Wednesday, August 06, 2008
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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.
1 comment:
What a nifty piece of equipment that is!
Thanks for sharing that sweet video. You are such a great family! Nathan is a lucky guy to have you all there right by his side.
Take good care and enjoy the rest of the summer.
~The Potter family
Laurie, Mark, Murphy, & Anders
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