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Our latest Newsletter

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

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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.

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Play 4 Purpose Community Lottery

ENTER for the chance to win $250k first prize pack, in the latest Play 4 Purpose community lottery. Buy your online ticket for the chance to win, while supporting Craniofacial Australia.

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Research study publication

A research study funded by the generosity of Craniofacial Australia donors and supporters has been published

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.


Discover more about Craniofacial Australia here.

How you can get involved


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What we do

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

Abby was born with a Haemangioma. Haemangiomas are malformations of blood vessels. At just three months of age Abby underwent steroid treatment after a medical team advised that they were worried about Abby’s eye.

Each year it is estimated that one in every eight hundred babies is born with a facial cleft, ranging in severity from a split lip to a grossly bisected face and palate that makes life impossibly difficult. Cecilia was one of those babies.

Selva was born with a rare craniofacial cleft, a severe deformity of the face and head that affects both bones and soft tissue. Some of the complications for children with a rare craniofacial cleft include trouble eating and breathing, making life impossibly difficult.

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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