• Slide title

    Give the gift of hope this Christmas

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  • Read Zuhrah's Journey...

    from Pakistan to Australia

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    Care & support for the craniofacial community

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    View Photos from our 40th Anniversary Gala Lunch

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Our latest Newsletter

Explore all the latest news with "Changing Faces, Changing Lives", our quarterly Newsletter. Spring 2024 Edition is out now.

Leave a Gift in your Will

Leaving a gift in your will, is a gift that lasts a lifetime. It transforms lives. Thank you for considering Craniofacial Australia in your Will.

WIN a $250k First Prize Pack!

Buy your ticket here for the chance to win a $250K First Prize Pack!


Closes 8pm (AEST) Thu 12 Dec 2024
Drawn 9am (AEST) Fri 13 Dec 2024

Annual Impact Report

We are thrilled to share the Craniofacial Australia Annual Impact Report for the 2023/24 Financial Year. 

Who we are:


Founded in 1984 by Professor David David AC, Craniofacial Australia supports craniofacial patients, scientists, surgeons and families to achieve extraordinary outcomes.


We promote and fund research directed at improved patient outcomes, develop and implement training and teaching courses worldwide and support patients and families when they need it most.


Your generosity continues to make a difference to the lives of many. Thank you. Together, we are changing faces and changing lives.

How you can get involved


Fundraise in your community

Volunteer

Workplace Giving

EMBRACE YOUR FACE

Our community joined the journey and here is what they had to say

Now you can

Join the Journey.


We want to hear about your journey and what "Embrace Your Face" means to you.


You may have seen our incredible ambassadors Selva, Abby and Cecilia on billboards and social media.


Now you can join them!


Join the journey and be a part of our Community Billboard or join them on social media.

Join the Journey

Craniosynostosis:

Metopic and Sagittal Fusions.


This is Attila’s story:
“Attila was born with an egg-looking head shape, which clinicians thought was due to the vacuum and forceps used during birth. Shortly after, they struggled to find his fontanelle so they sent us for an ultrasound. About two weeks later, they advised that he might have Craniosynostosis.

Apert Syndrome


This is Zuhair's story:

"We named our daughter Zuhrah, an Arabic name meaning "Venus" or "the morning star. As first-time parents, we were overjoyed, anticipating the boundless joy our little star would bring into our lives. But nothing could have prepared us for the unimaginable challenges we would face.

Nager Syndrome


This is Mariam's story:

Mariam was born with Nager Syndrome, a rare and debilitating condition that affects development of the lower face, jaw and mouth.


EMBRACE YOUR FACE

Our community joined the journey and here is what they had to say

Now you can

Join the Journey.


We want to hear about your journey and what "Embrace Your Face" means to you.


You may have seen our incredible ambassadors Selva, Abby and Cecilia on billboards and social media.


Now you can join them!


Join the journey and be a part of our Community Billboard or join them on social media.


Join the Journey
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