andreaa30's Blog

Hi, how are you guys?  Let me start by saying that i love your show, it is very interesting how the cohosts go back and forth on issues.  The reason of my email is to ask for help.  I have a 13 year old severly handicapp child, she has Angelman Syndrome.  It is a very rare disease only about 1500 kids have it in north america, because theres not that many cases the foundation doesnt get funding for testing.  On may 17th there will be a walk-a-thon to raise money for the study of Angelman Syndrome.  Please take the time to go to www.angelman.org and find out more about it.  This is my daughters page www.firstgiving.com/valerieaki   i'm just a regular stay home mom because my baby girl requires 24/7 care, and i realize that i can't reach as many people ase you guys can so this is my reason for writting.  If theres anything you guys can do please pass the information to anyone that would like to help us.  The Angelman Syndrome Foundation is in New York City. 1-800-IF ANGEL.   Our walk will be in San Diego, and there will be 16 other sites around the country.  Have a bless day, and thank you so very much for your time.

Andrea Aki