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Tag Archives: Anger (Upon Disclosure of Diagnosis
Experiences of the Patient Journey into Alzheimer’s Disease (Alzheimer’s Society)
Summary This research report, from Lilly UK and the Alzheimer’s Society, explores the experience of progression through stages in the development of dementia, from the early signs to diagnosis and beyond. Full Text Link Reference The ‘patient journey’ for people … Continue reading →
Posted in Acute Hospitals, Alzheimer's Society, Charitable Bodies, Community Care, Diagnosis, For Carers (mostly), For Doctors (mostly), For Nurses and Therapists (mostly), For Researchers (mostly), For Social Workers (mostly), Management of Condition, National, Patient Care Pathway, Person-Centred Care, Personalisation, Practical Advice, Quick Insights, UK, Universal Interest
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Tagged Age-Related Memory Loss, Alzheimer Experience, Anger (Upon Disclosure of Diagnosis, Assessment and Diagnosis, Barriers to Early Diagnosis, Carer's Experience of Dementia, Carers’ Experiences of the Dementia Journey, Coping Mechanisms, Coping Strategies, Coping with Memory Loss, Dementia Diagnosis, Diagnosis and Referral, Diagnosis of Alzheimer's Disease, Diagnosis of Dementia, Disclosure, Disclosure of Diagnosis, Eli Lilly, Emotions (Upon Disclosure of Diagnosis, Experiences, Experiences of Diagnosis, Experiences of the Transition to Dementia, Fear (Upon Disclosure of Diagnosis, Frustration (Upon Disclosure of Diagnosis, Impact of Diagnosis, Initial Onset and Diagnosis, Lilly, Lilly UK, Living Well After Diagnosis, Loss (Upon Disclosure of Diagnosis, Mapping the Patient Journey, Memory Clinics, Memory Lapses, Memory Loss, Memory Services, Mild Memory Problems, NHS Memory Clinics, Patient Experience, Patient Journey into Alzheimer's Disease, Post-Diagnosis Support, Psychological Coping Skills, Service User Experience, Support and Coping Mechanisms, upon, User Experience
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GP’s Dementia Guide: Living Well After Diagnosis (Alzheimer’s Society)
Summary A Dementia Guide has been produced for GPs and psychiatrists to help them provide more support to patients diagnosed with the condition (and better support for their carers). This free booklet, produced by the Alzheimer’s Society and sponsored by … Continue reading →
Posted in ADASS, Alzheimer's Society, Charitable Bodies, Community Care, Department of Health, Diagnosis, For Carers (mostly), For Doctors (mostly), For Nurses and Therapists (mostly), For Researchers (mostly), For Social Workers (mostly), Integrated Care, Management of Condition, Mental Health, Models of Dementia Care, National, NHS, Non-Pharmacological Treatments, Patient Care Pathway, Person-Centred Care, Pharmacological Treatments, Practical Advice, Quick Insights, Royal College of Psychiatrists, Standards, UK, Universal Interest
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Tagged All-Party Parliamentary Group on Dementia, Alzheimer's Society, Anger (Upon Disclosure of Diagnosis, Anxiety, APPG on Dementia, Association of Directors of Adult Social Services (ADASS), Barriers to Early Diagnosis, Care and Support Planning, Care Planning, Caregiver Support, Carer Support, Community Support, Coping with Memory Loss, Dementia and Driving Guidance, Dementia Research, Depression, Disclosure of Diagnosis, Driving, Driving and Dementia, Early Diagnosis, Experiences of Diagnosis, Family Support, Fear (Upon Disclosure of Diagnosis, Financial Issues, Financial Planning, Frustration (Upon Disclosure of Diagnosis, GP’s Dementia Guide, GPs, Living Well After Diagnosis, Living Well with Dementia, Loss (Upon Disclosure of Diagnosis, Medical Research, Memory Loss, Post-Diagnosis Support, RCGP, Recent Diagnosis, Royal College of General Practitioners (RCGP), Signposting, Support, Support for Carers, Support Networks, Supportive Environments, Timely Diagnosis, Unlocking Diagnosis
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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
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Tagged Anger (Upon Disclosure of Diagnosis, Assessment and Diagnosis, Autonomy and Safety, Barriers to the Diagnosis and Management of Patients with Dementia in Primary Care, Breaking Bad News, Burden of Dementia, Burden on Caregivers, Care Transitions, Case Finding for Patients with Dementia, Centre for Research in Primary and Community Care: University of Hertfordshire, Coping Strategies, Dementia Case Finding, Dementia Case Finding Scheme, Dementia Diagnosis, Diagnosis, Diagnosis and Assessment, Diagnosis of Alzheimer's Disease, Disclosure, Disclosure of Diagnosis, Early Diagnosis, Emotional Strategies, Experiences of Diagnosis, Experiences of the Transition to Dementia, Family Support, Fear (Upon Disclosure of Diagnosis, Feelings of Loss Anger Fear and Frustration, Frustration (Upon Disclosure of Diagnosis, Identity, Loss (Upon Disclosure of Diagnosis, Maintaining Identity, Managing Transitions, Patient and Carer Experiences of Dementia Diagnosis and Treatment, Patient and Carer Experiences of Diagnosis, Patient Experience, PLoS Medicine, Positive Mindsets, Practical Strategies, Reminders, Sense of Identity, Social Strategies, Strategies for Living, Survival After Diagnosis of Dementia, Transition, Transition from Cognitive Impairment to Dementia, Transition to Dementia: Individual and Family Experiences, Unequal Relationships, University of Hertfordshire
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