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Treatment

Articles that highlight the treatment experience

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Love keeps shining strong with the Clements twins

Children's Cancer Foundation / 20/06/2020

Carlee shared her sibling experience of childhood cancer with us, after her brother Hayden’s battle with a brain tumour.

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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.

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Early Identification Provides Hope

Children's Cancer Foundation / 01/10/2018

Application of a genetic screening technique – RNA sequencing – is helping to identify cancer cells early on.

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After the Diagnosis: Advice for Parents, Friends and Family

Children's Cancer Foundation / 28/08/2018

Heather, mother of Mia who was diagnosed with Wilms’ tumour in 2014, shares her advice for how you can navigate the days, weeks and months after the diagnosis.

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More Clinical Trials Equal More Treatment Options

Children's Cancer Foundation / 06/07/2018

Funding from the Children’s Cancer Foundation increases clinical trials offered to patients at Monash Children’s Hospital.

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.