Disability: social aspects Books

Book SynopsisNew to the world of AuDHD?You're probably familiar with autism or with ADHD by now: an increase of information online has helped more people advocate for assessments. However, much of the discussion around the two conditions centres on their neurological differences. But what about those diagnosed with both? Where do the two conditions intersect and overlap?Explaining AuDHD is a straight-talking guide for those trying to understand Autism and ADHD as a combined diagnosis. Using real-life stories of people living with AuDHD, this book offers advice for those grappling with a diagnosis, and provides a framework for readers to advocate for themselves and discuss it with loved ones.Written in accessible prose by Dr Khurram Sadiq, Explaining AuDHD is a worthwhile read for anyone questioning their own neurodiversity, undergoing assessment, or making sense of their recent diagnosis.

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Book SynopsisEliza Fricker gets it. Describing her perfectly imperfect experience of raising a PDA child, with societal judgements and internal pressures, it is easy to feel overwhelmed, resentful and alone. This book's comedic illustrations explain these challenging situations and feelings in a way that words simply cannot, will bring some much-needed levity back into PDA parenting. Humorous anecdotes with a compassionate tone remind parents that they are not alone, and they're doing a great job. If children are safe, happy, and you leave the house on time, who cares about some smelly socks? A light-hearted and digestible guide to being a PDA parent covering everything from tolerance levels, relationships and meltdowns to collaboration, flexibility, and self care to dip in and out as your schedule allows to help get to grips with this complex condition. This book is an essential read for any parent with a PDA child, to help better understand your child, build support systems and carve out some essential self care time guilt free.Trade ReviewIn The Family Experience of PDA Eliza Fricker shares her heartfelt insights through an accessible illustrated volume that will be helpful to parents as they support, encourage, and manage their children who may have features of PDA. The book through words and pictures provides the important lessons she has learned about the sensitivities and regulatory capacity of her child. Eliza shares the basic principles that enabled her child and family to feel safer and to mutually enjoy daily interactions. We learn the power of softening the edges of restrictive parenting, which may function in more resilient children with higher thresholds to be reactive but is disastrous with a child with feature of PDA. We learn that a gentler less demanding, accepting, and positive playful parental strategy will lead to more cooperative behaviors and mutually rewarding co-regulatory interactions. -- Stephen W. Porges, PhD, Professor Department of Psychiatry, University of North Carolina at Chapel HillThis book is the perfect tonic for frazzled loved ones of children with PDA. Perfectly imperfect, quirky and always en pointe, Eliza will make you nod and smile with her descriptions and illustrations whilst also providing you with a tonne of practical ideas without once seeming preachy. -- Dr Pooky Knightsmith, Child and Adolescent Mental Health ExpertTable of ContentsForeword by Ruth Fidler; Introduction; Tolerance Levels; Meltdowns; Relationships; Sensory; Anxiety; Collaboration; Flexibility; Prioritising; Positives; Self Care

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Book SynopsisAnalyses popular Japanese manga published from the 1990s to the present that portray the everyday lives of adults and children with disabilities in an ableist society. The book focuses on five representative conditions currently classified as disabilities in Japan, and explores the complexities and sociocultural issues surrounding each.

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Book SynopsisCombining medical knowledge with sympathetic common sense, this completely updated comprehensive handbook offers help and advice to all parents and carers of children with Down''s syndrome, and shows them how to help their children flourish and reach their full potential. Written in association with the Down''s Syndrome Association, this book goes beyond the average introduction to Down''s syndrome and addresses the questions, practical or otherwise, that parents will often find themselves asking, and also offers information and advice on a wide variety of related issues, including:--current medical knowledge about the condition--advice on the special care of babies and young children--education and training--emotional and sexual development--integration into societyTrade ReviewA must for parents of children with Down's Syndrome * Baby & You *

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Book SynopsisGreg Marshall''s early years were pretty bizarre. Rewind the VHS tapes (this is the nineties) and you''ll see a lopsided teenager limping across a high school stage, or in a wheelchair after leg surgeries, pondering why he''s crushing on half of the Utah Jazz. Add to this home video footage a mom clacking away at her newspaper column between chemos, a dad with ALS, and a cast of foulmouthed siblings. Fast forward the tape and you''ll find Marshall happily settled into his life as a gay man only to discover he''s been living in another closet his whole life: he has cerebral palsy. Here, in the hot mess of it all, lies Greg Marshall''s wellspring of wit and wisdom.Leg is an extraordinarily funny and insightful memoir from a daring new voice. Packed with outrageous stories of a singular childhood, it is also a unique examination of what it means to transform when there are parts of yourself you can''t change, a moving portrait of a family in crisis, and a tale of resilieTrade ReviewThis hilarious and wholly unique memoir by Greg Marshall tackles many subjects: disability, family relationships, and coming out (twice). With signature wit and humor, Marshall takes material that could be morbid in the hands of a lesser writer, and dares his readers not to laugh. He knows he's had an unconventional life, but there's no self-pity here. Instead, he embraces the absurdity of it all and leans into it, making one hell of an entertaining book. * Buzzfeed, Most Anticipated LGBTQ+ Book of 2023 *Smart and heartfelt ... His honesty and clarity in writing about disability makes this debut one to watch. * LitHub, Most Anticipated Books of 2023 *Greg Marshall's Leg has all the ingredients of an addictive memoir. But what separates this book from the pack is Marshall's rich and rare perspective navigating the world as a queer disabled person. Marshall delves into his unique life experiences to illustrate the all-too-relatable struggle to be your authentic self and he does it with unflinching honesty. He's one of the most exciting new voices in non-fiction. I could get lost in his brilliant brain forever. * RYAN O’CONNELL, author of Just by Looking at Him *

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Book SynopsisImagining anti-ableist liberation beyond the rubrics of access and inclusion In the thirty years since the Americans with Disabilities Act was signed into law, the lives of disabled people have not improved nearly as much as activists and politicians had hoped. In Crip Negativity, J. Logan Smilges shows us what’s gone wrong and what we can do to fix it.Leveling a strong critique of the category of disability and liberal disability politics, Smilges asks and imagines what horizons might exist for the liberation of those oppressed by ableism—beyond access and inclusion. Inspired by models of negativity in queer studies, Black studies, and crip theory, Smilges proposes that bad crip feelings might help all of us to care gently for one another, even as we demand more from the world than we currently believe to be possible.Forerunners: Ideas First is a thought-in-process series of breakthrough digital publications. Written between fresh ideas and finished books, Forerunners draws on scholarly work initiated in notable blogs, social media, conference plenaries, journal articles, and the synergy of academic exchange. This is gray literature publishing: where intense thinking, change, and speculation take place in scholarship.

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Book SynopsisThe first book to be written on the Judge Rotenberg Center and their use of painful interventions to control the behavior of children and adults with disabilities. For more than forty years, professionals in the field of disability studies have engaged in debates over the use of aversive interventions (such as electric shock) like the ones used at the Judge Rotenberg Center. Advocates and lawyers have filed complaints and lawsuits to both use them and ban them, scientists have written hundreds of articles for and against them, and people with disabilities have lost their lives and, some would say, lived their lives because of them. There are families who believe deeply in the need to use aversives to control their children’s behavior. There are others who believe the techniques used are torture. All of these families have children who have been excluded from numerous educational and treatment programs because of their behaviors. For most of the families, placement at the Judge Rotenberg Center is the last resort. This book is a historical case study of the Judge Rotenberg Center, named after the judge who ruled in favor of keeping its doors open to use aversive interventions. It chronicles and analyzes the events and people involved for over forty years that contributed to the inability of the state of Massachusetts to stop the use of electric shock, and other severe forms of punishment on children and adults with disabilities. It is a long story, sad and tragic, complex, filled with intrigue and questions about society and its ability to protect and support its most vulnerable citizens. Trade Review"A history of the notorious Judge Rotenberg Center in Massachusetts, and the fight to ban the use of electric shock treatment and other severe punishments on disabled children and adults. This is a historical case study that remains sadly relevant, as aversion therapies are still encouraged in many places." * The Bookseller *“. . . . An in-depth, riveting, and devastating account of violent treatments known as aversives, used at the Judge Rotenberg Center. Nisbet’s painstakingly detailed history insists that we must not look away—as too many have done—from these horrific stories.” * Isis *“A history of the notorious Judge Rotenberg Center in Massachusetts, and the fight to ban the use of electric shock treatment and other severe punishments on disabled children and adults… An incredibly well-documented book.” * Masslive *"This important book brings to light the shameful history of torturous methods used on individuals with developmental disabilities. If animals or prisoners of war had been subjected to this torture, the perpetrators would have been charged with felony cruelty to animals or war crimes. I am hopeful that by exposing what has occurred at the Judge Rotenberg Center, this work will finally bring this sad chapter of our history to an end." -- Temple Grandin, author of Thinking in Pictures"Nisbet provides important insights into the present-day use of aversive interventions and the ongoing struggle for disability justice. Highly recommended. General readers through faculty; professionals.” * Choice *Table of ContentsList of IllustrationsForewordAcknowledgmentsChapter I. A Long StoryChapter II. How We Got to This PlaceChapter III. Encouraged to Expand to CaliforniaChapter IV. Pushing BackChapter V. The Death of VincentChapter VI. The Food and Drug Administration Permits the Use of Electric Shock on People with DisabilitiesChapter VII. Here Comes National Institutes of Health: A National Outcry After the Office for Children’s and Mary Kay Leonard’s Loss to BRIChapter VIII. Staging the Next BattlegroundChapter IX. Bad Faith or Responsible Government: Another Attempt to Limit the Use of AversivesChapter X. ContemptChapter XI. More Legal Issues and Advocates Take Action: Weiss and NisbetChapter XII. The FDA Bans the Electric Shock Device: A Final Ruling? Weiss and NisbetEpilogueChronologyEndnotesBiographical Note

