5K for Spinal Muscular Atrophy Support

In this WYMT Television video, learn more about Kirsten’s family, who saw their lives change when she was diagnosed with spinal muscular atrophy (SMA). The family is determined to keep fighting, and to do so, they host an annual 5K in support of researching, and hopefully one day curing, the disease.

Read five frequently asked questions about spinal muscular atrophy.

Spinal muscular atrophy (SMA) is the most common cause of mortality in infants linked to a genetic mutation and affects between 1 in 6,000 and 1 in 10,000 people.

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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