Healthier lives for all
Canadians with CF.
Healthier lives for all Canadians with CF.
Healthier lives for all Canadians with CF.
Achieving the next wave of impact for cystic fibrosis requires a comprehensive approach.
$2 million over four years
Galvanize collaboration and speed up the pace of discovery by bringing together multiple research teams across the country to tackle a single topic of importance to the CF community.
$300,000 over three years
Support rising stars in CF research to create the next generation of CF research talent in Canada.
$300,000 over three years
Yield the incremental gains that breakthroughs are built upon through laboratory and clinical research that responds to the CF community’s research priorities.
$50,000 over one year
Encourages out-of-the-box thinking by balancing higher-risk, more innovative work with lower budgets and shorter timeframes.
Dr. Christine Bear is looking for evidence that Trikafta can improve lung health for those who have been denied access due to their rare mutations.
A McGill University research team led by Dr. Dao Nguyen is tackling the problem of bacterial infections in the lungs of people with CF.
Amid the challenges of the pandemic came an opportunity to give the CF community a stronger voice in the research we fund.
We refuse to lose the extraordinary momentum we’ve established in our work to improve and lengthen the lives of Canadians with CF.
Learn more about our vision for thoughtful and comprehensive research investment that will create the future we know is possible.
COMMUNITY STORIES
"All we want is for Sebastian to have a full, long, adventurous life that he deserves. This disease is still a ticking clock for us and others.”
"…It was like a punch in the gut to learn [this new treatment] wouldn't help any of my children. Now I'm worried my kids will be left behind."
“We strongly believe our time will come for a ‘miracle’ drug, and that’s because one thing has kept us going all these years: Hope.”
COMMUNITY STORIES
“All we want is for Sebastian to have a full, long, adventurous life that he deserves. This disease is still a ticking clock for us and others.”
“…It was like a punch in the gut to learn [this new treatment] wouldn't help any of my children. Now I'm worried my kids will be left behind."
“We strongly believe our time will come for a ‘miracle’ drug, and that’s because one thing has kept us going all these years: Hope.”
for research advances that will drive improvements in treatment and care for all with CF.
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