Meet Our Champions
Meet Meg
Meg's journey began with developmental delays, which led to diagnoses of Cerebellar Hypoplasia, Cerebral Palsy Ataxia and a rare genetic disorder CTBP1. These conditions impacted her mobility and speech which presented unique challenges. Meg's family found a team dedicated to her progress at Carilion Children's, supported by Children's Miracle Network Hospitals. Through therapies, surgeries, and assistive devices including a wheelchair, Meg's light shone bright, radiating love and positivity to everyone around her while she climbed every mountain.