08/10/2026
WOW! WHAT A DAY 🎗️
A few months ago, Charlie’s Rainbow received a generous donation.
When I reached out to say thank you, I learned they were supporting their son’s best friend, Isaac, who was in Sydney undergoing treatment for AML. We spoke about the research, and I offered a tour of the lab whenever the time felt right.
Then on Father’s Day, I received a message from Isaac’s mum. Isaac had passed away. My heart sank as I realised this was the same boy we’d been thinking about and hoping would make it home.
As an AML bereaved mum, there are conversations no parent should ever have to have. We spoke about honouring Isaac through donations, and I reminded her that the invitation to visit the lab would always be there.
Today was that day.
Isaac’s family and support crew joined us in the lab, where our incredible research team welcomed them, shared their work, answered questions, and showed firsthand what your support makes possible.
Hearing stories about Isaac was such a gift. A larger-than-life teenager with a wicked sense of humour who loved playing pranks on the nurses. The more I heard, the more I smiled. I couldn’t help but think that if Isaac and Charlie had met, they would have kept everyone on their toes.
Today was a reminder of why Charlie’s Rainbow exists. It brought together another family, loyal friends, and passionate researchers, all united by the determination to change the future for children diagnosed with AML.
Here is Isaac’s support team checking out the cells in the lab today.
For Charlie. For Isaac. For every child and family facing AML 💙🌈
If you’d like to help us continue funding lifesaving paediatric AML research, please consider donating via the link in our bio. Every dollar brings us closer to better treatments, kinder treatments, and more children making it home 💙