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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.
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2 comments:
Mine too!
Nana Barb
Hi Trey and Jen,
Thank you for your blog. It has touched me for many reasons, mostly because you talk about important people and issues I care about. As a reward, I left you a present on my blog – I’ve nominated you for the Lemonade Stand Award. To accept, you must comply with the following conditions:
- Put the Lemonade logo on your blog or within your post. You can lift it off my blog, http://www.empowerpeoplechangelives.com.
- Nominate at least 10 blogs with great attitude or gratitude.
- Link the nominees within your post.
- Let the nominees know they have received this award by commenting on their blog.
- Share the love and link to the person from whom you received this award.
Please accept the award. I can’t wait to see and follow the people you give it to.
Thanks for your dedication to blogging!
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