In August 2021, after years of specialist appointments, genetic testing, and searching for answers, our world changed when my son, Christopher, was diagnosed with KAT6B syndrome, a rare genetic neurodevelopmental disorder. From birth, we knew he was different. He was a beautiful baby, but as he grew, developmental delays, coordination struggles, and communication difficulties became more apparent. His list of disabilities kept growing, While his KAT6B diagnosis gave us clarity, it also meant adjusting to a future filled with complex disabilities, therapies, and lifelong support needs.

Now, in 2025, Christopher is 10 years old. Every day brings battles, but through it all, he remains the strongest, most resilient little boy I know.

His journey is not just one of struggle, it is a story of resilience, determination, and unconditional love. And that is something truly worth celebrating.

Grateful for the KAT6 Foundation

Through all these struggles, we are incredibly grateful for the KAT6 Foundation and the strong, supportive community it has built. When Christopher was diagnosed, we felt lost, unsure of where to turn. But through the foundation, we found resources, expert guidance, and most importantly other families who truly understand.

The foundation has given us hope, showing us we are not alone. There are others, just like us, fighting the same battles and celebrating the same victories, no matter how small.

We are forever thankful for this incredible community and the strength, love, and advocacy it provides.

Jade Greatbatch

South Australia

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