Cystic Fibrosis Canada, Ontario

Cystic Fibrosis Canada, Ontario Cystic Fibrosis Canada is a national charitable not-for-profit corporation committed to finding a cure for cystic fibrosis (CF).

This is our page for Ontario and its 18 chapters as well as Nunavut. Please also follow your local chapters' pages.

Pipes for the People is a free, virtual program that introduces kids, teens and adults with CF to the chanter to encoura...
03/08/2026

Pipes for the People is a free, virtual program that introduces kids, teens and adults with CF to the chanter to encourage lung health. The chanter is a beginner-friendly instrument connected to bagpipes. Through guided lessons, participants gain a fun, creative way to strengthen breathing, build confidence, and discover the joy of making music.

This unique initiative was launched by Keshav, a teen who experienced firsthand how playing the chanter supported his own breathing during recovery from a lung infection. Today, the program is proudly supported by Canadian pipe band partners SFU and RMM.
🎶 Learn more and sign up for free:
https://pipesforthepeople.com/

Explore fundraising events across Canada this month and help create a meaningful change in support of Cystic Fibrosis Ca...
03/08/2026

Explore fundraising events across Canada this month and help create a meaningful change in support of Cystic Fibrosis Canada.

- Frock Swap: March 8 (BC)
- Team Stefan’s Oscars Pool: March 15 (ON)
- Oscars Night at the Fox: March 15 (ON)
- Oscars Night at ByTowne Cinema: March 15 (ON)
- JazzFest: March 28 (QC)

Want to start your own fundraiser? Register now: https://changemakers.crowdchange.ca/

This International Women’s Day, we’re celebrating the women and those who identify as women across the cystic fibrosis c...
03/08/2026

This International Women’s Day, we’re celebrating the women and those who identify as women across the cystic fibrosis community.

From mothers and caregivers, to people living with cystic fibrosis, clinicians and clinic teams, and researchers advancing new discoveries. And to the volunteers, community leaders, and the women across the CF Canada team helping move this mission forward every day, thank you.

🚶‍♀️🚶‍♂️🌟 Come celebrate 65 years of progress at the Walk To Make Cystic Fibrosis History on May 31 and take the first s...
03/05/2026

🚶‍♀️🚶‍♂️🌟 Come celebrate 65 years of progress at the Walk To Make Cystic Fibrosis History on May 31 and take the first step towards changing the lives of people with CF! Register early and opt into our contests by selecting the $25 fee and you’ll not only contribute to a great cause but also get a chance to win an Apple iPad, valued at $564! Sign up, start fundraising, and winning big! 🏁🎉 https://bit.ly/3MwP8v0

Maxim is a fourteen-year-old girl living with cystic fibrosis and an ice dancing athlete, representing Team Quebec at th...
03/03/2026

Maxim is a fourteen-year-old girl living with cystic fibrosis and an ice dancing athlete, representing Team Quebec at the Prospect level. She has never let CF stop her from living her dreams. Despite frequent hospital visits and daily CF care routine, she lives her life to the fullest, with the support of her family. “Every day should be lived like it’s a win”, says Maxim’s mom, Marie-Eve.

Maxim’s passion is what keeps her focused on her health and pushing forward in her journey as a figure skater with CF.

Read Maxim’s story on our blog here: https://bit.ly/4cftndz

“Together, we can and will make a difference,” says Hailey, captain of the Strong & Salty team. Hailey knows this first-...
03/02/2026

“Together, we can and will make a difference,” says Hailey, captain of the Strong & Salty team. Hailey knows this first-hand as she is living with cystic fibrosis and has been participating in the Walk To Make Cystic Fibrosis History for over 20 years, showing that every step truly matters.

Every registration fuels the vital work Cystic Fibrosis Canada does to improve and lengthen the lives of people living with CF. When you register and fundraise for the Walk, you’re helping drive breakthrough research, strengthen world-class care and advance access to the treatments for those who need it most.

