Inclusion Now Articles Issue 7
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Inclusion at Tuckswood Community First School
Creating Circles of Friends - Book Review
Now We Are All Middle Class - Poem
Hidden Voices - Notes from a Consultation with the
Visions of a Demon Race - Article by Maresa Mackeith
One For All - Consultation group of young people
Listening to the Asian Community - DEE Conference Report
Reasonable Adjustments - DRC Code of Practice
No More League Tables - NUT Campaign against SATs
and League Tables
The Green Paper - Every Child Matters
General Certificate of Segregated Education - Poem
Report of Direct Action by People with Down's Syndrome
at Screening Conference
Tuckswood Community First School serves an area of socio-economic
deprivation - lots of unemployment, free school meals and single families
etc. However - none of that really describes our community! The people (adults
and children) are honest and 'sparky' and have a big say in the running of
For the past eight years we have been working hard to develop the school as an inclusive learning organisation - a Community of Enquiry. At the heart of our curriculum (which we have redesigned, more or less within the requirements of Curriculum 2000) is the development of the ability to think as effectively and creatively as possible - again, adults and children.
We run weekly Philosophy for Children sessions and encourage a Socratic enquiry approach to learning; much of the curriculum is taught through drama using Mantle of the Expert strategies; School Council and Council Committees help with the decision making process of school; work in biodiversity and using the environment enhances what we do. We also teach the children to read, write and do their sums!! We run a Nurture Group, Basic skill groups and have a Light Sensory Room, one to one counselling for children who need it and try to offer one to one teaching for as many children as possible - very difficult at the moment with the funding crisis, but not impossible with a bit of creative thought. We also do lots of work in various ways with our parents.
In terms of inclusion we simply want to provide an opportunity for every child to show us what they are able to do. We work in a way which is 'needs led' and often re-look at what we provide to see if we can make it better. I guess we are unashamedly child-centred! They are, after all, at the centre of what we do. Children have their needs met anywhere within the school and the outside environment that is appropriate - we don't see inclusion as having to keep children in the immediate classroom if that is not going to be effective for them. Thus inclusion for us means inclusion within the school community.
We have lots of visits out to access community and natural environments for the children. We also have lots of visitors in to school and different people sharing their skills and passions with the children.
We try hard to encompass all intelligences and learning styles, looking to develop each child's ability to use as much of their whole brain as possible. We have never done the Literacy hour, although we use some of the strategies. The way our curriculum is organised enables every child to take part in their own way. It's quite hard to precis what the school is all about without sounding glib!!
There are many things we do with particular regard to inclusion. Readers might find it useful to have a look at our website:
A peer support and inclusion workbook
by Colin Newton and Derek Wilson:
This excellent book produced by Inclusive Solutions has been updated and now includes a chapter on Secondary Schools. Vanessa's Story is taken from that new chapter.
"I use this book in my teaching of future teachers, when I work with parents, and when I interact with government and other decision-makers whose mandate is to support people with disabilities in achieving their potential. It is amazing how much powerful thought and creativity is packed within the pages of this slim volume"
Gary Bunch, Principal Investigator, Faculty of Education, York University, Toronto
"Colin and Derek of 'Inclusive Solutions' have worked with a number of key groups here in Oxfordshire, including Teachers, Officers and Members.They have been exceptionally skilled at helping us to clarify and develop our vision for inclusion. Their passionate belief in the human value of inclusion is underpinned by a thorough understanding of the common constraints and a solid experience of the successful practice that can work in finding imaginative solutions. Circle of Friends is a powerful technique; it has been used extensively, with great success."
Chris Sey, Principal Educational Psychologist, Oxfordshire
Vanessa was a year 10 pupil attending an inner-city secondary school. Over the previous two terms, her life had become, in her words, "a living nightmare" as a result of the bullying and victimisation she was experiencing. Vanessa reported herself close to suicide. Her self-esteem and confidence were at rock bottom. She no longer believed that she had any real friends or that anyone really trusted or valued her. As a result she trusted no one.
Carol had been making her life extremely difficult. Carol had been interviewed by school staff and the police in connection with anonymous phone calls, intimidating letters, vicious mobile phone texting to Vanessa and for threats and bullying carried out by groups of girls with Carol at the centre.
The head teacher of the comprehensive school, frustrated by his attempts to tackle this complex web of relationships, asked for some help in setting up a circle of friends for Vanessa.
