Stories of children and families impacted by childhood cancer
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 / 18/07/2018
At the 2018 Million Dollar Lunch, Father Joel Gniel shared how an Acute Lymphoblastic Leukaemia diagnosis changed his family forever.
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 / 30/08/2017
A sibling’s side of a cancer journey. How love and loss of her brother to leukaemia led Carly to become a change-maker
Children's Cancer Foundation / 16/05/2017
In June 2016 a large mass was discovered on the brain of thirteen year old Dylan. He was rushed to the Emergency Department for urgent surgery.
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