2022
DOI: 10.1080/09638288.2022.2155714
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A meta-ethnographic synthesis of the experiences of stigma amongst people with functional neurological disorder

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Cited by 15 publications
(12 citation statements)
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References 56 publications
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“…These perceived conflicts were also underpinned by perceptions of, and anticipation of, enacted stigma. The perceived stigma appeared to impact how participants viewed their own self‐identity, which is consistent with findings from a recent meta‐ethnographic synthesis (Foley et al, 2022). Stigma appeared to function across three levels: intra‐personally, interpersonally and structurally (Goffman, 1963; Link & Phelan, 2001).…”
Section: Discussionsupporting
confidence: 87%
See 1 more Smart Citation
“…These perceived conflicts were also underpinned by perceptions of, and anticipation of, enacted stigma. The perceived stigma appeared to impact how participants viewed their own self‐identity, which is consistent with findings from a recent meta‐ethnographic synthesis (Foley et al, 2022). Stigma appeared to function across three levels: intra‐personally, interpersonally and structurally (Goffman, 1963; Link & Phelan, 2001).…”
Section: Discussionsupporting
confidence: 87%
“…There is considerable research highlighting that broader mental health stigma impacts seeking and participating in mental health care (Corrigan et al, 2014). Additionally, a recent systematic review highlighted how individuals may attempt to manage FND stigma by adopting coping styles that inadvertently worsen their condition (e.g., self‐isolation; Foley et al, 2022). Although it is acknowledged that individuals with FND experience significant stigma, current research has focused predominately on experiences in medical settings.…”
Section: Introductionmentioning
confidence: 99%
“…Patients with FND are typically seen either in extremely busy general neurology clinics in acute hospitals or in general practices, where rushed consultations are likely to be unsatisfactory for clinician and patient alike. Patients with FND frequently report negative relationships with HCPs in Ireland and elsewhere (O'Keeffe et al., 2021 ; Rawlings & Reuber, 2016 ) and experience a sense of invalidation regarding symptoms (Foley et al., 2022 ). It is possible that these difficulties are amplified by insufficient clinic time.…”
Section: Discussionmentioning
confidence: 99%
“…Patients with FND often report delayed and poor communication in diagnosis, negative relationships with HCPs and challenges in accessing services and supports (O'Keeffe et al., 2021 ; Rawlings & Reuber, 2016 ). The patient experience can often involve feelings of stigma and a sense of invalidation regarding symptoms (Foley et al., 2022 ).…”
Section: Introductionmentioning
confidence: 99%
“…Earlier this year, a paper in the European Journal of Neurology ( Mason et al, 2023 ) cited a different SNSS paper ( Stone et al, 2009 ) to support the assertion that FND prevalence at outpatient neurology clinics was 5.4 %—far lower than the percentage needed to be the “2nd most common” diagnosis. Moreover, the authors of another paper ( Foley et al, 2022 ) have recently issued a correction for the same misstatement of FND prevalence from the SNSS findings as the one identified in Perez et al…”
mentioning
confidence: 91%