Cystic Fibrosis Canada - BC

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.

Your lived experience could make a difference.Peer Connect is recruiting Group Facilitators to help lead welcoming, incl...
09/11/2026

Your lived experience could make a difference.

Peer Connect is recruiting Group Facilitators to help lead welcoming, inclusive virtual conversations for people impacted by cystic fibrosis.

Working with a co-facilitator, you'll help create a space where community members can connect, share experiences, and support one another.

We're looking for people who:
โ€ข Live with cystic fibrosis
โ€ข Are a parent/guardian of someone living with CF

Donโ€™t worry - we provide training, resources, and ongoing support to help you succeed in the role.

Learn more and apply today: https://bit.ly/4r2Rkdv

Epic views. Unforgettable memories. A meaningful cause.Join a group of passionate legacy and new trekkers as they journe...
09/10/2026

Epic views. Unforgettable memories. A meaningful cause.

Join a group of passionate legacy and new trekkers as they journey through the iconic Scottish Highlands while raising funds and awareness for Cystic Fibrosis Canada.

Email [email protected] to find out how you can be part of this incredible experience.

09/10/2026

Jack is like any other four-year-old: he loves monster trucks, playing hockey, and spending time with his big brother.

But before he can play, cystic fibrosis comes first. Medications, enzymes, physiotherapy, and treatments are part of his routine every single day.

Your support helps fund research, strengthen care, and advocate for access to life-changing treatments. Together, we can give more children with CF the freedom to be children.

Donate now: https://give.cysticfibrosis.ca/page/195941/donate/1?ea_tracking_id=org-social

Making slime. Decorating pill boxes. Playing games. And meeting other young people who just get it. ๐Ÿ’™ That was Camp From...
09/01/2026

Making slime. Decorating pill boxes. Playing games. And meeting other young people who just get it. ๐Ÿ’™ That was Camp Fromaway 2026!

For one week this past July, youth living with cystic fibrosis joined us virtually from across Canada for activities, laughs and connection (don't worry, you can read all about it on our blog: https://bit.ly/461uJnP ).

A huge thank you to our campers, Upopolis, Brigadoon, facilitators and volunteers for making it such a great week. And.... weโ€™re already looking ahead! Save the date for Camp Fromaway 2027: July 12-16, 2027. More details to come!

08/28/2026

Summer might be winding down, but our Change Makers are just getting started!

This September, dedicated people from coast to coast are rallying their families, friends, and local communities to raise funds and awareness for cystic fibrosis. Find a fundraiser near you or create your own to help move us closer to a future without limits.

- YYC Energy Charity Classic โ€“ September 3 (AB)
- La Classique internationale de canots de la Mauricie (participation) โ€“ September 5 (QC)
- Fairway of Dreams โ€“ September 5 (SK)
- Face off with CF Gala โ€“ September 12 (AB)
- Jogging for Jovie โ€“ September 13 (AB)
- KISS CF Goodbye #10 โ€“ September 19 (ON)
- Strike out for CF โ€“ September 25-27 (BC)
- Rallye FK des Sylvain โ€“ September 26 (QC)
- GearUp4CF Kamloops โ€“ September 26 (BC)
- Shinerama, September 2026, at the University of Manitoba, Mount Allison University, WLU Brantford & Waterloo, and the University of Ottawa

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

Research funded in part by Cystic Fibrosis Canada has been published in Science.This exciting work from Dr. Bowen Li fro...
08/27/2026

Research funded in part by Cystic Fibrosis Canada has been published in Science.

This exciting work from Dr. Bowen Li from the University of Toronto and his team explores a new approach that could one day help people with rare cystic fibrosis mutations who don't benefit from today's therapies.

It's a powerful reminder that every breakthrough begins with research and every research project begins with supporters who believe progress is possible.

๐Ÿ”— Learn more: https://bit.ly/4wW5rm7

For Hailey, a 32-year-old from Quebec, cystic fibrosis has a constant and significant impact on her daily life. Her diag...
08/20/2026

For Hailey, a 32-year-old from Quebec, cystic fibrosis has a constant and significant impact on her daily life. Her diagnosis ignited a sense of urgency not only to support the CF community, but also to chase her dreams.

As the cystic fibrosis population continues to grow and age, ongoing investment in research, advocacy, and clinical care is more important than ever.

Create a lasting impact. Become a monthly donor today. Your ongoing support will help bring the CF community one step closer to a future without limits. https://bit.ly/4hIOasI

Nothing says back-to-school season like a new opportunity to make a difference! โœ๏ธNo matter your age, fundraising helps ...
08/17/2026

Nothing says back-to-school season like a new opportunity to make a difference! โœ๏ธ

No matter your age, fundraising helps support critical research, advocacy efforts, and programs for people living with cystic fibrosis. Getting involved can be as simple as organizing a Dress Down Day at your school! ๐Ÿ‘•

๐Ÿ’ก Looking for more inspiration? Explore our fundraising ideas: https://changemakers.cysticfibrosis.ca/fundraising-ideas

Together, we can make a meaningful impact. Whether your fundraiser is big or small, every contribution helps move us closer to a future without limits.

Start your own fundraiser and become a Change Maker today! https://changemakers.cysticfibrosis.ca/

Calling our friends across Canada! ๐Ÿ’™The 34th Annual Face Off with CF Gala is happening in Edmonton on September 12, and ...
08/13/2026

Calling our friends across Canada! ๐Ÿ’™

The 34th Annual Face Off with CF Gala is happening in Edmonton on September 12, and weโ€™d love to welcome supporters from across the country for an unforgettable evening in support of Cystic Fibrosis Canada.

โœˆ๏ธ Join us in Edmonton โ€” gather your friends, family or colleagues and make a weekend of it.

๐Ÿ’™ Canโ€™t attend? You can still make an impact by making a donation directly through the Face Off with CF Gala website.

Whether you join us in person or support from afar, youโ€™re helping create a future where everyone with cystic fibrosis can live W/O Limits.

๐ŸŽŸ๏ธ Attend or donate: cfgala.ca

๐Ÿ’ Join us for the 34th Annual Face Off with CF Gala!

One month away, on Saturday, September 12, weโ€™re bringing the CF community together at the JW Marriott Edmonton ICE District for an incredible evening in support of Cystic Fibrosis Canada.

With Honorary Chairs Ryan and Breanne Nugent-Hopkins, guests will enjoy an elegant dinner, live and silent auctions, special guests, inspiring stories and a Hot Stove Q&A.

Last year, this incredible community raised more than $264,000. Letโ€™s make an even bigger impact in 2026! ๐Ÿ’™

๐ŸŽŸ๏ธ Tickets are available now: http://cfgala.ca

Address

BC Area
Burnaby, BC

Opening Hours

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

Telephone

+16044361158

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