Recent PET scan showed tiny mets to lymph nodes and pelvis. No pain/symptoms as yet, just SEs from Lupron and Xtandi. Mostly slight fatigue, some loss of appetite, and occasional hot flashes.
Retired a little over a year ago. Since then have been traveling, biking, joined a softball league, and play a lot of pickleball. Also working out (weights) 3-4 times a week.
It has been very educational reading the various postings. Definitely gives context to where I am with PC. I also admire the "spunk" of many of you fellow travelers.
Written by
LaxMan75
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Welcome aboard friend!..Looks like your living positively through your adversity.... Lots of other very positive, helpful people here full of hope ... Glad to know you! 🙂🙏
welcome to the group brother … lots of top notch medical knowledge and experience found here and camaraderie between brothers and sisters too.
Post some of your travel or sports exploits under the header “ QOL , this is what my post is about “ . It helps uplift some of the depression here , encourages others and brightens up the natural darkness on groups like this. That we are all croakers is understood , but most of us still have enough health left to have some QOL enjoyment for ourselves and our loved ones.
AHHH thanks for noticing......6 months in the joint has made me a new MAN, if you catch my drift......I opted to be the husband..... but they made me the wife...........
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Completed LuPSMA Vision Trial. I hope my journey encourages someone on this site.
Almost 3 years on ADT + Erleada
Update on my journey so far
25+ Plus years but now on Lupron
New guy just looking for information as I start this journey.
