Stigma and quality of life in adults with sickle cell disease in Jamaica and the United States

Author:

Bulgin Dominique1ORCID,Asnani Monika2ORCID,Vorderstrasse Allison3,Royal Charmaine4,Pan Wei5,Tanabe Paula5

Affiliation:

1. Duke University School of Nursing, Duke University National Clinician Scholars Program Durham

2. Caribbean Institute for Health Research- Sickle Cell Unit, The University of the West Indies, Mona, Jamaica

3. University of Massachusetts Amherst College of Nursing, Amherst

4. Departments of African & African American Studies, Biology, Global Health, and Family Medicine & Community Health, Duke University, Durham, NC, USA

5. Duke University School of Nursing, Duke University School of Medicine, Durham

Funder

National Institute of Nursing Research

Publisher

Informa UK Limited

Subject

Psychiatry and Mental health,Applied Psychology,Clinical Psychology

Reference28 articles.

1. The Measure of Sickle Cell Stigma: Initial findings from the Improving Patient Outcomes through Respect and Trust study

2. Stigma of Sickle Cell Disease: A Systematic Review

3. CDC. (2016, August 31). Data & statistics on sickle cell disease | CDC. Centers for Disease Control and Prevention. https://www.cdc.gov/ncbddd/sicklecell/data.html

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