{
"$type": "site.standard.document",
"bskyPostRef": {
"cid": "bafyreihtunyochzaalweszshw5vt4ff2arzylvik6meegmn6szewkxvhwq",
"uri": "at://did:plc:oznbnvgr7dmvddiyvr7dih52/app.bsky.feed.post/3mejdohkxxqy2"
},
"coverImage": {
"$type": "blob",
"ref": {
"$link": "bafkreidxfuokpnrt5n7hdmdzzexw4yt3kcjha6efc4q6yzicxptms2tsbq"
},
"mimeType": "image/jpeg",
"size": 44105
},
"path": "/celebrity/jesy-nelson-twin-daughters-hospital-pictures-instagram",
"publishedAt": "2026-02-10T15:12:01.000Z",
"site": "https://www.gbnews.com",
"tags": [
"diagnosed last month with spinal muscular atrophy type 1",
"her daughters may never walk",
"Marc Anthony finally speaks out on Beckham family feud as he makes bold Brooklyn Beckham claim",
"Alex Armstrong dumbfounded as he makes surprise Dianne Abbott admission amid Labour chaos: 'Spot on'",
"Emily Carver ridicules university debating society over Reform UK campus ban with savage swipe",
"Ms Nelson and Mr Foster have since separated",
"campaigning for the NHS to include SMA screening in the standard heel prick test given to newborns.",
"The GB News Editorial Charter"
],
"textContent": "\n\n\nJesy Nelson has shared a heartbreaking update on Tuesday, revealing her nine-month-old twin daughters are back in the hospital.\n\nThe former Little Mix star posted an emotional photograph on Instagram showing Ocean and Story lying together in a hospital bed, their hands intertwined whilst watching television.\n\n###\n\n\n\n\nBoth babies can be seen with feeding tubes in their noses, covered by a blanket.\n\nThe 34-year-old singer captioned the touching image: \"Watching TV together holding hands. My heart.\"\n\n###\n\n\n\n\nTRENDING\n\nStories\n\nVideos\n\nYour Say\n\n###\n\n\n\n\nMs Nelson welcomed the twins with her ex-fiancé Zion Foster in May last year, with the girls arriving nine weeks premature at 31 weeks.\n\nThey spent their first weeks in hospital following their early arrival, but Ms Nelson has not disclosed the reason for their current hospital stay.\n\nThe twins were diagnosed last month with spinal muscular atrophy type 1, a devastating genetic neuromuscular condition that progressively weakens and wastes muscles due to the loss of motor neurons.\n\nSMA1 represents the most severe form of this rare disease, with sufferers typically unable to sit independently.\n\n###\n\n\n\n\n###\n\n\n\n\n###\n\n\n\n\nThe condition often proves fatal before the age of five.\n\nMs Nelson has been told her daughters may never walk and might not regain strength in their necks.\n\nThe feeding tubes visible in recent photographs are necessary because the condition creates severe difficulties with swallowing, sucking, and breathing.\n\nThe girls also faced complications before birth, suffering from twin-to-twin transfusion syndrome whilst sharing a single placenta in the womb.\n\n### LATEST DEVELOPMENTS\n\n\n\n\n * Marc Anthony finally speaks out on Beckham family feud as he makes bold Brooklyn Beckham claim\n * Alex Armstrong dumbfounded as he makes surprise Dianne Abbott admission amid Labour chaos: 'Spot on'\n * Emily Carver ridicules university debating society over Reform UK campus ban with savage swipe\n\n\n\n###\n\n\n\n\n###\n\n\n\n\nMs Nelson and Mr Foster have since separated following their daughter's diagnosis.\n\nSpeaking to the Daily Mail, Ms Nelson described the emotional toll of providing daily medical care for her babies.\n\n\"Every day is so full-on, I can speak about it, but I'll never be able to explain how intense it is until you see it,\" she said.\n\nShe further explained: \"They're so tiny and I have to do things which I know are doing them good but at the time when they're crying and screaming, it feels like I'm hurting them and I hate that I have to be the person to do that. I just want to be their mum.\"\n\n###\n\n\n\n\n###\n\n\n\n\nDespite the heartbreak, Ms Nelson remains hopeful her daughters will exceed expectations.\n\n\"My girls are the strongest, most resilient babies, and I really believe that they are going to defy all the odds,\" she told Jamie Laing on his Great Company podcast.\n\nThe twins have received a one-off gene therapy infusion to prevent further muscle damage, though it cannot reverse existing deterioration.\n\nMs Nelson is now campaigning for the NHS to include SMA screening in the standard heel prick test given to newborns.\n\n###\n\n\n\n\n###\n\n\n\n\nMs Nelson says the £1 test could have enabled earlier treatment that \"could have saved their legs\".\n\nThe singer met with Wes Streeting, the Secretary of State for Health and Social Care and MP for Ilford North, in January to discuss her daughter’s condition.\n\nMr Streeting admitted he \"didn’t know\" the full impact of SMA testing until hearing directly from Ms Nelson.\n\nHe added that it was \"hard to look SMA parents like Jesy Nelson in the eye\" knowing that a simple heel prick test could prevent such devastating outcomes.\n\n###\n\n\n\n\n\n\n\n\n\n\n**Our Standards:The GB News Editorial Charter **",
"title": "Jesy Nelson shares heartwarming new pictures of twins in hospital as they continue rare health battle: 'My heart!'"
}