Graham Stringer
Main Page: Graham Stringer (Labour - Blackley and Middleton South)Department Debates - View all Graham Stringer's debates with the Department for Education
(6 years, 2 months ago)
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I draw Members’ attention to the fact that our proceedings are being made available for people who are deaf or hearing-impaired. The interpreters are using British Sign Language, and Parliament TV will show a live, simultaneous interpretation of the debate. We are also trialling live subtitling for the first time on channel 15 on parliamentlive.tv. I call Jim Fitzpatrick to move the motion.
I beg to move,
That this House has considered deaf children’s services.
It is a pleasure to see you presiding over today’s debate, Mr Stringer. I am grateful to the Backbench Business Committee for granting us time to raise this matter with the Minister. I look forward to his response and to those of the shadow Minister, my hon. Friend the Member for South Shields (Mrs Lewell-Buck), and the Scottish National party spokesperson, the hon. Member for Lanark and Hamilton East (Angela Crawley). I am also grateful to colleagues from the all-party parliamentary group on deafness, who supported the bid for the debate—it is good to see a number of them here. Finally, I am grateful to the House authorities for ensuring that, as you mentioned, Mr Stringer, the debate is transmitted live with signed simultaneous translation. Surely that is the future.
The title of the debate is “Deaf Children’s Services”. I intend to concentrate on educational support for deaf children, and I am grateful to the National Deaf Children’s Society for the briefing that will form the bulk of my comments.
Deaf children are 42% less likely to achieve the top grades than their hearing peers, but there is no reason a deaf child should do any worse than a hearing child if given the appropriate teaching. That is the historical perspective. The worry for the deaf community, and many colleagues here, is not only that the situation is deteriorating, but that it looks unlikely to improve.
In addition to their educational disadvantages, deaf children can be more susceptible to mental health issues. NHS England has said that around 40% of deaf children suffer from mental health problems, in contrast to 25% of hearing children. Continuing into adulthood, people with hearing loss are twice as likely to suffer from depression and anxiety-related issues. Investment in early life would likely lead to healthier adults, without the need for employment support or NHS attention.
The NDCS briefing predicts that more than a third of local authorities in England plan to cut £4 million from their budgets for education support for deaf children this year. At the same time, the number of teachers of the deaf, who provide vital support for deaf children, has fallen by 14% over the last seven years. Those figures are drawn from freedom of information requests, as detailed in the House of Commons Library briefing.
The NDCS “Stolen Futures” campaign is calling on the Government to step in and tackle that growing crisis. Cuts are putting the education of thousands of deaf children at risk, leaving their futures hanging in the balance. Vital services for deaf children must be adequately funded, both now and in the next spending review. That review has led to today’s debate.
There are more than 50,000 deaf children and young people in the United Kingdom. More than 90% of deaf children are born to hearing parents who have no prior experience of deafness. Those parents rely on advice from specialist teachers of the deaf to support their child’s language and communication skills. Around 80% of deaf children attend mainstream schools, where they may be the only deaf child. Teachers of the deaf play a key role in helping all teachers to understand how to differentiate the curriculum and provide effective support.
Despite the fact that deafness itself is not a learning disability, deaf children underachieve throughout their education. That is demonstrated in the early years foundation stage, where only 34% of pre-school deaf children were reported as having achieved a good level of development, compared with 76% of other children. At key stage 2, less than half of deaf children achieved the expected standard for reading, compared with 80% of other children. At key stage 4, deaf children achieve, on average, a whole grade less in each GCSE subject than other children, and in recent years that attainment gap has widened. Finally, 41% of deaf young people achieved two A-levels or equivalent by the age of 19, compared with 65% of other young people.
Most deaf children do not have an education, health and care plan. The NDCS estimates that less than a fifth—19%—of deaf children have their support confirmed through a statutory EHC plan. The NDCS has been researching what is happening on the ground, and believes that services are clearly under threat. The NDCS has tracked local authority spending on specialist education services for deaf children since 2011. This year alone, more than a third of local authorities—37%—have told the NDCS that they plan to cut funding for those vital services. Deaf children in those areas will lose £4 million of support this year, with local authorities cutting 10% on average from deaf children’s services.
