Children and Families Bill Debate
Full Debate: Read Full DebateEdward Timpson
Main Page: Edward Timpson (Conservative - Eddisbury)Department Debates - View all Edward Timpson's debates with the Department for Education
(11 years, 6 months ago)
Commons ChamberI beg to move, That the clause be read a Second time.
With this it will be convenient to discuss the following:
New clause 8—Support for children with specified health conditions—
‘(1) The governing body of a mainstream school has a duty to produce and implement a medical conditions policy that defines how it plans to support the needs of children with specified health conditions.
(2) The medical conditions policy must include provision about—
(a) the means by which records of the specified health conditions of children at the school are to be recorded and maintained; and
(b) the preparation of an individual healthcare plan for each child with a specified health condition which sets out the needs of that child arising from that condition.
(3) The medical conditions policy must include requirements relating to the provision of appropriate training for school staff to support the implementation of individual healthcare plans.
(4) In preparing an individual healthcare plan the governing body must—
(a) consult the parent of the child concerned and, where appropriate, the child about the contents of the plan; and
(b) there shall be a duty on NHS bodies to co-operate with the governing body in its preparation and implementation of individual healthcare plans.
(5) Local authorities and clinical commissioning groups must co-operate with governing bodies in fulfilling their functions under this Act.
(6) The Secretary of State may by regulations define “specified health conditions” for the purposes of this section.
(7) For the purposes of this section “NHS bodies” has the same meaning as in the Health and Social Care Act 2012.’.
New clause 21—Inclusive and accessible education, health and social care provision—
‘(1) In exercising a function under Part 3, a local authority and NHS bodies in England must promote and secure inclusive and accessible education, health and social care provision to support children, young people and their families.
(2) Regulations will set out requirements on an authority and its partner NHS commissioning bodies to promote and secure inclusive and accessible education, health and social care provision in its local area, in particular through—
(a) the planning;
(b) the design;
(c) the commissioning or funding;
(d) the delivery; and
(e) the evaluation of such services.’.
New clause 24—Publication of information relating to Special Educational Needs tribunal cases—
‘(1) The Secretary of State must collect information on all cases related to special educational needs which are considered by the Tribunal Service, including—
(a) the local authority involved;
(b) the cost to the Tribunal Service;
(c) the amount spent by the local authority on fighting each case;
(d) the nature of each case; and
(e) the outcome of each case.
(2) The Secretary of State must collate and publish information collected in the exercise of his functions under subsection (1) once a year.
(3) The following bodies must make arrangements to provide such information to the Secretary of State as is necessary to enable him to perform his functions under this section—
(a) the Tribunal Service;
(b) local authorities.’.
Amendment 59, in clause 19, page 18, line 22, at end add—
‘(e) the right of the parent to make their own arrangements for some or all of the special educational provision under section 7 of the Education Act 1996.’.
Amendment 39, in clause 21, page 19, line 16, leave out ‘wholly or mainly’.
Amendment 60, in clause 23, page 19, line 29, leave out ‘may have’ and insert ‘probably has’.
Amendment 61, page 19, line 32, leave out ‘may have’ and insert ‘probably has’.
Amendment 46, in clause 27, page 22, line 3, at end insert—
‘(2A) If the education and care provision provided as part of the local offer is deemed insufficient to meet the needs of children and young people under subsection (2), a local authority must—
(a) publish these findings;
(b) improve that provision until it is deemed sufficient by—
(i) those consulted under subsection (3); and
(ii) Ofsted.’.
Amendment 62, in clause 28, page 23, line 29, at end insert ‘;
(n) Parent Carer Forums.’.
Amendment 66, in clause 30, page 24, line 21, leave out ‘it expects to be’ and insert ‘which is’.
Amendment 67, page 24, line 24, leave out ‘it expects to be’ and insert ‘which is’.
Amendment 30, page 24, line 34, at end insert—
‘(f) arrangements to assist young people and parents in managing a personal budget should they choose one.’.
Amendment 68, page 24, line 39, at end insert ‘, including in online communities.’.
Amendment 69, page 25, line 7, at end insert—
‘(7A) The Secretary of State shall lay a draft of regulations setting out the minimum level of specific special educational provision, health care provision and social care provision that local authorities must provide as part of their local offer, and the regulations are not to be made unless they have been approved by a resolution of each House of Parliament.
(7B) Once regulations under subsection (7A) have been made, the Secretary of State must—
(a) issued guidance to local authorities on how to meet these regulations, and
(b) publish information on these regulations accessible to the families of children and young people with special educational needs on the Department’s website, and in any other way he sees fit.’.
Amendment 65, in clause 36, page 28, line 21, at end insert—
‘(1A) A person acting on behalf of a school or a post-16 institution (“A”) must request an EHC needs assessment for a child or young person (“B”) as soon as A becomes aware that B has been diagnosed with epilepsy or a related condition.’.
Amendment 40, page 29, line 20, leave out subsection (10).
Amendment 44, in clause 37, page 30, line 8, leave out from ‘provision’ to end of line 10 and insert
‘required by the child or young person.’.
Amendment 41, page 30, line 13, leave out subsection (4).
Amendment 45, in clause 38, page 30, line 35, at end insert—
‘(g) an institution of higher education which the young person has accepted an offer from.’.
Government amendment 17.
Amendment 37, in clause 42, page 33, line 6, at end insert—
‘(2A) If the plan specifies social care provision, the responsible local authority must secure the specified social care provision for the child or young person.’.
Amendment 63, page 33, line 13, leave out ‘suitable alternative arrangements’ and insert
‘arrangements suitable to the age, ability, aptitude and special needs of the child or young person and has chosen not to receive assistance with making provision.’.
Amendment 42, in clause 44, page 34, line 3, leave out subsection (5).
Amendment 43, in clause 45, page 34, line 37, leave out subsection (4).
Amendment 64, page 34, line 39, at end insert—
‘(4A) A local authority must not cease to maintain an EHC plan on the sole ground that the child or young person is educated otherwise than at school in accordance with section 7 of the Education Act 1996.’.
Government amendments 18 to 20.
Amendment 70, in clause 48, page 36, line 21, at end add—
‘(6) This section will not have effect until an Order is made by the Secretary of State, subject to affirmative resolution by both Houses of Parliament.
(7) Before making an Order under subsection (6), the Secretary of State must lay a copy of a report before both Houses of Parliament detailing findings from the pathfinder authorities established under the Special Educational Needs (Direct Payments) (Pilot Scheme) Order 2012, including but not limited to—
(a) the impact on educational outcomes for children and young people;
(b) the quality of provision received by children and young people;
(c) the value for money achieved;
(d) the impact on services provided for children and young people without EHC plans, or those for whom direct payments were not made.
(8) The Secretary of State may not prepare a report under subsection (7) until September 2014.
(9) An Order made under subsection (6) may amend this section as the Secretary of State deems necessary to ensure the effective operation of personal budgets, having had regard to the finding of the report produced by virtue of subsection (7).’.
Government amendment 21.
Amendment 38, in clause 50, page 37, line 18, at end insert ‘;
(g) the social care provision specified in an EHC plan;
(h) the healthcare provision specified in an EHC plan.’.
Amendment 47, in page 48, line 35, leave out clause 69.
Amendment 71, in clause 65, page 45, line 37, leave out ‘19’ and insert ‘25’.
Amendment 72, page 46, line 11, leave out ‘19’ and insert ‘25’.
Amendment 73, in clause 67, page 47, line 21, leave out
‘such persons as the Secretary of State sees fit’
and insert
‘publicly, for a period of not less than 90 days’.
Amendment 74, page 47, line 22, leave out ‘by them’ and insert
‘as part of that consultation’.
Amendment 75, in clause 67, page 47, line 23, leave out subsections (3) to (8) and insert—
‘(3) A code, or revision of a code, does not come into operation until the Secretary of State by order so provides.
(4) The power conferred by subsection (3) shall be made by statutory instrument.
(5) An order bringing a code, or revision of a code, into operation may not be made unless a draft order has been laid before and approved by resolution of each House of Parliament.
(6) When an Order or draft of an order is laid, the code or revision of a code to which it relates must also be laid.
(7) No order or draft of an order may be laid until the consultation required by subsection (2) has taken place.’.
Amendment 48, in clause 72, page 49, line 46, leave out from ‘education,’ to end of line 1 on page 50.
Government amendments 22 to 25.
Part 3 of the Bill introduces a much stronger framework for supporting children and young people with special educational needs. These reforms have been widely welcomed, and I am grateful to Members in all parts of the House for their interest in and support for them. We can be sure in the knowledge that the Bill has been significantly strengthened since draft clauses were published last autumn.
