Read the results from the 2024 cost burden survey


([link removed])


Earlier this year, the Cystic Fibrosis Foundation and Dartmouth College, asked you to share your experiences with health care costs and how they may impact you and your family. You generously shared your experiences, and the results are now available.


SEE RESULTS ([link removed])


The survey, Cystic Fibrosis Outcomes, Social Factors, Tradeoffs Due to Cost and Financial Burden (COST-CF), revealed that while each person's experience with CF may vary, the burden of the disease can be felt regardless of geography, employment status, or insurance coverage.

The Cystic Fibrosis Foundation uses this valuable data to shape support programs and tools designed to help the community navigate the challenges of health care costs. Our goal is to ensure that no one has to make difficult tradeoffs when managing their disease.


READ MORE ABOUT SUPPORT PROGRAMS ([link removed])


We acknowledge that conversations around financial hardships are sensitive and the Foundation thanks those in our community who graciously shared their experiences to help inform how we can better serve you and your needs.


([link removed])


www.cff.org ([link removed])

4550 Montgomery Avenue, Suite 1100N | Bethesda, MD 20814 US


DONATE ([link removed])


WE WILL NOT REST UNTIL WE FIND A CURE


([link removed])
% link:[link removed] name="[link removed]" content="" %]
% link:[link removed] name="[link removed]" content="" %]
% link:[link removed] name="[link removed]" content="" %]
% link:[link removed] name="[link removed]" content="" %]


This email was sent to [email protected].
To continue receiving our emails, add us to your address book.

Got this as a forward? [Sign up]([link removed]) to receive our future emails.

[Opt out of this mailing list]([link removed] "opt out of this mailing link")

Opt out of all CF Foundation emails ([link removed])