My own borough of Tower Hamlets, which is regarded as a model of excellence, has among the highest figures in England for hearing impairment and special educational needs and disability. It comments that it is difficult to make fair and equitable decisions for all children with special educational issues. The NDCS says that cuts are likely to affect my local services too, and believes that those cuts are being driven by wider pressure around SEND funding. I know that the Department for Education has protected high-needs funding to support children with SEND in cash terms, but I also know that the budget has not been adjusted to reflect several key aspects.
First, the number of children and young people requiring additional support is rising. Government figures show that more than 30,000 more children had statements or EHC plans in 2017 than in the previous year. Secondly, local authorities have greater responsibilities to support young people with SEND aged between 16 and 25, following the SEND reforms introduced through the Children and Families Act 2014. Since 2014, they have seen significant increases in the number of 16 to 25-year-olds with a statement of special educational needs or an EHC plan. Finally, there is a trend towards many more children being placed in special schools. The number of children in special schools rose by 12.5% between 2014 and 2017.
The NDCS has published more background material to back up its concerns, and the Local Government Association has also recognised the funding pressures, saying:
“we are calling for an urgent review of funding to meet the unprecedented rise in demand for support from children with special educational needs and disabilities.”
As we head towards the next spending review, the needs of some of the most vulnerable children in society must not be forgotten. A failure to invest in deaf children’s futures will likely result in a generation of lost potential.
The NDCS raised a number of issues with me that I know its representatives have already communicated to the Minister and his team. The Department responded that £6 billion is the highest budget on record. Nobody disputes that, but the demand outstrips the supply, and that is the fundamental question for the Minister to respond to. There is more money in the budget—it is the highest it has ever been—but the demand is even higher. I would be grateful if he would address those figures.
The NDCS has raised other issues and put forward some suggestions. For example, it wants to explore with the Department whether the ring fence on the schools block can be relaxed or removed. The national funding formula means that 99.5% of the schools block is now ring-fenced. The remaining 0.5% can be transferred to the high-needs block, which funds SEND support services, only with the agreement of the local schools forum.
That ring-fencing makes it harder for local authorities to move funding in response to growing SEND pressures, as evidenced by the large number of local authorities that have applied to the Department for permission to overrule the schools forum locally and/or go beyond the 0.5%. The NDCS understands that 27 local authorities made a formal request for disapplication of the ring fence, 15 of which were allowed to proceed. I would be grateful if the Minister could comment on those figures and on that principle. I would also welcome his views on whether there is more we can do to ensure that the local school forums include more representation around special educational needs and disabilities.
The NDCS wants the gaps in the specialised SEN workforce addressed. As I have described, teachers of the deaf play a key role in supporting deaf children, their families and other teachers. Where services are working well, they ensure that deaf children start primary school with age-appropriate language and communication skills and that they are effectively supported and included within mainstream schools. In 2017, there were 913 qualified teachers of the deaf working in a peripatetic role or in resource provision. That total has fallen by 14% in the past seven years. In addition, more than half of teachers of the deaf are over the age of 50 and hence are due to retire in the next 10 to 15 years. Many services are telling the NDCS that they cannot recruit. In 2017, 45% of services reported difficulties in recruiting new teachers of the deaf or arranging supply cover over the previous 12 months.
The NDCS believes a national systemic approach is needed to address this growing crisis. There is little incentive for local authorities to be proactive in ensuring there are sufficient numbers of teachers of the deaf being trained to meet future needs. Many will not be able to meet the financial cost of training new staff while also employing someone who has yet to retire. In 2016, the Department for Education commissioned a report from the National Sensory Impairment Partnership on the supply of specialist teachers, which recommended a central bursary scheme. However, the NDCS is not aware of any action taken in response, and I would be grateful if the Minister could indicate if there is any progress in that regard.
The NDCS asks whether there is a way to incentivise or even require local authorities to work together to commission more cost-effective services for deaf children. Given that deafness is a low-incidence need, it is important that local authorities, and particularly smaller authorities, work together to commission specialist services and provision. There are too many services employing just one or two teachers of the deaf, who are trying to meet the diverse needs of deaf children in their area. There are just nine consortiums delivering education support services for deaf children in England—the largest is in Berkshire. There has been no noticeable increase in recent years in the extent to which services and provision for deaf children are regionally commissioned. I would be grateful if the Minister might comment on that suggestion.
The NDCS welcomes the fact that the Department has asked Ofsted how schools can be better held to account for how they support children with SEND, but it has concerns about whether more could be done to strengthen the accountability framework around specialist services for deaf children.
