Hi Everyone,
I live in Connecticut in the US , have PV (exxon 12 mutation) and have been on pegasys for about 3 years. I now am on an every other week dose of 45 mcg. I am in a Medicare Advantage program. I was supported by a PAN copay program which has apparently run out and am confronted with a $500 monthly copay.
Just looking for advice as to whether I should switch to regular medicare and get a Part D drug program or other possible alternatives that might be out there.
Also since I see people on different dosing intertervals and I pay per dose apparently - wonderting if 45 every two weeks the same as 90 monthly for a drug like interferon (and can the body handle that).
thanks