Non-fiction

"Lauren "Lolo'' Spencer provides a candid and real inside look into the life of being a person with a disability. This disability advocate embarks on the importance of visibility for the disabled community because representation matters! Words from someone doing the work. Lolo Spencer gained popularity as a YouTube personality. On her platform, Sitting Pretty, she encourages viewers to achieve their dreams through making strong choices. Lolo shares how she navigates daily life with Amyotrophic Lateral Sclerosis (ALS). You are more than your limits. Choosing to see herself as more than a person with a disability and wheelchair user, Lolo chooses to live a bold and courageous life now because representation matters. She created this intersectional guide to provide tools for people with disabilities to thrive in personal growth, independence, and community building. Add this guide to your list of inclusion books!Inside, you'll find: An intersectional guide on how to grow personally and professionally. Tools for people with disabilities to live a full life despite limitations and expectations. Words from the inspiring Lauren "Lolo" Spencer, your favorite disability advocate."--Amazon.com.

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"One of the most influential disability rights activists in US history tells her personal story of fighting for the right to receive an education, have a job, and just be human. A story of fighting to belong in a world that wasn't built for all of us and of one woman's activism--from the streets of Brooklyn and San Francisco to inside the halls of Washington--Being Heumann recounts Judy Heumann's lifelong battle to achieve respect, acceptance, and inclusion in society."-- Provided by publisher.

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Beryl Potter was a reserved working-class mother of three living a decent life, or so it seemed, when a harmless slip and fall marked the unravelling of everything that she had known about herself and the world around her. Over the course of six years, she endured unimaginable pain. As doctors raced to save her life, her limbs and eyesight were taken from her one by one. In the span of a few years, she lost nearly half her body, her financial security, her home, her husband, and any semblance of a recognizable future. A survivor of more than one hundred surgeries, a dangerous opioid addiction, and multiple suicide attempts, Beryl Potter devoted herself to bettering the lives of other people with disabilities and made a tremendous contribution to disability awareness from the 1970s to 1990s. In this unparalleled biography, Dustin Galer demonstrates how Beryl Potter seemed to crack the code of the social system that oppressed her. By wading into the weeds of her complicated life before and after her accident, Galer leaves readers with a complex portrait of a woman who defied and challenged gender and disability norms of her time, paving the way for disability justice.

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"A witty, winning, and revelatory personal narrative of the author's transition from sightedness to blindness and his quest to learn all he can about blindness as a distinct and rich culture all its own. We meet Andrew Leland as he's suspended in the strange liminal state of the soon-to-be blind: He's midway through his life with retinitis pigmentosa, a condition that ushers those who live with it from complete sightedness to complete blindness over a period of years, even decades. He grew up with full vision, but starting in his teenage years, his sight began to degrade from the outside in, such that he now sees the world as if through a narrow tube. Soon-but without knowing exactly when-he will likely have no vision left. Full of apprehension but also dogged curiosity, Leland embarks on a sweeping exploration of the state of being that awaits him: not only the physical experience of blindness but also its language, internal debates, politics, and customs. He also negotiates his changing relationships with his wife and son, and with his own sense of self, as he moves from sighted to semi-sighted to blind, from his mainstream, "typical" life to one with a disability. Part memoir, part historical and cultural investigation, The Country of the Blind represents Leland's determination not to merely survive this transition, but to grow from it-to seek out and revel in that which makes blindness enlightening. His story reveals essential lessons for all of us, from accepting uncertainty and embracing change to connecting with others across difference. Thought-provoking and brimming with warmth and humor, The Country of the Blind is at once a deeply personal journey and an intellectually exhilarating tour of a way of being that most of us have never paused to consider-and from which we have much to learn"-- Provided by publisher.

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Crip Up: a term used by disabled disability rights advocates and academia to signal taking back power, to lessen stigma, and to disrupt ableism as to ensure disabled voices are included in all aspects of life. With 50 recipes that make use of three key tools - the electric pressure cooker, air fryer, and bread machine - Jules Sherred has set out to make the kitchen accessible and enjoyable. Includes pantry prep, meal planning, shopping guides, kitchen organization plans, and tips for cooking safely when disabled, all taking into account varying physical abilities and energy levels.

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Disabled people are the world's largest minority, an estimated 15 percent of the global population. But many of us - disabled and non-disabled alike - don't know how to act, what to say, or how to be an ally to the disability community. This is a friendly handbook on important disability issues you need to know about, including how to appreciate disability history and identity, how to recognize and avoid ableism (discrimination toward disabled people), and how to appropriately think, talk, and ask about disability.

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"An eye-opening portrait of the diverse disability community as it is today and how attitudes, activism, and representation have evolved since the passage of the Americans with Disabilities Act (ADA)"-- Provided by publisher.

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A groundbreaking collection of first-person writing on the joys and challenges of the modern disability experience: Disability Visibility brings together the voices of activists, authors, lawyers, politicians, artists, and everyday people whose daily lives are, in the words of playwright Neil Marcus, "an art ... an ingenious way to live." According to the last census, one in five people in the United States lives with a disability. Some are visible, some are hidden--but all are underrepresented in media and popular culture. Now, just in time for the thirtieth anniversary of the Americans with Disabilities Act, activist Alice Wong brings together an urgent, galvanizing collection of personal essays by contemporary disabled writers. There is Harriet McBryde Johnson's "Unspeakable Conversations," which describes her famous debate with Princeton philosopher Peter Singer over her own personhood. There is columnist s. e. smith's celebratory review of a work of theater by disabled performers. There are original pieces by up-and-coming authors like Keah Brown and Haben Girma. There are blog posts, manifestos, eulogies, and testimonies to Congress. Taken together, this anthology gives a glimpse of the vast richness and complexity of the disabled experience, highlighting the passions, talents, and everyday lives of this community. It invites readers to question their own assumptions and understandings. It celebrates and documents disability culture in the now. It looks to the future and past with hope and love

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Girma grew up with her family in the Eritrean city of Asmara during Eritrea's thirty-year war with Ethiopia. Defining her disability as an opportunity for innovation, she learned non-visual techniques for everything from dancing salsa to handling an electric saw. She developed a text-to-braille communication system that created a new way to connect with people. Pioneering her way through obstacles, Girma graduated from Harvard Law, and now uses her talents to advocate for people with disabilities. This is a testament to her determination to find the keys to connection. -- Adapted from jacket.

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"Annie Liontas suffered multiple concussions in her thirties. In Sex with a Brain Injury, she writes about what it means to be one of the "walking wounded," facing her fear, her rage, her physical suffering, and the effects of head trauma on her marriage and other relationships. Forced to reckon with her own queer mother's battle with addiction, Liontas finds echoes in their pain. Liontas weaves history, philosophy, and personal accounts to interrogate and expand representations of mental health, ability, and disability-particularly in relation to women and the LGBT community. She uncovers the surprising legacy of brain injury, examining its role in culture, the criminal justice system, and through historical figures like Henry VIII and Harriet Tubman. Encountering Liontas's sharp, affecting prose, the reader can imagine this kind of pain, and having to claw one's way back to a new normal. The hidden gift of injury, Liontas writes, is the ability to connect with others. For the millions of people who have suffered from concussions and for those who have endeavored to support loved ones through the painful and often baffling experience of head trauma, this astonishing and compassionate narrative offers insight and hope in equal measure."-- Provided by publisher.

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Growing up as a paralyzed girl during the 90s and early 2000s, Rebekah Taussig only saw disability depicted as something monstrous, inspirational, or angelic. None of this felt right. 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.

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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. More than 15 percent of people worldwide live with a disability, and many of them are also parents. 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.

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