Kids Wish Network is hard at work planning an incredible experience for Taliyah; make sure to stay up to date by checking back soon for all of the details of their once-in-a-lifetime wish!
Tag: Spinal muscular atrophy
“Mynia loved visiting Disneyland and going down the water slides” Mynia is a happy and eager 8-year-old who loves Disney’s “Princess and the Frog,” and cannot believe she finally got to meet Princess Tiana when her wish to Disneyland was granted by Kids Wish Network. Mynia was born with a degenerative disease commonly referred to […]
Name: Luke Age: 18 State: SC At just 14 months old, Luke was diagnosed with spinal muscular atrophy, a genetic disease that causes ongoing muscle degeneration and weakening for which there is currently no cure. Because of this, Luke has never had the ability to walk and has been in a wheelchair since the age […]