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When Wade was 4 months old, we were concerned that he was developmentally delayed. After many doctor visits and over a month later, he was diagnosed with Spinal Muscular Atrophy (SMA) type 1. SMA is a genetic disorder that affects the muscles, causing extreme weakness. A child with type 1 will never sit, crawl, walk or be very verbal. 95% of babies do not live to see their second birthday.This blog is to raise awareness for SMA and to update how Wade is doing.
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