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Showing 1 - 20 of 4366 items
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Disabilities, Social issues
Human-narrated audio, Human-transcribed braille
People with disabilities (PWDs) have the same aspirations for their lives as you do for yours. The difference is that…
PWDs don’t have the same access to education, employment, housing, transportation and healthcare in order to achieve their goals. In The Disability Experience you’ll meet people with different kinds of disabilities, and you'll begin to understand the ways PWDs have been ignored, reviled and marginalized throughout history. The book also celebrates the triumphs and achievements of PWDs and shares the powerful stories of those who have fought for change.
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Disabilities, Sports biography, Sports and games, Canadian travel and geography
Synthetic audio, Human-transcribed braille
An uplifting and engaging celebration of Paralympic champions and the sports they dominate
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Disabilities, Sports biography, Sports and games
Human-narrated audio, Human-transcribed braille
It's time to cheer for the inspiring athletes of the Paralympic Games! As the Opening Ceremony for the 1948 Summer…
Olympic Games commenced in London, a similar sporting competition was taking place a few miles away. But the men at Stoke Mandeville weren't your typical athletes. They were paralyzed World War II veterans. The games at Stoke Mandeville were so successful that they would eventually lead evolve into the Paralympics. Participants from all around the world vie for the gold medal in a variety of sports, including archery, basketball, swimming, speed skating, and ice hockey. Author Gail Herman highlights their achievements, describes how these athletes train--both mentally and physically--for the games, and gives the reader a better understanding of what makes the Paralympic Games one of the world's most viewed sporting events.
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Disabilities, General non-fiction, Addiction and substance abuse
Human-narrated audio, Human-transcribed braille
? “Informative, diverse, and highly engaging; a much-needed addition to the realm of mental health.”—Kirkus Reviews, starred review Featuring real-life…
stories of people who have found hope and meaning in the midst of life’s struggles, Heads Up: Changing Minds on Mental Health is the go-to guide for teenagers who want to know about mental health, mental illness, trauma and recovery. For too long, mental health problems have been kept in the shadows, leaving people to suffer in silence, or worse, to be feared, bullied or pushed to the margins of society where survival is difficult. This book shines a light on the troubled history of thinking about and treating mental illness and tells the stories of courageous pioneers in the field of psychiatry who fought for more compassionate, respectful and effective treatments. It provides a helpful guide to the major mental health diagnoses along with ideas and resources to support those who are suffering. But it also moves beyond a biomedical focus and considers the latest science that shows how trauma and social inequality impact mental health. The book explores how mental health is more than just “in our heads” and includes the voices of Indigenous people who share a more holistic way of thinking about wellness, balancing mind, body, heart and spirit. Highlighting innovative approaches such as trauma-informed activities like yoga and hip-hop, police mental health teams, and peer support for youth, Heads Up shares the stories of people who are sparking change.
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Disabilities, Journals and memoirs
Human-narrated audio, Human-transcribed braille
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.
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Disabilities, Anthologies, Biography of persons with disabilities
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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.
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Journals and memoirs, Disabilities, Travel and geography
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One morning at breakfast, while gawking at his phone and feeling increasingly disconnected from family and everything else of importance…
in his world, it strikes writer Bruce Kirkby: this isn’t how he wants to live. Within days, plans begin to take shape. Bruce, his wife Christine, and their two children—seven-year-old Bodi and three-year-old Taj—will cross the Pacific by container ship, then travel onward through South Korea, China, India and Nepal aboard bus, riverboat and train, eventually traversing the Himalaya by foot. Their destination: a thousand-year-old Buddhist monastery in the remote Zanskar valley, one of the last places where Tibetan Buddhism is still practised freely in its original setting. Taken into the mud-brick home of a senior lama, Tsering Wangyal, the family spends the summer absorbed by monastery life. In this refuge, where ancient traditions intersect with the modern world, Bruce discovers ways to slow down, to observe and listen, and ultimately, to better understand his son on the autism spectrum—to surrender all expectations and connect with Bodi exactly as he is. Recounted with wit and humility, Blue Sky Kingdom is an engaging travel memoir as well as a thoughtful exploration of modern distraction, the loss of ancient wisdom, and the challenges and rewards of intercultural friendships.
