Posts Tagged ‘Special Needs’

Children with SEN Statements are 9 times more likely to be excluded

Statistics published by the Department for Education today show that pupils with statements are nine times more likes to be permanently excluded from school than those pupils without any SEN. Meanwhile, the number of pupils with statements of SEN receiving one or more fixed period exclusions is six times higher than for pupils with no SEN. The Statistical First Release (SFR) provides information about exclusions from schools and exclusion appeals in England during 2010/11. It reports national trends in the number of permanent and fixed-period exclusions together with information on the characteristics of excluded pupils such as age, gender, ethnicity, free school meal eligibility, and special educational needs (SEN) as well as the reasons for exclusion. The key points from the latest release are: There were 5080 permanent exclusions from state-funded primary, state-funded secondary and all special schools in 2010/11. In 2010/11 there were 271,980 fixed-period exclusions from state-funded secondary schools, 37,790 fixed-period exclusions from state-funded primary schools and 14,340-fixed period exclusions from special schools. The average length of a fixed-period exclusion in state-funded secondary schools was 2.4 days, for state-funded primary schools the average length of a fixed-period exclusion was 2.1 days. The permanent exclusion rate for boys was approximately three times higher than that for girls. The fixed-period exclusion rate for boys was almost three times higher than that for girls. Pupils with SEN with statements are around nine times more likely to be permanently excluded than those pupils with no SEN. Children who are eligible for free school meals are nearly four times more likely to receive a permanent exclusion and around three times more likely to receive a fixed-period exclusion than children who are not eligible for free school meals. What are we to make of these statistics?

A mainstream school it would seem is, quite often, unable to cope with the high level of demands placed upon it by children with special educational needs and challenging behaviour and for these children, inclusion is the last thing they need. They need a specialised environment that can help them overcome difficulties of background or learning style or hidden disability so they have the same chance of a successful life as everyone else. Timely intervention is crucial for these children so that they can be identified and assisted long before things get to the stage of an exclusion being considered. When thinking specifically of children with statements, I wonder what percentage of these SEN children, or of children with SEN but without statements, were excluded for persistent disruptive behaviour compared to the other reasons above. A child displaying persistent disruptive behaviour almost certainly has underlying issues, whether BESD, ADHD, ASD etc, that prevents them from accessing the curriculum and hence makes them feel that school is a waste of time. A large percentage were also recipients of free school meals, which also indicates that poor children (with or without SEN) are hugely at risk of not getting the support they need in a mainstream school environment. Many may come from difficult family backgrounds and would be much more suited to a nurture group environment such as those set up by child psychologist Charlie Mead, if only they existed more widely.   See http://www.wordswell.co.uk/tapf-conference/october-charlie-mead.php

There is much interesting analysis that can be taken from these stats aside from the startling SEN figures, for example the comparatively high ratio of exclusions for traveller children (who may or may not have SEN). These would take far more time to ponder than I have available, but I hope someone does and lets me know.

First published by Tania Tirraoro on Special Needs Jungle where you will find links to all the stats

share save 120 16 Children with SEN Statements are 9 times more likely to be excluded
 

Children in a Care-less Society: Vulnerable – but not eligible

 Today Tania Tirraoro of Special Needs Jungle has continued her post regarding the presentation by Charlie Mead, Educational and Child Psychologist at the Towards a Positive Future SEN conference on 16th June 2012.

‘He spoke powerfully about the plight of these ‘Looked After Children’ or, as it would appear, not very well looked after children. Charlie works in many children’s homes in the Midlands and South West of England and if you want to know about how he sees the state of provision of children in care – our most vulnerable members of society – please read on, share it, reblog it, quote it on your own blogs, anything you can do to help highlight it. ‘

“Children are being ignored, abandoned and abused within the care system. The tension between available finances and how they are spent is at the cost of children’s development. Children in care are some of the most vulnerable people in this country yet they are given no more priority (in many cases less) than privileged young people from stable and wealthy backgrounds. They are denied access to the basic rights of most children. The right to security, protection, opportunity and equality.

We now have over 73,000 children in care in England and Wales – but we are losing some every day. Sometimes physically – they disappear; but also socially and emotionally. We lose them as potential contributors to society – as ‘net gain adults’ in HMRC speak. The number is an increase of 12 per cent since 2008 and rising since the case of Peter Connolly.

■56% of all children in care are there because they were abused or neglected

 ■26% are in children’s homes.

