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1.
J Appl Res Intellect Disabil ; 34(1): 200-210, 2021 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-32939930

RESUMO

BACKGROUND: People with intellectual disabilities are at increased risk of forced marriage compared to those without intellectual disabilities. In the UK, this risk is particularly, though not exclusively, associated with South Asian communities and is linked to the desire to secure long-term care. METHOD: Focus groups and semi-structured interviews were undertaken with South Asian parents and family carers (n = 22) of adults with intellectual disability and the resultant data thematically analysed. RESULTS: Although securing care for their intellectually disabled relative was identified as a key motivator for forced marriage, other important themes also emerged. These included cultural and religious beliefs about disability and marriage, and limited understanding of relevant laws. Factors militating against forced marriage were also identified, including fears of abuse and neglect. CONCLUSIONS: Implications for the provision of services and the need for improved access to information on forced marriage of people with intellectual disabilities are highlighted.


Assuntos
Deficiência Intelectual , Deficiências da Aprendizagem , Adulto , Cuidadores , Grupos Focais , Humanos , Reino Unido
2.
J Appl Res Intellect Disabil ; 33(3): 354-363, 2020 May.
Artigo em Inglês | MEDLINE | ID: mdl-31621174

RESUMO

BACKGROUND: A common factor in the abuse of people with intellectual disabilities in residential settings has been the failure of care staff and frontline managers to recognise poor practice at an early stage and prevent its development into a culture of abuse. In this context, staff understandings of abuse and poor practice in residential services for people with intellectual disabilities were explored. METHOD: Semi-structured interviews (n = 56) were undertaken with care staff and frontline managers working across England. Interviews included the use of vignettes, based on real-life experiences of people with intellectual disabilities, to prompt discussion. RESULTS: Staff struggled to define either "abuse" or "poor practice", focussing more on individual acts or omissions than on institutional practices. When faced with vignettes, staff demonstrated a lack of agreement regarding what constitutes either abuse or poor practice. CONCLUSIONS: The implications for practice in residential care settings and for safeguarding training are discussed.


Assuntos
Atitude do Pessoal de Saúde , Deficiência Intelectual/enfermagem , Competência Profissional , Relações Profissional-Paciente , Instituições Residenciais , Violência , Adulto , Inglaterra , Feminino , Humanos , Masculino , Pesquisa Qualitativa
3.
Br J Soc Work ; 46(5): 1301-1317, 2016 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-27559229

RESUMO

Increasing numbers of adults in the UK are living with acquired brain injury (ABI), with those affected requiring immediate medical care and longer-term rehabilitative and social care. Despite their social needs, limited attention has been paid to people with ABI within the social work literature and their needs are also often overlooked in policy and guidance. As a means of highlighting the challenge that ABI presents to statutory social work, this paper will start by outlining the common characteristics of ABI and consider the (limited) relevant policy guidance. The particular difficulties of reconciling the needs of people with ABI with the prevailing orthodoxies of personalisation will then be explored, with a particular focus on the mismatch between systems which rest on presumptions autonomy and the circumstances of individuals with ABI-typified by executive dysfunction and lack of insight into their own condition. Composite case studies, drawn from the first author's experiences as a case manager for individuals with ABI, will be used to illustrate the arguments being made. The paper will conclude by considering the knowledge and skills which social workers need in order to better support people with ABI.

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