The Irish Government has formally agreed to establish a statutory public inquiry into spina bifida and complex scoliosis services, following years of mounting concern from families, advocacy groups, and medical professionals about the quality and accessibility of care.
Initial Steps
On Tuesday, 18 November 2025, the Department of Health confirmed that a facilitator will be appointed to consult with stakeholders and scope the potential terms of reference. This process will involve close collaboration with the Office of the Attorney General to ensure the inquiry is legally robust and comprehensive.
Scope and Objectives
The inquiry will be time-bound, but officials acknowledged that significant preparatory work is required to define its scope. The Government stressed the importance of carefully considering the wide range of issues raised by families and stakeholders, with the ultimate goal of delivering clear, actionable outcomes that improve patient care and accountability.
Next Steps
Once the scoping exercise is complete, the Government will seek final approval for the terms of reference, paving the way for the inquiry to begin. The process is expected to examine systemic failures, treatment delays, and the broader impact on children and families affected by spina bifida and scoliosis.
Broader Context
Calls for an inquiry intensified after repeated reports of surgical backlogs, inadequate resources, and inconsistent standards of care in Ireland’s scoliosis and spina bifida services. Advocacy groups have argued that only a statutory inquiry can deliver the transparency and accountability needed to restore public trust.
Outlook
The inquiry represents a significant step toward addressing long-standing concerns in Ireland’s healthcare system. Families and campaigners say they hope it will lead to meaningful reform, improved services, and justice for those affected.