We have all met constituents who have had to battle to get the special educational support that their child needs. These reforms are ambitious; they aim to ensure that in future, children, young people and their parents are at the heart of the system, and that special educational provision builds around them, instead of asking them to adjust to the system. It will not always work perfectly in every case, but the pathfinders that I have visited have convinced me that we have a really exciting reform under way—one that challenges local authorities to design a system around those who use it, rather than conform to existing structures and processes. The reforms are also ambitious as regards personal aspirations. The new system will support young people through further education and training, up to the age of 25 for those who need it, and focus much more strongly on independent living and helping them to find paid employment. The provisions extend support to younger years as well, so that children are supported as soon as their needs are identified, from birth onwards, instead of having to wait until they reach school to be assessed.
The reforms provide the foundation for a system in which children and young people’s needs are picked up early; parents know what services they can reasonably expect their local schools, colleges, local authority, and health and social care services to provide, without having to fight for the information; those with more severe or complex needs have a co-ordinated assessment built around them and a single education, health and care plan from birth to 25; and parents and young people have greater control over their support. I believe these ambitions are shared across the House.
We had a wide-ranging, constructive debate on Second Reading, and the Committee sittings were passionate, knowledgeable and helpful. I hope that today we can build on the broad consensus that has characterised the debate to date.
We have also listened carefully to the views expressed by Members of the House, parents and young people, and many of the organisations supporting them, and we have acted to improve the SEN provisions following pre-legislative scrutiny and as the Bill has made its way through the House.
The Minister may recall that he kindly met me to discuss my particular concerns about children who had suffered from cancer and perhaps missed quite a large amount of school but did not fit in with the SEN criteria. What level of support could they expect under these proposals?
I recall the constructive meeting that I had with the hon. Gentleman and he will remember that I gave a commitment then to work with him and with organisations with which he has been working with great astuteness to see what more we can do through the code of practice and other means to provide the additional support that we all want to see so that no child, particularly a child with cancer, misses out on the opportunity to fulfil their potential, and I will continue to work with him to achieve that.
Following the Education Committee’s thorough and well-argued report—another one—in December, we amended the Bill in several ways. By virtue of clause 19, we introduced a requirement for local authorities when exercising a function under part 3 to have regard to the views, wishes and feelings of a child and his or her parent, or of the young person, and the importance of them participating as fully as possible in decisions, and being provided with information and support to enable them to do so—an important set of transcending principles.
We have clearly specified the right of parents and young people themselves to request an assessment for special educational needs, to remove any uncertainty. We have ensured that young people on apprenticeships can receive support through an education, health and care plan. We have enabled independent special schools and specialist colleges to apply to be on a list of institutions for which parents and young people with education, health and care plans could express a preference. We have changed our approach to mediation so that parents and young people must consider mediation but do not have to take it up and can go straight to appeal to the tribunal if they wish without prejudicing their position.
To ensure that services are responsive to families’ needs we added a requirement for local authorities to involve children, young people and parents in reviewing the local offer and to publish their comments about the local offer and what action they will take to respond, and we made provision for the SEN code of practice to be approved by Parliament by way of negative resolution.
I apologise for missing the first two minutes of the Minister’s speech. He outlines responsibilities that have rightly been referred to various public agencies, but I find it somewhat confusing that nowhere can I find, either in the new clause or in the amendments, any reference to advocacy. I might have missed something, but what role do the Government see for advocates in the situations that we are discussing?
The right hon. Gentleman raises an important point. Advocacy comes in different forms. We have advocacy in relation to the legal process, and legal aid will still apply up to the point of tribunal for those who require legal advice. There is also advocacy in terms of trying to navigate the system. One thing that we are doing in relation to the pathfinders is to see who can help co-ordinate and navigate for parents and young people in a system that often has been too impenetrable, labyrinthine and drawn out. That could be through a key working role or through the work that the special educational needs co-ordinators carry out so effectively in so many of our schools. It is a practical response to the problem that we know exists while ensuring that the advocacy that is currently available for the legal process continues into the future. We set that out in Committee and I encourage the right hon. Gentleman to look carefully at what we said.
Will the Minister reassure some local authorities that the proposal will still ensure integration between the 1970 legislation, the Children Act 1989 and this Act, and make sure that there is not a silo system that does not have the integrated service that we all so want?
My hon. Friend touches on the heart of the Bill, which is to tackle the perennial problem of special educational needs, in that education, health and social care have tended to work in parallel rather than in conjunction with one another. In many of the clauses, both through the general duty to co-operate, the joint commissioning clause, and now the duty on health as well as the duty to consult parents and children themselves, there is already, with the pathfinders, a growing involvement of each of those different agencies in coming together and concentrating on the central and most important issue, which is the child. I hope he will see that the Bill gives local authorities an opportunity to nurture and grow their relationships with health and other agencies, and ensure that as a consequence they are providing better services for children in their local area.
I thank my hon. Friend on behalf of the Education Committee for taking such a positive and constructive approach to our pre-legislative scrutiny report, and implementing so many of the proposals, as he has just listed.
My hon. Friend appeared before the Committee this morning in our inquiry into school sports, and he suggested that he would consider looking at the code of practice to ensure that rather than disabled children being sent to the library while others are doing sport, as we heard in evidence sometimes happens, they have access to sport in schools, and that that is part of an overall package to meet their needs.
As ever, I am grateful to the Chair of the Education Committee for raising a crucial element for many young people with a disability, and that is access to other activities outside those of the classroom. I am mindful of that and as I told the Committee this morning have seen for myself, at a special school in Chislehurst only last week, how the integration of sport in schools, where children with both physical and other disabilities are able to participate, can have a huge knock-on effect in other areas of their life. It would not always be appropriate through the identification of the needs and therefore the support for each child in relation to their plan to have a built-in element that incorporates and encompasses physical activity, but clearly we want to provide as much opportunity for them as for any other child. The schools should be doing it anyway under the Equality Act 2010 and the reasonable adjustments for which they are responsible, but it also makes good sense, as we know. I am happy—I made this commitment to the Committee—to look at that in the context of the code of practice, but also to work with many of the organisations and charities who are already out there, through the project ability scheme and others, to see what more they can do to spread good practice in this area. I am happy to keep my hon. Friend informed of that process.
As has been mentioned, the Select Committee held a series of pre-legislative scrutiny meetings. Is the Minister satisfied that there are sufficient accountability mechanisms for agency co-operation, and that the appropriate agency will automatically take the lead? How will that work out in different cases?
Briefly to disaggregate my hon. Friend’s two points, clearly it is important that we know what is happening in schools on the delivery of SEN provision, and since September 2012 we have had a strengthened Ofsted framework that seeks to do that. I and my colleague in the Department of Health want to explore what more we can do to try to bring about a more multidimensional accountability and inspection regime for special educational needs that goes beyond the school gates and looks at it across education, health and social care, so there is more that we can do in that area. The Education Department is also looking at some of the destination measures in schools as a way of ensuring that we do not miss out on understanding the progress of children who sometimes fall below the radar because they do not count towards any of the measures of success that the school is being marked against. We need to get around that and make it more explicit that every child needs to be making progress whatever their ability, and there is no reason why all of them should not be doing so, and every school has a responsibility in that regard.
We made further changes in Committee, where I was pleased to include a specific duty requiring those responsible for commissioning health provision to secure the health care provision education, health and care plans. This is a hugely significant change and has been widely welcomed. Srabani Sen, board member of the Every Disabled Child Matters campaign and chief executive of Contact a Family, when giving evidence to the Committee on 5 March, said that
“it was phenomenally good news to hear this morning about the duty on health to provide. One of the things that that helps with enormously is bringing people together to work together at a service delivery level”—
a point that my hon. Friend the Member for Hexham (Guy Opperman) made—
“but it also gives parents something solid that they can use when they are having these discussions with their service providers about how they get the right services for their child. I do not think we can overestimate the potential of what you”—
I think that means me—
“announced this morning. It is phenomenally useful.”––[Official Report, Children and Families Bill Public Bill Committee, 5 March 2013; c. 47-48, Q103.]
The new duty builds on the joint commissioning duty set out in the Bill, which requires local authorities and clinical commissioning groups, and NHS England where relevant, to assess the needs of the local population of children and young people with SEN and plan and commission services to meet them.
The Minister has referred several times to the role of local authorities, but the reality is that some local authorities give greater priority to this than others. Because this ought to be—I think that the Government agree—person-centred, considering the needs, rights and ambitions of young people, has he had an opportunity to speak with the Local Government Association, for example?
Yes, I have had a number of meetings with the Local Government Association, the Association of Directors of Children’s Services and other bodies that will be responsible for delivering education, health and care plans and, more widely, SEN provision within their local area. This has been a huge consultative exercise, and one that continues through the pathfinders. One of the messages we have been clear about throughout the process is that legislation, although a key component of long-term, sustainable reform, is not the whole solution. We also need to see—this is happening through the pathfinders and starting to spread outside them as we develop the changes in the system more widely—a recognition that those bodies must play their part at grass-roots level and recalibrate the sorts of relationships that in the past have not been good enough to help deliver the required provision.
