Hi! Afraid of change, per usual.
Anyone make this change previously?
The reason my oncologist suggested it was the side effects of letrozole (maybe Ibrance too) @ times put me down-as I feel like day after car accident feels or I’m 80-90 years old.
My reluctance to change is for following reasons:
1. Devil 😈 you know = better than 👿 Devil you don’t know.
2. The ONC said sometimes when you switch to another type of Aromatase Inhibitor (AI) the MS side effects will improve greatly—but the could actually become worse than they already are.
3. I did not like the numerous life threatening (sudden death) & worse potential side effects of listed Anastrazole vs only feeling like total Crap a few times a month & typically on my “off-IBRANCE” week!
4. The effectiveness of my current Med Regime = Ibrance/letrozole which has me @ no progression very early on intreatment; then 14 month-23rd month with no radiographic evidence all with minimum side effects. I’m absolutely afraid to change my current regime that’s working!
So, I’m reaching out to see:
1. if others have been on either of the 3 AI’s that are available in pill form & what side effects they’ve encountered.
2. Did you initially try Femara Ibrance then other oral AIs or just go right to Fulvestrant (I think that’s the name) shots?
3. How do the shots work and is it like an AI. Does anyone know about the progression free state is it shown to be longer with the traditional Ibrance/Femara combo or same with either one of the pill alternatives or Fulvestrant shots!
Thank you!