■That means more than 17,000 are looked after in children’s homes or accommodated in institutions (LA or Private), while the rest are in foster care.

■More than half of all children in care (53%) leave school with no formal qualifications

■13% get 5 A*- C grade GCSEs, compared with 47% of all children.

■6% enter higher education.

■20% of women who leave care between the ages of 16 and 19 become mothers within a year, compared with just 5% of the total population.

Parents who have been through the care system are twice as likely to lose the right to care for their own children.

I’ve seen cases of 14 year old girls serially sexually abused; criminalised boys; neglected young people; children who were heroin addicts from birth. But they DO have a voice and they let it be heard – believe me. They know what they want. And it isn’t institutionalised living. They want opportunities to develop relationships to build their own lives. So, I am asking why we can’t and won’t protect, educate and cherish children in care as our own? They have already experienced degrees of rejection and loss of control hard for others to imagine, before the system neglects their needs to the point of losing them altogether. In the area I work these are the most vulnerable groups of children – many do not have a voice of their own and their parents are ignored or dismissed, especially if they have learning difficulties or addictive behaviours of their own. Their social workers are ignored, their care workers are ignored… They don’t have the “opportunity-language” even if they were to be listened to…..they do not have the leverage. They have become part of the system as soon as the system decides they should be!

All children need: safety; security; health; continuity; routines; knowledge; opportunities; equality.

■73 %of school age looked after children have some form of special educational needs – especially social, emotional and behaviour difficulties

■In the 2009/10 school year, 130 children who had been looked after continuously were permanently excluded from school.

■7.9 % of looked after children who were aged 10 or over had been convicted or subject to a final warning or reprimand during the year

■4.3 % were identified as having a substance misuse problem during the year 2010.

Why are these simple basic rights not only denied children in care but are routinely flouted by a whole range of agencies? Even safeguarding issues are ignored if Duty Officers and social workers make wrong decisions based on lack of knowledge – and then D.O decisions are rarely rescinded

For example:

■The child who is allowed to return to their abusive and neglectful parents because they have made significant progress in care and the money is tight.

■The child who absconds, arrives home and is left there because there are no Social Workers on duty.

What is it that makes adults lack any sense of what they are doing and abdicate responsibility for the care of children.? Much of the answer lies in the stories of the children themselves. As a psychologist, I am driven by empirical evidence that is usually supported by strong theoretical hypotheses. In this case it is my theories that have been formulated and are driven by observable and measurable data taken from the circumstances around children in care. So, what evidence is there? These are the circumstances of just nine of the children that I am currently working with – when we can find some of them. They reflect the overall pattern and range of difficulties they face – some made more so by the response of adults who should be providing them with opportunities – not further rejection.

■Child 1: Secure unit – Children’s Home – disappeared

■Child 2: Looked After Child – drug runner – sexually exploited

■Child 3: Subject of physical abuse from boyfriend

■Child 4: Missed schooling – now costs the authority £1,500 a week

■Child 5: Withdrawn, self-harmer – low self-esteem

■Child 6: Sexually abused, absconds – returned home

■Child 7: No awareness of risk – in independent living

■Child 8: Intelligent – but no school will take her

■Child 9: Neglected, also bright – no support available

Where does it all go wrong? They have parents who are addicts or criminals, they are abused and have early exposure to that abuse and to criminality. For example two year old girls sold for drugs, five year olds who rob and steal. They live in an environment where failure, abuse and lack of normal behaviours are normal. They have a very low socio-economic status. The full range of normal opportunities can be denied children and they are constantly being rejected. And rejection results directly in lack of control…

Examples include:

■Failed parenting – even though children might not realise it at the time.

■Failure by the extended family: abuse, or relatives not believing children

■Failure of Social Workers: so many changes and missed appointments. Part-time staff with large case loads.

■Courts who have no understanding of what sending child in care to secure accommodation means.

■Schools that won’t let them in – ‘had one like you and it caused so much disruption’

■Friends – generally they don’t have many. Parents of peers are wary.

■Fellow children in care want to control them. If they don’t comply they are then bullied – possessions stolen etc. It’s about regaining control in an uncontrollable environment.

■Themselves: they’ve lost faith in their own abilities, except how to survive – so allow themselves to be exploited – sex, drugs, alcohol….and so on.

