▲ 7 r/Hemophilia
U.S. Medicare Question
Hello All — I’ll be transitioning to Medicare later this year and I’d like to tap this audience for any learnings and advice.
My understanding is that traditional Medicare Part B covers hemophilia treatment and clotting factors. With that in mind, I think I will be opting for traditional Medicare A and B — with part D drug plan and a Medigap policy (not an Advantage Plan).
Would anyone like to share experience or advice? Thanks!
I have Classic Severe Hemophilia A (no inhibitor).
u/Tight-Employment9420 — 10 days ago