TWINS

Heartbreaking new video of Jesy Nelson’s twins shows early symptoms experts missed

Jesy Nelson has opened up about her twin daughters’ devastating genetic condition and how they may never walk in an emotional interview on ITV’s This Morning

Jesy Nelson has revealed the extreme lengths she takes to make sure her twins can breathe at night following their devastating muscular atrophy diagnosis. The Little Mix star announced on Sunday that her twins had been diagnosed with the rare genetic condition spinal muscular atrophy and may never walk.

The 34-year-old welcomed daughters Ocean Jade and Story Monroe Nelson-Foster prematurely back in May with her musician fiancé Zion Foster, 27. Speaking in a video on Instagram at the weekend, Jesy told her fans that Ocean and Story have the most severe form of the disease, which sees muscles deteriorate over time, and that she’s now a nurse to the twins.

She added that she took them to the GP when her mum noticed they weren’t moving as much as they should. “The girls have been diagnosed with a severe disease called SMA type one. It stands for spinal muscular atrophy which affects every muscle in the body from legs, arms to swallowing,” she said.

Speaking on This Morning today, Jesy revealed that her twins exhibited early symptoms of SMA – but she didn’t know what they meant. Fighting tears, she told Ben Shephard and Cat Deeley: “That is the part that frustrates me the most. I knew and saw all of the signs before I knew what SMA was.

“It was weird because from when I was in NICU [Neonatal Intensive Care Unit], the way they used to lay on my chest, they would have frog leg position. I did say to my mum, ‘Isn’t their belly an unusual shape? They breathe from their belly.’

“That’s what frustrating – for me, if these were the cards I was always going to be dealt and there was nothing I could do about it, it would be easier for me to accept. But when you know there is something that can be done about it and it is lifechanging to your child, that’s the bit that I cannot accept.”

She added that it makes her “so sad” to watch videos which show the twins gradually losing use of their legs over the course of weeks. “That’s how quick it is and that is why it’s so important to get treatment from birth,” she said.

Jesy went on to reveal that her house was “looks like a hospital” with all of the medical equipment needed to keep the twins alive.

“Story has to be on a breathing machine at night because she isn’t strong enough to breathe by herself at night,” she said. “They have to have Cough Assist machines to help them cough, I have to put feeding tubes down their nose to get secretions off their chest.

“I’ve had to learn this within the space of a few days of getting their diagnosis. It’s so much to deal with while you’re also trying to deal with this horrendous thing that’s just happened.”

Sharing an update on the twins, she said that doctors have told her that they won’t be able to walk, regain neck strength and will be in wheelchairs. However, Jesy isn’t giving up hope.

“There have been so many stories where parents have been told this and then their children have gone on to do incredible things,” she said.

“So I believe you have to manifest this into existence. They’re still smiling, they’re still happy and they have each other.”

If you have been affected by this story, advice and support can be found at SMA UK. You can get in touch by phoning 01789 267520 or by emailing office@smauk.org.uk.

This Morning airs weekdays from 10am on ITV1 and ITVX.

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Jesy Nelson’s ex Chris Hughes shows support to ‘warrior’ singer after she revealed her twins’ heartbreaking diagnosis

JESY Nelson has been flooded with support after sharing the heartbreaking diagnosis of her twin girls – including her ex, Chris Hughes.

The former Little Mix star took to Instagram on Sunday to open up about her twins, Ocean Jade and Story Munroe, revealing they have been diagnosed with a rare muscle wasting disease that could be fatal.

Jesy has shared her twins have been diagnosed with a rare diseaseCredit: Instagram/Jesynelson
The star posted a heartbreaking video on Instagram to raise awareness to other mothersCredit: Instagram
The adorable seven-month-old babies are being looked after by Great Ormond StreetCredit: Instagram

Speaking from her home, Jesy said the pair have been diagnosed with SMA Type 1, or Werdnig-Hoffmann disease, the most severe form of Spinal Muscular Atrophy.

The tearful star told the camera: “If it’s not treated in time, your baby’s life expectancy will not make it past the age of two.”

Her stunningly honest discussion prompted a wave of support from celebrity pals, with Chris – who dated Jesy from 2018 to 2020 – one of the first to back her up and send her love.

