Cystic Fibrosis Foundation
| Formation | December 16, 1955 |
|---|---|
| 13-1930701 | |
| Legal status | 501(c)(3) nonprofit organization |
| Focus | Cystic fibrosis |
| Headquarters | Bethesda, Maryland, United States |
| Catherine C. McLoud | |
| Michael P. Boyle | |
Chair, Adult Advisory Council | KC White |
| Subsidiaries | Cystic Fibrosis Patient Assistance Foundation, Cystic Fibrosis Foundation Therapeutics |
| Revenue | $192,528,975 (2016) |
| Expenses | $299,650,531 (2016) |
| Employees | 731 (2016) |
| Volunteers | 250,000 (2016) |
| Website | www |
Formerly called | National Cystic Fibrosis Research Foundation |
The Cystic Fibrosis Foundation (CFF) is a 501(c)(3) non-profit organization in the United States established to provide the means to cure cystic fibrosis (CF) and ensure that those living with CF live long and productive lives. The Foundation provides information about cystic fibrosis and finances CF research that aims to improve the quality of life for people with the disease. The Foundation also engages in legislative lobbying for cystic fibrosis.