Articles that highlight the treatment experience
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.
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.
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.
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.
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.
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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