Safeguarding d/Deaf and disabled children and young people

Risk and vulnerability factors

There are several factors that contribute to disabled children and young people being at a greater risk of abuse.

Communication barriers

Children and young people with speech, language and communication needs (including those who are d/Deaf, or have a learning disability or physical disability) face extra barriers when it comes to sharing their worries and concerns.

• Adults may have difficulty understanding a child’s speech so they may not realise when a child is trying to tell them about abuse.
• Adults may not have the knowledge and skills to communicate non-verbally with a child, which can make it harder for children to share their thoughts and feelings.
• Communicating solely with parents or carers may pose a risk if the child is being abused by their parent or carer.
• It can be difficult to teach messages about what abuse is or how to keep safe to children with communication needs. Without this knowledge children may not recognise that they are being abused or won’t know how to describe what’s happening to them.

Increased isolation

Disabled children may have less contact with other people than non-disabled children, because they have:

• fewer out of school opportunities than their peers
• fewer opportunities for spontaneous fun with friends
• less access to transport
• less provision for appropriate toilets and changing facilities
• difficulty finding out about accessible events

(Franklin, 2016).

This means they have fewer people to turn to if they need help or support.

They may be further isolated if they:

• need carers to take them out
• have restricted independence because they use a wheelchair or require a sign language interpreter
• live away from home at a residential school.

Disabled children and their families may have limited access to support systems. Support may not be available due to lack of funding or it may not be appropriate for the child’s physical, emotional or cultural needs. This can make it difficult for parents to provide the care their child needs and add to the pressure of caring for a disabled child.

Dependency on others

Children with disabilities may have regular contact with a wide network of carers and other adults for practical assistance in daily living including personal intimate care.
This can increase the opportunity for an abusive adult to be alone with a child.

If a child is abused by a carer they rely on, they may be more reluctant to disclose abuse for fear that the support service will stop.

Caring for a child with little or no support can put families under stress. This can make it difficult for parents to provide the care their child needs and can lead to a child being abused or neglected.

Inadequate support

It can be difficult for any child who has experienced abuse to get the support they need, but disabled children may face extra problems.

• Disabled children are less likely to tell someone about experiencing abuse and more likely to delay telling someone than their non-disabled peers (Hershkowitz, Lamb and Horowitz, 2007).
• Adults may not understand and respond to a disabled child’s safeguarding needs.
• Communication barriers may prevent adults fully understanding what the child is telling them.
• Some adults may not focus on a disabled child’s views.
• If abuse is reported to the police and/or children’s social care, the response may be affected if professionals lack skills or experience in working with disabled children.

Misunderstanding the signs of abuse

It’s not always easy to spot the signs of abuse. In some cases, adults may mistake the indicators of abuse for signs of a child’s disability.

• A child experiencing abuse or attempting to disclose abuse may self-harm or display inappropriate sexual behaviour or other repetitive and challenging behaviours. If this is misinterpreted as part of a child’s disability or health condition rather than an indicator of abuse, it can prevent adults from taking action.
• Injuries such as bruising may not raise the same level of concern as they would if seen on a non-disabled child. Adults may assume that bruising was self-inflicted or caused by disability equipment or problems with mobility.

Lack of education on staying safe

Personal safety programmes and relationships and sex education (RSE) are not always made accessible to d/Deaf and disabled children, and not always taught in special schools. This can be for a number of reasons:

• teachers may not realise they need to teach RSE to children with disabilities
• parents and professionals may think young people with learning disabilities shouldn’t have relationships or sex
• teachers may feel they need more training about how to deliver RSE to children with disabilities
• school governors may not approve RSE being taught in a different, more accessible way
• the school may prioritise other subjects over RSE
• sex and relationships education may not be taught in a way that makes sense to young people with learning disabilities

(Garbutt et al, 2010).

As a result, a disabled child may not know how to recognise abuse or who to tell.

Who is at most risk of abuse?

Disabled children at greatest risk of abuse are those with behaviour or conduct disorders. Other high-risk groups include:

• children with learning difficulties/disabilities
• children with speech and language difficulties
• children with health-related conditions
• d/Deaf children

(Miller and Brown, 2014).

Safeguarding policies and procedures

The needs of all children with a disability should be incorporated into safeguarding policies and procedures.

