Children and Families Bill

Baroness Wilkins Excerpts

Tuesday 7th January 2014 Lords Chamber

[Baroness Morris of Yardley (Lab)]

My Lords, I support the amendments and, in particular, will comment on Amendments 30, 31, and 33D.

The amendments tabled by my noble friend Lady Jones, which deal with the “expects to be” versus “which is” dilemma, just make sense, as I do not think that anyone here would not want parents to know what is being offered rather than what might be offered. The Government’s concern appears to be that something innovative might happen during the year that could be added to the offer, but the Minister might reflect that, if the offer was a living document so that it could be updated as an innovation came through, was proven to work, accepted as best practice and added to the local provision, in a digital age it would not be difficult to update the offer. The notion of “which is” gives far more certainty to users of the service than the words “expect to be”. In that respect, I very much support those amendments.

I just want to comment on the amendment of the noble Lord, Lord Low. I see both sides of this argument. We want local authorities to be free to innovate, to reach for the stars and to be the best they can, and we do not want the local offer in every local authority area to look exactly the same regardless of where you are in the country. Neither do we want to give permission to local authorities to go for a basic minimum standard. I accept the concerns laid out by the noble Baroness, Lady Eaton, and the noble Lord, Lord Storey, but we are still left with a problem.

The code of practice talks a lot about the quantity that should be in the local offer. There is a whole list of things that the code of practice guarantees will be there. What is missing from the whole debate is something that guarantees quality. Amendment 33D attempts to do that, and I want the Minister to respond to it. None of us wants poor quality, and I do not think that we would be in politics and would certainly not be legislators if we did not know that we have to ensure quality. It does not happen by itself or through a free-for-all, and it will not happen if we just leave it to local authorities to do their best. We want more than that. Minimum standards are not in the amendment. I do not want to fetter those local authorities who will provide very well; I want to protect those people who live in areas where the local authority does not do very well. I am concerned about how we protect people against poor provision falling below those minimum standards.

Normally, government takes one of three actions. It leaves it to the market—the noble Lord, Lord Storey, mentioned just now that if people do not like it, they will complain and changes will be made. I do not think that that will happen with the local offer. The only way that the market usually works is if people are free to go elsewhere. Then the poor provision that they did not want withers on the vine, vanishes, closes down and gets off the playing field. That is not what we want here. We do not want a local offer to be squeezed out of the market so that people have to go over the local authority borders. I cannot see how the market works as a regulator of standards for the local offer.

Secondly, we inspect. That is another way to guarantee quality. I would be grateful if the Minister would give us an update on where the department is with Ofsted inspecting the local offer. In Committee, he undertook to write to me, and I must admit that I am not sure whether that letter has been sent; I have not seen it. I would accept it if the Government have decided to inspect the local offer to make sure that people are protected against poor provision.

If they do not want to do that, the next action is regulation. Amendment 33D, as tabled by the noble Lord, Lord Low, would put in regulation to protect people against poor standards. It really does not matter whether it is inspection or regulation—but I do not want it to be the market, which I think is where the Government are headed with this, because that will not work. We have to get the balance right between protecting people in areas where a local authority does not deliver the goods and leaving local authorities that are good, free to excel.

This is not just about safeguarding against low-quality provision: the Government should, equally, be incentivising innovation and high standards. If you only dampen down by inspecting, you will not get the high standards and innovation to which the noble Baroness, Lady Eaton, referred. We have had so many decades of experience in the delivery of public services, and there are good ways of incentivising innovation, rewarding high standards and making sure that those high standards are spread to include everyone else. That is my ideal— to do both. I think that we will see the good quality provision in the local offer to which the noble Baroness, Lady Eaton, referred, and that we will find ways of making sure that other local authorities know about it. Equally, for balance, we need something to set a basic standard below which local authorities’ local offer should not fall so that as regulators and legislators we can say that everybody, no matter where they live, is protected from a poor standard of provision. In that respect, I very much support the amendments that we are considering in this group.

[Baroness Wilkins (Lab)]

My Lords, I, too, support all the amendments in this group. If the Bill really is to improve the position of families of children with SEN in their struggle to give their children the best start in life then it must provide some certainty. Assurances of the provision which a local authority expects to be available are useless if they turn out to be just warm words. Parents need to know what is available, and families must know that there is a benchmark below which standards are not allowed to fall.

Let us not forget that the vast majority of people who find themselves as the parent of a disabled child will have no previous knowledge of the world of special educational need. They will not know what services that their child might need should be available and will have no knowledge of the structure of provision or the standards that they should expect. They will have to learn all of this at a time of great stress and amid all the other demands of family and work life. On Amendment 25E, I particularly support the comments of the noble Baroness, Lady Howe, on the importance of accountability regarding the local offer. As the Education Select Committee said, the importance of the local offer cannot be overestimated.

Given that Clause 30 relates to the local offer as an information offer and not to the actual provision contained in it, can the Minister explain exactly how local authorities will publish their response and what action they intend to take following parents’ comments about the local offer? How will that actually lead to improvements to the services being made? Unless the Minister agrees to move the Government’s Amendment 33C to Clause 27, what do the Government expect local authorities to do with comments from parents about service provision? Is there anything in the Bill to ensure that these comments will be fed into the review of service provision referred to in Clause 27? Moreover, will local authorities clearly explain to parents that they can comment on the local offer only as a source of information and not the provision itself?

As the noble Baroness, Lady Howe, stated, the local offer will be relied upon by 1.4 million children with SEN, namely those without a statement or an EHC plan. Can the Minister therefore clarify, if the child does not have a plan and a local authority publishes a response and follow-up action which was unsatisfactory to parents, are there any further mechanisms in place to ensure that parents’ concerns are addressed?

By the Government’s own figures, the total cost to the taxpayer of parents taking cases to an SEN tribunal is more than £30 million a year. Given this substantial cost, is it not imperative that disputes between parents and local authorities are resolved at the earliest possible opportunity? Amendment 25E, which requires parents, local authorities and others to work together and develop an action plan, would enable this to happen, and I urge the Government to accept it.

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[Baroness Howarth of Breckland]

My Lords, I want briefly to say what I have said several times. If you have a package for education and health, you cannot fail to include the social care element. What I am hoping is that the Minister will give the same answer that he has just given on my previous point—that such provision is contained in the Care Bill. Having looked at the progress made in the way that these services are delivered, that Bill will ensure that the social care element can be provided along with the health element. That is really important because the three are inseparable in the provision of services, particularly for very severely disabled young people. I therefore hope that the answer will be that such provision is already there in another piece of legislation.

[Baroness Wilkins]

My Lords, I, too, add my support for the amendment. For this system to be truly joined up, all parts of the education, health and care plan need to be enforceable; otherwise, social care will be, as has been described, the poor cousin—the element within the EHC plan that will be considered to be of least importance. This is of concern to a wide range of children and young people with SEN and disabilities. We know that parents, too, are concerned about this; in fact, more than 1,000 people have written to the Minister on the issue and asked the Government to ensure that social care will be an equal partner in education, health and care plans. I am therefore encouraged to learn that the Government are looking into the issue in more detail. I very much welcome this and look forward to the Minister’s response.

[Baroness Eaton]

My Lords, perhaps the Minister can clarify what I understood was the situation, whereby there is already in existence a statutory duty under Section 17 of the Children Act 1989 for local authorities to provide services in their area to meet the needs of children in need, including disabled children.

In the case of services for disabled children, under Section 2 of the Chronically Sick and Disabled Persons Act 1970, once the local authority is satisfied that it is necessary to provide assistance under that section, it is under a duty to provide the assistance. It is not, however, necessarily the case that services must be provided to meet every assessed need. Whether a children’s services authority has to provide services following assessment depends on the nature and extent of the need assessed, and on the consequences of not providing the service. These duties have already been the subject of significant litigation, and it may be that imposing a social care duty under the Bill would further complicate an already complex legal position.

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Moved by

[Baroness Wilkins]

48ZA: After Clause 68, insert the following new Clause—
“Inspection and review of local authority special educational needs provision
Services included in the local offer that are delivered or commissioned by the local authority for the provision of specialist education support for children with special educational needs under this Act shall be subject to inspection by an appointed regulator and the findings shall be published.”

[Baroness Wilkins]

My Lords, this amendment is in my name and that of the noble Baroness, Lady Howe of Idlicote, and the noble Lord, Lord Low of Dalston. It would require an independent regulator to be appointed to scrutinise the provision of local authority services for children with SEN and their families. It is a further attempt to address the widespread concern about the lack of accountability in this Bill. As my noble friend Lady Morris of Yardley said in Grand Committee, the whole Bill could fail if parents do not quickly have confidence in the offer. There must be a clear message to parents that there will be a voice speaking on their behalf to make sure that the offer is of good quality.

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[Baroness Wilkins]

I thank the Minister very much for that very full reply. I must admit that I need to take it in more thoroughly and shall read it. I am glad to hear that the department has not ruled out inspection of local SEN support services in the Ofsted review and that that will be heard this summer. However, that will be after the Bill has completed its course.

I thank all noble Lords who have taken part: the noble Baronesses, Lady Howe and Lady Sharp, and the noble Lords, Lord Low and Lord Ramsbotham. I am sure that noble Lords will want to reflect on what the Minister has said and perhaps follow up on the very interesting suggestion from the noble Lord, Lord Ramsbotham. However, for now, I beg leave to withdraw the amendment.

