Cystic Fibrosis Canada - Atlantic Region

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Cystic Fibrosis Canada - Atlantic Region

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This page represents the Atlantic Region of Cystic Fibrosis Canada. This page is run by Cystic Fibrosis Staff.

CF Canada is a national charitable not-for-profit corporation established in 1960, and is one of the world’s top three charitable organizations committed to finding a cure for CF. The Cystic Fibrosis Canada - Atlantic Region's page is an online community where people can share information, tell their story, and interact with one another. We share a national vision for ending CF, while elevating stories across Atlantic Canada here.

10/28/2026

November is here, and our Change Makers continue to show what's possible when communities come together. 🍂

Across Canada, people are finding meaningful ways to raise funds and awareness for cystic fibrosis. Whether you join an upcoming event or create a fundraiser of your own, every effort helps bring us closer to a future without limits.

- Marquer contre la FK – November 7 (QC)
- Souper Spectacle (Sacré-Coeur) – November 7 (QC)
- Edmonton Casino – November 7-8 (AB)
- Brews Brushes and Belly Laughs – November 13 (ON)
- Upcycle Christmas Craft Sale – November 14 (BC)

Find upcoming events on our website: https://cysticfibrosis.ca/events-hub

10/26/2026

📣 Calling all CF fundraisers, walkers, riders and go-getters! You make community fundraising happen, so help us shape what comes next. Tell us what motivates you, how you'd like to get involved, and what would make your experience even better.

Take our 5-minute survey: https://bit.ly/4smifBq

10/22/2026

Emma, a 24-year-old triathlete, spent years navigating long hospital stays, countless treatments, and the daily challenges of living with cystic fibrosis (CF). Thanks to progress in cystic fibrosis treatment, fueled by donors, she is now pursuing opportunities that once felt out of reach. But while treatments like Trikafta have changed the lives of many, CF is still not cured.

Read Emma’s inspiring story of resilience, progress, and hope. https://bit.ly/4iyH4qw

10/20/2026

Our research funding is helping uncover new ways to fight persistent lung infections in people with cystic fibrosis. 🔬

With support from Cystic Fibrosis Canada, Dr. Justin Di Trani and his team are identifying weaknesses in bacteria that cause difficult-to-treat infections, bringing us closer to understanding how future treatments could be more effective.

Read more about the discoveries they're making and what's next for this research: https://bit.ly/47Xvkrs

10/16/2026

Emma is chasing goals she once thought were out of reach, thanks to advances in CF research and care. But living with cystic fibrosis and CF-related diabetes means every day is still a balancing act.

New treatments changed Emma’s life, but they aren’t a cure. She still lives with this disease every day. Donate today to help fund the next breakthrough: https://bit.ly/4xt4JwU

10/15/2026

Today is Global Peer Support Day and we're celebrating the power of peer support and the volunteers who help make it possible.

Through our Peer Connect program, people with cystic fibrosis and caregivers can connect with others who understand the realities of life with CF, share experiences and support one another.

Whether you're looking to connect with the community or interested in helping others as a volunteer facilitator, learn more about upcoming Peer Connect sessions and volunteer opportunities: https://cysticfibrosis.ca/peer-connect

10/13/2026

"For me, clinical trials didn’t just extend my life. They gave me back my future. And that is worth it every time."

Élise has participated in clinical trials throughout her life, helping advance research that benefits the entire cystic fibrosis community. When her health took a dramatic turn, that research gave her a second chance. Today, she continues to chase her dreams and lives life to the fullest.

By becoming a monthly donor, you’ll help power the clinical trial network that could lead to breakthroughs like the ones that changed Élise's life. https://bit.ly/4hIOasI

10/13/2026

Grab your lederhosen and join the Kinsmen Club of Corner Brook for their 3rd Annual Kintoberfest on October 24th.

Make sure to register your teams with Keith Hobbs at [email protected] as they are maxing out at 16 teams!

With live music, costumes, prizing and curling fun, it's sure to be a great day!

A portion of proceeds are in support of Cystic Fibrosis Canada and will help\us go further to drive advancements in treatment, care, and advocacy for everyone impacted by cystic fibrosis.

10/12/2026

Halloween is just around the corner so here are three ways to fundraise for Cystic Fibrosis Canada this spooky season:

- Host a costume party
- Organize a pumpkin carving contest
- Turn your trick-or-treating adventure into a fundraiser

Even in their Halloween best, Change Makers are raising funds to help advance research, care, advocacy, and support for people living with CF across Canada. Join this incredible community, start your frightful fundraiser today and show us your best costume in the comments. 🎃🧡

https://changemakers.cysticfibrosis.ca/

10/10/2026

Pearl lives with cystic fibrosis (CF) and has undergone two double lung transplants.

Today, she is grateful every day for her organ donors and the second chance they gave her.

Pearl shares what it's like to live with CF and cystic fibrosis-related diabetes (CFRD), while pursuing her dream career as an athletic therapist and enjoying life with her beloved pets.

Read Pearl's story: https://bit.ly/3TzZzBs

Address

Dartmouth, NS

Telephone

+19024252462

Website

http://www.cysticfibrosis.ca/atlantic-canada/

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