AND THEN REPEAT THE CYCLE. We MUST break the pattern – but who will do this? Not the targets of my evidence. This is the system…

■Government – not prioritising its resources for those most at risk; not supporting those that want to effect change and challenge the status quo; using its agencies (Ofsted, inspectorates) to create fearful institutions; and all the while definitely not doing what it preaches!

■Local Authorities – Child and Family Services – a multi-agency approach that is dysfunctional and buck passing – child deaths in Birmingham; CAMHS waiting lists; Education – refusing to encourage collaboration outside its own self-interest. Placement Panels…..hiding the gatekeepers.

■Communities: for tolerating complacency and not getting involved to enable change – for perpetuating bias and discrimination (targeting children’s homes for drugs in the local press)

■Agencies – who exploit the state of confusion in all of the above to suit their financial needs

■Charities – for putting their image before either its core clients or the people who work with them at the lowest paid levels. For presenting one face and delivering another

■Private providers who charge high fees and deliver low levels of service

Complex needs demand a complex solution and each of these points could be an area of research on its own. But to give an example, asked whether it was an appropriate use of government and national funding to support children in care achieve in school the answer was put in financial terms by the Minister for Children. All questions about costs for anything would be referred to as part of the national debate on the deficit – budgets being the principle behind all policy decisions. So, children in care are better not educated, especially after 16 – but kept in residential care units where costs can be kept down. It is symptomatic of a complete lack of understanding – even of simple financial expediency of children able to work paying taxes! This is short-termism – based on today’s budget NOT tomorrow’s costs. These are the dynamics – or lack of them – that come out of the evidence gathered around children in care. Simply put, decisions appear to be made and situations developed based on Assumptions and Opinions, Financial demands and Exclusivity. Not on research, need and the idea of doing the best for all. Generally the children in care themselves would prefer not to go to the types of school they find themselves in – mainly because they don’t see how those schools can help them. PRU’s, specials, units, PLS etc. They have been failed again and again. They don’t see the CARE they are supposed to get so why should they bother? The Problem is they can’t get into proper schools. Nearly all CiC are within the average band of intelligence and achievement and would be able to access the full national curriculum. However, many have missed school and are behind with reading, spelling and maths. Even if they are willing to catch up, schools won’t take them for fear of it affecting their results. Even those who are ahead of their peers in Literacy and Numeracy are not allowed in because of the fear, prejudice and discrimination against children in care. Schools, in my experience, go out of their way to find reasons NOT to take children. So these children get access to ASDAN and work experience at best – at worst – nothing. So it’s no wonder that private educational companies charge £1,500 a week for 1:1 programmes for young people unable to access any form of education. How can that be right in any sense – for either the child or the tax payer?

The System

There is the full range of quality of provision for CiC – from excellent to appalling. In the worst, children are locked up for eight hours a day with poor nutritional food – and the provision is different because no one provider, authority or government has a shared view of what constitutes a child in care and his or her need. Organisations are oppositional; Placement Panels are highly secretive and make fallible decisions. Commissioning officers then have to place children based on highest level of provision for the lowest cost – which is then not delivered by children’s homes. Children’s details are then circulated to a range of providers who make bids to deliver the resources able to be paid for. This will vary from residential care and may expand to include education, therapies, medical provision with varying levels of security and safeguarding needed. Costs vary from £1,500 a week to £7,000 a week. And if you can guarantee a minimum of 3 places from any one LA then bulk reductions in fees take place – but the provision is the same for all three children irrespective of their need.

In an interview with CEO of a major provider of care homes she made the following comments:

Local authorities want more for less;

children in most need are having provision withdrawn as money is reduced – and this affects holidays, education, therapy, training for staff and even food;

Education should be supporting children in care and social services, but they are opposing factions in a multi-agency joined up world that is fast becoming dysfunctional.

So, this is what I have seen over the past year. These are the difficulties children have faced in care. Some children not in care also face these difficulties – but not at the frequency or severity of CiC.

This is why the system is not working –

■Lack of principles

■Simplistic Solutions

■Wrong funding priorities

■Lack of engagement with children

■Lack of aspiration

■Lack of creative thinking

■Outdated measures and targets

So it is not a system then! The only part of the process that appears systematic is the inspection process that is beginning to flex its authority in the interests of children but is still pre-occupied with health and safety detail rather than addressing the issues here.

