Disponible en / Available in: Español
Cystic Fibrosis Worldwide. This is the CF World Organization, with approximately 60 members, Spain among them. Website in English.
European Cystic Fibrosis Society. It is a partnership of European and international experts in the different fields of research of Cystic Fibrosis. Website in English.
Cystic Fibrosis Foundation. Cystic Fibrosis Association of America. Website in English.
Cystic Fibrosis Trust. Cystic Fibrosis Association of UK. Website in English.
Cystic Fibrosis Australia. Cystic Fibrosis Association of Australia. Website in English.
Canadian Cystic Fibrosis Foundation. Cystic Fibrosis Association of Canada. Website in English and French.
Association Vaincre la Mucoviscidose. Cystic Fibrosis Association of France. Website in French.
The Mukoviszidose e.V. Cystic Fibrosis Association of Germany. Website in German.
Asociación Argentina de Lucha contra la Enfermedad Fibroquística del Páncreas. Cystic Fibrosis Association of Argentina. Website in Spanish.
Cystic fibrosis research INC. NGOs focused on raising funds for Cystic Fibrosis research. Website in English with Spanish translations.
Adult Cystic Fibrosis Committee of Quebec. Provincial Committee of Adults with Cystic Fibrosis. Organization representing adults with CF in Quebec (Canada). Of special interest is the official magazine SVB (Santé Vous Bien). Website and magazine in English and French.
United States Adult Cystic Fibrosis Association. American Association for Adults with Cystic Fibrosis. Website in English.
MedlinePlus. Health Information contrasted by American Institutes of Health. Website in English.
Cysticfibrosismedicine.com. English page with information about the management of people with Cystic Fibrosis.
The Cochrane Cystic Fibrosis & Genetic Disorders Review Group. International network of researchers and health professionals who prepare and disseminate systematic reviews of randomized trials in the treatment of cystic fibrosis and other diseases.
Federación Europea de Enfermedades Raras EURORDIS. Federation of patient organizations and individuals active in the field of rare diseases led by patients. Eurodis’ mission is to build a pan-European community of patient organizations and people living with rare diseases, to be their word spokesperson at European level, and directly or indirectly, to fight the impact of rare diseases on their lives. Website published in six languages, including Spanish.