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Archive for March, 2018

CONNECTIONS WINTER 2018

Cystic Fibrosis Canada is proud to publish the winter 2018 edition of Connections magazine! It is published exclusively online. This edition is full of the…

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The reality of living with a rare disease

Today is International Rare Disease Day, a great initiative that raises awareness of rare diseases, and highlights the daily lives of patients, families, and caregivers…

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Then and Now: Our impact (1960-2017)

Since 1960, Cystic Fibrosis Canada has invested more than $244 million in leading research, care and advocacy, resulting in one of the world’s highest survival…

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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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November is Diabetes Month: Let’s Talk about Cystic Fibrosis-Related Diabetes

As more people with cystic fibrosis (CF) are living longer, a greater percentage of the community is developing cystic fibrosis-related diabetes (CFRD). CFRD is distinct…

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Happy Halloween!

It’s the time of year for goblins, witchcraft, candy, horror movies, and ghosts. For us here at Cystic Fibrosis Canada, it is the perfect time…

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