Search

Effective solutions to biodiversity loss are multidimensional, requiring engagement from diverse stakeholders across various sectors and commitment levels. In this context, voluntary actions from community members emerge as a valuable addition to the large‐scale nature conservation activities conducted by states and municipalities. Such actions complement biodiversity protection measures and legal requirements aimed at companies. This article delves into the rescaling of biodiversity offsetting to the community members level and explores it from the perspective of community members. Through workshops organized in four Finnish municipalities, participants were prompted to reflect on biodiversity offsetting in their daily lives. The results show community members' limited resources to conduct pro‐biodiversity actions and highlight their diverse interpretations of the topic. Beyond direct biodiversity‐enhancing action, like maintaining rural biotopes, eradicating alien species, or protecting forests, workshop participants called for indirect actions. These included education, eco‐taxes, and the development of sharing economies. Thus, rather than solely focusing on biodiversity offsetting or the mitigation hierarchy, these suggestions underscore the need for diverse pro‐biodiversity actions at the community member's level. Furthermore, the results highlight the need for support that enables community members and communities' work for biodiversity. Introducing the concept of nature amends addresses this need, enhancing the mitigation hierarchy's capacity to incorporate community members in nature conservation endeavors. [ABSTRACT FROM AUTHOR]

Objectives were (a) to understand a community‐informed narrative, as told by community members (CMs) and community partners (CPs), about the strengths, experiences, and perspectives of public housing communities; and (b) to analyze similarities and differences between CMs' and CPs' experiences and perspectives. Qualitative interviews were conducted with 22 CMs of public housing (ages 26–58, 100% female caregivers, 96% Black, 4% multiethnic) and 43 CPs (ages 28–78, 67.4% female, 81.4% Black and African American). Four themes were derived from the CM and CP interviews: (1) counters to public narratives, (2) disinvestment begets disinvestment, (3) community conditions should be better, and (4) community cohesion and connection. Findings from this study present community‐centered narratives and experiences that were counter to stereotyped public narratives and could influence public perceptions and behavior to inform policy changes related to improving living conditions and supporting CMs in public and low‐income housing communities. [ABSTRACT FROM AUTHOR]

Introduction: To investigate the association between individual and community‐level measures of HIV stigma and HIV incidence within the 21 communities participating in the HPTN (071) PopART trial in Zambia and South Africa. Methods: Secondary analysis of data from a population‐based cohort followed‐up over 36 months between 2013 and 2018. The outcome was rate of incident HIV infection among individuals who were HIV negative at cohort entry. Individual‐level exposures, measured in a random sample of all participants, were: (1) perception of stigma in the community, (2) perception of stigma in health settings and (3) fear and judgement towards people living with HIV. Individual‐level analyses were conducted with adjusted, individual‐level Poisson regression. Community‐level HIV stigma exposures drew on data reported by people living with HIV, health workers and community members. We used linear regression to explore the association between HIV stigma and community‐level HIV incidence. Results: Among 8172 individuals who were HIV negative and answered individual‐level stigma questions at enrolment to the cohort, there was no evidence of a statistically significant association between any domain of HIV stigma and risk of incident HIV infection. Among the full cohort of 26,110 individuals among whom HIV incidence was measured, there was no evidence that community‐level HIV incidence was associated with any domain of HIV stigma. Conclusions: HIV stigma is often cited as a barrier to the effectiveness of HIV prevention programming. However, in the setting for the HPTN 071 "PopART trial," measured stigma alone was not associated with the risk of HIV infection. [ABSTRACT FROM AUTHOR]

