Latest news & stories

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.

We are thrilled to announce The Kids' Cancer Project’s founder Col Reynolds OAM is the winner of Research Australia's 2024 Advocacy Award.

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.

In a world that often seems overwhelmed by challenges, there are individuals and communities that rise above, showing unwavering dedication to a cause close to their hearts.

Thanks to years of research funded by people like you, Tommy is on track to recover from acute lymphoblastic leukaemia. But having been diagnosed at just 19-months-old, the pain, trauma and side effects of treatment have impacted him all the same. His special bear, donated by a kind person like you, has been by his side throughout his cancer journey, giving him the courage he needs to face the scary world of cancer.

The Kids' Cancer Project first Christmas fundraising luncheon raised $100,000 to help children with many different types of cancer. Read more about how to get involved in this year's event.

With an investment of over $7.9 million, The Kids’ Cancer Project is ensuring that some of the best and brightest young researchers in Australia can further their careers and most importantly, their impact on childhood cancer research. Read more about the recipients here.

Read how your support has helped save lives and is pushing kids' cancer research further than ever before.

At just eight-weeks-old, Matilda's chances of surviving acute lymphoblastic leukaemia (ALL) hung at less than 20%.

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.