Literature DB >> 28407536

"Rare place where I feel normal": Perceptions of a social support conference among parents of and people with Moebius syndrome.

Kathleen R Bogart1, Erika Frandrup2, Taylor Locke2, Hanna Thompson2, Natalie Weber2, Jacqueline Yates2, Nicholas Zike2, Amanda R Hemmesch3.   

Abstract

BACKGROUND: Moebius syndrome is a rare congenital disorder resulting in impaired facial and eye movement. People with rare diseases like Moebius syndrome experience stigma and a lack of specialized information. Support conferences may provide important forms of social support for people with rare disorders. AIMS: To examine reasons for attending, benefits, and limitations of support conferences. METHODS AND PROCEDURES: 50 adults with Moebius syndrome and 57 parents of people with Moebius syndrome completed open-ended items in an online study. OUTCOMES AND
RESULTS: Mixed- methods content analysis revealed that companionship and informational support were most frequently mentioned as reasons for and benefits of attending. Finances were the most frequently mentioned reason for not attending. Parents were more likely than people with Moebius to describe instrumental support as a conference benefit. When describing conference limitations, parents were significantly more concerned by lack of information relevance, while people with Moebius noted more often that conference attributes were not relevant to their age. CONCLUSIONS AND IMPLICATIONS: Being surrounded by others who share one's condition offers a unique opportunity for destigmatizing companionship support, which normalizes, reduces isolation, and promotes solidarity. Ways to increase facilitators and decrease barriers to accessing support for rare disorders should be investigated.
Copyright © 2017 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Companionship support; Facial paralysis; Moebius syndrome; Rare disease; Social support; Stigma

Mesh:

Year:  2017        PMID: 28407536     DOI: 10.1016/j.ridd.2017.03.014

Source DB:  PubMed          Journal:  Res Dev Disabil        ISSN: 0891-4222


  7 in total

1.  Healthcare access, satisfaction, and health-related quality of life among children and adults with rare diseases.

Authors:  Kathleen Bogart; Amanda Hemmesch; Erica Barnes; Thomas Blissenbach; Arthur Beisang; Patti Engel
Journal:  Orphanet J Rare Dis       Date:  2022-05-12       Impact factor: 4.303

2.  The Caregiving Experiences of Fathers and Mothers of Children With Rare Diseases in Italy: Challenges and Social Support Perceptions.

Authors:  Paola Cardinali; Laura Migliorini; Nadia Rania
Journal:  Front Psychol       Date:  2019-08-05

Review 3.  Psychosocial Considerations for the Child with Rare Disease: A Review with Recommendations and Calls to Action.

Authors:  Leslee T Belzer; S Margaret Wright; Emily J Goodwin; Mehar N Singh; Brian S Carter
Journal:  Children (Basel)       Date:  2022-06-21

4.  Narrative identity among people with disabilities in the United States during the Covid-19 pandemic: The interdependent self.

Authors:  Jonathan M Adler; Robert B Manning; Rachel Hennein; Julia Winschel; Alessandra Baldari; Kathleen R Bogart; Michelle R Nario-Redmond; Joan M Ostrove; Sarah R Lowe; Katie Wang
Journal:  J Res Pers       Date:  2022-09-28

5.  Acceptance and commitment therapy meets peer-support. Development of a supportive self-care intervention for patients with rare diseases: a multistage development process.

Authors:  Miriam K Depping; Natalie Uhlenbusch; Bernd Löwe
Journal:  BMJ Open       Date:  2021-07-02       Impact factor: 2.692

6.  Health-related quality of life among adults with diverse rare disorders.

Authors:  Kathleen R Bogart; Veronica L Irvin
Journal:  Orphanet J Rare Dis       Date:  2017-12-07       Impact factor: 4.123

7.  Web-based sensitivity training for interacting with facial paralysis.

Authors:  Nicole Zhang; Kathleen Bogart; John Michael; Luke McEllin
Journal:  PLoS One       Date:  2022-01-21       Impact factor: 3.240

  7 in total

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