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Boomer Esiason Foundation
A resource for those affected by this disease. Includes details about the organization, fund raising, events and a newsletter. |
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Chicago Cystic Fibrosis Awareness Day
Provides information about the annual educational awareness day for people with CF and their families living in the greater Chicago area. Includes links, clinical trial and archives. |
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Cystic Fibrosis Australia
Information about the organization and its aims and objectives, CF facts, events, links and contact details. |
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Cystic Fibrosis Foundation
Seeking the means to cure and control cystic fibrosis and to improve the quality of life for those with the disease. Providing information about the disease, treatment options, clinical trials, research, and public policy. |
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Cystic Fibrosis Trust
National charity in the United Kingdom which funds research into the disease and provides information and support for patients and families. |
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Cystic Fibrosis Victoria Inc
Current information on Cystic Fibrosis, Cystic Fibrosis Victoria the organisation, online chat room, message board, '65 Roses Magazine', SSL Secure Online Shop and donations, events |
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Cystic Fibrosis Worldwide
International Association of Cystic Fibrosis Adults web site and International Cystic Fibrosis Mucoviscidosis Association. |
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Elizabeth Nash Foundation
Supports causes reflective of Elizabeth Nash's interests and values with a specific emphasis on efforts that improve the lives of those affected by Cystic Fibrosis. |
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European Cystic Fibrosis Society
ECFS, aims to achieve the best possible treatment and the highest quality of life for the patient with cystic fibrosis by the development and distribution of knowledge in the field of cystic fibrosis |
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European Cystic Fibrosis Thematic Network
Creates a platform for scientists involved in fundamental CF research, for the more than 160 genetic diagnostic laboratories, for CF associations of families, patients and clinicians, legal experts and representatives of the industry. |
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I.C.F.M.A.
A not-for-profit organization for increasing cystic fibrosis awareness. |
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Milan Foundation
Created in the name of Milan Brown who, at the age of 3 1/2, was diagnosed with Cystic Fibrosis. Includes a calendar, stories and poems about CF, how to donate, and the foundation's mission. |
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New Jersey State Organization of Cystic Fibrosis
NJSOCF provides direct, hands on financial assistance to CF patients throughout the state, counseling, referrals and educational materials to patients and their families. Includes a Q&A's, news, services offered and coming events. |
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Reaching Out Foundation
Provides information on the programs provided by this foundation, a personal story of a person with CF who had a double lung transplant, general information on CF, and how you can donate. |
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The Genentech Endowment for Cystic Fibrosis
An independent, non-profit endowment dedicated to expanding access to Pulmozyme? (dornase alpha) therapy to qualifying un-insured and under-insured CF patients. Find the eligibility and how to apply. |
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Victoria Chapter, Canadian Cystic Fibrosis Foundation
The Victoria Chapter, one of 51 Chapters of the Canadian Cystic Fibrosis Foundation, works to provide a brighter future for every person born with cystic fibrosis. It assists in the quest to find a cure or control for the disease. |
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