Cystic fibrosis (CF) is the most common, fatal genetic disease affecting Canadian children and young adults. There is no cure for cystic fibrosis. CF is a multi-organ disease, primarily affecting the lungs and digestive system.
The Canadian Cystic Fibrosis Foundation (CCFF) raises and distributes funds for research projects to improve treatment and help find a cure, or control, for the disease. It also promotes public awareness of CF and provides incentive grants to transplant centers and CF clinics across Canada, to ensure quality care and treatment.
Each province in Canada has active Chapters. There are a total of 50 chapters located in Canada. Individual chapters are made up of volunteers who are deeply committed to finding a solution to CF. They organize and stage fund raising activities, raise awareness of CF in their local communities, and support family and friends who are coping with CF daily.
