Cure4 Cystic Fibrosis Foundation

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.

When you support Cure4CF Foundation through Play For Purpose Raffle 33, you're not just in the running for amazing prize...
31/08/2026

When you support Cure4CF Foundation through Play For Purpose Raffle 33, you're not just in the running for amazing prizes, you’re helping fund life-changing cystic fibrosis (CF) research.

🎟️ Buy your tickets by 11:59pm AEST, Wednesday 2 September and you'll automatically go into the draw to win a $10,000 Flight Centre voucher in the Early Bird Bonus Draw!

Plus, you'll still be in the running to win the incredible $350,000 First Prize Pack!

Every ticket helps bring us closer to a future free from CF.

Get your tickets today and don't miss your chance to win while making a real difference: www.playforpurpose.com.au/cure-4-cf

There’s probably something on your to-do list that’s been there for a while…“Write my Will” may be one of those things. ...
30/08/2026

There’s probably something on your to-do list that’s been there for a while…
“Write my Will” may be one of those things.

We get it. It’s not exactly the most exciting job, and it can be easy to keep thinking, “I’ll get around to it.” But what if you could get it sorted completely free?

From 7–25 September, Cure4CF supporters can write or update their Will online for FREE through our partnership with Safewill as part of Free Wills Charity Week.
It takes around 20 minutes and can give you something pretty valuable in return: peace of mind.

Knowing your wishes are clear.
Knowing the people you love are looked after.
Knowing one important thing is finally ticked off your list.
And yes, there is absolutely no pressure to leave a gift to Cure4CF.

But if you do choose to remember us in your Will, it would make a meaningful difference to the research we fund.

So, consider this your little heads-up. Free Wills Charity Week starts 7 September.
Maybe this is the year you finally tick it off. More details coming soon.

Could the bionic pancreas change the way cystic fibrosis-related diabetes (CFRD) is managed?At the 2026 Australasian Cys...
26/08/2026

Could the bionic pancreas change the way cystic fibrosis-related diabetes (CFRD) is managed?

At the 2026 Australasian Cystic Fibrosis Conference, Dr Putman from Boston shared insights into why CFRD can be so complex to detect and manage, and how new technologies could help change that.

From continuous glucose monitoring and automated insulin delivery to the emerging “bionic pancreas”, the future of CFRD care is moving fast.

In our latest blog, we explore the research, the potential of these technologies and why equitable access to CGM matters for people with CF in Australia.

Read the full article: www.cure4cf.org/diabetes-in-cf/

Meet Lauren, our newest Cure4CF Ambassador 🧡We’re so excited to welcome Lauren Cooper to the Cure4CF Ambassador family.L...
25/08/2026

Meet Lauren, our newest Cure4CF Ambassador 🧡

We’re so excited to welcome Lauren Cooper to the Cure4CF Ambassador family.

Lauren was diagnosed with cystic fibrosis (CF) at just 10 days old. At 16, a serious infection destroyed around 50% of her lung function, and after years of declining health, she was eventually listed for a double lung transplant.

Then, research changed the course of her life.

Compassionate access to Trikafta helped Lauren regain lung function, come off the transplant list and build a future she once thought might not be possible. She completed her studies, began her career, became a mum and married her husband.

Today, Lauren is passionate about sharing her story and helping others understand why continued investment in CF research matters.

Because while treatments like Trikafta have transformed what is possible for many people with CF, they are not a cure. There is still so much more to discover.

Lauren’s hope for the future? That one day we can say: “We’ve done it, we’ve found a cure.”

We’re incredibly proud to have Lauren using her voice to help make that future possible. 🧡

Welcome to the team, Lauren!

Kinda chic to fund the science.Kinda chic to back the breakthroughs.Kinda chic to be relentless.
23/08/2026

Kinda chic to fund the science.
Kinda chic to back the breakthroughs.
Kinda chic to be relentless.

We’re proud to be partnering with Lung Foundation Australia to support and strengthen research into bronchiectasis in cy...
21/08/2026

We’re proud to be partnering with Lung Foundation Australia to support and strengthen research into bronchiectasis in cystic fibrosis (CF).

Together, we’re offering a $5,000 travel award to support an early or mid-career researcher or health professional working on bronchiectasis in CF to attend the 2027 World Bronchiectasis Conference in Hanover, Germany.

