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To read previous Canadian CF Registry Annual Data Reports, click below:
Cystic Fibrosis Canada has launched a Trends Report that examines key trends in Canadian CF health data.
2020 was anything but typical. For those who monitor the state of cystic fibrosis (CF) in Canada, it will be remembered as a year filled with uncertainty, optimism, and change. Cystic Fibrosis Canada’s Canadian Cystic Fibrosis Registry 2020 Annual Data Report shed light on how the events of this unusual year as well as advancements in treatments and access to new drugs over the last decade have impacted people who live with cystic fibrosis. Here, we explored three trends that emerged from the data in 2020 and asked what they might mean for the Canadian CF community. It is important to note that we did not conduct scientific studies and aren’t able to draw any specific conclusions, however, we can ask some intriguing questions given the observed data.
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Certain PDF documents may not work with current assistive technologies because they use outdated technologies that do not support accessibility. Cystic Fibrosis Canada will convert documents to new formats upon request within 5 business days. Please contact accessibility@cysticfibrosis.ca for support.
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Dedicated volunteers in Kitchener, ON are excited to announce their first annual Cystic Fibrosis Gala in support of Cystic Fibrosis Canada. The event will feature a buffet dinner with a cash/card bar, dance and a live performance from Windjammers, a 45-piece band.
*See event listing to learn more & purchase tickets today!
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My name is Mia Gaudenzi and I’m 12 years old. I was born a seemingly healthy baby until around 3 years old when I became ill with pneumonia regularly. Doctors just thought I was unlucky until I had my sweat chloride tests to rule out CF.
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