Amendment 48ZA withdrawn.

Children and Families Bill

Baroness Wilkins Excerpts

Tuesday 17th December 2013 Lords Chamber

[Baroness Warnock (CB)]

My Lords, I have added my name to the amendment of my noble friend Lord Low for reasons that I think are a worry for everybody who is concerned with Part 3 of the Bill; namely, the lack of clarity as to how children who do not get an EHC plan will be placed, and the processes by which they are placed. This must be a worry for parents with moderately disabled children as well as for people who are concerned with the clarity—as we hope—of the legislation.

I am not a wholehearted, ideological supporter of inclusion for all children. I think that special schools are enormously important, and there was a time when it looked as though we were going to have specialist special schools, beacon special schools and special schools whose expertise would flow over into mainstream schools much more readily than it does at present. Therefore, I am by no means concerned to uphold a view that would end with all children with disabilities being educated in the mainstream. In some cases, it is very difficult to ensure that children with disabilities do not interrupt or destroy the possibility of the education of other children in the school—this, of course, goes particularly for children with behavioural and emotional difficulties.

The Bill needs to be much clearer on how children will be placed within their local authority area if they do not have a plan made out especially for them—I think that that is still a matter of lack of clarity. Parents find it very difficult to make the decisions and choices that the Bill very properly emphasises, because of the difficulty of access to exactly what the ordinary, mainstream school will be able to offer their child. I know that a large number of parents want mainstream education for their children whatever their disabilities, whether they are going to get the best possible education and the best possible chances or not—it is a fixed belief that it is a right for a child to be educated in the mainstream and for parents to make that demand.

Parents who are genuinely interested in finding the right school for their child who has a disability, but may not be severely disabled or have a complex disability that speaks for itself, need the means to make a properly informed choice. That is why I like the wording of my noble friend’s amendment—although I find the grammar rather difficult—and why I strongly support it.

[Baroness Wilkins (Lab)]

My Lords, I speak in strong support of the amendment of the noble Lord, Lord Low, which is set out so comprehensively and to which I added my name. If accepted, it will reassure those of us who are concerned that elements of Part 3 of the Bill could weaken the right of disabled children and young people with SEN to be included in mainstream education. Sadly, the noble Baroness, Lady Campbell of Surbiton, is not able to be in her place today because, like many people, she has a bad cold. But many noble Lords will have heard her give eloquent testimony of the blight that her segregated education laid on her life. It was not necessary, and it is something that has never left her.

It would be welcome if the amendment were further strengthened by extending the duty to post-16 providers, to ensure consistency for disabled learners across the educational experience. Local authorities such as Nottingham, Calderdale and Newham have used such duties to good effect. They have provided specialist support services and training for mainstream schools so that those schools are confident in implementing inclusive educational practice. This has increased the number of disabled children and young people with a wide range of impairments and health conditions being included in mainstream education. But while some local authorities have been proactive in promoting inclusive education at a strategic level, a lot of work still needs to be done to support the development of inclusive education across the country, especially when half of our disabled children and young people with SEN are still being placed in segregated educational provision.

I am very concerned that without an explicit duty, local authorities will become complacent—and, more worryingly, will revert to the practice of investing increasingly limited resources in existing segregated, rather than inclusive, educational provision. For instance, Kent County Council is already investing heavily in special school provision. Nigel Utton, a Kent County Council primary school head teacher and the chair of Heading for Inclusion, is quoted as saying:

“About half the children with statements in Kent are in special schools, with so much resource being targeted at special provision (not to mention the huge transport costs incurred) mainstream schools are left with a very small proportion of the special needs budget. The pressure on mainstream schools to achieve high academic standards, combined with budgetary pressures, is forcing many to not accept children with SEND statements or to persuade parents to leave”.

Such investment in special schools is not compatible with the Government’s Article 24 obligations. One such obligation is to develop and promote inclusive education across the country by building the capacity of mainstream schools to support the inclusion of disabled learners. The situation will only worsen if the Bill, and the draft SEN code of practice, do not include the explicit duty to promote inclusive education practice. I urge noble Lords to support the amendment.

[Baroness Lister of Burtersett (Lab)]

My Lords, I am glad to be able to follow my noble friend, who has made a powerful case. As a member of the Joint Committee on Human Rights, I simply want to put on record my thanks to the noble Lord, Lord Low, for taking the committee’s recommendation forward and for making the case for it so cogently. The committee saw this as a matter of principle. It is a principle that the Government do not disagree with, and I am at a loss as to why they have been so resistant to accepting that it should be in the legislation. I hope that the Minister will think again.

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Moved by

[Baroness Wilkins]

18C: After Clause 22, insert the following new Clause—
“Data on the number of children and young people with special educational needs and disabilities
(1) A local authority in England must publish information annually within the local offer on the number of children and young people in its area who have special educational needs and disabilities.
(2) Information under subsection (1) must be published by type of special educational need and disability.”

[Baroness Wilkins]

My Lords, I hope that the Government will agree to this amendment. Clause 22 requires local authorities to identify children with special educational needs. This amendment would require the local authority to publish these data within its formal offer. I have tabled the amendment because I am concerned about the availability of good-quality data on children with SEN and disabilities. It is an important issue, which could well determine the success of the Government’s proposed reforms.

Accurate data on the number of children in their area is vital for local authorities effectively to plan and deliver services. The draft SEN code of practice, particularly in the section on joint commissioning, outlines the importance of local data sets in identifying the needs of children with SEN and in informing their decision-making. Without good-quality data, it is difficult to see how the Government or local authorities can effectively plan and commission services for children with SEN and disabilities. It also means that we have a very weak basis on which to determine the long-term impact of these changes.

I am pleased to see that the Government will be amending the Bill so that local authorities have a clear duty to identify children with disabilities, as well as those with SEN. However, there is compelling evidence that existing data sets are failing accurately to identify all children with SEN and disabilities. Currently, data from different sources for the same area can vary widely. Using deafness as an example, I know that different figures on the number of deaf children vary by as much as 30,000: according to the disability register, there are 7,500 deaf children; according to the school census, there are 16,000; and, according to the National Deaf Children’s Society’s survey of all 152 local authorities in England, there are 37,500 deaf children.

Sense has also identified a widespread failure accurately to identify numbers of children who are deafblind. In the local authority of Kensington and Chelsea, Sense has found that, according to the prevalence data, there should be around 10 deafblind children. However, the local authority has identified four. How many have been identified by the school census? The answer is none. These children urgently need specialist SEN support, so why is the system not capturing them?

In Grand Committee, the Minister enumerated the various sets of data that are published but failed to acknowledge that the existing data sets are inadequate. For example, the Special Educational Needs in England report does not cover all children with SEN and so misses more than 40% of school-age deaf children. A single data set is needed to bring together all the data from different sources into a format which would ensure well informed commissioning decisions.

It is difficult to see how the Minister’s department will meet the ambitions set out in the Bill unless we have a reliable and single data set that accurately captures all children with an SEN and disability. The current state of affairs cannot be allowed to continue whereby 152 local authorities are left failing correctly to identify and record all children with SEN and disabilities. I hope that the Minister will give the House reassurance that the urgency of this matter is recognised and that work is in hand to ensure that commissioning can rely on accurate data before this Bill comes into force. I beg to move.

[Baroness Howe of Idlicote]

My Lords, I support the amendment tabled by the noble Baroness, Lady Wilkins. Good quality data on children with SEN and disabilities must be in place before we proceed with these reforms. Unless action is taken, there is a clear risk that some children will continue to fall through the net. The department’s draft SEN code of practice acknowledges that issue and specifically highlights the importance of quality data on children with low incidence needs. Given that these children’s needs are relatively less common, there is an even greater need to establish their needs and whether local provision is sufficient to meet them.

However, as the noble Baroness, Lady Wilkins, has pointed out, existing data sets are flawed. The code of practice refers to the disability register. However, in the case of deaf children, I understand that it is identifying only around 7,000 to 8,000 children, whereas other estimates suggest that 40,000 would be closer to the truth. I understand that the department recently published guidance to local authorities on implementation of the new nought to 25 special needs system. In that, the Department for Education asks local strategic leaders to consider what their data tell them about local outcomes for children and young people with SEN.

My concern is that, whatever these data tell them, they are not going to give a reliable or accurate impression of children with SEN because the underlying data sets and systems are so fundamentally flawed. I hope that the Minister will be able to reply positively in support of this amendment or indicate that positive action is being taken to address these concerns.

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[Lord Nash]

My Lords, I would like to thank the noble Baroness, Lady Wilkins, for raising this important issue and noble Lords who have spoken on this matter. I accept noble Lords’ concerns on this. I understand that the noble Baroness’s purpose behind tabling the amendment is to put, as the noble Baroness, Lady Howarth, has said, local authorities and schools in a better position to make good commissioning decisions. Good commissioning is clearly an important underpinning to the reforms that we are making and the Bill already provides for joint commissioning arrangements across education, health and care for the provision that is reasonably required for local children and young people with SEN. That commissioning will be informed by the local joint strategic needs assessment and the data that are already available on these children and young people.

I accept absolutely that good data need to be available to inform commissioning, but I do not think that the local offer is the right place to publish that data. The purpose of the local offer is to set out what provision children, young people and families can expect in their local areas and it is to be used as a vehicle for discussion about the development of local services. It is not designed to publish information on the numbers of children and young people in the area with different types of SEN. It would not be appropriate to clutter up the local offer with such data. We accept that that information will be material to discussions about the development of provision in the local area, but that information is available elsewhere.