Finally, the NDCS raises the question of a review of post-16 funding. SEND funding for mainstream post-16 providers is given where a young person has been commissioned a place, using high-needs funding. In practice, that means that, in many areas, colleges will receive funding for young people only if they have an EHC plan.
Government figures suggest that more than 85% of deaf young people do not have an EHC plan. If SEND funding is, in practice, restricted to those with an EHC plan, a large number of deaf young people are less likely to get the support they need to access the curriculum, such as a radio aid to help with additional amplification, or notetakers. In further education, deaf young people are twice as likely to drop out as their peers, and one quarter do not gain any qualification. Teachers of the deaf are unable to provide advice to mainstream college staff or support young people there, as they are not funded. Again, I would welcome comments from the Minister, and I hope he would be prepared to look at that point.
A number of individuals have been in touch with me directly. I apologise for not being able to mention their cases, but there is just not enough time—there are so many colleagues who want to contribute to this important debate. The House Facebook post for the debate was seen by nearly 64,000 accounts, had over 6,000 post clicks and 1,700-plus engagements covering funding, accessing support, good experiences, geographical differences and lack of understanding. There are some very poignant accounts, especially from parents. I hope the Minister has a chance to view them, if he has not done so already.
There are some very able deaf young people out there who can be huge assets to UK plc. If we do not allow them to develop—if we do not encourage and support them as they mature—we are not just denying them their birthright, but robbing our country of a significant contribution from some highly skilled and intelligent individuals. We owe them more than that.
Order. Eight people wish to speak in the debate, and we have 45 minutes. I am not going to impose a time limit straightaway. I hope people will do the arithmetic and follow that. If not, I will have to impose a time limit. I call Peter Aldous.
I thank the hon. Gentleman for that intervention. The resource bases in Suffolk, both in primary and secondary schools, are very popular and go down very well—the feedback from pupils who are not deaf is that they welcome the provision. They are incredibly proud of the young people in those units. The problem in Suffolk is that there are three resource bases at primary level—in Ipswich, Bury and Lowestoft—but at secondary level there is a resource base only in Bury St Edmunds. They need to be put out across the whole county, particularly in the north.
The hon. Member for Poplar and Limehouse is a champion for the deaf and the hard-of-hearing community, but it is important to highlight the sterling work of another such champion, Ann Jillings from Lowestoft, who has been working tirelessly with passion and determination to secure the best possible education for her son Daniel. In doing so, she is campaigning for other parents of deaf children in north Suffolk. Ann chairs the Waveney Deaf Children’s Society and, along with Daniel, has been campaigning for the introduction of a GCSE in British Sign Language as soon as possible. They made their case firmly and passionately but politely to the Minister for School Standards, my right hon. Friend the Member for Bognor Regis and Littlehampton (Nick Gibb), at a meeting in March. I hope that the Department for Education will continue to do as much as it can to support the development of the new GCSE, and I would welcome the Minister’s reassurance on that point.
Daniel was born deaf. Following a diagnosis through the newborn hearing screening programme, Ann receives support from a person she describes as a “fantastic” teacher of the deaf, who acted as an advocate for the family as Daniel grew up. Daniel has been able to make excellent progress throughout his education. Ann is very clear that that is because of the support he received from specialist teachers of the deaf and communication support workers. That confirms that, provided that deaf children receive the right support from the start, there is no reason why they cannot thrive and break through any glass ceilings that get in their way.
Getting support for Daniel has been a challenge. Ann comments that she has fought tooth and nail for it, which has put the whole family under incredible stress. She highlights that it took 50 weeks to complete the transfer from a statement to an education, health and care plan—more than twice the statutory deadline. She points out that initially the local education authority did not agree with the advice that Daniel would need to continue to have support from a teacher of the deaf in his school. Only when she stated that she would take up her right of appeal was it accepted that a full-time teacher of the deaf was needed. She says:
“Getting the support for your deaf child is a battle which parents should not have to fight, and I do wonder what happens to the children whose parents cannot persevere in the same way as we have.”
I have got a lot to say, Mr Stringer, but I sense I am preventing others from speaking.
To help the hon. Gentleman, there were roughly five and a half minutes for everybody if they self-allocated. He has now been speaking for six and a half minutes.
