Cystic Fibrosis Canada is a national charitable not-for-profit corporation committed to finding a cure for cystic fibrosis (CF). What is Cystic Fibrosis? · Living with Cystic Fibrosis · Kin Canada · Ways to Give

It is estimated that one in every 3,600 children born in Canada has CF. More than 4,300 Canadian children, adolescents, and adults with cystic fibrosis attend ...

The Canadian Cystic Fibrosis Foundation (CCFF) is a national, non-profit organization dedicated to helping individuals with cystic fibrosis (CF) and their ...

Cystic Fibrosis Canada's mandate is to help individuals with cystic fibrosis, principally by funding cystic fibrosis research and care.

Cystic fibrosis (CF) is the most common, fatal genetic disease affecting young Canadians. Cystic fibrosis mainly affects people's lungs and digestion.

Kin Canada and Cystic Fibrosis Canada have shared in many exciting accomplishments, including the discovery of the gene responsible for cystic fibrosis in 1989.

60 years of Shinerama For 60 years, students across Canada have come together to support Canadians living with cystic fibrosis, raising over $29 million!

The CF Foundation is the world's leader in the fight against CF, and our scientific portfolio reflects our drive to provide effective treatments and — one day — ... Intro to CF · Explore Career Opportunities · Local Chapter · Support

Cystic Fibrosis Canada is a Canada-wide health charity helping Canadians with cystic fibrosis live longer, healthier lives.

Approximately 1 in 25 Canadians is a carrier of the defective gene with approximately 1 in 3600 live births diagnosed with cystic fibrosis.