Cystic Fibrosis Canada

Did you know that Cystic Fibrosis is the most common fatal genetic disease in Canada? Cystic Fibrosis impacts all the major organ systems, including the respiratory and digestive systems. Over 4,300 children and young adults in Canada are living with this devastating disease. There is no cure.

Cystic Fibrosis Canada (CFC) is a national not-for-profit organization and one of the world’s top three charitable organizations committed to finding a cure. Investing $150+ million in leading research, innovation and care, resulted in CF Canadians having one of the highest median survival rates in the world.

We need your help and support! We rely on your generous support to improve the lives of Canadians living with cystic fibrosis, and ultimately find a cure for this devastating disease. Thank you!

Register or Donate Today!
Registration #:106845100RR0001

Join our TC10K Team: Cystic Fibrosis Canada RUN4CF

Learning more about Cystic Fibrosis and Cystic Fibrosis Canada at: https://www.cysticfibrosis.ca

Contact: Adena Brettler, TC10K Liaison for Cystic Fibrosis Canada (Victoria Chapter)
Email: cfcanadavic@gmail.com