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I am so excited. Saturday morning the kids and I are participating in a walk-a-thon. It is to benefit
the Angelman Syndrome Foundation. Campbell’s teacher has a daughter that was born with
this genetic disorder and his teacher let her class know about the walk-a-thon so that those who
wanted to participate could sign up. Mrs. Evans is very well-known and respected nationally
and internationally with the Angelman Syndrome Foundations. We are just thrilled to be able
to participate. Jacob was planning to walk with us, but his current trip to Mexico leaves the
kids and I to go it ourselves. I stayed up way too late last night reading all about AS and being
in awe at these sweet children (they are known as Angels) and their amazing parents.
What a privilege to have a small part in it. We cannot wait.
the Angelman Syndrome Foundation. Campbell’s teacher has a daughter that was born with
this genetic disorder and his teacher let her class know about the walk-a-thon so that those who
wanted to participate could sign up. Mrs. Evans is very well-known and respected nationally
and internationally with the Angelman Syndrome Foundations. We are just thrilled to be able
to participate. Jacob was planning to walk with us, but his current trip to Mexico leaves the
kids and I to go it ourselves. I stayed up way too late last night reading all about AS and being
in awe at these sweet children (they are known as Angels) and their amazing parents.
What a privilege to have a small part in it. We cannot wait.
