It is a real pleasure to serve under your chairship, Ms Jardine. I thank my hon. Friend the Member for Bexleyheath and Crayford for securing this important debate. Adults with cerebral palsy make up a significant but often overlooked part of our population—around 130,000 people across the UK. Although cerebral palsy is a lifelong neurological condition, we frequently see well-structured, multidisciplinary paediatric care systems simply evaporating when people reach the age of 18. Adults are left navigating a fragmented system with no clear pathways, limited specialist input and inconsistent recognition of their needs. The updated neurology service specification ensures that cerebral palsy is embedded within a broader national framework, strengthening national expectations for adult cerebral palsy care. One of the most important ways we are strengthening support for adults with cerebral palsy is by improving awareness and understanding within primary care. The service specification now requires integrated care boards and specialist centres to work much more closely with GPs, strengthening communication and clarifying referral pathways so that primary care clinicians understand when an adult with cerebral palsy requires specialist review or escalation. NHS England's revised service specification for adult specialised neurology services, which was published in August last year and comes into effect next month, represents an important step forward in improving care for adults with cerebral palsy. It sets clear expectations for how people with lifelong neurological conditions, including cerebral palsy, should move between general practice, community services and specialist centres. The 10-year health plan will ensure that people with complex needs are supported to be active participants in their own care. As part of that, 95% of people with complex needs or long-term conditions will have an agreed personalised care plan by 2027. The 10-year health plan's focus on personalised and proactive care will support integrated care boards to improve access to reviews as part of a more consistent offer for adults with cerebral palsy. The plan will also ensure that no young person is lost in the gaps between children's and adult services, a point at which many families tell us that they feel most vulnerable. NHS England's children and young people transformation programme provides a clear nought-to-25 model of care to achieve that. For young people with cerebral palsy, that means earlier preparation for transition, co-ordinated support from a multidisciplinary network and clearer expectations for how professionals should plan and hand over care.