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A toddler wearing a cute dinosaur Halloween costume

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

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Blog & News

A family of three laughing while baking in their kitchen.

Save the date! December 3rd is GivingTuesday

November 19, 2024
Blog
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A grandmother holding her grandchild.

Trikafta funding recommendation for rare cystic fibrosis mutations brings hope to some, but falls short for others, says Cystic Fibrosis Canada

November 6, 2024
News
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Dr. Stephanie Cheng smiling in front of a poster.

Discover Key Insights from the 2024 NACFC

November 1, 2024
News
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Cystic fibrosis occurs when a child inherits two defective copies of the gene responsible for cystic fibrosis (one from each parent). Canadians with cystic fibrosis consume a large number of enzymes, about 20 pills a day, to help absorb nutrients from food Over 2,000 different mutations of the CF gene
Upcoming Events
November 26, 2024
2024 Decant - IronGate Annual Fine Wine Benefit Auction

Get ready to bid and raise crucial funds for Cystic Fibrosis Canada!

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December 1-24, 2024
Wrapping for A Cure - Winnipeg 2024

Wrapping for A Cure

Join us this holiday season in Wrapping for a Cure at Kildonan Place in Winnipeg.

Volunteers will be gift wrapping - by-donation - with all proceeds going to Cystic Fibrosis Canada.

Love to wrap? Wanting to create a FUN holiday tradition - join us as a volunteer! 

Individuals, teams, and workplace employees can give a little back during the Holiday season by volunteering to wrap gifts. Funds raised from Wrapping for a Cure go back into the local community.

Click for more details!

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CF Champions
Mia Gaudenzi
Age 12, Toronto, Ontario

My name is Mia Gaudenzi and I’m 12 years old. I was born a seemingly healthy baby until around 3 years old when I became ill with pneumonia regularly. Doctors just thought I was unlucky until I had my sweat chloride tests to rule out CF.

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