SUMMARY: Objective: To describe local perceptions of blood transfusion for children with severe anaemia in Uganda. Background: Blood transfusion is a common emergency treatment for children with severe anaemia and saves millions of lives of African children. However, the perceptions of transfusion recipients have not been well studied. A better understanding of the perceived risk may improve transfusion care. Methods: A qualitative study based on 16 in‐depth interviews of caregivers of transfused children, and six focus group discussions with community members was conducted in three regions of Uganda between October and November 2017. Results: Caregivers of children and community members held blood transfusion in high regard and valued it as life‐saving. However, there were widespread perceived transfusion risks, including: Human immunodeficiency virus (HIV) transmission, too rapid blood infusion and blood incompatibility. Other concerns were: fatality, changes in behaviour, donor blood being 'too strong' and use of animal blood. In contrast, recent transfusion, older age, knowledge of HIV screening of blood for transfusion, faith in God and having a critically ill child were associated with less fear about transfusion. Respondents also emphasised challenges to transfusion services access including distance to hospitals, scarcity of blood and health workers' attitudes. Conclusion: Perceptions of the community and caregivers of transfused children in Uganda about blood transfusion were complex: transfusion is considered life‐saving but there were strong perceived transfusion risks of HIV transmission and blood incompatibility. Addressing community perceptions and facilitating access to blood transfusion represent important strategies to improve paediatric transfusion care. [ABSTRACT FROM AUTHOR]

ABSTRACT There are many constraints to implementing comprehensive health insurance in the context of Sub-Saharan Africa. Mutual health organizations are under pressure to resolve the inadequacies, accordingly. The objective of this study is to explore the extent to which the mutual health organizations constitute facilitators and/or barriers to the successful implementation of the health insurance scheme nationwide. Data were gathered through interviews and review of literature. The findings of the empirical data were analyzed using theories of health seeking behaviour and reflexive communities. The findings of the paper suggest that the mutual health organizations are beneficial to their communities as they have broadened the understanding of the community members, regarding what the concept of health insurance was in Ghana, a country where it was a relatively new concept in public health financing and delivery. However, the paper also observes that the mutual health organizations are facing problems that are likely to affect sustainability overtime under a national health insurance scheme. Therefore, the need for continuous public education to sustain the enthusiasm among community members is recommended. [ABSTRACT FROM AUTHOR]

Introduction: The African American church is a highly influential institution with the potential to greatly increase the reach of HIV prevention interventions and address HIV‐related stigma in US African American communities. However, there are few studies on HIV‐related stigma and African American church populations. This study explored HIV‐related stigma among church and community members participating in an HIV education and testing intervention pilot study in African American churches, named Taking It to the Pews. Methods: Four African American churches located in Kansas City, MO and KS, were randomized to either intervention or comparison groups. Churches assigned to the intervention group received religiously tailored HIV education, testing and compassion messages/activities (e.g., sermons, brochures/church bulletins, testimonials) via the Taking It to the Pews HIV Tool Kit. Comparison churches received non‐religiously tailored HIV information. HIV‐related stigma was assessed with 543 church members and with community members served through church outreach services (e.g., food/clothing pantries, social services) in the four churches. Participants completed surveys at baseline, 6 months and 12 months to assess their HIV‐related stigma beliefs, exposure to intervention components and satisfaction with the study. Results: At baseline, HIV‐related stigma beliefs were similar across experimental groups and were quite low. Mean HIV‐related stigma scores were not significantly different between experimental groups at 6 months (p=0.92) or at 12 months (p=0.70). However, mean HIV‐related stigma scores within both groups showed decreasing trends at six months, which approached significance. Analysis of previously studied HIV‐related stigma factors (e.g., age, gender, income, HIV knowledge, religiosity) did not yield changes in the null findings. Intervention group participants were highly exposed to several intervention components (sermons, HIV resource tables, posters, brochures/church bulletins). Overall, participants were highly satisfied with the intervention pilot study. Conclusions: African American churches may be well positioned to increase the reach of HIV prevention interventions to church and community members and could serve an important role in addressing HIV‐related stigma in their church communities. Future research is needed on measuring HIV‐related stigma beliefs and on testing intensive, scalable, religiously tailored HIV interventions to impact HIV‐related stigma in African American churches. [ABSTRACT FROM AUTHOR]