The department already collects data from schools and local authorities on the number of children with special educational needs and publishes this annually on the department’s website. This includes data about the number of children by type of special educational need and we will be expanding this information. At present, we publish data by type of need for children at school action plus and with SEN statements. However, as we move to the new system for school-based SEN support, we will also publish data by type of need for children who are currently at school action.

For disabled children, local authorities are already under a duty to maintain a register of disabled children and young people under Section 17 of, and Schedule 2 to, the Children Act 1989. The draft, new SEN code of practice reminds local authorities of that duty. The department also collects data on children in the early years through the early years census. For post-16, the Education Funding Agency and the Skills Funding Agency also collect data on young people in the further education sector, through the individualised learner record on a range of types of need. Requiring local authorities to publish this data in the local offer would just replicate data that is already available.

So far as bringing together these different data sets into one place is concerned, as I said, I do not believe that the local offer is the appropriate place to do this, and I do not think it is right that central government should impose on local authorities something that they should already be doing. Some local authorities may well be poor at carrying out their duties in this regard, but that is not a legislative issue: it is a matter of practice. We have made it clear in the code that local authorities have this duty.

The noble Lord, Lord Low, talked about incomplete data. It is true that SEN data from the early years census, although available on request, is not routinely published publicly, but we will make sure in future that it will be and will be linked up to the main SEN statistical publication. I assure noble Lords that the department is thinking about what the new arrangements in the Bill imply for data collection and we are seeing where there are possibilities for greater clarity and the joining up of data sets. The post-16 data that are collected by the department, the Education Funding Agency and the Skills Funding Agency are publicly available on a number of websites, and we are looking at ways to bring these together for greater clarity.

Indeed, more generally, we are looking to see how data can be brought together to reflect the new nought to 25 arrangements under the Bill. We will also consider whether there should be a collection of disability data from schools. I would be happy to discuss this further with the noble Baroness and any other noble Lords who are interested. On that basis, I ask the noble Baroness to withdraw her amendment.

[Baroness Wilkins]

My Lords, I thank the Minister for that reply. Unfortunately, agreement has not continued from previous amendments. I thank all other noble Lords who contributed to this debate, but I find the Minister's reply extremely disappointing. He said that the local offer was not the place to put this information and that it would be cluttered up by it. But he then went on to enumerate various forms of collection of the data which fail to recognise that it is the quality of the data that are collected that is so criticised at the moment: it is failing to provide its purpose. It seems key that, without reliable data, local authorities will not be able to commission the services that are needed.

I will read what the Minister has said in Hansard and consider this further. As I said, I am disappointed in his reply, but, for the moment, I beg leave to withdraw the amendment.

Amendment 18C withdrawn

Children and Families Bill

Baroness Wilkins Excerpts

Wednesday 6th November 2013 Grand Committee

[Baroness Wilkins (Lab)]

My Lords, I add my strong support to Amendment 181. My noble friend Lady Hughes has just refereed to Jane Raca. Anyone who has read her book, Standing Up for James, will know that there is an urgent need to improve the current system of support for families with disabled children. However, the Government’s proposals for appeals risk creating an even more complex system than already exists, with different appeals or challenges having to be made simultaneously, as we have heard, about different parts of the EHC plan to different bodies.

In her book, Jane Raca recounts the situation of her local vicar’s family. The Tomlinsons have six children, including Edmund, who is 14 and severely autistic. Ed does not speak and has no sense of danger or of what is socially appropriate, He is very often awake at night, meaning that Matthew and Joanna, his parents, have very little sleep. Although Ed’s statement provides for him to attend a weekly boarding school for autistic children, he is at home every weekend and all school holidays. Despite that, his parents receive just 27 nights’ respite a year, which they try to eke out during the school holidays. They got that only when they broke down completely in front of their GP.

That is far too little support but, as Joanna Tomlinson says, she just did not have the strength to fight for what the family needed and for Ed’s needs to be looked at holistically. The Bill holds out hope for that. Joanna knew that her local authority would not have agreed to fund both the education and the social care provision, and that she would have had to fight to appeal on both fronts. The Bill will perpetuate that unless we accept these amendments. If we do not, parents will still have to face three different processes if they wish to challenge the content of EHC plans. I urge the Minister to accept this amendment.

[Lord Touhig (Lab)]

My Lords, I will just add a few words. This multilayered system of appeal is absolutely insane and crying out to be altered. In Wales, we have a word, “dwp”, which means stupid or daft in the head. If a Nobel prize were awarded for daft bits of red tape, this would get it. Surely the Government must see the common sense and logic of reducing this down to one system of appeal and stopping all the battles that people who have children with special educational needs or disabilities, or children who are autistic, must have to appeal a decision that they think is not just, right or in the interests of their child.

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[The Countess of Mar (CB)]

My Lords, I, too, support the noble Lord, Lord Addington. The noble and learned Baroness, Lady Butler-Sloss, hit the nail on the head when she said that she has relatives who have been to university and got degrees, with assistance, because they are dyspraxic. My granddaughter has dyspraxia. She is at the University of Lincoln at the moment and doing very well. She is getting “ones” right across the board because she is given extra time to do her written work. That has been accepted. Why do we not do it with apprenticeships? It seems ridiculous that we are putting these kids on the scrapheap. We criticise young people for not going out to work, and when they try to get qualifications, we fail them. To fail is disillusioning for these youngsters. They will not want to go to work if they think nobody wants them. The noble Lord, Lord Addington, and the noble Baroness, Lady Walmsley, have a very valid point.

[Baroness Wilkins]

I support this group of amendments. I am mildly dyslexic, and I assure noble Lords that in terms of daily frustration, it is a million times more frustrating than being in a wheelchair. There is a great deal of support for being in a wheelchair, but there is very little support for being dyslexic. The Government are to be admired for their commitment to apprenticeships, and it seems a tragedy that it should be undermined in this way, so I beg the Minister to accept these amendments.

[Lord Low of Dalston]

My Lords, the noble Lord, Lord Addington, has had a pretty good run for his money and has got not only unanimous but very voluble support from the other Members of the Committee. I would not detract from that one whit. I support every word he said and what others have added, but I wonder whether I may crave the Committee’s indulgence to make a slight change of subject.

I shall speak to Amendment 192 in this group, which is tabled in my name and the names of the noble Lord, Lord Touhig, and the noble Baroness, Lady Sharp. It is a probing amendment which would require schools to retain the current system of school action and school action plus. We may not have formulated the amendment perfectly, and I am sure there is room for plenty of discussion about how it might be focused or targeted more precisely. I am anxious to learn more about the Government’s thinking in seeking to abolish the current stages of school action and school action plus. As we know, the Government are replacing that graduated approach with a single SEN category. The amendment refers to schools, but my concerns also relate to how early years settings and post-16 institutions will meet the needs of children and young people with SEN.

My reason for tabling this amendment is that, like the Government, I believe that policy should be developed on the basis of robust evidence. Changing the way the SEN system operates in every English school and early years setting could be very disruptive. We need to be sure that any change will genuinely improve outcomes for children and young people before we embark on what is quite a major change. From what we have heard so far, it seems that the Government’s intention here is to improve the identification of special educational needs. The Ofsted report, A Statement is not Enough, published in 2010, suggested that some children and young people were being wrongly identified as having special educational needs.

Improving the identification of special educational needs is a goal everyone would support. However, my understanding is that the Ofsted report did not in any way indicate that the problem resided in the graduated approach of school action and school action plus. The same is true of the Lamb inquiry, which also picked up on the issue of identification, but did not indicate in any of its 51 recommendations that the problem arose from school action and school action plus. Neither of these important investigations proposed the removal of the current system, so I wonder on what evidence the Government are basing their decision to move to a single category of SEN. Everyone has been encouraged by the reference in the recently published draft code of practice to “a graduated response”. Since the Government remain committed to a graduated response, which is provided by school action and school action plus, one wonders why they are so insistent on the need for this change.

I should also like to pick up on the fact that the draft code of practice removes guidance on the use of individual education plans. IEPs were a key feature of the school action and school action plus system. They set out educational targets, the agreed SEN support and how progress would be measured. They require schools to involve children, young people and their parents in the process and are vital for parents when holding schools to account. When used properly, IEPs are a simple and effective way of recording targets, putting support in place and tracking the child’s progress. While they might not always be used as effectively as they might be, would it not be better to seek to improve the way IEPs are used than to scrap them altogether?

The Government are not opposed to schools retaining these types of records. The draft code says that schools should keep records and that these can be shared with parents. Again, therefore, one is prompted to ask why the Government are getting rid of something so valued by parents when they continue to support the principles behind it. I would be extremely grateful if, when he responds to the debate, the Minister could set out the Government’s thinking and give us the rationale for these changes and, in particular, the evidence on which they are based. It seems that the Government still support the principles of a graduated approach and keeping good records, so it is important that we understand why we need what is really quite a major change.

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[Baroness Howe of Idlicote]

My Lords, this amendment would insert a new clause imposing a duty to secure sufficient communication support for parents of children with hearing loss. The amendment would create a new duty on local authorities to ensure that families with deaf children have access to communication courses on communicating with their children. Some 90% of deaf children are born to hearing parents, many of whom have little or no prior experience of deafness. As well as the usual emotions that parents face when they learn that their child is disabled, parents of deaf children face a battle in learning how best to communicate with that child, particularly if they need to learn sign language.