“A warrior Jess. Be easy on yourself,” he told her. “Sending prayers to you all, everyone behind you guys 🤍”

BRAVE BOY

My son has the same disease as Jesy Nelson’s twins & was given one year to live


‘DADDY LOVES YOU’

Jesy Nelson’s partner Zion speaks out on twins’ devastating diagnosis

Amy Childs added: “I’m so sorry jesy what your going through ❤️xx sending love and strength to you and your beautiful girls xxx”

Megan McKenna wrote: “My heart is breaking for the pain you are in right now. Sending so many prayers and love to your beautiful girls ♥️♥️”

Jess Wright also commented, telling Jesy: “Sending you so much love Jesy. Love & strength ❤️❤️❤️❤️❤️❤️❤️”

Ashley James also noted: “Jesy I’m so sorry. I’m thinking of you and your girls and sending love ❤️❤️’

“Jes, There are no words big enough for how unfair and heartbreaking this is. I am so deeply sorry,” wrote I’m A Celeb star Shona McGarty. “My heart aches for you and for your beautiful little girls.

“Please know that their lives, no matter what, are already filled with love because of you. That love matters. It always will.

“You don’t have to be strong, and you don’t have to find the right words. However you feel, whatever you need, it’s okay.

“You are not alone in this, Jes. You are so loved, and your girls are so loved. I’m holding you all in my heart. 💔🤍”

While Shaughna Phillips also added: “Sending you and your girls so much love and positive prayers, you are a superwoman and they are lucky to have you ❤️❤️❤️”

Jesy’s Journey

Jesy has shared that her babies had to endure “months and months” of doctors appointments before finally getting diagnosed with SMA Type-1.

Spinal Muscular Atrophy: Signs and symptoms

Spinal muscular atrophy is a disease which takes away a persons strength and it causes problems by disrupting the motor nerve cells in the spinal cord.

This causes an individual to lose the ability to walk, eat and breathe.

There are four types of SMA – which are based on age.

  • Type 1 is diagnosed within the first six months of life and is usually fatal.
  • Type 2 is diagnosed after six months of age.
  • Type 3 is diagnosed after 18 months of age and may require the individual to use a wheelchair.
  • Type 4 is the rarest form of SMA and usually only surfaces in adulthood.

What are the symptoms?

The symptoms of SMA will depend on which type of condition you have.

But the following are the most common symptoms:

• Floppy or weak arms and legs

• Movement problems – such as difficulty sitting up, crawling or walking

• Twitching or shaking muscles

• Bone and joint problems – such as an unusually curved spine

• Swallowing problems

• Breathing difficulties

However, SMA does not affect a person’s intelligence and it does not cause learning disabilities.

How common is it?

The majority of the time a child can only be born with the condition if both of their parents have a fault gene which causes SMA.

Usually, the parent would not have the condition themselves – they would only act as a carrier.

Statistics show around 1 in every 40 to 60 people is a carrier of the gene which can cause SMA.

If two parents carry the faulty gene there is a 1 in 4 (25 per cent) chance their child will get Spinal muscular atrophy.

It affects around 1 in 11,000 babies.

The twins, which Jesy shares with Zion Foster, were born two months premature in May 2025, following a difficult pregnancy that saw her diagnosed with twin-to-twin transfusion syndrome (TTTS), a rare but serious condition in which blood flows unevenly between identical twins sharing a placenta.

In her newest video, Jesy revealed that her mother, Janice, raised concerns after the twins didn’t show much movement in their legs.

While their initial concerns were chalked up to the twins being premature and therefore unlikely to hit milestones at the same pace as other children, Jesy and Zion pushed for more tests after they had trouble feeding.

Jesy and Chris dated from 2018 to 2020Credit: Getty
Chris Hughes led the messages of support in her commentsCredit: Refer to source
Jesy looked heartbroken as she opened up about what her girls had gone throughCredit: Instagram

According to Jesy, it took three to four months of appointments before they finally got a diagnosis, with the pair then being treated at Great Ormond Street Hospital.

“I feel like I’ve almost had to become a nurse in the space of two weeks,” Jesy added, explaining how she has had to put her daughters on breathing machines.

“The reason I wanted to make this video was because, the last few months has honestly been the most heartbreaking time of my life. I feel like my whole life has done a 360.

“I’m grieving a life I thought I was going to have with my children,” she emotionally said, before acknowledging that she is grateful to have them.

“I truly believe that my girls will defy all odds. And with the right help, they will fight this, and go on to do things that have never been done.”