The system, in its complexity:

■Abdicates responsibility by passing the buck

■Blames the children for who they are

■Refuses them opportunities to develop

■Does not engage with local people and communities or allow CIC to take part in local activities

■Where staff even buy into the failures…“There’s no point in getting her up-she’s late for school already”

So, what would work and how can we replace the problems with solutions that may have a more positive impact on the outcomes for CIC. Research suggests CiC respond best to localised, dynamic groups of adults that focus on their needs.

Complex problems need complex solutions – which means individualised assessments and recommendations that can be delivered immediately and locally.

■We need to give care staff responsibility for the outcomes of CiC – how much they are involved in local community for example.

■We should fund the child not the place. With flexibility to move if necessary.

■And we should involve the children – and not just lip service.

If it’s working – keep children where they are. We have been putting this model into practice for the past three months and have already seen positive outcomes for children. Vulnerable children are by their nature the most vulnerable people in our society – but we continue to under resource and under prioritise their needs. Apart from the waste they have a right to a life. Positive change can be made when priorities are identified and addressed. Resources can be limited but positive management can influence outcomes for the better . This leads to hope, high expectations, self-esteem and value for money! It also increases educational and work prospects, decreases crime and addiction, improves individual and group safety and security. Children develop the ability to build relationships and improved social behaviours. These positive changes also lead to improved health and increased life expectancy all of which helps break the cycle of failure and despair.

What is stopping this happening?

I would suggest it is mainly the lack of will and the dishonesty of governments and agencies to face up to the fact that they have continually failed. By giving the appropriate weight and resources to this issue they would flag their own failures even more. As if that were possible. So, we must make a change – it could be any type of change but it cannot be the same system that has failed for so long. Because if we don’t, children will continue to be lost, uncared for and barely provided for. It is absurd that we are still having to fight for the rights of anyone in this day and age – but if we can’t do that for children we can’t do it for anyone. And if we can do it for children – we can do it for everyone. ”

Charlie Mead, June 2012

CPS For Children

share save 120 16 Children in a Care less Society: Vulnerable – but not eligible
 

Crucial support for vulnerable children and adults lost as special needs funding is withdrawn by the Government

“Shouldn’t it be every child’s right to communicate?”, says mother

Crucial support for thousands of people living in Oxfordshire, Hampshire, Surrey, Sussex, Kent, Bedfordshire, Devon and Guernsey, who are unable to communicate without the aid of assistive technology, is scheduled to come to an end on 30th June this year when The ACE Centre in Oxford closes its doors for the last time.

The latest casualty of government cuts, The ACE Centre along with hundreds of other charities and specialist services across the country, has seen funds used to support the 260,000 children and adults in the UK who require Augmentative and Alternative Communication (AAC) provision reduced or withdrawn.

“Communication should be a right for every individual”, said Jenny Malone whose daughter Claire, despite battling with Cerebral Palsy, a condition that affects her speech and motor control, has realised her full potential and is now studying Physics at Imperial College London thanks to the provision and support of appropriate technology recommended by The ACE Centre.

Since it opened in 1984, The ACE Centre has provided support for over 5,000 people like Claire who struggle to communicate, by carefully assessing their needs and recommending the right technology that literally enables them to speak, write and access education. The Centre also provides essential training and free information services for parents, carers and professionals within education and health services.

Claire, who was first assessed by The ACE Centre in early childhood and continues to be supported by them, has been able to realise her full potential as a result of a range of communication aids designed to meet her complex needs. In addition to using a specialised joystick to control onscreen software, Claire uses Eyegaze technology , an eye-operated communication and control system to communicate and interact with the world around her. With this, Claire can speak, write, interact with information technology and even control systems in her home or at University. (See further down this page for more information and a video about Claire)

A recent AAC Report to the Government’s Communication Council by the former Communication Champion, Jean Gross CBE found that there is a significant under-provision of local and regional AAC services with a pressing need to build capacity within the sector to ensure its sustainability. Unless the Government tackles the issue, other charities and specialist services that address complex physical and communication difficulties will be forced to close, further disadvantaging those in need.

Bill Nimmo, Trustee, The ACE Centre, Oxford, said:

“Vital services like ours that provide so much support through high levels of expert knowledge and understanding of people’s needs cannot be allowed to close and we ask the Government to urgently review the sustainability of these essential services.

“ The ACE Centre Advisory Trust staff and Trustees are deeply saddened that the Centre is scheduled to close at the end of June 2012. Despite significant efforts to ensure the sustainability and future of our Centre, we are unable to continue to operate in the current financial climate.”

