Repeated exercise, or wasting, can change the way key genes work.

A MUM, whose eight-year-old son has Spinal Muscular Atrophy (SMA), says families have been ‘ignored for years’ as singer Jesy Nelson calls ...

SMA patients in Kerala urge government to allocate funds for free drug distribution to combat the rare genetic disorder.

Biogen has secured European regulatory approval for a high-dose regimen of its Spinraza drug for the neuromuscular disease spinal muscular atrophy, or SMA. Biogen on Monday said the European ...

Jesy Nelson shocked fans when she recently revealed that her twin baby daughters have been diagnosed with the rare genetic ...

Some secrets won't stay buried. In this irresistibly twisty drama, a suburban garden club’s perfect world starts to crumble ...

Sam agreed, and said: "Unless you've lived it, it's hard to understand it, so having a sibling who can not only understand, ...

I don't think I'll ever get over it or accept it, but all I can do is try and do my best and try and make change." Although the babies have undergone gene therapy, the 34-year-old star explained the ...

The former Little Mix singer posted an emotional video to Instagram on Sunday, vowing that the girls will "fight all the odds ...

The Little Mix singer, 34, revealed her eight-month-old daughters suffer from a severe muscular disease and will likely be ...

A mother whose son was diagnosed with spinal muscular atrophy (SMA) when he was ten days old has urged singer Jesy Nelson to ...

A County Down mother, whose five-year-old daughter has Spinal Muscular Atrophy (SMA), has said singer Jesy Nelson should know "there is light at the end of the tunnel". The former Little Mix star ...