• Check out our new shop!

    Featuring Muco, the CF Fighting Monkey, new 65 Red Roses products and Lace Bite, the DVD.

  • Emma is two years old.

    Like most other children with cystic fibrosis, Emma spends the equivalent of four months of full-time work doing life-sustaining treatments every year.

  • Canadian CF care is among the best in the world, giving Rina full access to innovative new treatments.

    There are 4,000 Canadians living with cystic fibrosis.

  • Cystic Fibrosis Canada has invested over $140 million in research and care.

    Thanks to these investments Canadians living with cystic fibrosis, like 52-year old Colleen Kohse, are living longer lives than ever before.

We’re Moving!
Please note our new office address, effective January 12th, 2015 will be
Unit #301, 3185 Willingdon Green, Burnaby, BC V5G 4P3

 

NHLRaffle Register for the 2015 GearUp4CF today!
Every year family and friends of Canadians with cystic fibrosis come together for GearUp4CF to cycle and raise funds in support of life-giving research. 2014 boasted its largest year with over 100 riders and more than $375,000 raised. Since its inception nine years ago, GearUp4CF has raised over $1.5 million for vital cystic fibrosis research and clinical care.

GearUp Mark your calendars for Sunday, May 31, 2015!
Cystic Fibrosis Canada is making great strides, because others take strides. Every year across Canada, friends, family and colleagues of Canadians with cystic fibrosis lace-up their walking shoes to participate in the Great Strides™ walk, our flagship national fundraising event.

My dream for CF…
In this heartfelt video that was shown at the 13th Annual 65 Roses Gala, CF patients, physicians and families share their dreams for cystic fibrosis. Together, we will find a cure or control for this devastating disease.

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