Articles that highlight the treatment experience
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 / 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.
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.
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.
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