Skip To Content

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

20 years of Walking Strong! Register for the 20th Walk today!

Register now
A young walker, smiling big.

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.

CYSTIC FIBROSIS CANADA CALLS ON PROVINCES AND TERRITORIES TO IMMEDIATELY EXPAND FUNDING OF TRIKAFTA FOR 2-5 YEAR OLDS

Learn More
Cystic fibrosis occurs when a child inherits two defective copies of the gene responsible for cystic fibrosis (one from each parent). 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
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
May 11, 2024
Decant Gala Invitation photo
Decant Gala & Fine Wine Auction

join us at the 10th annual Decant Gala & Fine Wine Auction - Cheers to 10 Years! on Saturday, May 11, 2024 at the Delta Hotels Toronto. Our 10th anniversary celebration promises to be a special evening filled with dining, dancing, fundraising, and special messages from CF community champions.  

Read More
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.

Read More