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It’s about equality!” Disability advocacy in the UK

Bibliographic Data

ID12314196
AuthorsRebecca Fish (0000-0003-1933-1769, University of Lancashire, corresponding author), Alexander Wilde (0000-0003-1583-3833, Northumbria University), Ruth Malkin (Independent researcher)
Year2025
Volume41
Issue4
Pages1040-1059
Publication date2025-11-26
Open AccessYes
TypeARTICLE
VenueDisability & Society (JOURNAL)
Journal identifiersISSN: 0968-7599 • E-ISSN: 1360-0508
PublisherTaylor & Francis (PUBLISHER • GB)
DOI10.1080/09687599.2025.2586677
OpenAlexW4416715597
LanguageEN
References cited22

Advocacy means taking action to support people to secure their rights, pursue their interests, and obtain services they need. This study aimed to find out people’s knowledge and experiences of advocacy, as well as their recommendations for the improvement of advocacy services. Forty-six people from various regions of the UK were interviewed online, and 193 people completed a survey. Participants had different impairments, and some were family members of disabled people, most of whom experienced impairment and disability themselves. People said that they would like more access to advocacy services to support them with many areas of their lives, such as to reduce isolation, accessing employment and healthcare, support with benefits and help with documentation, financial support and advice, and to challenge inaccessibility and discrimination. There is a need for improved general statutory advocacy that involves disabled people as advocates, along with greater awareness of what is offered

Action (physics · Disabled people · Family support · Patient advocacy · Self-advocacy · Statutory law · Disability Rights and Representation · Healthcare innovation and challenges · Social Work Education and Practice

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Highly citedNo

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