The Care Act Information Duty in a digital age: What do we need to consider for improving both the information and our practice?

The internet

Background Since the implementation of the Care Act 2014, information has been a statutory duty of Local Authorities. Under the Care Act section 4 of the Care Act, Local Authorities (LAs) have particular responsibilities around providing information to carers and care and support recipients, however how that information is, or should be, provided, as well [read the full story…]

Sharpening the focus: viewing self-harm images online – harmful and protective?

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Jo Lockwood, Camilla Babbage and Ellen Townsend consider a systematic review exploring the impact of viewing self-harm images online, which finds that images can trigger powerful emotions and may relate to a change in cognition, affect and behaviour.

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Online experiences: a risk factor for suicide?

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Louise La Sala and Jo Robinson review a UK-wide case series study of young people who died by suicide, which explores their previous suicide-related online experiences.

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Talking to young people about online safety: the who, what, when and how

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In his debut blog, Luke Bayliss explores a Delphi study that will help mental health practitioners to converse with young people about their online activities and impact on mental health.

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Mental health stigma and online social support for bipolar disorder: what can we learn from Twitter?

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Charlotte Walker explores an online ethnography study that explores how Twitter users discuss mental illness, particularly bipolar disorder, and in what context; focusing specifically on the areas of stigma and social support.

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