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Posted: 27 April 2005 | Subscribe Online


By the time a hearing child is three it will have a vocabulary of about 700 words. A deaf child of the same age - whose hearing loss has not been detected - will know fewer than 25. And a quarter of the estimated 840 babies born every year with a permanent hearing loss are still undiagnosed by the age of three and a half.
It is vital to diagnose deafness as soon as possible after birth, because delay can have a ruinous impact on a deaf child's ability to learn language and communication skills, says the National Deaf Children's Society (NDCS).

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Millie was hardly speaking at two and a half, but shouted a lot. A community audiologist tested Millie but told her mother, Nicola, that she was "just a naughty child". Then in August 2003, a month after her third birthday, a consultant's tests showed she had sensorineural hearing loss, moderate to severe in both ears, for which she could get hearing aids.

Nicola was shocked by the diagnosis and angry that she had been told so often that her daughter didn't have a problem. Millie, now four, is at a mainstream school with a hearing unit and Nicola says: "Because she was diagnosed so late, she is quite far behind the other children in language... I was hoping she'd have caught up more by now, but she's not."


How many have deafness?

All told, there are an estimated 30,000 children and young people in the UK with permanent deafness, ranging from moderate to profound. Other children have mild deafness and some have deafness that affects only one ear (unilateral deafness), while up to one in five children experience temporary deafness caused by glue ear. Some children are born deaf and others become deaf later on, sometimes following an infectious disease. But few children are totally deaf; most can hear some sounds at certain pitches and volume.

Types of deafness

There are two main types of deafness:

Conductive deafness (the most common type), means the sounds cannot pass through the outer and middle ear to the cochlea and auditory nerve in the inner ear. This is often caused by fluid in the middle ear (glue ear). It can either clear up spontaneously and quickly, or can develop into a long-term condition needing surgery or a hearing aid. Children under five are the largest group affected by glue ear.

Sensorineural deafness usually means that the cochlea (inner ear) is not processing the sound effectively. This can be the result of: an inherited condition; an infectious disease such as rubella, mumps, measles or meningitis; or a shortage of oxygen at birth. Children can have a mixture of the conditions.

How to communicate?

Communication options depend on the individual child's needs, but the three main methods are:

Auditory-oral, using hearing aids, radio aids and cochlear implants to amplify residual hearing to develop spoken language. These can also include lip-reading, but not sign language or finger-spelling.

Sign bilingualism, where the child learns to use two languages at the same time: a sign language (using hand-shapes, facial expressions, gestures and body language) and a spoken or written language. Finger-spelling allocates a sign to each letter of the alphabet and is used for signing names and places.

Total communication (TC) entails choosing the most appropriate communication method for the child at any one time. Sign language is used to support but not replace oral communication and the use of residual hearing in developing speech and language skills.


How to identify deafness

If you have concerns about a child's hearing, encourage the parents to visit their GP and ask for a referral for further tests if deafness is suspected.

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Pointers to deafness include:

  • Delay in learning to speak.
  • Lack of clarity in speech, slurring of words, incorrect pronunciation.
  • Intent focus on the face/lips.
  • Reluctance to speak, eg nodding or shaking head rather than saying 'yes' or 'no'.
  • Temper tantrums.
  • Incorrect verb tenses.
  • Constantly asking for repetition.
  • Continuing with an activity when everyone else has stopped.
  • Making little or no contribution to group discussions.
  • Shouting or talking too loudly.
  • Speaking very softly.
  • Frequently asking for help from peers.


And some practical advice for working with children with deafness

  • Position the child with their back to the window so they can see you.
  • Make sure you have their attention before starting to talk.
  • Speak clearly, naturally and at a normal rate - don't shout.
  • Face them when you are talking to them and keep a distance of between one and two metres for signing or lip-reading purposes.
  • Try not to walk around while you are speaking.
  • Repeat what other people say.
  • Encourage parents to reinforce what you do at home.
  • Statistics and information supplied by the NDCS


'I had to pull myself together' 

James and Damian live with their parents, Vicki and Owen. James, now four, was eight months old when he was diagnosed as severely to profoundly deaf. His mother, Vicki, says it was devastating.  Having worked with children with communication problems, Vicki knew fingerspelling and wanted him to be able to choose how he wanted to communicate. By the age of two he had around 50 spoken words but could sign 250, she says.

James's pre-school arranged for a signer to be his one-to-one communication worker. She taught all the other children and all the other teachers have recently passed their BSL stage 1. "They do a lot of signing at school now, and the kids have taken it home and the parents are all wanting to learn it as well." 

James now has a statement so he will have sign provision at school. When James's brother Damian was born 14 months ago, his parents thought they were prepared, but it was still a shock when they found he, too, was deaf. Says Vicki: "I had to pull myself together and start again." 

Damian was tested at two weeks, diagnosed with moderate deafness and received his hearing aids when he was 10 weeks' old. 

Says Vicki:  "We recently got married, after 16 years together, and as a special treat the boys had glitter earmoulds."She adds: "I hope that I can encourage the boys to always speak up if they don't understand something so they don't miss out on things... Owen and I want them to have the best of both worlds."

  • All names have been changed
  • Featured on the NDCS website: www.ndcs.org.uk

 

 



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