Safeguarding policy statements should:

• include an equality statement with a commitment to anti-discriminatory practice
• recognise the increased vulnerability of disabled children to abuse and neglect and the barriers they may face
• include additional safeguards to protect disabled children
• consider the need of d/Deaf or disabled children in making it easier for them to report abuse to a trusted adult
• cover any safeguarding issues that are specific to a child’s disability such as intimate care and safe touch.

> Find out more about writing a safeguarding policy

Intimate care

Children with certain disabilities or medical issues may need help and support with intimate personal care including going to the toilet and washing.

There should be a separate policy on how intimate care plans are written, carried out and reviewed. This should include making sure children and young people are including in the development of care plans.

The policy should cover safeguarding concerns around intimate care including:

• how records of intimate care are kept
• a statement about the responsibility of all staff to report any child protection concerns arising from intimate care
• a statement that recognises that staff carrying out intimate care may be at increased risk of allegations of abuse
• a statement that recognises that perpetrators of abuse can include members of staff as well as others known to the child
• how the organisation will respond to allegations of abuse related to intimate care.

Training

Everyone working with children should receive regular child protection training.

Training should highlight the reasons disabled children are at increased risk of abuse and neglect and why additional safeguards are needed to protect them.

It should provide guidance on what to look out for and how to respond early to the needs of disabled children.

> Find out more about how our specialist consultants can provide support to your organisation

Direct work

Assessment

In any assessment of a disabled child professionals should assess all the needs of the child and their family, not just those related to the child’s disability.

• Professionals should ensure that parents understand and are supported to meet the additional needs of caring for a disabled child.
• Professionals across all agencies should be aware of safeguarding issues for disabled children.
• Professionals should be aware of the range of services available to families and disabled children. Families and children should be referred to these services accordingly (NSPCC, 2016).

Best practice

Learning from case reviews about disabled children emphasises the importance of child focused practice, highlighting the need for a holistic approach to supporting disabled children and their families (NSPCC, 2016).

Listening to the child

• Make sure the child’s voice is heard. Where there are safeguarding concerns, speak to children alone and don’t use parents as interpreters.
• If a child’s disability means verbal communication is difficult or impossible, make every attempt to communicate by other means.
• Consider how a child may communicate through their actions. Consider whether distressed or disruptive behaviour is due to the child’s disability or if the child is upset for another reason.
• Tailor tools and resources to the child’s needs. Check that the child has understood what you’ve told them and is able to apply it – don’t make assumptions about what they have understood.

Information sharing

Professionals should have a shared understanding of the nature of a child’s disability, the services their family are receiving and the risk of harm. This information should be used by all agencies to distinguish between disability and child protection issues.

Interagency cooperation

• Specialist disabled children services should be embedded within wider support services and children and families.
• Every family should be designated a lead professional to coordinate work across services and provide a single point of contact (NSPCC, 2016).

Working with British Sign Language interpreters

Every d/Deaf child is different and every family is different with its own complexities and needs. As part of assessing a family’s needs it’s essential to establish the d/Deaf child’s preferred method of communication. They may use:

• British Sign Language (BSL)
• some signs with speech
• speech, lip reading and gestures.

It’s essential for social care practitioners to establish how the child communicates with their family and others. They should also see if there are any trusted adults that the child or young person communicates directly with. This could be:

• another member of the family
• a teacher
• a youth club leader.

Social care practitioners should discuss the need for a British Sign Language interpreter with the child and their family and make sure one is found as soon as possible if needed.

There is no ‘ideal’ way to facilitate communication between safeguarding professionals and d/Deaf children. 

• Consider whether a child protection assessment or discussion is better with or without a third party. Would the child rather sign directly to a trusted individual or have a third party in the room?
• Reflect on your own language limitations and don’t assume you can communicate “well enough”. Even when a d/Deaf child can use spoken language this may not be the method of communication they’re most comfortable with.
• It’s likely that sign language interpreters will be more familiar with d/Deaf culture than most social workers. Recognise sign language interpreters as having cultural knowledge that can help you gain optimal understanding and participation.
• Sign language interpreters are highly skilled professionals, but may not be used to working in safeguarding and child protection situations. You should meet with the interpreter in advance to help them understand the issues and the concerns to make sure they are able to explain all the necessary concepts to the child and their family.
• It’s important to consider communication where there are d/Deaf parents with hearing children. Parents need to be given every opportunity to communicate in their own language.
• Always prioritise the child’s strengths, requirements and needs, whether working with an interpreter or not.