________________________________

About Claire

Claire uses a ruggedised tablet computer that she accesses with a joystick and switch. It contains a dongle which enables her to send and receive text messages – essential for coordinating a busy student social life! Although she often relies upon her own speech, she uses synthesised speech as a back up, or when she is giving talks or presentations.

*    Watch a video about Claire (scroll down page) <http://tinyurl.com/ace-casestudy>

Claire is studying physics at degree level and therefore requires powerful customised onscreen grids to enable her to produce the complex calculations required. During tutorials, her study assistant writes notes onto a DigiMemo that can be shared amongst other students. Interestingly, Claire’s tutor finds that the students engage much more with Claire’s assistive technology than with the conventional whiteboard that they had all found a bit daunting!
What this helps the individual to achieve: Claire has been a high flyer throughout her academic career and has aspirations to pursue a PhD. She also uses her technology to manage her social life.

Those contributing to the video: Claire talks eloquently about her assistive technology and what it has enabled her to achieve. We also hear from Claire’s study assistant and tutor about her experiences at university. David, a teacher from the ACE Centre in Oxford, also contributes to the story as he has known Claire since she was four.

share save 120 16 Crucial support for vulnerable children and adults lost as special needs funding is withdrawn by the Government
 

Review of Towards a Positive Future: stories, ideas and inspiration from children with special educational needs, their parents and professionals – published by J&R Press on 14th October 2011

 

As an SLT working both for the NHS, Privately and for a major Charity I must say a huge thank you for all the time you have invested writing this book.

 

Put simply it’s a fantastic reference point for any professional working with children and adolescents with SEN and their families.

 

I like how the vastly complicated process of statementing is clearly described in terms of not simply what happens but when it should happen. When I was a newly qualified SLT I wish I had such a resource to refer back to as it has taken years of experience to get my head around (and I still don’t feel overly confident). I will definitely recommend this resource to NQT (and experienced) professionals who work with children with SEN.

 

Whilst the book does not expect a particular level of prior understanding of SEN having some certainly helps. The majority of (affected) families greet having more information on the SEN ‘with open arms’ however I do feel that due to the complexity of the process, and hence the complexity of the book itself, it is not accessible to all families. Personally I would recommend reading particular chapters to some of my families and the whole book to others.

 

I think the icing of the cake are the inspirational stories. Whilst they are heart breaking at points, the positive messages found are clear. I like the way they are categorised into SLCN diagnoses/disorders as it helps the reader to relate to particular children they know.

 

Finally, with all the cuts and changes happening across the UK it is very easy to become disillusioned; the ‘making it happen’ has lit my fire of enthusiasm and I can’t wait to go into work tomorrow and begin to make a difference!

by Chris Wade

share save 120 16 Review of Towards a Positive Future: stories, ideas and inspiration from children with special educational needs, their parents and professionals   published by J&R Press on 14th October 2011
 

Review of the Conference – Towards a Positive Future – 14th October 2011 by ‘Special Needs Mum’ Tania Tirraoro and orginally published on her site ‘Special Needs Jungle’

The event was held at the Mary Hare School for hearing impaired children near Newbury. The school does inspirational work in providing an education for its pupils, helping each through individually designed hearing equipment. As a non-maintained state school, the school’s head, Tony Shaw, said they are ‘not considered to be part of inclusion’ and have had their funding cut by central government. This, despite the Education Secretary, Michael Gove, himself having a sister with a hearing impairment.

The school has had to diversify to survive, establishing an ear mould lab that services the NHS. Despite this, Mr Shaw says they never forget what they’re there for. He said, “At the core are the children we have the passion of serving.”  It’s a sad fact that, in the politics and cost-cutting of government both local and national, this message is too often overlooked.

Another speaker was Kevin Geeson, CEO of Dyslexia Action, who talked about the opportunities and risks of the Green Paper. He highlighted concerns about the assessment of hidden disabilities such as dyslexia in that it may not be picked up early enough and the question of who will control the personal budgets given to children to provide for their SEN. Mr Geeson said the Green paper brought an opportunity to provide the proper skills and support for teachers to include all children in the curriculum. He said, “Good teaching for children with hidden disabilities is good teaching for all.”

Education solicitor, Inez Brown of Anthony Collins solicitors, set out the legal framework and funding of special needs and pointed out the problem with parents appealing against SEN decisions for children at the new Academies because the Academies do not fall within the Education Act. She also pointed out that the Green paper removes speech and language and occupational therapy out of educational provision – something every parent of a statemented child should be aware of. This means that the local authority cannot be challenged about these things at a Tribunal.  