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Disabilities
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This ground-breaking volume considers what it means to make claims of disability membership in view of the robust Disability Rights…
movement, the rich areas of academic inquiry into disability, increased philosophical attention to the nature and significance of disability, a vibrant disability culture and disability arts movement, and advances in biomedical science and technology. By focusing on the statement, "We are all disabled", the book explores the following questions: What are the philosophical, political, and practical implications of making this claim? What conceptions of disability underlie it? When, if ever, is this claim justified, and when or why might it be problematic or harmful? What are the implications of claiming "we are all disabled" amidst this global COVID-19 pandemic? These critical reflections on the boundaries of disability include perspectives from the humanities, social sciences, law, and the arts. In exploring the boundaries of disability, and the ways in which these lines are drawn theoretically, legally, medically, socially, and culturally, the authors in this volume challenge particular conceptions of disability, expand the meaning and significance of the term, and consider the implications of claiming disability as an identity. It will be of interest to a broad audience, including disability scholars, advocates and activists, philosophers and historians of disability, moral theorists, clinicians, legal scholars, and artists.
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Biography, Social issues, Biography of persons with disabilities, Politics and government, Disabilities, Health and medicine
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The story of a mid-century working-class housewife whose extraordinary physical transformation empowered her to become a dynamic social activist who…
fueled a movement to create a more inclusive future for people with disabilities.
Braille (Contracted), Electronic braille (Contracted), DAISY Audio (Direct to Player), DAISY Audio (Zip), DAISY text (Direct to player), DAISY text (Zip), Word (Zip), ePub (Zip)
Disabilities
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The first major anthology by parents with disabilities. How does a father who is blind take his child to the…
park? How is a mother with dwarfism treated when she walks her child down the street? How do Deaf parents know when their baby cries in the night? When writer and musician Eliza Hull was pregnant with her first child, like most parents-to-be she was a mix of excited and nervous. But as a person with a disability, there were added complexities. She wondered: Will the pregnancy be too hard? Will people judge me? Will I cope with the demands of parenting? More than 15 percent of people worldwide live with a disability, and many of them are also parents. And yet their stories are rarely shared, their experiences almost never reflected in parenting literature. In We’ve Got This, parents around the world who identify as Deaf, disabled, or chronically ill discuss the highs and lows of their parenting journeys and reveal that the greatest obstacles lie in other people’s attitudes. The result is a moving, revelatory, and empowering anthology that tackles ableism head-on. As Rebekah Taussig writes, ‘Parenthood can tangle with grief and loss. Disability can include joy and abundance. And goddammit — disabled parents exist.’
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Health and medicine, Politics and government, Biography, Disabilities, Social issues, Biography of persons with disabilities
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The story of a mid-century working-class housewife whose extraordinary physical transformation empowered her to become a dynamic social activist who…
fueled a movement to create a more inclusive future for people with disabilities.
Braille (Contracted), Electronic braille (Contracted), DAISY audio (Direct to player), DAISY audio (Zip), DAISY text (Direct to player), DAISY text (Zip), Word (Zip), ePub (Zip)
Disabilities, General non-fiction, Arts and entertainment
Human-narrated audio, Human-transcribed braille
The remarkable story of Sins Invalid, a performance project that centres queer disability justice. In recent years, disability activism has…
come into its own as a vital and necessary means to acknowledge the power and resilience of the disabled community, and to call out ableist culture wherever it appears. Crip Kinship explores the art activism of Sins Invalid, a San Francisco Bay Area-based performance project, and its radical imaginings of what disabled, queer, trans, and gender-nonconforming bodyminds of colour can do: how they can rewrite oppression, and how they can gift us with transformational lessons for our collective survival. Grounded in the disability justice framework, Crip Kinship investigates the revolutionary survival teachings that disabled, queer of colour community offers to all our bodyminds. From their focus on crip beauty and sexuality to manifesting digital kinship networks and crip-centric liberated zones, Sins Invalid empowers and moves us toward generating our collective liberation from our bodyminds outward. Includes a foreword by Patty Berne, co-founder, and executive and artistic director of Sins Invalid.
