Cure4 Cystic Fibrosis Foundation

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Cure4 Cystic Fibrosis Foundation Raising funds to find a cure for cystic fibrosis.

Raising funds to support research into the development of a cure for the airway disease caused by cystic fibrosis.

We’re so lucky to have the ongoing support of the Johns' Print Centre  team, who recently brought these fantastic Cure4C...
14/10/2026

We’re so lucky to have the ongoing support of the Johns' Print Centre team, who recently brought these fantastic Cure4CF banners to life for us.

From event signage and campaign materials to all the printing that helps us share our story, their generous support helps us show up professionally and bring Cure4CF to our community.

As a small charity, support like this makes a huge difference and means more of our fundraising can go directly towards funding life-changing CF research.

Thank you, Johns Print Centre, for being such an important part of the Cure4CF community. We’re so grateful! 🧡

Could GLP-1 medicines have an unexpected role in cystic fibrosis (CF) research?GLP-1 medicines are making headlines arou...
12/10/2026

Could GLP-1 medicines have an unexpected role in cystic fibrosis (CF) research?

GLP-1 medicines are making headlines around the world, but a new Australian study has researchers asking a different question: could these medicines have an impact on lung function in people with CF related diabetes (CFRD)?

The small exploratory study found improvements in lung function and blood glucose control among people taking GLP-1 receptor agonists alongside insulin. The findings are interesting, but more research is needed.

So, why does this matter? Because sometimes the most valuable research doesn't give us an answer. It gives us a better question.

Read our latest blog to explore the findings, what they could mean for future CF research, and why following the science matters: www.cure4cf.org/dont-fear-the-glp-1ra/

This World Mental Health Day, we're recognising the importance of mental health for people living with cystic fibrosis (...
09/10/2026

This World Mental Health Day, we're recognising the importance of mental health for people living with cystic fibrosis (CF) and the need for research and care to evolve alongside the changing experience of the condition.

CF has changed. Our approach to mental health needs to change with it.

For people living with cystic fibrosis, the mental health burden can be significant. CF brings a demanding daily treatment regimen, uncertainty, hospitalisations, pain, social isolation and the challenge of navigating relationships, work, family and life alongside a lifelong condition.

And now, in the era of CFTR modulators, there is another dimension to understand.
For many people, modulators have brought remarkable improvements in health, wellbeing and hope. But emerging research indicates that a smaller group experience new or worsening symptoms after starting treatment, including anxiety, depression, irritability, sleep disturbance or cognitive symptoms. The reasons are not yet understood and require further research.

This isn't about questioning the enormous benefits of CFTR modulators.
It's about making sure we understand the whole experience of living with CF.

The latest psychosocial research identifies understanding the neuropsychiatric effects of CFTR modulators, improving screening, and developing better psychosocial support as important priorities for CF research and care.

At Cure4CF, we believe research needs to keep pace with the changing reality of CF.

Because better CF care isn't only about lung function.
It's about helping people live longer — and live well.

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🧡 If you need support:

Living with CF can be challenging, and it's okay to ask for help. If you're struggling with your mental health, please speak with your CF care team, GP or a mental health professional.

You can also contact Lifeline on 13 11 14 or Beyond Blue on 1300 22 4636 for support.

🧡 D-DAY is on the horizon, and we’re building something big.This December, the Cure4CF community will come together for ...
06/10/2026

🧡 D-DAY is on the horizon, and we’re building something big.

This December, the Cure4CF community will come together for 24 hours of action, generosity and hope, raising vital funds for life-changing CF research.

We’re looking for businesses, corporates and philanthropists to be part of D-DAY as Match Donors. Could this be you?

For 24 hours only, every donation will be matched, turning the generosity of our supporters into twice the impact.

As a Match Donor, you’ll be at the heart of something bigger:

✨ Inspire our community to get behind D-DAY
✨ Give supporters an even bigger reason to donate
✨ Double the impact of every community gift
✨ Help fund research bringing us closer to a future where CF no longer limits lives

Could you help us make this year’s D-DAY our biggest one yet?

📩 Get in touch with Gemma at [email protected] or send us a DM to find out more.

04/10/2026

Cure4CF recently brought our 20th anniversary celebrations to Sydney, with a special evening at Doltone House Signorelli, hosted by Penfolds Global Ambassador Jamie Sach.

The evening brought together long-time supporters, researchers, partners, members of the business community, and friends of Cure4CF to celebrate two decades of progress in cystic fibrosis (CF) research and the community that has made so much of that progress possible.

Guests heard powerful stories about the impact of research and what Cure4CF’s work has meant to people living with CF, their families and the broader CF community. It was also an opportunity to reflect on how far we have come, while looking ahead to the research and discoveries still needed to achieve a future without CF.

