What we do

Our key focus areas

  • Programs and services: providing support programs and services that help to enhance the quality of life and meet the needs of over 1,000 members
  • Research: promoting and facilitating research into improved treatments and therapies for people with cystic fibrosis, and fundraising to support the Australian Cystic Fibrosis Research Trust
  • National unity and collaboration: participating in cooperative initiatives between CF organisations across Australia
  • Public awareness and communications: maintaining and improving relations and communications with members, the wider CF community, and other key stakeholders
  • Information, education and advocacy: delivering information and education services to key stakeholders, and representing individuals and groups on issues that require government or institutional action
  • Fundraising: a commitment to generating a regular stream of income to meet program delivery objectives, support research initiatives and remain financially viable in the future
  • Governance and transparency: providing balanced, transparent and proactive governance and delivery of positive program outcomes through a highly productive workforce.