First cosodex then injections of Zolodex If it progresses Enzalutamide
First cosodex then injections of Zolodex If it progresses Enzalutamide
My brother had back pain similar to your description. Turns out a blood test suggested multiple myeloma which was causing high calcium in blood due to bones leaching out calcium. His vertebrae were collapsing causing back pain. Good News, he survived 7 good years beyond the point at which they told him he had 3 months to live. He used Chemo, new age meditation, diet modification, exercise, and a lot of prednisone. Not easy, but 7 good years.
I wish you the best going forward.
I’m 82 and, even though it has metastasized to various locations, I never felt better. It’s dormant thanks to the medications. I also believe that continuing my exercise program, and Pickleball, have been very helpful for my attitude and physical well being.
I was diagnosed with pc in 2009. Went through 25 sessions of radiation and Bracytherapy in 2010. Evaluated through 2015 and psa
I had my prostrate removed in the year 2009. Have cancer taking Lupron which I am still taking. Lupron has stopped working Dr. says I keep taking Lupron. Had been taking xtandi but Johnson and Johnson quit furshing the medicine to me anymore, Took Erleada for two weeks my feet swollen plus I just felt so terrible I told my Dr. that was not going to take it any more. I been having little TIA's 80% blockage of some of my arteries,so now have to blood thinners. Back hurts not eating very good. Weigh 133 with my clothes on. Thank you fdor listening to me. Butch
Forgot to mention I am 83 years old. butch
Enzalutamide works psa dropped from9.8 to 1.7 in 2.5 months
Keep Zolodex injections
Add calcium
Sorry Butch that you are experiencing so many side effects. I pray that some how you can win this battle. I am on Eligard and Xtandi, which has given me some nasty side effects too.
I did Xgeva and lupron for 5 months andNeulasta and now I’m on Xtandi. Hot flashes are unbearable sometimes. I wish you luck, I’m on methadone for pain along with oxy 10 mg