A particularly meaningful part of the evening was honouring the legacy of CF Warrior Olivia Wood, with Olivia’s family joining us to mark this important milestone. Olivia was a passionate advocate for research and for the CF community, and her courage, warmth and determination continue to inspire the work we do. Having her family with us made the evening even more special and was a beautiful reminder of the people at the heart of our mission.

As we celebrate 20 years of Cure4CF, we are incredibly grateful to everyone who has been part of our journey.

To our supporters, partners, researchers, volunteers and friends, thank you for every donation, conversation, event and act of support. Together, you have helped drive research forward and create more hope and possibilities for people living with CF.

A special thank you to Macquarie for supporting our Sydney celebration, and to Jamie Sach for hosting such a memorable evening.

Thank you for being part of the last 20 years, and for helping shape what comes next.

10 years of Peaks4CF. One more mountain. 🚴 On 7 March 2027 Peaks4CF are back at Falls Creek to ride Peaks Challenge, 235...
01/10/2026

10 years of Peaks4CF. One more mountain. 🚴

On 7 March 2027 Peaks4CF are back at Falls Creek to ride Peaks Challenge, 235km and 4,000m+ of climbing, to raise funds for Cure4CF, raising funds for life-changing cystic fibrosis (CF) research.

We're looking for riders to sign up and join the team:
✅ Riding kit supplied by Peaks4CF sponsors
✅ Raise a minimum of $1,000 for Cure4CF (every dollar goes directly to the CF research)
✅ Cover your own Peaks Challenge entry, travel, and accommodation.

Can't ride? Please donate or share this post to help us find a team!

Head to https://peaks4cf-2027.raiselysite.com to sign up or find out more!

A HUGE SHOUTOUT TO MAE 🧡We want to take a moment to celebrate one of our incredible Cure4CF ambassadors, Mae Johnson.Mae...
01/10/2026

A HUGE SHOUTOUT TO MAE 🧡

We want to take a moment to celebrate one of our incredible Cure4CF ambassadors, Mae Johnson.

Mae is 23 years old and lives with cystic fibrosis (CF). This year, she took on the City-Bay Half Marathon to raise money for vital CF research, while running in honour of the CF warriors who are no longer here today.

And what an effort she made.

Mae raised more than $7,000 for Cure4CF, making her our highest fundraiser at City-Bay this year.

Incredibly, she was also the second highest individual fundraiser across City-Bay overall. 👏👏👏

Mae, thank you for putting your heart into this challenge, sharing your story and using your voice to help create a future without CF. We’re so proud to have you as part of the Cure4CF family. 🧡

Please help us celebrate Mae and the incredible impact she has made for CF research.

What if your $10 could help change the future of cystic fibrosis (CF)? For just $10, you could enter Raffle 33 for your ...
29/09/2026

What if your $10 could help change the future of cystic fibrosis (CF)?

For just $10, you could enter Raffle 33 for your chance to win an incredible $350K First Prize Pack with $5 from every ticket going towards CF research.

That means your ticket could help support research working towards better treatments, better outcomes and, ultimately, a future without CF.

And the prize? 👀

🚗 Lexus RX 450h+ valued at $138,087.76
🛍️ $36,912.24 in shopping vouchers
✨ $175,000 in gold bullion

⏰ Raffle 33 closes — Thursday 8 October at 8pm AEST.

🎟️ One ticket. A chance to win. And $5 helping fund the search for a cure: https://www.playforpurpose.com.au/cure-4-cf

This World Lung Day, we’re backing research into one of the biggest challenges facing people with cystic fibrosis (CF): ...
24/09/2026

This World Lung Day, we’re backing research into one of the biggest challenges facing people with cystic fibrosis (CF): lung health. 🧡

At Cure4CF, we’re focused on research in areas where there are still unmet needs. Bronchiectasis is one of those areas.

That’s why we’re proud to partner with Lung Foundation Australia to support the Cure4CF x Lung Foundation Australia Travel Award.

The award supports an early or mid-career researcher working on bronchiectasis in CF to attend the World Bronchiectasis Conference in 2027.

It’s an opportunity for researchers to share their work, learn from others working at the forefront of bronchiectasis and lung health research, and build connections that can help move research forward.

We’re proud to support the researchers working towards better outcomes for people with CF.

Applications are now open. Find out more and apply: https://app.eprocure.com.au/lungfoundation/home/public

Address

PO Box 313
Adelaide, SA
5125

Opening Hours

Monday 9am - 5pm
Tuesday 9am - 5pm
Wednesday 9am - 5pm
Thursday 9am - 5pm
Friday 9am - 5pm

Telephone

+611300131480

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