Abstract

This study examines the initial impact of the COVID-19 pandemic on adults with physical disabilities from marginalized communities in southeastern Michigan, one of the early pandemic epicenters in the United States. A purposeful sample of fifteen adults with moderate to severe physical disabilities were recruited, taking part in individual remote semi-structured qualitative interviews, which were recorded, transcribed, and coded for emergent themes using a thematic approach to coding and analysis. Three interrelated, overarching themes emerged: fear, feelings of isolation, and a sense of being invisible. These were identified in the contexts of health and healthcare, home care assistance, and access to resources. The findings help illuminate the experiences of those from socioeconomically and racially marginalized communities, populations that are often "always already" vulnerable. Participant narratives made visible the negative impact of the pandemic on physical and mental health as well as the lack of accommodations available. They showed that participants were faced with a dilemma between engaging in risky behavior to have their needs met or avoiding risk and not have those needs met. This knowledge can expand awareness and appreciation of how social, economic, and political systems impact adults with physical disabilities in lower-income and racially diverse communities and provide guidance in designing future clinical and emergency response policies.

Highlights

  • In early March 2020, the World Health Organization (WHO) declared the spread of coronavirus disease 2019 (COVID-19) a pandemic

  • Drawing from remotely conducted interviews with those living or working in lower-income and primarily African American communities in Metro Flint and Detroit in southeastern Michigan, this study aims to identify the barriers and facilitators that impacted their experiences of the pandemic

  • The aim of this study was to center the experiences that adults with long-term physical disabilities from lower-income and racially marginalized communities encountered in the early months of the COVID-19 pandemic, despite living active, engaged lives prior to the pandemic

Read more

Summary

Introduction

In early March 2020, the World Health Organization (WHO) declared the spread of coronavirus disease 2019 (COVID-19) a pandemic. By early April, Michigan had almost 19,000 confirmed cases and 845 deaths [1]. As of 14 January 2021, there were 14,325 deaths in Michigan, ranking it eighth in the country. The pandemic may appear to be indiscriminate; some groups are at far greater risk for severe complications and negative impact than others. The distribution of these risks within society are socially and structurally determined and include age, sex, socioeconomic status, racial identities, and disability [2–4]. Poverty and race/ethnicity are key epidemiological factors that put people at risk for a severe case of COVID-19 [5,6]

Objectives
Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call