The legal rights of an education that meets the needs of children and young people with special educational needs and deficiencies (send) are at risk. Many thousand children risk denying important provisions, or loss of education access to full education.
As new education changes are dragging, each sign from the government suggests the right to an education, the plan of health care and care (EHCP) to attend mainstream schools. Local authorities want EHCPs to decrease, or remove all, to relieve the duties they often find loved and sad.
About 85% of children who have to send educated in Mainstream settings. Over 270,000 of these children have EHCPs. These legal documents implemented detailed needs of a child or young, and the support to fulfill their individual potential. EHCPS allows children and young people with all kinds of disabilities to receive an education.
Without statutory support, set up with the necessary additional resources for schools, it is not possible that the ministers can achieve their intentions to many children with progress, or even survival, in the safety, in the safety, in the safety, in the safety, in the safety, in primary education. A reduced or complete snatching-away EHCPs in the main education does not mean their needs to be extinct. This, rather, add applications for overcrowded special schools or mean they are forced outside school.
We believe that the public is on our side, and we support the newly launched by our children’s rights (Socr) led by work forests, issues and others. This campaign calls for EHCPs to be maintained, now and in the future. Socr is recently petition The reflection of this purpose rapidly passed 100,000 signatures, which means that the issue will be considered for a parliamentary debate, and is growing.
For more than 40 years, children and young people who have special needs and deficiency and disability have a lawful right to an education that meets their needs. Put on disaster plans to cut benefits for disabled people, it raises the question of who we are as a country and the kind of society we want to live. Regardless of the shipping system problems, the answer is not to remove children’s rights and young people. Families cannot afford to lose valuable legal protections.
Ameel Algani Professor, School of Law and Social Justice, University of Liverpool
Elizabeth Archer CEO, PDA SOCIETY
Jane Asher President, National Autisted Society
Profter Simon Baron-Cohen Director, Autism Research Center, Cambridge University
Anna ant CEO, contact
Ian Birrell Campanist in the reporter and disability
Alison Bloomer Editor, Learning Learning Now
Carol Boys Chief executiveDown’s Syndrome Association
Lucy Bray Professor of Health Health Literacy, Spect Hill University
Jane Campbell Disability Campaign
Madeleine Cassidy CEO, moro (independent provider of special education advice)
Samantha Clark CEO, Learn to Lack of England
Lucas cleansed Cerebra Professor of Law and Social Justice, Leeds University
Dr Mine Conkbayir Early years of researcher, author and consultant
Justin Cooke Head of policy and influence, National Deaf baby child
Claire Cushions Director of fundraising and participation, children
Claire Brown CEO, National Association of Special Schools
Rachel Movies Builds, sends alliance with rights
Anita Franklin Professor of Childhood Studies, The Metropolitan University of Manchester
Carrie Grant Broadcaster and Send Parents
Gems come Head of policy, UK’s entitlement
Jane Harris CEO, speaking and language UK
John Harris Journalist, writes and send parents
Siela Hassiotis Intelleval disability professor, University College London
Ben Higgins CEO, PHOTOS
Cherylee Houston Actor and Capability
Dr Rhidian Hughes CEO, VOLUNTARY ORGANIZATIONS DISABILITY GROUP
Sarah Johnson President, Prussian
Dr Anna Kennedy Autism Charmity Founder and Campanist
Jolanta Lasota CEO, ambitious about autism
Dr Tony Lloyd former CEO, ADHD FOUNDATION
Christine McGuinness Broadcaster, campaignigner and send parents
David Mitchell Nevoholl and Ginio search
Rosa Monckton Lack and Send Campanisener
Emma Murphy Director handle, Infact (independent fetal anti convulsions of trust)
Chris Packham Broadcaster and Neurodirida Hella
Scarlet Page Photographers and send parents
Liz Pellicano Professor of Autism Research, University College London
Sally Phillips Actor, Come and Send Parent
Sharon Pratt Founder member, Sending National Crisis
Tom Siger CEO, Autism Action
Brian Roberts Director of Education and Wellness, National Association for the Fetal Alcohol Spectrum Disorder, and Send Parents
Katherine Runshick-Cole Professor and Educational Chair, University of Sheffield
Sara Ryan Professor of social care, Markropolitan University
Saba Salman Journalist and Campanist
Melissa Simmonds Autistic Campaignerigner and Send Parents
Tom Shakespeare Professor of Disability Research, London School of Purity & Tropical Medicine
Stephanie Shirley Autism philanthropicist and trader
Caroline Stevens CEO, NATIONAL AUTISTED SOCIETY
Jon Kickss CEO, painting
Rachel Stevenson CEO, reverse right
Tania Tirraoro and Renata Watts Co-directors, special need forest
James Watson-O’Neill Chief executive, senses
Eleanor Wright Legal Officer, SOS! Sen
Stephen Unwin Director, writer and send parent
Suzy Yardley CEO, AUTISM UK
and 50 more (full list of www.saavourchildrensrights.org.uk)
