Tag Archives: Patient and Carer Experiences of Diagnosis

The Subjective Impact of Cognitive Impairment Upon People with Parkinson’s Disease (Parkinson’s Disease)

Summary Qualitative research which explores the subjective impact of cognitive impairment on people with Parkinson’s Disease and their carers / families. Full Text Link Reference Lawson, RA. Collerton, D. [and] Taylor, JP. [et al] (2018). Coping with cognitive impairment in … Continue reading

Posted in Community Care, For Carers (mostly), For Nurses and Therapists (mostly), For Researchers (mostly), For Social Workers (mostly), Person-Centred Care, Quick Insights, UK, Universal Interest | Tagged , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , | Leave a comment

Factors in Patients’ and Carers’ Experiences of Dementia Diagnosis and Treatment (PLoS Medicine)

Summary Early diagnosis and intervention for people with dementia is becoming a priority, as has been reflected in the “Dementia Case Finding Scheme”. Some GPs are concerned about the effects of early diagnosis and disclosure on patients and carers, however. … Continue reading

Posted in Community Care, Diagnosis, For Carers (mostly), For Doctors (mostly), For Nurses and Therapists (mostly), For Researchers (mostly), For Social Workers (mostly), Quick Insights, Systematic Reviews, UK, Universal Interest | Tagged , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , | Leave a comment