Literature DB >> 17291319

'Building a new normality': mothers' experiences of caring for a child with acute lymphoblastic leukaemia.

E A Earle1, S A Clarke, C Eiser, L Sheppard.   

Abstract

BACKGROUND: Treatment of childhood cancer occurs over a 2- to 3-year period, with initial intense phases of chemotherapy followed by less severe treatment periods. From first diagnosis, families are encouraged by healthcare professionals (following government guidelines) to try to maintain a normal life. The aim of this paper is to contribute to our understanding of how 'normal' family life is compromised from the perspective of the families themselves during this period of extreme stress and concern for the health and well-being of their child.
METHODS: This study was longitudinal and involved a cross section of 32 mothers of children recently diagnosed with acute lymphoblastic leukaemia (ALL) currently participating in the Medical Research Council ALL-97 randomized control trial. Mothers were interviewed at three time points (3-4 months post diagnosis, 15 and 27 months) using a semi-structured format with open-ended questions. A qualitative methodology was employed to analyse interview data using Thematic analysis.
RESULTS: Mothers reported understanding the importance of achieving normal life, but described how this was difficult to realize. At first interview, mothers were optimistic that they could achieve the 'normal life' as advised by healthcare workers. At 12 and 24 months, although all mothers reported that life was not back to normal, there were differences in how they perceived this lack of normality. Whereas some families experienced frustration and disappointment, others had adjusted and managed to accept the new order.
CONCLUSIONS: Families felt encouraged on diagnosis to be told that despite the severity of the disease and treatment regime, a normal life was possible and should be pursued. Our findings indicate that over time, more concrete information is needed to guide parents through the treatment process in order to help them achieve this.

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Mesh:

Year:  2007        PMID: 17291319     DOI: 10.1111/j.1365-2214.2006.00638.x

Source DB:  PubMed          Journal:  Child Care Health Dev        ISSN: 0305-1862            Impact factor:   2.508


  11 in total

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Journal:  J Clin Psychol Med Settings       Date:  2011-03

2.  Exploring sleep-wake experiences of mothers during maintenance therapy for their child's acute lymphoblastic leukemia.

Authors:  Madalynn Neu; Ellyn Matthews; Nancy A King
Journal:  J Pediatr Nurs       Date:  2014-01-11       Impact factor: 2.145

3.  Parental perceptions of health-related quality of life in children with leukemia in the second week after the diagnosis: a quantitative model.

Authors:  Marta Tremolada; Sabrina Bonichini; Gianmarco Altoè; Marta Pillon; Modesto Carli; Thomas S Weisner
Journal:  Support Care Cancer       Date:  2010-03-13       Impact factor: 3.603

4.  Depression in parents of children with leukemia in southern China accompanied by the prevalence of type D personality.

Authors:  Jie Chen; Yang Liu; Qingqing Cai; Yimin Liu; Tong Wang; Jingfeng Wang; Wei-qing Chen; Hui Huang
Journal:  Support Care Cancer       Date:  2013-12-11       Impact factor: 3.603

5.  The personal experience of parenting a child with juvenile Huntington's disease: perceptions across Europe.

Authors:  Virginia Eatough; Helen Santini; Christine Eiser; Marie-Louise Goller; Wioletta Krysa; 'Annunziata' de Nicola; Matteo Paduanello; Martina Petrollini; Maria Rakowicz; Ferdinando Squitieri; Aad Tibben; Katie Lee Weille; Bernhard Landwehrmeyer; Oliver Quarrell; Jonathan A Smith
Journal:  Eur J Hum Genet       Date:  2013-02-27       Impact factor: 4.246

6.  Longitudinal analysis of quality-of-life outcomes in children during treatment for acute lymphoblastic leukemia: A report from the Children's Oncology Group AALL0932 trial.

Authors:  Daniel J Zheng; Xiaomin Lu; Reuven J Schore; Lyn Balsamo; Meenakshi Devidas; Naomi J Winick; Elizabeth A Raetz; Mignon L Loh; William L Carroll; Lillian Sung; Stephen P Hunger; Anne L Angiolillo; Nina S Kadan-Lottick
Journal:  Cancer       Date:  2017-11-07       Impact factor: 6.860

7.  Patterns of family management of childhood chronic conditions and their relationship to child and family functioning.

Authors:  Kathleen A Knafl; Janet A Deatrick; George J Knafl; Agatha M Gallo; Margaret Grey; Jane Dixon
Journal:  J Pediatr Nurs       Date:  2013-04-19       Impact factor: 2.145

8.  Effects of illness representation, perceived quality of information provided by the health-care professional, and perceived social support on depressive symptoms of the caregivers of children with leukemia.

Authors:  Ozlem Bozo; Selin Anahar; Gizem Ateş; Evren Etel
Journal:  J Clin Psychol Med Settings       Date:  2010-03

9.  Parents' Experiences with Home-Based Oral Chemotherapy Prescribed to a Child Diagnosed with Acute Lymphoblastic Leukemia: A Qualitative Study.

Authors:  Étienne Camiré-Bernier; Erwan Nidelet; Amel Baghdadli; Gabriel Demers; Marie-Christine Boulanger; Marie-Claude Brisson; Bruno Michon; Sophie Lauzier; Isabelle Laverdière
Journal:  Curr Oncol       Date:  2021-11-01       Impact factor: 3.677

Review 10.  Children's and Parents' Conceptualization of Quality of Life in Children With Brain Tumors: A Meta-Ethnographic Exploration.

Authors:  Emma Beecham; Richard Langner; Darren Hargrave; Myra Bluebond-Langner
Journal:  Qual Health Res       Date:  2018-07-25
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