Hunter
Sports-mad Hunter came into the Cure Kids family by winning a competition to have lunch with the All Blacks. A dream come true and something positive for him to focus on after being diagnosed with type-1 diabetes suddenly that same year.
Hunter is an active kid who loves playing soccer and rugby! He is also a keen fisherman who has caught his fair share of fish. Hunter has always eaten a balanced healthy diet and tried a wide variety of foods without fuss. Because Hunter was such an active, fit and healthy kid, it was a massive shock to his family when he got diagnosed.
Having very little knowledge of type-1 diabetes, his parents hadn’t picked up on the symptoms. Hunter was always thirsty, and his moods changed. He would cry at the drop of a hat, which was entirely out of character. A flyer in the mail about diabetes awareness alerted his mum Rebecca to get him checked by the doctor. From there, they went straight to Starship and Hunter was diagnosed with type-1 diabetes.
Despite the initial shock, Hunter has handled the diagnosis well, and his parents say he has not once complained about his diet change and that he even injects himself with his insulin - so brave!
Hunter lives with his older sister, mum and dad.
Other special ambassadors
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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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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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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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MelaMela is diagnosed with an incredibly rare condition called Moebius syndrome
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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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JeremyBorn at 29 weeks and 5 days, Jeremy is one of the approximately 700 babies born preterm each year.
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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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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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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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IsabellaBella was diagnosed with cystic fibrosis at her Mothers 27-week anatomy scan
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EvaEva was born with only half a diaphragm after suffering a diaphragmatic hernia during fetal development.
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CorinCorin lives with a very rare genetic heart condition
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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.
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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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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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AddisonAddison was diagnosed with a staph infection, which caused damage to her heart.
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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.
