Thursday, July 26, 2007
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My name is Nathan Russell and I am forever 6 years old. In December 2003, at the age of 5 months, I was diagnosed with a neuromuscular genetic disorder called Spinal Muscular Atrophy - Type 1 (SMA) and fought as hard as I could until April 28, 2010. My parents created this site so that my family and friends can check up on me and my little brother, Owen.
2 comments:
This picture (and the one underneath it) is so very sweet! Nate, you have a beautiful smile and it looks like you love to share it with many people.
I hope you are enjoying the summer. Take care!
I am just here looking at your BEAUTIFUL FAMILY, and wanted to take the time to tell the 4 of you now, that the love, and admiration that is in your family is unmistakeable!!! I looked at this photo of Nate and his Daddy, and I am still crying tears of happiness..
Word's can not express how much love is so apparent in your little family.. Nate chose the PERFECT peopl to become his parent's..
So keep on doing what you do, and little (or should I say) big, lol, Owen is going to have a wonderful life as well..
God Bless your family, Stephanie (Mommy to ^Malia Simone George^, angel SMA Type 1, and Taye SMA free..)
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