Jesy Nelson moved to tears as SMA1 petition hits 100,000 signatures

Jesy Nelson's petition for newborn SMA1 screening reached 100,000 signatures, triggering eligibility for a House of Commons debate; her twin daughters, born prematurely in May 2025, were later diagnosed with SMA1.

Jesy Nelson broke down in tears after a petition she began calling for SMA1 screening at birth reached 100,000 signatures. That milestone makes the petition eligible to be debated by MPs in the House of Commons. Nelson welcomed twin daughters, Ocean Jade and Story Monroe, prematurely in May 2025 and the children were later diagnosed with spinal muscular atrophy type 1. She has said she has paused her music career to focus on caring for the twins and on campaigning for the screening change. Key facts: - The petition reached 100,000 signatures, which triggers consideration for debate in the House of Commons. - The article reports the signature total has since risen to more than 120,000. - Nelson’s twin daughters were born prematurely in May 2025 and were later diagnosed with SMA1. - Nelson has called for the newborn heel‑prick blood test to be expanded to screen for SMA1 and noted the test costs around £1. Summary: The petition’s referral for debate brings newborn SMA1 screening into parliamentary discussion and raises the public profile of the issue. Jesy Nelson has shifted her public focus to campaigning and to caring for her daughters. The next procedural step reported is a possible debate by MPs in the House of Commons.