Spinal Muscular Atrophy Treatment at Nationwide Children's -- Brett & Paige

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As the holidays approach, the Kingsley family has much to be thankful for and is counting its blessings. Their little miracle, 6-year-old Brett, has beaten the odds and continues to do so every day. Diagnosed as a baby with Spinal Muscular Atrophy (SMA) Type 1, Brett's family heard the word no family should ever hear. Terminal. SMA is the leading genetic killer for children under the age of two. Today, as a feisty 1st grader, Brett is one sweet, determined little boy who makes the most out of each day. As we've gotten to know Brett over the years, we've also come to love his whole family. They are strong, inspirational and tireless advocates for Brett and SMA research. And big sister Paige is loving and fiercely protective of her little brother, but never treats him differently than any other kid. 

Here at Nationwide Children's, our researchers are hard at work looking for a cure for Spinal Muscular Atrophy. For Brett and every child with SMA. With your help, every dollar gets us one step closer to the day the Kingsley's know will come. The day we find a cure, and the day Brett finally "tackles" his sister.