Jesy Nelson, the former Little Mix singer, is taking a significant step in advocating for newborns by launching a petition in Parliament aimed at ensuring that every newborn in the UK is screened for spinal muscular atrophy (SMA). This initiative comes in conjunction with the Mirror and the charity SMA UK, highlighting the critical need for early detection of the disease, which can lead to devastating consequences if not identified early. Nelson's twin children are affected by SMA, which has profoundly influenced her commitment to this cause.

In her campaign, Nelson emphasizes the heartbreaking reality faced by families dealing with SMA and the potential for change that a simple £5 blood test at birth could bring. She believes that by having SMA screening included in the NHS heel prick test, many families would be spared the challenges her own family has faced, including the knowledge that her children will never walk. By leveraging her platform, Nelson aims to raise awareness and garner public support for the initiative, indicating that personal experiences can drive powerful advocacy.

This petition and the broader campaign reflect a growing movement in the UK to improve health outcomes for newborns through preventive measures. As more public figures like Nelson join the fight, there is significant potential for increased attention on genetic disorders like SMA, ultimately leading to policy changes that could make a difference in countless lives. Nelson's involvement not only sheds light on the issue but also inspires others to advocate for health reforms that benefit vulnerable populations, particularly children.