Jesy Nelson Splits from Fiancé Zion Foster Following Twin Daughters’ SMA Type 1 Diagnosis
Jesy Nelson, the former Little Mix singer, has reportedly ended her engagement with rapper Zion Foster just weeks after the couple revealed their twin daughters had been diagnosed with spinal muscular atrophy (SMA) Type 1. This heartbreaking news has not only impacted their personal lives but has also sparked Jesy’s passionate campaign to raise awareness about this severe neuromuscular disorder. Despite the split, Jesy and Zion remain committed to co-parenting their daughters, Story and Ocean, as they navigate the challenges ahead.
Jesy Nelson and Zion Foster’s Relationship and Recent Split
Jesy Nelson and Zion Foster’s relationship has been in the public eye since they began dating three years ago. The couple got engaged in September 2025, sharing their joy with fans worldwide. However, recent developments have taken a difficult turn. Reports indicate that Jesy and Zion have decided to part ways romantically, though they continue to maintain a strong friendship and co-parenting partnership.
Jesy was seen without her wedding ring during a recent appearance on the popular daytime show This Morning, where she openly discussed the devastating diagnosis of their daughters. The decision to split comes amid the emotional strain of caring for their children’s complex medical needs, but sources close to the couple emphasize that their focus remains firmly on their daughters’ health and happiness.
Understanding SMA Type 1 and Its Impact on Families
Spinal muscular atrophy (SMA) Type 1 is the most severe form of SMA, a genetic disorder characterized by progressive muscle weakness and loss of motor function. Symptoms typically manifest in infancy and can include difficulty swallowing, respiratory complications, and extreme muscle weakness. Unfortunately, SMA Type 1 is life-threatening and requires intensive medical care.
For Jesy Nelson and Zion Foster, the diagnosis of their twin daughters Story and Ocean has been a life-altering moment. The couple has been vocal about the challenges they face and the urgent need for better screening and treatment options. Jesy has taken on an advocacy role, campaigning for the inclusion of SMA Type 1 in newborn screening programs to enable earlier diagnosis and intervention.
Jesy Nelson’s Campaign for SMA Type 1 Newborn Screening
In response to their daughters’ diagnosis, Jesy Nelson has launched a petition urging health authorities to add SMA Type 1 to the newborn blood spot screening test, commonly known as the heel prick test. Early detection through newborn screening can significantly improve outcomes by allowing timely access to treatments that can slow disease progression.
Jesy’s campaign highlights the importance of raising public awareness about SMA and the need for systemic changes in healthcare screening protocols. By sharing her family’s story, she hopes to inspire other parents and policymakers to support this critical cause.
Jesy’s advocacy work has garnered widespread support from fans and medical professionals alike, emphasizing the power of celebrity influence in driving social change. Her dedication to her daughters and the SMA community underscores her resilience during this challenging period.
Looking Ahead: Co-Parenting and Family Support
Despite their split, Jesy Nelson and Zion Foster remain united in their commitment to their daughters. Sources close to the family confirm that both parents are focused on providing a loving and supportive environment for Story and Ocean. Their shared priority is ensuring the twins receive the best possible care and emotional support.
Jesy’s openness about her family’s struggles has resonated with many, shedding light on the realities faced by families affected by rare diseases. Her journey serves as a reminder of the strength found in unity and the importance of advocacy in the face of adversity.
Conclusion
Jesy Nelson’s recent split from fiancé Zion Foster marks a difficult chapter in her life, especially following the devastating SMA Type 1 diagnosis of their twin daughters. However, their unwavering dedication to co-parenting and Jesy’s passionate campaign for newborn SMA screening demonstrate hope and resilience. If you want to support Jesy’s mission and raise awareness about SMA Type 1, consider signing her petition and sharing her story to help make a difference for families affected by this condition. Together, we can advocate for early detection and better care for all children diagnosed with SMA.
