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CF Canada President and CEO Kelly Grover and Dr. Theo Moraes, a researcher at The Hospital for Sick Children

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FORWARD TOGETHER: A REPORT ON CYSTIC FIBROSIS CANADA’S IMPACT IN 2023-24

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A collage of community CF Canada community members
Over 2,000 different mutations of the CF gene 73.5% of Canadians newly diagnosed with cystic fibrosis in 2019 were diagnosed through newborn screening Of the Canadians with CF who died in the last three years, half were under 34 years of age
Upcoming Events
October 18 & 19 | 25 & 26
Ghostly Greenhouses 2024

Join us for a spooktacular event in support of Cystic Fibrosis Canada. Ghostly Greenhouses is back this Halloween!

*See event listing to learn more!
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October 19, 2024
2024 Fusion - An Evening in Rome

Over the past 21 years, the Fusion Gala has successfully raised over $4.5M for cystic fibrosis research and care.

Join us at 2024 Fusion – An Evening in Rome for a very special evening of dining, dancing, and fundraising, with lively entertainment, and the chance to participate in our exceptional silent and live auctions, as well as our Key to a Cure auction.

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CF Champions
Kelly Ann Quinlan
Age 19, St. John's, Newfoundland and Labrador

My name is Kelly Ann Quinlan and I am 19 years old. I was diagnosed with cystic fibrosis at birth. My 24-year-old brother Michael also has cystic fibrosis, which is a challenge, as we both live in the same home but must live separately to a degree. We are very close to our parents and sometimes they struggle with the extra duties and constant cleaning that comes with raising two CF children.

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