Cystic Fibrosis Canada / Fibrose kystique Canada
Catharine Dunn is a seasoned professional with extensive experience in executive assistance and administrative roles across various sectors. Currently serving as an Executive Assistant at Cystic Fibrosis Canada since May 2023, Catharine previously held the position of Head Secretary at Durham District School Board from July 2013 to June 2023. Prior experience includes positions as Production Manager and Unit Manager at Bell Media, and multiple roles at CTVGlobemedia and CTV Inc., including Executive Assistant and Communications Coordinator. Catharine began their career with a focus on student relations at the University of Manitoba Students' Union and earned a Bachelor of Arts in Women's Studies from the University of Manitoba. Additionally, Catharine completed high school in French Immersion at Institut Collegial Vincent Massey Collegiate.
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Cystic Fibrosis Canada / Fibrose kystique Canada
Cystic Fibrosis Canada is a national not-for-profit corporation and one of the world’s top three charitable organizations committed to improving and lengthening the lives of people living with cystic fibrosis. In our 60 year history, we have advanced cystic fibrosis research and care that has more than 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. Today, CF Canada is a leading organization with a central role engaging people living with cystic fibrosis, parents and caregivers, volunteers, researchers and healthcare professionals, government and donors. We work together to change lives through treatments, research, information and support. * Fibrose kystique Canada sommes un organisme de bienfaisance national à but non lucratif et l’un des trois principaux organismes de bienfaisance au monde voués à l’amélioration et au prolongement de la vie des personnes fibro-kystiques. Au cours de nos 60 ans d’histoire, nos avancées dans les domaines de la recherche et des soins ont plus que doublé l’espérance de vie des Canadiens fibro-kystiques. Nous avons contribué à l’ensemble des connaissances mondiales sur la FK et financé des réalisations en recherche, notamment la cartographie du gène responsable de la fibrose kystique en 1989. Nous avons également fait progresser l’accès aux médicaments révolutionnaires contre la FK au Canada, grâce à notre travail constant de défense des droits et de relations avec les gouvernements. Aujourd’hui, FK Canada est un leader quant à l’engagement des personnes touchées par la maladie : celles qui vivent avec la maladie, les parents, les aidants, les bénévoles, les chercheurs et les professionnels de la santé, les gouvernements et les donateu