| Contact Information |
Mrs. Cathleen Morrison, CEO
Cystic Fibrosis Canada
Address:
2221 Yonge Street
Suite 601
Toronto, ON M4S 2B4-
CANADA
Email:
Telephone:
1-416-485-9149
Fax:
1-416-485-0960
Website:
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CANADA
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ASSOCIATION:
Cystic Fibrosis Canada |
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Mission
The mission of Cystic Fibrosis Canada is to help people with cystic fibrosis.
To this end, CF Canada: funds research towards the goal of a cure or control for CF, and supports high quality CF care; promotes public awareness of cystic fibrosis; and raises and allocates funds for these purposes. |
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RELATED ARTICLES
The Canadian Cystic Fibrosis Foundation is changing its name and logo
As of February 2011, the Canadian Cystic Fibrosis Foundation is changing its name and logo
 Full Article
Hope is in the air
Staying current and contemporary in a highly competitive market is not only a challenge for the profit sector, but charities as well. Cystic Fibrosis Canada (formerly known as the Canadian Cystic Fibrosis Foundation) is changing its look in an effort to build recognition for the cause, and raise vital funds for research.
Full Article
CF Canada announces the appointment of Maureen Adamson as Chief Executive Officer
Maureen joins Cystic Fibrosis Canada with noteworthy experience in the healthcare sector. She was an Assistant Deputy Minister and the CAO for the Ministry of Health in Ontario and Vice President and CAO for Women’s College Hospital in Toronto.
Full Article
Canada: Martinis in May - 12 May 2006
The Evening is designed to raise money - but also to bring together lots of fun people for a very fun night. There will be fantastic food, great music / dancing and drinks! You also have a chance to win an All-Inclusive Trip for 2 to Cuba...courtesy of my great friends in the travel industry!
Full Article
CYSTIC FIBROSIS IN CANADA
Unwilling to wait for a miracle, the parents set about creating a miracle themselves. Over time, they enlisted the interest and support of caring physicians, health professionals, and scientists. With the passage of time, countless ordinary Canadians were captivated by their vision, and rallied to their side.
Full Article
FIBROSE CÍSTICA NO CANADÁ
Em 1960, os líderes fundadores da Canadian Cystic Fibrosis Foundation (CCFF) tinham um ideal – que suas pequenas crianças enfermas sobrevivessem e pudessem ir à escola. Eles se recusaram a aceitar que seus bebês – carentes de médicos, clínicas, tratamentos e medicamentos – morressem na infância.
Full Article
LA FIBROSIS QUÍSTICA EN CANADÁ
En 1960 los creadores de la Fundación Canadiense de Fibrosis Quística (CCFF) tuvieron una ilusión: que sus niños enfermos y frágiles debían de sobrevivir para ir al colegio. Ellos rechazaron aceptar que sus bebés, sin médicos ni clínicas, sin tratamientos ni medicaciones, debían morir en la infancia.
Full Article
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5 for 5 Campaign
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