I would like to build on the comments my right hon. Friend the Member for Coatbridge, Chryston and Bellshill (Mr Clarke) made about the role of local authorities. The Royal National Institute of Blind People has raised specific concerns about the registration of visually impaired children—it is worried that some local authorities will do it but some will not. Has the Minister had an opportunity since that was discussed in Committee to have any further conversations with either the RNIB directly or local authorities on that issue?
I will be corrected if I am wrong, but my understanding is that there have been ongoing discussions. We are aware of the issue. As with all organisations that have expressed an interest in the Bill, we have been keen to keep an open dialogue with the RNIB to see what solutions we can find. Many of the solutions will be found at local level. We must accept that some conditions have a high incidence and some have a low incidence, and that can affect the sort of provision available right across the country. The beauty of trying to develop the local offer is that it will make it far more transparent not only in a local area, but across a regional area, so parents and young people will have a greater understanding of what is available to them, how they can access it and, if they are unable to do so, how they can make a complaint, which in the past has been quite a convoluted and impenetrable process. We must ensure that they have the power to make those decisions.
I am not sure whether I need to, but I will make a declaration: I have represented about 100 applicants for statements at special educational needs and disability tribunals, and local authorities still owe me money for some of them from before 2010. The simple question that my constituents in Northumberland would like answered, if that is possible, is this: will these proposals make it easier to gain a statement for those parents who have been trying to do so for so long, given that the process has been so convoluted and difficult over the years, as we have all found?
The short answer is yes. That is the intention of the Bill. There are a number of reasons for saying that. One of the complaints from parents about the statementing process relates less to the statement itself and more to early identification and the need for much greater effort from different agencies in co-ordinating the assessment and the plan. Everything in the Bill tries to encourage that and, in some circumstances, cajole the different bodies to come together and work with the family, rather than, as we have heard far too often, the family feeling that they are working in a different environment from those around them. By ensuring that that happens, we will reduce the prospect of conflict, misunderstanding and, therefore, the road to tribunal, which we all want to avoid. That is why we included the mediation process, albeit on a voluntary basis, to give parents and those responsible for providing services every opportunity to work together, co-operate and consult at every stage, but particularly in the early stages, in order to avoid unnecessary discord and damage further down the line.
While the Minister is on the subject of conflict between local authorities and parents, may I press him, as many of my amendments do, on home-educating parents, who all too often have been subject to misinformation and abuse of power by local authorities? Will he give serious consideration to including a provision stating that parents who home educate are not to have their children’s SEN support removed and that local authorities, despite their duty to find children with SEN, do not have their powers to demand access to children strengthened? We should reinforce the primacy of parents in deciding what should happen to their children and ensure that local authorities are the servants of families, not their masters.
I have a strong memory of spending a late night in the House a few years ago when my hon. Friend managed to get more than 100 of us to present petitions on behalf of many of those parents who decided to home educate their children. I know that he, as chair of the all-party group on home education, has been a great advocate on their behalf. Clearly we want to ensure that every child with SEN, however they are educated, during the period of compulsory age and beyond, from nought to 25, gets the support they require to meet their full potential. That should be no different in the circumstances he describes. I will be able to respond in more detail when we debate his amendments, and I am happy to continue that conversation with him outside the Chamber.
On home education and the obvious issues relating to special educational needs, what consideration has the Minister given to registration of those children who are home educated?
I am straying slightly outside my portfolio, but where it impinges on special educational needs clearly we want to ensure that those children receive the support they require. There were attempts in the last Parliament to bring about some form of registration, which was eventually put out to grass. I think we have the balance right at this stage, but of course it is something that my ministerial colleagues who are responsible for these matters will no doubt keep under review.
The new duty in the Bill relating to health commissioning also brings in joint commissioning arrangements, which must include those for securing education, health and care needs assessments and the education, health and care provision specified in the education, health and care plans. The new health duty requires health commissioners to ensure that the health elements of those plans are provided for each individual, thus providing direct clarity for parents that the support their child needs will be provided
We have taken an open approach to the Bill, listened carefully to the views of a wide range of people and made changes to improve it. I know that is the approach that my ministerial colleagues in the other place, including Lord Nash, intend to continue when the Bill makes its way to them. However, before it does we have some important business to conclude in this House today.
I will begin our consideration of the Bill’s SEN provisions by speaking to new clause 9 in a little more detail and to Government amendments 17 to 25. These amendments clarify responsibilities and make consequential amendments to legislation as a result of provisions in the Bill. With regard to new clause 9, it is important that the responsibilities of local authorities are clear when a child or young person with an education, health and care plan moves from one area to another. The new clause provides for regulations to specify those responsibilities. Regulations will make it clear that the new local authority is treated as though it had made the plan. This ensures that plans do not lapse when children and young people move from one area to another and that support for their special educational needs is maintained. I therefore urge the House to support new clause 9.
Amendment 17 to clause 41 has been tabled at the request of the Welsh Government. It would enable independent schools that are specially organised for making provision for children and young people with special educational needs, and specialist post-16 institutions in Wales, to apply to the Secretary of State for Education to be on a list of independent institutions that those with education, health and care plans can ask to be named on their plan. If independent schools in Wales wish to put themselves forward for approval, the amendment will be of benefit to children and young people who live close to the Welsh border whose needs would be best met in a Welsh independent school or those who would be appropriately placed in independent boarding provision in Wales. I urge the House to support the amendment.
On amendments 18 to 20 on personal budgets, I signalled our intention to table these consequential amendments when we debated clause 48 on personal budgets in Committee. The changes they make are necessary because of the changes we made to clause 42 in Committee by placing the duty in clause 42(3) on health commissioners to secure the health provision identified in an education, health and care plan. The amendments allow health commissioners to discharge their duty to make health care provision specified in EHC plans when this provision is secured using a direct payment. This replicates the equivalent provision on local authorities set out in clause 48(5). The amendments clarify that when parents or young people exercise their direct payment, this allows the commissioning body to discharge its statutory duty. The proposed use of the words “having been” in clauses 48(5) and 48(7) makes it clear that the duties on commissioning bodies and local authorities to secure provision are discharged only through the use of a direct payment when the child or young person has actually received the provision, in a manner in keeping with the regulations. I urge the House to support these amendments.
Government amendment 21 relates to clause 49, which inserts new section 17ZA into the Children Act 1989, giving local authorities a power to continue to provide services they have been providing under section 17 to a young person before their 18th birthday to that young person when they are 18 and over. This is a technical amendment that makes it clear that the power in section 17ZA applies only to local authorities in England.
Government amendments 22 to 25 relate to schedule 3 and make further amendments to existing legislation as a consequence of the Bill’s provisions—for example, replacing references to statements and learning difficulty assessments throughout. These are necessary changes to ensure the proper implementation of the reforms in part 3, and I therefore urge hon. Members to approve them.
It is a pleasure to debate this Bill again, this time on the Floor of the House. In Committee we had some excellent debates on this part of the Bill, in particular. A large number of amendments were tabled by hon. Members on both sides of the Committee, but we were at all times united in our ambition for the children and young people to whom the Bill applies.
It is crucial that children and young people with special educational needs and disabilities be given the support they need to access education and reach their potential, academically and in terms of their physical, social and emotional development. It is not just a moral imperative that leads us to seek those better outcomes for all children; there is also a financial imperative for the whole country. A young person who makes a successful transition to adulthood and has achieved as much as they can educationally is likely to be less in need of welfare, health and social care support and more likely to be able to work and contribute their skills to the economy and their taxes to the Treasury. We support a great many of the reforms that the Government are making to achieve these better outcomes, but we have sought at all stages to ensure that we are going as far as we can, that current rights and entitlements are protected and built on, and that children and young people, and their families, are at the very heart of the changes made and are able adequately to hold agencies to account where they do not get the support they should.
We support the introduction of personal budgets to allow families a greater degree of choice in securing the choice that their child needs. As I said in Committee, I would have greatly welcomed such an opportunity when I was trying to get my severely dyslexic son the support he needed to get through his GCSEs. However, there are serious and abiding concerns about whether they can work in the sense of improving outcomes while providing value for money for the taxpayer, and there are still questions about how the market for support that this reform will create will really look. The Government are running pathfinders in an effort to answer these questions, but they have not been answered yet. Parliament is therefore being asked to legislate for something that we do not know will work and could well be a costly failure.
