If You Dont Put it in Your Mind, then it Dont Matter: A Phenomenological Study of Coping Self-Efficacy in African American Women Diagnosed with Lupus

• Published in: Diversity and equality in health and care 2018, Vol.15 (4)
• Main Authors: Tyler M, Singleton, Nikki, Wooten, Trevor D, Faith, Edith M, Williams
• Format: Article
• Language: English
• Subjects: Activities of daily living; African Americans; Age; Arthritis; Autoimmune diseases; Chronic illnesses; Coping; Cultural awareness; Data analysis; Disease management; Empathy; Empowerment; Health care access; Human agency; Interviews; Lupus; Medicaid; Medical diagnosis; Minority & ethnic groups; Mortality; Patients; Perceptions; Quality of life; Relatives; Religion; Self awareness; Self care; Self-efficacy; Selfawareness; Spirituality; Stigma; White people; Women; Womens health
• ISSN: 2049-5471; 2049-5471; 2049-548X
• DOI: 10.21767/2049-5471.1000167

Lupus is a chronic debilitating rheumatic autoimmune disease that disproportionately affects African American women. A phenomenological approach was used to conduct confidential semi-structured qualitative interviews to explore “lived experiences” of coping and self-efficacy among 10 African American women diagnosed with lupus. Six major themes identified included self-awareness, religion and spirituality, a sense of connectedness, stigma, empowerment, and peer perceptions. These themes highlighted human agency and coping self-efficacy exhibited by African American women that facilitate chronic disease management and self-care. Perceptions of coping self-efficacy varied and the women’s “use of self” was instrumental to their individualized way of coping with their lupus diagnosis. Study findings increase cultural awareness, understanding, and potentially empathy from providers, employers/colleagues, and family members about African American women’s experiences of living with lupus.