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Notes for parents from ANZCED 2006

Meet the PoDs
Microtia Australia Group Support 
Implants make sound sense to Mitchell  
Notes for parents from ANZCED 2006

The 23rd Conference for Australian and New Zealand Educators of the Deaf was held at Royal Lakeside Novotel in Rotorua, New Zealand from the 11th to the 14th of January 2006. This conference is for teachers of the deaf, families of deaf children and young people, deaf and hearing impaired people and other professionals working in the area of childhood deafness.

Damian Lacey, CEO of Deaf Children Australia and Ann Porter, Board Member of Deaf Children Australia, attended this conference. Ann has summarised various papers presented which may be of interest to families of deaf and hearing impaired children.

These notes are extracts from the presentation slides used at the conference and includes links to articles where Ann has been able to find them. The summaries of the papers may prompt you to ask questions of your audiologist, classroom or visiting/itinerant/advisory teacher of the deaf or other service provider and Deaf Children Australia encourages you to do so. This is not professional advice but pieces of information that Ann felt parents may find useful and interesting.

Read more...

Meet the PoDs

September 2005

A new support and advocacy group for families of deaf children has been set up in Lismore NSW with the assistance of the Deaf Society of NSW - Lismore office.

PoD (Parents of Deaf) aims to provide families with all they need to make informed decisions about their child's welfare. All choices are respected and this offers a fantastic opportunity for the parents of northern NSW to share experiences and ensure the available services meet the needs of your deaf or hearing impaired child and family.

PoD (Lismore) meet on the last Friday of every month at 6.30pm. The next meeting is on Friday September 30 at the Gonellabah Early Intervention Centre. Pack the kids into the care and join other parents and kids for a fun and informative evening.

For more information...

Microtia Australia Group Support

My son was born with no ear, two and a half years ago and since then, I haven't been able to find much relevant information or support, if any, in Australia for this. I felt so alone and uninformed on the subject and have never seen, met,or heard of Microtia before.

Because I couldn't find anything to help me, I thought I would try and provide some sort of support for others, so they don't have to feel and go through what I already have.

I am wanting contact with others with Microtia or parents of children;pre and post surgery; for friendly support or simply just to chat.

Get support and help me support others.

I would love to hear from you.
Rebecca
http://groups.msn.com/MicrotiaAustraliaGroupSupport

Implants make sound sense to Mitchell
Joondalup Community News - August 21,2003

Last updated: April 18, 2008

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