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The Experiences of Carers of Adults With Intellectual Disabilities During the First COVID-19 Lockdown Period.
Patel, Varsha; Perez-Olivas, Gisela; Kroese, Biza Stenfert; Rogers, Gemma; Rose, John; Murphy, Glynis; Cooper, Vivien; Langdon, Peter E; Hiles, Steve; Clifford, Clair; Willner, Paul.
  • Patel V; Birmingham Community Healthcare NHS Foundation Trust Unit 3 Priestley Wharf, Holt Street Birmingham B7 4BN UK.
  • Perez-Olivas G; Hertfordshire Partnership University NHS Foundation Trust 99 Waverley Road, St Albans Hertfordshire AL3 5TQ UK.
  • Kroese BS; University of Birmingham, School of Psychology Edgbaston Birmingham B15 2TT UK.
  • Rogers G; Kent and Medway NHS and Social Care Partnership Trust, The Tarentfort Centre Bow Arrow Lane, Dartford Kent DA2 6PB UK.
  • Rose J; Division of Psychiatry University College London Maple House, 149 Tottenham Court Road London W1T 7BN UK.
  • Murphy G; University of Birmingham, School of Psychology Edgbaston Birmingham B15 2TT UK.
  • Cooper V; University of Kent Tizard Centre, Cornwallis North East Canterbury Kent CT2 7NF UK.
  • Langdon PE; Challenging Behaviour Foundation, The Old Courthouse New Road Avenue, Chatham Kent ME4 6BE UK.
  • Hiles S; Centre for Educational Development, Appraisal and Research University of Warwick Coventry CV4 7AL UK.
  • Clifford C; Centre for Mental Health and Wellbeing Research, Warwick Medical School University of Warwick Coventry CV4 7AL UK.
  • Willner P; Coventry and Warwickshire Partnership NHS Trust, Wayside House Wilsons Lane Coventry CV6 6NY UK.
J Policy Pract Intellect Disabil ; 18(4): 254-262, 2021 Dec.
Article in English | MEDLINE | ID: covidwho-1234251
ABSTRACT

Background:

The recent COVID-19 pandemic led to widespread international restrictions, severely impacting on health and social care services. For many individuals with an intellectual disability (ID) this meant reduced access to services and support for them and their carers.

Aim:

The aim of this study was to gain insight into the ways parents of adults with ID coped during the first 2020 lockdown period.

Methods:

Eight parents of adults with ID were interviewed. The recordings of these interviews were subjected to a thematic analysis.

Results:

Four main themes were identified powerless and unappreciated; coping under lockdown; support; and the impact of lockdown on well-being.

Conclusions:

The parents of adults with ID who made up our sample reported that they received little support from services and experienced a sense of powerlessness. Nevertheless, they were open to accepting support from family and friends and showed remarkable resilience. These findings are discussed in the light of the Willner et al. (2020) survey results on parental mental health and coping, and suggestions for future service provision during pandemic conditions are proposed.
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Full text: Available Collection: International databases Database: MEDLINE Type of study: Observational study / Qualitative research Language: English Journal: J Policy Pract Intellect Disabil Year: 2021 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Observational study / Qualitative research Language: English Journal: J Policy Pract Intellect Disabil Year: 2021 Document Type: Article