Cystic Fibrosis organisations in Australia provide support and services to people with Cystic Fibrosis (CF) and their carers and families. This is complemented by a commitment to research and a quality improvement program focussing on improved clinical care for people with CF.
Every four days a baby is born in Australia with cystic fibrosis (CF) and more than one million Australians are carriers of cystic fibrosis. Cystic Fibrosis Australia (CFA) is committed to improving clinical practice and patient outcomes through its quality improvement programmes and research with the aim of extending life expectancy from 37 to 50 years by 2025.
Cystic Fibrosis is a recessive genetic condition. It primarily affects the lungs and digestive system because of a malfunction in the exocrine system, responsible for producing saliva, sweat, tears and mucus.
In addition to working for a cure, Cystic Fibrosis Australia also provides support and advocacy to improve the lives of people with cystic fibrosis. Get involved by raising awareness about CF, participating in a fundraising event or volunteering.
Cystic Fibrosis Australia has established a consistent approach to advocacy across Australia and is now a subject matter expert for government, industry and the media.
The Australian Cystic Fibrosis Research Trust (ACFRT) is managed by Cystic Fibrosis Australia (CFA). Since 1989 it has funded more than 300 projects valued at over $6,000,000.
Visit the media room to browse through number of resources including media representatives, press releases and reports.
If you're looking for a great night of frivolous fun, brain teasing trivia and lots for laughs then get on board the Trivia Extravaganza coming to the Meat Market on Saturday, 26 May!
If you have a family member who has recently being diagnosed with CF, you are invited to join us in Melbourne on Saturday 2 June 2018 at 2.30pm
If you have a family member who has CF, you are invited to join us in Wodonga on Wednesday 20 June 2018 at 6.30pm
Join Cystic Fibrosis Community Care (CFCC) for a night of frivolous fun in support of Victorians living with cystic fibrosis.
A Night for CF is CFCC's premium fundraising event. Funds raised from the evening will allow the organisation to continue to provide vital support and services to Victoria's CF community.
Support for the CF community takes many forms including emergency financial assistance, supplementing the cost of expensive physiotherapy equipment and support for those receiving lifesaving lung transplants. CF affects the lungs, pancreas and reproductive systems. The average life expectancy is only 38. There is no cure.
You're invited to join us at our CF Community Conference in Melbourne on Saturday 18 August 2018
If you have a grandchild who has CF, you are invited to join us in Southbank on Saturday 28 April 2018 at 2.00pm
All members of Cystic Fibrosis Community Care Ltd (CFCC) are invited to attend our 2018 AGM on Sunday 15 April 2018 at 2.00pm
If you have a family member who has CF, you are invited to join us in Ballarat on Wednesday 14 March 2018 at 6.30pm