Rebuilding muscle mass post-Lupron
I was on Lupron for 12 months and received my last six-month shot in June 2022. I underwent proton radiation treatment in March/April 2022. My PSA dropped from 45 pre-Lupron and radiation to undetectable in November 2022.
With my doctor's agreement, I did not receive another Lupron shot in December 2022 because I wanted to build up muscle mass for a long-planned four-day hike to Machu Picchu in May 2023.
I continued daily exercises and hikes throughout my treatment, but I am conscious that my strength and endurance have dropped significantly. I'm currently working with a personal trainer, but I still feel much less strength on long uphill sections of my daily hike. I'm really concerned that I may not have the leg strength to complete my fairly demanding four-day hike in May.
I'd love to hear others' advice on how long it takes to rebuild muscle mass after the effects of Lupron have moved out of the system.
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Diagnosed with Prostate cancer in 2004 , age 54, PSA 9.5, had Robotic surgery and 36 radiation treatments. Surgery (showed seminal vesicle spread but not lymph system and) left me impotent. No detectable PSA for 6 years. Had periodic Lupron / Eligard shots from 2010 to 2020. Since then had two PSMA scans, no tumor visible, with intent to use salvage radiation to zap tumor.
As there seems to be no track history for when energy comes back after shots (mine hasn't) I remain hopeful of putting shots off as long as I can!
To what do you attribute getting your testosterone high, post-Lupron treatments?
Don't know. I am hoping that my testosterone is getting back to "normal" after ceasing the Lupron treatments. All I really know is that for me, my body does not adhere to the allopathic theory that high testosterone equals high PSA. Perhaps the changes in diet and exercise are having a positive effect.
It testosterone isn’t back to normal, do you expect the CA to come back too, or will it stay in remission?
Testosterone is currently very low, not at all back to "normal", but I have been on the merry go round more than once with Eligard shots where there did not seem to be any real relationship between low testosterone and PSA levels. Not in remission. In the middle of my Pluvicto treatments. Will get scans updated when finished with Pluvicto and that will give me a current read on actual condition. Until then I just keep on keeping on, one day at a time, coping with reduced strength and stamina and occasional pain.
I am very interested in this discussion of how long the effects of Lupron stay after the Lupron shots stop. I had my last shot 3 months ago. I remember reading about all the side effects of Lupron and loss of muscle mass was the one I feared most. Even though I was 83 when diagnosed I was very physically active, taking care of a large yard by myself, repairing decks, hauling everything from a hundred bags of mulch to 60 lb bags of sand and paver base. I also went to the gym 3 days a week for 2 to 3 hours lifting weights.
My mineset after the diagnosis was that I would continue, as usually, everything I did before the the prostate cancer. Even during radiation, I'd get off the table and go to the gym. I'd arrive feeling tired but feel almost normal when I left. My ability to lift the same amout of weight has not dimished. It may be that I could have increased the weight w/o the lupron but at least my strength and muscle mass does not seem to have changed.
I take additional vitamins to helf prevent bone loss and I have a small very quiet fan I found on Amazon that keeps me cool at night for the hot flashes.
I am a firm believer that my getting angry sometimes, and forcing myself to overcome the bad hand that was dealt, is the primary reason I do not suffer as much from the side affects of Lupron as some on this site have.
Believe me. I have had to deal with other side effects from the intense radiation to kill the cancer which had spread to my lymphnodes. The mild lymphedema, the rectal bleeding.
But my mineset has made my life with advanced prostate cancer better than I could have hoped for. And there is another benefit, after a hard days work.........happiness that you did it and that you feel as good as you do. I reward myself with something I enjoy just about every afternoon/evening. The company of my wonderful, lovely wife, a stiff drink and a cigar, while lisening to our favorite music.
Dear Weak But Strong,
I appreciated your story because it echoes mine. I am a former athlete who has worked out all my life until Stage 4 metastatic cancer was diagnosed 5 years after radical prostatectomy in 2017.
I am 20 months into my treatment with Multiple Meds, bicalutamide, Lupron shots, Abiraterone, 39 radiation treatments prednisone, etc. All to say, I am tired most of the time and although disappointing I have hope of regaining my strength. But that may not be in the future, but like you, it is my faith in Jesus the Christ that is my source of strength.
I read this daily and it is helpful to me...Therefore we do not lose heart. Though outwardly we are wasting away, yet inwardly we are being renewed day-by-day. For our light and momentary troubles are achieving for us an eternal glory that far outweighs them all. So we fix our eyes not on what is seen, but on what is unseen, since what is seen is temporary, but what is unseen is eternal.
Blessings and Thanks for posting,
John from Texas
What an inspiration you are for the rest of us!
Thanks so much for sharing
your journey
Good thoughts!
Interested in the "not fun" comment. Please expound.
77 y.o. PC Dx 9/23 with PSA of 27 (interesting that I asked my PCP for the PSA test, otherwise would have done it). Bx mixed 3/4-4/3. Body CT negative. PSMA scan confined to the prostate. First Lupron injection 1/31/24. Within a couple of weeks excruciating thigh, hams, and glut pain. Nearly impossible to get to the bathroom, etc. RT, seemed surprised and suggested Excedrin extra strength to little avail.
Prior to Dx and Lupron, 25 mile a day bike rider until 5/23 Achilles, then to PT and gym 4 days a week with mild-moderate weights, stationary bike and swimming. Second Lupron in June coinciding with radiation.
Severe cramps persist complicated by peripheral neuropathy affecting balance, etc., but mostly the pain.
Question: Does this pain subside over time or persist?
Question: Starting to feel leg weakness climbing stairs, etc.
What to do?
My best guess: try Trelstar injection instead of Lupron. My injection Nurse told me : Lupron injection uses a bigger needle and more fluid to inject into the body. I get mine every 3 months and don t have the side effects you described vividly. Best of luck. I m 18 months into the Trelstar doing ok, just tired out a lot but NO PAIN.