Navigating cerebral palsy from childhood to adulthood: The importance of effective transition

Cerebral Palsy (CP) is a non-progressive neurological disorder originating from early brain injury, with an incidence of 1.4–3 per 1000 live births. While primarily a neuromotor condition, it often includes associated impairments such as epilepsy, intellectual disability, and communication challenges. Advances in care have significantly increased life expectancy, with most individuals with CP now living into late adulthood. As a lifelong disorder, management requires individualised intervention strategies tailored to current motor function and potential participation restrictions. In paediatric services, early and regular intervention is critical to optimise developmental milestones and support musculoskeletal growth enabling children to reach their full potential. In adulthood skilled timely management is essential to address evolving challenges such as musculoskeletal complications, pain, and fatigue. Transitioning to adult care however unfortunately often highlights gaps in continuity and expertise, leaving individuals navigating fragmented healthcare systems with unmet needs. Effective transition planning, initiated in collaboration with the young person and their family is crucial to empower and equip individuals with the skills and confidence to navigate adult care, reduce complications and enhance quality of life across the lifespan.