Georgia Gould

I confess that I think I have committed to go to every constituency in the country, but I will do my best. [Laughter.] I cannot promise that every single ask will be responded to quickly, but I want to get to every community, and we will also be doing a number of online events as part of the consultation to ensure that everyone has the chance to feed in. To respond to the hon. Member’s questions, first, it is important to make clear that we are not saying that children do not need a diagnosis. Diagnosis plays an important part in the system for children and young people, but it cannot and should not be a barrier to accessing support in the education system. Schools must have the tools to identify and respond to need, and the resource and well-evidenced interventions to wrap support around children without a diagnosis. However, we are committed to working with Health colleagues on improving the whole system, and the SEND consultation document is clear about that further work on accountability —not just for local authorities, but for integrated care boards. The hon. Member will know about the review of some of the inequalities in access to diagnosis. The point about care co-ordinators and parental support is well made—that is something I have heard a lot from families. Within the consultation, we have asked a question about how that can be better delivered, and we are committed to doing more in that space. Lots of different ideas have come forward from different disabled children’s organisations and from parents, but I want to use the consultation to hear directly from parents about what is most helpful for them. In some models, parents who have been through the system are paid to support other parents, and the special educational needs and disabilities information advice and support service already exists. We want to look at all the different models, and I would welcome insights from across the House. I want to provide some important reassurance to those parents who the hon. Member for Runnymede and Weybridge (Dr Spencer) talked about who are concerned about the changes. First, any child at a special school will remain there for as long as they want. We have deliberately taken a careful and staged approach and are putting investment up front, so we are building a new system before we look to transition into it. We are also asking the Children’s Commissioner to take an independent view of system readiness. Secondly, we are clear that any child transitioning from an education, health and care plan must move on to an individual support plan, with the wraparound support I have mentioned.