Eight volunteers were gathered together by the form tutor and a meeting was held with Colin as the outside facilitator. This initial meeting was extremely powerful. Each of the volunteers explained clearly to Vanessa that she was:
A good friend
Someone they trusted
Someone who was always there for them when they had a problem
Someone they cared a lot about
The eighth volunteer simply hugged Vanessa when asked why she had volunteered with the simple expression, "she's my mate ain't she!"
Strategies agreed were relatively simple and centred on the theme of 'being there' for Vanessa and of encouraging her to speak to circle members about her concerns and worries rather than to bottle these up. The volunteers made it clear that they would help Vanessa work through the dilemmas she was facing and that the regular circle meetings would form an initial structure for this dialogue.
The affirmation of positive regard along with the clear statement of friendship from these individuals must have been extremely powerful for Vanessa. The messages of support, trust and acceptance plus the willingness to work with her on difficult social issues were impressive. Vanessa had not been able to hear any of this up to this point. In fact one of the circle members actually described Vanessa as having "words going in one ear and out the other" because she was so preoccupied with her own problems. On the day of the initial meeting Vanessa heard. She will always be stronger for that moment in time. The memory of those expressions of friendship from her peers is unlikely ever to be forgotten.
Preferably with stars
That is the only way to be
It's the only point of school
The stiff competition
In the global market
Makes it necessary you see
To raise the standards
To such a degree
That we can all be free
Of the need
To be working class
No, we won't need houses
Hospitals or schools.
Buildings are now unnecessary
And so are tools.
No bricks will need laying
No pipes to be plumbed,
No wood to join,
No tiles to be laid,
No walls to be plastered,
No sockets to be wired.
No roads, no rails,
No phone lines, cables or masts.
All that is in the past now
We are no longer working class
No more oil rigs,
No more gas,
No more wind power
Turbines, generators or grids
No more electricity,
Petrol at the pumps,
No more servicing or maintenance
No more mechanics for our cars,
No more clothes to be sewn
No more washing, ironing or putting away,
No more hair to be cut.
Nothing will need making,
And nothing will ever break,
All that is in the past now
We are no longer working class
No more babies to be cuddled,
No more patients to be healed,
No more Home Care, Child Care or Meals on wheels,
No more sadness to be noticed,
No more messes to be cleaned,
No more food to be farmed,
No more meals to be cooked
No more heat, no more light,
No more fires to be put out
No more deaths to be grieved
The future is in the City
Now that we are all middle class
Notes from a consultation meeting held
between disabled special school survivors and representatives of the DfES,
The Government have published their report of the Working Party on the Future Role of Special Schools. This report recommended the continued existence of special schools as a 'valuable part of an Inclusive Education System'. Disabled people, especially those who have experienced segregated education, were angry that they had not been consulted in any formal way about proposals which will affect a whole new generation of young disabled people. After much pressure, representatives of the DfES agreed to meet a group of disabled people and to accept their contribution as part of their consultation process. The following excerpts come from a full report of this meeting.
"There is no place for special schools in inclusive education. The more we segregate children from mainstream into special schools it doesn't reflect real life - an artificial environment for children of the same class, ability. I strongly believe you should rip it up and start the whole thing again, from mainstream schools."
"I'm a special school survivor, visually impaired. From being in the mainstream, I was given the choice between going away to special school or staying at home - no choice really. There was no cultural awareness - I was separated from family and friends - the first four years were traumatic, I cried myself to sleep every night - I can't believe the government will entertain the idea of carrying on with special schools - I'd have them burnt or pulled down - I will fight this as hard as I can."
"When I was 5 at one special school and there was one nursery nurse teacher doing this stuff and I took them home to my mother and said I didn't do these - brown rabbits and things - what's the point of teachers doing the work for you? Special schools should be dumped. They're out of fashion nowadays."
"In special school you're encouraged to think inside a narrow field."
"I'm a special school survivor and system survivor. I was in one in Durham from age 9 to 16 which took all I needed to know about life and living away from me - skills, everything. It was dehumanising. I couldn't function even in a day centre. The only route available was a day centre. That whole journey was 40 years. How can we advocate for continuation of special schools? The agenda needs to be led by special school survivors, not teachers. I want to make a few points - (1) Parents choosing special schools - no-one chooses special schools - parents don't know other options, they're not in touch with positive role models of disabled children and adults - it isn't choice. (2) Special school teachers leading the mainstream - no way! The whole system is corrupt and medicalised - do we want that taken into the mainstream?"
