When Lewis was born, he needed emergency surgery in hours. Soon after, doctors discovered he had cystic fibrosis — a genetic condition that can cause severe breathing problems, chronic lung infections and a reduced life expectancy.
Lewis’s journey began in his earliest days and today, at 12, he is thriving. He spends his time outdoors, takes on new challenges, and recently received the Grey Wolf Award, one of the highest honours in Scouts Victoria. His determination has shaped his journey — and through his involvement in research at MCRI, his experience is helping shape answers for other children too.
A child’s future. Your impact.
As Murdoch Children’s Research Institute (MCRI) marks 40 years of discovery, Lewis’s story shows just how far sustained research has brought us — and why continued breakthroughs matter.
Advances in genetics and targeted treatments means Lewis now has access to medications that help protect his lungs and give him every chance to enjoy a healthy, active childhood. But many children with cystic fibrosis are still waiting for answers.
Why the next breakthroughs can’t wait
MCRI, researchers work across more than 150 childhood conditions, including cystic fibrosis. Teams are using genomics to deliver earlier diagnoses, developing stem cell-derived “mini lungs”, and rapidly testing medicines that could protect vulnerable airways before infection takes hold.
The Director’s Fund helps ensure promising discoveries don’t stall — giving researchers the freedom to move quickly when children’s futures are on the line.
Four decades of discovery at MCRI has changed what’s possible for children. Together, we can ensure the next 40 years are just as transformative.
Please give before 30 June to help bring the next breakthrough closer for children like Lewis.
Thank you for your generosity — and for helping create stronger futures for children. For all. Forever.
Banner image: Lewis as a toddler on dad Nick’s shoulders with mum Justine. Credit: Nicole Anderson.