Wednesday, September 14, 2011

Kayli is 28 months and is Loving Life with Full Trisomy 18!  The purpose of this blog will be to make other T18 parents or parents to be AWARE of the AWESOME life to live with the Diagnosis of Trisomy 18 (Edward's Syndrome).  I (Kayli's Mommy, Kelly) am new to blogging, so please be patient as I create a wonderland for Kayli's blogspot. 

1 comment:

  1. I am so thankful that I saw the article about Kayli in the newspaper. I was hoping that I would see her at the "Santa's House" event that was held by the Lions Club at the Cary firehouse. I'm the woman who takes photos and I have never forgotten you and your family. Your daughter is a "hero and a warrior" and so are you! The love that your family shares is inspirational!