Feb 14 • 12:17 UTC 🇬🇧 UK Mirror

Jesy Nelson makes honest admission about twins' future amid heartbreaking health ordeal

Jesy Nelson expresses her emotional journey following her twins' Spinal Muscular Atrophy diagnosis and her advocacy for increased newborn screenings for the condition.

Jesy Nelson, the former Little Mix star, has shared an emotional update regarding her twin daughters who were diagnosed with Spinal Muscular Atrophy (SMA) Type 1 shortly after their premature birth. The twins, Ocean Jade and Story Monroe, were born in May 2025, following serious health complications related to twin-to-twin transfusion syndrome (TTTS). The alarming diagnosis was first suspected by Nelson's mother due to the girls' lack of movement, leading the family to seek medical attention and ultimately discover the severity of the condition.

SMA Type 1 is a debilitating and progressive muscle condition that poses a significant threat to affected infants, as it can lead to fatal outcomes if not treated promptly. In light of her daughters' diagnosis, Jesy has passionately campaigned for the inclusion of SMA screenings in standard newborn blood tests, a cause she believes is vital to prevent similar suffering in other families. Following her public advocacy efforts, Nelson's petition to include these screenings has amassed over 100,000 signatures, highlighting a strong public support for enhanced health screenings.

The emotional weight of her twins' health struggles has deeply impacted Jesy, who has been open about her feelings, even shedding tears in public as she reflects on their journey ahead. As she navigates the challenges of motherhood alongside her ex-partner Zion Foster, Jesy remains focused on raising awareness about SMA and the urgent need for screening to ensure timely interventions that could change the future for infants diagnosed with this condition. Her story not only sheds light on the reality of SMA but also serves as an inspiring call to action for better healthcare practices for vulnerable children.

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