All over the world, families and communities are key providers of care and support. This is particularly true in relation to serious illnesses such as HIV and AIDS. Yet families and communities can also stigmatise their members, leaving people to die in the most appalling conditions. This book examines the diversity of family and community responses to HIV and AIDS. By examining contexts such as nuclear, extended and refugee family households, and gay community networks and structures, it offers insight into the factors which lead to positive responses and those which trigger negative ones.

First Published in 1989. Routledge is an imprint of Taylor & Francis, an informa company.

First Published in 1990. Routledge is an imprint of Taylor & Francis, an informa company.

All over the world, families and communities are key providers of care and support. This is particularly true in relation to serious illnesses such as HIV and AIDS. Yet families and communities can also stigmatize their members, leaving people to die in the most appalling conditions. This book looks at the diversity of family and community responses to HIV and AIDS. By examining contexts as diverse as nuclear, extended and refugee family households, and gay community networks and structures, it offers important insight into the factors which lead to positive responses and those which trigger negative ones.

From the start of the AIDS epidemic there have been calls for greater solidarity between affected groups and communities, and public health services. This can be seen both in the move towards healthy alliances in health service work, and in the demands of AIDS activists worldwide. This text brings together specially selected papers addressing these and related themes given at the Eighth Conference on Social Aspects of AIDS held in London in late 1995. Among the issues examined are profession and policy; the heightened vulnerability of groups such as women and younger gay men; and issues of drug use, disability and HIV prevention.

From the start of the AIDS epidemic there have been calls for greater solidarity between affected groups and communities, and public health services. This can be seen both in the move towards healthy alliances in health service work, and in the demands of AIDS activists worldwide. This text brings together specially selected papers addressing these and related themes given at the Eighth Conference on Social Aspects of AIDS held in London in late 1995. Among the issues examined are profession and policy; the heightened vulnerability of groups such as women and younger gay men; and issues of drug use, disability and HIV prevention.

Some 12 years into the epidemic, with an effective preventive vaccine or therapy against HIV disease still to be found, this book reflects on the contributions of social and behavioural research to the development of interventions for prevention. After over a decade's work documenting HIV and AIDS-related knowledge, attitudes and behaviour, social researchers have begun to focus more clearly on perceptions of sexual safety and risk, and the factors that contribute to these. The issues addressed by the book were examined during three major conferences in 1994: the annual conference of the British Sociological Association, the 2nd International Conference on the BioPsychoSocial Aspects of AIDS and the Xth International Conference on AIDS. The book brings together key papers presented at each of these conferences, documenting issues of focal concern to social researchers, policy makers and health educators in the mid-1990s.

Some 12 years into the epidemic, with an effective preventive vaccine or therapy against HIV disease still to be found, this book reflects on the contributions of social and behavioural research to the development of interventions for prevention. After over a decade's work documenting HIV and AIDS-related knowledge, attitudes and behaviour, social researchers have begun to focus more clearly on perceptions of sexual safety and risk, and the factors that contribute to these. The issues addressed by the book were examined during three major conferences in 1994: the annual conference of the British Sociological Association, the 2nd International Conference on the BioPsychoSocial Aspects of AIDS and the Xth International Conference on AIDS. The book brings together key papers presented at each of these conferences, documenting issues of focal concern to social researchers, policy makers and health educators in the mid-1990s.

HIV and AIDS have posed new challenges to societies, communities and individuals. In many parts of the world, existing health and social services have been hard pressed to cope with the dermands of the epidemic. In hospitals and in the community, new approaches to health education, support and care have been developed. Non-governmental and community organizations have had a central role to play in responding to the challenge of HIV and AIDS. "AIDS: Foundations for the Future" highlights progress made over the last decade, and offers an agenda for future activism and research. This book examines the extent to which sound foundations for the future have been laid in public, private and voluntary sector action. It focuses on topics as diverse as workplace policy on HIV and AIDS, voluntary sector responses, the reactions of health care workers, the experience of living with AIDS, outreach work and community action, patterns of male prostitution, and new interventions to promote and maintain safer sex and safer drug use.

In February 1989, the 3rd conference on Social Aspects of AIDS took place at South Bank Polytechnic. Social researchers working in psychology, socio logy, anthropology and education were represented, along with health care workers and members of statutory and voluntary organisations. The confe rence's themes emphasised the individual, cultural and policy dimen sions of HIV disease, and under these broad headings a wide range of paper s were given. This book contains many of the papers given at this conference as well as a number of additional contributions. The book is representative of a range of research currently under way. Some of the chapters are empir ical in their emphasis, some are more concerned with reporting on parti cular health education and health policy interventions, and some begin to develop a critique of some of the assumptions that operate in and aroun d contemporary social research agendas.

First Published in 1989. Routledge is an imprint of Taylor & Francis, an informa company.

AIDS: Rights, Risk and Reason contains a mix of papers linking research with the development of theoretical frameworks in a readable and accessibole style. Issues examined include: perceptions of risk and risk-taking behaviour; rights and responsibilities; and the rationality that underpins individual and collective responses to HIV/AIDS.