Of course, sign language will not be appropriate for all families and children, but that option must be there if parents are to be able to play their important role in developing their children’s language and communication skills. I do not need to stress to the Minister how important and fundamental communication within the family is. It is the strongest influence on language development at age two. Money spent here to achieve those skills can be an absolutely invaluable investment. Indeed, failure to support communication within the family is a false economy. It condemns deaf children to a life of frustrated potential. We already know that by the time they start school, four out of five deaf children have failed to achieve a good level of development within the early years foundation stage.

The National Deaf Children’s Society believes that supporting families with deaf children on communication is more than just common sense and should be regarded as a basic human right. We must do more to ensure that families with deaf children can communicate with those children. Sadly, at present, I do not believe that we are doing enough. In a survey in 2011, the NDCS found that more than half—56%—of local authorities did not provide any support to families who needed to learn sign language to communicate with their children. The other half were found to be patchy and uneven in terms of exactly what they provided.

Some families have faced an agonising choice of deciding whether the mother or the father would be able to learn sign language, because local authorities have made funding available for only one person or because there is no childcare funding available. When this matter was raised elsewhere, the Government, alas, left it to the local authorities, saying that it was a matter to them to decide. Is the Minister confident that local authorities understand how important communication support for families is? Is he as concerned as I am, and as many others are, that more local authorities do not already make it available?

I acknowledge that the department has funded a range of projects to improve sign language provision to families, including the I-Sign consortium. That is welcome and certainly much appreciated. I also acknowledge the department’s hope that the Bill will address some of these difficulties, particularly through local offers and personal budgets. However, I would welcome the Minister’s views on whether he thinks this is likely to lead to the step change in provision that deaf children badly need—not in the future but here and now.

Is he confident that sign language courses will be included in local offers? Is he confident that courses would even be available to families should they wish to use their personal budgets for this purpose? Is he confident that local authorities will engage with, and listen to, families with deaf children on this matter? We must remember that deafness, as we have already heard from the noble Baroness, Lady Walmsley, is a low-incidence disability. Many local authorities are unlikely to be familiar with the needs of deaf children, who will always be one of a range of competing needs. Therefore, without a clear duty on local authorities, I and many others are concerned that sign language provision for families will continue to be patchy and progress will continue to be piecemeal. Surely, deaf children and their families deserve better and I hope that the Minister will seriously consider this amendment and its implications. I beg to move.

[Baroness Wilkins]

My Lords, I will speak briefly to support the amendment moved by the noble Baroness, Lady Howe. She has made a strong and clear case for action. This issue has been raised elsewhere several times and the fact that it continues to be raised must show the Minister the strength of feeling on it. The current approach of asking voluntary bodies to support improvements in individual local areas is just too piecemeal. The progress being made is far too slow, and deaf children are suffering because of it. Access to communication support for families with deaf children and young people is fundamentally important; the Government must send a clear signal to local authorities that it should be provided where needed. Otherwise, we will be here in 10 years’ time, still having this debate about the lack of sign language provision for families. I beg the Committee to support this amendment.

[Baroness Walmsley]

My Lords, I, too, rise to support the amendment of the noble Baroness, Lady Howe, and agree with the points that she has already made. In July 2011, the Prime Minister said in response to a Question from my right honourable friend Sir Malcolm Bruce MP:

“We do a lot to support different languages throughout the UK. Signing is an incredibly valuable language for many people in our country. Those pilot schemes were successful”.—[Official Report, Commons, 13/07/2011; col. 308.]

The scheme that the Prime Minister was referring to was the I-Sign consortium, which has piloted family sign language classes in two regions. NDCS, with support from the Department for Education, continues to work to support the development of sign language courses. However, local authorities cannot be compelled to provide sign language support because there is no duty to do so. As has already been outlined, a very high percentage of deaf children are born into hearing families who have no previous first-hand experience of deafness. These families really need support to communicate with their child, particularly where sign language is chosen.

It has been estimated that where deaf children need to communicate in sign language, eight out of 10 parents of deaf children never learn how to communicate with their child through sign language. Without the right support from the start, deaf children and young people are vulnerable to isolation, abuse, bullying, poor self-esteem and low levels of attainment. We have already heard from the noble Baroness, Lady Howe, how local authorities are very patchy in their provision of sign language services.

The SEN reform in this Bill offers the potential to generate a step change in the provision of sign language courses for families. For example, personal budgets may enable families to pay for this support themselves. However, while SEN reform might generate more demand for sign language courses, it really will be useless while local authorities can walk away, which is very damaging to deaf children and their families.

Children and Families Bill

Baroness Wilkins Excerpts

Monday 4th November 2013 Grand Committee

[Lord Low of Dalston (CB)]

My Lords, I have added my name to Amendments 137, 145, 165 and 173, but I do not propose to speak to them in any detail because we have been on this debate for a good long time. We have heard a number of full and eloquent speeches and I do not wish to go over what noble Lords have said. However, I should like to add a couple of points.

The Government are presumably worried that parents and young people will assume that they have an automatic right to an education, health and care plan up to the age of 25, but that is not something that the Government need to be too worried about. Most young people will not want to stay in education until they are 25. As the noble Lord, Lord Touhig, said, these amendments do not seek a blank cheque for continuing education for all young people to the age of 25 regardless of the type and purpose of the course they are pursuing; rather, they envisage local authorities supporting young people to achieve their agreed education, health and care plan outcomes, allowing them to progress to a job, develop their independent living skills, make an economic contribution to their community and avoid swelling the ranks of those who are not in education, employment or training.

I do not think that age needs to be mentioned at all, as the noble Baroness, Lady Howarth, just said. Most young people will achieve their education, health and care plan outcomes well before the age of 25, as they do now. Young people must have the opportunity to continue their educational programmes to achieve their agreed outcomes in age-appropriate settings in order to make the transition to adulthood, including work and independent living. These amendments will ensure that the existing protections for 16 to 25 year-olds are not lost.

In that connection, Ministers have stated that no one should be worse off as a result of the Bill. Currently, the learning difficulty assessment statutory guidance requires local authorities to maintain learning difficulty assessment and support to allow the young person to achieve their potential in employment and independent living up to the age of 25. That is in part a recognition of the fact that some disabled people may take longer to reach their potential.

The Bill should therefore not derogate from what is provided for in the current learning difficulty assessment guidance. As the noble Baroness, Lady Cumberlege, told us, independent specialist providers support many students who need a longer period to complete their studies or training. Many such providers also have significant numbers of students who become disabled for the first time as they approach adulthood, which obviously delays their educational progress. Decisions about whether to maintain a young person’s education, health and care plan beyond the age of 19 should be based solely on the young person’s progress in relation to their planned outcomes. Their age up to 25 is not the most significant factor. Focusing disproportionately on age will divert attention from supporting the young person to achieve the agreed outcomes in their education, health and care plan, which should be the prime consideration throughout.

[Baroness Wilkins (Lab)]

My Lords, I support Amendment 172 tabled by the noble Baroness, Lady Howe. I will not extend much further this excellent debate. It is very important that the Bill and the accompanying guidance is clear on the need to maintain specialist support when this is needed. It should not simply be cut when a child starts to do well. On this point, it seems that there is an inherent tension in the draft code of practice that needs to be resolved. I would be grateful if the Minister would look into this.

On the one hand, the definition of special educational needs includes children or young people who have a disability which prevents or hinders them from making use of the educational facilities of a kind generally provided for others of the same age. There are some groups of children, such as those who are deaf, to which this particularly applies. The implication is that these children have a special educational need by virtue of the fact that they are in need of specialist support to enable them to access those same educational facilities. However, there are times in the code of practice, from the tone of what is being said, when the reader can be forgiven for thinking that only children who are not making progress should be regarded as having a special educational need. For example, on page 75, it is suggested that SEN specialists should be involved when it becomes apparent that the child is making little or no progress. Many believe that this reflects a tension between the special educational needs framework of supporting children who fall behind and the disability equality framework of taking proactive steps to support disabled children.

Will the Minister look again at this to make sure that it is crystal clear that no local authority should cut support for a child because they are making good progress when it is only because they are receiving that support that they are able to make that good progress? I would also welcome his clarification for the record that children who need specialist support, such as deaf children, should be regarded as having a special educational need regardless of whether they are falling behind or making good progress.

[Lord Nash]

My Lords, I am grateful to all who have spoken in this important debate. I know that we all share the same concern to ensure that young people who need educational provision up to the age of 25 will receive it. I hope that I can offer some reassurance and will be delighted to discuss the matter further with my noble friends Lady Cumberlege and Lady Sharp, the noble Baronesses, Lady Howe and Lady Howarth, and others if that is not the case. I will first respond to those amendments regarding the genuine worry that the various clauses which require local authorities to “have regard” to a young person’s age when they are over 18 will give local authorities the ability to refuse to assess a young person or to cease their plan based solely on age.

From the outset, I would like to state categorically that this concern is unfounded. Local authorities cannot make decisions based on a young person’s age alone. The legislation requires local authorities to maintain EHC plans while it is necessary for special educational provision to be made for the young person in accordance with a plan. The draft code of practice makes this completely clear, stating in Chapter 7 that local authorities must not make decisions based only on the fact that a young person has turned 18.

