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What do we do? - Website

Cystic Fibrosis Worldwide operates a multi-lingual website and online newsletter distributing information about CF globally. The website also hosts forums on our website that allow for the exchange of information internationally and contact with trained CF specialists, something not available in many countries, for parents of children with CF and adult CF patients. The CFW website also offers publications such as the Joseph Levy Lecture, the IPG/CF physiotherapy manual and WHO guidelines for the management of CF. We have over 164 translators that help to eliminate language barriers and open lines of communication globally, publications and the latest news and developments in the CF community. The CFW website receives over 70,000 visitors monthly and we look forward to continuing to provide an international platform for the exchange of information.
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5 for 5 Campaign
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