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Archive for September, 2017

ADVOCACY IN ACTION: BC residents lose access to life-changing cystic fibrosis medication

Province doesn’t cover cost, private insurance cut them off   As a result of swift and unexpected changes to their health insurance coverage, two BC…

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Transitioning to Adult Care

Transitioning towards adulthood is a challenge for anyone, add in a huge shift in treatment and care for people living with cystic fibrosis and it…

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Shine On!

September is synonymous with Shinerama around the CF Canada office! Shinerama is Canada’s largest post-secondary fundraiser in support of Cystic Fibrosis Canada. Over 35,000 student…

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A Sincere Thank You and a Warm Welcome

Helen Meinzinger has completed her 2-year term as the Chair of the Kin Cystic Fibrosis Canada Liaison Committee. Her dedication and support for the CF…

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Back to School!

Happy belated Labour Day and welcome to September! It’s back to school season which can be overwhelming and exciting for students with CF and parents…

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“Kin”gratulations to this year’s Bill Skelly and Ian F. McClure awardees

Kin Canada is Cystic Fibrosis Canada’s longest standing partner whose continued commitment has made a difference in the lives of Canadians with cystic fibrosis. Since…

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Collaborating with the Cystic Fibrosis Trust

International partners Cystic Fibrosis Canada and the Cystic Fibrosis Trust are thrilled to announce an international collaboration on the paediatric feasibility study for the Cystic…

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Why Canada Needs A Rare Disease Strategy

Approximately, one in every 3,600 children born in Canada has CF, making CF a rare disease. While each rare disease affects only a very few…

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CONNECTIONS SUMMER/FALL 2017

Cystic Fibrosis Canada is proud to publish the Summer/Fall 2017 edition of Connections magazine! It is published both online and in print. This edition is…

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