Jump to content

Former Little Mix star Jesy Nelson has said she is “proud” of having reached a “major milestone” as a rollout of screenings for spinal muscular atrophy (SMA) is to begin earlier than expected.

The singer, 34, campaigned for all newborn babies to be screened for SMA after her twins, Ocean Jade and Story Monroe Nelson, were diagnosed with the rare condition, which causes progressive muscle wastage.

In a letter addressed to Nelson and Giles Lomax, the chief executive of the charity SMA UK, health secretary Wes Streeting confirmed that screenings will be rolled out earlier than planned and begin as part of in-screening evaluations (ISE) from October 2026 instead of January 2027.

Read full article.

Source: The Independent, 2 April 2026

0 Comments


Recommended Comments

There are no comments to display.


Create an account or sign in to comment

You need to be a member in order to leave a comment

Create an account

Sign up for a new account in our community. It's easy!

Register a new account

Sign in

Already have an account? Sign in here.

Sign In Now
×
  • Create New...

Important Information

We have placed cookies on your device to help make this website better. You can adjust your cookie settings, otherwise we'll assume you're okay to continue.