Aphasia Bill of Rights

The author, who has lived with aphasia for more than 30 years, offers a personal perspective on the “Aphasia Bill of Rights,” adopted by the National Aphasia Association Board of Directors.

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Bibliographic Details
Published in:Rehabilitation nursing Vol. 36; no. 4; pp. 136 - 137
Main Author: Liechty, John
Format: Journal Article
Language:English
Published: Oxford, UK Blackwell Publishing Ltd 01-07-2011
Lippincott Williams & Wilkins Ovid Technologies
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Summary:The author, who has lived with aphasia for more than 30 years, offers a personal perspective on the “Aphasia Bill of Rights,” adopted by the National Aphasia Association Board of Directors.
Bibliography:ark:/67375/WNG-0NHJFR2S-8
ArticleID:RNJ80
istex:623F1ACB2E399B5B96C4184C358BF89C047F5A6B
John Liechty, MSW, works as a housekeeper at Oaklawn Psychiatric Hospital. He has been active as an advisory board member and volunteer with National Aphasia Association and helped form the Goshen, IN, Community Aphasia Support Group. Since 2000, he has presented to regional and national health‐related organizations about aphasia. More recently, working with several collaborators, he has published articles about aphasia in a variety of journals and periodicals. John received the 2009 Aphasia Advocacy Award from National Aphasia Association in recognition of his speaking and writing on behalf of people with aphasia. He was assisted by Donald Garber, a freelance writer and editor.
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ISSN:0278-4807
2048-7940
DOI:10.1002/j.2048-7940.2011.tb00080.x