Here is a really great resource for those cg's out there (or cboys or transplant patients in general, or actually a whole list of chronic expensive diseases)-that are having trouble paying for medications, whether due to lack of health insurance, high copays or co-insurance, or medications being denied by insurance as experimental or non-generic.
The Patient Access Network Foundation
They grant temporary benefits, in some cases, while verifying your financial resources- so this is a great resource to go to for short-term /emergency aid while other agencies might be stalling you. They have coverage for CF, transplant, diabetes, and a whole list of covered diseases.
(I have no professional or medical relationship with them, btw, just putting some info out there!)
L'Chaim!
CG
The daily ponderings of Beth Peters as she writes about Cystic Fibrosis and lung trasnplant.
Subscribe to:
Post Comments (Atom)
New Blog and Site
Yo Old Friends! It's me, Beth Peters / CysticGal / the artist actually known as Mary ElizaBeth Peters . I am moving on from this bl...
-
I've been thinking a lot about the way that our bodies handle stress when we are physically challenged. I am obviously hanging on by a s...
-
1. To the guy that broke up with me right after I got out of the hospital: You are cowardly, and selfish, and also bald*. 2. To the neighbor...
-
In my explanation of UnBlog , I told you the "Why" of UnBlog , and those invited were instructed on the "Where" of UnBlo...
No comments:
Post a Comment
Thanks for commenting! Your comment will be posted ! (probably)