Lanterman Developmental Disabilities Services Act With 1988 Amendments
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Author | : California. Legislature. Senate. Subcommittee on Mental Health, Developmental Disabilities, and Genetic Diseases |
Publisher | : |
Total Pages | : 122 |
Release | : 1989 |
Genre | : Developmentally disabled |
ISBN | : |
Author | : California |
Publisher | : |
Total Pages | : 396 |
Release | : 2015 |
Genre | : Developmentally disabled |
ISBN | : |
Author | : |
Publisher | : |
Total Pages | : 148 |
Release | : 1992 |
Genre | : Developmentally disabled |
ISBN | : |
Author | : |
Publisher | : |
Total Pages | : 160 |
Release | : 1992 |
Genre | : Developmentally disabled |
ISBN | : |
Author | : California. Legislature. Assembly |
Publisher | : |
Total Pages | : 1116 |
Release | : 1987 |
Genre | : Bills, Legislative |
ISBN | : |
Author | : California. Legislature. Senate |
Publisher | : |
Total Pages | : 1362 |
Release | : 1987 |
Genre | : Bills, Legislative |
ISBN | : |
Author | : California |
Publisher | : |
Total Pages | : 2294 |
Release | : 1988 |
Genre | : California |
ISBN | : |
Volumes include: Statutory record.
Author | : California State Library |
Publisher | : |
Total Pages | : 468 |
Release | : 1989 |
Genre | : California |
ISBN | : |
Author | : Daniel Pateisky |
Publisher | : Routledge |
Total Pages | : 199 |
Release | : 2021-03-23 |
Genre | : Social Science |
ISBN | : 100036710X |
This book provides insight into the globally interlinked disability rights community and its political efforts today. By analysing what disability rights activism contributes to a global power apparatus of disability-related knowledge, it demonstrates how disability advocacy influences the way we categorise, classify, distribute, manipulate, and therefore transform knowledge. By unpacking the mutually constitutive relations between (practical) moral knowledge of international disability advocates and (formal) disability rights norms that are codified in international treaties such as the UN Convention on the Rights of Persons with Disabilities (CRPD), the author shows that the disability rights movement is largely critical of statements that attempt to streamline it. At the same time, cross-cultural disability rights advocacy requires images of uniformity to stabilise its global legitimacy among international stakeholders and retain a common meta-code that visibly identifies its means and aims. As an epistemic community, disability rights advocates simultaneously rely on and contest the authority of international human rights infrastructure and its language. Proving that disability rights advocates contribute immensely to a global culture that standardises what is considered morally and legally ‘right’ and ‘wrong’, thereby shaping the human body and the body politic, this book will be of interest to all scholars and students of critical disability studies, sociology of knowledge, legal and linguistic anthropology, social inequality, and social movements.
Author | : John J. Pitney |
Publisher | : Rowman & Littlefield |
Total Pages | : 191 |
Release | : 2015-08-06 |
Genre | : Political Science |
ISBN | : 1442249617 |
In the first book devoted exclusively to the contentious politics of autism, noted political scientist and public policy expert John J. Pitney, Jr., explains how autism has evolved into a heated political issue disputed by scientists, educators, social workers, and families. Nearly everything about autism is subject to debate and struggle, including its measurement and definition. Organizational attempts to deal with autism have resulted in not a single “autism policy,” but a vast array of policies at the federal, state, and local levels, which often leave people with autism and their families frustrated and confused. Americans with autism are citizens, friends, coworkers, sons, daughters, fathers, and mothers. No longer simply the objects of public policy, they are active participants in current policy debates. Pitney’s fascinating look at how public policy is made and implemented offers networks of concerned parents, educators, and researchers a compass to navigate the current systems and hope for a path towards more regularized and effective policies for America’s autism community.