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Diabetes‐related stigma affects the quality of life of people living with diabetes mellitus in S witzerland: implications for healthcare providers
Author(s) -
Gredig Daniel,
BartelsenRaemy Annabelle
Publication year - 2017
Publication title -
health and social care in the community
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.984
H-Index - 68
eISSN - 1365-2524
pISSN - 0966-0410
DOI - 10.1111/hsc.12376
Subject(s) - stigma (botany) , distress , quality of life (healthcare) , psychological intervention , gerontology , psychology , social support , health care , social stigma , clinical psychology , qualitative research , psychological distress , medicine , mental health , social psychology , psychiatry , nursing , family medicine , social science , human immunodeficiency virus (hiv) , sociology , economics , economic growth
Abstract There is a growing body of scientific evidence that stigma represents a reality for many people living with diabetes ( PWD ). However, little is known about the impact of experienced stigma. Against this background, the present study aimed to establish, by means of an in‐depth consideration of the situation in Switzerland, whether and how experienced and perceived stigma impact the quality of life of those PWD affected. In this cross‐sectional study, an anonymous paper‐and‐pencil self‐administered questionnaire ( SAQ ) was used for data collection. The SAQ drew on a qualitative elicitation study and was distributed in 2013 to the readers of a Swiss journal destined to people living with diabetes. Data were analysed using descriptive statistics and structural equation modelling. The sample included 3347 people (response rate of 16%) with type 1 and 2 diabetes, aged 16–96. Respondents who reported higher levels of perceived stigma reported higher levels of psychological distress (β = 0.37), more pronounced depressive symptoms (β = 0.33) and less social support (β = −0.22). Higher psychological distress (β = −0.29) and more pronounced depressive symptoms (β = −0.28), in turn, predicted lower quality of life. Findings suggest that stigma should be considered as an additional predictor of quality of life in PWD . Therefore, healthcare providers should support PWD 's fight against stigma. Especially, social workers are called to engage in advocacy to reduce discrimination against PWD and claim equal chances for them. They are also called to develop and implement interventions to correct stereotypes about PWD .