Jesy Nelson shared an adorable upload of one of her twin daughters enjoying a cuddle and kiss, and the former Little Mix star couldn’t resist filming the sweet moment
Jesy Nelson with her baby(Image: Prime Video)
Jesy Nelson has shared a sweet clip of her baby daughter amid the tot’s health woes. The Little Mix singer posted the adorable upload on Instagram as the youngster smiled and giggled as she got cuddles and kisses from Jesy’s mum.
Jesy could be heard laughing in the background as she gushed: “aww” at the sweet interaction. And in another touching clip, Jesy is seen sweetly showing off her child’s hair as she laughs at the mullet that is growing.
“She’s got a little mullet,” Jesy admitted as she flicked the baby’s cute curls. “Look at this little mullet.” As she laughed, she said: “She’s got little curly tufts and then a little straight mullet.
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Jesy posted the sweet video(Image: jesynelson/Instagram)
She showed off her tot’s cute hair(Image: jesynelson/Instagram)
“Have you ever seen. Oh my gosh. Look at you. Look at this little barnet…She’s like a little cabbage patch doll.” Jesy has been vocal about her twins’ condition and started a petition to have SMA screenings added to the newborn blood screening test. The petition quickly received over 100,000 signatures.
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Her twin girls were her sadly diagnoses with Spinal Muscular Atrophy (SMA) Type 1. The 34-year-old gave birth prematurely to daughters Ocean Jade and Story Monroe in May 2025, after complications with twin-to-twin transfusion syndrome (TTTS).
The condition was spotted after her mother noticed that something wasn’t right with the girls’ lack of movement. The musician then raised her concern and after undergoing medical tests, the family learned after the twins’ diagnosis.
SMA is a genetic condition that affects the motor neurons, causing progressive muscle weakness and wasting (atrophy). According to the NHS, the condition can affect a child’s ability to sit up, crawl, or walk.
Itmay also cause difficulties with their breathing and swallowing. The condition is thought to occur in an estimated one in 10,000 births. Around 60 per cent of cases are type 1.
For those children with type 1 SMA who don’t have breathing support, they can die before their second birthday. However, the NHS states that more are now surviving due to advances in treatment.
Jesy has revealed her twins have received a one-off gene therapy infusion. It’s used to try to help preserve any muscles that are still functioning.
She continues to share her motherhood journey and give updates on her kids on social media. She also released a documentary following her pregnancy.
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