About Cystic Fibrosis

Cystic Fibrosis is the most common life threatening recessive genetic condition affecting Australian children and young adults today.

  • There are approx 3,000 people living with CF in Australia.
  • CF seriously affects breathing and digestion.
  • People with CF may need to have up to 2 hours intensive chest physiotherapy (to help break up the mucus in their lungs so they can breathe) and up to 40 enzyme tablets (to help their digestion) every day just to survive.
  • Due to advancements the average life expectancy of someone living with CF is now mid thirties, but there are still many children who do not reach adulthood.
  • Approximately one in every 2,500 babies will be born with CF.
  • There are a million genetic carriers of CF in Australia.
  • As yet there is no cure.

Why 65 Roses?

"65 Roses" comes from the folklore story of a little boy’s effort to pronounce his sister’s condition. Find out more.

Cystic Fibrosis Q & A

Frequently asked questions and answers about Cystic Fibrosis. Find out more.

About Cystic Fibrosis Australia

Cystic Fibrosis Australia (CFA) is a national body comprising Cystic Fibrosis (CF) state organisations. Find out more.



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About Cystic Fibrosis Australia
Why 65 Roses?
65 Roses Song
CF Research
Cystic Fibrosis Q & A
Media
Joels Story

Testimonials

"This year sees LJ Hooker celebrating 11 years as national sponsor of Cystic Fibrosis Australia. Our mission is to utilise our extensive national network to raise public awareness and funds for CF research.  To this end we have raised over $3 million through a myriad of fundraising activities large and small. I encourage everyone to support this worthwhile cause"

Alan Lambert - LJ Hooker Managing Director


National Sponsor of
Cystic Fibrosis Australia