Muscular Dystrophy Association Marks Rare Disease Day by Spotlighting Community Stories Driving Progress in Research, Care, ...

In an age where screens dominate our lives, the importance of regular physical movement has never been more critical.

The mother of a four-year-old boy with a rare muscle disease says screening newborn babies for the condition could "save ...

Nelson's twin daughters, Ocean Jade and Story Monroe, have been diagnosed with spinal muscular atrophy (SMA) Type 1 ...

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 ...

More than two years after the Government committed to adding SMA to newborn testing, families are still waiting ...

On January 4, former Little Mix singer Jesy Nelson took to Instagram to reveal that her twins have been diagnosed with spinal muscular atrophy (SMA) type 1, which is a genetic neuromuscular condition ...

The 34-year-old singer recently shared the devastating news that her children have Spinal Muscular Atrophy Type 1, which ...

LITTLE Mix star Jesy Nelson has revealed that her baby twins have been diagnosed with a severe form of Spinal Muscular Atrophy. In a heart-breaking Instagram post ...