Tag: Spinal muscular atrophy

Wish Kid Taliyah - Kids Wish Network

Wish Kid Taliyah

December 2016

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!  

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Mynia’s Princess Vacation

November 2013

“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 […]

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I Met Brian Williams!

November 2011

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 […]

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48,632 kids helped this last fiscal year through our many programs and services.

Our Mission

Kids Wish Network is a charitable organization dedicated to infusing hope, creating happy memories, and improving the quality of life for children having experienced life-altering situations. Kids Wish Network assists children and their families through several key programs.