Empowering d/Deaf and disabled children and young people

Social attitudes and assumptions about disability can lower a child’s self-confidence and make them feel disempowered.

Building a child’s self-esteem can help to promote their safety. A child who feels empowered is less likely to blame themselves if they experience abuse and more likely to seek support.

Help empower disabled children by:

• consulting them on their views and wishes about their life and care in order to meet their needs
• giving them access to advocacy services
• providing them with communication support and opportunities to express themselves
• helping them to build a supportive relationship with a trusted person – this can increase the chances of a child disclosing abuse to that person (Taylor et al, 2015)
• providing accessible education on topics such as keeping safe, sex and relationships and online safety
• providing information in accessible formats.

Resources

Our PANTS resources help parents talk to their children about how to stay safe from abuse. We’ve developed resources which are tailored to the needs of children and parents with disabilities, including a BSL video.

> See our PANTS resources

Our Love Life films and supporting resources help young people with learning disabilities explore topics such as:

• personal identity
• feelings
• relationships
• different kinds of love
• privacy and boundaries
• online safety.

> Find out more about Love Life

Activities

Activities that can help improve disabled children’s wellbeing include:

• Peer support and social activities. Opportunities for recreational and social interaction can enable children to explore issues with their peers. Activities can also build on children’s confidence and reduce isolation.
• Creative therapies. Activities like art and music can provide children with opportunities to express themselves through indirect and non-verbal means.
• Building relationships. Supportive and trusting relationships can help make a child feel safe and confident and know that they have someone to talk to.
• Improving communication. Helping a disabled child to communicate with trusted adults can help them express their views and tell someone if they need help.

Childline

> d/Deaf children and young people can contact Childline through a qualified BSL interpreter using Sign Video

Legislation on safeguarding d/Deaf and disabled children

Statutory guidance across the UK highlights the responsibility of those in education, community and care sectors to safeguard all children from all forms of abuse and neglect.

The statutory guidance in all nations includes sections on safeguarding disabled children and young people. Find out more about child protection in:

• England
• Northern Ireland
• Scotland
• Wales

See also Key guidance for schools in the UK.

Key legislation

The key legislation relating to the safeguarding of d/Deaf and disabled children in England is the Children and Families Act 2014. Part 3 establishes help for children with special educational needs and disabilities, including a single assessment process and personal budgets.

Under Section 17 of the Children Act 1989, local authorities in England must also safeguard and promote the welfare of children in need. A child in need is a child who is unlikely to have, or have the opportunity to have, a reasonable standard of health and development without any support provided by a public authority. This may include having a disability.

In Northern Ireland, The Children (Northern Ireland) Order 1995 sets out how children in need and their families are supported, including giving information about the assessment of carers of disabled children.

In Scotland, Sections 23 and 24 of the Children (Scotland) Act 1995 refer specifically to disabled children. The Act requires local authorities to give disabled children the opportunity to lead lives which are as normal as possible. It also requires local authorities to promote the welfare of children in need.

In Wales, Section 15 of the Social Services and Well-Being (Wales) Act 2014  requires local authorities to minimise the effects of disabilities on disabled people.

The Rights of Children and Young Persons (Wales) Measure 2011 embeds the UN Convention on the Rights of the Child into Welsh law, including giving disabled children the right to protection, participation and service provision.

Discrimination

In England, Scotland and Wales, the Equality Act 2010 provides protection from discrimination against disabled people, requiring service providers to make sure their service is accessible for disabled people to the same standards as non-disabled people.

The Disability Discrimination Act 1995 provides protection from discrimination against disabled people in Northern Ireland. Schedule 8 prohibits discrimination against disabled people relating to goods and services.

Section 75 of the Northern Ireland Act 1998 requires public authorities to promote equality of opportunity between disabled and non-disabled people.

Special educational needs

In England, Scotland and Wales, Part 6 of the Equality Act 2010 states that schools must not discriminate against a disabled person when conferring qualifications.

