Academies Bill [Lords]

The amendment is on a really important matter, and the fact that so many Members are present after 4 o'clock on Thursday shows how important. Given my background in this area, I wish to start by saying that a lot of it is about definitions. I welcome what the Minister has said, but as someone who is steeped in the issue and has worked in special educational needs for many years, I have to say that I am sorry, but it just is not enough. SEN is a notional term—it is almost in the eye of the beholder. It is not defined in law. There is a huge code of practice intended to give the term feel and shape, but that code of practice is nothing more than guidance. It mentions the responsibilities of local authorities, but not necessarily those of schools or academies. If we are to rely on the code of practice, it will need to be rewritten with those things specifically stated. SEN is also a disputed term. The very fact that we have an SEN tribunal, with which local authorities struggle all the time, and which is large, growing and very costly, and that SEN cases are in the courts all the times, suggests that the term is not defined now and will become less defined in future. I have gone into many schools, some of which achieve incredibly highly, and found that 50% of their children are on their SEN register. That is clearly nonsense, and there are all kinds of reasons for it. It is the teacher in the classroom, or the head teacher, who defines whether a child has SEN and places them at school action or school action plus. In many cases, they do not even advise the parent. That is illegal, but it happens. Head teachers do that for myriad reasons, including that they feel it will improve the school's contextual value added and its standing with Ofsted. Some local authorities still delegate funding on the basis of school action and school action plus, however stupid that may seem, as I tell them. The number of children who are at school action or school action plus or defined as having SEN depends on so many different contextual issues in different places. That brings us to the comments about who gets a statement and who does not. In defence of my former colleagues, I have never dealt with services that do not want to do a good job or want to prevent children from getting the support that they need. However, they are rationed services and they have to prioritise. No matter how much money the previous Government and the Government before them put into the more severe and complex end of SEN, which is growing, it inevitably drifted off to the less severe end. That is why there is a problem of children with statements who should not have them, and others who need them but do not get them. I hope that the Government can resolve it, but previous Governments have not been able to do so. One can put as much money as one likes into the hard end of SEN, it will inevitably drift off to the mild end of the spectrum. As the Chair of the Select Committee rightly pointed out, low incidence SEN is exactly that—SEN that occurs rarely. It is sometimes called, ““low incidence; high need; high cost.”” Low incidence SEN services are generally classified as services for deaf and hearing impaired children and for blind or partially sighted children. Autistic spectrum disorder is not classified as low incidence SEN. It was in the past, but it is the fastest growing SEN. What will happen to autism services? If the provision is not defined, services for children with autism may be delegated.