Parents Karin and Steve know all too well the stress and trauma that comes with a craniofacial deformity. Their son Jacob was born premature, underweight, and then diagnosed with Craniosynostosis.


“It wasn’t easy to see Jacob go through his journey with craniofacial surgeries and what he had to endure. It was hard to see the pain and suffering. However, Jacob has had the best people looking after him. As tough as it was, we knew that Jacob was going to come out the other side healthy and able as he did.”

People just like Jacob need your support. Please, will you give $25 this tax time?

Yes, I'd like to help people just like Jacob

As little as $25 can give the gift of hope


Your past generosity has helped fund crucial services like:


  • Financial assistance to over 10 families, to the value of over $35,000
  • A Family Support Coordinator. Claire ensures that families are looked after and supported from the time of diagnosis, and throughout their journey
  • 50 care packs, 43% more compared to the previous financial year
  • $75,000 in Patient Support, including financial assistance and care packs
  • $200,000 into research grants
  • A medical fellowship in the UK and continued our online training program for Indonesian surgeons, to the value of over $96,000


These programs are life-changing. For you, our supportive community, giving the gift of hope is pretty special. That’s why we ask you today: please will you give a gift of $25 or more for our Tax Appeal?
 

*Data 22/23 FY

YES, I'd like to donate this Tax Time

Celebrating 40 years of care

This year, we celebrate 40 years of helping thousands of people proudly face the world.

People like Jacob go through their infancy, childhood years and sometimes adult years having to undergo grueling treatment. Jacob explains:


“It has been a very challenging journey. I have spent a lot of time in and out of hospital, on a feeding tube, home oxygen, experienced developmental delays, hearing impairment, other medical issues and learning difficulties. I am now 18 years old and have been through so much. I have overcome a lot of obstacles in my life.”

Your support is needed so that people like Jacob can face a brighter future. As we close out the financial year, the need for our services remains high.
Would you consider making a gift in support of the craniofacial community? 

YES, I'd like to help people face a brighter future

Working for a better today and a better tomorrow


We know first-hand that a better future is well within our reach, but change is not easy or quick. It's about investing time and money into research for a better tomorrow We are working hard to find new ways to improve more lives, sooner.

• we could develop the delivery of medicines to stimulate new bone formation, eliminating the need for invasive surgery?

• we could identify the very genes that are potentially responsible for craniofacial development?

• we could contribute to the largest cohort of cleft lip and palate data in the world?

we could develop the delivery of medicines to stimulate new bone formation, eliminating the need for invasive surgery?

we could identify the very genes that are potentially responsible for craniofacial development?

we could contribute to the largest cohort of cleft lip and palate data in the world?

Your kindness shows how these thrilling possibilities could become a reality.
 

Will you join us by leaving a tax-deductible gift before June 30? 

DONATE to make a difference
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