Care home or home care? : difficult decisions for people with dementia and their carers

Article

WORTLEY, Michael

The majority of people, including people with dementia, would prefer to be cared for in their homes until the end of their lives. However, that is often dependent on the ability of an informal carer (a family member or friend) to provide care at home. Caring for a person with dementia, particularly as the condition progresses, can be very stressful, both physically and psychologically. If the carer receives insufficient support, then the person with dementia is often admitted to a care home. When carers are no longer able to maintain care at home, they can experience negative emotions, such as guilt, sadness, shame and loss. This article will discuss reasons why family/friends of people with dementia want to care for their loved one at home, their perceptions of care homes, the need to open up discussions about place of care early in the disease trajectory and some of the advantages of care homes. In so doing, it will draw on issues raised by carers who participated in Alzheimer's Society's Carer Information and Support Programme. It is hoped that the article will provide both health and social care workers with insight into the difficulties experienced by the family/friends of people with dementia.

http://dx.doi.org/10.1136/eoljnl-2016-000022

Voir la revue «END OF LIFE JOURNAL, 6»

Autres numéros de la revue «END OF LIFE JOURNAL»

Consulter en ligne

Suggestions

Du même auteur

Care home or home care? : difficult decisions...

Article indépendant | WORTLEY, Michael | END OF LIFE JOURNAL | n°1 | vol.6

The majority of people, including people with dementia, would prefer to be cared for in their homes until the end of their lives. However, that is often dependent on the ability of an informal carer (a family member or friend) to ...

Care home or home care? : difficult decisions...

Article indépendant | WORTLEY, Michael | END OF LIFE JOURNAL | n°1 | vol.6

The majority of people, including people with dementia, would prefer to be cared for in their homes until the end of their lives. However, that is often dependent on the ability of an informal carer (a family member or friend) to ...

De la même série

Managing breathlessness in palliative care : ...

Article | LOPES DE SOUSA, Flavio Gil | END OF LIFE JOURNAL | n°1 | vol.7

Breathlessness is a symptom frequently experienced in end of life. The assessment and management of breathlessness can present a challenge to healthcare professionals due to its complexity and multidimensional character. Current r...

Going for Gold : the Gold Standards Framework...

Article | CLIFFORD, Collette | END OF LIFE JOURNAL | n°1 | vol.7

Primary care teams are pivotal in caring for patients in the final year of life, enabling more to live well and die where they choose. They face increasing pressures from an ageing population, rising mortality and limited resource...

Lessons from an incomplete implementation pro...

Article | RANDALL, Kirsty | END OF LIFE JOURNAL | n°1 | vol.7

The AMBER care bundle was formally adopted in 2015 by the National Health Service (NHS) Improving Quality and provides a systematic approach to managing the care of hospital patients who are facing an uncertain recovery and who ar...

Undergraduate nursing students’ constru...

Article | ADESINA, Oluwatomilayo (Tomi) | END OF LIFE JOURNAL | n°1 | vol.6

Background: Nurses have a key role to play in ensuring that high-quality care is given to patients throughout their disease trajectory, including at the end of life. An increase in the ageing population in Western countries means ...

Experiences of palliative care nurses in the ...

Article | DWYER, Irene | END OF LIFE JOURNAL | n°1 | vol.6

Background/ Palliative sedation, or bringing about a state of decreased or absent awareness (unconsciousness), is one of the therapies used in end-of-life healthcare settings in order to manage refractory symptoms such as pain, d...

Chargement des enrichissements...