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Issues in Comprehensive Pediatric Nursing Volume 33, 2010 - Issue 2
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Research Article

Exploring Parent-Sibling Communication in Families of Children with Sickle Cell Disease

J. Carolyn Graff Ph.D., RN University of Tennessee Health Science Center, College of Nursing and Boling Center for Developmental Disabilities, Memphis, TN, USACorrespondence[email protected]
,
Jane S. Hankins M.D., MS St. Jude Children's Research Hospital, Department of Hematology, Memphis, TN, USA
,
Belinda T. Hardy M.S.S.W., L.C.S.W. University of Tennessee Health Science Center, Boling Center for Developmental Disabilities, Memphis, TN, USA
,
Heather R. Hall Ph.D., MSN University of South Alabama, College of Nursing, Mobile, AL, USA
,
Ruth J. Roberts Ed.D., MA St. Jude Children's Research Hospital, Department of Hematology, Memphis, TN, USA
&
Susan L. Neely-Barnes Ph.D., MSW University of Tennessee, College of Social Work, Nashville, TN, USA
Pages 101-123 | Received 14 Nov 2009, Accepted 14 Jan 2010, Published online: 12 Apr 2010

Citations (12)

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Read on this site (1)

Heather R. Hall, Susan L. Neely-Barnes, J. Carolyn Graff, Taylor E. Krcek, Ruth J. Roberts & Jane S. Hankins. (2012) Parental Stress in Families of Children with a Genetic Disorder/Disability and the Resiliency Model of Family Stress, Adjustment, and Adaptation. Issues in Comprehensive Pediatric Nursing 35:1, pages 24-44.
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Articles from other publishers (11)

Winnie Samanú Lima Lopes, Martha Cristina Nunes Moreira & Romeu Gomes. (2023) The sickle cell illness experience under the qualitative lens. Ciência & Saúde Coletiva 28:9, pages 2489-2500.
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Winnie Samanú Lima Lopes, Martha Cristina Nunes Moreira & Romeu Gomes. (2023) A experiência de adoecimento falciforme pelas lentes qualitativas. Ciência & Saúde Coletiva 28:9, pages 2489-2500.
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Delphine Hoegy, Ronald Guilloux, Nathalie Bleyzac, Alexandra Gauthier‐Vasserot, Giovanna Cannas, Yves Bertrand, Arnaud Hot, Claude Dussart & Audrey Janoly‐Dumenil. (2020) Sickle cell disease perceptions of caregivers, adolescent, and adult patients: Barriers and facilitators to medical care adherence. Journal of Advanced Nursing 76:9, pages 2391-2400.
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AdedoyinA Fetuga, MobolanleRasheedat Balogun & AdeseyeMichael Akinsete. (2020) Knowledge of SCD and psychosocial burden experienced by caregivers of children with SCD at a secondary level hospital in Lagos, Nigeria - A cross sectional study. Journal of Clinical Sciences 17:4, pages 113.
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Nancy Havill, Louise K. Fleming & Kathleen Knafl. (2019) Well siblings of children with chronic illness: A synthesis research study. Research in Nursing & Health 42:5, pages 334-348.
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Badr M. Madani, Rajaa Al Raddadi, Soad Al Jaouni, Mohab Omer & Marie-Isabelle Al Awa. (2018) Quality of life among caregivers of sickle cell disease patients: a cross sectional study. Health and Quality of Life Outcomes 16:1.
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Mariam Kayle, Paula Tanabe, Nirmish R. Shah, Lynne Baker-Ward & Sharron L. Docherty. (2016) Challenges in Shifting Management Responsibility From Parents to Adolescents With Sickle Cell Disease. Journal of Pediatric Nursing 31:6, pages 678-690.
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Maria O’Shea, Mary Hughes, Eileen Savage & Clare O’Brien. 2016. Children and Young People’s Nursing. Children and Young People’s Nursing 93 110 .
Rebecca Okashah, Kelly Schoch, Stephen R. Hooper, Vandana Shashi & Nancy Callanan. (2014) Parental Communication and Experiences and Knowledge of Adolescent Siblings of Children with 22q11.2 Deletion Syndrome. Journal of Genetic Counseling 24:5, pages 752-759.
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Jerlym S. Porter, J. Carolyn Graff, Alana D. Lopez & Jane S. Hankins. (2014) Transition From Pediatric to Adult Care in Sickle Cell Disease: Perspectives on the Family Role. Journal of Pediatric Nursing 29:2, pages 158-167.
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J.Carolyn Graff, Jane Hankins, Rebecca J. Graves, Kimberly Y. Robitaille, Ruth Roberts, Katherine Cejda, Belinda T. Hardy, Margery Johnson & Jerlym S. Porter. (2012) Exploring Family Communication About Sickle Cell Disease in Adolescence. Journal of Pediatric Oncology Nursing 29:6, pages 323-336.
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