The Diamond Babies project will follow a number of families with deaf children as they grow up. It will ask them to share their stories and experiences to help other families with a deaf child. Around 90% of deaf babies are born to hearing parents with little experience of deafness, although the project will involve deaf and hearing parents from a range of backgrounds across the UK.
Amy Skipp, NDCS Head of Research explains:
“We want to look at the experiences of families with deaf children, from diagnosis and at different ages as they grow up. How do parents deal with the day-to-day issues that come up and what outlook do they have for their deaf child?
“From interviews carried out so far, we know how stressful and upsetting it can be for many parents when their child is first diagnosed. But we are also learning from parents of older children what a fulfilling and rewarding experience having a deaf child can be. We hope the Diamond Babies project will offer families stories to encourage and reassure them that their deaf child can lead a happy and fulfilling life.”
The project is part of the charity’s Diamond Anniversary celebrations themed ‘Language without limits – a future without barriers.' Participating families will be interviewed each year about some of the issues, practicalities and successes they have. It will include how they felt when their child was first identified as being deaf, the challenges and achievements the whole family experiences in daily life, and their hopes for the future. Their stories will be shared with other families through the NDCS website (www.ndcs.org.uk) and later in the project all the stories will be published in a book. The interviews will also provide NDCS with information on what families really need support with, which stages of childhood are most challenging, and will help to inform future service provision.
Already some common themes are emerging – the worry at receiving test results, concern at lack of experience of deafness, and parents’ anxiety and hopes that their child will lead a happy and fulfilling life. Many parents admit they hadn’t even met a deaf person before and really needed more information and reassurance. But the strongest theme is the parents’ wishes for their children’s happiness, and their commitment to doing whatever they can to help their child.
Baby Chloe, aged six months, had her first hearing aids fitted when she was just nine weeks old. Her mum says:
“I’d like her not to see her deafness as something that will stop her from doing whatever she wants to do in life. We don’t want there to be any barriers to her reaching her full potential. We hope she will feel she can do anything she puts her mind to.”
Mirage is 12 years old and was identified as being deaf when she was eight months old. Her dad says:
“I’d love to speak to other parents of deaf children and tell them not to worry about their child not achieving or not getting on in schools. I hope my daughter will go to college and then perhaps university. It’s her choice though. I don’t know about work because I’m aware there is a lack of provision to support deaf people in the workplace. I just hope she is successful and happy in whatever she does.”
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Notes to editor
For further information or an interview with one of the families please contact Sarah Etwell T: 020 7014 1144 sarah.etwell@ndcs.org.uk or Paula Whitworth T: 020 7014 1146 paula@ndcs.org.uk
The National Deaf Children’s Society is the only UK charity solely dedicated to supporting deaf children, deaf young people, their families, carers and professionals working with them.
Parents can contact the charity’s freephone helpline on 0808 800 8880 (voice and text)
http://www.ndcs.org.uk/news_media/ndcs_press_releases/whats_it_like.html
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I find this web site program quite interesting, it may help alot of hearing parents out there to know what to do on how to rasie a deaf child, and what's it like to have a deaf child too...
Amy Skipp, NDCS Head of Research explains:
“We want to look at the experiences of families with deaf children, from diagnosis and at different ages as they grow up. How do parents deal with the day-to-day issues that come up and what outlook do they have for their deaf child?
“From interviews carried out so far, we know how stressful and upsetting it can be for many parents when their child is first diagnosed. But we are also learning from parents of older children what a fulfilling and rewarding experience having a deaf child can be. We hope the Diamond Babies project will offer families stories to encourage and reassure them that their deaf child can lead a happy and fulfilling life.”
The project is part of the charity’s Diamond Anniversary celebrations themed ‘Language without limits – a future without barriers.' Participating families will be interviewed each year about some of the issues, practicalities and successes they have. It will include how they felt when their child was first identified as being deaf, the challenges and achievements the whole family experiences in daily life, and their hopes for the future. Their stories will be shared with other families through the NDCS website (www.ndcs.org.uk) and later in the project all the stories will be published in a book. The interviews will also provide NDCS with information on what families really need support with, which stages of childhood are most challenging, and will help to inform future service provision.
Already some common themes are emerging – the worry at receiving test results, concern at lack of experience of deafness, and parents’ anxiety and hopes that their child will lead a happy and fulfilling life. Many parents admit they hadn’t even met a deaf person before and really needed more information and reassurance. But the strongest theme is the parents’ wishes for their children’s happiness, and their commitment to doing whatever they can to help their child.
Baby Chloe, aged six months, had her first hearing aids fitted when she was just nine weeks old. Her mum says:
“I’d like her not to see her deafness as something that will stop her from doing whatever she wants to do in life. We don’t want there to be any barriers to her reaching her full potential. We hope she will feel she can do anything she puts her mind to.”
Mirage is 12 years old and was identified as being deaf when she was eight months old. Her dad says:
“I’d love to speak to other parents of deaf children and tell them not to worry about their child not achieving or not getting on in schools. I hope my daughter will go to college and then perhaps university. It’s her choice though. I don’t know about work because I’m aware there is a lack of provision to support deaf people in the workplace. I just hope she is successful and happy in whatever she does.”
-ends-
Notes to editor
For further information or an interview with one of the families please contact Sarah Etwell T: 020 7014 1144 sarah.etwell@ndcs.org.uk or Paula Whitworth T: 020 7014 1146 paula@ndcs.org.uk
The National Deaf Children’s Society is the only UK charity solely dedicated to supporting deaf children, deaf young people, their families, carers and professionals working with them.
Parents can contact the charity’s freephone helpline on 0808 800 8880 (voice and text)
http://www.ndcs.org.uk/news_media/ndcs_press_releases/whats_it_like.html
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I find this web site program quite interesting, it may help alot of hearing parents out there to know what to do on how to rasie a deaf child, and what's it like to have a deaf child too...