Questions and Answers Related to our Advocacy Work
We recently invited our online community to ask us questions about our advocacy work. We responded in the comments sections. We made a round-up of…
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All for fair drug prices and access to medicines
A life-changing drug that can help 90% of people living with cystic fibrosis is stuck in a complicated web of Canadian bureaucracy. Trikafta has been…
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Advocacy Update From the Desk of the CEO
Improving access to the new life-changing cystic fibrosis (CF) medications is a priority for Cystic Fibrosis Canada (CF Canada) and we have been working hard,…
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Spotlight: He would move heaven and earth to create a world without cystic fibrosis
Today, as we continue our overview of the donors and fundraisers working tirelessly for Cystic Fibrosis Canada across the country, we’re stopping in Quebec to…
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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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