"I'm a special school survivor, from age 7 to 12 in a special school in Oxford. I had no formal education - I educated myself when I left school at 16. Our son is 7. He went to mainstream to start with and it didn't work. At the SEN tribunal we felt as if we were pushed into a corner between a special school or home education, and I couldn't stand that so I had to send him to special school."
Dzifa Afonu (young ally):
"I feel really angry that the government chose who I should be educated with and have as my first friends. Everyone in society misses out, the arguments are weak for having special schools - the argument is that mainstream schools are not good enough. So let's improve mainstream schools"
"I'm the youngest here so the most recently out of the system. There is nothing more damaging that you can do to young people than separate them. It is the cause of all conflict between young people all over the world. I was in mainstream until 16/17. I got 10 A-C GCSEs. Did 5 AS levels then left to do performing arts. I was advised through Connexions to go to this super 'inclusive' college in Coventry - but actually it was a segregated institution with no contact with the college next door. Supposed to be the most inclusive place! The only included students were NVQ Care students. They suggested I did 1 AS over 2 years and then work towards sheltered employment! The problem is not lack of resources but the resources put in the wrong place."
"I went to Elizabeth Fry school in Newham. Went to segregated school because no option - I was told I was 'too fragile' for mainstream - even in the special school I wasn't allowed to do PE or woodwork. We got the reject teachers. People from the mainstream next door come in and see you playing music for the day - 'how wonderful!' These things are not cool. I came out with no friends. You feel like a nerd on the street, begging for a friend. Not able to communicate with non-disabled people. In school - I spent time in rehab, not learning or having fun."
"I went to special school at two and a half. I saw physical and mental abuse every day. We were fully institutionalised, nowhere to go - being controlled not educated. In a class of eight - I was the only one with a small number of O levels, which made me isolated - no one to talk to about exams. I left despising myself, my impairments and other disabled people. Then I went to mainstream college and met these alien non-disabled people. Nothing in school prepared us for this. Twenty years down the line people are experiencing the same oppression. They don't have a place in a civilised society. Your understanding of inclusion is not mine."
"When I left school in 1979 when the Tories came in I went to a day centre for 6 months, because I had nothing to do. I wasn't educated properly for life at all. The education system let me down, has discriminated against me from living a normal life. I've had to fight for my rights.... I work at a college. Most of my education was self-taught."
"My daughter is 18 and is one of those people who the government thinks special schools should be kept for. To enter a hostile world, to find role models is difficult - that is the legacy of segregation. Parents are in the most difficult position - you want to love your child and do your best but are trapped in a corner. Going to special school is not a real choice - it happens after assessment and statementing - they're not open door institutions - you are sent there. There's a lack of reality. People have created their own sense of wonderfulness by being carers. The special school heads lobby must be examined for motives for retaining the place of special schools. Creating two parallel worlds has got to stop."
"I feel extra frustration that the word 'inclusion' has been taken and redefined to mean segregation - it's corrupted the point of our struggles - the dream of relationships is inclusion, it's about the world changing."
The main points to come out of the meeting were:
Contrary to public opinion, the move to inclusive education is already very slow.
Adult ex - users of special education have the benefit of hindsight and are a vital voice in the debate about the future of education for children with special educational needs.
This voice is not being recognised or heard.
All the survivors present felt segregation had been harmful and limiting to them.
Non-disabled young people have a right to be educated with the full diversity of people with whom they will live as adults.
There is no argument for the continuation of segregated education. There is only an argument for improving mainstream education until it becomes inclusive.
Special schools have no expertise in inclusion. Successful inclusive schools are the resource which is needed by trainee teachers and anxious Heads.
Parents do not choose special schools unless forced by the lack of trustworthy alternatives.
I think that to have an education system that leaves out some
of its young people, hidden away in the so called care of special people,
is to create a "demon race" that can't be handled by ordinary people.
This "demon race" will in turn be surrounded by a mystique, which
sanctifies those who "care" for them, and creates a separate class
of crazy subhuman beings who can't have ordinary friends and make ordinary
mistakes in learning how to live.
The more elite we get, in making a cream of academic young people, who are pushed through a system of circus hoops to get a recognition they should have anyway, the more there will be people who, the system will think, are too much trouble or beyond the pale.