I thank my hon. Friends the Members for South Swindon (Mr Buckland), for Romsey and Southampton North (Caroline Nokes), for Beverley and Holderness (Mr Stuart) and for Torbay (Mr Sanders) and the hon. Member for Walsall South (Valerie Vaz) for the amendments they tabled. I thank in particular the hon. Member for Washington and Sunderland West (Mrs Hodgson) for embodying in her approach the very essence of this part of the Bill, in that she has demonstrated a lot of co-operation and constructive consultation and has, I suspect, sometimes strayed into the occasional bit of joint commissioning, which I welcome. I also thank other Members who have spoken in this debate on the SEN provisions. I will do my best to respond to the amendments and the key points that have been made.
Amendments 30, 46, 62 and 66 to 69 and new clause 21 are concerned with arrangements for improving local provision. I hope I will be able to address the concerns that are behind amendment 30—as just raised by my hon. Friend the Member for Romsey and Southampton North—through regulations and the code of practice. Draft regulations under clause 48 would require local authorities to provide information, advice and support in relation to personal budgets, including information about independent organisations. Draft regulations made under clause 36 would require local authorities to provide any support they consider necessary for parents or young people to take part effectively in the education, health and care assessment, and regulations made under clause 30 would require local authorities to include in their local offer sources of information, advice and support for children and young people with special educational needs and their families. The indicative code of practice—which my hon. Friend the Member for South Swindon helpfully pointed out was made available in Committee and proved invaluable as a consequence—clarifies that this should include information, advice and support available in relation to personal budgets.
I share the aim of my hon. Friend’s amendment 46, which is to ensure that education and social care provision is sufficient to meet the needs of children and young people with SEN and to promote improvements in that provision, but that should be balanced with the need to retain local decision making; that point seemed to unite the House in the debate we have just had. Local authorities, schools and other services must determine spending on provision for children and young people with special educational needs, taking account of their legal responsibilities. Clause 27(3) would require local authorities to consult a wide range of people and organisations in reviewing provision, including, importantly, children and young people with special educational needs and their parents, but placing a specific legal duty on them to improve special educational and social care provision until everyone consulted agrees it is sufficient would be impractical, as views of different people and groups would inevitably differ. Local authorities will be able to reflect the outcomes of the reviews they undertake under clause 27 in the local offer, which also requires the close involvement of children and young people with special educational needs and their parents in its development and review.
On amendments 66 to 69, I can assure the hon. Member for Washington and Sunderland West and other hon. Members that the local offer will not be a speculative document. It will set out what the local authority expects will actually be available. The local authority does not have control of all the services set out in the local offer, so it can only set out what it expects to be available. If it can only reflect what is currently available, that will prevent the local offer from setting out, for example, what provision it expects to become available in the near future. This could, for example, include new provision in a school, which parents or young people will want to know about in advance.
On amendment 68, I agree that online communities can be a valuable way to socialise, and perhaps that is especially true for young people with special needs. Only yesterday I had the opportunity to visit Springfield special school in my constituency. The children being educated there were keen to show me first their school’s IT suite, where they had developed some important skills in a number of innovative ways. I agree that online communities have their dangers, and that young people should be equipped to socialise over the internet safely. I repeat the commitment I gave in Committee: I will consider including a reference to online communities in the code, in the context of preparing for adulthood. I do not believe it is necessary to amend the Bill in order to achieve what Members want, but I think what I have said demonstrates the importance of this area both now and in the future.
Amendment 69 concerns minimum standards in the local offer. The key to the success of the local offer in each area will be the transparency of information, and the involvement of local parents, children and young people in developing and reviewing the local offer. Central prescription would stifle the very innovation and responsiveness we want to see the local offer trigger, and stipulating minimum standards for the local offer would weaken local accountability. They would constrain parents’ ability to influence a local authority, which could point to meeting minimum requirements to end further discussion. That is a potential “race to the bottom” that we must avoid; my hon. Friend the Member for South Swindon raised that point in Committee. I hope that detail about what will be in the offer and the strength of the processes for agreeing it will reassure Members that such a potentially counter-productive minimum standard is not necessary.
Amendment 62, from my hon. Friend the Member for Beverley and Holderness, the Chair of the Education Committee, reflects the view expressed by his Committee about the importance of parent carer forums, whose national network I believe I am meeting tomorrow. I share my hon. Friend’s views about the importance of parents helping to shape local policies for supporting children and young people with special educational needs. The indicative SEN code of practice makes clear reference to that and to the value of parent carer forums, but as they are not legally constituted bodies we cannot include them in the list in clause 28 of organisations with which a local authority must consult when carrying out its functions under the Bill.
Provision has been made in clause 27 for local authorities to consult children and young people with special educational needs and parents of children with SEN, along with
“such other persons as the authority thinks appropriate”,
when carrying out their statutory duty to keep their special educational provision and social care provision under review. I am sure that local authorities will want to consult parent carer forums as they carry out that duty, which is reflected in the draft code of practice. The SE7 pathfinder, for example, is working closely with its local parent carer forums to develop the local offer, to ensure that it reflects the needs of children, young people and parents.
Turning to new clause 21, local authorities aim to provide services close to home, and I know how important it is for families for provision to be made locally. However, as has been said, that is not always practical for those who require specialist support that is available only in very few places. Clause 27 requires local authorities to consult children and young people with special educational needs and their parents when they are reviewing their special educational provision and social care provision. Local authorities, clinical commissioning groups and NHS England must develop effective ways of harnessing the views of their local communities, and they will undoubtedly want to engage with Healthwatch organisations, patient representative groups, parent partnerships, parent carer forums and other local voluntary organisations and community groups.
Clause 30 requires local authorities to involve children and young people with special educational needs and their parents in developing and reviewing the local offer. That will ensure a continuing dialogue between local authorities and their partners, including children, young people and families, and keep a focus on the need for local provision. I recently discussed these issues with Scope, which has a good deal of experience in this area, and undertook to consider how the guidance in the SEN code of practice could best encourage the development of services that are responsive to local needs.
Amendments 44, 37 and 39, tabled by my hon. Friend the Member for South Swindon, are all concerned with ensuring an integrated approach to meeting the needs of children and young people. I share the goal of amendment 44—integrated health and social care support—but cannot agree that it is the best way to achieve it. Under the Bill, the support that must be available to the child or young person is that reasonably required by his or her special educational needs.
Local authorities and health commissioners have the power to include other social and health care if they feel it is appropriate. So a child with special educational needs arising from cerebral palsy who needs a wheelchair would have that in their plan. If the child developed an unrelated minor infection, any prescribed medication would not normally be included. Amendment 44 would add unnecessary bureaucracy and hinder pragmatic decision making. I am alive to the case studies that my hon. Friend brought to the House’s attention and will look carefully at them in understanding the consequences of the point he makes. I am happy to continue to discuss that with him, but as things stand I am not convinced that his amendment is necessary.
Amendment 37 seeks a specific duty on authorities to deliver social care provision in EHC plans. As I said in Committee, existing duties in section 17 of the Children Act 1989 provide important protections. I understand concerns that this is a general, not an individual duty, but I fully expect that local authorities will provide care services to meet assessed needs. In the case of disabled children, the Chronically Sick and Disabled Persons Act 1970 applies, and once the authority is satisfied it is necessary to provide support and assistance, it is required to do just that. I do not think it right to prioritise, as a matter of course, children with EHC plans over all other children in need, who would then risk being marginalised—I am thinking, for example, of children suffering neglect or abuse.
On amendment 39, I know that my hon. Friend has concerns about clause 21, and my hon. Friend the Member for Peterborough (Mr Jackson), among others, has also raised this issue. Clause 21(5) fulfils an undertaking I gave during pre-legislative scrutiny of the Bill that we would maintain existing protections, including case law. The subsection was included to preserve the current position whereby, of course, there is no duty to secure the health provision in plans. Amendment 39 goes further than current case law and would define all social care and health care provision made for a child or young person with SEN as special educational provision, if it was in some way for the purposes of education or training.
The logic throughout what the Minister has set out has been about bringing together providers to offer one point of contact with families and young people affected. If, as the pilots continue and this policy is brought into effect, it emerges that it might be preferable for there to be some kind of unified appeal process, would there be the mechanism to bring that about subsequently through secondary legislation? Alternatively, for that to happen would it need to be in the Bill?
My hon. Friend makes a point about the importance to the parents and the young person of having a single point of access into any complaints procedure. That is why we are looking at how there can be a single point of interface for them, providing them with the information and navigation they require to find themselves in the right part of that complaints process. Clearly, as my hon. Friend the Member for South Swindon said, there are tribunal rules in place and there are always practical ways in which we can look at trying to enmesh more clearly together the various strands in the complaints mechanisms. We need to develop that through the pathfinders and, as we hopefully reduce the number of cases that end up in the tribunal system, see whether that has had an effect. We will keep that under close review.
