Jesy Nelson has revealed her emotional Prime Video series documenting her pregnancy with her twin daughters will be released next month, days after sharing her babies' heartbreaking health diagnosis.
The Little Mix star, 34, shared a picture of a clapperboard announcing her new show, Jesy Nelson: Life After Little Mix, will be released on February 13.
The show will see the star navigate the journey of motherhood as she prepares to welcome her twins.
Last week, Jesy revealed that her daughters, Ocean Jade and Story Monroe, have been diagnosed with Spinal Muscular Atrophy (SMA1).
'Spinal muscular atrophy (SMA) is a rare genetic condition that can cause muscle weakness. It gets worse over time, but there are medicines and other treatments to help manage the symptoms,' according to the NHS website.
The singer, who shares her children with fiancé Zion Foster, took to Instagram on Saturday with a heartwarming video with one of her children.
Jesy Nelson has revealed her emotional Prime Video series documenting her pregnancy will be released next month, after sharing her twins' heartbreaking health diagnosis.
Last week, Jesy revealed that her daughters, Ocean Jade and Story Monroe, have been diagnosed with Spinal Muscular Atrophy (SMA1).
And now she will release a new series on Amazon that will show a rare insight into the pop star's life and her difficult pregnancy.
A synopsis for the show reads: 'Expecting twins, Jesy opens up about the joy, vulnerability, and fear that comes with carrying two little lives.
'The series follows Jesy through the emotional roller coaster of pregnancy complications, including Twin-to-Twin Transfusion Syndrome, a rare and potentially life-threatening condition.
'With weekly hospital visits, candid conversations, and the unwavering support of her loved ones, Jesy navigates the highs and lows of pregnancy, confronting her deepest fears while embracing a newfound strength.
'But this journey isn't just about motherhood; she needs to confront her past, too. In this series, she will open up about the life-altering decision to leave Little Mix in 2020, breaking her silence on the relentless pressures of fame, her battle with mental health, and the controversies that followed.'
Ahead of the release, Jesy told Amazon: 'We opened the doors fully, and I'm really looking forward to letting you all in as I navigate my way to becoming a first-time mum to our beautiful baby girls, Ocean and Story.
'I'll be honest, it's not been easy as it's been such a high-risk pregnancy, so you'll see all the highs and lows and rollercoaster of emotions we have been going through.
'I hope you will all join me on this journey as I really open up and say goodbye to the past and enter this new chapter in my life. I hope you love it as much as we do.'
The Navy Bee direct show will see the star navigate the journey of motherhood as she prepares to welcome twins.
Jesy broke down in tears on Wednesday's episode of This Morning as she shared a heartbreaking update on her twin daughters' muscle disease.
The singer admitted that her home now 'looks like a hospital' after learning how to look after her twins and cater to their complex needs as she shared the most difficult aspects of the diagnosis.
Getting very emotional about her girls, Jesy said: 'We've been told that they will probably never walk, they'll probably never regain their neck strength. They are gonna be in wheelchairs.
'There's been so many stories where parents have been told this, and then their children have gone on to do incredible things, so I believe that you've just got to manifest that.
'They are still smiling; they're still happy. They have each other, and that's like the main thing that I'm like so grateful for because they could be doing this by themselves, but they're twins, and they're going through this together.
'My whole life has just completely changed. If you came to my house, it looks like a hospital.
'My whole hallway is filled up with medical stuff and it’s just crazy how you can go from one extreme to the next.
'Story has to be on a breathing machine at night because she isn’t strong enough to breathe by herself at night; they have to have cough assist machines to help them cough; I have to put feeding tubes down their nose to like get out secretions off their chest.
'I’ve had to learn this within the space of a few days of getting their diagnosis, and it’s just so much to deal with while you’re also trying to deal with this like horrendous thing that’s just happened and still be a mum as well.
'That’s the part that I really, I’m still struggling with it, I won’t lie, but that is the part that, like, really gets me, is I just want to be their mum; I don’t want to be a nurse.
'All I can do is just try my best to be there for them. Give them positive energy.'
Looking back over the signs that the two girls had been battling the condition before their diagnosis, she added: 'I actually knew and saw all of the signs before I even knew what SMA was.
'But when I left the NICU, it was hammered home to me, 'Don't compare your baby, they're not going to reach the same milestones, take them as they are' because they were premature.
'When I took them home from NICU, the only thing I was really concerned about at that time was checking their temperature, making sure they were still breathing. I'm not checking to see if their legs are still moving...
'And that's what's frustrating, knowing that for me, if this was the cards I was always going to get dealt and there was nothing I could do about it, then it's almost easier for me to accept.'
Heaping praise on her mum for spotting the signs that eventually prompted her to take further action, she said: 'It took for my mum to be like, 'They don't move their legs how they should be moving'.
'Bless my mum, she’s a worrier, and I just thought my mum was being a worrier - but I noticed they were moving [their legs] less and less and less until it just stops.'
'That is why it’s so important and vital to get treatment from birth and that it’s detected from birth.'
Opening up on her decision to share her story with the world, Jesy continued: 'I wanted it to get as much reach as possible to raise awareness about it; it's what I wanted to do.
'If I'd seen someone else's video maybe just maybe I could have prevented this from happening if I'd have seen a video and caught it early enough.
'Yes I could have dealt with it privately but at the same time I'm like I have this platform and I almost feel like I've got a duty of care to raise awareness about it.'
Jesy's daughters Ocean Jade and Story Monroe have been diagnosed with Spinal Muscular Atrophy (SMA1)
'I don't know if this is even crazy to say this but it feels selfish to keep this to myself and not potentially save a child's life. I'm going to shout to the rooftops about this.'
'I could have saved their legs... I don't think I'm ever going to get over this or accept it but I'm going to try my best to make a change.'
Jesy has also revealed that she has put a petition in to try and get newborn babies screened from birth for SMA from birth and is 'determined and ready to fight' to see it approved.
If SMA1 is treated pre-symptomatically (at or near birth), the disease can be largely prevented, and many children develop with minimal or no symptoms.