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Home | Cystic Fibrosis Foundation The Cystic Fibrosis Foundation is the world's leader in the search for a cure for CF and supports a broad range of research initiatives to tackle the disease from all angles
About Us - Cystic Fibrosis Foundation 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
About Cystic Fibrosis | Cystic Fibrosis Foundation Diagnosing cystic fibrosis is a multistep process, and should include a: Newborn screening; Sweat test; Genetic or carrier test; Clinical evaluation at a CF Foundation-accredited care center; Although most people are diagnosed with CF by the age of 2, some are diagnosed as adults
Research and Clinical Trials - Cystic Fibrosis Foundation The Cystic Fibrosis Foundation is the world's leader in the search for a cure for CF, and supports a broad range of research initiatives to tackle the disease from all angles
Managing CF - Cystic Fibrosis Foundation Managing cystic fibrosis can feel overwhelming at times — but we’re here to help Learn how to navigate life with CF below
Support - Cystic Fibrosis Foundation The Foundation is here for you Whether you're looking to talk to someone, find your local chapter or care center, or read some additional information, we have plenty of resources to help
Intro to CF - Cystic Fibrosis Foundation Cystic fibrosis is a genetic disorder that affects the lungs, pancreas, and other organs Keep reading to learn how to treat and live with CF
Our History - Cystic Fibrosis Foundation Since our founding in 1955, we have worked alongside the cystic fibrosis community to effectively transform a genetic disease in a single generation — making CF one of the most amazing stories in medicine today Read about the milestones we've achieved in pursuit of a cure for cystic fibrosis
Annual Report - Cystic Fibrosis Foundation We continue to learn about the CF population through our Patient Registry — representing about 80% of people with CF in the U S — including health status and their lives beyond CF Here are some highlights from the latest report:
News - Cystic Fibrosis Foundation Public Policy Cystic Fibrosis Foundation Urges Congress to Reject Harmful and Reckless Cuts to Medicaid Medicaid is a lifeline for nearly 40% of people living with cystic fibrosis May 13, 2025 | 2 min read