NJ girl is a true ‘Wonder’ and the focus of a movie
We were joined by Suzanne Ashby Friday, who is the mom of Olivia, a young girl suffering from Treacher Collins syndrome which is a craniofacial disorder.
I was introduced to the family by the executive director of Make-A-Wish New Jersey Tom Weatherall when my wife Jodi and I were participating in the "Walk for Wishes" with our friend Rob Dekanski.
The story of struggle for a girl with a disfiguring disease and a fight for life is part of the inspiration for a new movie. The family is hosting a screening of the movie "Wonder" at the AMC New Brunswick 18 theaters on Route 1 in New Brunswick Saturday at 3 p.m. Tickets are only $20 and all proceeds will benefit the Children's Craniofacial Association.
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