Literature DB >> 31765628

"There Are Hills and Valleys": Experiences of Parenting a Son With X-Linked Retinoschisis.

Amy Turriff1, Rosalie Nolen2, Celeste D'Amanda2, Barbara Biesecker3, Catherine Cukras4, Paul A Sieving5.   

Abstract

PURPOSE: To explore the experiences of parents of sons with X-linked retinoschisis (XLRS).
DESIGN: Mixed methods-qualitative interviews with quantitative survey.
METHODS: Parents of sons with XLRS who were evaluated at the National Eye Institute between December 2017 and January 2019 were eligible for this study. Participation involved engaging in a semistructured interview and completing a survey assessing optimism, anxiety, personality traits, and sociodemographics using valid and reliable scales. Interview transcripts were coded and analyzed thematically, and scales were scored and used descriptively.
RESULTS: Eleven mothers and 8 fathers from 13 families participated. Optimism, anxiety, and personality traits fell into the normative ranges for the scales. Parents described a process of continuous adaptation to their son's condition. The initial diagnosis was characterized by shock, grief, and "devastation" for most parents. Maternal guilt was common, but usually lessened over time. As parents adjusted to life postdiagnosis, they attempted to achieve a state of normalcy while balancing a desire to protect their sons. Significant sources of stress included decisions around sports participation and driving. Among all parents, the fear of retinal detachment was an ongoing concern. Most parents did identify perceived benefits from their experiences, such as feelings of gratitude or family cohesion.
CONCLUSIONS: Most parents viewed XLRS as a significant challenge in their sons' lives, but one that could be overcome. Clinical encounters may be enhanced for families with XLRS by providing accurate information, preparing families for potential challenges, anticipating stressful decisions, and meeting other families with XLRS. Published by Elsevier Inc.

Entities:  

Mesh:

Year:  2019        PMID: 31765628      PMCID: PMC8696984          DOI: 10.1016/j.ajo.2019.11.023

Source DB:  PubMed          Journal:  Am J Ophthalmol        ISSN: 0002-9394            Impact factor:   5.258


  31 in total

1.  Psychometric properties and population-based norms of the Life Orientation Test Revised (LOT-R).

Authors:  Heide Glaesmer; Winfried Rief; Alexandra Martin; Ricarda Mewes; Elmar Brähler; Markus Zenger; Andreas Hinz
Journal:  Br J Health Psychol       Date:  2011-07-21

2.  The Natural History of Congenital X-Linked Retinoschisis and Conversion between Phenotypes over Time.

Authors:  Edward H Wood; Itsara Lertjirachai; Benjamin K Ghiam; Nicole Koulisis; Stavros N Moysidis; Ali Dirani; Kimberly A Drenser; Antonio Capone; Michael T Trese
Journal:  Ophthalmol Retina       Date:  2018-08-24

3.  Benefits and burdens of genetic carrier identification.

Authors:  J K Williams; D L Schutte
Journal:  West J Nurs Res       Date:  1997-02       Impact factor: 1.967

4.  Ultimate success in epilepsy--the patient's perspective.

Authors:  J W Sander
Journal:  Eur J Neurol       Date:  2005-11       Impact factor: 6.089

Review 5.  Children's experiences of congenital heart disease: a systematic review of qualitative studies.

Authors:  Lauren S H Chong; Dominic A Fitzgerald; Jonathan C Craig; Karine E Manera; Camilla S Hanson; David Celermajer; Julian Ayer; Nadine A Kasparian; Allison Tong
Journal:  Eur J Pediatr       Date:  2018-01-11       Impact factor: 3.183

6.  Alone in a Crowd? Parents of Children with Rare Diseases' Experiences of Navigating the Healthcare System.

Authors:  Jennifer Baumbusch; Samara Mayer; Isabel Sloan-Yip
Journal:  J Genet Couns       Date:  2018-08-21       Impact factor: 2.537

7.  Development of personality in early and middle adulthood: set like plaster or persistent change?

Authors:  Sanjay Srivastava; Oliver P John; Samuel D Gosling; Jeff Potter
Journal:  J Pers Soc Psychol       Date:  2003-05

Review 8.  The experience of living with a chronic illness during adolescence: a critical review of the literature.

Authors:  Rachel M Taylor; Faith Gibson; Linda S Franck
Journal:  J Clin Nurs       Date:  2008-12       Impact factor: 3.036

9.  How does the mode of inheritance of a genetic condition influence families? A study of guilt, blame, stigma, and understanding of inheritance and reproductive risks in families with X-linked and autosomal recessive diseases.

Authors:  Cynthia A James; Donald W Hadley; Neil A Holtzman; Jerry A Winkelstein
Journal:  Genet Med       Date:  2006-04       Impact factor: 8.822

10.  Australian children living with rare diseases: experiences of diagnosis and perceived consequences of diagnostic delays.

Authors:  Yvonne Zurynski; Marie Deverell; Troy Dalkeith; Sandra Johnson; John Christodoulou; Helen Leonard; Elizabeth J Elliott
Journal:  Orphanet J Rare Dis       Date:  2017-04-11       Impact factor: 4.123

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