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.
