To facilitate and promote the provision of optimal care to all people affected by Cystic Fibrosis and ensure they have the best possible quality of life.
To promote change in federal policies or laws which are prejudicial to the rights or well-being of persons with Cystic Fibrosis.
To be a co-ordinating body in the production and dissemination of national and international developments on research and matters of interest to CF organisations.
To build an international network of contacts with acclaimed Cystic Fibrosis researchers, centres of learning and kindred organisations.
To administer national research monies.
To administer national community awareness and education programs. To administer, with co-operation of the States, national fundraising efforts and programs.