Literature DB >> 33886382

An inductive qualitative content analysis of stigma experienced by people with rare diseases.

Marla Munro1, Abigail M Cook2, Kathleen R Bogart2.   

Abstract

OBJECTIVE: There are more than 6,000 known rare diseases (RDs), which are often serious, chronic, and progressive conditions. Cumulatively, having a RD is actually common, impacting an estimated 300 million people worldwide. While the stigmatization of some specific RDs has been studied, examining stigma in a large sample of many RDs allows for a broader understanding of patterns.
DESIGN: We used inductive qualitative content analysis to analyze survey responses to an open-ended question about challenges of living with a RD among 384 people with 178 distinct RDs.
RESULTS: We identified eight codes which were organized under the following three themes: structurally enacted, interpersonally enacted, and felt stigma. People with RDs experience structurally enacted stigma in the forms of healthcare stigma, education/workplace stigma, and an overall lack of accessibility. They also face interpersonally enacted stigma, including insufficient social support, a lack of understanding from others, and capitalist norms of productivity and self-sufficiency. Additionally, they experience felt stigma related to shame and the pressure to pass as able-bodied.
CONCLUSION: Possible solutions to RD stigma include increased education about RDs for healthcare professionals, a societal shift towards prioritizing accessibility, strengthened legal protections for disabled people, and expanded disability justice-focused community organizing.

Entities:  

Keywords:  ableism; disability; rare disease; rare disorder; stigma

Mesh:

Year:  2021        PMID: 33886382     DOI: 10.1080/08870446.2021.1912344

Source DB:  PubMed          Journal:  Psychol Health        ISSN: 0887-0446


  5 in total

1.  Healthcare access, satisfaction, and health-related quality of life among children and adults with rare diseases.

Authors:  Kathleen Bogart; Amanda Hemmesch; Erica Barnes; Thomas Blissenbach; Arthur Beisang; Patti Engel
Journal:  Orphanet J Rare Dis       Date:  2022-05-12       Impact factor: 4.303

2.  Understanding the ecosystem of patients with lysosomal storage diseases in Spain: a qualitative research with patients and health care professionals.

Authors:  Juan de Dios García-Díaz; Mónica López-Rodríguez; Montserrat Morales-Conejo; Antoni Riera-Mestre
Journal:  Orphanet J Rare Dis       Date:  2022-01-14       Impact factor: 4.123

3.  Treating rare diseases with the cinema: Can popular movies enhance public understanding of rare diseases?

Authors:  Jan Domaradzki
Journal:  Orphanet J Rare Dis       Date:  2022-03-05       Impact factor: 4.123

4.  'It was Supposed to be a Secret': a study of disclosure and stigma as experienced by adults with differences of sex development.

Authors:  Line Merete Mediå; Lena Fauske; Solrun Sigurdardottir; Kristin J Billaud Feragen; Charlotte Heggeli; Anne Wæhre
Journal:  Health Psychol Behav Med       Date:  2022-07-22

Review 5.  Psychosocial Considerations for the Child with Rare Disease: A Review with Recommendations and Calls to Action.

Authors:  Leslee T Belzer; S Margaret Wright; Emily J Goodwin; Mehar N Singh; Brian S Carter
Journal:  Children (Basel)       Date:  2022-06-21
  5 in total

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