• 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.

GearUp Sign up for Great Strides walk 2014!
Mark your calendars for Sunday, May 25, 2014! 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. Click here to register for this year’s Great Strides walk!

21st Annual Mike Cassidy Legacy CF Golf Classic
You are invited to participate in the 21st Annual Mike Cassidy Legacy CF Golf Classic, to be held on Thursday, May 8th, 2014, at the Newlands Golf and Country Club in Langley. Enjoy a day of golf and an evening of fine food and drink. If golf is not your game, you can still support the tournament by donating goods or services for the live or silent auction. We look forward to seeing you on the green! Register today here.

NHLRaffle NHL Raffle raises $49,500 for BC!
The winning names were drawn on February 14th, 2014 and we are please to announce that John W. Macmillan from Kamloops won the grand prize! Thanks to the dedication of volunteers across the province who supported our cause, we raised $49,500 to further research and awareness in British Columbia. Click here to find the names of the 2nd and 3rd prize winners…

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.