New clause 24, tabled by the hon. Member for Washington and Sunderland West, was discussed in Committee, following which I wrote clarifying what information was already published. The effect of the new clause would be that details were published by individual case. It would not be appropriate to publish information that could identify details of private cases. Clearly, we want to reduce contention. Publishing information on individual cases is likely to extend the contention beyond the delivery of the tribunal’s judgment.
Information would have to be published on the tribunal service and authorities’ costs, and that raises the question whether information would also have to be published on the relative complexity of cases to justify what may be a proportionate expense. The wish to publish information on the cost to authorities may be based on the misapprehension that authorities usually engage legal representation. The most recent figures show that authorities were legally represented at only 15% of hearings, and in most cases authorities would just be providing information on officer time costs. Publishing seemingly simple information on costs without proper context may well lead to greater confusion, therefore, but I have no doubt that the hon. Lady will want to return to that area in due course.
New clause 8, tabled by my hon. Friend the Member for Torbay, and amendment 65, tabled by the hon. Member for Walsall South (Valerie Vaz), both concern children with health conditions. It is right that every child with a long-term health need is entitled to a high-quality education. Their needs must be identified and addressed promptly, so that they can achieve their full potential. Imposing further statutory duties on schools to ensure that is not necessarily the answer, however.
The right hon. Member for Wentworth and Dearne (John Healey), in a powerful and passionate speech, demonstrated an acute knowledge of life as a Minister and the response that he was likely receive as to current provision. The Education Act 2002 already places a duty on the governing body of a maintained school to promote the well-being of pupils and, as the right hon. Gentleman said, schools are already under a duty through the Equality Act 2010 not to discriminate against pupils with long-term health problems that have an adverse effect on their ability to carry out their normal day-to-day activities. Nor should we require schools and further education institutions to request an EHC assessment for everyone with epilepsy or a related condition.
In a recent written answer to a parliamentary question, I announced that the “managing medicines” guidance would be issued this year, which will further clarify schools’ responsibilities. I am confident that it will address the right hon. Gentleman’s concerns. However, I take what he said extremely seriously and will look closely at the details of what he and others have proposed. I would be more than happy to discuss these matters with him as we consider how we can improve practice in our schools, some of which is still below the level that we should be seeing. We know from figures cited by my hon. Friend the Member for Torbay that the number of children affected by conditions that require support in school is not small, so every effort needs to be made to improve practice on the ground.
The statistics seem to show that while there are provisions in previous legislation that are supposed to work, they are not working for large numbers of children with these medical conditions. That is the point of new clause 8.
I understand the intention behind the new clause, but when the raft of legislation directly or indirectly related to the point that my hon. Friend raises is still not bringing about the required support for children in our schools, one wonders whether additional legislation is necessarily the answer. We are seeking to provide the best possible guidance to schools on managing medicines, set against the current legislative framework; and under the new Ofsted inspection of schools, safety is a key feature.
I find the Minister’s answer inadequate. It is shameful that successive Governments have gone for so many years with a significant minority of children simply not having their needs met in school. When they have a condition or a flare-up that requires action, they get sent off to hospital, or their parents get called, whereas if the school had trained someone up, it could meet that need. This is not good enough. The Minister has done so much under the Bill; this is another area where there could be an historic, positive settlement coming out of the legislation. It would be a shame if the opportunity were missed.
I had been doing so well with my hon. Friend, throughout the day. He is quite right to continue to challenge us, and schools, on this point. The question that has to go back to schools is why some are able to manage medicines effectively and others are not. That suggests to me that there is not necessarily a direct relation to the legislative framework that they are working under, and that it is down to differences in practice and to the school’s commitment to dealing with the issue. As I say, I am not stopping the discussion at this juncture. I am sure that there will be other opportunities for us to explore what more we can do. Reissuing the guidance is an important step, because it will provide very clear advice to schools on how they should approach this important issue. We will follow that up closely, both through Government channels and through Ofsted’s work in its role as inspector.
My hon. Friend tabled amendments to part 3 in respect of children who are home-educated. I know, because we have discussed the issue, that he takes a keen interest in these matters, both as the chair of the all-party parliamentary group on home education and as the Chair of the Select Committee on Education. He recently wrote to the Secretary of State about the Bill’s implications for home educators. He will receive a reply shortly. In the meantime, I reassure him that the Bill will bring benefits to all children and young people with special educational needs, including those who are home-educated. In particular, clause 19 says that in exercising their functions under this part of the Bill, local authorities have to have regard to parents’ views, wishes and feelings, which might, of course, include a wish for home education.
Parents will still have the right to educate their children at home. Where local authorities draw up education, health and care plans that say that home education is right for the child, the local authority will have a duty to arrange the special educational provision set out in the plan, in co-operation with the parents.
I was impressed by almost everything that the Minister said until he got to the words, “local authorities have to have regard to”. Does he not feel that that is rather a weak way to challenge local authorities? Is it possible that people will look at that in another place?
As to the right hon. Gentleman’s second point, I am sure that they will; that is the beauty of the process that we find ourselves in. We are content that we have the right balance. We also need to be alive to the fact that home-educated children require support—this goes to the earlier point about proportionality and reasonableness—that fits in with their education. Clearly, every child’s needs have to be assessed, and local authorities should have that in mind.
Where a child has a plan that names a school as the appropriate environment in which to receive his or her education, parents will still be able to decide to home-educate; that is an important point. If they do, the local authority must assure itself that the parents are providing an education in accordance with section 7 of the Education Act 1996—that is, a full-time education that is suitable for the child’s age, ability, aptitude and special educational needs. If the local authority is so assured, it will be relieved of its duty to make the special educational provision set out in the plan, just as it is now with regard to statements. However, local authorities will continue to have the power to help parents to make suitable provision in the home by providing support services. To take on the right hon. Gentleman’s point, I would strongly encourage local authorities to consider exercising that power when making decisions about whether the provision being made by parents is suitable.
My hon. Friend says that local authorities must assure themselves that parents are delivering the education in accordance with 1996 Act. I do not think that that is the case. They have to act if they have reason to believe that parents are not providing suitable education. They have no such overarching duty to assure themselves that every single home educating parent is doing so. The parent, not the local authority, has primacy in the education of their child. The local education authority acts only if it finds out that there is a problem. It does not have to seek it.
I hope that our differentiation is based simply on the semantics of some of the vocabulary that is being used, but clearly we need to have absolute clarity on the role of each agency in the life of a child, whether they are educated within the school sector or at home. I will write to my hon. Friend to ensure that he has chapter and verse on precisely that point.
I come now to amendments 60 and 6l. I understand from my hon. Friend that home educators are concerned that clause 23 will mean that local authorities will have to assess every home educated child to see if they have SEN, which takes us back to the previous Parliament, where we had many of these discussions. I can assure him that this is not the case. Clause 23 sets out which children and young people local authorities are responsible for under this part of the Bill. These will be children and young people who have already been identified by the authority or who have been brought to the authority’s attention as having, or possibly having, SEN. There is not that overarching forensic exercise of trying to locate each child.
Amendment 63 seeks to tie the definition of the suitability of any alternative arrangements that parents make for children with an EHC plan more closely to the definition of parents’ right to home educate as set out in section 7 of the Education Act 1996. However, this is unnecessary as the provision in the amendment is already contained within the phrase “suitable alternative arrangements”, so does not need to be spelled out in this way. Similarly, while I understand the concern that amendment 64 seeks to address, it is not necessary. Where a child has a plan that says that education provided in the home is the right provision for the child, the local authority could only cease the plan when it felt it was no longer necessary to meet the child’s needs, as set out in the legislation.
Where parents take a child out of school to home educate and are making suitable provision, as is the case now with statements, the local authority will be under a duty to review the plan annually to ensure that the provision that the parents are making continues to be suitable. The local authority could cease to maintain the plan only where it was decided it was no longer needed to meet the child’s needs. Moreover, the new duty on commissioning bodies to arrange the health provision in the plan and the greater expectation that the social care provision will be made will mean that parents can expect that these will continue to be provided. There is further scope within the code of practice to provide clarity on these issues for local authorities, and no doubt my hon. Friend will want, through his connections with the home education lobby, to contribute to that consultation, which will be happening later this year.
On amendments 40 to 43, I find myself completely agreeing once again with my hon. Friend the Member for South Swindon that some young people with special educational needs require more time to complete the education that other young people have already finished by the age of 18. The Bill rightly enables them to do so, but we want to avoid the expectation that every young person with SEN has an entitlement to education up to 25—a point that I think he accepted in Committee—regardless of whether they are ready to, or have already made, a successful transition into adult life. The Education Committee recommended that we clarify whether there is an entitlement to special education provision up to age 25. The requirement to have regard to age makes it clear that there is not. However, I can categorically assure my hon. Friend that no young person who needs an education, health and care plan to complete or consolidate their learning can be denied one just because they are over 18. Local authorities must rightly consider a range of matters in coming to these important decisions.
