We have one powerful community! 💙 As we celebrate this new year, we’re reflecting on what’s possible when people come together with a shared purpose. From incredible events to life-changing programs, you helped write a new cystic fibrosis story. Join us as we continue to push for an even greater impact by hosting your own fundraising event this year. Click here to learn how you can get started: https://changemakers.cysticfibrosis.ca/become-a-changemaker | Cystic Fibrosis Canada - Atlantic Regio

"It's kind of surreal to see people supporting your cause, because essentially they're supporting your life." In this short documentary, CF Champion Tara Bourque is sharing her journey living with cystic fibrosis. Visit our website and help us achieve a world without CF: http://www.cysticfibrosis.ca/ | Cystic Fibrosis Canada

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

🎁🎁Double Your Gift ➡️➡️Double the Impact. Stephanie Stavros, a CF warrior, knows firsthand how critical treatments like Trikafta are. Make a gift today and your donation will be matched, ensuring even more people living with CF get the care they need to live W/O Limits. Donate today and change lives. 🌟 | Cystic Fibrosis Canada

Want to know what CF related clinical trials are happening in Canada? Check out our Clinical Trial Finder tool: https://trialfinder.cysticfibrosis.ca/ | Cystic Fibrosis Canada

Canada's CF community knows well that life-changing treatments have brought uncharted territory and a range of new needs to be met. How is Cystic Fibrosis Canada evolving to meet those needs today and tomorrow? Our President & CEO Kelly Grover joined last week's episode of Sickboy with answers. Tune in now for this far-ranging discussion that's grounded in the commitment and needs of the CF community: https://spoti.fi/4efsNLd | Cystic Fibrosis Canada

Nominations are now open for the 2025 Cystic Fibrosis Canada Community Awards! Every achievement in the CF community is powered by people who give their time, energy, and heart. Their dedication, leadership, and generosity create a stronger, more connected community and helps us improve the lives of Canadians living with CF. Now is your chance to celebrate them - someone whose contributions inspire others and make a lasting impact. Nominations close November 1, 2025! Don’t wait, nominate today:

Cystic Fibrosis Canada is on a mission to raise $100,000 this Giving Tuesday, December 2. And we need your help! Your gift is essential to our work. We’ve come so far, but we’re at risk of losing momentum if we stop investing in research, care, and support. Today, people with CF are living longer – but that brings new challenges. Many now face complex health issues like CF-related diabetes, heart disease, and mental health struggles. The financial burden of lifelong treatment is growing, and car