Spinal Muscle Atrophy

Spinal muscular atrophy explained

What is spinal muscular atrophy? As Jesy Nelson shares twins’ diagnosis

Former Little Mix star Jesy Nelson revealed on social media that her twin girls have been diagnosed with a rare genetic condition called Spinal Muscular Atrophy (SMA) and may never be able to walk.

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Spinal Muscular Atrophy: Symptoms to life expectancy after Jesy Nelson's heartbreaking news

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Little Mix alum Jesy Nelson’s 8-month-old twins diagnosed with severe muscle disease, may never walk

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Little Mix's Jesy Nelson says twins may never walk amid rare diagnosis

Jesy Nelson, a one-time member of the British girl group Little Mix, is opening up about the rare genetic condition her children are facing.

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Our children waited too long for the same diagnosis as Jesy Nelson's twins

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What Is SMA Type 1? Jesy Nelson’s Twins’ Diagnosis Explained

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Former Little Mix singer Jesy Nelson says her twin babies may never walk

“We were told that they’re probably never going to be able to walk, they probably will never regain their neck strength, so they will be disabled, and so the best thing we can do right now is to get t...

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Jesy Nelson told her twin babies may 'never walk'

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Jesy Nelson Says Rare Disorder May Prevent Her Twin Daughters From Walking

The Independent on MSN

What is spinal muscular atrophy?

Spinal muscular atrophy explained after Jesy Nelson reveals her twins’ diagnosis - The singer shared an emotional update about her twins’ health on Sunday and that ‘time is of the essence with this di

5don MSN

Boy, 5, Born with Rare Genetic Disorder Walks by Himself After Receiving World’s Most Expensive Drug

A 5-year-old boy who was born with a rare genetic condition is now able to walk by himself, his mother has said, after receiving the world's most expensive drug, which costs around $2.4 million.