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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 Learn about cystic fibrosis, a genetic disorder that affects the lungs, pancreas, and other organs, and how to treat and live with this chronic disease
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
Research and Clinical Trials - Cystic Fibrosis Foundation Research by dedicated scientists and clinicians from a wide range of disciplines is expanding our knowledge of cystic fibrosis, translating discoveries and insights into vital new treatments and clinical care practices for people living with CF
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 Mission - 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
News - Cystic Fibrosis Foundation The U S Food and Drug Administration (FDA) today approved the expansion of Trikafta (elexacaftor tezacaftor ivacaftor) to people with cystic fibrosis ages 2 and older who have at least one of 94 rare mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene
Annual Report - Cystic Fibrosis Foundation 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 fibrosis