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In Occupied Palestinian territory (OPT), which is in a complex political situation and has limited access to resources, there is a critical need to deepen the understanding of how children with life-limiting and life-threatening illnesses are cared for. This study explores the experiences of parents caring for more than one child with a chronic or serious illness. A qualitative descriptive method was adopted, with data collected from several paediatric units in two OPT cities, Tulkarm and Ramallah. Semi-structured, face-to-face interviews were conducted with 16 parents (each interview was of an individual parent). Data were analysed using thematic analysis, and the analysis unearthed seven major themes that reflected the parents' experiences. These were as follows: Significant life changes with the first child's illness; the second experience; becoming stronger; support systems; economic difficulties; social stigma; and social isolation. Data analyses suggest that there is a significant need for emotional and physical support to be provided to parents, and culturally salient social service provisions should be implemented to alleviate the burden placed on these parents.
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http://dx.doi.org/10.1177/13674935251375126 | DOI Listing |
Omega (Westport)
September 2025
Department of Clinical Medicine, Aarhus University, Aarhus, Denmark.
Pregnancy loss is a traumatic experience, and the quality of care can vary significantly across healthcare settings. However, evidence on the impact of different types of care on psychological outcomes is limited. This study examined the relationship between specialized care for parents experiencing pregnancy or neonatal loss and the level of Prolonged Grief Disorder (PGD) and Post-Traumatic Stress Disorder (PTSD) symptoms, as well as the role of midwifery support, one month post-loss.
View Article and Find Full Text PDFBone Jt Open
September 2025
Kadoorie, Oxford Trauma and Emergency Care, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, Oxford University, Oxford, UK.
Aims: We sought to explore staff experience of a paediatric randomized controlled trial (RCT), comparing operative fixation and nonoperative treatment for displaced medial epicondyle fractures.
Methods: A total of 20 staff (eight surgeons and 12 research delivery staff) recruiting to the RCT in 18 NHS Trusts across the UK took part in a telephone/online qualitative interview. Interviews were informed by Heideggerian Phenomenology and thematic analysis.
Women Birth
September 2025
Department of Women's and Children's Health, Uppsala University, Uppsala, Sweden; Department of Nursing, Mid Sweden University, Sundsvall, Sweden.
Background: Few parents experience stillbirth in Sweden, and their perspectives on the grieving process remain largely unknown.
Objective: To explore parents' perspectives, memories, reflections and insights in the grieving and recovery process six months after stillbirth.
Methods: A mixed-method study involving nine in-depth interviews and responses to eleven quantitative statements.
Cien Saude Colet
August 2025
Universidade Federal da Paraíba. João Pessoa PB Brasil.
The scope of this article was to comprehend discourses and attitudes that permeate care relationships in the reproductive journeys of women with physical disabilities. The qualitative research, conducted in the metropolitan area of João Pessoa-PB, was based on ethnography, interviews, and biographical accounts of 14 female interlocutors between 26 and 54 years of age. The theoretical-analytical framework was anchored in the intersectional perspectives of care studies and disability studies, considering gender, class, and disability oppressions.
View Article and Find Full Text PDFGerontologist
September 2025
Department of Psychiatry, University of Rochester Medical Center, Rochester, NY, 14642, USA.
Background And Objectives: Over 12% of older Latinos in the United States have Alzheimer's disease and related dementias (ADRD), facing earlier onset of the disease and severe symptoms compared to non-Hispanic Whites. These disparities in ADRD among Latinos can lead to significant caregiver strain and burden in Latino ADRD caregivers. Notably, Latino ADRD caregivers have poor overall health outcomes and face systemic inequities including limited access to quality dementia care resources that impact their well-being significantly.
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