Just four days before news of their breakup, Jesy Nelson’s ex-boyfriend, Zion Foster, praised her as ‘the definition of a superwoman‘ in a heartfelt social media post.
People close to the couple have shared that they ended their engagement shortly after learning their eight-month-old twin daughters have a serious muscle disease.
The musician referenced a shared connection, writing ‘we are all one’ in a post dedicated to his former partner, shortly after she revealed their twins’ medical diagnosis.
He shared a poem he created for Ocean & Story, expressing the idea that we are all connected. He also praised Jesy for bravely highlighting a major problem within the healthcare system, calling her a role model.
The current situation is unacceptable and must be improved. With groundbreaking treatments now available, the UK should begin newborn screening for Spinal Muscular Atrophy (SMA).
We’re grateful to the SMA community and everyone facing difficult challenges for welcoming, supporting, and standing with us.
Zion wrote and shared a poem about learning to accept the daily challenges of raising his eight-month-old daughters, who have a medical condition.
He explained that doctors had warned them it was unlikely their child would ever walk or talk, and might not even be able to hold their head up. He and Jesy had been told this diagnosis was Spinal Muscular Atrophy Type 1.
‘And it became so clear, doctors only go near what they can measure, so what’s certain?
I cherish your smiles, like fleeting but beautiful sunsets. Hearing you talk – even just your everyday chatter – feels like listening to the most wonderful music. It makes me think: when I constantly try to shape you into who I want you to be, am I truly loving you, or am I just acting on my own anxieties?
If I love and accept you completely, exactly as you are, without wanting you to change anything about yourself, am I truly showing you love and acceptance?
He asked Story if she was alright, and Ocean how she was feeling. He said he could hear their resilience even in their tears, calling them two little fighters who already knew how to be strong.
I’m not really concerned with hitting certain life goals or rushing things. My real concern is much more personal – it’s about truly accepting and loving you exactly as you are, without any expectations or conditions.
‘No matter what tomorrow brings, and no matter what yesterday was.’
News broke on Sunday that Jesy and Zion have separated, but they’re still friends and prioritizing their children.
They told The Sun that their daughters’ well-being is their main concern, and they are working together as parents.
Daily Mail contacted Jesy Nelson and Zion Foster’s representatives for comment.
As a lifestyle commentator, I noticed something during Jesy Nelson’s recent appearance on This Morning. She wasn’t wearing her engagement ring, which definitely got people talking. She was bravely sharing her family’s story – how her daughters, Ocean and Story, are living with Type 1 Spinal Muscular Atrophy – and it was a really moving conversation. It’s always tough when personal details like that become public, but she handled it with such grace.
Type 1 Spinal Muscular Atrophy (SMA) is the most serious form of the condition. Symptoms usually start in babies and include severe muscle weakness, trouble swallowing, and breathing problems.
Jesy is now working to include screening for Spinal Muscular Atrophy type 1 (SMA1) in newborn screenings. She’s started a petition to add the condition to the heel prick test, which is a routine blood test given to newborns.
Jesy recently discussed the problem on the show This Morning, explaining she feels a responsibility, given her public platform, to help people understand it.
A part of me worries it’s selfish to not share this information, especially if it could help save a child’s life.
The NHS offers a newborn screening test to all babies around five days old. A blood sample is taken to check for nine uncommon but potentially serious health problems.
Jesy shared that she’s been incredibly touched by the reaction to her recent announcement. She explained she hoped to reach as many people as possible to raise awareness, and she’s amazed by how supportive everyone has been.
‘I could have prevented this from happening if I’d have seen a video and caught it early enough.’
As someone who’s dedicated to helping families thrive, I truly believe that when we discover a solution that can dramatically improve a child’s life, we have to act. It’s something I feel incredibly passionate about, and I’m committed to raising awareness and advocating for these kinds of impactful changes. Knowing there’s something we can do – and it makes all the difference for a child – is why I’m so driven to share this with everyone.
Jesy explained that her life has changed dramatically since her diagnosis, and her home now feels more like a hospital than a family space. She expressed a simple desire: to be a mother to her children, not a full-time caregiver.
‘They’ve had treatment now, thank God, that is a one-off infusion.
This treatment works by reintroducing a missing gene into the patient’s body, which helps prevent further muscle loss. However, it can’t restore function to muscles that have already deteriorated.
‘I just want to reiterate that if this is caught from birth, it’s just life-changing.’
Currently, the UK doesn’t routinely screen newborns for Spinal Muscular Atrophy (SMA), but Scotland plans to begin screening babies this spring.
Currently, the UK National Screening Committee doesn’t advise screening for this condition. However, they are reviewing this decision because of recent improvements in treatment options.
Jesy became well-known after winning the TV show The X Factor in 2011 as a member of the group Little Mix, with Leigh-Anne Pinnock, Perrie Edwards, and Jade Thirlwall.
After almost ten years with the band, she departed in December 2020 and has since launched a solo career, releasing the songs “Boyz” (featuring Nicki Minaj) in 2021 and “Bad Thing” in 2023.
In September, Zion proposed to Jesy on a romantic beach trip at sunset. Jesy shared a photo of the beautiful diamond ring on social media.
Alongside the post, she wrote: ‘Just got engaged to my best friend.’
Jesy and Zion started dating in January 2022 and have had an on-again, off-again relationship ever since. They got engaged in September.
Earlier this month on This Morning, Jesy became emotional while sharing a sad update about how she’s doing.
After learning to care for her twins and manage their complicated medical needs, she said her house now feels more like a hospital. She also opened up about the hardest parts of receiving their diagnosis.
Jesy became very upset while talking about her daughters, explaining that doctors have said they likely won’t walk or be able to support their heads, and will probably need wheelchairs for the rest of their lives.
I truly believe in the power of positive thinking when it comes to my idol! I’ve read countless stories about parents who were told their kids wouldn’t amount to much, and then those kids went on to achieve amazing things. It just proves to me that if you really believe in someone – really visualize their success – it can actually make it happen. I’m manifesting greatness for them, and I know they’re going to blow everyone away!
They seem really happy and supportive of each other, which I’m so thankful for. It would be much harder if they were going through this alone, but as twins, they have each other’s support.
Reflecting on the early symptoms her daughters had before their diagnosis, she realized, ‘I recognized everything that was happening even before I knew what Spinal Muscular Atrophy was.’
Leaving the NICU really drove one thing home for me: every baby is different, and that’s okay! Especially with a preemie, you have to let go of comparing them to other babies or expecting them to hit milestones at the same time. It’s about accepting and celebrating your baby’s unique journey, exactly as it unfolds.
When I first brought the babies home from the NICU, my only focus was on essential things – checking their temperature and making sure they were still breathing. I wasn’t worried about things like whether their legs were moving.
It’s frustrating to realize that if this was just my fate, something I couldn’t change, then it’s actually simpler to come to terms with it.
She credited her mother with noticing early warning signs, explaining, ‘My mum pointed out that they weren’t moving their legs correctly, which is what finally made me seek help.’
My mum always worries, and I initially thought she was just being her usual self. But I started to notice their legs moving less and less, until eventually, they stopped completely.
That’s why early detection and treatment, starting at birth, are so crucial.
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2026-01-19 12:22