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Disabilities, General non-fiction, LGBTQ+ biography
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In The Future Is Disabled, Leah Laksmi Piepzna-Samarasinha asks some provocative questions: What if, in the near future, the majority…
of people will be disabled - and what if that's not a bad thing? And what if disability justice and disabled wisdom are crucial to creating a future in which it's possible to survive fascism, climate change, and pandemics and to bring about liberation? Building on the work of their game-changing book Care Work: Dreaming Disability Justice, Piepzna-Samarasinha writes about disability justice at the end of the world, documenting the many ways disabled people kept and are keeping each other - and the rest of the world - alive during Trump, fascism and the COVID-19 pandemic. Other subjects include crip interdependence, care and mutual aid in real life, disabled community building, and disabled art practice as survival and joy. Written over the course of two years of disabled isolation during the pandemic, this is a book of love letters to other disabled QTBIPOC (and those concerned about disability justice, the care crisis, and surviving the apocalypse); honour songs for kin who are gone; recipes for survival; questions and real talk about care, organizing, disabled families, and kin networks and communities; and wild brown disabled femme joy in the face of death. With passion and power, The Future Is Disabled remembers our dead and insists on our future.
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Biography of persons with disabilities, Disabilities, Blindness and visual impairment
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"I lost everything that mattered in my life because I went Deaf and Blind. It was then, in the depths…
of challenges, that I found salvations. It took my disabilities to help me realize what an incredible life I could lead. Sport. Philanthropy. Storytelling. This book is about reaffirming that anyone and everyone needs to know anything is possible and no matter how tough things get, there is always going to be another tomorrow." -- cover.
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Biography, Disabilities, Biography of persons with disabilities, Social issues, Journals and memoirs, Family and relationships, Canadian authors (Non-fiction)
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"A tender, beautifully written essay collection that is about so much more than parenting a child with a disability." —…
Erin Pepler, author of Send Me Into The Woods Alone A raw and intimate portrait of family, love, life, relationships, and disability parenting through the eyes of a mother to a daughter with Down syndrome. With the arrival of her daughter with Down syndrome, Adelle Purdham began unpacking a lifetime of her own ableism. In a society where people with disabilities remain largely invisible, what does it mean to parent such a child? And simultaneously, what does it mean as a mother, a writer, and a woman to truly be seen? The candid essays in I Don't Do Disability and Other Lies I've Told Myself glimmer with humanity and passion, and explore ideas of motherhood, disability, and worth. Purdham delves into grief, rage, injustice, privilege, female friendship, marriage, and desire in a voice that is loudly empathetic, unapologetic, and true. While examining the dichotomies inside of herself, she leads us to consider the flaws in society, showing us the beauty, resilience, chaos, and wild within us all
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Disabilities, Canadian non-fiction, Laws and statutes
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Ce guide vise à synthétiser les lois qui régissent l’accès et l’utilisation du matériel protégé par le droit d’auteur pour…
les personnes ayant une déficience perceptuelle au Canada. Le guide précise comment ces lois sont mises en oeuvre, présente une liste de contrôle des principales exigences de ces lois, fournit de bonnes pratiques et des conseils pratiques pour les situations de tous les jours, donne des indications sur l’élimination des pratiques antérieures et contient un glossaire des termes qui peuvent être peu familiers pour certains lecteurs et lectrices. Il est destiné aux producteurs et productrices de formats de substitution, aux bibliothèques, aux archives, aux musées, aux galeries, aux écoles, aux collèges, aux universités et aux institutions similaires et/ou aux organisations sans but lucratif agissant au profit des personnes ayant des déficiences perceptuelles, ainsi qu’aux utilisateurs et utilisatrices eux et elles-mêmes, conformément aux articles 32, 32.01, 32.02 et 41.16 de la Loi sur le droit d’auteur1. Il peut également être une source d’information pour les titulaires de droits (éditeurs et éditrices et autres titulaires de droits d’auteur) sur l’interprétation de la loi concernant la création d’oeuvres sur formats de substitution pour les personnes vivant avec une déficience perceptuelle, afin que les titulaires de droits puissent comprendre comment les producteurs et productrices de formats substituts opèrent et comment les aider au mieux dans ce processus. Les éditeurs et éditrices sont engagés dans un effort et continu de création de contenu accessible dès leur publication qui peut réduire le temps et les efforts requis pour la production de formats de substitution, et, dans l’intervalle, ce guide est destiné à orienter les producteurs et productrices de formats de substitution lorsque des oeuvres accessibles dès leur publication n’existent pas sur le marché