Let me be clearer still: our vision is for a system that is ambitious for children and young people with special educational needs. There is no hidden agenda to cut costs or to reduce the number of families we want to help. Instead, we want a system that raises the aspirations not only of children, young people and their parents, but of those professionals working with them, and that has high expectations about what children and young people with SEN can achieve. Our ambition is that with the right support and opportunities, many more of these young people will have completed their education and made a successful transition to adulthood at the age of 18, along with their peers. Our vision is that where young people need longer to complete or consolidate their learning, they are able to remain in education and continue to receive co-ordinated help and support through their EHC plan—until the age of 25 if necessary.

What we must not do is create an expectation in law that all young people with SEN will simply stay in formal education until age 25. Creating an automatic right for all young people with EHC plans to remain in education for that long would dilute the focus on outcomes that we want throughout the new system and particularly from year 9 onwards. Local authorities could delay proper consideration of outcomes until after age 18, by which time it is likely to be too late, and many young people will simply drop out of the system at that point, as happens now. Worse, it could create a cliff-edge at age 25, when support would have to end for all those with EHC plans regardless of whether outcomes had been met. Surely the focus must instead be on supporting them to achieve outcomes and make a successful transition to adulthood, wherever possible, along with their peers. We need to end the presumption of failure attached to special educational needs and make sure that local authorities are doing all that they can to help many more children and young people with SEN achieve positive outcomes by age 18.

Turning to the point made by my noble friend Lady Cumberlege about the word “must”, we think that adding it to Clause 45 would serve to create an expectation that all young people with EHC plans should remain in education until after 25. On the question of why we refer to 18, and not 19, a young person aged over 18 has the legal meaning of a person who is aged 19 to 25, and it is our intention for the clause to apply to 19 to 25 year-olds. I hope that that provides some clarification.

The noble Baroness, Lady Howarth, asked why we use the phrase “have regard to age” at all. Following pre-legislative scrutiny, the Education Select Committee stated that there was confusion about whether the Bill created an entitlement for young people with EHC plans to remain in education until 25. It recommended that we make that clear in the Bill. Including the phrase “have regard to age” is our best solution to address that recommendation. It simply requires local authorities to take a young person’s age into account as part of a range of things that they must consider when making decisions. All other suggestions that we have had err on the side of creating a presumption that young people should remain in education until 25 unless certain conditions are met.

Young people with SEN over the age of 18 must be supported to remain in formal education where this will enable them to complete or consolidate their learning, achieve outcomes and make a successful transition to adulthood. Local authorities must, in consultation with young people, consider whether that has already been achieved by the time compulsory participation ends at age 18 or whether the young person needs, and indeed wants, further support through an EHC plan. We have made it clear in the draft assessment and plan regulations and code of practice that the EHC plan process should prepare and support young people for adulthood, facilitating a successful handover to new opportunities and support in the adult world. That transition planning must start from year 9 of a child’s schooling and continue until they have left formal education and made a successful transition to adulthood. This includes enabling young people to access learning opportunities, such as those offered by the Chailey Heritage Foundation, which prepare young people to live more independently. Such opportunities are a vital part of what is needed and I am grateful to my noble friend Lady Cumberlege for enabling me to see at first hand, in an extremely impressive and moving visit to Chailey, what a difference such approaches can make to the lives of those with complex needs.

Not only do our reforms protect the current position for those aged 19 to 25, they go further by creating a legislative requirement for local authorities to focus on outcomes and prepare young people for adulthood. In addition, where young people disagree with decisions made by local authorities, they now have—for the first time—the right to appeal to the tribunal.

It is right that once these educational outcomes have been achieved, local authorities should no longer be required to maintain EHC plans. Young people with ongoing health and social care needs will continue to receive those from the relevant services; that will not stop simply because they no longer have an EHC plan. Young people who have made a successful transition to adulthood and are now in employment, higher education, adult learning and so on will continue to receive support in those settings to enable them to maintain and build on the outcomes achieved while in formal education. For example, Access to Work is available for those in employment, Disabled Students’ Allowances for those in higher education and so on.

Children and Families Bill

Baroness Wilkins Excerpts

Tuesday 2nd July 2013 Lords Chamber

[Baroness Wilkins]

My Lords, I welcome the Government’s intention to reform the special educational needs system in England. However, I share the disability sector’s concerns, echoed by many noble Lords, that the Bill still requires major improvement if it is to deliver better outcomes for children and young people with special educational needs or disabilities. Worryingly, in some areas the Bill does not protect existing rights and risks making matters worse. I will not repeat the points made by many other noble Lords. I will concentrate on the further action needed to address the challenges and difficulties faced by children with sensory impairments.

We sometimes talk about children with special educational needs as if they were a single entity to which we can apply single, catch-all solutions. That is clearly not the case, as is demonstrated by children with sensory impairments. Sensory impairment is a low-incidence need. Most mainstream professionals are unlikely to have regular contact with such children with which to build up expertise on how to meet their needs. Instead, this expertise is likely to be centred in relatively small, specialist support services and teachers.

It is not clear to me that the department’s proposals on SEN reform fully recognise the importance of specialist SEN support services. Further action is badly needed to ensure that these services are able to do their job—ensuring that every child with a sensory impairment is able to fulfil their potential. We first need to look at the funding of these vital services. The National Deaf Children’s Society has established that in this year alone 29% of local authorities are making cuts to specialist education services for deaf children. RNIB and Sense believe that similar cuts are taking place in other sensory impairment services. These cuts are having a devastating impact. Distressed parents who have fought so hard for their child to get the support they need are now seeing support being taken away. They talk of their children’s futures being stolen.

Last year, just 37% of deaf children achieved five good GCSEs, compared to 61% of children with no identified special educational need. That is a massive attainment gap. It is painfully unnecessary when you consider that deafness is not a learning disability and that deaf children should be doing as well as other children. Deaf children and other children with sensory impairments need more support, not less. When this was raised during the passage of the Bill in the other place, the Parliamentary Under-Secretary of State for Children and Families indicated that his department would not intervene and that it was for local communities to challenge any such cuts. This is shamefully complacent. The department has made a commitment that funding for these services will be protected and yet seems unperturbed that 29% of local authorities are not doing so in relation to deaf children.

What assurances can the Minister give on the success of the Bill, knowing that there is a clear risk that in many areas funding cuts will fatally undermine its ambitions and result in children getting less support? Where are the specialist teachers to advise on a child’s education, health and care plan going to come from unless there is action to protect these services? Who will provide early intervention services? What will families buy with their personal budgets? Without adequate funding to provide these services and staff, it is extremely difficult to see how SEN reform can be made a success. Parents of children with sensory impairments deserve better than this complacency when it comes to their futures. They need the department to take action, not pass the buck to local authorities and communities.

That brings us to accountability. Many of these measures place the burden of holding local authorities to account almost entirely on the shoulders of parents. Not all parents will be able to, or necessarily want to, take this role. The vast majority were not knowledgeable about the world of special educational needs and disability, and are desperately feeling their way, trying to discover what will best help their child. They are busy being parents to all their children, and the parents of children with special educational needs have plenty to do already.

I am surprised to learn how little information is available to parents or professionals on the quality of SEN support services in their area and how little the Bill does to address this. There is no specific requirement to publish information about local authority SEN support services, despite the importance of these services to children with sensory impairments. It does not appear that local authorities would have to publish information by type of need, and they might therefore simply publish generic information about SEN. Nor does it appear that the Government will require the local offer to follow a set format—most importantly with clear expectations for minimum provision—which will make it harder for parents to compare provision in different areas. I understand that the department has been considering representations that Ofsted should inspect specialist SEN support services. I hope that the Minister will be able to update us on the department’s considerations on these concerns and that progress can be made before we further discuss this Bill.

Crucially, will the Minister ensure that the department does much more to ensure that children with sensory impairments get the help that they need from specialist SEN support services? These are the issues that he must address if he wishes us to have confidence that the Bill will make a positive difference to all children, including those with sensory impairments.

Academies Bill [HL]

Baroness Wilkins Excerpts

Tuesday 13th July 2010 Lords Chamber

Moved by

[Baroness Wilkins]

2: Clause 2, page 2, line 43, at end insert—
“( ) In Schedule 1 to the School Finance (England) Regulations 2008, after paragraph 8 insert—
“8A Where a child is a registered pupil at an Academy, expenditure in respect of services for making provision for pupils with low incidence special educational needs or disabilities.”
( ) Where a local authority fails to secure satisfactory provision for pupils with low incidence special educational needs or disabilities, the Secretary of State may make alternative arrangements.”

[Baroness Wilkins]

My Lords, this amendment is also tabled in the name of the noble Baroness, Lady Howe of Idlicote. Both in Committee and on Report I have spoken about my concerns that a large increase in the number of academies will have the unintended consequence of dispersing funding for children with low incidence or complex special educational needs. As a result, vital support services for these children and their parents will become untenable, and there could be large numbers of deaf and blind children and others with multi-sensory impairments who do not get the support they need.

These concerns have received the support of all sides of the House and I am grateful to all noble Lords who have spoken. They are also shared by the National Sensory Impairment Partnership, the Special Educational Consortium and, particularly, the National Deaf Children’s Society, RNIB and Sense. I should like to thank the noble Lord, Lord Hill, and his officials for taking the time to meet with me yesterday afternoon, as he offered to do on Report, and it is therefore with regret that I must speak again to say that these concerns have still not been addressed. Sadly, while the Government are willing to recognise that the problem is real, they have shown no real urgency in coming up with a way forward. As the Special Educational Consortium points out in its briefing, the Government should recognise that there is a need to address the impact of the Academies Bill on individual children currently receiving specialist provision when a number of schools convert to academy status in September 2010.

