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Being parents with epilepsy: thoughts on its consequences and difficulties affecting their children
OBJECTIVE: Parents with epilepsy can be concerned about the consequences of epilepsy affecting their children. The aim of this paper is to describe aspects of what it means being a parent having epilepsy, focusing the parents’ perspectives and their thoughts on having children. METHODS: Fourteen adu...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Dove Medical Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4455853/ https://www.ncbi.nlm.nih.gov/pubmed/26064047 http://dx.doi.org/10.2147/NDT.S74222 |
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author | Gauffin, Helena Flensner, Gullvi Landtblom, Anne-Marie |
author_facet | Gauffin, Helena Flensner, Gullvi Landtblom, Anne-Marie |
author_sort | Gauffin, Helena |
collection | PubMed |
description | OBJECTIVE: Parents with epilepsy can be concerned about the consequences of epilepsy affecting their children. The aim of this paper is to describe aspects of what it means being a parent having epilepsy, focusing the parents’ perspectives and their thoughts on having children. METHODS: Fourteen adults aged 18–35 years with epilepsy and subjective memory decline took part in focus-group interviews. The interviews were conducted according to a semi-structured guideline. Material containing aspects of parenthood was extracted from the original interviews and a secondary analysis was done according to a content-analysis guideline. Interviews with two parents for the Swedish book Leva med epilepsi [To live with epilepsy] by AM Landtblom (Stockholm: Bilda ide; 2009) were analyzed according to the same method. RESULTS: Four themes emerged: (1) a persistent feeling of insecurity, since a seizure can occur at any time and the child could be hurt; (2) a feeling of inadequacy – of not being able to take full responsibility for one’s child; (3) acknowledgment that one’s children are forced to take more responsibility than other children do; and (4) a feeling of guilt – of not being able to fulfill one’s expectations of being the parent one would like to be. CONCLUSION: The parents with epilepsy are deeply concerned about how epilepsy affects the lives of their children. These parents are always aware that a seizure may occur and reflect on how this can affect their child. They try to foresee possible dangerous situations and prevent them. These parents were sad that they could not always take full responsibility for their child and could not live up to their own expectations of parenthood. Supportive programs may be of importance since fear for the safety of the child increases the psychosocial burden of epilepsy. There were also a few parents who did not acknowledge the safety issue of their child – the authors believe that it is important to identify these parents and provide extra information and support to them. |
format | Online Article Text |
id | pubmed-4455853 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-44558532015-06-10 Being parents with epilepsy: thoughts on its consequences and difficulties affecting their children Gauffin, Helena Flensner, Gullvi Landtblom, Anne-Marie Neuropsychiatr Dis Treat Original Research OBJECTIVE: Parents with epilepsy can be concerned about the consequences of epilepsy affecting their children. The aim of this paper is to describe aspects of what it means being a parent having epilepsy, focusing the parents’ perspectives and their thoughts on having children. METHODS: Fourteen adults aged 18–35 years with epilepsy and subjective memory decline took part in focus-group interviews. The interviews were conducted according to a semi-structured guideline. Material containing aspects of parenthood was extracted from the original interviews and a secondary analysis was done according to a content-analysis guideline. Interviews with two parents for the Swedish book Leva med epilepsi [To live with epilepsy] by AM Landtblom (Stockholm: Bilda ide; 2009) were analyzed according to the same method. RESULTS: Four themes emerged: (1) a persistent feeling of insecurity, since a seizure can occur at any time and the child could be hurt; (2) a feeling of inadequacy – of not being able to take full responsibility for one’s child; (3) acknowledgment that one’s children are forced to take more responsibility than other children do; and (4) a feeling of guilt – of not being able to fulfill one’s expectations of being the parent one would like to be. CONCLUSION: The parents with epilepsy are deeply concerned about how epilepsy affects the lives of their children. These parents are always aware that a seizure may occur and reflect on how this can affect their child. They try to foresee possible dangerous situations and prevent them. These parents were sad that they could not always take full responsibility for their child and could not live up to their own expectations of parenthood. Supportive programs may be of importance since fear for the safety of the child increases the psychosocial burden of epilepsy. There were also a few parents who did not acknowledge the safety issue of their child – the authors believe that it is important to identify these parents and provide extra information and support to them. Dove Medical Press 2015-05-27 /pmc/articles/PMC4455853/ /pubmed/26064047 http://dx.doi.org/10.2147/NDT.S74222 Text en © 2015 Gauffin et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Gauffin, Helena Flensner, Gullvi Landtblom, Anne-Marie Being parents with epilepsy: thoughts on its consequences and difficulties affecting their children |
title | Being parents with epilepsy: thoughts on its consequences and difficulties affecting their children |
title_full | Being parents with epilepsy: thoughts on its consequences and difficulties affecting their children |
title_fullStr | Being parents with epilepsy: thoughts on its consequences and difficulties affecting their children |
title_full_unstemmed | Being parents with epilepsy: thoughts on its consequences and difficulties affecting their children |
title_short | Being parents with epilepsy: thoughts on its consequences and difficulties affecting their children |
title_sort | being parents with epilepsy: thoughts on its consequences and difficulties affecting their children |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4455853/ https://www.ncbi.nlm.nih.gov/pubmed/26064047 http://dx.doi.org/10.2147/NDT.S74222 |
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