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Parents perspectives

Stories from parents of children affected by cancer

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Our newest Board Member – The Hon. Jaala Pulford

Children's Cancer Foundation / 15/02/2023

We are pleased to announce that former Victorian member of parliament Jaala Pulford, will take up a position on the Children’s Cancer Foundation Board.

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Labor MP Jaala Pulford lost her daughter Sinead to cancer shortly after the election

Million Dollar Lunch / 01/10/2021

Three months after her shock cancer diagnosis, 13-year-old Sinead died. Her mum had just fought a state election and been made a Victorian Government minister.

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Hayden’s a hero in our book

Children's Cancer Foundation / 23/09/2020

Hayden has been fighting hard following a brain tumour diagnosis in 2015. Mum Simone shares his long, painful and sometimes frustrating road to recovery.

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The Foundation welcomes Tracey Danaher to the Board

Children's Cancer Foundation / 23/06/2020

We extend a warm welcome and congratulations to Tracey Danaher to the Board of the Children's Cancer Foundation.

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A Wilms tumour diagnosis at Christmas time

Children's Cancer Foundation / 06/12/2019

On Christmas Eve 2014, two-and-a-half-year-old Mia was diagnosed with cancer. Her mother Heather shares the family’s experience of Wilms' tumour, and how it changed their lives.

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A remarkable family’s fight against a rare form of children’s cancer

Children's Cancer Foundation / 17/10/2018

This is Cassandra Howcroft’s story about her son Lochie’s battle against Philadelphia +ve, a very rare form of Acute Lymphoblastic Leukaemia.

How can you help?

When you love someone deeply you want them to shine in your life always. You will do anything to protect them. Children’s cancer shouldn’t happen – but sadly, it still does. With your help, we're funding game-changing research projects that will help eliminate children’s cancer.