CONNECTIONS WINTER 2019
Cystic Fibrosis Canada is proud to publish the winter 2019 edition of Connections magazine! It is published online only. In this edition, we introduce our…
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Living with an unpredictable disease
When you have CF, life can often be unpredictable. A simple cold can turn into an infection and an infection can lead to a long…
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Practical Tips to Stay Organized during March Break – Caregivers Edition
March Break is such a fun time of year! Children are on break from school, and some parents /guardians take vacation time to spend it…
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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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