Abstract
Stigma remains a weight those with epilepsy have to carry and a defining feature of their identity. This article highlights recent studies published in the area of stigma, knowledge, attitudes, and practices regarding epilepsy. First, recent studies addressing the frequency of stigma and factors associated with stigma are discussed. Second, tools developed to ascertain stigma in epilepsy, or knowledge, attitudes, and practices, are examined. Lastly, we discuss interventions recently studied to reduce stigma in epilepsy.
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Acknowledgements
Kirsten M. Fiest is funded by an Alberta Innovates Health Solutions (AIHS) studentship. Nathalie Jette holds a Canada Research Chair in Neurological Health Services Research and an AIHS Population Health Investigator Award. Gretchen L. Birbeck is funded by the US NIH to conduct epilepsy-associated stigma research in Zambia. Ann Jacoby holds the Chair in Medical Sociology in the Department of Public Health, University of Liverpool, UK.
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Kirsten M. Fiest, Ann Jacoby, and Nathalie Jette declare that they have no conflict of interest.
Gretchen L. Birbeck has received grants from the NIH and travel/accommodation expenses from the WHO and the NIH.
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This article does not contain any studies with human or animal subjects performed by any of the authors.
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Fiest, K.M., Birbeck, G.L., Jacoby, A. et al. Stigma in Epilepsy. Curr Neurol Neurosci Rep 14, 444 (2014). https://doi.org/10.1007/s11910-014-0444-x
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DOI: https://doi.org/10.1007/s11910-014-0444-x