Tuesday, May 29, 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.
1 comment:
Oh my goodness! He is so handsome and growing so tall!
I would love to include Nathan in the 2008 SMA Calendar, benefiting Marshall's Miles (www.marshallsmiles.com) and SMA Support (www.smasupport.com). The only months not available, currently, are May, July, and September. Let me know if you would like to be included. Hope you are doing well!
MJ
tweetyroll88@aol.com
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