Spinal muscular atrophy (SMA) is a genetic disease that affects mostly children. Sadly, SMA leads to shortened life span. The severe neuromuscular disease causes the inability to participate in daily life functions like walking, eating, or even breathing.
In this riveting, yet heartwarming video shared by USA Today, one of 14-year-old Jerika’s last wishes before she goes “on hospice” is to attend a prom. Her family and friends all work to make that happen. Jerika was diagnosed with type 2 spinal muscular atrophy at just eight months old and was crowned prom queen in Appleton, Wisconsin last month.
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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