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The mission of the Cystic Fibrosis Foundation is to cure cystic fibrosis and to provide all people with CF the opportunity to lead long, fulfilling lives by funding research and drug development, partnering with the CF community, and advancing high-quality, specialized care.
Members of the council lend their voices to convey the hopes, needs, and aspirations of the CF adult community.
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.
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.