Jesy Nelsons Twins Star in Chart-Topping Documentary!

Jesy Nelsons Twins Star in Chart-Topping Documentary!

Advertisement

shared an adorable new video of her twin daughters after her documentary about their heartbreaking health battle topped the Amazon viewing charts on Monday.

The star, 34, welcomed twin daughters Ocean Jade and Story Monroe, whom she shares with ex Zion Foster, prematurely in May 2025, and last month she revealed they've been diagnosed with Spinal Muscular Atrophy Type 1 (SMA1).

On Friday, Jesy released her documentary Life After Little Mix, where she spoke about her babies' diagnosis, as well as the truth behind her decision to leave the band in 2020.

And in a post on Instagram Stories, Jesy celebrated the news that her documentary was number one in Amazon's viewing charts.

Posting a video of her baby daughters as well as her TV with the documentary at the top of the charts, Jesy wrote: 'Still can't believe it, thank you everyone.'

Since sharing her twins' diagnosis, Jesy has been demanding the NHS expand the standard heel prick test to check for SMA1 and says the test, which costs around £1 each, could have saved [her twins'] legs' by giving them access to earlier treatment. 

Advertisement

Jesy Nelson shared an adorable new video of her twin daughters after her documentary about their heartbreaking health battle topped the Prime Video viewing charts on Monday 

The Little Mix star revealed last month that her twins Ocean and Story have been diagnosed with spinal muscular atrophy 

Now taking to Instagram the singer shared a clip of herself and a group of pals watching the signatures rise, before finally hitting 100,000 leaving them all collapsing into both cheers and tears - the total has since risen to way over 120,000. 

An emotional Jesy captioned the post: 'I cannot actually put into words how grateful I am that this moment has just happened right here! And it is all thanks to you guys'.

'Thank you to every single person that took time out of their day to sign this petition. You have no idea how much this means to me and the SMA community. This is the first hurdle but we bloody did it and I truly believe that together we are going to make change!'. 

As she continues to campaign for screening for the condition to be included in the newborn blood spot test, she's revealed she has parked her music career.

Advertisement

Appearing on Heart FM's Breakfast show on Thursday, Jesy told and her focus is now solely on the twins.

She explained: 'Look listen I’d never say never say never to music, but for me, my girls are my main focus, I’ll be honest with you, I’ve not got time, I really don’t.

'They are my whole heart and soul and my main focus, and I want to continue advocating for them and getting this heel prick test changed and getting them strong, that’s my main focus.

'Because that’s going to determine their future. That’s my main focus right now.'

In a post on Instagram Stories, Jesy celebrated the news that her documentary was number one in Amazon's viewing charts

The star shared a video that showed her doting on her baby girls, after opening up about their diagnosis in the series

Advertisement

Since sharing her twins' diagnosis, Jesy has been demanding the NHS expand the heel prick test to check for SMA1, and last week she celebrated her petition reaching 100,000 signatures

She added: 'Mentally, I'd got myself ready and I was like, "Right , I want to sit down with the girls now and I want to chat to them and tell them why I did what I did, and how I've been feeling, and just really explain to them, and try to make them understand how I was feeling." 

'And then my manager called, and she was like, "So, I've spoken to the girls, and they are happy to chat with you, but they don't feel comfortable being in a room with you unless there's a therapist there."

'I was like, "What? I've just come out of hospital, this is the time I need you the most." I didn't feel like they were my sisters. It's been five years now; everytime I think about it I'm like, "Was it them, or was it the management?" I will never know that because we never got to have that conversation. 

'And then eventually there was a phone call, and it was really awkward. It was just so weird because it was like talking to strangers. 

'It was the most uncomfortable phone call I've ever had, no one knew what to say, and that was the last time I ever spoke to them as a group.' 

Advertisement

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.

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

Advertisement

Advertisement