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Treatment

Articles that highlight the treatment experience

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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.

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Super Mum in the City

Children's Cancer Foundation / 22/05/2018

Mum Sharon shares the story of a chance accident led to the discovery of a tumour in her daughter Kasey’s leg, and how this regional family managed her cancer treatment.

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A Creative Mind

Children's Cancer Foundation / 07/12/2017

Five-year-old Caleb was diagnosed with T-Cell Lymphoma in early 2017. During the long hospital stays, Caleb feeds his creative mind with music and play therapy.

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Marcus: A beautiful, funny, but short life

Children's Cancer Foundation / 23/10/2016

Parents Marisa and Fabian share a beautiful tribute to their son Marcus, who lost his battle with Ependymoma in 2014.

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Brooke: “Each day is special”

Children's Cancer Foundation / 03/03/2016

A sore leg was the first sign that something was wrong with nine-year-old Brooke. Tests were taken and within days Brooke’s parents received the news.

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.