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?
As little as $25 can give the gift of hope
Your past generosity has helped fund crucial services like:
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
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?
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?
Address: 204 Melbourne Street
North Adelaide SA 5006
Postal: PO Box 1138, North Adelaide SA 5006
Phone: (08) 8267 4128
Email: info@acmff.org.au
Monday - Friday: 9am - 5pm
Saturday - Sunday: Closed
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Welcome to the Craniofacial Australia family. We are thrilled to have you join this incredible craniofacial community of ours. At the centre are our families affected by a wide range craniofacial conditions, but an equally important part are our amazing donors, supporters, volunteers, researchers and medical professionals. Thank you for joining our community.
You will now receive our quarterly Newsletter – Changing Faces Changing Lives.
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If you have any questions about our work or want to find out how you can get involved further, please do not hesitate to contact us direct.
Many thanks,
Craniofacial Australia
P: (08) 8267 4128
Registered Charity: CCP2573 | ABN: 29 008 155 780
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