Written evidence from Anonymous (SEN 101)

 

Education Committee

Solving the SEND Crisis

 

Why I am responding

I am grandmother to, and advocate for, 2 young people with additional needs:

 

 

 

SEN support in mainstream schools should be on a statutory footing.

Agreed.

 

Improving outcomes for young people with SEND

Government, local authorities and educators must create, and role model a culture of inclusion and high expectations for SEND students.

 

The law relating to SEND is currently good. However, it is systematically and deliberately ignored by local authorities as there is no enforcement or penalties.

The single most impactful and cost-effective way to improve outcomes would be to hold Local Authorities to account, mandating that they correctly apply and uphold the law, with rigorous enforcement and punitive penalties for failure.

 

It is shocking that parents currently win 92-98% of all tribunals across the UK. Local authorities waste millions of pounds annually by forcing families to tribunal to have their children’s legal rights upheld. They do this to ‘save money’ as the SEND teams are not accountable for the council’s legal budget. If they delay providing support to a child they see it as a ‘win’.  Yet the long term consequences for the fiscal purse are dire with children failing to reach their potential, becoming unemployable, unable to live independently and reliant on statutory services. Imagine how your life would be if you had been denied 50+ weeks of education.

 

This happens routinely to our children, including my eldest grandson. We went to tribunal as the local authority refused to issue an EHCP. Just 2 weeks before the tribunal date they conceded, issued an EHCP and he is now not only within a special school, but within a nurture hub within this in a class of just 5 children. His needs, as set out by the Educational Psychologist report at the time, are complex. His case worker proudly told me that by forcing me to tribunal they had saved 51 weeks of support costs. My grandson lost a full year of education. We, as his full time carers suffered immense stress and also unnecessary cost. His case is not an isolated anomaly, but part of a stated strategy by our local authority – refuse to assess, then refuse to issue and see which parents fight this. This discriminates against our most vulnerable children where their families lack the ability and resources to fight the local authority.

 

Local authorities waste millions more in unnecessary correspondence, meetings and complaints arising directly due to their failure to act within the law. This is not isolated to our local authority, but endemic across all local authorities as evidenced by the tribunal statistics. This money would more than pay for the support our children need.

 

Their teams appear not to understand and/or correctly apply the law which leads to poorer outcomes. This has not changed in the 7 years I have had the misfortune of dealing with them. For example, just last week in response to a formal complaint I made over failure to adhere to legal EHCP timescales my local authority told me that they are proud that they meet the legal timeframes in 75% of cases. In their eyes failure to comply with the law in 25% of cases is not only acceptable, but to be applauded. Each delay results in additional weeks, months and in some cases years, that children’s outcomes are negatively impacted.

 

It is essential that sufficient funds are allocated to enable our children to receive the support they need in an appropriate education setting. Our local authority tells me that their unlawful approaches are in part driven by lack of budget to provide the support our children need. To stay within budget they are knowingly and intentionally depriving children of the support they are entitled to. Every child should receive the support they need. If the experts, including educational psychologists, occupational therapists, and school staff identify necessary support for these vulnerable children, then this must be provided.

 

It is likely that I shall be forced to tribunal again for my eldest grandson this year as the local authority is refusing to provide his special school with the funding needed to deliver his Section F provision. This then triggers a costly and time consuming process, including multiple communications, an emergency review, and then an expedited tribunal as he is in his GCSE years.  The combined costs of these are far greater than the funding required. This is a total waste of money and has life-long detrimental consequences for our child whose GCSE attainment, college place and future career are now all in jeopardy.

 

There is a dearth of appropriate special schools. This must be addressed. Our eldest grandson travels out of city because there is no special school in the city that provides a full GCSE curriculum to children with his level of autism and ADHD needs. This adds travel stress to his day and cost to the fiscal purse as his transport costs are higher. Proper analysis of needs and provision in localities with forward planning to ensure sufficient provision of the right type for children coming through the educational system is totally lacking.