I am alarmed that the Government should seek to pass this Bill knowing that potentially it could damage the educational prospects of some of the most vulnerable children in the country. The number of children may be small and the impact may not be immediate, but that is no excuse for failing to come up with a solution that will reassure parents and children that they will get the support they need. The National Sensory Impairment Partnership believes that the Government should set up a working group to consider solutions. The working group should be time-limited and have clear terms of reference to consider this issue and make urgent recommendations. The group must be led by Government and its recommendations must be communicated by the Government to all local authorities and schools across the country. I stress that the working group should also include representatives of the parents of children with sensory impairments, and I strongly urge the Government to accept the recommendation.

I hope that the Minister can give a positive reply before the Bill moves to the other place. But in the absence of that positive response, I have spoken to Members of the other place who have said that they will continue to raise this matter until we are certain that the educational prospects of disabled children will not be damaged by these proposals. I beg to move.

[Baroness Howe of Idlicote]

My Lords, I, too, support this amendment, as I have done on previous occasions. It is sad indeed that the Minister has not yet been able fully to satisfy our concerns. Disabled children and those with SEN often need specialist support to ensure that they achieve positive learning outcomes. These services are crucial for pupils with a wide range of disabilities and have a unique role to play in the education of children with low incident disabilities such as blindness, partial sight and hearing impairments.

Specialist support services are not focused solely on the delivery of the curriculum. They also provide much-needed training and skills to support independent living, and examples of some of those specialist services give a clear view. I cite the teaching of Braille and of British sign language, independent living training to enable independent personal care skills and home skills, mobility instruction and pre-employment support. Local authorities have traditionally provided specialist support services to all schools, using funds retained from school budgets to ensure adequate provision throughout their areas. There are strong concerns that, as academies move out of local authority control, so will their revenue, reducing the amount available overall to specialist support services and relying on academies to commission the services they require. I hope that while the Bill is still with us, we will have further assurances from the Minister. Otherwise, as the noble Baroness, Lady Wilkins, said, the issue will come up again in the other place.

--- Later in debate ---

[Lord Hill of Oareford]

My Lords, I am grateful for the points that have been raised in this debate. We have, rightly, spent a lot of time on this Bill talking about various sensitive issues to do with our most vulnerable children. As I said in Committee and on Report, I accept the practical concerns raised by the noble Baroness, Lady Wilkins, and others. When we met yesterday, we went through some of those. I hope that some of the answers I can give this afternoon may take us a little further. However, I certainly recognise the concerns that she has raised.

The noble Baroness, Lady Wilkins, and others have been kind enough to accept that, with the parameters within which I am operating, I have sought in general to approach SEN issues throughout this Bill with an open mind and, so much as I have been able, taken concerns on board. I hope that, in some cases, I have gone further than perhaps noble Lords thought was likely to be the case when this process started.

On the specific point of low-incidence SEN, I can say to the noble Baroness that, as part of looking at funding for academies from 2011 onwards, we will work closely with local authorities. I accept the point made by the noble Lord, Lord Hunt, about the importance of local authorities and other parties in this area. I can confirm that we will look specifically at the funding of low-incidence SEN. This work will start during the autumn. I have today instructed officials to ensure that the Special Educational Consortium is kept abreast of developments and is able to make its views known. It is extremely important that it has that opportunity and we shall reflect on the points that it makes to us. We are committed to ensuring that children with sensory impairments in both the maintained and academies sectors receive the services that they require.

We have also established an advisory group to help us work through the issues particular to SEN and special schools in relation to the establishment of academies. We want to use the practical expertise in that sector and the group will include heads and governors from special schools and mainstream schools with specialist units, as well as local authority representation at officer and political level. As I said on Report, and as I underlined to the noble Baroness, Lady Wilkins, and to the noble Baroness, Lady Howe, yesterday when we met, I am very happy to put on the record our undertaking to monitor the impact of increasing numbers of academies on local authority sensory impairment services. We will continue to work with local authorities to ensure that adjustments to their funding in respect of academies properly reflect their continuing responsibilities. Our officials will also work with organisations such as the National Sensory Impairment Partnership on this.

Listening to the debate, I am very conscious that I am not expert on SEN, and I am not the Minister responsible. However, as part of the advisory groups and the work we will be taking forward, I would be very happy to enable a proper exchange with the relevant Minister in the department so that we can work through these issues, using the experience and expertise of noble Lords, to make sure we come up with practical solutions that meet the concerns that noble Lords have raised. So I am alive to the concerns. I hope that the noble Baroness will feel that that provides some slight further reassurance from yesterday. In the light of that I ask her kindly to withdraw her amendment.

[Baroness Wilkins]

My Lords, I am most grateful to all Members of the House who have spoken in support of this amendment and to the Minister for the reassurances that he has tried to give. Unfortunately, it does not meet the needs of those children who are going to be at school in September. Given the strength of feeling in the House, I would like to test the opinion of the House.

Academies Bill [HL]

Baroness Wilkins Excerpts

Wednesday 7th July 2010 Lords Chamber

[Lord Low of Dalston]

My Lords, I wish to speak to Amendments 12 to 14 and to Amendment 39, all of which are in my name. I very much welcome government Amendment 11, to which the Minister has just spoken. In Committee, there was a widespread concern throughout the Chamber to ensure that academies were put on the same footing as maintained schools as regards admitting and meeting the needs of pupils with special educational needs. The Minister said then that he would reflect and come back with proposals on how parity could be achieved. As we have heard, he has been as good as his word. I am very grateful to him for this and for the time and trouble that he has taken to meet Peers to discuss their concerns. I am also most grateful to officials for the time that they have taken to make sure that we get this absolutely right.

For my part, I think that we have very nearly got it right, but not quite. That is why I have put down the amendments to which I am speaking this evening. I spoke on this at some length in Committee, so I shall not weary the House by going over the same ground all over again. The Minister has met very many of the concerns that I raised in Committee, but one or two issues still remain. The first is whether the new provisions will relate to existing as well as new academies. In moving his amendment, the Minister has clarified that because he has said that they will do so. However, I think he said that they would apply to existing academies when they entered into a new agreement. That could be some years away. I hope that the Minister can reassure us that steps will be taken to apply the new provisions to existing academies at the earliest possible date and not necessarily waiting several years before doing so.

Secondly, there is the question of whether obligations that are equivalent to the SEN obligations in the Minister’s amendment are the same in their effect as the SEN obligations. If not, it will be argued in court that Parliament’s decision not to make these obligations direct statutory obligations must indicate an intention to permit variation from the statutory framework. I should therefore be grateful if the Minister could confirm that the intention is for academies to be subject to exactly the same obligations as maintained schools as regards admitting and meeting the needs of pupils with special educational needs, which the notion of parity would imply.

My main concern is with the enforceability of the rights implied by these obligations. The Minister has chosen to confer the obligations by importing the statutory SEN framework into the contractual framework of academy arrangements. These are contractual agreements between the Secretary of State and an academy to which parents and pupils are not a party. There is a complex legal argument as to whether the duties imported into academy arrangements by this means are enforceable by parents or pupils. I shall spare the House all the legal technicalities, but there are essentially three ways that one might seek to ensure that the duties are enforceable.

The first is by laying on academies the same statutory obligations as those laid on maintained schools directly by statute, not by statutorily importing them into a contract. That is what my Amendment 14 would do and I still think that it is the simplest and surest way to achieve my aim, which is why I have tabled that amendment again and why it would save a lot of bother by putting everything beyond doubt, if the Minister agreed to it.

Assuming that the Minister’s preference is to proceed by the contractual route and to maintain the contractual relationship with academies, there are two further ways that one might seek to enforce the contractual obligations. One is through a complaints procedure and the other is by making it clear that pupils and parents can enforce their rights by judicial review.

As for complaints procedures, complaints would presumably be made to the Secretary of State, but there is nothing that establishes such a procedure and nothing is proposed. Even if there were, it would need to be clear that if the Secretary of State found that an academy had not complied with the relevant provisions of the academy arrangements, he would require the academy to comply, and the arrangements would need to make clear that he could compel compliance. This would place a considerable additional burden on the Secretary of State, whose process for dealing with complaints is already widely perceived to be slow and ineffective—as is illustrated by the fact that it is never suggested by defendants in proceedings for judicial review that the court should decline jurisdiction because a complaint to the Secretary of State would provide an effective alternative remedy.

As for judicial review, the availability of this remedy could be put beyond doubt simply by making clear that the rights accorded to pupils and parents under academy arrangements could be enforced through judicial review. This could be done on a narrow basis relating to SEN only, as is provided for in Amendment 12, or on a wider basis covering all rights given to parents and pupils, as provided for in Amendment 13. Amendment 12 would sort out the problem relating to special educational needs, but would, if anything, weaken the position in relation to other rights—say, those relating to admissions—because it would imply that those rights could not be enforced through judicial review.

The Minister has shown himself to be very accommodating of our concerns in the quest to achieve full parity between academies and maintained schools. I hope that further discussion may be possible before Third Reading, with a view to finding a formula which would ensure that enforceability is not only a reality, but is seen to be a reality, either through a robust complaints procedure or by putting it beyond doubt that judicial review is available as a remedy.