How can we reap the good thinking of those who don't fit the present system, if we make them into outsiders? Do we really want the world to stay the same, with its horrendous discrimination and fear of impairment?
Resources now going into eliminating impairment, could be put into assisting those of us, who need help to express our thinking. Our world could then move on to a place, where it could see the craziness of backing war and destruction, when our children have no opportunity of making relationships with people who have different needs from their own, or of negotiating where time and energy would be most profitably used.
Maybe it is worth trying to reduce the crime on our streets by making people feel they are a success. By putting energy into helping people make friends, we would learn to care with skills that very few people dare to look at learning, enabling the world to see that people's worth is not in what they can do.
We are looking at a future, not making past mistakes invisible with a pretence that they weren't made.
I am a Special School Survivor. Mistakes were made with me.
It was ordinary teachers and ordinary young people who had the confidence to listen to me. Yes, we need expertise. I needed an unusual speech therapist, who had had to leave her job in the system so she could gain the skills she needed to help me. We need the expertise in the context of real inclusion, not added on to an already selective system of who is worth teaching and who is not. I was not considered worth teaching.
I want to give to the world. I watch, listen, and think. I am not distracted by endless things "to do", as I can't do them. I need help to express myself, as I can't talk on my own, and if I didn't have physical help I would die. I can still give. The experience of being hidden away, with the assumption that I was worthless, still haunts me with a terror I can't describe. Nobody should be put through that. Yet there are hundreds forcibly excluded from life everyday.
Listen to us, we can teach you.
I think if you don't, the world is truly on its way to destruction.
Maresa MacKeith, June 2003
'One for All' are a consultation group who can offer a variety
of friendly, informative equality training workshops and meetings, like no
other training organisation to date! We have some of the leading disability
training organisations in the country such as Disability Equality in Education,
Inclusive Solutions and EQuality Training supporting our work. Fundamentally
we have experience - the key to understanding these issues and more importantly
we are part of the evolving education system in mainstream today. Our aim
is to promote the social model of disability, which sees society's systems
and attitudes as the problem, not an individual's impairment. We are not seeking
to place blame or find 'quick fixes' but instead find long term solutions.
Ultimately we are the proof that inclusion does work!
Who are 'One for All'?
"My name is Maresa MacKeith. I have Cerebral Palsy and no speech. As a result I was denied access to mainstream education for many years but I am now studying for my A'Levels at Clarendon College. I have a passion for inclusion as I believe other disabled young people should not miss out on the benefits of mainstream education and schools should not miss out on getting to know disabled young people."
"My name is Lucy Fisher and I too have Cerebral Palsy. I am also studying for my A' Levels at Clarendon College where I met Maresa. Whilst I was accepted into mainstream education I discovered many barriers and think it is important for me to share my experience to stamp out discrimination."
"My name is Lindsey Wallace. I am a non-disabled young person who met Maresa at school. She taught me a lot about disability issues so I feel inspired by her to promote inclusion and understand the benefits it will have to the non-disabled community. I am currently studying for my A' Levels at High Pavement Sixth Form College."
One for All can be contacted at:
PO Box 7612, Nottingham, NG8 3ZY
Phone 0115 9297526
A report on a day conference run by
Disability Equality in Education:
The work in this project has focussed on North West London with visits to Mosques, Gunwara's and Temples, appearances on Desi Local Radio and a number of meetings with local community groups culminating in 'An Equal Education For All' Day held at the Asian People with Disabilities Alliance in Brent on 17th May 2003. Krishna Birdy, the DEE worker in this area put in a great deal of work to make the day a success, aided by four other DEE trainers some 20 parents and 10 young people attended. The young people had their own workshop and activities including identifying their dreams and the barriers, a drumming workshop and presentations to parents. The parents did a more detailed path.
Some of the issues identified in the Asian community, prior to the day:
A very high proportion of Asian disabled children attend special schools.
Parents were not aware of the options available to them with regards mainstreaming.
Parents were not happy with transition options at post-16.
Parents did not feel confident to question the decisions of 'professionals'.
Parents were not aware of the support agencies that exist.
Parents were not aware of the statutory process of statementing.
In many cases parents had not been involved in Annual Reviews.
Overall, parents felt very isolated and unsupported.
When the young people reported back, one young man felt his parents did not like him and said his "dream was to play cricket with his dad". Later on his father came over and said " I never thought of playing cricket with my son." This was something he intended to do.