 

Earlier diagnosis and identification of additional needs is required. This enables children to receive support at the earliest opportunity thereby increasing their life chances and reducing reliance on statutory support. This is also essential to enable proper planning for appropriate provision, budgets, and school places.

 

Wrap multi-agency support (e.g. school, physical and mental health, social services, etc.) around children and families. It is so disjointed and siloed that children routinely fall through cracks and conditions worsen resulting in greater need.

 

The local authority’s relationship with families is adversarial whereas it should be a partnership to wrap support around each child. We feel we are in constant battle with the local authority to uphold our children’s legal rights. We never have a case worker for more than few months. They never meet our child, and typically only speak to us once a year at our EHCP annual review where it is clear that they haven’t even read the case file. As such meaningful discussions about how children could be better supported, including through community provision never take place.

 

Mainstream school staff receive insufficient training to identify and implement appropriate strategies to enable children with additional needs to access their education. Many of these are no/low cost inclusivity adaptations (environment, teaching resources, and approach), and would benefit all children, but require a skilled teacher to apply them. When in a mainstream primary school my elder grandson’s teachers received just 2 hours of training in autism and ADHD which was woefully inadequate.

 

School staff need comprehensive training in Autism, ADHD, dyslexia, adverse childhood experiences, trauma-informed approaches, emotional coaching, attachment theory, mental health first aid, etc. They also need comprehensive training in strategies to apply to create truly differentiated teaching and inclusive classrooms.

 

Schools need to be inclusive environments. Smaller class sizes, quiet corridors, places to eat away from dining halls which result in sensory overload, quiet spaces, ear defenders, visual prompts, precision teaching techniques, nurture hubs, differentiated curriculum and teaching, and similar need to be standard. All children would benefit from this approach.

 

For this to work schools need sufficient budget (which will pay back in the longer term through reduction in reliance and use of other services), sufficient qualified and experienced staff, and also immediate access to external expertise when needed. For example they need access to an Educational Psychologist to advise schools and support teachers as they implement strategies. It is impossible for schools to get ad-hoc advice from an Educational Psychologist or other experts when needed. Increasingly parents are told to apply for an EHCP as this is the only way to get and Educational Psychologist assessment. This was the case for our younger grandson where school’s requests for an Educational Psychologist visit were refused for 2 years. We will never know if getting support earlier might have reduced the level of need he has now.

 

Invest in evidence-based approaches that support SEND students, increasing their educational attainment, improving their mental health and wellbeing, and building critical life skills e.g. the mentoring programmes provided by charity Power2. Make these available to schools. Early intervention improves outcomes and reduces longer-term reliance and use of statutory services.

 

Address the CAMHS crisis. Children with additional needs frequently have social, emotional and mental health needs. Failure to address these has well evidenced repercussions.

Invest in assistive technology and make this available within schools to support students who would benefit from this.

 

Develop supported pathways for SEND students transitioning to further education, employment, or supported living. Transport must be provided as part of this for these young people. Many young people with SEND cannot take up their college place as transport is not provided and they cannot travel independently and/or by public transport (e.g. due to sensory or social communication challenges).

 

Rigorous inspection of SEND provision in mainstream and special schools with sharing of best practice.

 

Published outcomes data by local authority with ranked tables.

 

Education, Health and Care Plans  

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

What can be done to reduce the disproportionately high exclusion rates for students with SEND?

 

 

 

What steps can local authorities take to ensure funding is in place to meet the transport needs of post-16 students with SEND?

 

Whilst I don’t know the answer to this, as a parent I can emphasise how important it is. Our child wants to go to college. However, he cannot travel independently and neither can he travel on public transport due to sensory overload. Our local authority’s policy is not to fund his transport. This would prevent him from going to college, which in turn would prevent him from pursuing his chosen career (which is a realistic aspiration), and living independently.

 

January 2025