WORLDWIDE WALK TO MAKE CF HISTORY: PERU EDITION
Emotional, amazing, unreal, life-changing, incredible. These are words people have used to describe Cystic Fibrosis Canada’s first ever Worldwide Walk to Make Cystic Fibrosis History…
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Food and CF – Caregivers’ Perspective
For a caregiver, understanding the needs of the person you care for is very important. As we highlighted earlier this month, food and nutrition are…
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Clinical trials: A CF parent’s perspective
My name is Lina Bhardwaj and my 13-year-old daughter Rianna lives with cystic fibrosis. Rianna was diagnosed at two months old and luckily, she’s been…
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Clinical trials: A patient’s perspective
My name is Mark Becker and I’m 36-years-old. I’m a secondary school teacher for students with autism and I live with my wife Ana and…
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Spotlight: Sandra Dery
Who am I? I’m a 31-year-old woman named Sandra. Not “I have cystic fibrosis, and my name is . . . ” This is how several people choose…
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Adapting Your Diet to Summer
Food and nutrition are very important for people living with cystic fibrosis. But as the temperature rises and we approach summer, it’s an even more…
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2019 Broken Arrow Conference
Cystic Fibrosis Canada’s 17th Broken Arrow Conference, hosted in Toronto from May 2nd – 4th, was a great success. The event brought together many of the…
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Thank you for making history!
What a month! As we close Cystic Fibrosis Awareness Month we want to say THANK YOU for mobilizing, motivating, encouraging, fundraising, recruiting and caring. Thank…
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Walk for Kadeem
My name is Kadeem Morgan, I’m 22 years old and live in Pickering, Ontario. I was diagnosed with cystic fibrosis at one year old. I…
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