In Northern Ireland, the Special Educational Needs and Disability (Northern Ireland) Order 2005 provides guidance on safeguarding against the discrimination of disabled children in schools and educational settings and places a duty on schools to make ‘reasonable adjustments’ for disabled pupils to participate in education.

Intimate care

Across the UK, the activities associated with providing intimate care to a child fall under ‘regulated activity’ if they are carried out without supervision. This means that anybody carrying out these activities as part of their work must have an enhanced (with barred list) vetting and barring check before they can begin. The activities include:

• taking a child to the toilet
• dressing a child
• washing or bathing a child.

This law is particularly important to disabled children who may require a greater level of intimate care than other children.

In England and Wales, procedures for intimate care are outlined in Section 64 of the Protection of Freedoms Act 2012.

In Northern Ireland, Part 1 of Schedule 2 of The Safeguarding of Vulnerable Groups (Northern Ireland) Order 2007 outlines intimate care and regulated activities with disabled children.

In Scotland, the Protection of Vulnerable Groups (Scotland) Act 2007 lays out the statutory guidance for regulated work with children, including intimate care.

> Find out more about vetting and barring checks in our safer recruitment section

Special measures for disabled child witnesses

Across all four nations in the UK, there are statutory ‘special measures’ that can be used for the purpose of taking evidence from a vulnerable witness, including disabled children.

These include:

• screening the witnesses from the accused
• giving evidence by live link
• giving evidence in private.

If a young witness is disabled, they may have particular difficulties attending court and giving evidence. In England and Wales, the Youth Justice and Criminal Evidence Act 1999 introduced a range of measures to help children in these circumstances. Section 16 specifies the grounds on which a child may be eligible for assistance.

The Criminal Evidence (Northern Ireland) Order 1999 makes provision for assistance such as communication for witnesses who are disabled. The Justice Act (Northern Ireland) 2011 raised the maximum age for eligibility for assistance from 17 to 18.

The Vulnerable Witnesses (Scotland) Act 2004 defines and outlines the provisions for vulnerable witnesses in Section 1.

> Sign up to CASPAR to stay up-to-date with new legislation and guidance

References and resources

References

Franklin, A. (2016) Friendship opportunities for disabled children and young people (PDF). Coventry: Children and Families Research, Coventry University.

Garbutt, R. et al (2010) Final report: talking about sex and relationships: the views of young people with learning disabilities (PDF). Leeds: CHANGE.

Hershkowitz, I. Lamb, M.E. and Horowitz, D. (2007) Victimization of children with disabilities. American Journal of Orthopsychiatry, 77(4): 629-635.

Jones, L. et al (2012) Prevalence and risk of violence against children with disabilities: a systematic review and meta-analysis of observational studies.The Lancet, 380(9845): 899-907.

Miller, D. and Brown, J. (2014) ‘We have the right to be safe’: protecting disabled children from abuse. London: NSPCC.

NSPCC (2016) Deaf and disabled children: learning from case reviews. London: NSPCC.

Taylor, J. et al (2014) An investigation into the relationship between professional practice, child protection and disability (PDF). Edinburgh: The Scottish Government.

Taylor, J. et al (2015) Deaf and disabled children talking about child protection. London: NSPCC.

Childline

If a child or young person needs confidential help and advice direct them to Childline. Calls to 0800 1111 are free and children can also contact Childline online or read on the Childline website:

• living with a disability 
• dyslexia and learning disabilities
• Deaf Zone 
• British Sign Language (BSL) advice videos
• Contacting Childline using Sign Video 

You can also download or order Childline posters and wallet cards.

Further reading

For further reading about parental mental health, search the NSPCC Library catalogue using the keywords "children with disabilities"; "children with multiple disabilities"; "children with physical disabilities"; "deafness"; "safeguarding".

If you need more specific information, please contact our Information Service

Related NSPCC resources

Read our leaflets specifically for d/Deaf adults on recognising and reporting concerns if a child is being bullied or abused:

• Telling about bullying
• Telling about abuse.

Our summary of learning for improved practice from case reviews working with d/Deaf and disabled children provides several key findings.

Read our commissioned report summarising research on d/Deaf and disabled children’s experiences of the child protection system.