
To act boldly for all Canadians living with cystic fibrosis so they can live longer, healthier, fuller lives.
To live fully, beyond the limits of cystic fibrosis.
Cystic Fibrosis Canada is a national non-profit dedicated to improving and extending the lives of people living with CF. Since 1960, the organization has been a global leader in funding specialized research and clinical care, significantly increasing life expectancy for Canadians. They focus on securing equitable access to breakthrough medications and managing the Canadian CF Registry to monitor health trends.
Today, the organization supports over 4,500 individuals while pivoting toward the challenges of an aging CF population. Their current mission prioritizes mental health resources and finding solutions for patients with rare genetic mutations. By combining community advocacy with scientific investment, they strive to transform CF from a fatal diagnosis into a manageable condition.