Family Caregiver Suffering in Caring for Patients with Amyotrophic Lateral Sclerosis in Korea
Bibliographic Data
| ID | 15466768 |
|---|---|
| Authors | Juyeon Oh (0000-0002-9843-4928, Dankook University), Jung-A Kim (Hanyang University), Min Sun Chu (0000-0003-0276-1682, Seoul Women's College of Nursing, corresponding author) |
| Year | 2021 |
| Volume | 18 |
| Issue | 9 |
| Pages | 4937-4937 |
| Publication date | 2021-05-06 |
| Open Access | Yes |
| Type | ARTICLE |
| Venue | International Journal of Environmental Research and Public Health (JOURNAL) |
| Journal identifiers | ISSN: 1661-7827 • E-ISSN: 1660-4601 |
| Publisher | Multidisciplinary Digital Publishing Institute (PUBLISHER • CH) |
| DOI | 10.3390/ijerph18094937 |
| PMID | 34066364 |
| OpenAlex | W3159022955 |
| Language | EN |
| Citations received | 1 |
| References cited | 30 |
The purpose of this study was to describe the meaning of the suffering experience of Korean ALS family caregivers. This is a descriptive phenomenological study that included ten participants using convenience sampling with maximum variation in a tertiary hospital in Seoul, South Korea. Colaizzi's data analysis method was used to inductively determine themes and formulate meanings. The three main themes derived from analysis were: "frustration with seeing a patient suffering", "burnout at the cost of a life of dedication", and "desperate need for help". Caregivers experience high levels of suffering, which can come in various forms depending on the circumstances of the particular patient and family. Especially, distress from seeing a loved one suffering was another aspect of suffering in Korean ALS caregivers, reflecting strong family ties. At the same time, patients are in desperate need of help and support from their families. Thus, it is essential to provide care to lessen the causes of distress and meet the needs of not only patients, but also caregivers through family-centered care to improve overall quality of life for all involved
Amyotrophic lateral sclerosis · Caregiver burden · Dementia · Disease · Distress · Family caregivers · Mental health · Psychiatry · Psychological distress · Quality of life (healthcare · Amyotrophic Lateral Sclerosis Research · Clinical Psychology · Family Support in Illness · Medicine · Nursing · Palliative Care and End-of-Life Issues · Psychology
| Citations per year | 1 |
|---|---|
| Citation span | 2025 - 2025 (1) |
| Highly cited | No |