Archive for December, 2018
Anne-Sophie Barrette: How can I not keep smiling?
My name is Anne‑Sophie, I’m 26 years old and I’m a pastry cook. I have two extraordinary parents, who are more loving, devoted and generous than you…
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Navigating the Holidays with CF
The holidays are an exciting time of year, but they are also a very busy time and for some people, it can even be quite…
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The McDougall Family: Time is Precious
My name is Twyla McDougall. I live in Regina, Saskatchewan. My husband Christopher and I are blessed to have three daughters: Ella, Soleil, and Allegra….
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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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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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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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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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Preparing for Cold Season with CF
Despite the beauty of the Canadian cold seasons, the climate can have a negative effect on the health of people with cystic fibrosis. This is…
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Late Summer Melancholy – Guest Post from Audrey
As usual, we can see the summer galloping away. Yes, it’s with great sadness that I must declare dehydration season over. Of course, this means…
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