“They probably will never regain their neck strength, so they will be disabled,” she revealed, adding it’s also unlikely they’ll ever be able to walk.

“So the best thing we can do right now is get them treatment and just hope for the best.”

Jesy then said that she wanted to make the video because if the disease is detected early enough in the first few months of a baby’s life “a lot of this stuff could be prevented”.

Shortly after Jesy shared the highly emotional video, her partner Zion Foster spoke out about their daughters’ diagnosis.

Taking to his Instagram page, Zion shared a photo of his daughters in what looked a stroller.

With tubes attached to their noses, the two tots could still be smiling widely.

Alongside the photo, Zion wrote: “Still smiling through all the challenges. Daddy loves you so much.”

Jesy and Zion welcomes their twins in May 2025Credit: jesynelson/Instagram
The star hoped that her experience would help others see the warning signs in their babiesCredit: Instagram

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Jesy Nelson’s partner Zion Foster speaks out on twins’ devastating diagnosis after emotional video

THE partner of Little Mix star Jesy Nelson has spoken out after she shared a devastating health diagnosis over the couple’s baby twins.

Zion Foster delivered a touching message to his baby daughters after partner Jesy’s emotional video revealing the seven-month-old girls were suffering from a rare and potentially deadly type of Spinal Muscular Atrophy.

Zion shared the sweet snap and moving words after Jesy’s admission on SundayCredit: Instagram/zionfoster
Jesy and Zion are parents to twin girls Ocean Jade and Story MonroeCredit: Shutterstock

Taking to his Instagram page, Zion shared a photo of his daughters in what looked a stroller.

With tubes attached to their noses, the two tots could still be smiling widely.

Alongside the photo, Zion wrote: “Still smiling through all the challenges.

“Daddy loves you so much.”

SPOT THE SIGNS

The six ‘red flag’ signs of SMA as Jesy Nelson reveals baby twins’ diagnosis


STAR’S HEARTACHE

Little Mix’s Jesy Nelson reveals her baby twins’ devastating diagnosis

Jesy welcomed twins Ocean Jade and Story Monroe prematurely at 31 weeks on May 15, 2025.

In a video she shared on Sunday, the former Little Mix star broke down as she described how the devastating diagnosis emerged.

The twins, she said, had now been diagnosed with a condition called SMA Type 1, or Werdnig-Hoffmann disease, the most severe form of Spinal Muscular Atrophy.

The lifelong disabling condition causes dramatic muscle weakness with severe breathing and swallowing issues and is commonly fatal without radical treatment.

Tearful Jesy said: “If it’s not treated in time, your baby’s life expectancy will not make it past the age of two.”

She later added: “When they assessed the girls at Great Ormond Street, we were told that they will probably never be able to walk.

“They probably will never regain their neck strength, so they will be disabled.

“So the best thing we can do right now is get them treatment and just hope for the best.”

Jesy then revealed that the girls, now seven and a half months old, have had their treatment, which she is “so grateful for, because if they don’t have it, they will die”.

Though Jesy was upset, she felt hopeful for the future.

Jesy took to social media on Sunday to reveal the devastating ordealCredit: Instagram
The two baby girls, who are almost 8 months old, have been diagnosed with SMA Type 1Credit: Instagram/JesyNelson

“I truly believe that my girls will defy all odds. And with the right help, they will fight this, and go on to do things that have never been done,” she said.

The singer said that she wanted to make the video because if the disease is detected early enough in the first few months of a baby’s life “a lot of this stuff could be prevented”.

Jesy explained how the treatment is where the gene, that they don’t have, is put back in the body.

But Jesy affirmed how “there is no cure for SMA” but added how the treatment can help.

She then detailed some of the symptoms to look out for in babies, such as “floppiness” and not being able to hold their head up on their own.

“If any one is watching this video and they think they see these signs in their child, then please, please take your child to doctor, to the hospital, because time is of the essence.”

Jesy and Zion’s twins were welcomed into the world last MayCredit: jesynelson/Instagram

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George Clooney, wife Amal and twins get French citizenship

George Clooney, wife Amal Clooney and their 8-year-old twins are officially citizens of France, as of the day after Christmas.

The news was reported by multiple French outlets as well as the Guardian, all citing an announcement published in a French government journal.

The Clooneys bought property in France — a farm, he recently told Esquire — in August 2021, when their twins were 4. He said it was a “much better life” there for Ella and Alexander.

