Jesy Nelson calls plan to test newborns for deadly muscle condition a 'victory'

Jesy Nelson calls plan to test newborns for deadly muscle condition a 'victory'Image source, PAImage caption, Former Little Mix singer Jesy Nelson was told her twin daughters may "never walk" PublishedJust nowAll newborn babies in England will be tested for the genetic disease spinal muscular atrophy (SMA), as part of a major study.Former Little Mix singer Jesy Nelson has been campaigning for screening since her twin girls were diagnosed with the condition. Nelson described the announcement as a "victory for every family" affected by SMA.Early treatment for SMA can transform babies' lives.SMA causes muscle weakness. This affects movement such as the ability to walk, but it also affects the muscles needed to breathe and to swallow.In the most severe cases it is fatal before the age of two.However, there are pioneering gene therapies that can correct the genetic defect that causes SMA.They need to be given before symptoms emerge as they cannot undo any damage that has already been done – hence the call for testing newborns.Jesy Nelson told her twin babies may 'never walk'Published4 JanuaryEarlier this year, Nelson revealed she had been told her daughters Ocean Jade and Story Monroe Nelson-Foster would "probably never walk".The singer recently posted on social media about how her twins needed to wear spinal jackets and foot splints in the middle of a heatwave.And in a trailer for her forthcoming documentary Jesy Nelson: Life Changing on Prime Video, she said: "I feel like I'm going to feel heartbroken for the rest of my life."This Instagram post cannot be displayed in your browser. Please enable Javascript or try a different browser.View original content on InstagramThe BBC is not responsible for the content of external sites.Skip instagram postAllow Instagram content?This article contains content provided by Instagram. We ask for your permission before anything is loaded, as they may be using cookie...