(12 years, 8 months ago)
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Thank you, Mr Weir. I congratulate the hon. Member for Luton North (Kelvin Hopkins) on securing this important debate. I have a ten-minute rule Bill, which is barely alive, on special educational needs, with particular focus on dyslexia and pragmatic language disorders. I thank both Front-Bench spokeswomen for allowing me to say a few words. I apologise for being late; I have been in a Committee.
My Bill was motivated by the enormous amount of casework in my constituency. There are very sad cases of extremely large numbers of children who have low to medium educational needs that are not being met by the local authority. I was dealing with about 30 cases, including a young lad with a very mild disability; he has had no assessment yet, so no one really knows what his needs are. He is supposed to be taking his GCSE options next year, but he has never been to a secondary school because a suitable place is not on offer. People do not understand what his issues are and there is no funding for a travel grant, which might open up some options for him. There are large numbers of extreme cases.
My Bill suggests that, common to all the cases I am dealing with, a wider burden of proof for parents to be able to demonstrate that their child has SEN would be extremely helpful. The old statement route catered for people with medium to high need, but did not help to provide leverage for parents whose children had lesser needs. In one case, a young girl with a reading age four years below her age was not considered to be significantly falling behind. If parents have paid for, or got a charity to make, an independent assessment from a qualified assessor, that should be enough to require the local authority to take action.
Teacher training has been mentioned, but training for those in local education authorities is also important. Part of our frustration in getting cases resolved was due to people not understanding what CReSTeD—Council for the Registration of Schools Teaching Dyslexic Pupils—accreditation was, or what the different levels meant for a particular individual. We were not really dealing with educationalists, which was partly due to staffing problems at the local education authority, so I echo the comments of the hon. Member for Washington and Sunderland West (Mrs Hodgson). Training should be extended to the LEA.
The local education authority should already be required to publish what provision is available in its area, but many do not, yet such a requirement would help parents tremendously. When the LEA has decided that a need will be catered for under school action plus, it should send the parents a quality letter, not simply one that tells them that the need will be covered in school action plus, so they should not worry. They should get detailed information about what that will mean for their child week by week.
I congratulate the hon. Lady on her ten-minute rule Bill. I hope that it moves to the next stage and influences Government. She said that she wanted detailed letters from the local authority, which not only say, “Your child is falling behind and has a problem”, but identify the problem. There is sometimes an overlap between dyslexia, dyspraxia, low academic ability and other conditions that can confuse the diagnosis, but the local education authority should be able to define dyslexia when it writes the letters.
The hon. Gentleman is absolutely right. Getting an assessment to start with is a battle for parents, and then they must have confidence in it and in the remedial action that should be taken. Many parents I have been dealing with have not had satisfaction on any of those fronts.
I would be grateful if the Minister could say more about the statutory responsibilities of the Department for Education and the discussions she may have had with the Department of Health. We need to strengthen the tools available to parents and other advocates for these children. My constituents certainly believe that they pay their taxes to ensure that the education system we provide gives every child the education they need to reach their full potential.
One of my final points relates to costs. Where we have not been able to get a school place for some of the children in my constituency, we have actually funded placements for them, and I should like to place on record my thanks to a number of London livery companies and local Rotarians for providing funds to allow that to happen. In just one year, the girl I mentioned at the start, who was four years behind her expected reading age, has caught up. She is a bright girl, and having been given the proper, full-time dyslexia teaching that she needed, she is now doing really well.
An argument that is often thrown back at us is that providing all the top-notch SEN provision that children need costs too much and that the state cannot possibly afford it, but that is a bit of a myth. The placement that we have funded for the child I mentioned cost less than the provision that the local authority would have had to put in place in the school that it chose for her. It is possible to do these things, and they will often save the state money not only initially, but, as has been mentioned, in the long term, given all the problems and issues that people have if they do not get the help that they need.