All about Cystic Fibrosis Canada
We were founded by parents of children with cystic fibrosis in 1960. Since then, we’ve worked closely with the cystic fibrosis community to dramatically change the cystic fibrosis story, for the better. But we’re not done yet.
Cystic fibrosis is in a time of great change.
New drugs are available and can help many people with cystic fibrosis live longer and healthier lives than ever before. But others don’t see that same promising future.
We celebrate our 65-year history and the extraordinary achievement of having doubled life expectancy for Canadians living with cystic fibrosis. We’ve contributed to the global body of CF knowledge, funding research achievements such as mapping the gene that causes cystic fibrosis in 1989. And we’ve advanced access to life-changing CF medicines in Canada through relentless advocacy and government relations work. For most young children diagnosed in the next few years, their experience with cystic fibrosis will be different, and most likely a more hopeful story. But today, there is still an immense burden for many Canadians, and we work hard on their behalf.
Help build lives without limits
Yes, we’ve come a long way. Many Canadians are living healthier, longer lives. Yet, there is no cure. Some still face an immense daily burden and others can’t benefit from the new treatments we helped bring to this country. We are working to that day when all Canadians with cystic fibrosis can live healthier, fuller lives with your help. Our 2024-27 Strategic Plan outlines how we’ll do it:
Influence health and financial support systems so that:
Drug access is improved and more equitable across the country
People have a reduced financial burden
Advance knowledge about CF in priority areas so that:
There is better understanding of how to manage or treat priority health issues
There are more clinical trials available for those with the greatest health need
Connect people and resources so that:
Emotional impacts of the disease are reduced
People with CF are informed about priority issues related to their disease
Drive action around needed care so that:
The burden of care, including mental health issues, is reduced
The clinical care model is adapted for current and future needs
Our mission
To act boldly for all Canadians living with cystic fibrosis so they can live longer, healthier, fuller lives.
Our vision
To live fully, beyond the limits of cystic fibrosis.
Our values
As we work together with Canada’s cystic fibrosis community to achieve our mission, we are committed to these four core values:
Connected
We are strongest when we collaborate well with our team and are connected to our community.
Impactful
We are intentional in our focus to ensure we create a better future for people living with CF in Canada.
Inclusive
We nurture a diverse and inclusive environment where everyone feels valued, and is heard, seen and respected.
Bold
We think and act boldly to inspire the best outcomes for people living with CF in Canada.
Our approach
As the only national organization with a legacy like ours and valuable data from our Canadian Cystic Fibrosis Registry, we are in a unique position to leverage our strengths, partnerships and expertise throughout Canada to prioritize the greatest need, drive change and provide much needed support to our community.
Invest in the right research
Our research roadmap is a five-year plan for thoughtful and impactful investment in research. Listening to people living with cystic fibrosis to help determine the most urgent priority health issues, we will invest in areas of unmet need, attract bright scientific minds to fuel innovation and create impact sooner.
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Evidence based
Having health data through our Registry on almost every person diagnosed with cystic fibrosis in Canada provides us with a unique ability to be deeply anchored in real world evidence and experience. We are always informed by our cystic fibrosis community and as we learn more, we will better position ourselves for the future.
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Advocacy & Government Relations
Our ability to mobilize the community across Canada continues to be important as we drive change in the system, ensuring all levels of government are focused on making sure everyone who can benefit from new treatments does.
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Community Engagement
We count on our people across the country to advance the cystic fibrosis story through volunteering, participating in clinical trials, fundraising, donating, sharing personal stories and contributing CF insights through our Elevate program and other opportunities.
Explore Elevate
Milestones of success
We thank our founding families, the Summerhayes and the Moutons, for their leadership and drive for change. And our community – people in Canada living with cystic fibrosis, parents and caregivers, donors, partners, volunteers, researchers, healthcare professionals and staff - for contributing their time, talents and insights to advance cystic fibrosis research, treatment and care in Canada.
There are many important milestones that mark our sixty-five-year journey (above are just a few). They’ve been accomplished with the passionate participation of our cystic fibrosis community across the country, our generous supporters and volunteers, and the committed researchers and clinicians who work to help people with cystic fibrosis live longer, healthier lives.
Read about the CF Story in CanadaBeyond Further: our new key concept
Along with our 2024-27 strategic plan, a new concept supports our work. We used FURTHER for the last three years to reflect our push to keep moving toward success and overcome obstacles on behalf of the cystic fibrosis community. Now we go even further. Look for the W/O Limits logo and messaging in our communications and campaigns. Some context:
Cystic fibrosis tests limits every day. It has pushed people of all ages, held them back. Closed doors on dreams. And taken away far too many people we love. But the cystic fibrosis community continues to persevere. We continue to push back. Break free. Open those doors to dreams and walk right through. Cystic fibrosis will never limit our drive.
It will never limit our relentless search for breakthroughs, the kind that have dramatically changed the cystic fibrosis story in Canada since our founding in 1960. But limits continue to be tested. There are far too many people still without treatment and facing painful daily struggles.
So, we’re planting our flag in the ground to declare that we won’t stop until everyone with cystic fibrosis can live without limits.
Cystic Fibrosis Canada publications
We produce several robust annual publications that reflect the latest in CF research and statistics, personal stories and profiles, and updates on all the ways Cystic Fibrosis Canada helps our community live without limits. You’ll find our latest publications on our Publications & Financials page and other helpful information in our Resources Hub.
2022 Annual Data Report and 2022 HighlightsAudited financials
Cystic Fibrosis Canada is committed to transparency and accountability of financial information. We are thankful for the support of our donors and steward this support strategically, ensuring we invest in the most important priorities to make change for people living with cystic fibrosis.
View the 2022/2023 Audited Financial Statements
Charities are legally required to file a Registered Charity Information Return (T3010) to the Canada Revenue Agency (CRA). Read the most recent T3010 for Cystic Fibrosis Canada.
View Cystic Fibrosis Canada's statement regarding contributions from the pharmaceutical industry.
Our partners
Cystic Fibrosis Canada relies on the incredible generosity and support of our corporate partners to help make a vital difference in the lives of those living with CF.
Learn more about corporate partnership.There are so many ways to make a difference
Whether you choose to make a single or monthly donation, become a corporate partner, volunteer at an event, create change as an advocate, provide peer support, host a fundraiser or share your cystic fibrosis story, you are helping the CF community live without limits. So, thank you!
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