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Cystic Fibrosis Community Care
2021 Christmas Appeal

Your generous support will give families living with cystic fibrosis the gift of togetherness this Christmas.

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Introducing CFStrong

CFStrong is now live! We recently launched our new website and have had an amazing response. The CFStrong project has delivered a comprehensive website covering topics and content relevant to Australian adults living with CF.

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Buy Socks Here!
What is CF?

Cystic fibrosis is a genetic condition

Cystic fibrosis (also called CF) is the most common, life-limiting genetic condition affecting Australians. 

CF causes an abnormal build-up of thick and sticky mucus in the lungs, airways and digestive system. Treatment requires intensive daily physiotherapy to clear the lungs and airways, countless medications and frequent hospitalisations.

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Living with CF

Everyone's experience with CF is different

Children

Learn more about CF so you can be confident in managing your child's condition.

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Young People

During your teenage years, you start to take over more management of CF from your family.

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Adults

Tools, information and advice to support you to live your life while managing CF.

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Carers

When you care for someone living with CF, looking after yourself needs to be important part of the plan.

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Fundraise for us

It takes a community to care for CF

Every donation received and every dollar raised no matter how big or small, has the power to make a difference to the life of someone living with cystic fibrosis. All funds raised for Cystic Fibrosis Community Care help us to deliver support services and improve the lives of people living with CF, their families and carers.

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Our impact

We provide practical support

870

 subsidised items of physiotherapy equipment

6,497

responses to requests for information, support & advocacy

353

responses to requests for emergency financial assistance

626

educators have undertaken CFSmart online learning

Who are the people living with CF?

3,500 people are living with CF in Australia and 1 in 25 people carry the recessive CF gene change. Babies born today with CF can expect to live well into adulthood. There is no cure but advances in treatment and care are helping people to better manage their CF.

Latest News View all news

A roadmap to living with risk

News

As COVID restrictions lift be gentle with yourself as you consider what you want next. It is okay to be apprehensive or anxious. Take things slowly and consider an individualised pathway based on your own situation and needs.

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Cystic Fibrosis Related Diabetes

News

Do you live with CFRD? If so, then we need your support. CFCC is collaborating with CF Queensland and we are asking the CF community to write letter of support seeking for all people living with CFRD to be included in the NDSS today.

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Trikafta update

News

Trikafta® (elexacaftor/tezacaftor/ivacaftor) is a new triple combination therapy that may benefit many people living with CF.

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COVID-19 (coronavirus) resources

News

Cystic Fibrosis Community Care is working to keep everyone in our community safe during the COVID-19 (coronavirus) pandemic. We have compiled a list of up-to-date resources on websites for you to visit, depending on what questions you might have.

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Cystic Fibrosis Community Care
admin@cfcc.org.au

VIC (03) 9686 1811 

282 Neerim Rd, Carnegie VIC 3163

NSW (02) 8732 5700

Suite 2A, 5 Belmore St, Burwood NSW 2134

Cystic Fibrosis Community Care acknowledges the Traditional Custodians of the land on which we work, live and gather, and we pay our respects to Elders past, present and emerging.

VIC
NSW

© 2022 Cystic Fibrosis Community Care

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