
A two-year-old girl from Melbourne, Australia, has been diagnosed with an ultra-rare genetic disease that has left her parents devastated. Mila Taylor is one of just 150 people worldwide to be diagnosed with Infantile Neuroaxonal Dystrophy (INAD), a neurological disorder that has no known cure or treatment.
Mila’s parents, Stephanie, 29, and Andrew, 32, had an easy pregnancy and a healthy baby at birth. But when Mila turned eight months old, they started noticing she wasn’t reaching typical milestones like crawling. Despite being reassured by their GP, the couple felt something was wrong and continued pushing for answers.