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Patient organizations and social health movements offer one of the
most important and illuminating examples of civil society
engagement and participation in scientific research and research
politics. Influencing the research agenda, and initiating, funding
and accelerating the development of diagnostic tools, effective
therapies and appropriate health-care for their area of interest,
they may champion alternative, sometimes controversial, programs or
critique dominant medical paradigms. Some movements and
organizations advocate for medical recognition of contested
illnesses, as with fibromyalgia orADHD, while some attempt to
"de-medicalize" others, such as obesity or autism. Bringing
together an international selection of leading scholars and
representatives from patients' organizations, this comprehensive
collection explores the interaction between civil society groups
and biomedical science, technology development, and research
politics. It takes stock of the key findings of the research
conducted in the field over the past two decades and addresses
emerging problems and future challenges concerning the
interrelations between health movements and patient organisations
on the one hand, and biomedical research and research policies on
the other hand. Combining empirical case studies with conceptual
discussion, the book discusses how public participation can
contribute to, as well as restrict, the democratization of
scientific knowledge production. This volume is an important
reference for academics and researchers with an interest in the
sociology of health and illness, science and technology studies,
the sociology of knowledge, medical ethics or healthcare management
and research, as well as medical researchers and those involved
with health-related civil society organizations.
Patient organizations and social health movements offer one of the
most important and illuminating examples of civil society
engagement and participation in scientific research and research
politics. Influencing the research agenda, and initiating, funding
and accelerating the development of diagnostic tools, effective
therapies and appropriate health-care for their area of interest,
they may champion alternative, sometimes controversial, programs or
critique dominant medical paradigms. Some movements and
organizations advocate for medical recognition of contested
illnesses, as with fibromyalgia orADHD, while some attempt to
"de-medicalize" others, such as obesity or autism. Bringing
together an international selection of leading scholars and
representatives from patients' organizations, this comprehensive
collection explores the interaction between civil society groups
and biomedical science, technology development, and research
politics. It takes stock of the key findings of the research
conducted in the field over the past two decades and addresses
emerging problems and future challenges concerning the
interrelations between health movements and patient organisations
on the one hand, and biomedical research and research policies on
the other hand. Combining empirical case studies with conceptual
discussion, the book discusses how public participation can
contribute to, as well as restrict, the democratization of
scientific knowledge production. This volume is an important
reference for academics and researchers with an interest in the
sociology of health and illness, science and technology studies,
the sociology of knowledge, medical ethics or healthcare management
and research, as well as medical researchers and those involved
with health-related civil society organizations.
Dass Gedachtnis, Erinnern und Vergessen eine koerperliche Seite
haben oder sogar koerperliche Vorgange sind, ist eine Einsicht, die
auch von der Soziologie geteilt wird. Gesellschaftliche und
gesellschaftlich gepragte individuelle Erlebnisse hinterlassen ihre
Spuren im Koerper, Spuren, die an Vergangenes erinnern und
Verhalten wie Handeln in Gegenwart und im Hinblick auf die Zukunft
zu orientieren vermoegen. Die in diesem Band enthaltenen Beitrage
nehmen sich der Frage nach dem Koerpergedachtnis jenseits der
Vorstellung eines Koerper-Geist-Dualismus an. Dabei werden sowohl
sozialtheoretische Fragen des Zusammenhangs von Koerper und
Gedachtnis als auch unterschiedliche Facetten des
Koerpergedachtnisses in konkreten praktischen Zusammenhangen
behandelt.
Das Buch mochte mit den beiden Konzepten "Soziologie des
wissenschaftlichen Nichtwissens" und "Science Assessment" einen
Beitrag zur Analyse der gegenwartigen Situation der
Wissensgesellschaft leisten und damit neue Perspektiven fur die
Wissenschaftsforschung sowie Impulse zur politischen Gestaltung des
Verhaltnisses von Wissenschaft und Gesellschaft geben."
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