Another theme that came out strongly from the day was of how much the young people felt their lives had been wasted in special schools. Sapna Ramnani who has significant Cerebral Palsy, a special school survivor until she was 17, who transferred by accident to mainstream school and then went on to university and has recently completed her MA said. "My teachers thought I did not understand anything. Its not that special schools have low expectations of you, its that they have no expectations."
The Way Forward:
To provide more opportunities for parents to meet and discuss their concerns about their disabled children.
To provide more opportunities for young disabled people to express their dreams and hopes for the future; give them space to talk and take control of aspects of their lives; have an opportunity to form new friendships.
To make a video for the Asian community showing how inclusion can work.
The report of the Conference is available from DEE for £2.
Disability Equality in Education (DEE) have been commissioned
by the Department for Education and Skills and the Disability Rights Commission
to produce a practical guide for teachers, which will help schools to make
reasonable adjustments for their disabled pupils and prospective pupils (as
detailed in Part IV of the Disability Discrimination Act 1995).
As part of the project, DEE will be asking schools across England to self-nominate their examples of good practice. We want schools who have made adjustments for the first time as well as those who have more experience in making reasonable adjustments to tell us about what they have done and how they did it.
The nomination questionnaires, and more information about the project, are available on the Department's SEN website:
www.teachernet.gov.uk/accessibleschools Alternatively you can ring 020 7359 2855 to request a paper copy of the nomination questionnaire.
Please bring this article to the attention of your Head Teacher if you wish the school to be considered for this project. We would like to receive nominations by Tuesday 25th November, but would welcome any submissions after this date. The guide will be produced in Spring 2005.
Examples of Reasonable Adjustments taken from the DRC Code
of Practice 2002:
"A large secondary school is opening a special unit for pupils with speech and language impairments. They plan to include the pupils from the unit in mainstream lessons. One of the challenges is how to enable the children from the unit to follow the timetable. They might otherwise be at a substantial disadvantage. The school has an established 'buddy system' as part of its anti-bullying policy. After discussions with pupils, parents and the speech and language specialist teacher, the school extends its buddy system. It provides training for additional volunteer buddies to guide the disabled pupils from class to class. This is likely to be a reasonable step that the school should take."
"A school operates a policy of not permitting staff to volunteer to administer medicines to pupils in any circumstances. The school reviews its policy. Following assurances that staff are indemnified by the education authority's insurance policy, the school changes its policy to permit suitably trained staff to volunteer. This is likely to be a reasonable step that the school should take."
Disabled people and parents pledge support for the campaign
against SATs and League Tables initiated by the National Union of Teachers:
"Well over 90% of these mass testings could be killed instantly with no loss whatsoever. The most valuable form of testing for pupils and teachers is informal diagnostic tests, revealing what has and has not been learned and on which children are given feedback." Ted Wragg, Professor of Education
The Alliance for Inclusive Education has issued a press release acknowledging that the existence of SATs and the publication of National League Tables in England have, and continue to, work against the principles and practice of Inclusive Education.
The latest Audit Commission report, 'SEN - a Mainstream Issue', relates yet again how teachers and head teachers are unwilling to include children with SEN into their schools because of the perceived lowering of standards as measured by such narrowly defined academic targets:
"Almost every head teacher interviewed raised the issue of 'league tables' of school performance. This lay behind the reluctance of some to admit children with SEN for fear they would 'drag down' the school's position; and could have a damaging impact on staff morale; failing to reflect the considerable achievements of some of the hardest to teach children and their teachers. This was seen (by the Audit Commission) as perhaps the key issue the Government in England needed to address if committed to pursuing its policy of greater inclusion". SEN - A mainstream issue, Audit Commission 2002
We also acknowledge that in a 'British Social Attitudes' survey of parents carried out in November 2002 only 1% of 20,000 said that they thought exam results were a reliable measure of a good school. Parents of children with special educational needs or disabilities are particularly clear about the detrimental effect of the inflexibility of the 'Standards Agenda' on their children.
Parents for Inclusion, a leading educational charity says:
"We know from our helpline and inclusion groups in schools that SATs and the league tables are the biggest barrier to teachers being able to throw themselves wholeheartedly into welcoming our children."
In this light, the Alliance for Inclusive Education has resolved to lend support to the campaign initiated by the National Union of Teachers to abolish SATs and The National League Tables in England, and to promote instead broader measures of success based on 'value-added' and inclusion.
