Half of all children with cystic fibrosis and a third of all adults with CF rely on Medicaid to afford the treatments and care they need to live a healthy life. Some proposed policy changes have the ...

In 2023, the Cystic Fibrosis Foundation celebrated continued achievements and milestones toward our mission of curing CF. With your support, we are transforming what it means to live with cystic ...

You have reached this page because you submitted a form that required JavaScript to be enabled on your browser. This protection is in place to attempt to prevent ...

Following Joe’s passing, longstanding volunteers Kate O’Donnell and Amy Barry stepped forward to carry the torch as Co-Chairs ...

Growing up, I participated in Great Strides in honor of my cousin who has CF. Today, I stride with even more purpose — now for my son, who was diagnosed with CF.

The CF Foundation expresses grave concern and strong opposition to the proposed cuts to Medicaid considered by Congress, ...

In early 1998, a teenager with cystic fibrosis from Florida posed a question to a CF community email listserv, “Why is there no national cystic fibrosis awareness day?” Dozens of community members ...

On behalf of the 272 undersigned organizations committed to the health of our nation’s mothers, infants, children, and families, we express our deep concern over the Administration’s recent decision ...

Dear Speaker Johnson, Minority Leader Jeffries, Majority Leader Thune, Minority Leader Schumer, Chairman Guthrie, and Ranking Member Pallone: The undersigned 37 organizations represent millions of ...