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This May 31, join Mariette and countless other parents, loved ones, and supporters at our annual Walk To Make Cystic Fibrosis History.
Dr. Augusto Zani, along with Dr. Hartmut Grasemann, are leading a pioneering effort to use extracellular vesicles – tiny droplets released by cells – to understand, diagnose, and potentially even treat chronic lung infections in people living with CF.
Living with CF has been a part of Jacklyn’s life for as long as she can remember. Both she and her older sister were born with CF, and growing up with the disease became her normal. What Jacklyn never imagined was navigating pregnancy, motherhood, and raising children—one of whom also has CF—while managing her own health.
Testing News - limited to 3 posts
Cystic Fibrosis Canada is proud to recognize 17 individuals, families, and groups from across the country whose dedication and generosity have made a meaningful difference in the lives of Canadians affected by cystic fibrosis.
Breathless Season 2 returns May 6, sharing real stories of life with cystic fibrosis—exploring new treatments, mental health, and the evolving future of the CF community.
Cystic Fibrosis Canada’s signature event, the Walk To Make Cystic Fibrosis History, will take place on Sunday, May 31 at 40 locations across the country.
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This May 31, join Mariette and countless other parents, loved ones, and supporters at our annual Walk To Make Cystic Fibrosis History.
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Join us for a night of dancing for a good cause! The Dance for CF - Casino Royal (James Bond) is organized in support of Cystic Fibrosis Canada for a 4th year.
Apr 25, 2026
Brew’s n’ Blokes is a night of live music, great food and fun. Join the live band 'The Decent Blokes' at Shawn & Ed’s Brewery for an unforgettable evening in support of Cystic Fibrosis Canada.
Apr 25, 2026
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Join us for a night of dancing for a good cause! The Dance for CF - Casino Royal (James Bond) is organized in support of Cystic Fibrosis Canada for a 4th year.
Apr 25, 2026This May 31, join Mariette and countless other parents, loved ones, and supporters at our annual Walk To Make Cystic Fibrosis History.
Apr 23, 2026