What is the Canadian Cystic Fibrosis Foundation?
The Canadian Cystic Fibrosis Foundation is a national, non-profit voluntary health agency that was set up in 1960 by parents, relatives, and other volunteers. The Foundation’s goal is to help people with Cystic Fibrosis by raising money for research into improved care and treatment, seeking a cure or control for CF, and promoting public awareness of the disease. The Foundation has 52 Chapters across Canada and raises about $10 million a year.
