At the Cystic Fibrosis Foundation, we commit to equity, racial justice, diversity, and inclusion as core principles guiding our efforts to provide all people with CF the opportunity to live long, fulfilling lives.
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Learn more about President and Chief Executive Officer Michael Boyle, MD.
Alongside the cystic fibrosis community, we advocate for policies and programs that promote access to highly specialized CF care and that help advance research and drug development.
View the Cystic Fibrosis Foundation's Board of Trustees and Advisors.
We want to hear from you. Learn how you can contact the Cystic Fibrosis Foundation.
Learn more about KC White, chair of the CF Foundation’s Board of Trustees.
Ad hoc patient advocacy coalition provides comments to Pennsylvania’s Insurance Commission to inform decision making regarding the state’s essential health benefits benchmark plan.
The CF Foundation writes to Michigan’s House Committee on Insurance and Financial Services to provide comments on SB 483: The Prescription Drug Cost and Affordability Review Act, which would create a prescription drug affordability board in the state.