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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.

06/09/2026

What could you do with 20 minutes today?
Have a coffee ☕
Scroll social media for a bit 👀
Or finally write your Will…
For FREE.

Free Wills Charity Week is officially here, and from today until 21 September, you can write or update your Will online through Cure4CF’s partnership with Safewill.
No cost. No appointment. No putting it off until “one day”.

Just around 20 minutes to put something important in place.
Your Will can help you:
🧡Look after the people you love
🧡Make your wishes clear
🧡Give yourself peace of mind
🧡Think about the legacy you want to leave

And if Cure4CF is a cause close to your heart, you can also choose to leave a gift to help fund research towards a future where cystic fibrosis no longer limits lives.

There is absolutely no expectation to leave a gift to us.

We’re simply grateful to be able to offer our community this opportunity, and we’d hate for you to miss out.

👉 Write your FREE Will: https://bit.ly/4cptJ0q
Available until 21 September.

05/09/2026

This Father's Day, we're celebrating all the dads, fathers, grandfathers and father figures who show up, support, encourage and love unconditionally. 🧡

For many families impacted by cystic fibrosis (CF), that support is felt in the everyday moments, the appointments, the treatments, the tough days and, most importantly, the moments of joy in between.

Today, we celebrate all the incredible father figures in our CF community and beyond.

Happy Father's Day from all of us at Cure4CF.

05/09/2026

JOIN KATE & CALLUM’S CREW! 🏃‍♀️🧡

City-Bay is just around the corner, and there are some BIG reasons to get involved!

💪 TOP 3 FUNDRAISERS
Each win a 5 class pack from STRONG Kensington Park!

🏏 RAISE $600 & GO INTO THE DRAW to win an incredible Adelaide Strikers experience on 6 January, including 2 x tickets to Adelaide Strikers vs Melbourne Renegades + 4 hour food & beverage package

🕶️ FUNDRAISE & WIN!
Be the top fundraiser by 9am, 7th September and score a pair of Smith Optics Australia glasses!

Whether you run, walk, fundraise or cheer us on, there’s a place for you in Kate & Callum’s Crew!

🧡 Every dollar helps Cure4CF fund vital cystic fibrosis research.

Can’t run? Walk.
Can’t walk? Donate.
Can’t donate? Share.

👉 Join Kate & Callum’s Crew today and make every step count! https://citybay26.grassrootz.com/cure4-cystic-fibrosis-foundation/kate-callum-s-crew

02/09/2026

A huge thank you to the incredible team at Pro Health Care! We were so lucky to join the team for their staff quiz night and see everyone come together for a fun evening while raising an amazing $3,700 for Cure4CF Foundation.

We’re incredibly grateful for the ongoing support from Pro Health Care over the past two years. Your generosity and commitment to helping fund vital cystic fibrosis (CF) research means so much to us and the CF community.

Thank you to everyone who took part, helped organise the night and contributed to making it such a success.

Here’s to great people, great nights and making a difference together! 💛

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

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.

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/

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!

23/08/2026

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

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

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

Website

https://linktr.ee/cure4cysticfibrosis

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