Beth Linker

"This book is a historical consideration of how poor posture became a dreaded pathology in the United States at the turn of the twentieth century. It opens with the "outbreak" of the poor posture epidemic, which began with turn-of-the-century paleoanthropologists: If upright posture was the first of all attributes that separated human from beasts - and importantly a precondition for the development of intellect and speech - what did it mean that a majority of Americans slouched? By World War I, public health officials claimed that 80% of Americans suffered from postural abnormalities. Panic spread, setting into motion initiatives intended to stem the slouching epidemic, as schoolteachers, shoe companies, clothing manufacturers, public health officials, medical professionals, and the popular press exhorted the public toward detection. Wellness programs stigmatized disability while also encouraging the belief that health and ableness could be purchased through consumer goods. What makes this epidemic unique is that, in the absence of a communicable contagion, it was largely driven by a cultural intolerance of disabled bodies, with notions of "ableness" taking hold for much of the twentieth century. The author traces this history through its consequential demise, as social movements of the 1960s prompted people to push back against invasive and discriminatory standards. Large-scale physical fitness assessments designed to weed out defective bodies relied on compliant participants, and the Civil Rights and Women's Movement, as well as the anti-Vietnam war protests and Disability Rights Movements eventually halted that supply, and in the 1990s a public outcry destroyed many of the archives and materials collected. Nevertheless, anxiety over posture persists to this day"--

Posture Panic in Modern America

Slouch

Nancy J. Hirschmann

An estimated one billion people around the globe live with a disability; this number grows exponentially when family members, friends, and care providers are included. Various countries and international organizations have attempted to guard against discrimination and secure basic human rights for those whose lives are affected by disability. Yet despite such attempts many disabled persons in the United States and throughout the world still face exclusion from full citizenship and membership in their respective societies. They are regularly denied employment, housing, health care, access to buildings, and the right to move freely in public spaces. At base, such discrimination reflects a tacit yet pervasive assumption that disabled persons do not belong in society. Civil Disabilities challenges such norms and practices, urging a reconceptualization of disability and citizenship to secure a rightful place for disabled persons in society. Essays from leading scholars in a diversity of fields offer critical perspectives on current citizenship studies, which still largely assume an ableist world. Placing historians in conversation with anthropologists, sociologists with literary critics, and musicologists with political scientists, this interdisciplinary volume presents a compelling case for reimagining citizenship that is more consistent, inclusive, and just, in both theory and practice. By placing disability front and center in academic and civic discourse, Civil Disabilities tests the very notion of citizenship and transforms our understanding of disability and belonging. Contributors: Emily Abel, Douglas C. Baynton, Susan Burch, Allison C. Carey, Faye Ginsburg, Nancy J. Hirschmann, Hannah Joyner, Catherine Kudlick, Beth Linker, Alex Lubet, Rayna Rapp, Susan Schweik, Tobin Siebers, Lorella Terzi.

Beth Linker

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