Little doctors take over PCH new Kids’ Clinic.
- Perth Children's Hospital Foundation
Little doctors take over PCH new Kids’ Clinic.
- Perth Children's Hospital Foundation
Seven remarkable Perth Children's Hospital Foundation (PCHF) ambassadors swapped patient gowns for doctor coats, taking over Perth Children's Hospital for PCHF's new Kids’ Clinic.
Nine-year-old Mikey and six-year-old Daisy formed part of the team of ‘Little Doctors’ who stepped into Kids’ Clinic to conduct a ‘check-up’ on some of Perth’s most well-known faces in a heartwarming experience designed to raise vital funds for WA’s sickest kids.
Kav Temperley (Eskimo Joe), Matt Kelly (Perth Scorchers), Jhye Richardson (Perth Scorchers), Katie Lamb (radio personality), Miranda DiGrande (international model) and Demi Skinner (TikTok circus sensation), were among the renowned patients who attended their health and happiness check-up, putting their balance, eyesight and even sense of humour to the test during the special appointment.
Carrick Robinson, CEO of Perth Children’s Hospital Foundation, said each Little Doctor’s journey is living proof of the importance of the Foundation’s commitment to ensuring WA’s sickest kids get well and stay well.
“Today’s Kids’ Clinic is a celebration of recovery, resilience and a reminder of the real-life, world-class specialists at PCH who make these stories of hope possible,” he said. “Seeing our Little Doctors smiling, confident and thriving is a powerful symbol of why we do what we do.”
The Kids’ Clinic also serves as a reminder of the urgent need for support during PCHF’s Tax Appeal, which runs until 30 June. Every donation made during this time will be doubled, helping the Foundation raise over $400,000 to fund state-of-the-art medical equipment for PCH.
“As WA’s specialist children’s healthcare charity, PCHF is vital in ensuring these experts have access to the cutting-edge equipment they need to give every child the best chance – not just in recovery, but in life,” Mr Robinson added. “Your support will help WA kids like Mikey, Daisy and Noah thrive.”
Hayley Hamilton, mother to 11-year-old Noah who was diagnosed with juvenile idiopathic arthritis at just two years old, said today is a light-hearted reminder to prioritise health. “You know your child better than anyone else and if something feels off, it’s really important to speak up and advocate – for them and yourself,” Ms Hamilton said.
“Noah’s regular check-ups for his juvenile arthritis have helped us to track pain – whether it was getting worse or moving to other joints. They also allowed the doctors to adjust the treatment when needed and make sure it was really working,” she said.
Meet the kids.
Mikey, 9
Born with seizures that caused brain damage and led to cerebral palsy, Mikey received pioneering ‘cooling therapy’ with equipment funded by the Foundation to limit the damage and help stabilise his condition. Despite this, Mikey doesn’t let his condition stop him from living life to the fullest.
Daisy, 6
Diagnosed with acute lymphoblastic leukaemia at just four months old, Daisy spent the first nine months of her life in hospital. After two years of chemotherapy, she is now in remission and set to celebrate five years cancer-free in January 2026.
Noah, 11
When Noah was two, he was diagnosed with Juvenile Idiopathic Arthritis. Despite constant pain and ongoing treatment, Noah never lets his condition slow him down; whether he’s surfing, playing footy, or dreaming of riding big waves at Pipeline with his surfing hero, Kai Lenny.
Anastasia, 8
Anastasia lives with cerebral palsy, a chronic condition that affects her movement abilities. She is one of the first kids to have signed up to the Move to Improve program, harnessing ‘movement as medicine’ to regain her confidence and strength in everyday activities.
Alexey, 16
Alexey’s medical journey began at just one month old, when he suffered a stroke due to a brain bleed, followed by the discovery of a tumour in his abdomen. He’s since undergone multiple surgeries, including the removal of half his brain. Today, Alexey continues to inspire others with his strength and determination.
Hailey, 6
Living with Type 1 Diabetes, Hailey is passionate about living life as normally as possible. Thanks to her insulin pump and the support she receives at PCH, Hailey is thriving and dreaming big.
Jordan, 7
Diagnosed at age two with Primary Ciliary Dyskinesia (PCD), a rare genetic condition that affects the lungs, ears, and sinuses, Jordan visits PCH weekly for physiotherapy, respiratory and immunology care. He jumps at every chance to feel like a ‘normal kid’ – and dreams of being Spider-Man for a day.
