Conquer Cystic Fibrosis
Sadly, there is still no cure for Cystic Fibrosis but we are fighting to change that. As a 100% volunteer run organisation, with no salaries or administration costs, we are able to channel every cent we raise directly into life saving research for people living with Cystic Fibrosis. Your support helps fund breakthroughs, accelerate new treatments, and bring hope to families who need it most.
Living With Cystic Fibrosis
Cystic Fibrosis affects the lungs and digestive system, causing thick, sticky mucus to build up in the airways and digestive tract. This leads to infections and progressive lung damage over time. Sadly, lung failure is the leading cause of death for people living with CF.
What is Cystic Fibrosis?
Cystic Fibrosis is the most common life‑threatening recessive genetic condition affecting Australian children today. Every breakthrough in research brings us closer to a future where children born with Cystic Fibrosis can live long, healthy lives.
Events and News
We host many events throughout the year, all helping to raise vital funds to support life‑saving research. From our annual Grand Ball, to weekly Bingo in Midland, Balcatta and Kingsway, plus Melbourne Cup lunches, movie nights, morning teas and sausage sizzles, there are countless ways to get involved. If you would like to hold an event, volunteer at an event, or receive advance notice of what’s coming up, we’d love to hear from you.