We are here to help

We know that receiving the diagnosis of deafness for your child can often be unexpected and unsettling, and that you will have many questions and concerns.

On this page we hope to reassure you and provide answers to some of the questions parents of newly diagnosed babies and children commonly ask us.

We will also show you some videos of parents and children at The Elizabeth Foundation, along with stories showing what young adults with hearing loss can go on to achieve.

A poem by parents, for parents

You might like to watch this short (1 min 20 second) video of a poem for parents of newly diagnosed deaf children.

This poem is written and spoken by parents of deaf children who have attended The Elizabeth Foundation's preschool intervention programme.

How we can help you

The Elizabeth Foundation has over 35 years of experience supporting parents and helping preschool deaf children learn to listen and speak. Find out more in the 'About us' section of the website.

We offer a wide range of services - including our Ofsted 'Outstanding' early intervention nursery services at our Family Centre in Cosham, Hampshire.

For families unable to attend our Family Centre on a regular basis, we offer a Residential Summer Course, individual Speech and Language Therapy services and our unique online Let's Listen and Talk programme.

If you would like to know more about the various ways we can help you and your child, please contact us.

Commonly asked questions

Parents of newly diagnosed babies and children ask us a wide range of questions about hearing loss and the impact it might have on their child.

These are the answers to some of the more commonly-asked questions, but please bear in mind that the level, type and impact of hearing loss will vary for every individual child.

If you have any other questions or concerns about your child, please contact us and we will try to help.

Most deaf babies are born to hearing families with no history of deafness – and it is a shock to them all. A diagnosis of hearing loss brings emotions of fear, loss, panic and huge sadness and parents can sometime receive conflicting information from different professionals when a baby’s hearing loss is first diagnosed. Once a reliable diagnosis is made, parents start learning about the many communication approaches available, about the modern hearing technology available (such as digital hearing aids cochlear implants), and about services and educational programmes available. It is a journey and the start of any new journey can be daunting, but don’t be put off – the sooner you start this journey the better it will be for you and your child. It will feel frightening at times! Don’t worry, this is normal. A really good starting point is the National Deaf Children's Society (NDCS) - and in particular their 'My baby has a hearing loss' webpage and booklet [1.3MB - click link to download]. You can find out more about the support and information the NDCS offers in the Family support section of their website.
There is no single cause of deafness in children. Some children are born with a hearing loss and in other cases they become deaf at some point after their birth. In some cases, the cause of deafness can be easy to determine. Heredity, high fevers, illnesses such as meningitis, complications during pregnancy or childbirth are some possible causes. In many other cases, the cause is more difficult to determine and may never be discovered. There may also be several other factors that contributed to the hearing loss. Perhaps there is no apparent reason for deafness. In such cases, the cause is listed as "unknown".
If by normal you mean, "Will my child run and play, go to school, learn to read, have friends, drive a car, have a job or career, get married?" the answer is almost certainly, "Yes." If it means, "Will my child be exactly the same as a hearing child?" the answer is, "No." There are differences between children with normal hearing and children who have a hearing loss. The primary difference is in the way they will learn to communicate.
Having a hearing loss can significantly affect a child's ability to communicate. However, with modern technology and appropriate intervention during their early years, most deaf children can - and do - learn to communicate clearly and effectively using spoken language.
There are lots of different methods of communication available to help your deaf child learn to communicate. However, one unifying factor is that they all involve you, their parents. No matter which method of communication you choose, you are the main educator for your child and may need to learn some new skills to support your child in learning to communicate and to enable you to communicate effectively with them. Deaf children who learn to communicate at an early age and who are included in family interactions have a good chance for success, both academically and socially. Learn all you can about all methods - this will help you decide which one is best for your family! No one method is right for every child. To learn more about some of the different methods of communication we would again recommend starting with the National Deaf Children's Society - and in particular their 'Communicating with your deaf child' webpage and booklet [1.3MB - click link to download].
Making a decision on which communication path to go down for your child is a very difficult thing. What you must remember is that they are too young to make this decision themselves and will be relying on you to make a choice for them. Making an informed choice is the best possible way forward, so spend time and effort getting as informed as you can. The most important thing to do is to make a decision, rather than no decision at all. Deaf children need early language and communication intervention to set the foundations so they can learn to communicate effectively. In making the choice for a method of communication, you must consider your child’s type and level of hearing loss and what suits your child and you as a family. Ask as many questions as you need to understand each of these factors. Talk with other parents and any professionals providing you with support, and compare the advantages and disadvantages of each possible approach for your child and your family. It’s extremely important to make a choice, maintain interaction, and provide your child with clear and consistent language input. But remember, no decision is irreversible. You may feel some consolation from knowing that you can review decisions about communication methods and educational programmes as your child grows older, and add to them or adapt them. You can change your decisions as necessary, to provide your child with the best chance to reach their full potential.
Most children with a sensorineural hearing loss are fitted with hearing aids right away. Through ongoing and consistent testing your child’s audiologist will help you find the best hearing aids and the correct setting for your child’s loss. Hearing aids do not cure a hearing loss, but depending on the type and level of hearing loss, many children can learn to detect and discriminate the sounds of spoken language through hearing aids. This will help your child learn to communicate through speech and be aware of the sounds around him. If hearing aids have been recommended for your child, it is important that your child builds up to wearing them on a full-time basis, as soon as possible, so they can hear and respond to everyday sounds and speech.. For some children, however, a type of technology called a cochlear implant (see below) will be more suitable.
For some deaf children who do not receive enough benefit from hearing aids, a cochlear implant may be the most suitable way for them to access sounds. Cochlear implants require surgery, which can take place from as early as around 12 months of age. You will need to work closely with your child's audiologist to find out whether or not your child is a candidate for this procedure.
Decisions regarding your child’s educational placement, now and in the future, will depend upon many factors. Deaf children should be placed in school programmes depending upon the needs of the individual child. You, the parents, will play an active role in making decisions regarding your child’s school programming and educational placement and the professionals working with you will give you support to do this. Some children who are deaf attend mainstream schools alongside their hearing peers. These children often require special support services so that they can benefit from their regular classroom settings such as a Learning Support Assistant. Some children who are deaf are placed in programmes with other deaf children because this is more appropriate for them, and which can be attached to a mainstream school in a ‘resource base’. Many children with hearing loss spend some of their day in classes with other deaf children, and some of their day with their hearing peers. The third option is for your child to go to a specialist school for the deaf. The most appropriate choice for your child will depend on their own unique circumstances.
From an early age, children with a hearing loss should receive educational support from their local government authority, alongside specialist audiological input (and any other relevant medical input) from local health providers. If you have not already heard from them, contact your local health authority and local government authority and enquire about their programmes and services to help you and your child. A deaf child might receive regular visits from a Teacher of the Deaf, ongoing appointments with an Audiologist, periodic assessments from an Educational Psychologist and input from a Speech and Language Therapist. The amount and range of the support you receive is likely to vary depending on where you live in the UK and the policies of your local education and health providers. You might also be able to join parent-run or charity support groups in your local area - the National Deaf Children's Society will be able to advise you.
If you and your child meet the eligibility requirements, you can apply for benefit payments to support the extra costs of looking after a young child who needs more looking after than a child of the same age who does not have a disability. The main one is called Disability Living Allowance (DLA) [click to find out more] which is paid to eligible families at a range of rates depending on the level of the child's needs and whether they have additional mobility needs alongside their care needs. If your child gets the middle or highest care rate of DLA and you spend at least 35 hours a week caring for them, you might also qualify for Carer's Allowance [click to find out more].
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