Hi! My name
is Angela. This is my son Noah.
Noah's
birthday is August 28, 2002. He is 3 years old.
Noah's
birthday is August 28, 2002. He is 3 years old.
He is the joy of our life. We found out he had Williams Syndrome when he was very small. He loves tractors and animals (especially cows and cats). He is a happy little guy. He received early intervention and now goes to a preschool program two mornings a week at Tallassee Elementary.
We have 2 other boys who are older. Luke is 12 years old and has DiGeorge Syndrome (not related in any way to Williams Syndrome). Samuel is 4 years old. I myself teach Kindergarten at our local school, Tallassee Elementary. My husband, Joe, is a dental lab technician. Our family is so blessed!!! All of our boys are doing well. If you would like to e-mail me, my address is angela.gantt@tcschools.com.
I am looking for alternatives to putting Noah in a public school setting. If anyone can help with information about how to deal with this, I would love to hear from you. As we all do, I want to do what is best for Noah. I also want to thank everyone who has helped establish the Williams Syndrome Foundation, because it has meant so much to me. With my older son, Luke, there isn't a foundation for DiGeorge Syndrome children. It helps to have others to share with.