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.
The Cystic Fibrosis Foundation is committed to finding new therapies and ultimately a cure for CF.
Please invite your friends to become a fan of the Cystic Fibrosis Foundation on Facebook, and help make “CF” stand for “Cure Found!”
About CF:
Cystic fibrosis is a life-threatening genetic disease that affects the lungs and digestive system of approximately 30,000 children and adults in the United States.
More than 10 million Americans are unknowing, symptomless carriers of a defective CF gene.
