Literature DB >> 7646829

The experience of South American mothers who have a child being treated for malignancy in the United States.

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Abstract

This phenomenological study examined the experience of South American mothers who brought their children to the United States for cancer treatment. Five mothers were interviewed twice about their subjective experiences. Data were analyzed using Colaizzi's method of phenomenology. Thirty-two significant statements were grouped into eight themes. The South American mothers brought their children to the United States in hopes of finding effective treatment, illustrating the major theme of our findings that no effort or sacrifice was too great to save their children's lives. The diagnosis of cancer had an overwhelming impact on the child and the family. This was made worse by the uncertainty of treatment outcome. Although the decision to come disrupted family life and caused economic and cultural hardship, it was uniformly believed to have been the right decision. The greatest challenges experienced by the mothers were language difficulties and the constant preoccupation with the child's illness. Through faith and a variety of coping strategies, these South American mothers succeeded in adapting. They transcended life disruption and focused on the critical goal of restoring their child's health. Central to their experience is that everything humanly possible be done to preserve the life of their child.

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Year:  1995        PMID: 7646829     DOI: 10.1177/104345429501200303

Source DB:  PubMed          Journal:  J Pediatr Oncol Nurs        ISSN: 1043-4542            Impact factor:   1.636


  6 in total

Review 1.  Cultural and religious considerations in pediatric palliative care.

Authors:  Lori Wiener; Denice Grady McConnell; Lauren Latella; Erica Ludi
Journal:  Palliat Support Care       Date:  2012-05-22

2.  On the road and away from home: a systematic review of the travel experiences of cancer patients and their families.

Authors:  Cecilia Vindrola-Padros; Eugenia Brage; Pinkie Chambers
Journal:  Support Care Cancer       Date:  2018-05-23       Impact factor: 3.603

3.  Understanding the health impact of caregiving: a qualitative study of immigrant parents and single parents of children with cancer.

Authors:  Anne F Klassen; Sonia Gulati; Leeat Granek; Zahava R S Rosenberg-Yunger; Lisa Watt; Lillian Sung; Robert Klaassen; David Dix; Nicola T Shaw
Journal:  Qual Life Res       Date:  2011-11-30       Impact factor: 4.147

4.  International adaptation: psychosocial and parenting experiences of caregivers who travel to the United States to obtain acute medical care for their seriously ill child.

Authors:  Rachel Margolis; Erica Ludi; Maryland Pao; Lori Wiener
Journal:  Soc Work Health Care       Date:  2013

5.  The 'radiation vacation': Parents' experiences of travelling to have their children's brain tumours treated with proton beam therapy.

Authors:  Sam G Cockle; Jane Ogden
Journal:  Health Psychol Open       Date:  2016-05-17

6.  Living with the Memories-Parents' Experiences of Their Newborn Child Undergoing Heart Surgery Abroad: A Qualitative Study.

Authors:  Ólöf Kristjánsdóttir; Annica Sjöström-Strand; Gudrún Kristjánsdóttir
Journal:  Int J Environ Res Public Health       Date:  2020-11-28       Impact factor: 3.390

  6 in total

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