Something along the lines of Amendments 12 or 13 would do the job for judicial review, and I have suggestions for a robust complaints procedure that I would be happy to put to the Minister. Amendment 39 begins the job, but even that requires fleshing out in some respects to reflect the ingredients of a robust complaints procedure. If the Minister would be happy to proceed along these lines, I am sure that we could reach an arrangement that would put enforceability beyond doubt and would be satisfactory to everyone. If full parity is the Minister’s aim, I cannot see a reason not to do this.

[Baroness Wilkins]

My Lords, I echo the thanks of the noble Lord, Lord Low, to the Minister for all his time and the concern that he has given to this issue. I support the noble Lord, Lord Low, in his amendments and hope that the Minister will meet his concerns and satisfy him fully.

[Lord Hunt of Kings Heath]

I, too, warmly thank the Minister for bringing his amendment. It certainly shows that he has listened to the House and we are grateful. I also support the noble Lord, Lord Low. He raises important issues in relation to JR and I am sure that the Minister will be able to respond positively.

I should like to raise a further issue on this group of amendments which relates to SEN funding. It arises from the potential decline in the ability of local authorities to fund support services for SEN pupils which would result from an increase in the overall number of academies.

At the moment, local authorities retain a proportion of funding related to the number of schools that they maintain for the provision of central services, including those for special educational needs. While the overall level of funding within a local authority area may well not fall as a result of this process, the reallocation of resources away from local authorities to individual schools can have potentially significant effects for children and young people with SEN.

We widely accept that the provision of special educational needs support is at the most expensive end, or at least the more expensive end, of the educational spectrum. A key feature of local authority provision is that it allows a local authority to ensure that finite resources are spent effectively through the ability of the local authority to generate economies of scale.

This matter will come up later in Amendment 21, to be moved by my noble friend Lady Wilkins, on low-incidence SEN. However, it actually raises a more general issue of principle. In the letter that the Minister circulated to us and to my noble friend, he states that academies are able to buy in SEN support services from their local authority, from neighbouring local authorities or from other providers. I understand that principle, but I ask him to reflect on the circumstances. Because there will clearly be no requirement for an academy to purchase services from its local authority, current services might be at risk. In particular, the expertise that individual local authorities have established might not be available to academies, because resources are no longer there to support it. There is also a risk that the provision of SEN support on an individual school basis might be more expensive than that which could be accessed by the local authority.

The noble Lord may say that the problem will not arise, that essentially he is proposing a market-based solution and that because of that the combination of academies making their own decisions will ensure a satisfactory outcome. I should mention again my NHS experience, because what is happening here is very much in parallel to the decentralisation that has been undertaken in the National Health Service. My experience has been that in that process specialist services can actually lose out and that if they do, the Government have to find some mechanism for intervention to make sure that those specialist services, as a whole, continue to be provided. I give advanced warning that I will raise this again in the debate on my noble friend’s amendment. It would be useful to have some indication from the Government that they understand the issue and that there is a mechanism by which they can deal with it. If the noble Lord had accepted my suggestion that a statutory duty of partnership might be laid on all parties, that might have been one way through.

Academies Bill [HL]

Baroness Wilkins Excerpts

Wednesday 7th July 2010 Lords Chamber

Moved by

[Baroness Wilkins]

21: Clause 2, page 2, line 35, at end insert–
“( ) In Schedule 1 to the School Finance (England) Regulations 2008, after paragraph 8 insert—
“8A Where a child is a registered pupil at an Academy, expenditure in respect of services for making provision for pupils with low incidence special educational needs or disabilities.”
( ) Where a local authority fails to secure satisfactory provision for pupils with low incidence special educational needs or disabilities, the Secretary of State may make alternative arrangements.”

[Baroness Wilkins]

My Lords, I speak to Amendment 21. In Committee, I spoke about my concerns that the Academies Bill will fatally undermine specialist support services for children with low incidence needs. I am grateful to the Minister for his letter of 2 July in response to these concerns, and to the noble Lord, Lord Wallace, for his reply in Committee. I particularly welcome the Government’s commitment that pupils in academies with low incidence SEN needs or disabilities will receive the support they require from specialist support services. But, unfortunately, my worries have not yet been allayed. The Special Educational Consortium, particularly the National Deaf Children’s Society, RNIB and Sense, share my concerns.

The funding arrangements for specialist support services may be complex but the problem is clear. If funding from the schools budget for specialist support services is to be dispersed widely to a large number of academies in a given area, this will reduce the funding available to existing specialist support services in local authorities. It takes away the pooling of resources that ensures services to children with low incidence needs can be met at reasonable value for money. As the noble Lord, Lord Hill, put it in his letter to me, this will result in “dis-economies of scale”. The noble Lord noted that academies will be able to buy back support from their local authority. However, a survey by the National Deaf Children’s Society raises serious concerns that this is simply not happening. The society found that of 66 local authorities where a deaf child with a statement of SEN was enrolled in an existing academy, in only 17 of these local authorities were the academies buying in support.

So what is happening to the deaf children in the other 49 local authorities? The society suspects that many local authorities are providing services free of charge, but that clearly will not be sustainable with greater numbers of academies. The worst case scenario is that children with sensory impairments are going without the support they need. NDCS is aware of examples where this is currently happening—for instance, in one local authority in Yorkshire and the Humber, where uncertainty over funding and buy-back has left deaf children totally unsupported.

In Committee, the Minister stated that he recognises this is a continuing problem, and that was very welcome. However, I would like him to go further and commit to finding an urgent solution to this problem. I recognise that it is not a new problem. However, if the Academies Bill is going to make matters worse, surely the Minister has a responsibility to act now before the Bill becomes law. In Committee, he suggested that “partnerships among schools” will clearly be the best way forward. Will he say a little more about how this will work in practice? How will these partnerships be funded? What support and guidance are being provided to schools to develop them? How many partnerships are there in place already? Most importantly, what evidence is there that these partnerships will ensure that every child with low incidence needs gets the support that they need?

The Minister also stated that academies will have access to top-up funding to cover the costs of support for children with low incidence needs. He went on to say that this will be funded by the local authority from its schools budget. Will he confirm that this is the same schools budget which will be cut if a large number of schools convert to academies? If so, how can these specialist support services be funded and provided on a reliable and sustainable basis?

The Minister stated that if the academy fails to secure the necessary support, it will be in breach of its funding agreement, and that the Young People’s Learning Agency can investigate, following a complaint. In Committee, the noble Baroness, Lady Sharp, made the important and obvious point that the YPLA is not an inspection agency. In response, the Minister stated that voluntary organisations will monitor the situation. However, surely he must agree that this is a very weak and unacceptable safeguard against the risk that children with low incidence needs will be denied the support they need. Many voluntary organisations simply do not have the capacity to monitor provision in large numbers of individual academies across England. It is not appropriate for such organisations to act as a watchdog, relying on them to make sure that the Government and academies fulfil their legal duties towards children with special educational needs.

My amendment would move funding for specialist support services out of the schools budget and into the LEA budget. This would protect these services from some of the unintended consequences to which I referred earlier. In Committee, the Minister did not set out his view on this. If it is his view that this amendment should not be passed, I should be grateful if he could explain why, and what alternative remedy will be put in its place. My amendment would also give the Secretary of State the power to make alternative arrangements if specialist support services in any particular area are inadequate.

In his letter, the noble Lord, Lord Hill, noted that academies will in future be free to buy in services from other providers. In light of the difficulties that some local authorities have in meeting the needs of children with low incidence needs, I recognise the appeal of this and hope that this option will be explored further, as I have no desire to prop up services that are not doing a good job. However, I stress that this needs to be fully thought through and fully planned for.

I very much welcome the fact that officials have met with the National Sensory Impairment Partnership, as the noble Lord, Lord Hill, pointed out in his letter. I have been told that the partnership also welcomes this and believes that there has been a useful discussion and exchange of views, which it is keen to continue. However, it does not believe that there has been sufficient progress in resolving the outstanding questions and concerns.

The partnership believes that the Government should set up a time-limited working group that will consider alternative arrangements and make urgent recommendations. This group should include representatives from the Department for Education, local authorities, professionals, head teachers of academies and maintained schools, and parents. I firmly agree with the partnership. If the Government wish to show that they are serious about addressing these important concerns about specialist support services and diseconomies of scale, it is imperative that a working group be set up immediately, and I very much hope that the Minister will give me a positive reply to this proposal, which would do much to alleviate the concerns.

Children with low incidence needs may, by definition, be fewer in number. That cannot be an excuse to pass a Bill which would potentially prevent many from getting the support that they need. I urge the Minister to do more than just recognise that there is a problem. He must find solutions before this Bill is allowed to pass. I beg to move.

[Baroness Howe of Idlicote]

My Lords, I support the amendment in the name of my noble friend Lady Wilkins, as I did with regard to her amendment in Committee. I agree with my noble friend and share her concerns on specialist support services for children with low-incidence needs. I also agree that the Minister has not yet, I fear, provided a satisfactory response on these important concerns. I also reiterate the point made by my noble friend that the Government’s desire to pass the Bill speedily must not be at the expense of children with low-incidence needs.