The conference also heard from internationally acclaimed academic, Professor Heather Van Der Lely who has developed an early-identification test for dyslexia called GAPS.  The professor pointed out that seven per cent of children have a specific language impairment – seven times the incidence of autism. She is trying to bring about the widespread use of GAPS which, she says, is quick, efficient and highly accurate. The crucial issue is, of course, that there are not enough Speech and Language Therapists to help all those that the test could identify.

Former Head Teacher, Charlie Mead is a consultant Child and Educational Psychologist, advising schools, the NAS and health and prison services about working effectively with young people with complex needs. He has a wealth of knowledge and experience in the field of helping children with special needs and makes the analogy of how the system is like an egg timer – with all the resources at the top not being able to filter down to those who need them at the bottom – ie, children. He spoke of how he had introduced nurture groups to a school in Birmingham where children with special needs were taught, mainly in the same classroom without the need to move around the school and given the help they needed, and how this had greatly improved their outcomes and allowed them to participate and be included within the mainstream of education. This is a fascinating idea that, with a some effort and will, could be adopted by every school in the country. It deserves greater public attention than it so far seems to have had.

One form of ‘hidden disability’ is that of acquired brain injury – that is, an injury not present at birth that occurs by illness or accident during childhood. Often these injuries present in a similar manner to developmental disorders. Every year it is estimated that at least 50,000 children and young people acquire a brain injury. Often, it is not until some time after the injury that a connection is made between a behavioural or learning deficit in the young person and the injury or illness that previously occurred. Research shows that 50% of those in custody have some kind of ABI. Louise Wilkinson, Training Manager of the Child Brain Injury Trust spoke at the conference of the issues faces by people with ABI. Her charity has been working to educate teachers on how to deal with such children. The charity is holding a conference in 2012 on the issue.

Finally, conflict resolution & NLP coach, Ian Ross and Lynne Kerry of Vievolve held a session about how to approach and deal with conflict and negotiations. They explained how to negotiate on ‘interests’ rather than ‘positions’ and how to maintain your cool when involved in a difficult discussion. One of the pieces of advice was to put yourself in your ‘opponent’s’ shoes and think what they are thinking. The company offers NLP coaching to businesses and individuals and has a number of courses at its South Oxfordshire venue coming up.

The site for the conference, where a DVD of the presentations will soon be available to purchase can be found here: http://www.wordswell.co.uk/conference/. Another event is being scheduled for next April.

All in all there was great concern over what the future for special needs might bring. It is clear that the green paper is far from perfect and that changes will need to be made. But it is heartening that there are plenty of people who are concerned with SEN that do not forget that the child is at the heart of everything. It is impossible to ignore the fact that money is always an issue, especially in these times, but our priority must surely be with the most vulnerable and childrenwith special needs are undeniably that.

   

 

share save 120 16 Review of the Conference   Towards a Positive Future   14th October 2011 by Special Needs Mum Tania Tirraoro and orginally published on her site Special Needs Jungle
 

What 10 things make the most difference to the families of children with special educational needs

When editing the forthcoming book ‘ Towards a Positive Future: Stories, Ideas and Inspiration from children with special educational needs, their families and professionals’ there were 10 things that cropped up repeatedly in the personal stories of the 14 families featured that made a positive difference to their well-being and the educational and life outcomes for the students.  These are:

  • having a clear description of all of the child’s needs
  • schools and services that focus on the child’s abilities and strengths
  • productive activity for the child throughout the day to promote learning rather than a differentiated but meaningless curriculum
  • safe, secure, appropriate physical environment which minimises the disability for the child and enables them to learn
  • integrated therapy and teaching
  • a positive and close relationship between parents and school
  • social care working in partnership with parents and schools
  • appropriate individual specialist programmes available as part of the curriculum
  • appropriate medication and nutrition available in school
  • access to specialist solicitors, barristers, advocates, representatives, expert witnesses and tribunal to achieve all of the above as early in the child’s life as possible

The book is available to pre-order from www.jr-press.co.uk and will be launched on Friday 14th October 2011.  To book your place at either the Book launch, the Conference or both please go to http://www.wordswell.co.uk/conference/

 

share save 120 16 What 10 things make the most difference to the families of children with special educational needs