Thank you for guiding me, Mr Stringer. I will cut to the chase and conclude with what I said at the end of the debate on deafness and hearing loss in this Chamber last November. Many barriers have been placed in Ann Jillings’s way in her pursuit of better education for Daniel. It is our duty and the duty of Government and local authorities to remove those barriers as soon as possible. Thank you for bearing with me, Mr Stringer.
It is probably easier if I impose a five-minute time limit on speeches.
It is a pleasure to serve under your chairmanship, Mr Stringer. I am grateful to my hon. Friend the Member for Poplar and Limehouse (Jim Fitzpatrick) for securing the debate, not least because it gives me an opportunity to present the cases of the many constituents who have been in touch about this issue. They and I are grateful for that opportunity.
I am privileged to have Elmfield School for Deaf Children in my constituency. It provides specialist services to early years and primary pupils in a specialist setting, but it has plans to integrate those into a mainstream setting. It also provides a secondary service, which is already integrated into Fairfield High School, a mainstream school in my constituency. Elmfield provides a full range of services, with signed bilingual educational approaches and an individual language profile for each pupil. I will say in a second why that is so important. However, like other schools, Elmfield struggles to meet demand. In the south-west, where there are more than 3,000 deaf pupils, there has been a 16% drop in the number of fully qualified teachers of the deaf and a 12% drop in the number of teachers training for that role. That is why, in Bristol and other places with vacancies, there are no guarantees that those specialist positions will be filled.
I picked two sets of constituents—Mr and Mrs Ward, and Mr and Mrs Bolton—at random from a number of families who got in touch with me. I thank them for doing so, and I will spend the rest of my speech telling their stories. Ella is the daughter of Mr and Mrs Bolton. She is in year 1 and is six years old. She has moderate hearing loss, which was diagnosed at birth, and wears hearing aids in both ears. I have met Ella, and her mum rightly describes her as a
“confident, creative, brave girl, who loves learning.”
She is bright and is expected to do well. However, because of the level of her hearing loss and the fact she appears to cope well in school, her disability is often overlooked when she is in a mainstream setting. The perception that it is not a serious condition or that she is coping or performing well means that the provision she requires to fulfil her potential is often missed. Ella has to put extra effort into hearing in the classroom, which gives her concentration fatigue. Because she has to focus so much on her teachers to be able to engage, on most days she is exhausted when she comes home. Her mum says it takes Ella until Sunday evening to fully recover before she starts again on the Monday morning.
Mrs Bolton says that deafness is not naturally understood by teachers, even with the best will in the world. Ella is an example of why specialist provision is required so much. However, as has already been said, this issue is not just about young people; it is about their families, too. Mrs Bolton told me how teachers of the deaf had helped the family come to terms with having a child who was deaf and with how best to support Ella at home and school. She wrote that teachers of the deaf played
“a pivotal role in providing and coordinating support and promoting deaf awareness”
among other staff and providers to Ella, and to the family.
Oli, the Ward family’s son, is much older and further down the track. They wrote that he had “a very mixed journey”, and that it felt like his choices narrowed and became more limited as he got older and progressed through the system. Mrs Ward says that specialist teachers of the deaf made a huge difference to Oli everywhere he went, not just in terms of education provision but in the way he navigated life socially in a mainstream setting. She says that teachers of the deaf were his lifeline on many occasions.
Oli moved around between specialist and mainstream provision while he was in secondary school, which caused him difficulties. Mrs Ward said she was told by a teacher that her son had outstanding GCSE results “for a deaf child.” She rightly makes the point that that should not be a distinction—just because someone is deaf does not mean a C is an outstanding grade for them if they have the potential to achieve an A. Mrs Ward wrote:
“Teachers of the deaf navigate schools and classrooms…in no end of subtle and clever ways”
to get the best out of her child, Oli, and so many other children, whom we want to flourish and do well.
I look forward to the Minister’s answers. There is cross-party support for getting this right. He has heard the stories of my constituents and those of local authorities on the frontline, which are really struggling to do the best, not just for children who are deaf but, as we have heard, for children with special educational needs. Many of my constituents face a struggle to get EHC plans in place, and schools cannot really afford to top up the money they get. This is a real slog. Parents, teachers and local authority staff are passionate about getting the best provision for deaf children and children with special needs to allow them to flourish, and I look forward to hearing how the Minister will help them do that.
