Emilia’s Story
17-month-old Emilia was born with a Unilateral Cleft Lip and Unicoronal Craniosynostosis. A Unilateral Cleft Lip occurs when one side of the lip has a gap, after failing to join together during pregnancy.
Darcy’s Story
Darcy was diagnosed with Sagittal Craniosynostosis at four months old. This was a scary and unknown time for our family, however our Paediatrician and the whole Cranio team were incredible. They went above and beyond to make us feel at ease and provide enough information on the matter / process going forward, this was especially important to us as we had never heard of the condition.
Daisy’s Story
We are incredibly blessed to have our own beautiful Cranio-Warrior, Daisy. Daisy is 2.5 years old and was born with a rare genetic syndrome; Apert Syndrome. Apert’s is caused by a mutation of the FGFR2 gene and because neither my husband or I have Apert’s, it’s a random mutation. The chances of having a rare gem like Daisy is 1 in 65000.
Cruz’s Story
When Cruz was born, mother’s instinct told Bec something wasn’t right. She shares with us her incredible story to find the right answers for her son and receive the treatment he needed for previously undiagnosed craniosynostosis.
Cathy’s Story
Cathy was born in 2020 in Adelaide, South Australia. At birth, it was noted that she had prominent ridging of the sagittal suture, along with dysmorphic features. She was immediately referred to the Craniofacial Unit, and had genetic testing recommended.
Benji’s Story
Weeks after second son Benji was born, Natalie’s world went into a spin. After being admitted to hospital for an unrelated virus, a paediatric doctor observed Benji’s head shape and referred him to a specialist team at the hospital.
Ava’s Story
Ava, now 2, was diagnosed at birth with Sagittal Craniosynostosis after nurses noted unusual ridging along her head. She was seen to promptly by the craniofacial unit.
Attila’s Story
Cranio-Warrior Attila has been through a lot in the first 6 months of his life.
Mum Katharina reached out to Craniofacial Australia in a bid to raise awareness. In doing so, she leaves an invaluable footprint for other families.
Courtney’s Story
When Courtney was born in Hobart, her skull had fused too early and she was missing bone in parts of her head. Since then, she has faced countless surgeries, long recoveries, and the emotional and financial challenges of travelling from Tasmania to Adelaide for specialist care. Yet through every setback, Courtney’s courage shines.