Cystic Fibrosis Canada is a national, not-for-profit health charity established in 1960, headquartered in Toronto, Ontario. The organization is dedicated to improving the lives of Canadians living with cystic fibrosis (CF) through funding research, providing care, and offering education and advocacy. With a mission to enhance health outcomes and quality of life for those affected by CF, Cystic Fibrosis Canada has invested over $260 million in research and care initiatives since its inception.

The organization funds approximately 50 research projects annually and provides grants to CF clinics and transplant centers to ensure high-quality care. It maintains a national registry with health data on nearly every person diagnosed with CF in Canada, which supports evidence-based research and care improvements. Cystic Fibrosis Canada also engages in advocacy efforts to improve access to treatments and raises public awareness through educational resources and community engagement initiatives.