336 related articles for article (PubMed ID: 30761947)
1. The experiences and needs of primary family caregivers of patients with multiple myeloma: A qualitative analysis.
Quiñoa-Salanova C; Porta-Sales J; Monforte-Royo C; Edo-Gual M
Palliat Med; 2019 May; 33(5):500-509. PubMed ID: 30761947
[TBL] [Abstract][Full Text] [Related]
2. Informal caregivers' needs on discharge from the spinal cord unit: analysis of perceptions and lived experiences.
Conti A; Garrino L; Montanari P; Dimonte V
Disabil Rehabil; 2016; 38(2):159-67. PubMed ID: 25858628
[TBL] [Abstract][Full Text] [Related]
3. Family Caregiver Experiences in the Inpatient and Outpatient Reduced-Intensity Conditioning Allogeneic Hematopoietic Cell Transplantation Settings: A Qualitative Study.
Gray TF; Do KM; Amonoo HL; Sullivan L; Kelkar AH; Pirl WF; Hammer MJ; Tulsky JA; El-Jawahri A; Cutler CS; Partridge AH
Transplant Cell Ther; 2024 Jun; 30(6):610.e1-610.e16. PubMed ID: 37783339
[TBL] [Abstract][Full Text] [Related]
4. The Experience of Myeloma Caregivers During Home-Based Oral Chemotherapy Treatment: A Qualitative Study.
Morris M; Marshall-Lucette S
Semin Oncol Nurs; 2017 Aug; 33(3):362-371. PubMed ID: 28751188
[TBL] [Abstract][Full Text] [Related]
5. Experiences of burden, needs, rewards and resilience in family caregivers of people living with Motor Neurone Disease/Amyotrophic Lateral Sclerosis: A secondary thematic analysis of qualitative interviews.
Weisser FB; Bristowe K; Jackson D
Palliat Med; 2015 Sep; 29(8):737-45. PubMed ID: 25762578
[TBL] [Abstract][Full Text] [Related]
6. Family caregivers' lived experiences of caring for epidermolysis bullosa patients: A phenomenological study.
Wu YH; Sun FK; Lee PY
J Clin Nurs; 2020 May; 29(9-10):1552-1560. PubMed ID: 32043289
[TBL] [Abstract][Full Text] [Related]
7. Living with multiple myeloma: experiences of patients and their informal caregivers.
Molassiotis A; Wilson B; Blair S; Howe T; Cavet J
Support Care Cancer; 2011 Jan; 19(1):101-11. PubMed ID: 19998045
[TBL] [Abstract][Full Text] [Related]
8. Relatives of people with spinal cord injury: a qualitative study of caregivers' metamorphosis.
Juguera Rodriguez L; Pardo Rios M; Leal Costa C; Castillo Hermoso M; Perez Alonso N; Diaz Agea JL
Spinal Cord; 2018 Jun; 56(6):548-559. PubMed ID: 29563575
[TBL] [Abstract][Full Text] [Related]
9. 'It's a traumatic illness, traumatic to witness': a qualitative study of the experiences of bereaved family caregivers of patients with cutaneous T-cell lymphoma.
Orlowska D; Selman LE; Beynon T; Radcliffe E; Whittaker S; Child F; Harding R
Br J Dermatol; 2018 Oct; 179(4):882-888. PubMed ID: 29451670
[TBL] [Abstract][Full Text] [Related]
10. Perceptions of family caregivers of cancer patients about the challenges of caregiving: a qualitative study.
Nemati S; Rassouli M; Ilkhani M; Baghestani AR
Scand J Caring Sci; 2018 Mar; 32(1):309-316. PubMed ID: 28869659
[TBL] [Abstract][Full Text] [Related]
11. The experience of the family caregivers' role: a qualitative study.
Lane P; McKenna H; Ryan A; Fleming P
Res Theory Nurs Pract; 2003; 17(2):137-51. PubMed ID: 12880218
[TBL] [Abstract][Full Text] [Related]
12. Experiences of family caregivers of patients with COVID-19.
Rahimi T; Dastyar N; Rafati F
BMC Fam Pract; 2021 Jun; 22(1):137. PubMed ID: 34187368
[TBL] [Abstract][Full Text] [Related]
13. Using photo-elicitation to explore the lived experience of informal caregivers of individuals living with dementia.
Rayment G; Swainston K; Wilson G
Br J Health Psychol; 2019 Feb; 24(1):102-122. PubMed ID: 30294928
[TBL] [Abstract][Full Text] [Related]
14. Understanding family caregivers' needs to support relatives with advanced progressive disease at home: an ethnographic study in rural Portugal.
Teixeira MJC; Abreu W; Costa N; Maddocks M
BMC Palliat Care; 2020 May; 19(1):73. PubMed ID: 32450848
[TBL] [Abstract][Full Text] [Related]
15. Living on the edge: Family caregivers' experiences of caring for post-stroke family members in China: A qualitative study.
Lu Q; Mårtensson J; Zhao Y; Johansson L
Int J Nurs Stud; 2019 Jun; 94():1-8. PubMed ID: 30928717
[TBL] [Abstract][Full Text] [Related]
16. Balancing needs as a family caregiver in Huntington's disease: a qualitative interview study.
Røthing M; Malterud K; Frich JC
Health Soc Care Community; 2015 Sep; 23(5):569-76. PubMed ID: 25471490
[TBL] [Abstract][Full Text] [Related]
17. Family caregivers' experiences of caring for patients with heart failure: a descriptive, exploratory qualitative study.
Etemadifar S; Bahrami M; Shahriari M; Farsani AK
J Nurs Res; 2015 Jun; 23(2):153-61. PubMed ID: 25967646
[TBL] [Abstract][Full Text] [Related]
18. Advantages and Challenges: The Experience of Geriatrics Health Care Providers as Family Caregivers.
Wohlgemuth CM; Auerbach HP; Parker VA
Gerontologist; 2015 Aug; 55(4):595-604. PubMed ID: 24381174
[TBL] [Abstract][Full Text] [Related]
19. The "sphere of care": A qualitative study of colorectal cancer patient and caregiver experiences of support within the cancer treatment setting.
Law E; Levesque JV; Lambert S; Girgis A
PLoS One; 2018; 13(12):e0209436. PubMed ID: 30586391
[TBL] [Abstract][Full Text] [Related]
20. Stroke family caregivers' support needs change across the care continuum: a qualitative study using the timing it right framework.
Cameron JI; Naglie G; Silver FL; Gignac MA
Disabil Rehabil; 2013 Feb; 35(4):315-24. PubMed ID: 22686259
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]