HIV/AIDS in Rural Communities


Book Description

This wide-ranging volume reviews the experience and treatment of HIV/AIDS in rural America at the clinical, care system, community, and individual levels. Rural HIV-related phenomena are explored within healthcare contexts (physician shortages, treatment disparities) and the social environment (stigma, the opioid epidemic), and contrasted with urban frames of reference. Contributors present latest findings on HIV medications, best practices, and innovative opportunities for improving care and care settings, plus invaluable first-person perspective on the intersectionality of patient subpopulations. These chapters offer both seasoned and training practitioners a thorough grounding in the unique challenges of providing appropriate and effective services in the region. Featured topics include: Case study: Georgia’s rural vs. non-rural populations HIV medications: how they work and why they fail Pediatric/adolescent HIV: legal and ethical issues Our experience: HIV-positive African-American women in the Deep South Learning to age successfully with HIV Bringing important detail to an often-marginalized population, HIV/AIDS in Rural Communities will interest and inspire healthcare practitioners including physicians, nurse practitioners, physician assistants, pharmacists, case managers, psychologists, social workers, counselors, and family therapists, as well as educators, students, persons living with HIV, advocates, community leaders, and policymakers.







Southeastern Conference on Rural Hiv/Aids, August 1997, Atlanta, Georgia


Book Description

Excerpt from Southeastern Conference on Rural Hiv/Aids, August 1997, Atlanta, Georgia: Issues in Prevention and Treatment (Conference Report) Faced with growing numbers of hiv and aids cases, service providers and volunteers in the rural Southeast have been forced to seek cre ative ways of building hiv service networks from meager resource bases. Although these net works are much smaller and less specialized than urban networks, they may ultimately be more enduring because they are part of the exist ing health and social structure rather than sup plements to it. Rural service providers have had to forge multiple linkages to be able to provide the array of services that are readily available from multipurpose clinics anol aids service organizations in large cities. In this sense, they are much more complex systems than their urban counterparts. About the Publisher Forgotten Books publishes hundreds of thousands of rare and classic books. Find more at www.forgottenbooks.com This book is a reproduction of an important historical work. Forgotten Books uses state-of-the-art technology to digitally reconstruct the work, preserving the original format whilst repairing imperfections present in the aged copy. In rare cases, an imperfection in the original, such as a blemish or missing page, may be replicated in our edition. We do, however, repair the vast majority of imperfections successfully; any imperfections that remain are intentionally left to preserve the state of such historical works.




HIV Screening and Access to Care


Book Description

Increased HIV screening may help identify more people with the disease, but there may not be enough resources to provide them with the care they need. The Institute of Medicine's Committee on HIV Screening and Access to Care concludes that more practitioners must be trained in HIV/AIDS care and treatment and their hospitals, clinics, and health departments must receive sufficient funding to meet a growing demand for care.




HIV Services in Rural and Remote Communities


Book Description

"Question: 1. What are the challenges and barriers to providing HIV/AIDS services in rural and remote AIDS service organizations in Canada? 2. What are some of the best practices for serving rural and remote populations"--Page [1].




Social Support and HIV/AIDS in Rural America


Book Description

Social support for people living with HIV in rural America remains a considerably understudied aspect of HIV/AIDS prevention. People living with HIV/AIDS (PLHA) require extensive support in order to remain in care, and reduce their viral suppression, and other disease complications. Without support, the likelihood that PLHA will refrain from or drop out of treatment options is gravely heightened, which consequently poses a significant threat for efforts to eliminate HIV as a public health issue. Using a mixed-method approach to Social Network Analysis, this study examines the principal role that social support plays in a person's likelihood to adhere to care and consequently, attain viral suppression. Specifically, it looks at the roles of the family, friends, partners/spouses, and healthcare providers. The study also explores how social relations serve as mediators to stigma and discrimination, especially for disproportionate groups. Closely linked to social support availability is the perceived level of significance of the type of support that is available to the subjects. The study therefore goes further to explore the subjects' perception of the support they receive (emotional, informational, and instrumental) and their satisfaction with it. This is imperative in that it sheds light on the role that the subjects' social relations plays in their retention in care. This research again takes an interdisciplinary approach by exploring the contribution of both communication and health communication strategies to effect behavioral change. It contributes to research on HIV/AIDS health equity, and infectious disease management. It also contributes to efforts to identify strategies to control the spread of HIV by proposing efficient ways to optimize social support through the stages of the Care Continuum and consequently, facilitate an increase in the number of people who attain viral suppression.