To improve the quality of life for people with CF and their carers.

In 1967 a group of parents of children with CF and medical personnel involved with treating the condition founded the organisation as the Cystic Fibrosis Association of New South Wales. Originally a parent self-help group the organisation has gradually employed a growing staff of professionals to provide a range of support services, an information and education service, and an advocacy service. We are dedicated to achieving the best possible care and quality of life for people with Cystic Fibrosis and their carers, now and in the future.

CF Clinics
Outreach
Equipment Hire
Financial Assistance
Mothers' Respite Weekends
Peer Support Program
Personal Trainer