Zelda McCollum, a parent and head teacher says:
"I am a nursery teacher and I believe strongly that National Curriculum Testing should be abolished. The desire for good results could motivate schools to teach to the test and not respond to particular learning styles, frustrating the learning potential of many children. This could then lead to poor self-esteem and exacerbate behavioural problems."
Micheline Mason, Director of the Alliance says:
"Standardised teaching and testing disadvantages non-standard children. What we need is to celebrate creativity, innovation and flexibility in the classroom and to reward teachers for those things instead."
"The time for a major turnaround in disabled children's
services is long overdue" states the Audit Commission Report, 'Services
for Disabled Children'. The Green Paper consultation however does not readily
address the needs of disabled children with it's five headings - 'Being Healthy',
'Staying Safe', 'Enjoying and Achieving', 'Making a Positive Contribution'
and 'Economic Well-Being'. However it is really worth spending a bit of time
responding to put disabled children at the centre of the consultation. Whether
it be Sure Start, inclusive education, support with direct payments being
used to pay for personal assistance at school, inclusive play, closure of
segregated services, effective transition or the development of extended day
and multi-service support centred on schools, there are many opportunities
to champion the rights of disabled children: http://www.dfes.gov.uk/everychildmatters/consultations.html
If every child matters then challenge New Labours utilitarianism by supporting the NUT boycott on compulsory testing. All parents and disabled people should be supporting the struggle against SATs and the struggle for more child centred education with a core emphasis on the development of emotional intelligence. Recent (2003)GCSE results for children in special schools show Yr 11 do over 50 times less well than children in mainstream schools(0.9%-52.6% 5 A-C) Even the measure of percentage getting 1A*-G has dropped since last year (37.2%-32%). This is an argument for a system based on valuing all young peoples achievements rather than normative tests and an argument for closing all special schools by 2020 so not only will every child matter, but also be a valued part of the community.
Why don't you mark me on
Who is he anyway
And why should we all
Be like him?
I'm not Norm,
My way is as good as your way
Or Norm's way
It's just a different way
Nothing to be scared of
Plenty to be proud of
While I'm waiting
For my education
I label you with
Lindsay Carter, 2002
By Simone Aspis and Anya Souza
Source: Human Genetics Alert, May 2003
On May 19th, a group of people with Down's Syndrome and their supporters disrupted the International Down's Syndrome Screening Conference at Regents College in London. This is the first time people with Down's Syndrome have made such a protest and is a major new step in the debate about genetics, eugenics and the rights of disabled people. As a result of the protest, the conference organisers allowed Anya Souza to speak from the platform. Ms Souza, who is a trustee of the Down Syndrome Association, told the doctors that she opposes Down's Syndrome screening and that people with Down's Syndrome are people not medical problems. Her speech was warmly applauded by the conference delegates
The protesters consisted of three people with Down's Syndrome, another disabled person with learning disabilities and their families and supporters. They had written to the conference organisers in advance and asked to speak, but were refused by the main organiser. It is unacceptable that doctors discuss better ways of preventing people with Down's Syndrome being born, whilst excluding their voices from the debate. This runs directly counter to one of the main demands of disabled people: 'Nothing about us without us'. The protesters expect that their action will persuade the conference organisers to ensure a full debate at next year's conference with proper representation of disabled people with learning difficulties. This should be the start of a national debate on prenatal screening.
Excerpt from Anya's speech:
"I can't get rid of my Down's Syndrome but you can't get rid of my happiness. You can't get rid of the happiness I give others either. It's doctors like you that want to test pregnant women and stop people like me being born. Together with my family and friends I have fought to prevent my separation from normal society. I have fought for my rights . I have the right to a job, to services when necessary, to a decent standard of living, to know about my medical problems, to speak my mind, to make choices about my friends, whether to have sex, and so on. To do this you have to be independent when you grow up and not get segregated from society . I may have Down's Syndrome, but I am a person first".
Kitty Gilbert also attended the demonstration. She had this to say:
"I enjoyed watching the conference although I was a bit scared of what the conference people were saying. I think Anya's speech was brilliant and she said it all so well. I think she's wonderful. I think screening pregnant mothers with Down's Syndrome babies is wrong. They are wanting their offspring to be able to enjoy their world around them and have endless happiness. I for one gave my mum pride and joy and I will continue to do so. I think that we should be treated fairly and equally, not being getting rid of because there is so much more in life that we can do. We are what we are and ask our opinion."