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Volunteer Advocate
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Spotlight: Putting An End To CF, One Pitch At A Time

Meet Neil Power and Grant Taylor. Both of these gentlemen work as provincial employees of the Government of Newfoundland and Labrador. They have both participated…

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Spotlight: Running, paddling and cycling the Trans Canada Trail for Cystic Fibrosis Canada

Kalea Mullett is raising awareness about Cystic Fibrosis Canada in memory of her sister, Lindsay. Recently, Kalea took on a 24,000 km challenge, spanning across…

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Advocacy in Action: An Open Letter to the Right Honourable Justin Trudeau: Please Save my Life

Dear Prime Minister Trudeau: My name is Melissa Verleg and I am a 36 year old mother of two young boys from Vernon. I live…

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Cystic Fibrosis: The Physical and the Mental

Recently, I’d been asked about how I take care of my mental health as it relates to living with cystic fibrosis (CF). I thought it…

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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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Transitioning to Adult Care

The transition from paediatric care to adult care is a big step in the life of a person with cystic fibrosis and involves many responsibilities;…

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Spotlight: The Vanstone’s Trek to the Great Wall of China

In September, 17 year old CF warrior, Madi Vanstone and her mom, Beth made the trek to China in support of Cystic Fibrosis Canada. For…

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Balancing Physical and Mental Health

People with CF spend a lot of time taking care of their bodies.  For many; nebulisers, inhalers, blood sugar monitoring, and insulin shots are part…

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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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