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‘There Are Other Educational Choices Too’

Parents’ responses are still being received by the team here, after the recent Derek Mooney radio interview with parent Eithne Carroll and Liam O’Dwyer of the CIDP.

 >> Listen to the podcast (RTE1, 2011).

This email response is from Orla Sexton, a parent in Cork.

Dear Derek,

I refer to your recent interview with Eithne Carroll and Liam O’Dwyer concerning services for deaf children in Ireland. It is my opinion that a very one-sided and biased viewpoint was presented and I feel compelled to express another and possibly more representative view of, in particular, educational supports available to deaf children in Ireland. I am the mother of 2 profoundly deaf children now aged 11 and 8, both deaf from birth. We made the decision that we wanted our children to speak if this was within their ability. We chose to have them wear hearing-aids and had our daughter fitted with a cochlear implant. Both of my children communicate orally and attend our local mainstream national school …

Read the full article (in PDF format) >>

Many other parents also wrote to Sound Advice after this broadcast, to share their own viewpoints. Some of their stories are shared below, in the comments section of this post.

Further Reading

  • Transcript of the Derek Mooney radio show (Feb 8th, 2011)
  • Home-Preschool Supports: A Mum’s Positive Story
  • The Visiting Teacher Service ‘Is Often Forgotten’
Feb 24, 2011Team Sound Advice

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Young Social Innovators Group Working With IDKIDK’s March 4th Information Session – Update
Comments: 2
  1. Brian
    12 years ago

    In relation to the interview on Derek Mooney’s radio show about the education of deaf children, we are the proud parents of a 5yo boy J, who was born June 05 profoundly deaf. Like a lot of parents of deaf children, we had no experiance of deafness in either of our families.

    J had an A.B.R. test in June 06 and we were told he was profoundly deaf in both ears.Our world fell apart that day.

    At this time we were referred to Beaumont’s cochlear department. And also we found out about the visiting teacher service at this stage.

    The V.T. came to our house every week and from then on felt we weren’t alone. Not only did she teach our son week in week out, she was our one stop to what services were out there for J. Any questions we had in regard to deaf services or deaf education, she would answer for us and if she had’nt got the answer she would find it for us.

    J got his implant in june 07 and while this was a success J has been diagnosed with verbal dyspraxia, which is delaying his ability to speak.

    When the time came to start J in school, our V.T. gave us all the options, including St Josephs in Cabra, mainstream school and a langauge unit attached to a nearby school.

    She took the time to accompany us when we visited each option, and supported us in our final decision. She continues to support J, his school teacher, SNA and us with regular meetings to discuss J’s progress and educational needs.

    We would like to stress that our V.T. was and is invaluable to our family. She has been a constant source of support to us all as a family, not just J. And we genuinely would be lost without her.

    Brian & Audrey

    ReplyCancel
  2. ide
    12 years ago

    Hi Brian & Audrey,

    It was really uplifting reading about J’s story. It is so important to highlight the fantastic work the VT does. These people are often not mentioned but in my view they are our backbone and I for one would be totally lost without our VT. Our son is doing extremely well with the help of our VT and my husband and I would like to thank her from the bottom of our hearts.

    ReplyCancel

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