Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2013 Oct;25(10):563-566.
doi: 10.1111/1745-7599.12008. Epub 2013 Feb 19.

The invisible and visible stigmatization of Parkinson's disease

Affiliations

The invisible and visible stigmatization of Parkinson's disease

Melinda Hermanns. J Am Assoc Nurse Pract. 2013 Oct.

Abstract

Purpose: To discuss the visible and invisible stigma shared by seven men and seven women with Parkinson's disease (PD), a chronic, progressive, neurodegenerative disorder characterized by overt physical and covert psychological manifestations.

Data sources: An ethnographic approach using interview data, participant observations, and fieldwork was used. Field data were generated from a 2-year exposure to two PD support groups in east Texas. The question "what does it mean to you to have Parkinson's disease"? illuminated the experience of everyday life and the existential meaning of what it means to live with this disease.

Conclusions: The invisible stigma was that of a changing self, a self with PD, a form of disability, which attested to the stigma and mounting isolation. Feelings of isolation were exacerbated by both the stigmatization associated with being different, coupled with the realization that life would never be the same. Facial masking was identified as one of the visible features that were commonly reported by all participants.

Implications for practice: Healthcare professionals can be more attuned to the visible and invisible manifestations of PD that are associated with stigma through the incorporation of a holistic assessment to identify perceived stigma in persons living with the disease.

Keywords: Qualitative; chronic illness; culture; family.

PubMed Disclaimer

References

    1. Conrad, P., & Barker, K. (2010). The social construction of illness: Key insights and policy implications. Journal of Health and Social Behavior, 51, 67–79.
    1. Mayor, V. (2006). Long-term conditions. 3: Being an expert patient. British Journal of Community Nursing, 11(2), 59–63.
    1. Moore, S., & Knowles, S. (2006). Beliefs and knowledge about Parkinson's disease. E-Journal of Applied Psychology: Clinical and Social Issues, 2(1), 15–21.
    1. Paterson, B., Thorne, S., Crawford, J. & Tarko, M. (1999). Living with diabetes as a transformational experience. Qualitative Health Research, 9(6), 786–802.
    1. Phillips, M. J. (1990). Damaged goods: Oral narratives of the experience of a disability in American culture. Social Science and Medicine, 30, 849–857.

LinkOut - more resources