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Book SynopsisAutism in women and girls is still not widely understood, and is often misrepresented or even overlooked. This graphic novel offers an engaging and accessible insight into the lives and minds of autistic women, using real-life case studies. The charming illustrations lead readers on a visual journey of how women on the spectrum experience everyday life, from metaphors and masking in social situations, to friendships and relationships and the role of special interests.Fun, sensitive and informative, this is a fantastic resource for anyone who wishes to understand how gender affects autism, and how to create safer supportive and more accessible environments for women on the spectrum.Trade ReviewAs a medical comic, an educational comic, it's really well done, imparting knowledge with ease, simple, clear, effective. Using comics for this (and make no mistake, this is, definitely, a comic), is a perfect fit, getting factual information through to many who simply either wouldn't be able to, or more likely, wouldn't wish to, access it through plain text... When it comes to autism, no matter how aware we think we are, there's always more to discover. Which is just what Camouflage does very well, breaking down the subject with a clarity and simplicity, yet without sparing any factual details or the personal experiences of women with autism. I guarantee that you'll finish Camouflage with a better understanding of an important issue. And in that sense, Camouflage is a hugely successful thing... Hopefully, this will be something that will be embraced by schools, libraries, medical practices, and should be an essential read for anyone with autism, or anyone affected by autism.And frankly, given that we're all on the spectrum somewhere, you will, definitely, know someone affected by autism. Isn't it time you knew a little more? -- Richard Bruton * Comicon *Using a combination of intriguing science facts and moving personal accounts, psychologist Bargiela explains why doctors more rarely identify autism in women than in men. Beginning with the history of autism research, Bargiela shows that studies don't focus enough on the differences between men's and women's brains and skills, such as women's greater talent for 'social mimicry,' and therefore miss the ways autism manifests in women. Bargiela ensures that the medical information is understandable, and when potentially confusing terms arise, quick and concise footnotes are provided. She includes interviews with three autistic women, in which she asked each the same four questions about her life experiences. The responses are revealing; one woman says her assumption that her romantic partners are truthful makes her vulnerable to those who want to take advantage of her. Standing's art is subtle, enhancing the information being shared without distracting from the subject matter. The artwork is reminiscent of art deco, with distinct illustrations and a calming color palette. This informative work has insights for those familiar with or new to autism studies, and readers will feel the interviews add an important perspective. -- Publishers WeeklyA fantastic, easy-to-digest book for anyone hoping to understand how we can create a safer, more accommodating environment for women on the spectrum. -- Bonnie Gifford * Happiful *Table of Contents1. Introducing Autism and Gender 2. 'You're not autistic' 3. Pretending to be Normal 4. From Passive to Assertive 5. Identity and Interests 6. Future Research

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Book SynopsisThis is the rise of the anti-capitalist neurodiversity movementTrade Review'This groundbreaking book fills a crucial gap in the discourse about neurodiversity, providing a deep history of the invention of the 'normal' mind as one of the most damaging and oppressive tools of capitalism, while not succumbing to the myths of the 'anti-psychiatry' movement. To read it is to see the world more clearly.' -- Steve Silberman, author of 'NeuroTribes: The Legacy of Autism and the Future of Neurodiversity''A vital book that kindles the flames of a Marxist neurodivergent revolution. Chapman boldly challenges us to envision a world liberated from neuronormative oppression, where dismantling capitalism is central to disabled, Mad, and neurodivergent liberation—a new radical approach to neurodiversity that is explicitly anti-capitalist.' -- Beatrice Adler-Bolton, co-author of 'Health Communism''An instant seminal text, Empire of Normality takes on the huge task of crafting a coherent, radical, Marxist approach to neurodivergence. Chapman impressively and critically assembles disparate philosophical, scientific and activist currents across time to carve out a new politics that pushes beyond liberal rights-based approaches, and guides us towards a liberated future.' -- Micha Frazer-Carroll, author of 'Mad World: The Politics of Mental Health''Empire of Normality argues that a radical politics of neurodiversity needs to be central to the struggle against capitalism. Chapman explains why this is necessary, not only for neurodivergent folk, but for our collective liberation. Thought provoking, challenging and compelling.' -- Professor Hel Spandler, Editor, 'Asylum: the radical mental health magazine''Engaging, impeccably researched, and a vital step in the emergence of a new social paradigm. Chapman uncovers the origins of the stifling norms that limit our collective potentials, and points the way toward a better and more creative future.' -- Nick Walker, author of 'Neuroqueer Heresies'Table of ContentsPreface Introduction 1 Rise of the machines 2 The invention of normality 3 Galton’s paradigm 4 The eugenics movement 5 The myths of anti-psychiatry 6 Fordist normalisation 7 The return of Galtonian psychiatry 8 Post-Fordism as a mass disabling event 9 The neurodiversity movement 10 Cognitive contradictions 11 After normality Notes Bibliography Acknowledgements Index

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Book SynopsisThis is not an inspirational memoir. This is not trauma porn. This is a memoir about the forces that impact our lives, both good and bad.Athena Stevens has never learned the name of the doctor whose lack of intervention at her birth lead to her cerebral palsy, but she feels the consequences of his actions and inaction every day. The factor observed first and foremost in her life will forever be the effects of what other people have done to her, rather than her accomplishments. And yet, she was groomed to believe that she would overcome any force that stood in her way.A memoir like no other, What's Done Cannot be Undone takes readers on a whirlwind journey through Athena's life, providing a profound insight into the realities of moving through the world as a disabled woman. From being born dead' to co-founding the Women's Equality Party; from not being picked to play the back of a cow to an Olivier Award nomination, this complex, lyrical, gut-punch of a memoir is laugh-out-loud funny, unrelentingly furious, and a powerful reminder that changing the world singlehandedly is as impossible as defying the laws of physics.

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Book SynopsisOliver Sacks is a physician and the author of many books, including The Man Who Mistook His Wife for a Hat, Awakenings (which inspired the Oscar-nominated film) and Musicophilia. Born in London and educated at Oxford, he held positions at Albert Einstein College of Medicine, New York University School of Medicine and was Professor of Neurology and Psychiatry at Columbia University. He is the first, and only, Columbia University Artist, and is also a Fellow of the Royal College of Physicians. In 2008, he was appointed Commander of the British Empire. His memoir, On the Move, was published shortly before his death in August 2015.Trade ReviewSeeing Voices is a manifesto, characteristically humane and impassioned; once more, Sacks proves he is the doyen of science with a human face. * Sunday Times *Empathetic, intelligent and compassionate. * Guardian *A passionate meditation on the richness of sign language. * Independent *Scholarly and carefully documented, Seeing Voices makes the gigantic leap so essential to understanding total deafness. * Sunday Telegraph *

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Book SynopsisThe devolution of social care policy has led to key differences emerging between the UK's four care systems. This book presents research on the perspectives of social care policy makers within the UK's four care systems, concluding that when given equal capacity to reform, the systems in each nation may take radically different shapes.Table of Contents1. Comparing Adult Social Care Systems in the UK 2. What Is Social Care Policy For? 3. What Is in Crisis? The Context of Care Policy in the Four Nations 4. The Mechanisms of Social Care Reform 5. The Outcomes of Social Care Reform 6. Territorial Policy Communities: Scale, Style and Scope 7. The Limits of Social Care Reform 8. Conclusion: Between Care Paradigms

