It’s Giving Tuesday! Today, we’re sharing a powerful video featuring three incredible stories – all deeply connected by cystic fibrosis. Their journeys show why your support truly matters. ⏱️ Countdown to midnight - help us reach our $100K goal! Every dollar is doubled today, meaning your gift goes twice as far to fund breakthroughs in research and life-changing CF care. Let’s do this together. 💙 Donate now https://heyor.ca/OAtKSE | Cystic Fibrosis Canada
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It’s Giving Tuesday! Today, we’re sharing a powerful video featurin…
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Families affected by cystic fibrosis face mental and physical challenges every day. Your donation today can fund programs and resources that help Canadians living with cystic fibrosis access the care they need.💙 Give healthcare without limits and help us reach our goal of $30K by February 28. https://bit.ly/3QpEpkp | Cystic Fibrosis Canada
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Families affected by cystic fibrosis face mental and physical challeng…
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Here's a first look at our three-part series where we take a deep dive into the latest Canadian CF Registry Annual Data Report with our Registry Director, Stephanie Cheng. The Canadian CF Registry monitors clinical trends in the CF population, aiming to help improve the quality and length of life for those with cystic fibrosis by aiding clinicians and researchers understand disease patterns. You can read more about the latest clinical trends in the full report here: https://bit.ly/3W7ySm0 | Cyst
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Here's a first look at our three-part series where we take a deep dive i…
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We urgently need your help to make sure your province is represented in our study on the financial and social impact of life with cystic fibrosis. For the results to be statistically significant, we need more people living with cystic fibrosis and caregivers to participate and there are only 3 days left to register. Participation is voluntary. The patient survey will take approximately 45-60 minutes to complete, while the caregiver survey will take 20-30 minutes to complete. Both do not need to
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We urgently need your help to make sure your province is represented …
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We are in the final stretch of the Walk To Make Cystic Fibrosis History! With only a few days left before the big day, we urge you to keep going. Every dollar you raise will help to support our programs to improve and lengthen the lives of Canadians with CF 💙 Haven’t registered for the Walk yet? There is still time, find a location near you: 🔗 bit.ly/41pNFLn | Cystic Fibrosis Canada
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We are in the final stretch of the Walk To Make Cystic Fibrosis Hist…
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Don’t miss out! Peer Connect, Cystic Fibrosis Canada’s new pilot program with small, virtual conversation groups, still has a few August sessions with space: - Aug 27: Moving out for the first time with Teresa & Mikayla, young adults with CF. - Aug 28: Connecting dads & father figures with Mitch & Austin, CF dads. Spots are limited! Register now before they’re gone! 👉 https://cysticfibrosis.ca/events-hub | Cystic Fibrosis Canada
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