We received the call this morning from Dr. Cyrus' office letting us know that OWEN IS SMA FREE!!!!!!!!
Thank you for all your prayers and support!!!!!
Trey
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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.
Donate to Nate's Memory and FSMA
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4 comments:
I knew it. Kisses to sweet NaRo and little O. Love to both of you as well. Ashley
AMEN! That is wonderful news. I'm so happy!
Yippee! Praise God.
I am so thankful, and am praising God as well!!! Susie
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