Family members in families with severe chronic disease play important roles in care-giving. In families affected by Huntington's disease (HD), caregivers encounter practical and emotional challenges and distress. Enduring caregiver burdens may lead to problems and caregivers are in need of social support and health services to deal with challenges. We wanted to explore coping strategies and behaviour patterns used by family caregivers to care for themselves, while caring for a family member with HD. Participants were recruited from hospitals and community-based healthcare. The sample represents experiences from care-giving in all stages of the disease. We conducted semi-structured interviews with 15 family caregivers in Norway. The transcri...
There has been little research into the psychosocial impact of Juvenile Huntington’s Disease on the ...
Background: People with Huntington’s disease (HD) can be affected by motor, cognitive and behavioura...
There has been little research into the psychosocial impact of Juvenile Huntington’s Disease on the ...
Family members in families with severe chronic disease play important roles in care-giving. In famil...
Aim: The objective of this study was to explore family caregivers' experiences with the impact of Hu...
Background: Huntington's disease (HD) is an autosomal-dominant inherited neurological disease charac...
Huntington's disease is a genetic, neurological disorder characterized by mid-life onset, involuntar...
Background: Collaboration between family caregivers and health professionals in specialised hospital...
Introduction. Despite the growing interest in the consequences of caring for patients with Huntingto...
The purpose of the study was to explore the experiences, challenges and needs of caregivers of a per...
Aim This paper is a report of a study conducted to examine the emotional experience of caregiving by...
disease, such as the unknown possibility of cure, the progressive loss of autonomy and life expectan...
Exploring supportive care for individuals affected by Huntington disease and their family caregivers...
ObjectivesThis study aims to provide more insight into possible barriers and facilitators caregivers...
Abstract Background Since Huntington's Disease (HD) is a familial disease with an average onset in t...
There has been little research into the psychosocial impact of Juvenile Huntington’s Disease on the ...
Background: People with Huntington’s disease (HD) can be affected by motor, cognitive and behavioura...
There has been little research into the psychosocial impact of Juvenile Huntington’s Disease on the ...
Family members in families with severe chronic disease play important roles in care-giving. In famil...
Aim: The objective of this study was to explore family caregivers' experiences with the impact of Hu...
Background: Huntington's disease (HD) is an autosomal-dominant inherited neurological disease charac...
Huntington's disease is a genetic, neurological disorder characterized by mid-life onset, involuntar...
Background: Collaboration between family caregivers and health professionals in specialised hospital...
Introduction. Despite the growing interest in the consequences of caring for patients with Huntingto...
The purpose of the study was to explore the experiences, challenges and needs of caregivers of a per...
Aim This paper is a report of a study conducted to examine the emotional experience of caregiving by...
disease, such as the unknown possibility of cure, the progressive loss of autonomy and life expectan...
Exploring supportive care for individuals affected by Huntington disease and their family caregivers...
ObjectivesThis study aims to provide more insight into possible barriers and facilitators caregivers...
Abstract Background Since Huntington's Disease (HD) is a familial disease with an average onset in t...
There has been little research into the psychosocial impact of Juvenile Huntington’s Disease on the ...
Background: People with Huntington’s disease (HD) can be affected by motor, cognitive and behavioura...
There has been little research into the psychosocial impact of Juvenile Huntington’s Disease on the ...