Articles that highlight the treatment experience
Million Dollar Lunch / 01/10/2021
Three months after her shock cancer diagnosis, 13-year-old Sinead died. Her mum had just fought a state election and been made a Victorian Government minister.
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 / 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 / 01/10/2018
Application of a genetic screening technique – RNA sequencing – is helping to identify cancer cells early on.
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.
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.Donate today