Jesy Nelson的早产双胞胎被诊断为罕见的SMA1, 面临90-95%的生存风险, Jesy Nelson's premature twins were diagnosed with rare SMA1, facing a 90-95% survival risk, leading her to advocate for awareness.

美国小组成员杰西·尼尔森在2026年2月13日首映的Prime Video纪录片预告片中分享,她的双胞胎在2025年5月早产,被诊断患有脊髓肌缩1型,这是一种罕见的遗传疾病. Former Little Mix member Jesy Nelson shares in a trailer for her Prime Video documentary, premiering February 13, 2026, that her twins, born prematurely in May 2025, were diagnosed with Spinal Muscular Atrophy Type 1, a rare genetic disorder. 她指出,他们有90%至95%的几率不可能存活,正在接受双对双输血综合症的紧急治疗,在医院住院10周。 She recounts facing a 90% to 95% chance their survival was unlikely, undergoing emergency treatment for twin-to-twin transfusion syndrome, and spending 10 weeks in the hospital. Nelson反思她的心理健康斗争、名声压力以及2020年离开该团体的决定, Nelson reflects on her mental health struggles, the pressures of fame, and her decision to leave the group in 2020, now finding purpose in advocating for SMA1 awareness and newborn screening.