Aphasia Association of New Zealand giving a voice to people with aphasia
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It is estimated that over 16,000 New Zealanders have aphasia. Anyone can acquire aphasia, including children. It affects not only the person with aphasia, but also their families and friends, and people in their community

     

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a·pha·sia (ay-faze-yuh) n. Partial or total loss of the ability to articulate ideas or comprehend spoken or written language, resulting from damage to the brain caused by injury or disease.

The Aphasia Association of New Zealand is a national organisation and registered charity, providing support, education, information and advocacy for the estimated 16,000 New Zealanders living with aphasia.

Our aim is to assist people with aphasia, their families, extended whanau, and the wider community to communicate effectively and reduce the barriers faced by people with aphasia.

We offer a range of resources, information, education and training programs which can be tailored to your needs.

Membership is open to individuals, families and businesses so please contact us as we welcome your interest and support.

Mission

To empower people with aphasia to participate in their own communities.

E-Newsletter

The Aphasia Association of New Zealand (AphasiaNZ) Incorporated database contains the details you submit to us via our online registration form.

2011 Aphasia Conference

A successful conference was held at Rydges Hotel and Conference Centre in Rotorua from the 16-18th of November 2011.

Approximately 100 people attended: people with aphasia, their spouse and family members, Speech Language Therapists, and other health professionals and those working with people with aphasia.

Our two international keynote speakers Dr Jenny Dautlich from the UK and Dr Robyn O'Halloran from Melbourne were a highlight for many.

Look out for our summer newsletter which will be out just before Christmas - lots of information about the conference will be included.

Stroke and Aphasia Guide

The Stroke and Aphasia Guide is here.  A first of its kind in New Zealand, this comprehensive book provides important information for people who have aphasia and their families. 

This is a free resource to members.  Contact us today for more information.

 

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