Metastic prostate Cancer Survivors - longevity and quality of life
I was just diagnosed at the beginning of January and of course the news hit me hard. I have found a lot of hope in the discussions within this group. I am curious to know how long ago people in this group were diagnosed with metastatic prostate cancer and what your quality of life is like. Right now I have no symptoms from the cancer itself other than weight loss (which I am actively monitoring and dealing with via extra eating) and I have no side effects from the medications the doctors are prescribing. I know that I am at the beginning of this journey and I hope that my current status stays the way it is for many years. We all need to have hope, and I am learning a lot about traditional and new Treatment options.
Interested in more discussions like this? Go to the Prostate Cancer Support Group.
I applied for SSD on June 30th and my application was approved within a few weeks since I have PC with mets to my hip and lower back. There is a 5 month waiting period before you get your first check. The SSD people were very helpful.
@round5 How are you doing? Your story is inspirational and gives me more hope. I was diagnosed with Stage 4 PC in January at age 54
7 months into this journey and I'm rereading the posts in this thread. I've learned so much about various treatments and options, and the posts from my fellow warriors are important and useful. I had 5 radiation treatments to my hip and lower back. I'm on ADT. I generally feel great, except for the libido issues and shrunken testicles. @dsingstock How are you doing?
Had metastasis to lymph nodes in 2018. Stage 4B. Did fine for 4 years. Now PSA up. Diagnosed at 65. Now 70. I believe some of the guys have been dealing with metastatic PC longer then me.
Equally inquisitive about how this stage 4 goes foreword.Currently on xytiga/orgovyx only side effect is fatigue. Care team seems fixated on radiating pelvic area where prostrate and lymph nodes were removed. I question efficacy of this as metastased cells will still need drug therapy which I am tolerating well now.Question is why do I voluantarily give up 7wks of my life for treatment and struggle to recover from radiation for a unknown period?Real quality of life issue.
When did the journey start with rad of prostate and now metastasis
I had it radiated 2017 It met to L 1 in 2020 Had that radiated In Jan 2023 L2 had 1 inch Put me on Xtandi and Xgiva PSA 1 to 9.8 to 1,7 to 2,3 and now 3 since Jan
On Zolodex last 3 years again
Scan bad. Just finished 6 cycles of Docetaxel and Carboplantin a couple weeks ago. Rescan Tuesday to see effectiveness. Lynzparza and Pluvicto on the table.
I’m 65 , Diagnosed Late June 2022. Stage 4 !! Been on Zytiga and prednisone with Lupron injections every 6 mos. My 3rd scheduled injection in 3 days !! I’m alive and dealing with the meds side effects !! It is what it is, as these are our only options if we want to Live !! Other health issues stole my 1st year 🙈 Hopefully the 2nd one is better ✌️ After that, that’s a whole different ballgame 🙈 and I’m told I’m the losing team 🙈 Not much to look forward to 🙈 Good Luck All
15 months into this journey, went thru docetaxel+nubeqa+Eligard every 3 months
So far so good, of course adt kills sex but I’m alive, working, traveling.
Newly diagnosed 6/2022 with PSA at 252 with several Mets age 47
There are 987 clinical trials going on, let’s hope one of them has the key to make this illness chronic!
Yes, lower back (iliac crest) and hip aches. Also lowest rib, right side. Radiologic bone scans show lesions in those places. (on my own I'm also trying soursop (graviola) herbal capsules which some people say are effective -- possibly!)