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Three young Walkers posing with a mascot.

CYSTIC FIBROSIS CANADA INVESTING MORE THAN $2 MILLION IN RESEARCH

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HEALTH CANADA APPROVAL SIGNALS SHIFT IN CF TREATMENT FOR NEWBORNS

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THE 2022 CANADIAN CYSTIC FIBROSIS REGISTRY ANNUAL DATA REPORT

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Individual with CF and mother.
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
April 26, 2024
CF Canada Community Forum: Unchartered Territories

Join us for the CF Canada Community Forum: "Uncharted Territories,"  taking place on April 26 from 4 PM to 5 PM EST or 1 PM to 2 PM PST.

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May 5, 2024
2nd Annual Amanda De Melo Bowl-A-Thon
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CF Champions
Gillian Maramieri
Caledon, Ontario

Gillian Maramieri has been involved with Cystic Fibrosis Canada for 10 years and is a working mother of two boys. Her youngest, Matthew, has cystic fibrosis and was the first to be diagnosed with CF in the family. He was diagnosed at birth after Gillian’s doctors noticed an echogenic bowel 18 weeks into her pregnancy. Her first words after the diagnosis were, "Ok, now what do we need to do?"

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