Stories of children and families impacted by childhood 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.
Children's Cancer Foundation / 02/10/2018
Elias' bright and cheeky personality "has everyone wrapped around his little finger", including the doctors and nurses at the Children's Cancer Centre.
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.
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