Worried about my life expectancy after AML diagnosis....
Worried about my life expectancy after AML diagnosis....
Hi ya ..
So sorry you've had to join our little chat room ... though it's amazing to have somewhere to talk about things that are on our mind ...
I think a lot depends on age with this ... but treatments have come on over the years ... so just know your not alone ... you'll always have a hand to hold along the way ... have you got a treatment plan in place yet .. l know it's a really scary time ... but try to take one day at a time ... and just sending a vertual hug to you ... Chrissie x
Hi, I have just joined here... my father was diagnosed this month with AML, his treatment is vidaza. What should I know apart of the vidaza leaflet? Which is not optimistic at all. Is anyone here who had this treatment and is alive more than... than it is mentioned everywhere?
Hello, how are you feeling now? My father was diagnosed in January with aml...
My husband has AML given an estimation of 15 months. In patient for approx 5 months. Including ICU. Now home, on chemo approx in 3 weekly intervals. He is Writing a book which is keeping him busy (good, as not focusing on AML). Finding this conversation hard, when good hearted friends ask is he feeling better!
obviously day by day.
I am type 1 diabetic for 50 yrs. We are both in our 70’s