In Committee, I highlighted my concerns about the impact of the Bill on the range of services delivered by specialist support services outside school. For example, many services provide pre-school support directly to families and children to aid language acquisition and to teach Braille. Support may also be given to ensure that children with visual impairments have the necessary independent living skills. Such support is essential if we wish to ensure that children with low-incidence needs are able to fulfil their potential and live independently later in life. The cost of failing to provide such support is likely to be prohibitive to individuals with low-incidence needs and also to the Government’s welfare budget. I am concerned that such services may be compromised if the schools budget for specialist support services is cut when a large number of schools convert to academies. When it comes to low-incidence needs, surely it is vital that our limited resources are pooled and used effectively to fund the services and ensure the best possible value for money.

I am concerned also that these unintended consequences will result not only in wastage but also in very poor value for money. These concerns are shared by the Special Education Consortium. I regret that the Minister did not address the concerns that I expressed in Committee that such preschool services would be undermined by the Bill. I strongly urge him to do so today.

--- Later in debate ---

[Lord Hill of Oareford]

My Lords, I will be fairly brief because in our earlier exchange I accepted the point made by the noble Lord, Lord Hunt, that as regards low-incidence SEN there is an issue that we need to look at.

I am grateful to the noble Baroness, Lady Wilkins, for referring to the work that my officials have been doing with her and the National Sensory Impairment Partnership. She made a powerful case, and I shall reflect on what she said and perhaps talk to her further about it. If she can spare the time we can meet officials to consider practical ways forward. I do not have an answer tonight and I cannot go further than I should, but I hope that she and others will accept that on the issue of SEN I have sought to be sensitive. I am not dismissive and if the noble Baroness will agree to meet, we can discuss her concerns. If she thinks that that is a fair and reasonable way forward, perhaps she will withdraw her amendment and we can meet outside the House.

[Baroness Wilkins]

First, I thank all noble Lords for their support for the amendment and for recognising and emphasising what a serious concern it represents. I am most grateful to the Minister for his awareness and the trouble that he has taken. I will definitely take up his offer to meet his officials, and I hope that we can reach a satisfactory conclusion. With that, I beg leave to withdraw the amendment.

Amendment 21 withdrawn.

Academies Bill [HL]

Baroness Wilkins Excerpts

Monday 28th June 2010 Lords Chamber

[The Earl of Listowel]

The reassuring words of the noble Baroness, Lady Perry of Southwark, are very helpful. When I visit special institutions for children with emotional and behavioural difficulties or children’s homes, I am concerned that often one finds that the children with the most severe difficulties are pooled together in one place. They become difficult to manage, difficult for each other, and difficult for those who are caring for them. When comparing Denmark and this country, one of the differences is that Denmark intervenes and takes children into care earlier. Children’s homes are used more and there is more of a mixed bag of children in them. Thus, the temperature of the place is lowered. As a result of this provision, I would not want to see the most difficult children pushed into one place. I hope that the Minister can reassure us that further thought will be given to how we can support head teachers in academies and non-academies to work together. For example, a small amount of resources could be put into a yearly local get-together where such people would be able to speak to and to meet each other.

[Baroness Wilkins]

Amendment 97 does not sit easily with the other two amendments in this group and is on a separate area. Therefore, we are moving on. This probing amendment seeks firm reassurance from the Government on how the Academies Bill may impact on specialist support services for children with low-incidence special educational needs and disabilities. I am focusing my remarks on specialist support services for deaf children, but these issues are applicable to other children with low-incidence needs, such as those with visual impairments.

The National Deaf Children’s Society, to which I am indebted for its advice on this issue, estimates that there are more than 35,000 deaf children in England, of whom 90 per cent attend mainstream schools. However, deafness is a low-incidence need. As a result, in many schools it may be many years before a deaf child enrols. The reality is that deaf children are spread unevenly in mainstream schools across any one area. There is no reason why a deaf child cannot achieve as well as their hearing friends, provided that they get the support that they need from the start. This support is normally provided through local authority specialist support services, which cover a wide range. They include providing the school with amplification equipment, such as microphones; ensuring that there are follow-up checks and maintenance; training mainstream teachers on how to support deaf children; and, most importantly, providing direct support to families to help with pre-school language development.

These services are normally funded by the local authority, but academies will be independent from them. I am therefore seeking reassurance that deaf children will still receive the support that they need in a school system with a greater number of independent academies. Currently, in local authority maintained schools, schools funding is allocated to local authorities by the Government. While most of the money is then delegated to schools, local authorities will usually retain or top-slice some money to fund services, such as the specialist support services for deaf children. The service then provides outreach support free of charge to all local authority maintained schools in its area. Where a school becomes an academy, any money retained or top-sliced will be taken away from the local authority and given straight to academies, which will be expected to buy in any specialist support that their pupils will need. But if a child has a low-incidence need, such as deafness, the cost of meeting this specialist support to one individual academy will be proportionately greater. The economies of scale that operate at a local authority level will not exist at individual academy level. I am deeply concerned that any extra funding that academies receive will not cover the costs for these necessary services, which may result in deaf children not getting the support that they need. This is not a theoretical risk.

The National Deaf Children’s Society is already aware of a number of cases in existing academies where deaf children have gone without the support that they need. Last year, when the NDCS did a survey of local authority specialist support services for deaf children, it asked whether any academies in their areas bought in support for any deaf children who were enrolled at those academies. I am shocked that nearly three-quarters of academies did not buy in any support, which raises alarm bells as to how deaf children in these academies are being supported, if at all. Surely, that is an inefficient way of funding specialist support services for deaf children. This top-slice money that academies will receive will go to all academies, even if they do not have a deaf child on their rolls. Does the Minister share my concern that this will be poor value for money?

My amendment aims to address these concerns. The first part would amend the School Finance (England) Regulations 2008 with the intended effect of moving funding for specialist support services for low-incidence special educational needs from the schools budget to the core LEA budget. This would prevent funding for specialist support services for low-incidence needs being top-sliced and spent inefficiently in the way in which I have described. I would welcome a statement from the Minister on how the department will address this matter.

I am all too aware that local authority specialist support services in some areas are not as good as they should be. For that reason, the second part of the amendment would also give the Secretary of State the power to make alternative arrangements if this is the case. I believe that the Government need to take urgent action to set up a working group to consider whether alternative arrangements, such as parent-led services, might offer a better way in those areas of delivering such services. I urge the Minister to ensure that any such working group includes representatives of children with low-incidence needs as well as their parents.

However, any alternative arrangements need to be carefully thought through and planned to ensure continuity in the service that deaf children receive. It is not good enough simply to throw our cards in the air and hope for the best. Government figures show that deaf children are already 42 per cent less likely to do as well in their GCSEs as other children. It is vital that this Bill helps us to ensure that deaf children get the support they need, regardless of the type of school they attend. I hope that the Minister will be able to reassure me on this. Should he not do so, I will return to this issue on Report.

[Baroness Howe of Idlicote]

My Lords, I very much support the probing amendment in the name of my noble friend Lady Wilkins. I agree with my noble friend and I am glad that she indicated that it is not suitably grouped. I share her concerns over the impact of the Academies Bill on specialist support services for low-incidence special educational needs and disabilities. I also am grateful to the National Deaf Children’s Society for its briefing.

In particular, I am concerned about the impact of the Bill on outreach services to pre-school children. Parents are at the heart of a child’s learning, as we would all agree, but the parents of a child with special educational needs or a disability need extra help, as well as the child. In many cases, this extra help is provided by the local specialist support services. We have heard about the important role that local authorities play in that. For example, the parents of children with communication difficulties need guidance and support on how to communicate effectively with their child. Without such support, it would be far more difficult for these children to acquire language and to develop communication skills at the same rate as their peers. A huge responsibility rests with helping the parents.

We risk condemning children with these communication difficulties to a life of underachievement before they even begin school. We have already heard from my noble friend Lady Wilkins just how far behind they can fall if they do not have early access to the services they need. Almost certainly, when such children start school, the school they attend will be forced to provide costly catch-up support.

There is a range of other pre-school services that families of other disabled children will find invaluable. I am very concerned that if funding for these services is delegated to academies, they may be unable or unwilling to invest in pre-school services. I am also concerned that it may be unsustainable for existing providers to do this if much of their funding is reduced as a result of the Bill. Like my noble friend Lady Wilkins, I would warmly welcome reassurance from the Minister that the Bill will not risk undermining these valuable pre-school services for disabled children. We are all urging the earliest possible testing for special needs. If ever there was a need, it is for this group of children.

--- Later in debate ---

[Baroness Morgan of Drefelin]

My Lords, on this occasion and given the hour, I have set aside my 2,000-word speech. I shall think carefully about what the Minister has said. I, too, was concerned by the contribution of the noble Baroness, Lady Perry, and the idea that we can just leave the matter to trust. We know that, of the academies that exist, a very large number—I do not have the exact number to hand—currently take part in behaviour partnerships and they work. However, it is the ones that do not do so that I am worried about.

I shall read the report of the debate. It has been a good discussion and helpful in clarifying for me the Government’s position. I was concerned to hear the arguments put forward by my noble friend Lady Wilkins and was interested in the noble Lord’s response. However, again, we come down to the academy agreement. When we are talking about a change from the number of academies being in the hundreds to potentially all schools in the country being academies, we have to think much more ambitiously about how we can make these partnerships work.

[Baroness Wilkins]

Before my noble friend withdraws her amendment, perhaps I may say that I regret that I am not reassured by the Minister’s words. However, I shall read them carefully and should like to consult my advisers. It is essential that the support services are kept together and maintained as a core service, but at the moment it does not sound as though they will be. I shall reflect on this issue.

[Baroness Morgan of Drefelin]

I was about to say that I am happy to withdraw my amendment.