
Family Support Service
The Family Support Service can provide information and support about the needs of your family member with a severe learning disability. Our support is confidential, and we won’t judge you or tell you what to do.
This page addresses issues of restraint and seclusion, and medication. Read about what these issues are, and the related activities the CBF has been involved in.
Jump to: Restraint and seclusion Medication
We are working together with a group of families to bring key national organisations together to develop a strategy to tackle the issue of restrictive interventions against children and young people across the UK. Our aim is to Reduce Restrictive Interventions and Safeguard Children (RRISC).
When we refer to restrictive intervention with children, we mean:
Restrictive Intervention of children and young people with SEN and disabilities during the pandemic: Results of Family Carer and School Staff Surveys
This report sets out the findings of two small scale surveys of families and schools which took place in the autumn of 2020 during the covid-19 pandemic. The aim was to try and gather some information about any impact of the pandemic (and associated restrictions) on disabled children’s experiences of restrictive interventions, such as physical restraint and seclusion. 48 family carers and 12 school staff responded.
Although the results are not nationally representative, they point to worrying trends which require further scrutiny.
Read the full report here: Pandemic survey report
And the data supplement here: Data supplement
In February 2020, we published an update report jointly produced by the Challenging Behaviour Foundation (CBF) and Positive and Active Behaviour Support Scotland (PABSS) and supported by the Reducing Restrictive Interventions and Safeguarding Children group RRISC. This report is an update to our January 2019 report ‘Reducing Restrictive Interventions and Safeguarding children’ and provides further analysis on additional case study data.
Reducing Restrictive Intervention of Children and Young People – update report
Our 2019 and 2020 reports shared family carers’ shocking accounts of their children’s experiences of restrictive intervention, shared through a survey and case studies. We found children are being injured physically and emotionally through the use of restraint, seclusion and other restrictive practices in schools. You can read the original 2019 report here.
We launched our update report at an event at the House of Lords on 10th February 2020 hosted by Baroness Sheila Hollins. The aim of the event was to raise awareness about this hidden issue and encourage different organisations, researchers and stakeholders across the UK to pledge to action to reduce restrictive interventions of children and young people.
Baroness Sheila Hollins opened the event by thanking all the families who shared their experiences for this report. The Baroness said: “I know it is traumatic to have to go over what happened, and we appreciate your bravery in bringing this issue to light.”
Elly Chapple, a family-carer whose daughter Ella lost her sight as a result of the traumatic impact of restrictive interventions, spoke about this life changing experience and how we should view children differently. Elly is also a founder member of the RRISC group and has worked in partnership with the CBF and PABSS to bring this issue to light.
Richard Hastings is the Cerebra Chair of Family Research and a Professor of Psychology and Education at the University of Warwick. He explained the research background and highlighted the findings of the report and the key recommendations.
Read Richard’s presentation here
Nick Hobbs, Head of Advice and Investigations at the office of the Children and Young People’s Commissioner Scotland (CYPCS), gave the final presentation. Nick explained the importance of focusing on restraint and seclusion as human rights issues and spoke about the current work taking place in Scotland.
A key feature of the day was when three parents described their experiences, the impact of Restrictive interventions and how we can support children well. You can see the short film here:
We asked all invitees to make a pledge to reduce restrictive intervention of children through a specific action. Pledges made at the launch begin to address all of the four main recommendations in the report.
Read all the pledges made here
Baroness Hollins closed the launch event highlighting the need to continue to ensure that the voices of families are heard
I hope we will look back on today as the start of a real process of change – Baroness Hollins
At a meeting of the RRISC group we filmed three parents talking about restrictive intervention experienced by their children, and the impact on the whole family. You can watch the short film we made:
A blog of one family’s experience, shared at our first meeting, can be found on the Paving The Way website.
The RRISC group have produced a series of key messages about the issues. The list includes five key asks that we believe, if carried out, will reduce the use of restrictive intervention on children and young people.
The key messages have been endorsed by the CBF, Positive and Active Behaviour Support Scotland, The Council for Disabled Children, National Association of Special Schools, Mencap, and NSPCC.
The CBF produced a briefing paper for the parliamentary debate on restrictive intervention of children and young people, held on Thursday 25th April 2019.
The RRISC group wrote to Michelle Donelan MP in October 2019, regarding the consultation on Restraint in Mainstream Settings and Alternative Provision.
You can read the RRISC group response here
We are still waiting for the outcome of this consultation to be published.
The CBF are concerned about ongoing issues of over-medication and inappropriate use of medication for children, young people and adults with learning disabilities. Antipsychotic medications are often prescribed for individuals with learning disabilities or autistic people when there is no related diagnostic reason for them, and may be prescribed for behavioural reasons.
The CBF were pleased to see the introduction of NHS programmes STOMP (Stopping Over Medication of People with a learning disability, autism or both) and STAMP (Supporting Treatment and Appropriate Medication in Paediatrics) in 2015, and have heard from families that, when applied as intended, these programmes have made a great difference for their relatives. However, we also head from many families to whom the programmes have had frustratingly slow progress. The experiences of families in touch with the CBF have been collected in our report.
Read the report: STOMP – A family carer perspective
There is also a risk of STOMP/STAMP being treated with diminished importance, and no longer appearing a policy priority for healthcare bodies. Since the introduction of the programmes in 2015, there has been limited distribution of information and training programmes, and safeguards to ensure that concerns are addressed has been limited. The CBF are committed to ensuring that addressing over medication and inappropriate medication remain on the health policy agenda.
To see what the CBF are doing to promote the STOMP/STAMP initiatives and to address overmedication and inappropriate medication, please visit the projects section of our website. This page includes information on our medication pathway resource, involvement with the development of training programmes, and our reports.
Medication used in response to someone’s behaviour can be a form of restraint. In June 2019 the CBF put together a briefing paper on medication, including background information about medication use and why it is important to avoid inappropriate medication.
The Family Support Service can provide information and support about the needs of your family member with a severe learning disability. Our support is confidential, and we won’t judge you or tell you what to do.
This information page answers four questions about what to do if you are worried about the safety of someone with a learning disability, and who you should tell. It also describes what happens when child and adult protection referrals are made.
The CBF aims to improve lives for individuals with severe learning disabilities who display behaviour that challenges through our project work, using new approaches and encouraging others to learn from this work and improve their practices.