implications of part 3 of the children and families act for children, young people, families and...
TRANSCRIPT
Implications of Part 3 of the Children and Families Act for children, young people, families and professionalsThe future of SEND in Hartlepool
Philippa Stobbs, Council for Disabled Children
• Broad purposes of the legislation
• What they mean for different groups
• How they might be realised
• First steps in implementation and how this might affect what we achieve longer term
• The views, wishes and feelings of the child and their parents, or the young person
• The importance of children, parents and young people participating ‘as fully as possible’ in decision-making
• The information and support necessary to enable participation
• Support to ‘achieve the best possible educational and other outcomes’
The culture change, s19
• Young people in their own right from the end of statutory school age
• Disability included in the strategic duties in Part 3
• Joint working across agencies, services and institutions: duties to co-operate, jointly commission and integrate
The culture change
• The big difference for children and families• Should feel listened to• Paperwork should reflect their views• Should be involved, in all the meetings where decisions are
made• Should feel in control
Participation in decision-making
• Listening to parents• Parents in the meetings where decisions are made• Involving parents in identification of SEN• Being able to reflect views of children, young people and
parents in reports• Bringing relevant evidence and expertise to the discussion• Additional time, SQW• Period for transfer from statements to EHC plans
What this means for professionals
Parent partnership services (PPS) become information, advice and support services (IASS) extended to include:
•health and social care
•IAS on disability
•children and young people
Provision of Independent Support for 2 years over the period of transfer form statements to EHC plans
Information and support to enable participation
• Developed with children, young people, parents, schools, colleges, other services including clinical commissioning groups, youth offending teams, early years providers, social services
• Builds on existing legal requirements (e.g. short breaks statement)
• Includes provision across education, health, social care, leisure, childcare, IAS services ..and much more
• Includes what schools and others expected to provide from their delegated budget
• Using comments on the local offer to inform future commissioning
Information and support: local offer
• Information about implementation of the school’s policy for pupils with SEN
• Must be on website• Must be updated annually• Includes a range of policies on: identification, involving
parents, support at transition, staff expertise and training, how specialist expertise secured, how children with SEN engage in activities with others
Information and support: Schools’ SEN Information Report
• EHC plans must focus on education and training, health and care outcomes that will enable progress
• Distinction between aspirations and outcomes• ‘A benefit or difference made to an individual as a result of
an intervention’• Personal and ‘not expressed from a service perspective’ and
not a description of a service being provided• What needs to be achieved by end of a phase or stage
Best possible educational and other outcomes
1. To be able to go out with my friends
2. To attend school 100%
3. To have three hours speech and language therapy a week
4. To be able to communicate with my friends at playtime
5. To enjoy school
6. To be able to travel to school on my own
7. To have 1:1 support so that I don’t mess around in the classroom
8. To get on to the college course I want
Best possible educational and other outcomes
Challenges for professionals:•Cultural and educational baggage•Expectations•Data•Equality Act and entitlement
Challenges for parents
Best possible educational and other outcomes
• Young people in their own right from the end of statutory school age• Rights to participate in decision-making transfer to young
people• Subject to mental capacity• Anticipated that ‘in the great majority of cases’ parents will
continue to be involved, or will be asked to act on behalf of their child
Young people in their own right
• Children and preparing for decision-making• Establishing child’s preferred method of communication• Challenges for parents and for young people• Challenges for professionals• Where there is disagreement
Young people in their own right
• Overlap: estimates suggest 75% disabled children may have SEN
• Children and Families Act 2014 and Equality Act 2010, SEND Code of Practice
• Section 100 C&FA, duties on schools in relation to pupils with medical conditions
• Individual benefits: thinking about reasonable adjustments and special educational provision together
• Strategic benefits: planning across both groups
Disability included in strategic duties in Part 3
Integrate services to promote the well-being
Joint commissioning by local authorities and clinical commissioning groups
Requirement to co-operate to meet EHC needs:• Schools• Colleges• Local authorities, including social care• Alternative provision• Health agencies
LAs to keep education & social care under review
Joint working across agencies
• The views, wishes and feelings of the child and their parents, or the young person• The importance of children, parents and young people
participating ‘as fully as possible’ in decision-making • The information and support necessary to enable participation• Support to ‘achieve the best possible educational and other
outcomes’
The culture change, s19
• Developing a common understanding and language
• Embedding change in strategic and individual planning
• Planning for success in early encounters
• Workforce development
• Building on existing mechanisms and creating new ones
Building a change in culture