The purpose of this study was to identify and describe the experiences of quality of life/life situation among those who were next of kin to persons with inoperable lung cancer. Data were collected in qualitative interviews, where 11 next of kin articulated their lived experiences, and were interpreted through interpretive phenomenology. Four themes were identified: changed life situation, experiences of uncertainty due to awareness of the ill person’s changed health status, interpersonal relationships, and false hopes due to health care professionals ’ treatment. These four themes gave a structure presenting the essence: balancing a changed life situation. The findings of the study point out the importance of promoting support for the next...
Primary caregivers are highly affected in the care of the terminally ill, especially if they are imm...
One cornerstone of palliative care is improving the family’s quality of life (QoL). The principles o...
There is a paucity of research exploring patients' and their informal carers' experience of coping w...
Objectives: The aim of the study was to illuminate the experience of life as next of kin to an elder...
Nursing research has been performed during the last 20-30 years, about the next of kin’s vulnerabili...
To assess if family care givers of patients with lung cancer experience the patterns of social, psyc...
The purpose of this qualitative research is to provide an in-depth exploration of the impact that a ...
This phenomenological study explored the lived experiences of middle-aged spouses who cared for thei...
This thesis explores the views and experiences of people with lung cancer, and family members, of di...
Lung cancer is associated with a wide range of symptoms arising from both disease progression and tr...
This study was designed to elicit the perceptions of families who are experiencing cancer in one of ...
Appraisal of the literature suggests that patients with lung cancer report more unmet supportive car...
The focus for this thesis has been significant others to patients with a life threatening cancer dis...
OBJECTIVES: Lung transplant patients and their next of kin share the experiences of illness but litt...
BACKGROUND: Chronic obstructive pulmonary disease (COPD) is an inflammatory and irreversible lung di...
Primary caregivers are highly affected in the care of the terminally ill, especially if they are imm...
One cornerstone of palliative care is improving the family’s quality of life (QoL). The principles o...
There is a paucity of research exploring patients' and their informal carers' experience of coping w...
Objectives: The aim of the study was to illuminate the experience of life as next of kin to an elder...
Nursing research has been performed during the last 20-30 years, about the next of kin’s vulnerabili...
To assess if family care givers of patients with lung cancer experience the patterns of social, psyc...
The purpose of this qualitative research is to provide an in-depth exploration of the impact that a ...
This phenomenological study explored the lived experiences of middle-aged spouses who cared for thei...
This thesis explores the views and experiences of people with lung cancer, and family members, of di...
Lung cancer is associated with a wide range of symptoms arising from both disease progression and tr...
This study was designed to elicit the perceptions of families who are experiencing cancer in one of ...
Appraisal of the literature suggests that patients with lung cancer report more unmet supportive car...
The focus for this thesis has been significant others to patients with a life threatening cancer dis...
OBJECTIVES: Lung transplant patients and their next of kin share the experiences of illness but litt...
BACKGROUND: Chronic obstructive pulmonary disease (COPD) is an inflammatory and irreversible lung di...
Primary caregivers are highly affected in the care of the terminally ill, especially if they are imm...
One cornerstone of palliative care is improving the family’s quality of life (QoL). The principles o...
There is a paucity of research exploring patients' and their informal carers' experience of coping w...