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New
Voices: Self-Advocacy by People with Disabilities.(1996).
Edited by Gunnar Dybwad & Hank Bersani Jr. To date the most thorough
account of the self advocacy movement, "New Voices" covers the US and international
self advocacy history, experiences of movement leaders and their support
persons, and its legacy.
We Can Speak for Ourselves: Self-Advocacy by Mentally Handicapped People. (1982). by Paul Williams & Bonnie Shoultz. The first historical account of the self advocacy movement, this book looks at its origins; tells the stories of its development in Britain and Nebraska (Project Two), USA with input of the first members there; describes its principles, a self advocacy curriculum, and resources; and, finally, includes numerous personal stories of many people with disabilities who were leaders and the first members of the movement.
The Self-Advocacy Movement by People with Developmental Disabilities: A Demographic Study and Directory of Self-Advocacy Groups in the United States. (1993). by Nancy Anne Longhurst. This is Longhurt's official report of a survey study she carried out to look at the US self advocacy movement, in terms of its growth, membership, meeting locations, and activities. Also included is a list of self advocacy organizations contacted.
Beliefs,Values and Principles of Self-Advocacy. (1997). by Barb Goode with contributions of Ake Johansson. Here, Goode -- first president of one of the first People First (PF) groups in Canada, co-founder of PF of Canada, and first recipient of the Rosemary Dybwad Award, and Johansson -- former president of the Swedish national organization, reflect on self advocacy.
Count
Us in: Growing Up with Down Syndrome. (1994). by Jason
Kingsley, Mitchell Levitz, & Andy Bricky. Based on over 50 conversations
with Kingsley and Levitz, two young men proud to have Down syndrome, talk
about their successful lives as people with disabilities. Seeing
life with a disability as being about "a half-full glass," not one that
is "half-empty," they discuss their views on friendship, sex, marriage,
politics, independence, their beliefs, among other topics.
Beyond
Ramps: Disability at the End of the Social Contract.
(1998). by Marta Russell. "Vividly written... goes to the heart of
many matters, starting with the profound desire of 'normal' people, many
of them supposedly broad-minded types squarely within the liberal tradition,
to reach for the sterilizing knife, or the medicine cabinet of Doctor
Kevorkian when confronted with an affront to their sense of the 'normal.'"
(cited from Amazon.com). Using examples such as these the author
critically analyses the so-called reform of the social safety net under
which for so many years people with disabilities have been forced to live.
Disability
Politics: Understanding Our Past, Changing Our Future. (1996).
by Jane Campbell & Mike Oliver. "Is disability a civil rights
issue?" While accounting the history of the disability rights movement
for people with physical disabilities in the UK, the authors also delve
into the question of this movement being a civil rights movement, and if
so what sort of social movement? Examples of questions they ask include:
is this a new social movement? what is disability consciousness, and is
it "a new vision or existing order?"
ABC
Clio Companion to the Disability Rights Movement.
(1997). by Fred Pelka. Although focusing on the US, to date this
is the most thorough encyclopedia of the Disability Rights Movement.
Included are descriptions/entries on anything and everything related to
the movement from ADAPT, to inclusive education, to the origin of the term
"developmental disability."
No
Pity: People with Disabilities Forging a New Civil Rights Movement.
(1994). by Joseph P. Shapiro. Written by the respected Washington
Post journalist Shapiro, this book accounts the history of the Disability
Rights Movement -- by themes rather than just dates -- until the 1990 signing
of the Americans with Disabilities Act in a most readable style.
Chapter titles include "You Just Don't Understand," "Tiny Tim's, Supercrips,
and the End of Pity," and "The Screaming Neon Wheelchair." A short
chapter on People First, based on interviews with TJ Monroe, is also included.
Nothing
About Us Without Us: Disability Oppression and Empowerment.(1998).
by
James I. Charlton. Based on his study of, and interviews with, disability
rights movement history and leaders from around the world, Charlton looks
from an international perspective at the attitudes of able-bodied people
and how these have, and do still, contribute to the oppression of people
with disabilities.
The
Ragged Edge: The Disability Experience from the Pages of the First Fifteen
Years of The Disability Rag. (1994). Edited by Barrett
Shaw. A celebration of the 15 years publication anniversary of Ragged
Edge, one the two key disability rights grass-roots magazines, this
collection contains pieces that have appeared over the years. Authors
include Mary Jane Owen, Cheryl Marie Wade, Anne Finger, Carol Gill, and
Billy Golfus.
Extraordinary
Bodies: Figuring Physical Disability in American Culture and Literature.
(1996). by Rosemarie Garland Thomson.
The
Body and Physical Difference: Discourses of Disability in the Humanities
(The Body, in Theory - Histories of Cultural Materialism). (1997).
Edited by David T. Mitchell and Sharon Snyder. This edited book starts
with a discussion of Disability Studies, as a discipline, and how we study
representation of disability (mainly physical disability). The first
half of the book includes studies of past representations, such as, "Constructions
of Physical Disability in the Ancient Greek World" (Edwards) and "In Search
of Al Schmid: War Hero, Blinded Veteran, Everyman" (Gerber). The
second half deals with modern-day representations, such as, "Disabled Women
as Powerful Women in Petry, Morrison, and Lorde: Revising Black Female
Subjectivity" (Garland Thomson), and Muteness and Mutilation: The
Aesthetics of Disability in Jane Campion's The Piano" (Molina).
The
Disability Studies Reader. (1999). Edited by Lennard J. Davis.
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