Jesy Nelson Shares Adorable Giggling Baby Moment — After Being Brought to Tears by a Painful Reminder in Her Twins’ Devastating Health Battle 💔

The Little Mix star, 34, who welcomed daughters Ocean Jade and Story Monroe prematurely in May 2025 - revealed last month that both girls had been diagnosed with Spinal Muscular Atrophy Type 1 (pictured last month)For Jesy Nelson, joy and heartbreak are now living side by side — often within the very same day.

On Thursday, the former Little Mix star shared a tender, heart-melting video of one of her baby daughters giggling uncontrollably as she cuddled up to her grandmother, Janice. The baby’s laughter filled the screen — a fleeting moment of light in a journey otherwise marked by fear, exhaustion and unimaginable strength.

But just days earlier, Jesy had admitted she was in floods of tears, shaken by what she called “another reminder of another obstacle we have to tackle” amid her twins’ devastating health battle.

Jesy Nelson has shared a heartwarming video of one of her daughters giggling with her mother, Janice on Thursday, after revealing that she broke down in tears at the weekend amid her twins devastating health battle💕 A Giggle That Stopped the Scroll

In the short Instagram Story clip, Jesy’s daughter squeals with laughter as her nan gently nuzzles into her neck. Jesy can be heard laughing along, clearly soaking in the rare, precious moment.

In another sweet post, Jesy joked about one twin’s adorable mullet hairstyle, while affectionately comparing the other to a Cabbage Patch doll as she ran her fingers through her soft, curly hair.

For fans who have followed every step of her journey, the clips felt deeply emotional — proof that even in the darkest chapters, joy still finds a way in.

On Thursday, she took to her Instagram Story to show followers an adorable clip of her daughter giggling away as her nan, Janice, nuzzled her face into her neck💔 The Reminder That Broke Her

Those heartwarming moments came just after Jesy revealed she had broken down in tears over the weekend when her daughters’ special feeding chairs arrived at her home.

Because of their condition, Jesy’s twins — Ocean Jade and Story Monroe — require feeding tubes and specially designed chairs to support their posture, breathing and swallowing.

Sharing a photo of the chairs, Jesy wrote honestly:

“So the girls need special feeding chairs that came yesterday and I couldn’t help but burst into tears when I saw them.”

“It just made me feel so sad as it’s just another reminder of another obstacle we have to tackle. Do any other SMA mummies feel this way?”

The post struck a nerve with parents across the UK, many responding to say they recognised the same mix of grief, love and resilience.

In another sweet clip, Jesy couldn't help but chuckle over her daughter's sweet mullet hairstyleA Diagnosis That Changed Everything

Jesy welcomed her twin daughters prematurely in May 2025 with her ex-fiancé Zion Foster.

Last month, she revealed the devastating news that both babies had been diagnosed with Spinal Muscular Atrophy Type 1 (SMA1) — the most severe form of the rare genetic condition.

The disease affects the motor nerve cells in the spinal cord, leading to progressive muscle weakness and, without treatment, a tragically short life expectancy.

Jesy first opened up about the diagnosis in her documentary Life After Little Mix, and has since continued to share raw, unfiltered updates on social media — choosing honesty over silence.

While she compared her other twin daughter to a cute Cabbage Patch doll as she ran her fingers through her curly dark hairFighting for Change — While Holding Her Girls Together

Alongside caring for Ocean and Story’s complex medical needs, Jesy has become a fierce campaigner — pushing for the NHS to expand the standard newborn heel-prick test to include SMA screening.

She has said that if the £1 test had been done at birth, earlier treatment could have saved her daughters’ leg function.

Her petition has already surpassed 100,000 signatures, forcing Parliament to consider the issue for debate.

Despite the momentum, Jesy admits the emotional toll is relentless.

“Some days are really fing s*,”* she previously told the Mail.
“Other days are lighter. It’s a rollercoaster — it’s never steady.”

The heartwarming posts come after Jesy revealed that she had burst into tears on Saturday when she saw the girls' special feeding chairs“I Just Want to Be Their Mum”

Jesy has spoken candidly about the daily procedures her babies must endure — and how painful it feels to be the one causing them discomfort, even when she knows it’s saving their lives.

“They’re so tiny,” she said.
“I have to do things that are helping them, but when they’re crying and screaming, it feels like I’m hurting them. I hate that I have to be the one to do that. I just want to be their mum.”

She has also addressed the devastating prognosis that SMA1 can bring — but insists she refuses to give up hope.

“My girls are the strongest, most resilient babies,” Jesy said.
“I really believe they’re going to defy the odds.”


Choosing Her Girls Over Everything

As she continues to fight for her daughters, Jesy has quietly put her music career on pause.

Speaking recently on Heart FM, she said simply:

“My girls are my whole heart and soul. That’s my focus. Their future depends on this.”


💔➡️💞 From tears over feeding chairs… to giggles in her mum’s arms.
Jesy Nelson’s days are heavy, fragile and fiercely hopeful — all at once.

And for now, every laugh is a victory.