A disability advocate debuts with a collection offering potent rejoinders to ableism. Tracing memories from childhood to the present, Taussig, who has a doctorate in disability studies, explores her life story and relationship with her body as well as attendant concerns of confidence, belief, and hope. Even though she grew up "after the passage of the 1990 Americans With Disabilities Act," the author, who was paralyzed at age 3 following a lengthy, deleterious cancer-treatment regimen, faced many difficult situations related to her disability, from confronting lowered expectations at a youth camp to navigating awkward moments with friends and acquaintances. She investigates what accessibility really means and how it relates to housing, employment, and health care--"The older I got," she writes, "the more I cringed at the bills my body created"--and she looks at dating challenges and the difference between finding marriage and finding love, exposing many of the mechanics behind traditional social scripts. Constantly questioning the damaging illogic of nonaccessible public spaces, Taussig confronts the insidious nature of "stigma, isolation, erasure, misunderstanding, skepticism, and ubiquitous inaccessibility." Introducing many key themes of disability studies throughout the narrative, the author pushes for nuanced awareness and understanding of fluid rather than fixed needs, essential for a more effective intersectional approach to social solutions. Taussig goes beyond empty inspirational jargon, forcing readers to consider the value of the real-world improvements that can emerge from centering underrepresented voices. An engaging, up-close view of the need for structural change regarding disabilities in this country, the text is a solid combination of theory and personal experience. "We should bring disabled perspectives to the center," she writes, "because such perspectives create a world that is more imaginative, more flexible, more sustainable, more dynamic and vibrant for everyone who lives in a body." A fierce and fabulous revision to entrenched ableist scripts. Copyright (c) Kirkus Reviews, used with permission.

Disability is often seen by the able-bodied population as something to be fixed, something to be pitied. With Taussig's memoir, readers are given a different perspective--one of someone seeking to bring awareness and education to the world around her. Taussig, with both a PhD in disability studies and the lived experience of having a disability herself, is able to meet readers where they are, whether they are disabled themselves or are curious to learn. However, Taussig states up front that she is not representative of all disabled people and that this book is not exhaustive. Rather, it is a personal account, and one that is organized as a book of essays, each a vignette of an experience where disability informed Taussig's experiences: her romantic relationship with an able-bodied person, teaching an experimental disability theory class for high schoolers, discussing her life experiences with her family, and more. VERDICT Taussig's narrative style is highly conversational, making it feel like one is chatting with a lifelong friend. Her ability to bring levity to a topic some may find taboo is certain to help spread her message of acceptance and love.--Ahliah Bratzler, Indianapolis P.L.

Treatment for childhood cancer led to paralysis at age three, but that didn't stop Taussig. She adapted. Nonetheless, she grew up in a world that didn't see her or welcome her or represent her. It was and is a struggle. The average annual income of a disabled person, she notes, is $25,400, less than a nondisabled person's. She describes how a disabled person navigates things nondisabled people take in stride: dating, marriage, the workplace. But she also places the onus on the nondisabled world, asking us not to look at disability as a limitation: "What if a lack of imagination was the actual barrier?" Taussig maintains that it is "our affinity for familiarity that traps us." She is more than her disability. If the disabled are marginalized, she continues, it is because of society, and society "has the power to change that." The epilogue's annotated list of resources includes "very cool people" who also happen to be disabled, books, television shows, and Instagram hashtags. An invaluable, eye-opening look at disability from a firsthand perspective.

Taussig debuts with a pull-no-punches memoir about life in a wheelchair. She insists up front that she doesn't speak for everyone with a disability ("I would be doing us all a great disservice if I led you to believe that the conversation starts and ends with bodies and experiences that look just like mine") and provides a frank look into her life with "a body that doesn't work," one that she's lived in since surviving an aggressive cancer as a 14-month-old. She analyzes sex and disabilities; her marriage to her first husband, which came about only because she was afraid it would be her only chance (she eventually found love with her second husband); unintentional ableism; online dating; and what she sees as the disempowering message from Hollywood that characters with disabilities are "always longing for a 'whole' body through a fantasy sequence." Taussig's refreshing, matter-of-fact tone makes it clear that she's not asking anyone to feel sorry for her; rather, she's asking for just the opposite--to not be defined by her wheelchair. Her smart and witty observations about living with disabilities will be enlightening and eye-opening for readers. (Aug.)