Spinal Muscular Atrophy Genetics

Jesy Nelson, Spinal Muscular Atrophy

Jesy Nelson Reveals Twins' Rare Diagnosis—What Parents Need To Know About Spinal Muscular Atrophy

British singer Jesy Nelson recently took to Instagram to share a devastating update about her 8-month-old twin daughters.

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Wes Streeting supports Jesy Nelson’s call for improved spinal muscular atrophy screenings

E! Online · 13h

Jesy Nelson Shares What Led to Her Twins’ Spinal Muscular Atrophy Diagnosis

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Jesy Nelson ‘right to challenge’ twins’ diagnosis process, says Streeting

The Health Secretary has said Jesy Nelson was “right” to challenge the screening process for spinal muscular atrophy (SMA) after her twins were diagnosed with the rare genetic condition.

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Jesy Nelson will 'shout from the rooftops' about baby muscle disease campaign

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Jesy Nelson shares update from hospital as she reveals she is fighting for SMA1 screening at birth after her twins' diagnosis because early treatment helps to prevent severe muscular disease

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Jesy Nelson Says She Noticed “Signs” Before Her Twins’ SMA Diagnosis

“I actually saw all of the signs before I knew what SMA was,” Jesy, 34, said during her Jan. 6 appearance on UK's This Morning.

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Jesy Nelson shares first warning signs she noticed that her babies may never walk

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Watch: Jesy Nelson breaks down over 'frustrating' reality of twin babies' life-changing SMA diagnosis

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

7don 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.

Medical Xpress

What you should know about spinal muscular atrophy

Spinal muscular atrophy (SMA) is a genetic neuromuscular disease affecting specialized nerve cells that control voluntary muscle movement, according to the Muscular Dystrophy Association (MDA). It can lead to severe physical disability, paralysis and life ...

Healio

Gene therapy slows progression of spinal muscular atrophy type 2

We were unable to process your request. Please try again later. If you continue to have this issue please contact [email protected]. Topline results from a phase 3 clinical trial showed an investigational gene therapy for young people with ...