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Archive for November, 2018

You can make a difference

When you are donating to CF Canada, you are supporting not only those who live with CF by helping us invest in research and care…

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Introducing Cystic Fibrosis Canada’s holiday giving campaign: Tough Questions

To celebrate Giving Tuesday, the global day for giving, Cystic Fibrosis Canada is excited to introduce the 2018 holiday giving campaign: Tough Questions. Having cystic…

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Advice for Parents of a CF child

Becoming a parent is one of the most emotional and overwhelming experiences for people, and a new cystic fibrosis diagnosis can be all-consuming. Cystic Fibrosis…

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Spotlight: Jenny Lalancette

What is the nature of your commitment to Cystic Fibrosis Canada (volunteer, donor, event organizer, etc.)? It all began in October 2015. I wanted to get…

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World Diabetes Day: Nutrition and CFRD

November 14 is World Diabetes Day. People living with CF have a unique type of diabetes called CFRD (Cystic Fibrosis-Related Diabetes) which is found in…

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Cystic Fibrosis Canada launches MyCFLifePortal

Cystic Fibrosis Canada is thrilled to announce the launch of MyCFLifePortal.ca. Canadians living with cystic fibrosis will now have the opportunity to access their CF…

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Coping with the loneliness of CF

Living with a rare disease can be lonely. There are a limited number of people who share in your lived experience, and despite how hard…

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The 2018 North American Cystic Fibrosis Conference

The North American Cystic Fibrosis Conference (NACFC) is the largest event of its kind, bringing together physicians, nurses, researchers, multidisciplinary healthcare providers, and others connected…

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2018 Newborn Resource Kits

In early October Cystic Fibrosis Canada staff came together to assemble 100 Newborn Resource Kits which are designed to support families during the time of…

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