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Book Synopsis‘Oliver Sacks is a perfect antidote to the anaesthetic of familiarity. His writing turns brains and minds transparent’ - ObserverWhen Oliver Sacks, a physician by profession, injured his leg while climbing a mountain, he found himself in an unusual position – that of patient. The injury itself was severe, but straightforward to fix; the psychological effects, however, were far less easy to predict, explain, or resolve: Sacks experienced paralysis and an inability to perceive his leg as his own, instead seeing it as some kind of alien and inanimate object, over which he had no control.A Leg to Stand On is both an account of Sacks’ ordeal and subsequent recovery, and an exploration of the ways in which mind and body are inextricably linked.Trade ReviewOliver Sacks is a neurologist, a man of humane eloquence, and a genuine communicator. The value of this book lies in its willingness to combine the technical and the demonic, to admit poetry and philosophy and the religious impulse. It is also intensely personal, and affirms the community of human experience. * Observer *In every way a marvellously rich and thoughtful tale. * Sunday Telegraph *A remarkable, generous, vivid and thoroughly intelligent piece of writing. * Sunday Times *

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Book SynopsisThis edited collection uses a critical theory perspective and draws on expertise from a range of contemporary policy and practice areas. Contributors include people with disabilities, family members, researchers, academics and practitioners. This book is an ideal text for students of social work, human services, child and youth care and disability studies. Chapters include first-person accounts from persons with disabilities, perspectives of families and historical perspectives, as well as a critical exploration of demographics, human rights issues, disability legislation and policy in Canada, theoretical approaches to disability, intersectionality and disability, Aboriginal people and disability, mental health disability, principles of anti-ableist practice, advocacy and strategies for change. This book offers as a fresh Canadian perspective on disAbility from a critical lens, challenging and inspiring students and practitioners alike to think outside the box and to examine their own attitudes and values toward disAbility, ensuring that they do not inadvertently impose ableist and oppressive practices on one of Canada s most marginalized populations."

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Book SynopsisWinner of the 2017 Margaret and John Savage First Book Award – Non-Fiction!Jen Powley was diagnosed with multiple sclerosis at fifteen. By thirty-five, she had lost the use of her arms and legs.Just Jen is a powerful memoir that tells the story of Powley's life at the time of her diagnosis, and the infinite, irrevocable ways it has changed since. Powley's writing pulls no punches. She is lively, bold and unapologetic, answering questions people are often afraid to ask about living with a progressive disease. And yet, these snapshots from Powley's life are not tinged with anger or despair. Just Jen is a powerful, uplifting and unforgettable work by an author who has laid her life - and her body - bare in order to survive.

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Book Synopsis"To think of PDA as merely involving demand avoidance is to me akin to thinking of tigers as merely having stripes."This book is a unique window into adult Pathological Demand Avoidance (PDA), exploring the diversity of distinct PDA traits through the voices of over 70 people living with and affected by the condition.Sally Cat, an adult with PDA, has successfully captured the essence of a popular online support group in book form, making the valuable insights available to a wider audience, and creating a much-needed resource for individuals and professionals. Candid discussions cover issues ranging from overload and meltdowns, to work, relationships and parenting. This is a fascinating and sometimes very moving read.Trade ReviewWith good humour and banter, this book demonstrates "the positive power of self-awareness" and understanding. Everyone should read it to appreciate what life is like for PDAers. Skilful Sally Cat enables PDAers to realise that other people feel the same. Shared experiences and coping strategies open the door to the realisation that they are not alone and feeling "different is ok". -- Anne Waterhouse, lifelong educationalist, self-identified as relating to PDA in her 70s after reading Sally Cat’s memesUnlike usual factual guides, this book brings a 'human touch' with moving tales, experiences and support from Sally Cat and her fellow PDAers. Alongside this are easy to follow and simple to understand graphs, memes and insights into the world of PDA. A wonderfully relatable book, full of humour and hope. -- Victoria Power, mother of two special needs children, self-diagnosed with PDAI think this is a great resource for understanding adult PDA. The NAS's website is all good, but it's only relevant to children. This book lifts the curtain. There are nuances to this condition! It itself is a spectrum I think. The parts of this book I've read have helped me to better understand some of my past behaviours. It was like looking in a mirror! -- Josh Bremner, 23-year-old sound engineering student exploring PDA through the Facebook Adult DA Support NetworkTable of ContentsIntroduction. 1: Demand Avoidance. 2: What sort of things are we driven to avoid?. 3: Anxiety and PDA. 4: PDA and Masking. 5: Intolerance of Uncertainty. 6: Control. 7: Meltdowns. 8: Overload. 9: PDA and People. 10: Hierarchy and Rules. 11: Fantasy and Role Play. 12: Wordplay. 13: Impulsiveness. 14: Routine. 15: School. 16: Work. 17: Coping Strategies. 18: Reasonable Accommodations. 19: Parenting. 20: Our Achievements

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Book SynopsisPathological Demand Avoidance Syndrome (PDA) is a developmental disorder that is being increasingly recognised as part of the autism spectrum. The main characteristic is a continued resistance to the ordinary demands of life through strategies of social manipulation, which originates from an anxiety-driven need to be in control.This straightforward guide is written collaboratively by professionals and parents to give a complete overview of PDA. Starting with an exploration into the syndrome, it goes on to answer the immediate questions triggered when a child is first diagnosed, and uses case examples throughout to illustrate the impact of the condition on different areas of the child's life. Early intervention options and workable strategies for managing PDA positively will make day-to-day life easier for the child, their family and peers. New problems faced in the teenage years and how to assist a successful transition from adolescence to adulthood are also tackled. The book concludes with a valuable resources list.Full of helpful guidance and support, this user-friendly introductory handbook is essential reading for families, carers and anyone who knows a child with PDA.Trade Review[This book] written by professionals and parents, it is highly accessible, illustrated by a wealth of case studies and provides practical strategies and approaches covering both the home and school context for managing children with PDA. In terms of addressing the underlying anxiety-driven need of these children, there is a useful section on developing emotional well-being and self-awareness in children with PDA. This book provides a very useful overview and practical resource which all educational psychologists should find helpful -- DebateThis book is a useful addition to the literature available on understanding and managing PDA in children and will be an excellent resource for those working and living with children with PDA on a daily basis. -- Child and Adolescent Mental HealthProfessionals working with children presenting PDA behaviour would be able to use the book as a "bible", since the sub-headings allow access to information quickly and easily... This book offers good guidance, understanding, advice and solutions to parents, teachers and everyone involved with a child presenting PDA. -- Special ChildrenThis book is full of helpful guidance and support for anyone caring for, or working with, children with Pathological Demand Avoidance Syndrome (PDS)... This is a comprehensive, user-friendly introductory handbook that offers practical advice for overcoming difficulties from diagnosis through to adulthood. -- CerebraPathological Demand Avoidance Syndrome, as a sub-group on the autism spectrum, is now recognised, as are the implications for management and support, particularly in education settings. This book is invaluable in helping parents and professionals identify, understand and support this very complex group. -- Dr Jacqui Ashton Smith, Principal, Helen Allison School, National Autistic SocietyTable of ContentsAcknowledgements. Introduction. 1. What is PDA? 2. Positive Everyday Strategies. 3. Living with PDA. 4. Providing the Best Education for a Child with PDA. 5. Developing Emotional Well-being and Self-awareness in Children with PDA. 6. Summing Up and Questions for the Future. Appendix 1: Useful Websites and Links. Appendix 2: Book List. References. Index.

