Français | Contact | Blog | Chapters |

CF Canada volunteers make every moment matter!

Learn more

Register for the Walk and raise $100 for a chance to win two Air Canada tickets!*

*Two (2) Economy Class tickets valid for travel to any Air Canada scheduled destination.

Register now
Three young Walkers posing with a mascot.

HELP US RAISE $10,000 TO FUND CF RESEARCH SO THAT NO ONE IS LEFT BEHIND

Donate Now
Photo of Amy and Allison and brother

HEALTH CANADA APPROVAL SIGNALS SHIFT IN CF TREATMENT FOR NEWBORNS

Learn More

THE 2022 CANADIAN CYSTIC FIBROSIS REGISTRY ANNUAL DATA REPORT

Learn More
Individual with CF and mother.

Blog & News

NEW SURVIVAL MILESTONE FOR CYSTIC FIBROSIS IS CAUSE FOR CELEBRATION BUT NOT INACTION

February 27, 2024
News
Read More

2022-24 Research Impact Report

December 14, 2023
Blog
Read More
Patricia holding up a photo of her younger self and Mac.

Patricia's Story

December 12, 2023
Blog
Read More
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 20, 2024
Brews N’ Blokes

BREWS N BLOKES is a night of live music, great food and fun!

All proceeds from ticket sales, raffle, silent auction and 50/50 draw will support Cystic Fibrosis Canada through Jaxson’s Village.

Read More
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.

Read More
View All Events
CF Champions
Nicki Perkins sitting on a bench smiling in a CrossFit gym with weights behind her.
Nicki Perkins
Nicki’s Fitness Journey: How CrossFit Changed my Life with Cystic Fibrosis

Nicki Perkins is a 50-year-old CrossFit trainer living with cystic fibrosis and 28% lung function.

Read More