“Yeah, we’re very lucky. … A good portion of my life growing up was on a farm, and as a kid I hated the whole idea of it. But now, for them, it’s like — they’re not on their iPads, you know?” he said in the interview, published in the magazine’s October/November issue.

“I was worried about raising our kids in L. A., in the culture of Hollywood. I felt like they were never going to get a fair shake at life. France — they kind of don’t give a s— about fame. I don’t want them to be walking around worried about paparazzi. I don’t want them being compared to somebody else’s famous kids.”

George Clooney married Amal Alamuddin in September 2014 in Venice, Italy.

Domaine Le Canadel in France is, according to Hello, “an enchanting and sprawling 425-acre Provence wine estate” that cost the Clooneys a reported $8.3 million. It has a pool, tennis court, gardens, a lake, an olive grove and a 25-acre vineyard, the outlet said. But, you know, it’s just a farm.

Other celebrity couples have put down roots in the area, of course, with less than charmed results over time. Then again, those folks weren’t French citizens, for the most part.

Clooney’s remarks about the French attitude toward fame echoed previous comments made by Johnny Depp, who years ago found refuge in France for himself and his children, Jack and Lily-Rose, until he split in 2012 from longtime partner Vanessa Paradis, a French singer, model and actor.

The country “afforded [Depp] the possibility of living a normal life. Really a simple life,” the “Pirates of the Caribbean” actor told SFGate in 2001.

In 2010, Depp told People, “With Vanessa and the kids, we live in a sort of little village in the south and I have the impression of being in paradise … and you know what I do there? Absolutely nothing.”

Depp, who started dating his “The Rum Diary” co-star Amber Heard the year he broke up with Paradis, listed his Provence property for sale for almost $26 million in June 2015, then reportedly put it on the market again in the years that followed for more than twice the price. However, despite containing an entire village in its 37 acres, the property appears not to have sold.

Heard and Depp married in 2015 but divorced two years later amid allegations of abuse. Of course, dueling defamation lawsuits followed. It got ugly.

Meanwhile, Clooney’s buddy Brad Pitt and Pitt’s ex, Angelina Jolie, have been battling in court for years over the 2021 sale of her half of their Provence wine estate, Chateau Miraval, which actually produces wine. The former couple signed a long-term lease on the property in 2008 and later bought a controlling interest in the company that owned it.

Pitt and Jolie married at Chateau Miraval in 2014 after meeting in 2004 on the set of “Mr. and Mrs. Smith” when he was still married to Jennifer Aniston. (They went official as a couple the following July after Aniston filed for divorce in March 2005.) Jolie and Pitt had kids and adopted kids together over the decade leading up to the wedding, but Jolie filed for divorce after only two years as husband and wife following a fight on a private plane. That also got ugly.

The story of the Pitt-Jolie court battle over the chateau and its winery is long and complicated, but it began with Pitt alleging that he and his ex had an agreement that if either wanted to sell their half of the place, the other would have to consent. Jolie, who sold her shares to Stoli’s wine division, Tenute del Mondo, said they had no such agreement in place.

Although the winery lawsuit remains active, Pitt and Jolie finally reached a divorce settlement in December 2024.

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EastEnders fans rejoice as Witches of Walford reunite on Christmas Day in ‘huge showdown’

EastEnders fans rejoiced as the Witches of Walford reunited in explosive scenes that played out in the BBC soap’s famous pub on Christmas Day as various truths were outed

EastEnders fans rejoiced as the Witches of Walford reunited in explosive scenes that aired on Christmas Day. The BBC soap aired its festive special on Thursday evening, and it was revealed exactly who had been tormenting Zoe Slater with threatening letters over the past few months.

Zoe made a much-anticipated comeback to the serial earlier this year, and it emerged later that she had twins almost 20 years ago. At the time, it was believed that the little girl had died and she had given her son away for adoption. Having been searching for her son for months, Zoe finally believed her son was about to turn up on Christmas Day, but it was all a wicked plot set up by a mysterious figure.

Earlier in the day, Zoe got into an altercation with Antony Trueman, the biological father of her children, at the top of the stairs in the Queen Vic which ended with her knocked out cold. In a surprise twist though, it was revealed that Zoe had woken up relatively unharmed and Anthony was dead.

