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How you’re helping

Every week in Aotearoa, three families are told the heartbreaking news that their child has cancer. Child Cancer Foundation is committed to supporting them every step of the way.

Child Cancer Foundation connects each newly diagnosed family with a dedicated Family Support Coordinator, who provides them with one-to-one support in the specific areas they need it.
 
We need to raise $6 million each year and we don’t receive any direct government funding, so these families rely on the generosity of their fellow Kiwis.
 

That’s why every dollar collected during our Street Appeal makes a difference.

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Your support will help families like Isla’s

Isla was diagnosed with leukaemia in 2020 when she was just three years old. Her family is just one of over 1,200 whānau who are currently being supported by Child Cancer Foundation.

Your support will help families like Isla’s

Hear it firsthand through these powerful stories.
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Roman’s story

Roman was just 11 months old when his mum Courtney found out that he was suffering from an extremely rare type of cancer.

“Hearing that my baby had cancer was my worst nightmare. But getting that news was just the beginning,” said Courtney.

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Maggie's story

In October 2021, six-year-old Maggie was diagnosed with T-cell lymphoblastic lymphoma, turning her family's world upside down. Thanks to the support of Child Cancer Foundation, Maggie and her whānau have received essential care throughout her courageous battle, from practical help to emotional support.

“All I could think about was the mass in Maggie’s chest. I just wanted them to get it out.” - Maggies mum, Emma

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Ellise's Story

Ellise’s life changed at just four years old when an 8.5cm by 8.5cm tumour was found in her brain. After two neurosurgeries and intensive treatment, she defied the odds by walking and talking again. However, new tumours have appeared, and her family remains determined to make the most of their time together.

“She went from being a happy, healthy girl – into ballet, gymnastics, really vibrant – to not being able to walk, and not being able to use the right side of her body.”

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We provide personalised, one-to-one support

No two families' experiences are the same, and neither is the support they need. That's why we are there for each whānau in the areas that will help them most.

Find out more
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How you will make a difference

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Funds a Family Support Coordinator to visit a family wherever they are

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Helps cover essential bills so a family can keep their phone and power on

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Covers travel costs to reunite a family separated by treatment

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Provides one full year of customised, wrap-around support for a family

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