About Us

Welcome to the Cystic Fibrosis Patient Assistance Foundation (CFPAF). We are a non-profit organization that helps patients and their families living with cystic fibrosis afford the medications and devices they need to manage complications of their disease. We know the challenges facing CF patients and their families - especially with rising prescription costs and the increasing complexity of insurance coverage. That's why we are here. The CFPAF offers the only national patient assistance program designed specifically for the CF community.

We offer a helping hand you can trust. Founded in 2008 as a subsidiary of the Cystic Fibrosis Foundation, We are committed to operating efficiently and to providing CF patients and their families the highest quality of service. Indeed, our mission is to ensure that all cystic fibrosis patients living in the US -- regardless of health insurance coverage or financial resources -- can obtain their prescribed FDA-approved drugs for inhalation and paired drug delivery devices(s) for the nebulized treatment of cystic fibrosis.

Meet Our Staff

Every member of our staff has received extensive training in insurance reimbursement, case management, patient advocacy, and patient assistance programs. Our case managers have extensive background in healthcare and customer service. Currently, Our staff includes:

Maria Thomas, CFPAF Manager	Yamini Saxena, CFPAF Team Lead
Minerva Flores, Case Manager	Linda Gough, Case Manager