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Pearl’s Story

My name is Pearl Cooley, I am 21 years old and I have Cystic Fibrosis. As some of you may know, Cystic Fibrosis is a…

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Living a Full Life: Alex’s Story

I have been LIVING with Cystic Fibrosis for 46 years and counting. At first glance I may appear fine – but I am not. I…

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The Miller Family Story

I tossed and turned — and worried — all night. I kept checking on my 11-month-old son, Ryan, fast asleep in his crib. The day…

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2016 Registry Annual Data Report

The 2016 Registry Annual Data Report is now available online in English and French. There are now over 4,200 Canadians with CF and the estimated…

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Share your Reason This December

Life is full of reasons that make it special. Time spent with loved ones, holding little hands on the walk to school, helping strays at…

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This Giving Tuesday, There are So Many Reasons to Give

If there’s one thing we know about our community of Canadians living with cystic fibrosis (CF) and their families, it’s that although they live with…

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2017 North American Cystic Fibrosis Conference: Plenary Sessions Overview

This year’s North American Cystic Fibrosis Conference (NACFC) took place November 2-4 in Indianapolis, Indiana. This is the largest cystic fibrosis (CF) conference in North…

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Q&A WITH CYSTIC FIBROSIS CANADA VOLUNTEERS, Anne‑Marie Tremblay and Claude Vachon

At Cystic Fibrosis Canada, we are lucky to have remarkable volunteers who have been working for the cause for several years. Today, we are pleased…

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Sweet Dreams

Sleep is one of the most important relationships we have with our body. Is your relationship with sleep impacted by CF? You’re not alone. Here…

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