The award can help cover:
✈️ Return airfares
🏨 Accommodation
🚕 Travel costs
🍽️ Daily incidentals and meals
🎟️ Full conference registration

By working together, we’re creating opportunities for researchers to connect, share knowledge and advance research that could lead to better treatments and outcomes for people living with CF.

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

20/08/2026

THE COUNTDOWN IS ON! With less than six weeks to go until , we’re calling on more runners and walkers to join Kate & Callum’s Crew!

Whether you’re a seasoned runner, a weekend walker or simply looking for a fun way to get moving and make a difference, there’s a place for you on our team.

And we’ve got some BIG fundraising incentives to keep you motivated! 🔥

👕 Raise $300 by 27 August at 9:00am → Get your personalised Cure4CF City-Bay team shirt
🎟️ Commit to raising $500 → We’ll cover your City-Bay registration fee*
💪 Top 3 fundraisers → Win a 5-class pack from STRONG
🏏 Raise $600 → Go in the draw to win an Adelaide Strikers experience, including 2 tickets + a 4-hour food & beverage package!
🕶️ Top fundraiser by 7 September at 9:00am → Win Smith Optics Australia sunglasses valued at $300!

Most importantly, every dollar raised helps fund vital cystic fibrosis research and work towards better outcomes for people living with CF.

Round up your friends, family or workmates and join Kate & Callum’s Crew (link in bio) or https://citybay26.grassrootz.com/cure4-cystic-fibrosis-foundation/kate-callum-s-crew

*Terms and conditions apply. A commitment and waiver form must be completed before Cure4CF purchases your City-Bay registration.

Three years. Three events. Over $20,000 raised for research. 💛🧡A huge thank you to the incredible Karlee Kerrigan, who h...
17/08/2026

Three years. Three events. Over $20,000 raised for research. 💛🧡

A huge thank you to the incredible Karlee Kerrigan, who has taken on a fundraising event for Cure4CF for the past three years, and this year, she tackled the Mornington Running Festival, raising an amazing $5,465.13! 🏃‍♀️

Across her three events, Karlee has now raised and donated more than $20,000 to Cure4CF, helping fund vital cystic fibrosis (CF) research and the search for better treatments and, ultimately, a cure.

But for Karlee, this is about so much more than fundraising. It’s about her son, Alfie.

Karlee is one of those people you want in your corner, fun, generous, fiercely determined and always ready to get behind a cause she believes in. She brings so much energy and heart to everything she does, and we feel incredibly lucky to have her in the Cure4CF community.

Every kilometre she runs, every dollar she raises and every challenge she takes on is helping create hope for a future where Alfie and everyone living with CF can live healthier, longer lives.

Karlee, thank you for putting your heart into this year after year. Thank you for showing up, going the extra mile and always finding a way to make a difference!

This National Science Week, we’re celebrating the science behind the search for a cure.Since 2009, Cure4CF has invested ...
17/08/2026

This National Science Week, we’re celebrating the science behind the search for a cure.

Since 2009, Cure4CF has invested more than $5 million in research with a clear pathway towards real-world impact.

Today, we’re funding researchers tackling some of the biggest challenges in cystic fibrosis (CF), from gene editing and gene therapy to new approaches to infection, airway clearance, CF-related diabetes and cancer detection.

There isn’t one path to a cure. There are many questions to answer, ideas to test and researchers pushing the science forward. Because CF is relentless. So are the scientists working to change its future.

Swipe through to meet some of the researchers and explore the work we’re currently funding. This is why we fund science.

You can read all about the research we are funding via the link in our bio.

This National Science Week, we're celebrating the science behind the search for a cure. Since 2009, Cure4CF has invested...
17/08/2026

This National Science Week, we're celebrating the science behind the search for a cure.

Since 2009, Cure4CF has invested more than $5 million in research with a clear pathway towards real-world impact.

Today, we're funding researchers tackling some of the biggest challenges in cystic fibrosis (CF), from gene editing and gene therapy to new approaches to infection, airway clearance, CF-related diabetes and cancer detection.

There isn't one path to a cure. There are many questions to answer, ideas to test and researchers pushing the science forward. Because CF is relentless. So are the scientists working to change its future.

Swipe through to meet some of the researchers and explore the work we're currently funding. This is why we fund science.

You can read all about the research we are funding at: www.cure4cf.org/current-research-projects

Address

PO Box 313
Adelaide, SA
5125

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

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+611300131480

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