Calls for SMA screening ignored before Jesy Nelson campaign, say families
For those who have spent years trying to raise awareness, Wes Streeting’s intervention is ‘bittersweet’When former Little Mix star Jesy Nelson announced her twins had been diagnosed with spinal muscular atrophy type 1 (SMA1), a rare genetic condition that causes muscle wastage, the news...
<p>For those who have spent years trying to raise awareness, Wes Streeting’s intervention is ‘bittersweet’</p><p>When former Little Mix star Jesy Nelson announced <a href="https://www.theguardian.com/society/2026/jan/04/little-mix-jesy-nelson-twin-babies-may-never-walk">her twins had been diagnosed with spinal muscular atrophy type 1 (SMA1)</a>, a rare genetic condition that causes muscle wastage, the news quickly made front page news.</p><p>The call for SMA to be added to newborn screening sprang to national attention and the health secretary, Wes Streeting, was quick to respond, saying Nelson was “right to challenge and criticise how long it takes to get a diagnosis”.</p> <a href="https://www.theguardian.com/society/2026/jan/11/uk-parents-jesy-nelson-sma-screening">Continue reading...</a>
Read the full article at:
The Guardian World →