Advocating for your deaf child in early education
Learn to advocate for your child in their early years education and childcare.
This information is for families of deaf children in England. Read our information for Northern Ireland, Scotland and Wales.
All children deserve the care and support they need to have the best start in life. This includes children with any type of hearing loss or levels of deafness.
Children learn and develop at a faster rate from birth to 5 years old than at any other time in their lives. Their experiences in early years have a major impact on their future life chances. Deaf children’s safe and happy experiences at home as well as, high-quality early learning are important. These provide the foundation they need to fulfil their potential.
You know your child. Sharing what works best for them with their early years provider can be helpful. It will help to build a strong foundation for their development and learning.
Understand advocating
Advocating for someone is when you stand up for what they need or is their right. Babies and young children are not able to fully advocate for themselves. Babies and young children may not have the language to describe how they feel. Older children may not feel comfortable letting an adult know if something is wrong.
Parents and carers of deaf children can be advocators for them. Knowing your child's rights in education and what you’re entitled to as a family can help. You can advocate for them to make sure they get the support they need. Sometimes, showing that you’re aware of your rights can make it easier to help solve problems.
It doesn’t come naturally to me to be a pushy parent, or to challenge professionals. We knew something wasn’t right, deep in our guts, and we needed to be Sybil’s voice. Knowing we were doing this for her pushed us on. When it came to choosing Sybil’s education we had to draw on our experience of advocating for her to ensure she was getting the right support.”
Holly is mum to Sybil (5), who is profoundly deaf and wears cochlear implants.
You can find tips on how to advocate for your child (Disabled Children Partnership).
Working in partnership with staff
Working in partnership with the professionals looking after your child can help. Building these relationships will help your child settle into their new environment. Being in the loop means that you can address any issues quickly.
As well as staff at the setting or provider, other professionals important to your child's early education may include:
Teacher of the Deaf (ToD)
Special education needs co-ordinator (SENCo)
a key person
Progress updates
Every early years setting or provider should be happy to meet with you to talk anything through. It’s expected that settings operate an 'open door' policy to welcome you when you need to speak with them.
They should also be able to provide you with regular progress updates. Progress updates allow you to work together to make sure your child is on track.
Deaf awareness
Some early years settings and provider may not have looked after a deaf child before. There are some things you can do to help them and raise deaf awareness.
Set up meeting with the professionals important to your child’s early education. This may include, your child's key person, their ToD if they have one and a SENCo if there is one.
Share our information, resources and training for early years education professionals.
Depending on your child's age, you can visit the setting or provider to talk about deaf awareness to the other children. You can discuss deafness, hearing technology and attention grabbers.
Share our deaf awareness videos for early years children. These short, fun, and colourful animated videos help young children understand how to support their deaf peers. The videos feature a diverse range of animal characters from our children’s book, Elephant and the Lost Blanket.
As your child makes friends, talk to the other parents about your child's deafness and how they like to communicate.
Share some deaf awareness resources with your child’s setting or provider.
Resources to share
Our postcards, posters and flyers can be a great way of raising deaf awareness. You can share them with the professionals and other parents in your child’s early years setting. They’re aimed at slightly older children, but it can still be helpful to have them around. These include posters and postcards with:
the British Sign Language (BSL) fingerspelling alphabet
tips for hearing children for when they’re talking to your deaf child
tips on communicating with your child for the adults working with them.
You can order copies or download these deaf awareness resources.
Share our resources for anyone working with deaf children in the early years. Including our ‘Deaf-friendly early education and childcare’ booklet. It includes a transition plan template they can use to record information about your child. You can also share the transition plan template separately:
Recognising the signs
It can be tricky to know if an early years setting or provider is meeting your child's needs. Being able to recognise the signs that it might not be the right environment for them is important. It can help you to solve issues quickly or ask for support. Especially as babies and young children may not have the language to tell you how they feel.
Here are some signs that may indicate that something isn’t quite right.
It’s always very noisy at drop off or pick up
Problems with your child’s hearing aids or implants. For example, coming home with dead batteries, damaged or switched off
The setting or provider is using Makaton instead of British Sign Language (BSL)
Noticeable changes in your child’s behaviour
Negative attitudes of the staff or childcare provider towards disability or deafness
Your child is being left out of things
Getting support
Every early years setting and provider is different. Your child has the right to be fully included. They may need some extra support to help them to take part in activities and experiences. Each deaf child is different and challenges they may face will vary. It’s important for staff not to make assumptions. They should consider each child individually and what works best of them.
Some deaf children benefit from additional support in early years education. If you think your child needs extra support, there are professionals you can talk to.
Teacher of the Deaf (ToD)
The main support you and your child may get is a ToD. If your child has a ToD, they will work in partnership with formal or informal settings or providers. ToDs can support:
staff at nurseries and pre-schools
nannies and au pairs
family members providing informal childcare.
A ToD can support by adapting the environment and curriculum to meet your child's needs. It’s important that your child’s setting or provider works with you and your ToD. Working together will make sure your child is getting the support they need. This may involve:
asking your ToD to support you when advocating for your child
asking your ToD to do some deaf awareness training with staff
sharing the importance of working with them with teachers, childminders, nannies, au pairs or family members.
Some deaf children do not have a ToD. If your child does not have a ToD, they may be eligible to one. If you have not been told about asking for a referral, speak to a professional working with your child. They should be able to start the process.
Special educational needs coordinator (SENCo)
Every education setting must have a special educational needs co-ordinators (SENCos). SENCos work in settings to support children with special educational needs or disabilities (SEND). Most, but not all, permanently deaf children may be viewed by their local authority (council) as having SEND.
Early years settings must identify a member of staff to act as a SENCo. Childminders are encouraged to have one.
SENCos work with families and professionals involved early education or childcare. They can:
co-ordinate meetings with these professionals, such as ToDs
make sure staff training is up to date
create targeted plans to support learning and development
put in place further support.
If you do not know who your child’s SENCo is, ask your child's setting or provider to put you in touch with them. If you think your child may have SEND, talk to the SENCo.
Find out more about deafness and SEND.
Full references for this webpage are available by emailing
informationteam@ndcs.org.uk