Clause 45(3) requires local authorities to consider whether the educational outcomes specified in the plan have been achieved when it is deciding whether it should cease to maintain a plan. The indicative code of practice, at section 6.18, says:
“local authorities must not simply cease to maintain plans once a young person reaches 18”.
They should consider whether young people have met their agreed outcomes, whether continued education will help them achieve those outcomes, and whether the young person wants to stay in education. Of course, in what we hope will be rare instances, a young person may appeal against a decision to cease their plan, a step forward from the current system.
My hon. Friend also tabled amendments 45 and 48. Securing a place at university is a positive outcome for any young person, and we are right to have high aspirations for children and young people with SEN and disabilities. However, it does not follow that higher education institutions must be part of this Bill. Local authorities are not responsible for the education of young people in higher education and it would be unreasonable to hold them accountable for securing special education provision while the young person is there. As my hon. Friend has already noted, the higher education sector has its own very successful system of support in the form of disabled students’ allowance. DSAs are not means-tested, are awarded in addition to the standard package of support and do not have to be repaid. We should not seek to duplicate or replace that system when it appears predominantly to be working well. In the academic year 2010-11, DSA provided 47,400 full-time students with support totalling £109.2 million. The Government also provided £13 million to HEIs in 2012-13 through the disability premium to help them recruit and support disabled students, and in 2013-14 that figure will rise to £15 million.
However, I agree that we must improve the transition to university. Draft regulations require that when a young person is within two years of leaving formal education a review of their EHC plan must set out plans for helping them make a successful transition to adulthood. We will make it clear in the code of practice that good transition planning includes sharing the EHC plan with the university, with the young person’s consent; ensuring that the young person is aware of DSA and has made an early application so that support is in place when their university course begins, on which the hon. Member for Washington and Sunderland West shared her experience with the Committee; and ensuring continuity of health and care services where those continue to be required by the young person. In addition, we will work with those conducting DSA assessments to ensure that they understand the EHC plans, as well as how they can assist and inform the assessment and ensure that details of DSA are included in the local offer so that all young people thinking of applying to university are aware of the support available to them.
Under proposals in the Care Bill, which is currently in Committee in the other place, 18-year-olds with eligible needs will receive a statutory care and support plan. The new legislation will ensure that there is no gap in provision as young people make the transition from children’s services to adult services and, when they move from one local authority area to another, that the new authority continues to meet their needs until it has undertaken its own assessment.
With regard to amendment 47, I agree with my hon. Friend the Member for South Swindon that all young offenders, including those with SEN, need to receive the right support and access to education, both in custody and when they return to their communities. Since our debate in Committee, I have considered the issue further and remain of the view that clause 69 is necessary, not because we are not committed to supporting young offenders, but because it prevents our legislation from coming into conflict with existing comprehensive statutory provisions governing how education support is delivered in custody, as set out in the Apprenticeship, Skills, Children and Learning Act 2009.
My hon. Friend the Member for South Swindon will know that the duties placed on local authorities by that legislation are currently fulfilled through the contracts held by the Education Funding Agency and that local authorities are often not involved. The Ministry of Justice, which funds that arrangement, is clear that the current system is not working, which is why it recently consulted on transformational reforms to how education and support in youth custody should be delivered in future. I have ensured that I have been kept in close contact with Justice Ministers so that the education element for children—not only those with SEN, but others in the care system and elsewhere—is being properly considered as part of the review.
Will my hon. Friend undertake to ensure that when the Bill goes to the other place a careful eye is kept on clause 69 and that the Ministry of Justice moves in a way that is properly co-ordinated so that we do not end up with the nightmare scenario of those young people simply falling through the gap?
I strongly share my hon. Friend’s view. I want to make progress on that, both in my Department and across Government. The commitment I gave him earlier will continue as the Bill moves on and other work is done by the Ministry of Justice on the consultation it has carried out, because it is important that we make as much progress on that as possible at an important stage of development in many of our institutions and within the secure estate.
Clause 69 also plays an important technical function by disapplying duties with the SEN clauses that it would be impractical to deliver while a young offender is in custody. For those reasons, I do not agree that we can simply remove the clause ahead of the significant reforms to education in custody that the Ministry of Justice is considering and the resulting changes that might need to be made to existing legislation. However, I have sought to reassure my hon. Friend the Member for South Swindon and hope that provides him with some confidence as we move forward.
Turning to amendments 71 and 72, tabled by the hon. Member for Washington and Sunderland West, we are continuing to strengthen our understanding of young people’s post-16 educational outcomes. The Department for Education will be publishing destination data on students with SEN at key stage 4 before the summer break, and later in the year for those at key stage 5. The Department for Business, Innovation and Skills already publishes data on participation and attainment in further education by students with SEN aged 19 and over, and that will continue. I do not think that it is necessary to place additional reporting requirements on the further education sector when those data are already being made public. However, as I have said previously, I am sure that she will continue to press that point as the Bill moves on to the other place.
On amendments 73 to 75, we will ensure that any code of practice laid before Parliament has been subject to proper consultation and that Parliament is given the opportunity to scrutinise new or updated versions. Clause 67(2) already ensures that the Secretary of State carries out sensible and proper consultation on the code of practice. We intend to publish a draft code of practice on the Department’s website for public consultation in the autumn of this year and to give ample time for comment, over and above the draft that we provided for the purposes of Committee. If we did not consult appropriately, there would be every reason for this House or the other place to resolve not to approve the code.
The Education Committee considered the careful balance between proper consultation and parliamentary scrutiny and keeping the SEN code of practice up to date during pre-legislative scrutiny. The Bill delivers on their recommendation that the draft should be subject to consultation and approved by Parliament using the negative resolution procedure. This brings the code into line with other statutory codes, such as the school admissions code, and enables an appropriate level of parliamentary scrutiny.
This debate has continued the good faith that has been a hallmark of the progress of this part of the Bill. Given what I have said, I hope that hon. Members will feel sufficiently assured not to press their amendments.
Question put and agreed to.
New clause 9 accordingly read a Second time, and added to the Bill.
New Clause 10
Childcare costs scheme: preparatory expenditure
‘The Commissioners for Her Majesty’s Revenue and Customs may incur expenditure in preparing for the introduction of a scheme for providing assistance in respect of the costs of childcare.’.—(Elizabeth Truss.)
Brought up, and read the First time.
I beg to move, That the clause be read a Second time.
I would like to speak briefly to amendments Nos 5, 6, 7 and 8, which seek to introduce greater flexibility and understanding of the 26-week target for care proceedings. Nobody in this place would deny that that target is very helpful and we hope that, in most cases, we will be able to meet it. But we know—for example from the Norgrove report—that, on average, cases take up to 61 weeks: 48 weeks in family court proceedings. The Justice Committee, of which I am a member, held an inquiry into the operation of family courts. In its evidence to us, Barnardo’s made the point:
“Two months of delay in making decisions in the best interest of a child equates to 1% of childhood that cannot be restored.”
For this reason, both the all-party group on child protection and the Justice Committee welcomed the Government’s aim of reducing unnecessary delay in the care system.
Care must be taken with regard to the target as well. Clause 14 provides the starting point for courts in setting a time for cases; proceedings should come to an end within 26 weeks, as I mentioned. But there is some ambiguity as to when courts should deem an extension appropriate. As the College of Social Work and the Family Rights Group have argued, there is a genuine risk that the proposed 26-week limit could result in too much focus on procedure and not enough on the welfare of the child.
The vast majority of cases will be concluded within six months, but deciding on permanent options can take longer for some children, not always due to problems with the court process or unnecessary delay. Social workers will attest that situations can change in the course of proceedings; for example, when relatives present themselves as possible carers late in the process. The Family Rights Group has pointed out that, under the new limit, if family members are late in offering themselves as carers there may well not be enough time for the relevant assessments to be carried out.
Equally, placing a child with grandparents, aunts, uncles, cousins or other siblings can reinforce aspects of a child’s identity. In many cases, however, relatives will be reluctant to offer this option if they think that there is still a chance that the child will be able to be returned to his or her parents.
I anticipate that Government Members will point out that the safeguard for granting extensions to cases is robust enough to allow for complications to be ironed out. Sadly, I have it on good evidence that judges are, in some cases, already imposing a 26-week deadline on proceedings even before the limit has been introduced. It is crucial that time considerations do not supersede the welfare of the child concerned. What is more, some intervention programmes take longer than 26 weeks due to parents undergoing treatment for substance misuse issues and similar problems. The pilot boroughs—Hammersmith and Fulham, Westminster, and Kensington and Chelsea—have estimated that 25 to 30 per cent. of all cases will take longer than the 26-week limit.
