Luca
When Luca was diagnosed with cystic fibrosis at just two weeks old, his parents had no idea what CF was or how much it would change their lives.
In his first three years, Luca has had countless hospital appointments and spent a huge portion of his little life on antibiotics. His daily routine includes twice-daily chest physio, nebulisers, medications and extra care to protect him from bacteria that can be dangerous for people with CF.
But CF is only a small part of who Luca is. He’s a cheeky, energetic three-year-old who loves playing with his big brother Beau and simply being a kid.
There is currently no cure, but advances in research and treatment are giving families like Luca’s so much hope. Every dollar raised helps give children like Luca the chance of a healthier, longer future
Other special ambassadors
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LucaWhen Luca was diagnosed with cystic fibrosis at just two weeks old, his parents had no idea what CF was or how much it would change their lives.
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BenBenjamin was diagnosed with Spina Bifida Myelomeningocele and Hydrocephalus at his Mum Catherine’s 20-week antenatal anatomy scan.
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LuccaLucca was diagnosed with an extremely rare and highly aggressive cancer called Epethelioid Inflammatory Myofibroblastic Sarcoma when she was just 16 months old.
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PaigePaige was born on December 6, 2021, entering the world prematurely at just 23 weeks and 4 days gestation, and weighing a tiny 525 grams
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EvaEva was born with only half a diaphragm after suffering a diaphragmatic hernia during fetal development.
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IslaIsla lives with type 1 diabetes. While type 1 diabetes is currently incurable, there are treatments available, but unfortunately all have a considerable impact on a person’s day-to-day life.
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RoryHe was diagnosed with type 1 diabetes at just six years old. It was an unforgettable day - he was picked up from school, sent for tests, and admitted to hospital.
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JeremyBorn at 29 weeks and 5 days, Jeremy is one of the approximately 700 babies born preterm each year.
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MelaMela is diagnosed with an incredibly rare condition called Moebius syndrome
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Amelia & GraceTwins Grace and Amelia were born prematurely at 27 weeks. They have extreme chronic lung disease and Grace had her first open heart bypass surgery at 8 weeks of age.
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CorinCorin lives with a very rare genetic heart condition
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AddisonAddison was diagnosed with a staph infection, which caused damage to her heart.
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IsabellaBella was diagnosed with cystic fibrosis at her Mothers 27-week anatomy scan
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HunterHunter was diagnosed with type 1 diabetes after his family noticed he was always thirsty and that his moods had changed.
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Matt JohnsonMeet Matt Johnson, a former midfielder for the Blues rugby team. Matt had rheumatic fever when he was 13 and has been experiencing severe heart problems ever since.
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SophieA urine test showed glucose, and a subsequent finger prick blood test showed elevated blood glucose.
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RichieHe had a persistent cough, had lost weight and become so lethargic he was short of breath even when lying flat on a bed.
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KaseKase lives with cystic fibrosis, a condition is typically detected at birth, but Kase was diagnosed at 8.
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JaideJaide lives with chronic asthma and type-1 diabetes.
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JacksonJackson had a tumour the size of a tennis ball attached to his optic nerve.
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FinnFinn was diagnosed with hypoplastic right heart, when his mother was 20 weeks pregnant.
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FinlayFinlay was diagnosed with type -1 diabetes at three-years-old.
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ChloeOur gorgeous little ambassador Chloe has suffered respiratory issues since she was an infant.
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BrookeAt six years old, Brooke was diagnosed with gelastic seizures.
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BraydenIn 2009, Brayden was cooking noodles when his t-shirt caught fire from the stove element. He received burns to 45 percent of his body.
