Jesy Nelson says her daughters’ ongoing treatment for spinal muscular atrophy (SMA) remains a “never-ending” and “life-changing” situation, according to reports. Nelson discusses the emotional impact of the condition as her family continues to manage multiple medical issues. She also reveals that her daughter Story has been diagnosed with scoliosis. In addition, Nelson says both of her twins require further operations, indicating additional planned care as the girls’ health needs develop. The coverage presents Nelson’s comments as a personal update about her family’s medical journey, emphasizing that progress in SMA care does not end the need for continued treatment and monitoring. The reports do not cite new test results or specific dates for the operations, but they describe the situation as ongoing and requiring further intervention. Overall, the articles focus on Nelson’s statements about her daughters’ health diagnoses and the expectation of additional procedures as part of their care.