December 2017 was diagnosed with Mets in several areas( NED since 2012) Dr took me off IBRANCE/ faslodex protocol( which shrunk all 8 original)tumors but is no longer effective and now have new tumors in T2,T9 and L4 and switched to Megesterole acetate and more radiation
Does anyone have experience with this drug for Mets? It is a really old drug I guess.
If / when this treatment stops working it may likely be chemo) 😕
SBRT pinpoint radiation is the kind I start this week - any advice on this strong type of radiation?
I am at peace with the cancer - don’t like how it’s affecting the kids ( all grown with kids of own) yet my youngest daughter told me just concentrate at taking care if myself and not worry about them ( the 8 of them support each other)
I read something on here this morning that is a good philosophy “live live live your life- the one they are trying to prolong “ go out, have some wine, talk to someone about thoughts, enjoy your new normal and make the best of every day ( I can and I will if I want to😂)
Thanks for letting me share