Macy (far left) used to have to regularly travel from Melbourne to Hobart with her mum Suzannah for treatment. Having treatment in Hobart means Macy’s sister Matilda (far right) gets more time with family too.
Tragically, sarcoma will return for one in three children even after surgery to remove the cancer - this high rate of relapse after treatment is a major cause of fatality. But with your kind support, Dr Ben Wylie and his team in Western Australia are developing a ground-breaking new treatment aiming to change that.
After losing seven members of her family to various types of cancer throughout her life, 91-year-old Coral from NSW decided that it was time to do something. By including a gift in her Will to The Kids’ Cancer Project, Coral hopes to help the next generation avoid the heartbreak her family have endured.
A generous grant of $91,000 made by Perpetual Trustees to The Kids' Cancer Project will help to fund a pioneering research project aiming to identify the 'culprit' genes behind childhood cancer.
July marks Sarcoma Awareness Month, a time when we shine a light on a cancer responsible for about 20% of childhood cancer diagnoses. Thanks to the ongoing commitment of our wonderful community, The Kids' Cancer Project is actively funding nine projects across Australia in order to develop better treatment options for those kids.
As The Kids’ Cancer Project continues to grow and commit more money to vital childhood cancer research, the role of our board is more important than ever. Here we get to know one of the board’s newest members, Tim Rose, and why he’s so passionate about making a difference to childhood cancer.
With a background in immunology, Dr Tessa Gargett is utilising her knowledge of the human immune system to tackle children’s cancer. Here, she explains how she’s maximising the potential of CAR-T cells to provide a treatment option specifically tailored to brain tumours.
Diffuse midline gliomas (DMG), including diffuse intrinsic pontine gliomas (DIPG), are the most lethal of childhood cancers primarily occurring in young children.
In March 2021, when she learned her beloved daughter had a life-threatening brain tumour, a mum made it her mission to raise the profile of childhood cancer.
Bec’s daughter Roxy was diagnosed with acute lymphoblastic leukaemia (ALL) when she was a four-year-old, and overnight, the family’s outdoorsy life quickly shifted to one of relentless appointments. But, thanks to supporters like you, Roxy got a new cuddly sidekick to help keep her smiling throughout her treatment.
Looking for a great way to stay active, and make a difference? You can be a community champion by fundraising with The Kids' Cancer Project. We've got some great outdoor events on offer, so read on to find the challenge event that suits you!
The Zero Childhood Cancer Program (ZERO), which has been supported by The Kids’ Cancer Project since 2015, is being expanded to all Australian's aged 0 to 18 years with any type of cancer.
Minister for Health and Aged Care, the Hon Mark Butler MP today announced the successful grant recipients to receive funding for innovative cancer research through the 2023 round of the Cancer Australia Priority-driven Collaborative Cancer Research Scheme (PdCCRS).
In the heart of Australia's vast outback, amidst the red sands and scorching sun, a remarkable journey is unfolding. Kiah Grillett, fuelled by compassion and determination, is gearing up to take on the ultimate challenge: a grueling two-day off-road dirt bike race spanning 226 kilometers each way on a multi through desert country from Alice Springs to and from the small Aputula (Finke) Community: The Finke Desert Race.
Behind all the laboratories and expert scientists it takes to create better kids’ cancer treatments are the systems and data in place to keep funding running smoothly. Thanks to The Kids’ Cancer Project’s ongoing partnership with SAS Analytics, now in its seventh year, we’re able to operate more efficiently and help commit even more money to vital kids’ cancer research.
When Ellalee’s daughter, Maia, was diagnosed with ALL, she prepared as best she could for the difficult journey ahead. Here, she opens up about the loneliness Maia faced during her cancer, and how the kindness of people like you has given her daughter a reason to smile during the hardest time of her life.
Now 17, Molly from Dubbo, NSW, is many things: a cancer survivor, a passionate advocate and fundraiser, and a teenager with dreams of netball coaching and university.
Since 2013, we’ve been honoured to have the support of the wonderful Tangalooma Island Resort. The team have raised over $53,000 to support kids’ cancer research through their whale watching tours.
We are thrilled to see the much-anticipated Sun Run is returning for 2024! A radiant fun run along the spectacular Northern Beaches coastline from Dee Why to Manly Beach in Sydney.
For Jessie Glew, the joint MD and COO of WOTSO, the simple idea that ‘we will find a cure’ drives her passion to help fund kids’ cancer research. Jessie’s infectious enthusiasm, clear drive to make a difference and wealth of business knowledge make her an invaluable member of The Kids’ Cancer Project’s board.
For Professor Matt Dun, his research into DIPG is more than just professional. In 2019, his daughter, Josie, sadly passed away from the aggressive form of childhood brain cancer, leading him to dedicate his career solely to developing treatments for the currently incurable disease. Today, with the help of your generous gifts, Prof. Dun and his team are making promising strides towards the first effective treatments for this devastating disease.