|
Home
|

Welcome to the Vancouver and Lower Mainland Chapter of the Canadian Cystic Fibrosis Foundation, a national, non-profit, voluntary health agency, established in 1960 by concerned parents, relatives, and other Canadians. The foundation works to help provide care for individuals with CF and to continue the search for a cure or control for CF. The CCFF raises and distributes funds for research projects to improve treatment and help find a cure, or control, for the disease. It also 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 activates, raise awareness of CF in their local communities, and support family and friends who are coping with CF daily. | | Supported by:
| |
| |
|