Wednesday, July 28, 2010
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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.
3 comments:
The room looks fantastic!!! What a great way to keep happiness there! And a fun place for Owen to remember his very special big brother! You did an awesome job!
Take your time with your decisions... in your time. As you said, God will show you. There is no set schedule or pattern on how things are to be done or when so do take the time to breathe and listen to the voice of God.
Have a blast in Vegas!!! May God rejuvenate your spirit!
Much Love!
Kim York
So glad you are finding peace. Making Nate's playroom makes perfect sense and you are right nate is looking down enjoying owen playing. have a wonderful time in vegas. Who knows maybe nathan will show up on his birthday in some wonderful way....a rainbow or bird or something :) Safe travels.
The room looks awesome!!! What a great thing to do...I am sure Nate is smiling down on it and helping to guide Owen!!
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