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Cystic Fibrosis Resources

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Cystic Fibrosis-Cystic Fibrosis Foundation
The Cystic Fibrosis Foundation is a donor-supported, nonprofit organization whose mission is to find therapies--and eventually a cure--for cystic fibrosis (CF), and to improving the quality of life for those with the disease. Established in 1955, the mission of the Cystic Fibrosis Foundation is to assure the development of the means to cure and control cystic fibrosis (CF) and to improve the quality of life for those with the disease.

Cystic Fibrosis-MedlinePlus
MedlinePlus will direct you to information to help answer health questions. MedlinePlus brings together authoritative information from NLM, the National Institutes of Health (NIH), and other government agencies and health-related organizations. A comprehensive source of links which provide news, overviews, diagnosing, symptoms, treatments, clinical trials, and related issues pertaining to CF.

Cystic Fibrosis: Cystic Fibrosis Trust
The Cystic Fibrosis Trust is the UK's only national charity that funds research into treating and curing Cystic Fibrosis and to ensure appropriate clinical care and support for people with Cystic Fibrosis. Cystic Fibrosis Trust Provides information, advice, support and, where appropriate, financial assistance to anyone affected by Cystic Fibrosis.

Cystic Fibrosis-Canadian Cystic Fibrosis Foundation
The Canadian Cystic Fibrosis Foundation (CCFF) is a Canada-wide health charity with more than 50 volunteer chapters. The Foundation’s primary objective is to fund cystic fibrosis research and care. The Canadian Cystic Fibrosis Foundation is one of the world’s largest non-governmental granting agencies in the field of cystic fibrosis research.

Cystic Fibrosis-Cystic Fibrosis Australia
Cystic Fibrosis Australia assists member organisations to achieve common objectives by developing national education programs and collecting and distributing information about Cystic Fibrosis (CF) at national and international levels. CF member organisations direct their activities to the provision of high quality health and welfare services to children and young adults with CF and their families.





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