Cystic Fibrosis Canada - BC

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Cystic Fibrosis Canada - BC We are dedicated to finding a cure for cystic fibrosis. We share a vision for ending CF, while elevating stories across BC and Yukon.

This page is run by Cystic Fibrosis Canada staff.

Emma, a 24-year-old triathlete, spent years navigating long hospital stays, countless treatments, and the daily challeng...
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

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

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

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

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

Pearl lives with cystic fibrosis (CF) and has undergone two double lung transplants.Today, she is grateful every day for...
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

Looking to connect with others who truly understand the realities of cystic fibrosis? Our Peer Connect sessions offer a ...
10/05/2026

Looking to connect with others who truly understand the realities of cystic fibrosis? Our Peer Connect sessions offer a welcoming virtual space to share experiences, learn from one another, and build meaningful connections within the CF community.

Here are the sessions taking place in October:
🔹 October 6: CF Adults Open Connection
🔹 October 8: Connecting Young Adults Living with CF
🔹 October 13: Connecting CF Parents and Guardians
🔹 October 29: CF Dads and Father Figures

Whether you're living with CF, parenting a child with CF, or supporting a loved one, these conversations are an opportunity to connect with others who understand your journey.

Register today: https://cysticfibrosis.ca/events-hub

Teresa lives with an ultra-rare form of cystic fibrosis (CF).From hours of treatments to hoping for a breakthrough treat...
10/03/2026

Teresa lives with an ultra-rare form of cystic fibrosis (CF).

From hours of treatments to hoping for a breakthrough treatment, Teresa’s journey reflects both the challenges many people with CF continue to face and the importance of continued progress.

Teresa shares her experience of living with CF, the sacrifices she’s made, and why continued research matters.

Read Teresa’s story now. https://bit.ly/4z7ImOO

09/29/2026

Teresa spends three hours every single day to manage her cystic fibrosis. Modulator therapies are not currently funded for her rare CF mutation. Your support helps bring us closer to a future where everyone living with CF has access to effective treatments—regardless of their mutation—by funding research, improving care, and strengthening advocacy efforts for everyone living with CF.

Create an impact. Donate today: https://bit.ly/4xt4JwU

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BC Area
Burnaby, BC

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Monday 9am - 5pm
Tuesday 9am - 5pm
Wednesday 9am - 5pm
Thursday 9am - 5pm
Friday 9am - 5pm

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+16044361158

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