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Book SynopsisThe first major anthology by parents with disabilities. ‘Being a disabled parent is a rebellious act. Disabled people should have the same right to parent as anyone else, but often when we decide to start a family we are met with judgement and discrimination. We are questioned rather than supported. We have to push up against the medical system. And we have to confront society’s model of parenting. Yet, despite all this, we still choose to parent. And we are damn good at it too!’ When writer and musician Eliza Hull was pregnant with her first child, like most like most parents-to-be she felt a mix of nerves and excitement. But as a disabled person, she faced added complexities. She wondered: Will the pregnancy be too hard? Will people judge me? Will I cope with the demands of parenting? In We’ve Got This, thirty parents who identify as Deaf, disabled, neurodivergent, or chronically ill discuss the highs and lows of their parenting journeys and show that the greatest obstacles lie in other people’s attitudes. The result is a moving, revelatory, and empowering anthology that celebrates the richness of disabled parenting in the twenty-first century. ‘Such an important book. Joyous, eye-opening, and deeply moving, these powerful stories will challenge long-held assumptions and hopefully shift societal attitudes towards disabled parents. Everyone should read this.’ Francesca Martinez, author of What the **** Is Normal?!Trade Review‘Moving … the essays are at their richest when the authors describe what ought to be mundane (for example, discussing how to adjust the height of a kitchen counter for a wheelchair) or when they are brutally honest.’ -- James Coney, The Sunday Times‘A brilliant, positive, and empowering read full of inspirational stories … really eye-opening.’ -- Anita Rani, Woman’s Hour on BBC Radio 4‘A luminous collection filled with stories of resistance, innovation, joy, and love, We’ve Got This shows that the biggest challenge disabled parents face is not their disability, but how ableist society is. I’m so glad this book exists!’ -- Eloise Rickman, author of Extraordinary Parenting‘We’ve Got This shows what’s possible — that disabled people make brilliant parents. Eliza Hull is a skilful curator. This book should be mandatory reading for healthcare professionals, educators, and everyone wanting to be a better disability ally.’ -- Carly Findlay OAM, writer, speaker and appearance activist‘We’ve Got This sparkles with insight that will make sense to every parent trying to figure out a way to live with whatever curveball the universe has thrown their way. Surprise is a constant. There is no such thing as normal. And it's not a sin to admit that you don’t always know what you are doing. The stories of disabled parents in this book prove that love and ingenuity are a powerful combination.’ -- Al Etmanski, author of The Power of Disability‘Eliza is a legend — and a great advocate for our community. This book will help a lot of people!’ -- Dylan Alcott, Paralympian‘We’ve Got This is the book I needed many years ago when I was considering whether to have children. Now, as I embark on motherhood, these stories from these incredible parents will teach me so much.’ -- Nas Campanella, journalist‘Such an important book. Joyous, eye-opening, and deeply moving, these powerful stories will challenge long-held assumptions and hopefully shift societal attitudes towards disabled parents. Everyone should read this.’ -- Francesca Martinez, author of What the **** Is Normal?!‘All parenting is a leap of faith: with a disability it’s a powerful affirmation of life — as the stories in We’ve Got This demonstrate.’ -- Virginia Trioli, journalist and radio/TV presenter ‘We’ve Got This challenges the narrow stereotype of what disability looks like. It shows that disabled people are parents too — and bloody good ones at that! Thank you, Eliza, for disrupting the discourse.’ -- Lisa Cox, media professional and disability advocate‘Full of deep, beautiful, important stories. I’ve learnt so much from this book.’ -- Clare Bowditch, musician, actress, and radio presenter‘Eye-opening and heartwarming, We’ve Got This will make you laugh, cry, and rethink disability entirely. A must-read.’ -- Holly Ransom, public speaker and author of The Leading Edge‘This is the book I needed on my pregnancy journey. It’s a source of affirmation and representation that disabled parents deserve.’ -- Alexis Hillyard, disability advocate, keynote speaker, and creator of Stump Kitchen‘An important and necessary read.’ * The Bookseller *‘Something I admire about Hull is that … She wants to do the best for the disability community as a whole.’ * The Saturday Paper *‘Everyone should find something empowering in this first major anthology by parents with disabilities. They show what’s achievable: disabled people make exceptional parents.’ * PS News *‘Parenthood can tangle with grief and loss. Disability can include joy and abundance. And goddammit — disabled parents exist.’ -- Rebekah Taussig‘We’ve Got This attests to the capacities of disabled parents and to the joys of parenting in an authentic way.’ * ArtsHub *‘Eliza Hull begins the book by stating that “being a disabled parent is a rebellious act”. What follows are riveting essays that explain why, all brimming with creativity and pluck.’ -- Louise Kinross, Editor of BLOOM and Special Projects Manager at Holland Bloorview Kids Rehabilitation Hospital in Toronto, Canada‘There are many myths and misconceptions surrounding disabled parents. One of ableism’s greatest myths questions our capacity to bring a child into our lives. For this reason there is so much joy in reading this book. Reading so many wonderful essays addressing how parenting plays out for other disabled parents opens doors to my own joy parenting. So open the book already!’ -- Neil Hughes, Paralympic snowboarder and disability advocate‘Being a disabled parent is a “rebellious act”, which is why We’ve Got This is so important. Although disabled parents exist in substantial numbers, they remain in the shadows. This groundbreaking anthology confronts this phenomenon by telling the stories of parents with disabilities and their families — in their voices. We’ve Got This is a must-read!’ -- Robyn M. Powell, disability advocate and Associate Professor at the University of Oklahoma College of Law‘As the mother of a daughter with a disability I am grateful for Eliza Hull’s We’ve Got This: essays by disabled parents. There is a lot I can give to my daughter, but perspective on what it’s like to be a disabled parent is not one of those things. Of course, these stories aren’t just for her: they’re for everyone! The world needs to become more deeply acquainted with the breadth and depth of humanity found within the stories and experiences of disabled individuals, including disabled parenthood. This book is a revelation and full of beauty, humour, and grace. It’s hard to be what you can’t see — thank you to Eliza and all the parents in this book sharing their stories to help my daughter, and others, see ever more possibility.’ -- Amy Webb, disability advocate and author of When Charley Met Emma and Awesomely Emma‘The rawness, vulnerability, and authenticity in these stories is refreshing! Too often in the disability community we don't feel reflected accurately in TV, news, and the media, and these stories shine a light on that. The need to be heard and respected is something we can all relate to, disabled or not, and these messages are exactly what we need to hear more of.’ -- Marco Pasqua, public speaker and accessibility consultant‘The collection includes authors from a wide variety of backgrounds and experiences … it also includes essays and interviews from parents with intellectual disabilities, a frequently missing discourse in disability spaces … As a disabled parent, this was such an affirming and moving read for me, though I think all parents will benefit from reading it.’ -- Margaret Kingsbury * Book Riot *‘[M]uch-needed … [W]onderfully intersectional … Eliza Hull has done a fantastic job of curating this book. The essays themselves are brilliant, written from the heart and are very informative … The wealth of experiences, knowledge and sense of community that We’ve Got This offers is invaluable … [A] necessary read.’ -- Heather T. * Just Geeking By *‘Beautiful.’ * PosAbility Magazine *

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Book SynopsisTrade Review"The Capacity Contract brings much-needed insights to both political theory and disability studies. Its original analysis calls for the fuller recognition of the contributions of the intellectually disabled and their social inclusion as citizens."—Kristin Bumiller, Amherst College"Most political theorists would agree with Rawls that citizens need to possess cognitive capacities ‘within some normal range,’ but Stacy Clifford Simplican argues that such a ‘capacity contract’ is wrong. She provokes us to disrupt these norms."—Joan Tronto, University of Minnesota"A very interesting read."—Catholic Medical Quarterly"Simplican presents a rich analysis of the role of capacity in classic political philosophy and offers a significant contribution to the field. "—Disability Studies Quarterly"The Capacity Contract should be required reading not just for political theorists but for everybody conscientious about being alerted to unconscious patterns of bias and exclusion in their everyday lives and practices."—The Review of PoliticsTable of ContentsContentsAbbreviationsIntroduction: Anxiety, Democracy, and Disability1. Locke’s Capacity Contract and the Construction of Idiocy2. Manufacturing Anxiety: The Medicalization of Mental Defect3. The Disavowal of Disability in Contemporary Contract Theory4. Rethinking Political Agency: Arendt and the Self-Advocacy Movement5. Self-Advocates and Allies Becoming EmpoweredAcknowledgmentsNotesIndex