The restraint on interventions and speeches means that we have gained a couple of minutes, so the Front-Bench spokespeople will have a generous 10 minutes each. I call Angela Crawley.
The SEND reforms are a topic I will refer to later in my speech, but my hon. Friend leads me aptly to my next point. When funding and support are denied in cases such as the ones we are talking about today, education is also denied.
In his response, the Minister will likely refer to the funding given to the National Sensory Impairment Partnership and other bodies, but that money does not address the falling number of teachers of the deaf. Having British Sign Language-trained teachers is vital to deaf children, a point that was well made by my hon. Friend the Member for Nottingham South (Lilian Greenwood), but some areas have only one specialist teacher per 100 students. I was sorry to hear from the hon. Member for Strangford (Jim Shannon) that that scarcity of teachers is the same in Northern Ireland, although I should say to him that I always follow every single word he says, and I love listening to his speeches.
None of that should come as any shock, since our schools are facing the first real-terms funding cuts in 20 years, with £2.8 billion cut from their budgets since 2015. As always in these austere times, specialist provision is the first to go. Bamburgh School is a specialist school in my constituency, which is now in the unenviable position of having to pay out of an existing budget for its existing teachers to learn BSL level 1 on a 30-week course, which will take the school into a deficit. On top of that, these dedicated teachers are completing the course in what little free time they have. However, their equally dedicated headteacher, Peter Nord, told me that he has a duty to the children he teaches, who, without BSL, would not get the full learning experience they deserve.
Not every deaf child or school will have a head and teachers as dedicated as we have at Bamburgh or the Elmfield School for Deaf Children in the constituency of my hon. Friend the Member for Bristol North West (Darren Jones). I wonder what will happen to those children. I appreciate that a review of the SEND workforce in schools is under way, but a report commissioned by the Department and published over two and a half years ago has already identified a drastic shortage of deaf teachers. Instead of yet another review to give the appearance of doing something, can the Minister please advise us when there might be a response to the review that was done nearly three years ago, and what the timescales are for the current ongoing review?
The decrease in support is taking place against the backdrop of an increasing number of children requiring it. In just the last year, the number of deaf children increased by 11%. Earlier this year, it was shown that the attainment gap between deaf children and hearing children has widened—the figures were ably shared with us by my hon. Friend the Member for Blaydon (Liz Twist).
Sadly, Government neglect of deaf children continues throughout their education, with post-16 funding bearing no resemblance at all to the number of deaf pupils without an EHC plan. Just last year, it was revealed that some county councils in England charge 16 to 19-year-old SEND students £1,500 a year for their transport. Since 2015, students have been required to pay a £200 contribution towards the cost of certain essential equipment that used to be covered by the disabled students’ allowance.
Parents have told me that support often only comes with an EHC plan, yet we have heard that most deaf children do not have such plans. Those who do, as outlined by the hon. Member for Waveney (Peter Aldous), have to fight, and suffer the exhaustion of taking on, the might of their local authorities. A recent damning report by the local government and social care ombudsman found that children and young people were missing out on provision, with health often a missing factor.
As we heard, 80% of deaf children and young people are not on EHC plans and rely on SEND support from their local authorities, which authorities struggle to provide following savage cuts that have resulted in up to 40,000 deaf children in England having no support at all. Deaf children and young people also remain stubbornly over-represented in alternative provision and exclusion figures. Schools, headteachers, support staff and parents work tirelessly every day under ever-challenging circumstances to give our deaf children the very best education, which they deserve. The Minister should be doing the same, and I look forward to his letting us know his plans.
I will end with a quick quote from Thomas Bailey, a 16-year-old pupil from Bamburgh School in South Shields. He sums up far better than I or anybody here could the damaging impact of the Government’s policies:
“Being deaf makes me feel depressed and very frustrated. Having no support in school is very mean. When I don’t have support, I don’t have that person to repeat and break down that information for me and to sign important key words, so I am not able to learn the same as other children in class. I feel left out. Improving equipment would make the sound easier and clearer for me to hear, but having no equipment makes everything very quiet and unclear. This means I’m not getting any important information, leaving me feeling annoyed and again left out. My life and learning becomes a blank.”
The Minister should know that, unless he takes urgent action, the despair and emptiness so well articulated by Thomas will continue to be felt by more and more deaf children across our country.
Before I call the Minister, I remind him that it would be helpful if he left a couple of minutes for the debate’s sponsor to wind up.