READ MORE: EastEnders’ Jasmine’s link to Cindy ‘explained’ as Chrissie’s secret family ‘revealed’READ MORE: EastEnders’ Tracy-Ann Oberman breaks silence on ‘obsession’ amid Zoe stalker hell

After Kat discovered them, she cleared out the pub and they were greeted by Chrissie Watts, who was last seen in 2024 driving away from the square following a long spell in prison for the murder of her husband Den. Chrissie, who had broken into the pub and fired up a karaoke microphone, said: “Ladies. Both of you. What a treat! Zoe pleaded: “Where’s my son?” as Chrissie confirmed: “He’s not coming I’m afraid…”

She added: “Torturing? With a few harmless games? I thought it was time we’d have a little reunion. It’s been so long. You’re not a drippy little girl anymore. Life has really toughened you up.” Zoe demanded to know why Chrissie was back on the scene, but she wouldn’t say anything without having a drink first.

It was then that Jasmine Fisher stepped into the pub and Chrissie confirmed that they knew each other. Zoe worked out that Jasmine was her daughter, even though she thought she had died several years ago. Jasmine said: “Only because you couldn’t be bothered to stick around the hospital long enough to hear me cry.” Through tears, Zoe pleased: “They took you away! You weren’t breathing,” but Jasmin continued: “Maybe I should be flattered because at least you didn’t just abandon me like you did my brother.”

“We’ve known each other a while, haven’t we, Jas? I was back in London seeing my parole officers. They can’t get enough of me, I’m a popular girl. Anyway, I bring up my phone, and there’s a picture of my old pal Zoe. You’d been through the wars. I thought it was a sign and decided to bring flowers. But when I got there, they wouldn’t let anyone near you and that’s when I bumped into this lovely one.”

“We both hate you. We wanted to teach you a lesson.” Jasmine raged that Zoe had never tried to find her once she knew she was alive but Kat reasoned: “We only found out today!” Chrissie twisted the knife further and brought up the fact that Zoe had slept with her husband Den several years ago.

Coldly, she added: “I pay for my crimes. And now you’re gonna pay for yours. But your punishment is gonna be in here. You’ve got a lovely little girl and you’re never gonna get to know her.”

Kat told Jasmine: “Look at her, she has really suffered, she has spent her whole life regretting this and yes, she makes bad decisions but she’s not a bad person. This here, Chrissie, she’s the evil one.” There was then another twist for fans as Sam Mitchell made her grand return to the soap by stepping out from behind the bar.

She said: “It’s not often that I side with Kat Slater. But she’s right. Chrissie Watts is evil.” Fans of the long-running BBC soap, which celebrated its 40th anniversary earlier this year, will know that Chrissie, Sam and Zoe formed the trio known as The Witches of Walford during their 2000s heyday.

At the time, an iconic storyline saw Chrissie instigating a revenge plot against her husband Den, and persuading Sam and Zoe to go along with her before she tried to frame them for Den’s murder.

Chrissie said: “The three of us. Back again. Who’s gonna turn up next? The ghost of Den?” Sam then asked Chrissie if she was related to Jasmine, and even though Zoe protested that she was the mother, Chrissie cut in to say: “She could’ve been mine! She’s the same age as the baby I lost in prison.”

Kat then demanded the three of them leave but Zoe, now in tears, tried to make her long-lost daughter see that Chrissie had simply goaded her into another revenge plot. Sam then brought up Chrissie’s manipulative ways to try to make Jasmin see sense.

Outside, Jasmine tried to get rid of Chrissie and insisted that she would be “better off” alone. Chrissie then warned Jasmine against mentioning her name to any law authorities, and walked back out of Albert Square. Jasmin and Zoe had a heart-to-heart, and when the police did arrive, Zoe stopped Kat from trying to cover for her and handed herself in as her mother wept.

Fans were quick to react to the reunion, with one fan writing on X: “Hahaha chrissie appearing like that in the Vic,” and a second added: “Kat, meet one of your first grandchildren!”

Another said: “This is vintage” and a fourth added: “Sam, Zoe and Chrissie in the same room in 20 years [crying emoji],” whilst another dramatically exclaimed: “THIS IS A HUGE SHOWDOWN!”

EastEnders airs Mondays to Thursdays at 7:30pm on BBC One and BBC iPlayer. * Follow Mirror Celebs and TV on TikTok , Snapchat Instagram , Twitter , Facebook , YouTube and Threads .



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