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Book SynopsisIn this wide-ranging and probing book Erin Manning extends her previous inquiries into the politics of movement to the concept of the minor gesture. The minor gesture, although it may pass almost unperceived, transforms the field of relations. More than a chance variation, less than a volition, it requires rethinking common assumptions about human agency and political action. To embrace the minor gesture''s power to fashion relations, its capacity to open new modes of experience and manners of expression, is to challenge the ways in which the neurotypical image of the human devalues alternative ways of being moved by and moving through the world—in particular what Manning terms 'autistic perception.' Drawing on Deleuze and Guattari''s schizoanalysis and Whitehead''s speculative pragmatism, Manning''s far-reaching analyses range from fashion to depression to the writings of autistics, in each case affirming the neurodiversity of the minor and the alternative politics it gestuTrade Review"Manning emphasizes a kind of affect that brings to the fore a feeling of being a part of a larger environment, something relational, something that helps people to see themselves as part of something bigger." -- Karen Simecek * Year's Work in Critical and Cultural Theory *"The Minor Gesture is a fascinating and intellectually challenging book that successfully problematises common-sense (neurotypical) understandings of perception, action and embodiment. In doing so it politicises mundane everyday experience and calls for sustained critique of normatively framed lifeworlds." -- Ben Simmons * Disability & Society *"A wide-ranging and carefully argued book. . . . Now that we know just how much mental activity escapes our conscious awareness and defies standard and dialectical accounts of knowledge, reason, and agency, efforts like Manning’s to better understand neurodiversity and to mobilize that understanding for research-creation and political activism alike are invaluable." -- Eugene W. Holland * Contemporary Political Theory *Table of ContentsPreface ix Introduction: In a Minor Key 1 1. Against Method 26 2. Artfulness: Emergent Collectives and Processes of Individuation 46 3. Weather Patterns, or How Minor Gestures Entertain the Environment 64 4. Dress Becomes Body: Fashioning the Force of Form 86 5. Choreographing the Political 111 6. Carrying the Feeling 131 7. In the Act: The Shape of Precarity 165 8. What a Body Can Do: A Conversation with Arno Boehler 189 Postscript: Affirmation without Credit 201 Notes 233 References 261 Index 269

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Book SynopsisThe role of disability and deafness in art Distressing Language is full of mistakeserrors of hearing, speaking, writing, and understanding. Michael Davidson engages the role of disability and deafness in contemporary aesthetics, exploring how physical and intellectual differences challenge our understanding of art and poetry. Where hearing and speaking are considered normative conditions of the human, what happens when words are misheard and misspoken? How have writers and artists, both disabled and non-disabled, used error as generative elements in contesting the presumed value of "sounding good"? Distressing Language grows out of the author's experience of hearing loss in which misunderstandings have become a daily occurrence. Davidson maintains that verbal confusions are less an aberration in understanding than a component of new knowledge. Davidson discusses a range of sites, from captioning errors and Bad Lip Reads on YouTube, to the deaf artist Christine Sun Kim's audiovisual installations, and a poetic reinterpretation of the Biblical Shibboleth responding to the atrocities of the Holocaust. Deafness becomes a guide in each chapter of Distressing Language, giving us a closer look at a range of artistic mediums and how artists are working with the axiom of "error" to produce novel subjecthoods and possibilities.Trade ReviewDrawing on his own experience of increasing deafness, Davidson provides an engrossing look into the ways that slips or unusual forms of language can unexpectedly lead to new meanings and beauty. Distressing Language expertly weaves together modern poetry and fiction, popular culture, sign language art, theory, politics, and history, and is often as funny as it is profound. * Christopher Krentz, author of Writing Deafness: The Hearing Line in Nineteenth-Century American Literature *A highly original account of language, meaning, and sound, all framed through hearing loss. In Davidson’s account, meaning and value come from things not working the way they are supposed to. But rather than fetishizing technical glitch or aesthetic failure, he processes meaning through a disability hermeneutic. Throughout Distressing Language, the lines between poetry, sound art, and music are intentionally blurred and violated, while the meaning of sound is foregrounded as something especially important for those who have limited access to it. * Jonathan Sterne, McGill University *

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Book SynopsisThis vital addition to carceral, prison, and disability studies draws important new links between deinstitutionalization and decarceration Prison abolition and decarceration are increasingly debated, but it is often without taking into account the largest exodus of people from carceral facilities in the twentieth century: the closure of disability institutions and psychiatric hospitals. Decarcerating Disability provides a much-needed corrective, combining a genealogy of deinstitutionalization with critiques of the current prison system.Liat Ben-Moshe provides groundbreaking case studies that show how abolition is not an unattainable goal but rather a reality, and how it plays out in different arenas of incarceration—antipsychiatry, the field of intellectual disabilities, and the fight against the prison-industrial complex. Ben-Moshe discusses a range of topics, including why deinstitutionalization is often wrongly blamed for the rise in incarceration; who resists decarceration and deinstitutionalization, and the coalitions opposing such resistance; and how understanding deinstitutionalization as a form of residential integration makes visible intersections with racial desegregation. By connecting deinstitutionalization with prison abolition, Decarcerating Disability also illuminates some of the limitations of disability rights and inclusion discourses, as well as tactics such as litigation, in securing freedom. Decarcerating Disability’s rich analysis of lived experience, history, and culture helps to chart a way out of a failing system of incarceration.Trade Review"Decarcerating Disability is a groundbreaking feminist study of the affinities, interrelations, and contradictions between prison abolition and psychiatric deinstitutionalization. Emphasizing the need for a more expansive field of critical carceral studies, Liat Ben-Moshe compellingly demonstrates the important lessons we can discover through serious engagements with radical disability movements. Scholars and activists alike should read this book without delay!"—Angela Y. Davis, University of California, Santa Cruz"In Decarcerating Disability, Liat Ben-Moshe carefully and incisively models an intersectional approach to abolition grounded in feminist, queer, and crip of color critique. Moving beyond demands for inclusion and critiques of overrepresentation, Ben-Moshe makes a powerful and persuasive case for a disability studies that recognizes state violence as central to its work and the carceral industrial complex as a site for queer coalitions for racial and disability justice. In so doing, she paves the way for thinking not only disability and disability studies differently, but also liberation itself."—Alison Kafer, University of Texas at Austin"Decarcerating Disability is a must-read for anyone interested in understanding and dismantling the interlocking systems of incarceration that shape the contemporary political landscape and shorten so many lives. Liat Ben-Moshe shows how the effectiveness of abolitionist work has been limited by the marginalization of disability and anti-sanism analysis and advocacy. She not only exposes how much contemporary abolitionists have to learn from historical struggles for deinstitutionalization, she also demonstrates a more truly intersectional method of abolitionist scholar-activism that we urgently need. This book is both a corrective intervention and a path-breaking tool for developing better strategy toward the world that those who seek liberation are fighting to build."—Dean Spade, Seattle University School of Law"Ben-Moshe outlines how people fought for a new paradigm in mental health treatment before. Beginning in the 1960s, widespread deinstitutionalization sparked by disability activists shut down asylums across the country. Many see this movement now as a failure because it led to more people with mental illness being herded into jails and prisons. But Ben-Moshe argues that this was a pivotal step in abolition by grassroots organizing."—Teen Vogue"Examining decarceration and deinstitutionalisation within the same frame is vitally important...the book challenges us to think about the range of carceral facilities that exist."—Race & Class"A groundbreaking connection between disability justice and prison abolition."—Public Books "Decarcerating Disability should be read not only by students and scholars of African-American studies, criminology, critical theory, gender studies, law, or sociology, nor only by policy makers, but by all who are concerned about disability, gender, or racial justice."—American Journal of Sociology "Each chapter of Decarcerating Disability serves as a fantastic example of the knowledges, perspectives, and genealogies that are made possible when disability and madness are the lenses through which a queer of color critique is engaged."—Disability Studies Quarterly"Decarcerating Disability is an impressive text that powerfully argues for robust coalitional politics to challenge the logic of incarceration. Entire syllabi and reading groups can be structured around this text as Ben-Moshe opens up much to consider, especially how to effectively demand carceral-free futures, while also valuing disability. "—Ethnic Studies Review"Decarcerating disability: Deinstitutionalization and prison abolition is abold and challenging critical intervention, which puts critical disability studies, deinstitutionalisation, decarceration, and abolition theory and scholarship into closer conversation with each other. In so doing, the book has pushed these fields forward in new and, interesting ways. The book’s strongest contribution is its attempt to transform, redefine, and reframe what disability studies is and can be about, its appeal to frame and address issues of incarceration and decarceration as disability and carceral abolition issues, and the generative groundwork laid for fostering coalitional, liberatory politics and ideas."—Australian & New Zealand Journal of Criminology"[A]n important book that offers both a sweeping genealogy of disability and itsentangled history with race and incarceration, and rallying cry for abolitionism."—Journal of Constructivist Psychology"Ben-Moshe offers a detailed history of institutionalization and incarceration primarily in the United States. In putting institutionalization and incarceration in conversation, Ben-Moshe offers a larger consideration around the systems that keep certain individuals enclosed and the implications of deinstitutionalization as a movement versus louder for total prison abolition. A major intervention of Ben-Moshe’s book is the different approaches to and opinions of institutions as opposed to prison systems across the United States."—Work in Critical and Cultural TheoryTable of ContentsContentsList of Abbreviations Introduction: The Case for Intersecting Disability, Imprisonment, and Deinstitutionalization1. The Perfect Storm: Origin Stories of Deinstitutionalization2. Abolition in Deinstitutionalization: Normalization and the Myth of Mental Illness 3. Abolition as Knowledge and Ways of Unknowing4. Why Prisons Are Not “the New Asylums”5. Resistance to Inclusion and Community Living: NIMBY, Desegregation, and Race-Ability6. Political and Affective Economies of Closing Carceral Enclosures7. Institutional and Prison Reform Litigation: From Politicization to the Governable Iron CageEpilogue: Abolition NowAcknowledgmentsNotesIndex

