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Stories Posts

Access to CF medicines in Canada – CF Canada blog circle

Access to medications is one of the most important priorities for Cystic Fibrosis Canada. Together with the Canadian CF community, our CEO, our advocacy program…

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Keeping CF kids healthy in winter: A Parent’s Perspective

It is a lot of work to keep our CF kids healthy throughout the winter, but the truth is, every year winter seems to be…

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Michel Desrochers: Wishing to Hear My Baby Breathe Easily

My son, Benjamin, is 9 months old and lives with cystic fibrosis (CF). He was one of the first newborns in Québec to have been…

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Gillian Bennett: My Wish to See My Son Live a Long and Healthy Life

My husband and I welcomed our son, John, into the world in May 2010. Two months later, on July 14th 2010, John was diagnosed with…

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Wishes for the holidays

The Holiday Season is here!  This time of year brings joy and happiness to many, but also has its own set of challenges for those…

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Samuel Moreau: My Wish to Thrive In Spite of CF

I was 4 and a half when I was diagnosed with cystic fibrosis (CF). Prior to my diagnosis, the doctors didn’t know what was wrong…

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Danielle Weil: My Wish is to Watch my Daughters Grow Up Together

My name is Danielle Weil and I live in Brantford, ON with my husband, Matt, and our two beautiful twin girls, Erin and Mary-Elizabeth (Emme)….

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World Diabetes Day: The CF-related diabetes (CFRD)

November 14th is World Diabetes Day. According to the 2017 Canadian CF registry, about 22.4% of people living with CF also have CF-related diabetes (CFRD)….

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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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