Entertainment & Celebrity News Today | 2 Min News | The Daily News Now! - Jesy Nelson's Mother's Day Tribute to SMA Babies
Episode Date: March 15, 2026Jesy Nelson, the former Little Mix singer, marked her first Mothers Day by honoring superhuman moms and advocating for her premature twins, Ocean and Story, who were diagnosed with Spinal Muscula...r Atrophy Type one. She shared photos from a campaign shoot and opened up about her emotional journey, including breaking down over their new feeding chairs. Jesy is campaigning for the NHS to add SMA screening to the standard newborn heel prick test, with her petition surpassing one hundred thousand signatures. She has stepped back from her music career to focus on her daughters and this advocacy, remaining hopeful theyll beat the odds with treatment. Support the show:Get a discount at https://solipillow.com/discount/dnn. Advertise on DNN:advertise@thednn.ai This is an automated, high-level news summary based on public reporting.Report issues to feedback@thednn.ai. View sources & latest updates:https://sources.thednn.ai/9a540b29b8102cac
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From the Daily News Now Network, this is entertainment and celebrity news today.
Jezie Nelson marked her first mother's day by honoring superhuman moms while facing a tough health
battle with her newborn twins. The former little mix singer, now 34, welcomed daughters' ocean
and story prematurely in May 2025 with her ex-fiancee Zion, Foster.
Last month, both girls received the diagnosis of spinal muscular atrophy type 1, the most severe
form that weakens muscles and affects breathing and swallowing, with a life expectancy under two years
without treatment. She shared photos from a campaign shoot featuring families with children
facing health challenges and disabilities. Jesse also acknowledged those finding the day hard
and paid tribute to people missing their own mothers. Earlier, she opened up about breaking down in
tears over the girls' new special feeding chairs, which help with their swallowing issues
and provide. Postural support amid progressive muscle weakness.
The reality of daily medical care has been an emotional roller coaster for GZ.
She describes struggling with procedures that make her tiny babies cry,
feeling like she's hurting them despite knowing it's necessary.
Many other SMA moms have shared similar feelings,
turning her journey into a shared support network.
Meanwhile, Jayzie is pushing hard for change by campaigning for the NHS to add SMA screening
to the standard newborn heel prick test, which costs just one pound.
her petition has to pass 100,000 signatures forcing Parliament to debate it.
She believes early detection could have saved her girl's leg muscles.
Right now, Gizi has stepped back for her music career to focus entirely on her daughters and this advocacy.
She remains hopeful they'll beat the odds with treatment, calling them the strongest babies she's ever known.
Her main priority is securing their future, one day at a time.
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