“Living and aging with CF comes with many complications. Which is why your decision to participate in the Walk means so much to every Canadian living with cystic fibrosis. [It] makes me feel like we have a team of people who surround and support us while we fight our lives with CF. ”

Join Hailey and your local community to make a difference today at the Walk To Make Cystic Fibrosis History!

➡️Read more about Hailey's story https://bit.ly/4shDl2H
➡️Register now for the Walk https://bit.ly/4beb6LF

02/27/2026

Early birds don’t just get the worm, they get the win!

You can NOW register for the 22nd Walk To Make Cystic Fibrosis History! By signing up and paying the $25 opt‑in fee by March 31, you'll be entered to win a 10.9 inch Apple iPad.

Don’t miss this chance to make a difference and win big! the best Walk yet on May 31! 🏆 https://bit.ly/3MwP8v0

"Although it has changed my life for the better, [Trikafta] is not a cure. Medications, treatments, and strict infection...
02/26/2026

"Although it has changed my life for the better, [Trikafta] is not a cure. Medications, treatments, and strict infection prevention measures remain part of my daily life - and many CF patients still do not have access to this therapy." - Tiffany

We’re entering a new era of cystic fibrosis care. We must ensure every person with CF —regardless of geography, age, socio-economic status, or access to modulators — receives personalized, quality healthcare as their needs evolve. Your support will help shape the future of cystic fibrosis, creating a world where all Canadians with CF like Tiffany live without limits.

It's your last chance to donate! Because CF isn’t cured yet. And until it is, your generosity is the lifeline families need. https://bit.ly/4apemEC

02/24/2026

Join Allie and other fundraisers for the Community & Fundraising Chat!

March 2nd at 1:00 PM (ET) | Live on Zoom

Whether you’re looking for new fundraising ideas or simply want to connect and share stories, this session is a great way to get inspired by others in the community.

Register now to learn how you can maximize your impact on event day. More details here https://bit.ly/3OYqsvW

See you there!

Cystic fibrosis affects families every day - both mentally and physically. Your donation will not only help advance the ...
02/23/2026

Cystic fibrosis affects families every day - both mentally and physically. Your donation will not only help advance the research that brings us closer to a cure, it will support equitable care and initiatives like the first ever Canadian guidelines for CF care, providing clinicians across the country with the tools they need to reduce burdens and adapt treatment plans to individual care needs.

Your generosity can have an immediate impact on someone’s life. Donate now. https://bit.ly/4apemEC

We are so back! Registration for the 22nd annual Walk To Make Cystic Fibrosis History opens February 27.Set your reminde...
02/21/2026

We are so back! Registration for the 22nd annual Walk To Make Cystic Fibrosis History opens February 27.

Set your reminder and a future without limits for all Canadians living with cystic fibrosis.

Find out more about the Walk: https://bit.ly/4rXlii2

“With more people living with CF than ever before, clinics are busier adapting their care and responding to the diverse ...
02/18/2026

“With more people living with CF than ever before, clinics are busier adapting their care and responding to the diverse needs of the CF community that is ageing for the first time”, says Dr. Paul Eckford, Chief Scientific Officer at Cystic Fibrosis Canada.

By donating today, you’ll help support initiatives like the first ever Canadian guidelines for CF care, a project Cystic Fibrosis Canada has developed alongside a national panel of clinicians and community members. You’ll help Canadians with CF receive world-class care, built for Canadians and their evolving needs.

Donate now! https://bit.ly/3ZfQSeI

Address

2323 Yonge Street Suite 800
Toronto, ON
M4P2C9

Telephone

1-800-378-2233

Website

Alerts

Be the first to know and let us send you an email when Cystic Fibrosis Canada, Ontario posts news and promotions. Your email address will not be used for any other purpose, and you can unsubscribe at any time.

Contact The Practice

Send a message to Cystic Fibrosis Canada, Ontario:

Shortcuts

Share

Share on Facebook Share on Twitter Share on LinkedIn
Share on Pinterest Share on Reddit Share via Email
Share on WhatsApp Share on Instagram Share on Telegram