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Book Synopsis''Incredible insight with a transgressive, witty, spirit.'' COURTNEY LOVE''The most sensational read of 2022!'' GEMMA COLLINS''A breath of fresh air... I want so many people to read this!'' TRAVIS ALABANZA''Visionary'' VIV ALBERTINEA STYLIST MUST-READ FOR 2022Wellness is oppressive, self-love is a trap, hustling is a health risk and it''s all the patriarchy''s fault. Poor Little Sick Girls is THE book for femmes who are online and want more from activism and life.Ione Gamble never imagined that entering adulthood would mean being diagnosed with an incurable illness. Watching identity politics become social media fodder from the confines of her sickbed Ione began to pick apart our obsession with self-care, personal branding, productivity and #LivingYourBestLife. Using her experience with disability to cast a fresh gaze on the particularly peculiar cultural moment in which young women find Trade ReviewA crystal-clear mirror held up to contemporary feminism . . . Ione Gamble examines feminism's fourth wave and its intersections with the internet and capitalism, to brilliant effect . . .Gamble inventively and accessibly explores the roots of feminism as it exists materially today. * i News *A clear-sighted, critically needed skewering of hustle culture, wellness and modern feminism's blind spots, Ione pulls no punches in Poor Little Sick Girls. Everyone - and I mean everyone - should read this book. -- Yomi AdegokeA sizzling insight into how tropes about sick women and unacceptable bodies have been constructed throughout history through a cultural and personal lens. Ione writes with warmth, honesty and nuance, inviting the reader into a conversation that has, up until now, been afforded little space for exploration. -- Liv LittleI inhaled Poor Little Sick Girls in one sitting. This book is smart, addictive, wry and insightful. At a time when online discourse feels so muddled, Ione manages to pick through the weeds with characteristic humour and nuance. This is the anti-girlboss Bible and I love it. -- Daisy JonesA thrilling exploration of the relationships between bodies, abstract forces like language and stereotypes, and the material conditions that shape young adults' lives. Ione Gamble's incisive analysis of the last 15 years of social media, pop culture, and online feminism both illuminate the sources of present-day challenges and model a more liberatory way forward. By tracing the pieces of her self to facets of her environment, she demonstrates how much of a responsibility we have to one another - and that, for all the cynical powers that make our world, we also have the power to remake ourselves. -- Tavi GevinsonWhere so much online is generic and conformist, Ione Gamble's aesthetic and vision is anything but. A style icon and writer who seamlessly blends the esoteric and the obscure with popular culture as well as a commitment to many forms of social justice, her forthcoming book Poor Little Sick Girls is bound to be a treat! -- Emma DabiriOne of the sharpest, wittiest and most incisive thinkers of her generation. I always want to hear Ione's perspective on feminism, culture, and art - or just about anything -- Sirin KaleIone is fiercely unapologetic and a defining voice of our generation. It's especially powerful to see how her own experiences of living as a sick person intersect with her discussions on feminism. This will resonate with anyone who has ever been seen as "unacceptable" and decided to think critically about that. -- Cat White

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Book Synopsis“A powerful, game-changing book. Tom''s approach is changing lives.”— Seth Godin, Author of This is MarketingDiscover how supporting employment for people with autism unlocked new ways of running a business—and revealed transformative lessons for all of us.Rising Tide Car Wash in Parkland, Florida, isn’t average in any way. When Tom D’Eri and his father John bought the location in 2013, they wanted to create employment opportunities for workers with autism. Like 1 in 54 Americans, Tom’s brother Andrew has autism, and he was facing lifelong unemployment. So the family set out on a mission to provide professional opportunities for people like Andrew, starting with one car wash. Now it’s one of the highest-volume washes in Florida. Its employee retention rate is five times that of its competitors. It has spun off into two additional locations that have been iTrade Review'Everybody who is interested in getting people with autism employed in a job that gives them a sense of purpose should read this book.' * Temple Grandin, Author of The Autistic Brain and Thinking in Pictures *'One of the top ten businesses books of 2023. The book goes way beyond a story of one business that is so exhilarating and stimulating you'll want to tell it to friends and colleagues. It ultimately provides essential advice for every manager in business, nonprofits, and government. The advice on hiring alone will have you hiring art teachers to engineers and nurses--in half the time with double your success.' * Chip Heath, Professor at Stanford Business School and coauthor of four NYT bestsellers including Switch and The Power of Moments *'This is a powerful, game-changing book, a book for anyone who has ever built a hiring process or managed a team. Tom's approach is changing lives.' * Seth Godin, Author of This is Marketing *'This provocative, informative, and engaging book contains the seeds of a revolution--an inclusive future in which businesses unlock the hidden potential of employees with autism and other neurodivergent conditions by redesigning onboarding processes and creating opportunities for them to shine. It's a template for a society in which everyone is given the best chance of success.' * Steve Silberman, author of NeuroTribes: The Legacy of Autism and the Future of Neurodiversity *'Tom's account of how he built Rising Tide Car Wash and the lessons he learned from hiring and managing a non-traditional workforce is riveting. Read it and learn how to overcome some of the most entrenched problems that hold companies back from scaling.' * Chris Yeh, Author of Blitzscaling *

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Book SynopsisEstimates suggest that up to 20% of employees, customers and clients might have a neurodivergent condition - such as dyslexia, autism, Asperger's, ADHD or dyspraxia - yet these individuals often struggle to gain and maintain employment, despite being very capable. This practical, authoritative business guide will help managers and employers support neurodiverse staff, and gives advice on how to ensure workplaces are neuro-friendly. The book demonstrates that neurodiversity is a natural aspect of human variation to be expected and accepted, rather than a deficit to be accommodated. Employer responsibilities are highlighted, including the 2010 Equality Act, and a range of strategies and policies are provided, including recruitment advice and the benefits of neurodiverse employees, along with advice on physical environments, interaction and communication, and working with clients and customers. This book is an ideal resource for all employers wanting to support and empower people with specific needs to help create a more inclusive workplace, benefiting both neurodiverse individuals and the companies employing them.Trade ReviewAs an HR Adviser in a University, I have become more aware of neurodiverse colleagues and students and consideration of reasonable adjustments. This book provides practical guidance on developing policies and processes which support neurodiverse employees by making simple adjustments to facilitate participation in a variety of tasks and situations. -- Anne Spence, HR AdviserThis is an excellent and very informative book celebrating and supporting diversity of people in one of our adult lives' most visited places, the workplace. It includes everything professionals, managers and neurodiverse people need to know about how to survive the demands of the workplace. It is a great follow up to The Neurodiverse Classroom and it is easy to read and follow the information. A must-read for all the professions who support and accept neurodiversity. -- Ioannis Voskopoulos, Psychologist, Social And Organisational Psychologist, SF practitioner TNA Space CliniqueTable of Contents1. Introduction2. Understanding neurodiversity3. Neurodivergent individuals4. Employer responsibilities5. Inclusive recruitment6. Communicating for neurodiversity7. Policies and practice for neurodiversity8. Neurodiverse-friendly environments9. Working with neurodivergent customers and clients10. Further resources11. References

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Book SynopsisThe COVID-19 pandemic has had a profound and potentially ever-lasting impact on our economy, society, and the way that we live. In response to this pandemic there has been a plethora of research published about COVID-19. However, within this fast-growing body of literature there are only scant references made to the impact that this pandemic has had on autistics, their families, and the healthcare professionals who support autistics. Autism and COVID-19 is a concise summary of the research, bridging the gaps in our knowledge about autism and the COVID-19 pandemic. Bennett and Goodall address vaccine hesitancy among autistics and parents raising autistic children, the experiences of autistics living with COVID-19 disease and parenting an autistic child during the COVID-19 pandemic, synthesising the data about the COVID-19 pandemic from the perspective of autistic, their families, and those that provide autistics with medical assistance. Autism and COVID-19 both reviews the existing literature and presents new findings from a survey distributed to autistics and parents of autistics during the pandemic, all of which offer a unique and timely contribution to researchers, academics, practitioners, and those working with autistics and their families.Table of ContentsChapter 1. Introduction Chapter 2. Methodology Chapter 3. Results Chapter 4. New perspectives about the COVID-19 pandemic for autistics

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Book SynopsisAt the beginning of the 1990s, Linda Grant's mother, Rose, was diagnosed with Dementia. In Remind Me Who I Am, Again Linda Grant tells the story of Rose's illness and tries to reconstruct the history of their Jewish immigrant family, stalking them from Russia and Poland to New York and London. Writing with humour and great tenderness, Grant explores profound questions about memory, autonomy and identity, and asks if we can ever really know our parents.

