This is a blog about Christopher's new diagnosis. We want to update our family, friends and other families we have connected with that have injured children or a child with a rare disease. I am hoping this blog will help all understand what it is like to be blessed with such a child.
Thursday, November 18, 2010
Ellen, over at Love That Max is hosting a favorite Photo
Carnival! I have so many favorite photos, but in this photo
I just love the expression on Cj's face the first time