Canadian Cystic Fibrosis Foundation
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Cystic Fibrosis Canada is a national charitable not-for-profit corporation established in 1960. Cystic Fibrosis Canada's mandate is to help individuals with cystic fibrosis, principally by funding cystic fibrosis research and care. The organization also provides educational materials for the cystic fibrosis community and the general public; undertakes
advocacy Advocacy is an activity by an individual or group that aims to influence decisions within political, economic, and social institutions. Advocacy includes activities and publications to influence public policy, laws and budgets by using fac ...
initiatives with, and on behalf of Canadians with cystic fibrosis, and raises funds to supports its programs.


Mission

Cystic Fibrosis Canada raises funds in order to promote public awareness and support research and high-quality cystic fibrosis care.


Research and care

Cystic Fibrosis Canada's primary objective is to fund CF research and care: the organization annually funds approximately 50 research projects, in addition to scholars, post-doctoral fellows, and students undertaking CF investigations. Each year, Cystic Fibrosis Canada awards more than $7 million in grants to CF researchers, and approximately $2 million in grants to the 42 CF clinics, and five transplant centres across the country. To help ensure consistent, high-quality care across the country, Cystic Fibrosis Canada provides support to clinicians through grants, training awards and access to statistical information through the online Canadian Cystic Fibrosis Registry. Canadian researchers are viewed as leaders in the global effort to find a cure or control for cystic fibrosis. In 1989, Canadian researchers, funded by Cystic Fibrosis Canada, discovered the gene responsible for cystic fibrosis, and they continue to play a leading role in developing new treatments.


Publications

As well as general information about cystic fibrosis in Canada and resources for teachers, parents, and health care professionals, Cystic Fibrosis Canada publishes newsletters and reports covering such areas as research and training grants, clinical services and annual data on patients with cystic fibrosis.


Kin Canada

Since 1964, Kin Canada, a Canadian service organisation, has supported Cystic Fibrosis Canada, raising over $42 million in support of cystic fibrosis research and care.


See also

* Shinerama *
List of cystic fibrosis organizations The following organizations assist people with or do research into cystic fibrosis, a hereditary disease affecting the lungs and digestive system, causing progressive disability and often early death. Australia * Cystic Fibrosis Australia (CFA), ...
*
Cystic Fibrosis Foundation The Cystic Fibrosis Foundation (CFF) is a 501(c)(3) non-profit organization in the United States established to provide the means to cure cystic fibrosis (CF) and ensure that those living with CF live long and productive lives. The Foundation p ...
*
Cystic Fibrosis Trust The Cystic Fibrosis Trust (stylised as Cystic Fibros''is''), is a UK-based national charity founded in 1964, dealing with all aspects of cystic fibrosis (CF). It funds research to treat and cure CF and aims to ensure appropriate clinical care and ...


References


External links


Cystic Fibrosis Canada Web siteCystic Fibrosis Canada Annual Report 2014/2015
{{Authority control Health charities in Canada Kin Canada Cystic fibrosis organizations Organizations established in 1960 Medical and health organizations based in Ontario