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News Posts

Cystic Fibrosis Resource Guide

WE HEARD YOU! BACK BY POPULAR DEMAND!  Cystic Fibrosis Canada is pleased to provide the 2019-2020 Cystic Fibrosis Resource Guide as a source of information…

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Whatever it takes; for myself, for my brother, and for everyone else living with CF

For most people, a cough is a temporary inconvenience. For me, and the thousands of other Canadians living with cystic fibrosis (CF), a cough is…

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Whatever it takes; for my daughter not to face this alone

Living in Canada, where many people receive the health care they need, is a privilege. But many people receiving care is not everyone – and…

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WORLD MENTAL HEALTH DAY

Today is World Mental Health Day, a day marked by the World Health Organization (WHO) to raise awareness of mental health issues globally and mobilize…

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Connections Summer/ Fall 2019 is now available!

Cystic Fibrosis Canada is proud to announce that the Summer/Fall 2019 edition of Connections is now published in print and online! In this edition, we…

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Whatever it takes; to be a mom for as long as I can

Many of us can relate to the daily stress and worry that comes with being a parent; scheduling play dates, juggling appointments, daily chores, making…

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CONGRATULATIONS TO THE 2019 IAN F. MCCLURE AND BILL SKELLY AWARD RECIPIENTS

Kin Canada is Cystic Fibrosis Canada’s longest standing partner whose continued commitment has made a difference in the lives of Canadians with cystic fibrosis. Since…

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Higher Education Financial Support Opportunities for the CF Community

It’s that time of the year again – back to school season! Post-secondary education can be expensive, which is why we gathered some financial support…

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Back To School Season: A CF Mother’s perspective

TIPS TO MAKE “BACK TO SCHOOL” A SEAMLESS EXPERIENCE FOR YOU AND YOUR CHILD.  The beginning of a new school year is fast approaching. For…

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