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The four walls of my freedom: Lessons I've Learned From A Life Of Caregiving
By Donna Thomson. 2014
Donna Thomson’s life was forever changed when her son Nicholas was born with cerebral palsy. A former actor, director, and…
teacher, Donna became his primary caregiver and embarked on a second career as a disability activist, author, and consultant. Thomson vividly describes her experience in treading delicately through daily care, emergencies, and medical bureaucracy as she and her family cope with her son’s condition while maintaining value and dignity (for Nicholas, too). She demonstrates the vital contribution that people with disabilities make to our society and addresses the ethics and economics of giving and receiving care. 2014.The disability rights movement: from charity to confrontation
By Frieda Zames, Doris Zames Fleischer. 2011
The cinema of isolation: a history of physical disability in the movies
By Martin F Norden. 1994
Film has often shown people with physical disabilities as deserving isolation from the rest of society. Norden examines hundreds of…
Hollywood and international movies and uncovers the industry's practices for maintaining this status quo, while offering an array of physically disabled characters who embody or break out of stereotypes. He observes the arrival of a new set of stereotypes tied to the growth of science and technology in the 1970s and 1980s, and underscores later movies that display a newfound sensitivity. Some descriptions of sex, strong language. 1994.The boy in the moon: a father's search for his disabled son
By Ian Brown. 2009
Walker Brown was born with a genetic mutation so rare that perhaps 300 people around the world also live with…
it. Walker turned twelve in 2008, but he weighs only 54 pounds, is still in diapers, can't speak and needs to wear special cuffs on his arms so that he can't continually hit himself. Expanded from Brown's Globe and Mail series about Walker, he sets out to discover his son. Some strong language. Canada Reads 2012. 2009.Rebuilt: how becoming part computer made me more human
By Michael Chorost. 2005
Science writer recounts his decision to get a cochlear implant, or a computer surgically imbedded in the skull, to artificially…
restore hearing after he became totally deaf in 2001. Describes his physical and mental changes and reflects on the implications of technological advances on the deaf community and on humanity. 2005.Explores the way disability activists in the United Kingdom and Canada have transformed their aspirations into legal claims in their…
quest for equality. It unpacks shifting conceptualizations of the political identity of disability and the role of a rights discourse in these dynamics. In doing so, it delves into the diffusion of disability rights among grassroots organizations and the traditional disability charities. 2011.Hit by an iceberg: coping with disability in mid-career
By Janet Freedman, Marie Howes. 2003
More people suffer a disability before age 65 than die before age 65. Shows how to manage a mid-career disabling…
experience from a personal, financial, and legal standpoint. A guide through government and private insurance and rehabilitation programmes, housing and living assistance, and legal and money management considerations. 2003.Critical disability theory: essays in philosophy, politics, policy, and law (Law and society)
By Ed Pothier Dianne, Richard F Devlin, Dianne Pothier. 2005
Twenty-four scholars from a variety of disciplines come together here to identify the problems with traditional approaches to disability and…
to provide new directions. The essays range from focused empirical and experiential studies of different disabilities, to policy analyses, legal interrogations, and philosophical reconsiderations. 2005.About Canada: disability rights (About Canada series)
By Deborah Stienstra. 2012
Through an examination of employment, education, transportation, telecommunications, and health care, this survey finds that, while important advances have been…
made, Canadians with disabilities still experience significant barriers in obtaining their human rights. Argues that disability is not about “faulty” bodies that need to be fixed but about the institutional, cultural, and attitudinal reactions to certain kinds of bodies, contending that neoliberal ideas of independence and individualism are at the heart of the continuing discrimination against “disabled” people. Achieving disability rights is possible through universal design, disability supports, social and economic assistance, and a sense of belonging. 2012. (About Canada series)After disability: a guide to getting on with life
By Lisa Bendall. 2006
More than 3.6 million Canadians are living with some sort of disability, with mobility-related issues affecting nearly one in ten…
people. This Canadian resource guide is geared to the rising number of adults who have experienced injury, stroke, disease, arthritis, or the effects of aging. Includes information on assistive devices and technology, accessible housing, financial concerns, health care, self-advocacy and the law, and family life and parenting. Some descriptions of sex. 2006.The world at her fingertips: the story of Helen Keller (Other or No Series)
By Joan Dash. 2001
A biography of the woman who overcame her disabilities to be an inspirational public figure. Discusses the cause of Helen…
Keller's blindness and deafness, her determination to lead a useful life, and the importance of her teacher, Annie Sullivan, throughout Helen's life. Grades 5-8. 2001.To the left of inspiration: adventures in living with disabilities
