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About the Nonprofit

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Over 60 years ago, Cystic Fibrosis Canada was founded by the parents of children living with cystic fibrosis. Since then, Cystic Fibrosis Canada has dramatically changed the cystic fibrosis story. They have advanced research and care that has more than doubled life expectancy and it has grown into a leading organization with a central role of engaging people living with cystic fibrosis, parents and caregivers, volunteers, researchers and healthcare professionals, government and donors. They work together to change lives for the over 4,300 Canadian children and adults living with cystic fibrosis through treatments, research, information and support. Despite their remarkable progress, there is still work to do so we all keep pushing and keep going further until all people with cystic fibrosis can experience and enjoy everything life has to offer.