Intensive family programmes, such as the NSPCC’s infant and family team, are another example. The programme was developed in the United States and is now being piloted in the United Kingdom. A four-year evaluation of the programme in the US showed improved outcomes for children and adults in all groups that undertook the programme. I will be unable to address that point as fully as I should like in the time allotted, but one of the motivations behind the amendments I am speaking to—by the way, I am hugely indebted to the NSPCC for its assistance in this matter—is that some cases should be exempted from the limit from the outset. Although the Bill as drafted would allow for incremental eight-week extensions, practitioners in the field have warned that they would need to know at the beginning of proceedings how much time they have to work with the family, in order to secure the best possible outcome.
Equally worryingly, practitioners warn that social workers could be deterred from seeking extensions other than in highly exceptional circumstances, as the “specific justification” test in clause 14(7) may be perceived as a barrier in borderline cases. That is why amendment 5 would allow courts to exempt certain cases from the 26-week limit from the very start of proceedings if evidence relating to a planned intervention or programme requiring a longer period was presented to the court, or if the court considered it necessary to permit additional time to safeguard the child’s welfare.
Amendments 7 and 8 relate to clause 17, which introduces significant reforms to the way in which courts scrutinise care plans. I do not have time to go into the context; all I would say is that I, too, am disappointed that our time is limited today. These are very important matters. I have skimmed through what I was going to say—I am grateful that I was able to catch your eye, Madam Deputy Speaker—and I know that the NSPCC and many other organisations will be bitterly disappointed that we have had to truncate such important debates in this way.
This group of amendments covers a wide range of issues relating to the care and protection of children. As I will be unable to address all the points made, I will endeavour to write to all hon. Members in response to their amendments and the questions they posed, particularly the hon. Member for Wigan (Lisa Nandy), who has been very convivial and constructive during the passage of this Bill, and my hon. Friend the Member for East Worthing and Shoreham (Tim Loughton), who has raised a number of important areas of debate, particularly in making some powerful points about returning home from care. I will look at those points extremely carefully and am happy to discuss them with him on another occasion.
I want to focus on a number of issues about which I have some important points to make. They are: care leavers, young carers, fostering for adoption, child witnesses and sex and relationships education. On carer leavers, new clause 4 considers “staying put” arrangements, where care leavers live with their former foster carer after they have left care. Many hon. Members have expressed their support for new clause 4, and I would welcome the opportunity to discuss how we can extend those arrangements. The legislative framework relating to care leavers is comprehensive and clear. I have written to all directors of children’s services asking them to prioritise “staying put” arrangements. We have also issued practical guidance on tax and benefits issues. We are monitoring “staying put” arrangements and reviewing local progress through Ofsted inspections and feedback from care leaver groups. If no progress is being made, I will consider whether legislation is required, but I do not believe we should make that change only two years after changing the statutory framework.
On young carers, in Committee we heard heart-felt arguments about the need to do more for young carers. I promised to reflect carefully on the arguments for legislative change. Since then I have discussed the matter with the Minister for care services, my hon. Friend the Member for North Norfolk (Norman Lamb), and we have agreed that our joint aim is to ensure that young carers are protected. We firmly believe that taking a “whole family” approach to the assessment of care needs will be the key to achieving just that. I have now given the matter careful thought and, with the changes being introduced by the Care Bill for adult carers, I am persuaded that the time is right to see what we can do to remove any barriers that may be preventing these vulnerable young people and their families from receiving the life-changing support they need.
I have asked officials to look at how the legislation for young carers might be changed so that rights and responsibilities are clearer to young carers and practitioners alike. We will also look at how we can ensure that children’s legislation works with adults’ legislation to support the linking of assessments, as set out in the Care Bill, to enable “whole family” approaches. We will ensure that interested parties, including hon. Members, are consulted on that work.
There is a strong consensus about the policy intention behind fostering for adoption: that children should be placed as early as possible in a stable placement. Amendment 33 would mean that clause 1 would bite too early for concurrent planning. I listened to the concerns raised in Committee about the impact on kinship carers, but there is no intention that kinship carers should be overlooked as a consequence of this clause. I am pleased to reassure hon. Members that I am giving consideration to amending the clause to be clearer that local authorities must first consider placing a child with relatives and friends before they consider a “fostering for adoption” placement. This is an issue that I expect to be returned to in the other place, and I know that Members will welcome that reassurance. I know that hon. Members will also be pleased by today’s announcement from the Secretary of State for Justice on child witnesses. That represents an important move forward.
On personal, social and health education, we all recognise that this is an important issue, but we do not have unanimity on what constitutes the best approach. The expectation that all schools should teach PSHE is outlined in the introduction to the framework of the proposed new national curriculum. It is not a statutory requirement, however, as we strongly believe that teachers need the flexibility to use their professional judgment to decide when and how best to provide PSHE in their local circumstances. The Government do not believe that the right of parents to withdraw their children from sex and relationships education should be diminished in the way proposed. We see no need to amend the existing legislation, which provides a clear and workable model for schools and parents. Moreover, the new provision would place a disproportionate burden on teachers, who would have to make and defend decisions on what constitutes “sufficient maturity”—
I beg to move, That the Bill be now read the Third time.
Let me begin by thanking all Members who served on the Public Bill Committee. The debate was constructive and—dare I say it?—mature, exceedingly thorough and all the more encouraging for being the first such Committee for many of the newly elected Members on both sides of the House. We had 19 sittings, 397 amendments were tabled, and every issue was thoughtfully scrutinised. I am sure that we all agree with the hon. Members for Washington and Sunderland West (Mrs Hodgson) and for Wigan (Lisa Nandy)—I extend to them my personal thanks for their responsible and fair-minded contributions —who told us that it was
“a hard-working, good-natured and somewhat consensual Committee. At times, we have agreed more than we have disagreed, which is for the good… the legislation we are shaping is extremely important for millions of our most vulnerable children now and in future.”––[Official Report, Children and Families Public Bill Committee, 25 April 2013; c. 815.]
I would also like to thank the Under-Secretary of State for Business, Innovation and Skills, my hon. Friend the Member for East Dunbartonshire (Jo Swinson), who has led jointly on the Bill with great aplomb in this House and before the four Select Committees that considered much of the Bill during pre-legislative scrutiny, even when the odd stray nut sought to scupper her endeavours.
The debates in Committee and today have reflected the importance of the issues the Bill seeks to address. It seeks to improve the lives of some of our most vulnerable children. Improving the life chances of every child, whatever their background, by putting their needs first in all that we do is at the heart of the Government’s agenda.
I will take a brief intervention, but I am mindful of the time and know that other Back Benchers wish to speak.
I, too, am mindful of the time, so I am grateful to the Minister for giving way—I understand why he could not do so during his speech on Report. I rise on behalf of a constituent who fosters three children. As a consequence of the Government’s decision to exempt only one bedroom from the bedroom tax for foster carers, she is required to pay £14 a week to carry on fostering. If she moved into smaller accommodation, she could foster only one of those three children, and there would be a cost of about £3,000 a week if the children went into care. Will he, together with the Minister responsible for welfare reform, look at the issue and reflect on whether they can give a further concession?
Of course I am happy to look at the specific case the hon. Gentleman raises in the context of the changes that have been made. As he and Opposition Front Benchers will know, I have worked hard, both before coming into government and since, to try to ensure that foster carers are given the best possible support in their endeavours, because we want to encourage more people to foster, and we know from the research we have done that many more would like to take up that opportunity. The Welfare Minister, Lord Freud, and I have written jointly to all local authorities to explain the importance of this, with regard to both the single room subsidy and making the discretionary housing fund available to foster carers where appropriate. We have committed to an independent review of that progress, and I will be keeping a keen and close eye on how that develops. I know that the Fostering Network, which has done some excellent work on the issue, will also take a lead in ensuring that we have a clear understanding of the impact of the changes.
The Bill will overhaul services for vulnerable children and support strong families. It will raise aspirations and place children and young people at the heart of decision making and support in the SEN system. It will reduce delays in the adoption system. It is part of a wider set of reforms to improve children’s services so that everyone involved in a vulnerable child’s life—teachers, social workers, health professionals and the police—has a proper sense of responsibility for the child’s prospects, not just focusing on their precise duties and whether they have followed the correct processes and ticked all the boxes, but looking at the child’s overall welfare. That means refocusing the system on the child’s needs in a child’s time frame, foremost among which must be the need to keep the child safe from harm.
