Craniofacial Australia

Craniofacial Australia We support the craniofacial community through patient care, education and research.

Founded by world-renowned surgeon Professor David David AC, Craniofacial Australia offers care and long-term support for patients, educates tomorrow’s best surgeons and invests in research that advances prevention, management and cures.

It’s almost EOFY, and if you’re thinking about making a tax deductible donation, but unsure where your money actually go...
12/06/2026

It’s almost EOFY, and if you’re thinking about making a tax deductible donation, but unsure where your money actually goes, let us show you. 🩷

As June 30 approaches, we wanted to share what your support makes possible for families facing a cleft or craniofacial diagnosis.

Every year, families reach out to Craniofacial Australia at some of the hardest moments they will ever face.

Sometimes it’s the moment everything changes with a new diagnosis. Other times it’s the overwhelming reality of travelling away from home for surgery, or simply not knowing what comes next.

In those moments, support matters. 🫶

Your EOFY gift ensures we can be there in those moments, offering practical support, care, and comfort when it’s needed most.

Every gift makes a real difference.

💌Donate today: https://craniofacial.com.au/donate/

💙 Run Melbourne. City2Surf. Bridge to Brisbane 💙Some of Australia’s biggest running events… but right now, we’re still a...
11/06/2026

💙 Run Melbourne. City2Surf. Bridge to Brisbane 💙

Some of Australia’s biggest running events… but right now, we’re still a little light on Craniofacial Australia representation.

And it matters.

Because this is more than just a run. It’s visibility. It’s awareness. It’s showing families they’re not alone. It’s helping change the conversation around craniofacial conditions in the most powerful way, out in the community.

The good news? It’s not too late. ⏰

If you’ve been thinking about signing up, this is your sign.

Run solo. Run with friends. Walk or wheel, everyone is welcome.

Every step helps raise awareness for families who need it most.

So… what are you waiting for?

Join us for Run Melbourne, City2Surf or Bridge to Brisbane and represent Craniofacial Australia this season. 💪

Run Melbourne 👉 https://raceroster.com/events/2026/110689/run-melbourne-2026

City2Surf👉 https://in.au.city2surf.com.au/2026-city2surf

Bridge to Brisbane👉 https://bridgetobrisbane.com.au/enter/

If you have any further questions, please contact Meg, our friendly Marketing and Fundraising Coordinator at [email protected] 🫶

At Craniofacial Australia, we're always looking for new ways to raise funds so that more families can access the support...
09/06/2026

At Craniofacial Australia, we're always looking for new ways to raise funds so that more families can access the support they need.

That's why we're excited to be part of Play for Purpose, Australia's biggest online charity raffle. Every ticket purchased through our charity partner page helps fund life-changing patient support programs, research and training opportunities, while giving you the chance to win an incredible prize.

Raffle 32 is now open!

You could win the ultimate $350K First Prize Pack including:

🚙 Land Rover Defender 110 valued at over $190K
⛽ Over $8K in fuel vouchers
💰 $150K in gold bullion

There's also 394 other prizes up for grabs valued at $50K!

Grab your $10 ticket in support of the charity of Craniofacial Australia and you'll also be entered into the Early Bird Bonus Draw to win a $10K VISA* Voucher!

For every $10 ticket purchased, 50% comes directly to Craniofacial Australia.

💙💙💙 Buy your tickets here 💙💙💙
https://www.playforpurpose.com.au/craniofacial-australia

T&Cs apply. Raffle 32 permits: ACT R26/00064, NSW GOCAU/2341, NT FNL1002, QLD 158466, SA M14995, VIC MG-R26344310, WA CC22649. *If Vic Resident, prize will be Woolworths voucher.

Every face has a story to tell.For families facing a craniofacial condition, that story often includes hospital stays, s...
05/06/2026

Every face has a story to tell.

For families facing a craniofacial condition, that story often includes hospital stays, surgeries, travel, uncertainty, and moments no parent expects to face.

Your support helps ease the financial and emotional burden, ensuring families can focus on what matters most, taking it one day at a time.

This Tax Appeal, your donation can help change faces and change lives. 💜

Donate before June 30.

Winter has officially arrived! and so has a fresh delivery of long-sleeve rompers and tees. 💜For many years, Jamie from ...
03/06/2026

Winter has officially arrived! and so has a fresh delivery of long-sleeve rompers and tees. 💜

For many years, Jamie from Cranio Warriors Australia has generously donated these much-loved products to support the families we serve.
These special tees are included in our Care Packs for children facing craniosynostosis, serving as a reminder of their bravery, strength and resilience. Each shirt carries a message of encouragement and support, and we know just how much our Cranio Warriors treasure them.

Do you know a family whose baby has recently been diagnosed with craniosynostosis? They can apply for a Craniofacial Australia Care Pack via the link in our bio or by visiting: https://craniofacial.com.au/care-packs/

Thank you, Jamie. Your ongoing generosity continues to make a meaningful difference to the families we support. 🫶

When a baby is born with a cleft lip or palate, one of the first challenges families can face is feeding. Something many...
02/06/2026

When a baby is born with a cleft lip or palate, one of the first challenges families can face is feeding.

Something many of us take for granted can become a source of worry, frustration and exhaustion as parents work hard to ensure their baby is getting the nutrition they need to grow.

That's why we're proud to share new research funded by Craniofacial Australia, led by Dr Nitisha Narayan and recently published in The Journal of Craniofacial Surgery.

