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Casper was diagnosed with achondroplasia, the most common form of dwarfism, as a newborn. Achondroplasia is a genetic bone disorder that affects one in 25,000 children. The condition slows bone growth in the limbs and spine and narrows the base of the skull, putting pressure on the spinal cord. To give Casper the best start in life, he was enrolled in the vosoritide clinical trial at Murdoch Children’s Research Institute (MCRI) when he was five months old. Casper's mum, Daisy, spoke to MCRI abou
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