Changing Faces, Changing Lives

Kate’s Story

Close up of baby with cleft lip and palate

It wasn’t until Kate was 19 years old that her father told her that he fainted at the sight of her as a baby. It is a significant moment, because it indicates just how far Kate has come. Her story is one of anguish and triumph – a craniofacial journey that will last her whole lifetime.

Born with a bilateral cleft lip and palate, Kate was only two days old when she first met Professor David David. He walked straight into the hospital room and immediately picked Kate up with a gleaming smile.

“It’s true that I owe my life’s happiness and contentment to Professor David David and his exceptional surgical and specialist team,”

Kate beams as she recalls the incredible journey she has been on. Kate has endured 13 operations over her lifetime, many of which have involved treating multiple issues at once. Until the age of 22 Kate would meet annually with specialists and have appointments that would often take two days to complete.

“I can still remember how busy the waiting room was, with every second or third chair seating a child, teenager or adult with a disfigured face. Then there were the babies sporting oxygen tubes taped to their nose, or paddle pop stick splints strapped to their arms so they couldn’t touch their sore little faces.”

Woman who had surgery for cleft lip and palate
Woman who had surgery for cleft lip and palate

When Kate talks about her journey, there are both physical and emotional scars. It wasn’t until she was 16 that she was able to talk about the way she looked, but now she shares how different her life is because of the treatment and care she received.

“They have given me a great gift, the gift of social acceptance. They not only change faces, they transform lives.”

Photo by The Dance Pad
Banner photo by Heidi Who Photos

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After her routine 20 week ultrasound scan, mum Angel was called in to her GP’s office. “The baby we’d been trying for, for almost three years would be born with a significant (1cm+) cleft lip and palate."
My daughter Briana was only 2 days old when she first met Professor David. I was in absolute shock when he walked in, knowing how busy he was. How amazing is it that this man cares so much about this little child that has just been born? When he held her on that first meeting, he said ‘You are the most beautiful little girl and we will do everything for you’.
Cecilia was born with a unilateral cleft lip and palate. She was inspired by the care given to her by medical staff during her treatment and is now a nurse herself. “Everyone is different and it can be hard, but when you grow up it’s not going to matter at all”.
Meet Flora – a bright and resilient little girl born with a bilateral cleft lip and palate. Her family received her diagnosis during a routine pregnancy scan, and from that moment, they began a journey filled with challenges, strength, and hope.
Meet Hunter - Born in May 2022, Hunter was diagnosed with cleft lip and palate and metopic craniosynostosis at birth. He had his lip repaired at 6 months and his palate repaired at 11 months old.
After her routine 20 week ultrasound scan, mum Angel was called in to her GP’s office. “The baby we’d been trying for, for almost three years would be born with a significant (1cm+) cleft lip and palate."
I was 6 years old when I first came to Australia from Pakistan where I was born. However, I was born with a birth defect called 'Cleft Lip Palate', 1 year later my father came to Australia by boat. He was a refugee and was finding it really hard to find a proper job (as he was uneducated) and to also support us back in Pakistan.
Meet Vallerie - Born with a bilateral cleft lip, she received her diagnosis during pregnancy and began treatment at just 14 weeks old. Over the years, Vallerie has undergone 7 surgeries, including a hip-to-face bone graft, Lefort 1 Maxilla Advancement, and septorhinoplasty - as well as over a decade of orthodontic care.
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