SMA: Scarlet’s Life

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In this WXYZ-TV Detroit video shared in March 2015, meet Scarlet and her loving family. Scarlet is a typical 2 1/2-year-old girl in many ways —  bright, funny, and very talkative — but she has spinal muscular atrophy.

Meet the Kingsley family and 6-year-old Brett who was diagnosed with spinal muscular atrophy (SMA) type 1 when he was just a baby

Diagnosed with Type 2 SMA at 10 months old when she failed to meet usual development milestones, Scarlet, unable to use her legs and has limited movement in her arms, is a treasure. The video reveals how the family deals with the disease.

Read about Reagan’s stem cell treatment and the hope it’s giving her family.

SMA News Today is strictly a news and information website about the disease. It does not provide medical advice, diagnosis or treatment. This content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or another qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on this website.

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