We often hear that the care system fails children, that it damages and betrays them. Too often it does, but, as I know from my family and the fostering and adopting we have undertaken, it can also transform lives. As the recent research report “Safeguarding Children Across Services” pointed out, when compared with those who are reunited with their birth families, the majority of maltreated children do better in care or accommodation. Looked-after children can and do achieve in care in a stable placement. We know, for example, that there is a marked correlation between the length of time in care and the stability of placements and achieving good educational outcomes at GCSE, yet we must remain resolute in ensuring that the child’s best interests, not administrative or personnel considerations, are always at the heart of the system.
Delays in care and adoption services mean that it currently takes, on average, 21 months to place a child. Those delays damage a child’s development and reduce their chances of finding the love and stability they need with a new family. The Bill will help to sweep away such barriers through measures designed to speed up the adoption process, help recruit more potential adopters and improve the support they can receive. It will enable children to be placed earlier with their potential adopters.
Building on the family justice review, we are tackling unacceptable delays in the courts, ensuring that children’s best interests remain at the heart of decision making, and encouraging parents to resolve disputes outside the court where possible. By introducing a 26-week time limit for care and supervision proceedings, the Bill will ensure that courts focus on the essentials and that the most vulnerable children are not damaged further by unnecessary drift and delay. This is already having an impact in our courts. As the president of the family division recently wrote to everyone involved in the family courts system:
“We must get away from existing practice. All too often, and partly as a result of previous initiatives, local authorities are filing enormously voluminous materials, which—and this is not their fault—are not merely far too long; too often they are narrative and historical, rather than analytical...I want to send out a clear message: local authority materials can be much shorter...and...should be more focused on analysis.”
We also want to improve support for children remaining in local authority care, and so the Bill will make the virtual school head a statutory role in local authorities. This sends out the strongest possible signal about the priority we attach to the educational attainment of looked after children. Changes to the Office of the Children’s Commissioner will help the commissioner act as a strong advocate for children, promoting and protecting their rights. For children and young people with special educational needs, the Bill will introduce a single system from birth to age 25; new education, health and care plans which ensure that health, education and social care are planned around the needs of the child or young person; new rights and protections for 16 to 25-year-olds in further education and training; and a clear focus on outcomes, including independent living and paid employment.
The most frequent complaint I have heard from parents about SEN is that the current system is opaque and inflexible, leaving children and families to battle for access to services in a fog of bureaucracy. By requiring local authorities to publish a clear and transparent local offer, families will, in future, know what support is available in their area and how to access it.
Crucially, the duty on clinical commissioning groups to secure provision of health services as part of an EHC plan strengthens the Bill’s creation of a more integrated approach to care and support, and it has been widely and warmly welcomed by the SEN charitable sector. I want to express my gratitude to the Secretary of State for Health and his ministerial team for their willingness to help to push the boundaries towards better health integration in SEN service provision.
We are committed to reforming child care substantially to increase the availability of high-quality, affordable provision. The enabling measures in the Bill will offer greater choice and flexibility for providers and parents. We are introducing shared parental leave, giving working parents greater choice over who looks after their child in the first year and offering fathers the opportunity to be more involved in caring for their children. Together with the extension of the right to request flexible working to all employees, these measures will make the labour market more flexible, equitable and family friendly.
We all share an ambition for this Bill to make a tangible, lasting difference to the lives of children and families. Many in this House and beyond have made important points about how we ensure that the Bill really achieves that. I am grateful for that valuable expertise and measured consideration. I particularly thank the Education Committee, the Justice Committee, the Adoption Legislation Committee and the Joint Committee on Human Rights for their valuable scrutiny of the Bill. I am grateful to the Office of the Children’s Commissioner for its children’s rights impact assessment and to the children’s rights director for his superb version of the Bill for children, which is so jargon-free that it should make all of us in Westminster and Whitehall blush. I thank the many organisations that gave and submitted evidence in Committee and worked with me, my officials and hon. Members across the House to make sure that the many important issues that the Bill touches on are properly understood in terms of its content and implementation.
Throughout the development and passage of the Bill, we have listened and made changes so that the Bill we now pass to the other place is an improved one. This is a detailed Bill and it is vital that we take time to consider the points made and get the legislation and implementation right. Therefore, as I indicated earlier, we will consider some key issues over the summer and hope that progress can be made in the other place. In particular, we will look at these issues: clarifying whether, before local authorities can consider a fostering for adoption placement, they must consider placing the child with a relative or friend; introducing new safeguards through regulations to ensure that a local authority notifies the child’s birth parents when considering a fostering for adoption placement; seeing what more we can do to improve outcomes for young carers, ensuring that our approach complements the changes being introduced through the Care Bill; and identifying further improvements to the support that young offenders with SEN receive in custody.
As the Bill moves on to the other place, I am confident that it will be viewed as a Bill that all of us in this House can look back on, in whole or in part, and feel sure that we did right by giving our most vulnerable children, who all too often have the weakest voice, the chance to be heard and respected and the prospect of a better future. I commend the Bill to the House.
I agree with my hon. Friend and will probably repeat some of the points that she has just made. I commend her for her tireless and excellent campaigning on behalf of young carers since she promoted her private Member’s Bill. I know that she will continue that work when this Bill goes to the other place.
As I pointed out to the Minister for children and families in Committee, the Minister of State, Department of Health, the hon. Member for North Norfolk (Norman Lamb), who has responsibility for care, promised my hon. Friend and those of us who were present for the Second Reading of her private Member’s Bill last September that young carers would be provided for in the Children and Families Bill, yet we are still waiting to see what those provisions will be. The Minister gave some warm assurances on that issue during his closing remarks, so we look forward to seeing it addressed in the Bill.
Just to clarify, if the hon. Lady looks back at Hansard she will see that just before the end of Report I gave some strong indications of the direction of travel I am persuaded to take with regard to young carers.
That is very good; I will do that.
At the very least, we need to ensure that agencies that come into contact with families know how to spot a child who might be providing care and how to refer that child and their family to the support that exists for the majority of young carers. That needs to happen in order to address the much poorer outcomes that such children have because of their responsibilities.
As the Children’s Society discovered recently in its “Hidden from View” report, about one in 20 young carers misses school because of caring responsibilities. Young carers attain the equivalent of nine grades lower than their peers at GCSE level and are consequently more likely than other young people to be classed as not in education, employment or training after school. There are also health implications. Young carers are one and a half times more likely to have a special educational need, a long-standing illness or a disability than their peers. Those who are dedicated to looking after someone else often do not take good enough care of themselves. That is particularly true of young carers.
There are 166,363 young carers in England according to the latest census data, which were released on 16 May this year. That is 166,363 young people who stand a much poorer chance of reaching their educational potential and a much greater chance of suffering poor health or being a NEET. It does not need to be that way. I know that the Minister has outlined measures, but he could make the changes to the Bill that we have suggested in the other place or bring forward his own changes to ensure that those young carers are given the support that they need.
The Minister will not be surprised that I am also keen for progress to be made on ensuring that children’s centres are better able to identify and help every family in their area who needs it by adopting the measures tabled by the hon. Member for South Northamptonshire (Andrea Leadsom). She has not made a speech today and I hope that she has a chance to do so in a moment. Those measures would require NHS trusts to share the live births register with Sure Start outreach workers and would roll out trials of births being registered in children’s centres. That would mean that all parents would have to visit their local children’s centre, where they would be shown all the opportunities and services that are available to them and their child. That would contribute greatly to ensuring that we reach out to and help the most vulnerable families and, once again, improve the outcomes of the children within them.
I know that many hon. Members are keen to speak, so I will bring my remarks to a conclusion. We will not oppose the Bill on Third Reading and we are as keen as Ministers for it to make speedy progress to the other place. However, I hope that the House and the Government are left in no doubt that there are a number of issues that my noble colleagues and, I am sure, peers on all sides in the other place will revisit. We are expecting big things from Ministers before then and I sincerely hope that they do not disappoint.
Most notably, we want measures to ensure that support is not denied to young offenders with special educational needs and measures to increase the chance of young carers being identified and given the support that they need in order to improve their outcomes. We hope that the Government reconsider their position on PSHE and, in particular, sex and relationships education, and that they bring forward measures to make it compulsory before the Bill reaches the other place.
I would like to take this opportunity to pay tribute to my hon. Friend the Member for Airdrie and Shotts (Pamela Nash) for her superb leadership through the all-party parliamentary group on HIV and AIDS in pursuing education on HIV and AIDS. One in four young people leaves school without being taught about HIV. The work that she has done in that area is commendable.
If all the issues raised by Her Majesty’s Opposition and hon. Members from all parts of the House in the preceding debate are addressed, the Minister will be able to answer the question posed by my hon. Friend the Member for Wigan on Second Reading and be confident that the Bill will improve the outcomes for millions of children, young people and families for a long time to come. In the hope that those improvements will be made, the Bill proceeds with our blessing.