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Book Synopsis''I'd encourage anyone who is aspirational for the lives of young people to draw from the wisdom and best practice in [these] pages.'' Oli de Botton, CEO of the Careers and Enterprise CompanyEverything you wanted to know about SEND, inclusion and careers (but were afraid to ask).?Whether you are a careers leader or adviser, school leadership team member, training provider, further education college representative, university staff member, employer, parent/carer or family member, or policymaker, this handbook is your essential guide to SEND careers. With actionable insights and practical advice, you can ensure that the most disadvantaged and vulnerable young people in our society have equal opportunities to succeed.Inside you''ll discover: Comprehensive strategies for supporting diverse career paths, from supported internships and accessible apprenticeships to higher education and entrepreneurship. In

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Book SynopsisJohn Barton used to live in the non-disabled world. Then he developed symptoms of an obscure inherited condition that affected his mobility, closely followed by Parkinson’s disease. And suddenly he found himself propelled into the kingdom of the disabled. There are two worlds, he writes: ‘In one lies power, privilege and validity, in the other, the supposed lack, shame and misery of the invalids. The barriers that separate them – physical, political and psychological – diminish us all. They cripple our societies.’ This is a book not about disability but about our shared humanity. Barton takes us on a journey through history, politics, sociology, medical science and psychology, to explore the meanings of disability. Why do we, as a species, find it so hard to share our common world with people who are different from us? When you meet a disabled person in the street, socially, or in your work, do you pass the Humanity Test? Read this book. You may learn something.Trade Review'This is a wise and fascinating account, written accessibly by someone who is a reliable guide to the worlds of disability and psychotherapy, because it’s exactly where he lives. I trusted him immediately and recommend this book to all.' Tom Shakespeare, Professor of Disability Research, London School of Hygiene and Tropical Medicine – 'The Humanity Test is a great book. John Barton has found a balance between being candid and learned about disability. This book acknowledges the emotional aspects of disability in an sensitive and intelligent manner. Each chapter is an accessible primer on interesting and relevant topics relating to disability, while bringing everything together in a carefully structured argument for social justice. There are many different ways of thinking about disability, Barton manages to acknowledge this while finding universalities for all disabled people.' Josh Hepple, disability equality activist and consultant – 'Barton shows how disability exposes us to ourselves in all our vulnerability, loneliness, incompetence and fear of disappearing. His research demonstrates how this can paradoxically lead to a deeper, more soulful humanity, so lacking in our contemporary world. The Humanity Test should be part of all therapeutic training.' Professor Emmy van Deurzen, existential psychotherapist and writer, Principal of the New School of Psychotherapy and Counselling and Director of the Existential AcademyTable of ContentsPreface, 1. Introduction: Failing the Humanity Test, 2. Biography: Getting on my nerves, 3. Disability: Who and what is disabled?, 4. Therapy: The search for a soulful life, 5. Spirituality: The transcendental turn, 6. Society: Uncivilization and its discontents, 7. Humanity: Passing the test

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Book SynopsisThis special issue brings together explorations of crip temporality: the ways in which bodily and mental disabilities shape the experience of time. These include needing to use time-consuming adaptive technologies like screen readers, working slowly during a pain flare-up, or only being able to look at a screen for short periods. Through accessibly written essays, art, and poems, contributors explore both the confines of crip temporality and the freedoms it provides. They offer strategies and narratives for navigating the academy as a disabled person; reclaim self-care as a tool for personal survival instead of productivity; and illustrate how crip time is mobilized in service of biopolitical projects. More than just a space of loss and frustration, they argue, crip time also offers liberatory potential: the contributors imagine how justice, connection, and pleasure might emerge from temporalities that center compassion rather than productivity. Contributors Moya Bailey, Amanda Cac

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Book SynopsisIn Crip Spacetime, Margaret Price intervenes in the competitive, productivity-focused realm of academia by sharing the everyday experiences of disabled academics. Drawing on more than three hundred interviews and survey responses, Price demonstrates that individual accommodations-the primary way universities address accessibility-actually impede access rather than enhance it. She argues that the pains and injustices encountered by academia's disabled workers result in their living and working in realities different from nondisabled colleagues: a unique experience of space, time, and being that Price theorizes as crip spacetime. She explores how disability factors into the exclusionary practices found in universities, with multiply marginalized academics facing the greatest harms. Highlighting the knowledge that disabled academics already possess about how to achieve sustainable forms of access, Price boldly calls for the university to move away from individualized models of accommodation and toward a new system of collective accountability and care.

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Book SynopsisElizabeth Barnes argues compellingly that disability is primarily a social phenomenona way of being a minority, a way of facing social oppression, but not a way of being inherently or intrinsically worse off. This is how disability is understood in the Disability Rights and Disability Pride movements; but there is a massive disconnect with the way disability is typically viewed within analytic philosophy. The idea that disability is not inherently bad or sub-optimal is one that many philosophers treat with open skepticism, and sometimes even with scorn. The goal of this book is to articulate and defend a version of the view of disability that is common in the Disability Rights movement. Elizabeth Barnes argues that to be physically disabled is not to have a defective body, but simply to have a minority body.Trade ReviewI am happy to unequivocally say that this text makes a fascinating and groundbreaking contribution to feminist and disability philosophy. I would enthusiastically recommend this text to anyone interested in disability and philosophy, and especially to those new to philosophy. * Tessa-May Zirnsak, Metapsychology Online Reviews *Elizabeth Barnes' new book offers a much-needed philosophical discussion of disability capitalizing on relevant research in bioethics, feminist philosophy and disability studies. * Elena Fell and Natalia Lukianova, The Philosophical Quarterly *Elizabeth Barnes has written an interesting and important book about disability . . . Barnes has brought a new level of precision to a popular slogan and has then set about defending it with all the familiar tools of contemporary analytic philosophy . . . it remains to be seen where the debate goes next, but wherever it goes, future discussion will need to engage with the work of Elizabeth Barnes. * Jennifer Hawkins, Ethics *It is a thoughtful, thorough, and rigorous argument that nevertheless has an accessible style. It is not a book for a generalist audience, but could work quite readily in both undergraduate and graduate courses. Her attempt to moderate a path between the physical body and social constructivism, and to combat a generalized skepticism in the field of philosophy about the possibility that disability might be a good thing for some people, or at least a neutral thing, that lives of disabled persons are generally as rich, valuable, and worth living as those of nondisabled persons, and that such skepticism is "rooted in--often knee-jerk unreflective--stereotypes about what disabled lives are like" is an unapologetic and strong case for disability positivity. It is a valuable contribution to disability philosophy in particular, and philosophy in general. * Nancy J. Hirschmann, Hypatia Reviews *The Minority Body is a fascinating and compelling study of the concept of disability. Barnes redefines disability as a social phenomenon in a fresh way. Her revolutionary ideas compel us to look at the minority body without making value-judgments. * The Washington Book Review *In her engaging, powerfully argued, and good-humored book, Barnes seeks to illuminate the nature of physical disability, challenge the view that it has a negative impact on well-being, and defend a mere-difference view of disability . . . it is a wildly creative, rigorous, and ground-breaking work that represents a significant contribution to the on-going inquiry into the nature and value of disability. It would not be an exaggeration to claim that it is the most important single-authored book in philosophy of disability to come out of the analytic tradition in a generation. * Stephen M. Campbell & Joseph A. Stramondo, Notre Dame Philosophical Review *Table of ContentsPreface Introduction 1: Constructing Disability 2: Bad-difference/Mere-difference 3: The Value-Neutral Model 4: Taking Their Word for It 5: Causing Disability 6: Disability Pride

