As people with cystic fibrosis live longer, there is a growing demand for physicians who are trained to address the unique medical needs of adults with CF and a need for greater participation from adult care programs in the clinical research enterprise.
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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.
8 min read
View the Cystic Fibrosis Foundation's Board of Trustees and Advisors.
1 min read
We want to hear from you. Learn how you can contact the Cystic Fibrosis Foundation.
2 min read
Since 2011, the Foundation has awarded $2.5 million across 35 different projects to improve cystic fibrosis newborn screening across the country.
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4 min read
We hold ourselves accountable to our donors, volunteers, people with CF and their families, and the public. Learn about our governance and policies.