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Make a Wish sends Wilmington girl to Disney World
A Wilmington girl with a rare form of dwarfism called Cockayne Syndrome is getting a dream come true. She and her family are off on a special vacation thanks to the Make a Wish foundation. Disclaimer: Comments posted on this, or any story are opinions of those people posting them, and not the views or opinions of WWAY NewsChannel 3, its management or employees. »N.C. Headlines |
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FOR THE PARENTS OF MAKAYLA.
We are so happy to see makayla on her trip to Disney Land she is beautiful.I have a little brother with the same syndrome.I had never seen another child with the same syndrome.I got suprised to see how much they look alike.My little brother is 7 years old and his name is ANTHONY. We would love to hear from you,you can e-mail us to daloserdeana@yahoo.com
GOD BLESS MAKAYLA & HER FAMILY.
To find out more about
To find out more about cockayne syndrome, go to Cockaynesyndrome.net
Makayla's make a wish
It is awesome that Makayla and her family get to go to Disney and spend time together! Make a wish a great organization and brings so much joy to the kids lives.
Makayla's Make A Wish
How Exciting for this Beautiful little Girl and what a wonderful story. We're so happy for this family!