Hey everyone,
I got a phone call from my transplant coordinator today saying that my insurance will not pay for my cellcept. She asked them why they would pay for it initially after my transplant but not now and they responded that as of 2010 they will not pay for it. My coordinator even explained to them that without the medication, the transplant was pointless and how could they authorize and pay for a transplant and not the meds that are required for afterwards.
I was just wondering if anyone else has had problems like this with their insurance. I looked up the price of cellcept online and it is almost $900 dollars a month without insurance...which I cant afford.
Thanks for any input.
I got a phone call from my transplant coordinator today saying that my insurance will not pay for my cellcept. She asked them why they would pay for it initially after my transplant but not now and they responded that as of 2010 they will not pay for it. My coordinator even explained to them that without the medication, the transplant was pointless and how could they authorize and pay for a transplant and not the meds that are required for afterwards.
I was just wondering if anyone else has had problems like this with their insurance. I looked up the price of cellcept online and it is almost $900 dollars a month without insurance...which I cant afford.
Thanks for any input.