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.

Thinking about leaving a legacy gift but unsure how it might affect your loved ones? You’re not alone. Our partners at W...
02/13/2026

Thinking about leaving a legacy gift but unsure how it might affect your loved ones? You’re not alone. Our partners at Will Power have created a short webinar that breaks down what to consider when writing your Will, how to give without taking away from family, and the tax benefits that come with smart planning: https://bit.ly/4aPBSL6

02/12/2026

Tiffany dreams of becoming a scientist. Living with cystic fibrosis means she works hard every day to stay healthy enough to chase that dream. High-quality CF care makes all the difference. Though progress has come a long way, Tiffany still faces the struggles of life with CF every day – infections, complications and uncertainty.

Your support helps ensure Tiffany and others can keep moving forward toward brighter futures.

Read Tiffany’s story on our blog and make a gift today: https://bit.ly/4qoq1Ir

Golf Charity Tournament Raises $181,855 for Cystic Fibrosis Canada!We’re so grateful for the generosity of Home Hardware...
02/11/2026

Golf Charity Tournament Raises $181,855 for Cystic Fibrosis Canada!

We’re so grateful for the generosity of Home Hardware Stores Limited. This remarkable contribution will help advance our mission to improve life with cystic fibrosis.

More than just an annual event, the Supplier Partnership Charity Golf Tournament, held in the Kitchener-Waterloo area, is a moment when the community comes together and takes one step closer towards a world without limits.

Learn more here: https://bit.ly/4r1rZjb

Alyftrek update: After Health Canada’s approval and a positive funding recommendation from Canada’s Drug Agency, Alyftre...
02/10/2026

Alyftrek update: After Health Canada’s approval and a positive funding recommendation from Canada’s Drug Agency, Alyftrek is now with the pan-Canadian Pharmaceutical Alliance (pCPA), which negotiates drug pricing on behalf of Canada’s public drug plans. In short: federal, provincial, and territorial drug plans can’t move forward until the pCPA process wraps up.

We’ve written to the pCPA, public drug plans and Vertex, the manufacturer of Alyftrek to stress the urgency of timely access. But more voices matter. Advocacy is critical to help ensure people living with cystic fibrosis can benefit from Alyftrek as soon as possible.

Are you interested in meeting with your provincial or territorial elected official to call for coverage of Alyftrek now? If so, please email advocacy@cysticfibrosis.ca with the subject line “Advocacy for Alyftrek”. A support package with key messages and materials will be provided to help guide the conversation.

Some private drug plans may already be covering Alyftrek. Please check with your plan provider to see if you are covered.

✨ We’re still feeling the magic from the 2026 Windsor Royal Ball last month!A massive congratulations to the incredible ...
02/09/2026

✨ We’re still feeling the magic from the 2026 Windsor Royal Ball last month!

A massive congratulations to the incredible organizing committee for raising more than $88,000 in support of Cystic Fibrosis Canada. This year, the team was also honoured with a special edition 65th anniversary plaque recognizing their dedication, passion, and outstanding impact. 💙

Interested in joining the planning committee for 2027? Email events@cysticfibrosis.ca for more information.

We are entering a new era of cystic fibrosis care where innovative treatments are changing what's possible. But even as ...
02/09/2026

We are entering a new era of cystic fibrosis care where innovative treatments are changing what's possible. But even as health outcomes improve for some, CF still requires enormous daily management: hospital stays, infections, CF-related diabetes, and mental health impacts remain common.

That's why high quality, specialized CF care is essential for all Canadians impacted by this disease. Your support helps to ensure CF care teams have the tools they need to reduce burdens, personalize treatment plans, and improve health outcomes.

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

Hey Ontario! The Walk to Make CF History is happening right here on May 31 and we’re recruiting the Walk Committees acro...
02/06/2026

Hey Ontario! The Walk to Make CF History is happening right here on May 31 and we’re recruiting the Walk Committees across the province to help bring it to life. Ready? Here’s what it takes:

- A few hours a week from now until Walk Day
- Remote planning meetings
- Be on-site May 31 to see it all come to life
- Must be 18+

Want to help build your resume or get in some volunteer hours while making CF history? Join the team: https://cfvolunteer.rosterfy.ca/roles/list

Cystic fibrosis is rare. But for more than 4,500 Canadians, it’s everyday life.Behind every number is a person navigatin...
02/05/2026

Cystic fibrosis is rare. But for more than 4,500 Canadians, it’s everyday life.

Behind every number is a person navigating daily treatments, frequent clinic visits and the uncertainty that still comes with this disease:

💛 Median age of death (past five years): 41.
💛 People with CF are 2–3x more likely to experience anxiety and depression.
💛 Not everyone can benefit from current therapies.

Progress is real. But it is not equal. And it is not finished. This Rare Disease Month and every month, we recommit to building a future without limits for everyone in our CF community.

Mark your calendar – Registration for the Walk To Make Cystic Fibrosis History opens in just a month, on February 27!   ...
01/27/2026

Mark your calendar – Registration for the Walk To Make Cystic Fibrosis History opens in just a month, on February 27! 📅

The 22nd annual Walk will take place on May 31 so get ready to a future without limits for all Canadians living with cystic fibrosis. 👟

Find out more about the Walk and how you can make a difference here: https://bit.ly/4rfzR0i

Don’t miss out!

With cutting-edge single-cell mapping, Dr. Justine Mathe is uncovering how different bacteria interact with lung cells –...
01/26/2026

With cutting-edge single-cell mapping, Dr. Justine Mathe is uncovering how different bacteria interact with lung cells – and why some areas of the lung become severely damaged while others don’t.

Read the full story of her research on our website: https://bit.ly/3Z0bkjC

We're hiring!Cystic Fibrosis Canada is looking for passionate new team members to join us. We have several opportunities...
01/24/2026

We're hiring!

Cystic Fibrosis Canada is looking for passionate new team members to join us. We have several opportunities available – primarily in event fundraising and annual giving – for individuals who want to make an impact and help Canadians live W/O Limits.

If you are interested or know someone who might be, please share or apply today: https://bit.ly/4blcihX

Address

2323 Yonge Street Suite 800
Toronto, ON
M4P2C9

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