Just 2 days ago I had a conversation with my transplant doctor about my concern that with a new administration that my medicare subsidy for my anti rejection medication would be at risk. And wondered what he thought if his patients would not be able to afford their medication, which usually runs about $1000 per month. Presently for those on Medicare 80% is paid by the program through part b and a supplement picks up the rest for me. His response was not to worry until the new HHS director is named. The director also oversees CMS also. So today I started to worry big time. politico.com/news/2024/11/1...
If you have any positive thoughts to deter this worry please share.
I realize this post is a little different than most. But I will not have any worry about medications or side effects or treatment if I cannot afford my medication and treatment.