Social media has facilitated the sharing of once isolated testimonies to an extent and with an ease never before possible. The #MeToo movement provides a prime example of how such pooling of individual stories, in large enough numbers, can fuel political movements, fortify a sense of solidarity and community, and compel public reckoning by bringing important issues into mainstream consciousness. In this timely and important study, Helga Lenart-Cheng has uncovered the antecedents of this phenomenon and provided a historical and critical analysis of this seemingly new but in fact deeply rooted tradition. Story Revolutions features a rich variety of case studies, from eighteenth-century memoir collections to contemporary Web 2.0 databases, including memoir contests, digital story-maps, crowd-sourced Covid diaries, and AI-assisted life writing. It spans the Enlightenment, the 1930s, and the twenty-first century—three historical periods marked by a convergence of mass movements and new methods of data collection that led to a boom in activism based in the aggregation and communication of stories. Ultimately, this book offers readers a critical perspective on the concept of community itself, with incisive reflections on what it means to use storytelling to build democracy in the twenty-first century.
This definitive reference work replaces Konigsmark and Gorlin's Genetic and Metabolic Deafness (1976). Whereas the earlier volume covered 151 genetic conditions related to hearing loss, this work covers 435. As before, the authors first discuss isolated hereditary hearing loss and then present hearing loss syndromes such as those involving the nervous system, eye, external ear and musculoskeletal system. The discussions are authoritative, practical and well-illustrated, and those of the most important syndromes are very detailed. Introductory chapters deal with the history of the field, clinical approach, embryology of the ear, tooth anomalies and hearing loss, and related endocrine and metabolic disorders. Throughout, the authors pay careful attention to nomenclature and classification. This will be an invaluable resource for all professionals concerned with genetic hearing loss, including medical geneticists, audiologists and otolaryngologists.
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