Jesy Nelson didn’t wear her engagement ring during emotional appearance on This Morning – almost two weeks before her split from fiancé Zion Foster was confirmed

Jesy Nelson tellingly didn’t wear her engagement ring during a recent appearance on This Morning – as her reported split from her fiancé Zion Foster is revealed.

Jesy and Zion are thought to have called it quits just weeks after revealing their eight-month-old twin daughters had been diagnosed with a severe neuromuscular disorder.

The former Little Mix star, 34, and rapper, 26, who got engaged in September 2025 after three years together, will remain ‘united as co-parents’ despite ending their romantic relationship. 

On January 7 Jesy appeared on the daytime show to discuss their diagnosis – and her sparkling diamond was clearly missing.

Posting about their engagement last year Jesy showed off the ring as she beamed in a sunset beach snap. 

But the sparkler was missing while she chatted on the show where she didn’t mention her relationship with Zion.

Jesy Nelson tellingly didn't wear her engagement ring during a recent appearance on This Morning - as her reported split from her fiancé Zion Foster is revealed

Jesy Nelson tellingly didn’t wear her engagement ring during a recent appearance on This Morning – as her reported split from her fiancé Zion Foster is revealed

Jesy and Zion are thought to have called it quits just weeks after revealing their eight-month-old twin daughters had been diagnosed with a severe neuromuscular disorder

Jesy and Zion are thought to have called it quits just weeks after revealing their eight-month-old twin daughters had been diagnosed with a severe neuromuscular disorder

On This Morning she discussed her daughters’ Ocean and Story’s Type 1 SMA (spinal muscular atrophy) diagnoses.

Considered the most severe form of SMA, Type 1 symptoms – which typically appear in infancy – include extreme muscle weakness, difficulties swallowing and respiratory issues.  

Jesy is now campaigning for SMA1 screening at birth and has started a petition to get the condition added to the newborn blood spot screening test, also known as the heel prick test.  

A source said of their split on Sunday: ‘She and Zion remain friends and are fully focused on their daughters’.

Before going on to tell The Sun: ‘Their priority continues to be the well-being of their daughters. They are fully united in co-parenting’.

Daily Mail have contacted Jesy Nelson and Zion Foster’s representatives for comment. 

Taking to Instagram on Thursday, Zion shared a self-written poem centred on acceptance as he comes to terms with the day-to-day reality of seeing his daughters with the condition, as well as praising Jesy as a mum. 

He read: ‘They said it’s unlikely you’ll walk, you may not be able to talk,  probably won’t be able to hold your head up, that’s what me and Jesy heard – SMA Type 1. 

‘And it became so clear, doctors only go near what they can measure, so what’s certain?

On January 7 Jesy appeared on the daytime show to discuss their diagnosis - and her sparkling diamond was clearly missing

On January 7 Jesy appeared on the daytime show to discuss their diagnosis – and her sparkling diamond was clearly missing

The former Little Mix star, 34, and rapper, 26, who got engaged in September 2025 after three years together, will remain 'united as co-parents' despite ending their romantic relationship

The former Little Mix star, 34, and rapper, 26, who got engaged in September 2025 after three years together, will remain ‘united as co-parents’ despite ending their romantic relationship 

What is spinal muscular atrophy?

Spinal Muscular Atrophy (SMA) is a disease that weakens a patient’s strength by affecting the motor nerve cells in the spinal cord.

It results in gradual muscle wasting and the severity of symptoms varies by type

Type 1 SMA is the most severe and is evident at birth. The weakening of muscles means sufferers cannot sit and usually leads to death by the age of five

Type 2  is intermediate with the sufferer being unable to stand

Type 3 is mild and makes it difficult to get up from a sitting position, while 

Type 4 sufferers don’t have symptoms until they are in their 20s or 30s

‘I watch your smiles like sunsets, not promised, but real. I listen to you babble the sweetest melodies, in the moment it makes me wonder, if I keep telling you who I want you to be, what I want you to do, what I expect from you, am I loving you, or am I loving my fear?

‘If I take you for how God knitted you, just as you are, nothing removed, am I loving you? Am I accepting you?’

He added: ‘Story, is your heart okay? Ocean, how’s your mind? I hear strength in your lungs every time you cry, two little warrior girls who already know how to fight.

‘Honestly, my worry isn’t the milestones, isn’t forcing life to live a different way. My worry is quieter than that, deeper. It’s about accepting you, loving you for who you are right now, without conditions.

‘No matter what tomorrow brings, and no matter what yesterday was.’ 

Captioning the post, he praised Jesy for highlighting England’s lack of birth screening for SMA Type 1. 

He wrote: ‘We are all one. Jesy addressing a huge flaw in our healthcare system is the definition of a superwoman.

‘Reality is, it’s indefensible and needs to be changed, simple. Test kids at birth for SMA in the UK now that there are revolutionary treatments available.

‘Thank you to the SMA community and wider community of those living with more unique challenges for accepting us, supporting us and fighting with us.’ 

Addressing the issue during a recent appearance on This Morning, Jesy, who has 9.7 million Instagram followers, said: ‘I have this platform, and I almost feel like I’ve got a duty of care to raise awareness about it.

‘A little part of me feels – I don’t know if this is even crazy to say this – it feels selfish to keep this to myself and not potentially save a child’s life.’

According to the NHS website, the test is offered to every baby at five days old, and involves taking a blood sample to find out if it has one of nine rare but serious health conditions.

Speaking about the response since she revealed the news, Jesy  said: ‘I’m actually overwhelmed because I wanted it to get as much reach as possible, to raise awareness about it, and just the response I actually can’t believe how amazing the response has been.

‘I could have prevented this from happening if I’d have seen a video and caught it early enough.’

She added: ‘When you know that there is something that can be done about it and it is life-changing to your child, that’s the part that I cannot accept and that is why I’m going to shout to the rooftops about this.’ 

Since the diagnosis, Jesy said her life has ‘completely changed’, and that her house looks like a hospital, adding: ‘I just want to be their mum, I don’t want to be a nurse.

‘They’ve had treatment now, thank God, that is a one-off infusion.

‘It essentially puts the gene back in their body that they don’t have and it stops any of the muscles that are still working from dying. But any that have gone, you can’t regain them back.

A source said on Sunday: 'She and Zion remain friends and are fully focused on their daughters' (pictured together on This Morning in July 2025)

A source said on Sunday: ‘She and Zion remain friends and are fully focused on their daughters’ (pictured together on This Morning in July 2025) 

‘I just want to reiterate that if this is caught from birth, it’s just life-changing.’

Newborn screening for SMA is currently not available in the UK, but Scotland has announced it will screen babies from the spring.

The UK National Screening Committee does not recommend screening but has commissioned work to reassess this due to developments in treatment.

Jesy rose to fame after winning The X Factor in 2011 with Little Mix alongside Leigh-Anne Pinnock, Perrie Edwards and Jade Thirlwall.

Source link

Related Posts

Load More Posts Loading...No More Posts.