The Lived Experiences of Caregivers of Children with Sickle Cell Disease: A Phenomenological Study
Author:
Affiliation:
1. Minority Behavioral Health Group, Akron, OH
2. Division of Psychology and Counseling, Governors State University, University Park, IL
Publisher
Informa UK Limited
Subject
Clinical Psychology,Social Psychology
Link
https://www.tandfonline.com/doi/pdf/10.1080/01926187.2021.1941420
Reference31 articles.
1. The Lived Experience of Parents of Children with Sickle Cell Disease: A Qualitative Study
2. American Academy of Pediatrics. (2014). Committee on Psychosocial Aspects of Child and Family Health. https://healthychildren.org/English/health-issues/conditions/chronic/Pages/How%20Chronic-Illness-Affects-the-Family.aspx
3. Parental Locus of Control and Family Functioning in the Quality of Life of Children with Sickle Cell Disease
4. Do Parental Coping, Involvement, Religiosity, and Racial Identity Mediate Children’s Psychological Adjustment to Sickle Cell Disease?
5. The Social and Cultural Context of Coping with Sickle Cell Disease: III. Stress, Coping Tasks, Family Functioning, and Children’s Adjustment
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Hidden stories of caregivers with children living with sickle cell disease in Uganda: experiences, coping strategies and outcomes;2024-01-17
2. Knowledge and nutrition-related practices among caregivers of adolescents with sickle cell disease in the Greater Accra region of Ghana;BMC Public Health;2023-03-06
3. Conceptualizing Sickle Cell Disease and the Family with Intergenerational Family Therapy;The American Journal of Family Therapy;2022-01-31
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