By Katherine Schneider. 2006
Millions of North Americans have chronic illnesses or disabilities requiring them to make accommodations in their lives. The author, a…
psychologist who has been blind since birth, hopes to help this adjustment with her own humorous life stories, as well as provide understanding of what life is really like for those with disabilities. 2006.To love this life: quotations
By Helen Keller. 2000
Quotations from speeches, letters, articles, and interviews by the author, lecturer, and humanitarian who became deaf-blind at nineteen months of…
age. Topics include the senses, faith, women in society, human nature, war and peace, education, happiness, friendship and love, and triumph over adversity. Includes a chronology of Keller's life from 1880 to 1968. 2000.Teacher: Anne Sullivan Macy : a tribute by the foster-child of her mind
By Helen Keller. 1985
Deaf-blind Helen Keller tells of her early years with Anne Sullivan, the Irish immigrant girl who became her teacher-companion. She…
also describes her years at Radcliffe, Anne's marriage to John Macy, and their work together for the blind. 1985.Creating a culture of accessibility in the sciences
By Mahadeo A Sukhai, Chelsea E Mohler. 2017
Provides insights and advice on integrating students with disabilities into the STEM fields. Features research and best practices that are…
interwoven with experiential narratives. The book is reflective of the diversity of STEM disciplines (life and physical sciences, engineering, and mathematics), and is also reflective of cross-disability perspectives (physical, sensory, learning, mental health, chronic medical and developmental disabilities). A useful resource for STEM faculty and university administrators working with students with disabilities, as well as STEM industry professionals interested in accommodating employees with disabilities. 2017.Until we have no tomorrows: "Dottie"
By Patricia Brudenell. 1999
Be a friend: children who live with HIV speak
By Lori Wiener, Aprille Best, A Pizzo. 1994
In these writings, children with HIV infection and AIDS tell how it feels to be different from other kids, how…
they face rejection if people learn they are sick and what it is like to lose friends and loved ones to AIDS.Care work: dreaming disability justice /
By Leah Lakshmi Piepzna-Samarasinha. 2018
Lambda Literary Award-winning writer and longtime disability justice activist and performance artist Leah Lakshmi Piepzna-Samarasinha explores the politics and realities…
of disability justice, a movement that centres the lives and leadership of sick and disabled queer, trans, Black, and brown people, with knowledge and gifts for all. Leah writes passionately and personally about creating spaces by and for sick and disabled queer people of colour, and creative "collective access"--access not as a chore but as a collective responsibility and pleasure--in our communities and political movements. Bringing their survival skills and knowledge from years of cultural and activist work, Piepzna-Samarasinha explores everything from the economics of queer femme emotional labour, to suicide in queer and trans communities, to the nitty-gritty of touring as a sick and disabled queer artist of colour. 2018.A World without Martha: A Memoir of Sisters, Disability, and Difference
By Victoria Freeman. 2019
Victoria Freeman was only four when her parents followed medical advice and sent her sister away to a distant, overcrowded…
institution. Martha was not yet two, but in 1960s Ontario there was little community acceptance or support for raising children with intellectual disabilities at home. In this frank and moving memoir, Victoria describes growing up in a world that excluded and dehumanized her sister, and how society’s insistence that only a “normal” life was worth living affected her sister, her family, and herself, until changing attitudes to disability and difference offered both sisters new possibilities for healing and self-discovery.Sitting Pretty: The View from My Ordinary Resilient Disabled Body
By Rebekah Taussig. 2020
A memoir-in-essays from disability advocate and creator of the Instagram account @sitting_pretty Rebekah Taussig, processing a lifetime of memories to…
paint a beautiful, nuanced portrait of a body that looks and moves differently than most.Growing up as a paralyzed girl during the 90s and early 2000s, Rebekah Taussig only saw disability depicted as something monstrous (The Hunchback of Notre Dame), inspirational (Helen Keller), or angelic (Forrest Gump). None of this felt right; and as she got older, she longed for more stories that allowed disability to be complex and ordinary, uncomfortable and fine, painful and fulfilling.Writing about the rhythms and textures of what it means to live in a body that doesn’t fit, Rebekah reflects on everything from the complications of kindness and charity, living both independently and dependently, experiencing intimacy, and how the pervasiveness of ableism in our everyday media directly translates to everyday life. Disability affects all of us, directly or indirectly, at one point or another. By exploring this truth in poignant and lyrical essays, Taussig illustrates the need for more stories and more voices to understand the diversity of humanity. Sitting Pretty challenges us as a society to be patient and vigilant, practical and imaginative, kind and relentless, as we set to work to write an entirely different story.