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Disabilities, Canadian non-fiction, Laws and statutes
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This guide aims to provide a summary of the laws that govern access to and use of material under copyright…
for people with a perceptual disability in Canada. The guide includes how these laws are applied, a checklist of the major requirements of these laws, best practices and practical advice for everyday situations, guidance on eliminating past practices that inadvertently add barriers to access and a glossary of relevant terms that may be unfamiliar to some readers. It is intended for use by alternate format producers, libraries, archives, museums, galleries, schools, colleges, universities and similar institutions and/or non-profit organizations acting for the benefit of people with perceptual disabilities, and for the users themselves, as specified by sections 32, 32.01, 32.02 and 41.16 of the Copyright Act. It also may be a source of information for rightsholders (publishers and other copyright holders) on the legislative interpretation for creating alternate format works for persons with perceptual disabilities so rightsholders can understand how alternate format producers are operating and how best to assist with the process. Publishers are engaged in ongoing work in creating born-accessible commercial content, which can reduce the time and effort required to produce alternate formats. In the interim, this document is intended to guide alternate format producers when born-accessible works do not exist commercially
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Poetry, Canadian non-fiction, Disabilities, Family and relationships
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Through public judgments, detouring dreams and unspoken prayers, Tell Them It Was Mozart, Angeline Schellenberg’s debut collection, traces both a…
slow bonding and the emergence of a defiant humour. This is a book that keens and cherishes, a work full of the earthiness and transcendence of mother-love. One of the pleasures of this collection is its playful range of forms: there are erasure poems, prose poems, lists, found poems, laments, odes, monologues and dialogues in the voices of the children, even an oulipo that deconstructs the DSM definition of autism. From a newborn "glossed and quivering" to a child conquering the fear of strange toilets, Tell Them It Was Mozart is bracing in its honesty, healing in its jubilance. Production note: This title was created through eBOUND's Accessible Conversion Project.
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Social issues, Disabilities
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How can I enjoy my hot disabled body whilst dealing with internalised ableism? How can I best navigate my sex…
life with mobility issues or a carer? Why are queer spaces so inaccessible - and what can I do about it? Andrew Gurza is seriously hot. He's also seriously disabled. Having spent a lifetime navigating the bars, clubs and apps of the queer scene, he's learned a thing or two about sparking queer crip joy amidst the hellscape of ableism, microaggressions and 'pity sex'. With advice on everything from sexual autonomy and self-pleasure to date-prep and disability disclosure - this is both a self-care bible and an urgent call for the queer community to do better
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Paranormal, Disabilities, Psychology, Self help
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Many of us have made our lives so noisy, overwhelming, sensory craving and data driven that we have somehow missed…
the most fundamental part about ourselves and our lives. Learning how to work with every process, every situation, every relationship intuitively; learning to love what is, to let go, to have faith and find stillness; to foster one&’s intuition and become creative in our own lives is something we can all achieve. To illustrate these concepts, Hajlmarsson calls on her decades of experience and work as a psychotherapist. But most significantly, her life as an autism parent, accounted for in her previous books, Finding Lina 2013 and Beyond Autism 2019, which has taught her where to find that elusive freedom and harmony: inside herself. Hjalmarsson believes that the solution to life's chaos, this freedom and harmony—this love—is accessible to all. She writes, "We don&’t earn freedom. We either realize who we are and how we can live free, connected, joyful and expansive lives or we don&’t. We can realize it some of the time and live a little bit connected and a little bit trapped. Or we can learn to realize it most of the time and spend most of our lives fully awake."