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Book SynopsisFINALIST FOR THE 2023 PULITZER PRIZE FOR MEMOIR''An exquisite exploration of disability, identity and the human capacity to do (and be) more than we''ve ever dreamed'' Time''Gorgeously, vividly alive'' New York Times''Challenges the unspoken social taboos about the disabled body, unpacking myths of beauty and our complicity in upholding those myths'' Lit HubBorn with sacral agenesis, a visible congenital disability that affects her stature and gait, Chloé Cooper Jones had always found solace in what she thought of as ''the neutral room'' - a dissociative space in her mind that offered her solace and self-protection, but also kept her isolated. When she became pregnant (disproving her doctor, who had assumed it impossible), something necessary in her started to crack, forcing her to reckon with her defensive positionality to the world and the people in it. This prompted an odyssey across time andTrade ReviewEasy Beauty is bold, honest, and superbly well-written. Chloé Cooper Jones is ruthless in probing our weakest and darkest areas, and does so with grace, humor, and ultimately, with something one seldom finds: kindness and humanity. * André Aciman, author of Call Me By Your Name *Graceful, soul-baring * Melanie Reid, The Times *Gorgeous, vividly alive... In rejecting the dismissive gaze of others, Jones stands in the light of her own extremely able self -- Books of the Year * New York Times *What a gift of a book ... Easy Beauty has the rigor and precision of Joan Didion and Maggie Nelson and a forthright humor and naked truth all its own. * Sarah Ruhl, author of Smile *Perceptive, stylish, and darkly funny, Easy Beauty is an act of grace, and a reckoning. Chloé Cooper Jones is a remarkable writer - I would follow her mind anywhere. * Anna Wiener, author of Uncanny Valley *Chloé Cooper Jones is a writer whose work I don't read, but enter: she weaves her brainy, crackling interior into the sinews of a reality that is forever reminding its participants of the difficulty of living inside a body. Easy Beauty is the most humane book I have read in a long time: in her insistence that we bear witness to each other, Jones calls forth a better, and indeed more beautiful world. I loved this book. * Kristen Radtke, author of Seek You: A Journey Through American Loneliness *I recommend Easy Beauty to anyone who has wanted beauty badly, even without knowing quite what it is, but who could never seem to access it. At least, I'm that sort of anyone, and I could feel and recognize parts of myself in every moment of this book. Chloé Cooper Jones' writing pierces right through and lets a light in. * Mitski, singer-songwriter *In this ambitious and elegant book about seeing and being seen, Chloé Cooper Jones invokes thorny, theoretical material about identity, the social order, and how we measure human value, but her clarity and compassion invite all readers in. She has created a forceful and fresh point of view from which to anatomize power, access, and perception in her precise, unsparing prose. A necessary, relentlessly honest book that feels both of the moment and timeless. * Whiting Foundation Judges citation *Jones is a magnificent guide, fiercely sharp and fiercely human. This book is for anyone who wants to immerse into a world of beauty, who wants to get real about the roots of their desire, and who can't quite kick the habit of admiring the structures-and humans-who harm them. The questions she raises will resound in your head for a long time to come. * Lulu Fisher, author of Why Fish Don't Exist and host of Radiolab *This book is utterly remarkable. I was spellbound by the style, the ideas, the vulnerability, the talent. * Lydia Kiesling, author of The Golden State *Dazzling . . . Chloe Cooper Jones challenges society's rules of attraction with razor-sharp wit and intellect . . .[and) makes a brilliant case for the beauty of complexity * Starred Publishers Weekly *Exquisite. Here Pulitzer finalist Jones reflects on our standards of beauty from the perspective of a disabled woman whose rare congenital condition affects her stature and gait, and leaves her in constant pain. But it's ultimately motherhood that liberates her, and prompts her to re-examine the limitations she has accepted as givens. * O Magazine *Jones challenges the unspoken social taboos about the disabled body, unpacking myths of beauty and our complicity in upholding those myths. Blending journalism, philosophy, and memoir, it's a book that everyone will be talking about. * Lit Hub *A memoir full of insight as the author tries to wrestle understanding and ownership of herself from a world still eager to assert its sovereignty over the female body. * Jarred McGinnis, author of The Coward *A soul-stretching, breathtaking existential memoir chronicles her reclaiming of body, mind, and self . . . Superlative writing, rendering complex emotion and unparalleled insight in skilfully precise language. Her debut is a game-changing gift to readers. * Booklist, starred review *Despite doctors' dire predictions that she wouldn't live, walk or have children, she has done these things and more. Here, she probes the ways a culture determines a person's value and embarks on a journey to understand the myth of beauty and her own unintentional complicity in it. * Washington Post *The multiple depths that Jones plumbs in Easy Beauty results in a memoir that can't easily be classified. The same can be said for the book's author. Jones is a Pulitzer Prize finalist, a philosophy professor and a writer, who delves into her journey as a daughter, mother, wife and her search for a new way of seeing the world. In other words, her story is about the complexity of the human experience and the questions of identity and belonging that plague us all. * People Magazine *Inspired in part by the shift Jones saw in others' perceptions of her during her pregnancy, Easy Beauty challenges deep-seated assumptions about who gets to be capable, trustworthy, and desirable. * Bustle Magazine *Candid and truth-seeking, this memoir charts the act of refocusing and realigning the ways we view and interpret ourselves * NB Magazine *Achingly felt, Jones's writing is a revelation * Publishers Weekly, Best Books of 2022 *Easy Beauty is an exquisite exploration of disability, identity, and the human capacity to do (and be) more than we've ever dreamed * Time *Touching and often humorous... explores life from the perspective of those who don't conform to conventional beauty standards -- Charlotte Heathcote * Daily Record *Genius... Shifted my understanding of a world I've only experienced while able-bodied -- Best Memoirs of 2022 * Vulture *Moving, incisive... Jones resists sentimentality and is as unsparing of herself as she is of other people, and yet she writes with such graciousness. A wonderful debut -- Tomi Obaro * Buzzfeed News *Gorgeous, concise and often very funny... a gripping memoir about parenting, disabilities and figuring out what to do next... a philosophical masterpiece, written in the tradition of those who see philosophy not as a dry academic subject but as a way of life * Coachella Review *A masterpiece ... Cooper Jones uses the particulars of her own experience to formulate ideas that are at once universally applicable and genuinely profound * Irish Times *

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Book SynopsisA dazzling performance (think Forrest Gump, think Curious Incident, think Anne Donovan''s Buddha Da) from one of Scotland''s brightest new talents.Adam Spark. Eighteen going on eight-and-a-half. Fast-food worker. Queen fan. Last in the queue for luck. On waking from an accident in which he saves a child, he has the distinct impression that all is far from right. What are these curious lights that seem to surround people? Why are animals and machines trying to speak to him? And can he really control time? Is it just his imagination, or has Adam Spark been chosen to become Scotland''s first, and only, superhero? This, however, is the least of his problems. The local gang is luring him into deeper and darker peril. His sister and lone carer, Jude, is giving all her love to another woman. And if Jude abandons Adam - or Adam drives her away - all the superpowers in the world won''t be able to save him.Trade Review'Bizarre, hilarious, moving' Big Issue in Scotland; 'Sparky is a terrific character' Sunday Herald; 'Sparky is a virtuoso literary creation... This is a fresh and exciting read' Scotland on Sunday * . *

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Book SynopsisPrison Health and Wellbeing blends theory with lived experience to explore the complex challenges and interventions that shape health and wellbeing for those living, working, and visiting prisons.People in prison are far from a homogenous group, yet epidemiological evidence consistently shows higher rates of ill health compared to the wider population. Historically, research has focused almost exclusively on individuals in custody, often overlooking the health needs of prison staff and others within these environments. This book addresses these gaps by offering comprehensive insights into the social, structural, and cultural factors that influence health in prison contexts. Moving beyond a narrow focus on disease, disability, and deficit, it adopts a salutogenic perspective â asking what keeps people healthy, not just what makes them ill. By reframing prison health through a holistic lens, this book provides a critical foundation for improving wellbeing in one of societyâs most challenging environments.Prison Health and Wellbeing is an essential resource for students and scholars of criminology, public health, and health promotion. It will also prove invaluable for policymakers, commissioners, and practitioners delivering health services in prisons.

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a huge range and FREE tracked UK delivery on ALL orders.

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a huge range and FREE tracked UK delivery on ALL orders.

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Book SynopsisAn ACT-based guide for practitioners working with adults with intellectual disabilities, with the aim of fostering self-advocacy and individual empowerment and centring their needs. With case studies and ideas for exercises, this is a clear roadmap for accessible ACT interventions.

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