A Forum on Rare Diseases in Quebec
On February 22, in Montreal, Cystic Fibrosis Canada, in collaboration with the Alliance des patients pour la santé and the Regroupement québécois des maladies orphelines (RQMO),…
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Sandy Stevens: I needed answers and the answer was advocacy
My 12-year-old daughter who has Cystic Fibrosis (CF) has been in the hospital many times with longer stays each time. They’re trying all the support…
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Spotlight: Gary and Colleen Donovan
What’s your involvement with CF Canada (are you a volunteer, donor, event organizer, participant etc.)? I am the current president of the Niagara Chapter. For…
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The unique challenges of caregiving
In honour of Family Day, we are excited to share this caregivers community blog post. We have reached out to parents and siblings of people…
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Love and Marriage and CF
Happy Valentines’ Day! Today is a special day to celebrate love in its many forms, and we wanted to take this opportunity to celebrate some…
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Spotlight: Lisa Hulbert
Lisa is participating in CF Canada’s Machu Picchu Walk. In this interview, she shares why she decided to fundraise in support of CF Canada. What’s…
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Is a clinical trial right for you?
Clinical trials test potential new drugs, treatments and devices to ensure they are safe, to assess how well they work, and to determine whether they…
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Adulting with CF
The transition from pediatric care to adult care is a big moment in the cystic fibrosis community, which involves shifts of responsibility, advocating for one’s…
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Fertility and Family Planning Webinar Series
Our Adult Cystic Fibrosis Advisory Committee (ACFAC) has been hard at work on a number of ongoing projects. Among these initiatives, we are pleased to…
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