Dr Narayan was Craniofacial Australia's Bristol (UK) Cleft Fellow in 2024, and this research formed part of her Fellowship. Through the Fellowship, she was able to undertake specialised cleft research and training, helping to advance knowledge that will ultimately benefit children and families affected by cleft conditions.

Drawing on data from The Cleft Collective, the United Kingdom's largest cleft research programme, the study examined growth outcomes in children born with cleft lip and/or palate and found that nearly 1 in 3 children experience poor weight gain in early life.

While outcomes have improved significantly over recent decades thanks to specialist cleft services and multidisciplinary care, the research shows that feeding and growth challenges remain a reality for many families.

💙Why does this matter?

Poor weight gain can affect a baby's overall health and development, increase stress and anxiety for parents, and in some cases impact the timing of surgery. The findings highlight the importance of early feeding support, access to specialist cleft teams, and ongoing monitoring during a child's first months of life.

Research like this helps clinicians better understand where support is needed most, identify children who may be at greater risk, and improve care pathways for future families.

Most importantly, it reminds us that beyond numbers, families navigate uncertainty, sleepless nights, feeding concerns and the emotional challenges that can come with a cleft diagnosis.

This important research was made possible thanks to the generosity of our supporters. Every donation helps fund research, education and training opportunities that improve care and outcomes for children living with craniofacial conditions.

A huge congratulations to Dr Narayan and the research team on this important publication and for her ongoing commitment to improving outcomes for children and families affected by cleft conditions 🎉

📖 Read the newly published research:
https://journals.lww.com/jcraniofacialsurgery/abstract/9900/faltering_growth_in_cleft_lip_palate__how_far_have.4143.aspx

💙 Thank you for helping us create a brighter future for children and families affected by craniofacial conditions.

For almost three decades, Sean has helped us continue changing faces and changing lives. 💜By donating to Craniofacial Au...
30/05/2026

For almost three decades, Sean has helped us continue changing faces and changing lives. 💜

By donating to Craniofacial Australia, you are helping families access vital emotional support, research and education for a brighter future, financial assistance with travel, accommodation, and meals during some of the most challenging moments of their lives.

This Tax Appeal, you can help our cranio warriors facing their journey.
If you’re able to give, your donation today will help us continue providing care, connection, and hope to families.

Please make a tax-deductible gift before 30 June and help us continue walking alongside families when they need it most.

👉 www.craniofacial.com.au/donate
👉 Or call (08) 8267 4128

Cranio mum Sarah shares why she decided to take part in the recent HBF Run For A Reason which ultimately raised over $10...
28/05/2026

Cranio mum Sarah shares why she decided to take part in the recent HBF Run For A Reason which ultimately raised over $1000 to help us continue supporting families facing craniofacial conditions.

"We choose to raise money for Craniofacial Australia in honor of Zoe, to show her how proud we all are of her and educate her in a positive way about her story with Metopic Craniosynostosis! so she can grow and be proud of her journey while being thankful for the love and support she has received along way."

💙 Every step helps build pride, awareness, and support 💙

If you are thinking about joining an upcoming fun run to walk, run of wheel for Craniofacial Australia, please contact our friendly Marketing and Fundraising Coordinator, Meg at [email protected] or 08 8267 4128.

CHANGING FACES CHANGING LIVES  2026 🤍Inside this edition, you’ll meet brave little Addie and read her family’s powerful ...
27/05/2026

CHANGING FACES CHANGING LIVES 2026 🤍

Inside this edition, you’ll meet brave little Addie and read her family’s powerful story of navigating craniosynostosis surgery in her first year of life.

You’ll also hear from Lou, our Family Support Coordinator, about what families really need during the toughest moments.

Plus updates on:
⭐️New research
⭐️Community fundraising
⭐️The impact your support is making across Australia.
⭐️Upcoming fun runs + More

📧 Subscribe if you haven't already:
https://www.craniofacial.com.au/

🌐 Read it online:
https://craniofacial.com.au/winter-2026/

These stories are why we do what we do.

⏰ Adelaide, one week to go for Early Bird pricing! 💙🏃‍♀️The countdown is on for the City-Bay on 20 September, and this i...
26/05/2026

⏰ Adelaide, one week to go for Early Bird pricing! 💙🏃‍♀️

The countdown is on for the City-Bay on 20 September, and this is your sign to lace up and join Team Craniofacial Australia. Run, walk or wheel at one of Adelaide’s most loved community events and be part of something bigger than the finish line.

With 27,000 participants last year and multiple distances selling out year after year, spots won’t last long.

💙 Adelaide families, let’s show up strong and proudly represent our cleft and cranio community.

⏳ Early bird pricing ends in just ONE WEEK – midnight 2 June. Don’t miss out!

🔗 How to join Team Craniofacial Australia:

Step 1: Register for the race
https://raceroster.com/events/2026/111162/city-bay-fun-run

Step 2: Set up your fundraiser
https://citybay26.grassrootz.com/join

Let’s show Adelaide the power of our community 💙

Address

204 Melbourne Street
North Adelaide, SA

Opening Hours

Monday 9am - 5pm
Tuesday 9am - 5pm
Wednesday 9am - 5pm
Thursday 9am - 7pm
Friday 9am - 5pm

Telephone

+61882674128

Alerts

Be the first to know and let us send you an email when Craniofacial Australia posts news and promotions. Your email address will not be used for any other purpose, and you can unsubscribe at any time.

Share