Literature DB >> 34096130

"Doctors can read about it, they can know about it, but they've never lived with it": How parents use social media throughout the diagnostic odyssey.

Natalie T Deuitch1, Erika Beckman1, Meghan C Halley2, Jennifer L Young2, Chloe M Reuter3, Jennefer Kohler3, Jonathan A Bernstein3,4, Matthew T Wheeler4,5, Kelly E Ormond1, Holly K Tabor2,3,6.   

Abstract

Parents of children with undiagnosed conditions struggle to obtain information about how to treat and support their children. It can be particularly challenging to find communities and other parents who share their experiences and can provide emotional and informational support. This study sought to characterize how parents use social media, both throughout the diagnostic odyssey and post-diagnosis, to meet their informational, social, and emotional support needs. We conducted qualitative semi-structured interviews with 14 parents from the Stanford site of the Undiagnosed Diseases Network (UDN), including five whose children had received a diagnosis through study participation. Interview recordings were analyzed using inductive, team-based coding and thematic analysis based in grounded theory using Dedoose qualitative analysis software. Through this process, we identified four key themes related to social media use. First, parents struggled to find the "right" community, often seeking out groups of similar patients based on symptoms or similar conditions. Second, though they found much valuable information through social media about caring for their child, they also struggled to interpret the relevance of the information to their own child's condition. Third, the social support and access to other patients' and families' lived experiences were described as both highly valued and emotionally challenging, particularly in the case of poor outcomes for similar families. Finally, parents expressed the need to balance concerns about their child's privacy with the value of transparency and data sharing for diagnosis. Our results suggest that the needs and experiences of undiagnosed patients and families differ from those with diagnosed diseases and highlight the need for support in best utilizing social media resources at different stages of the diagnostic odyssey.
© 2021 National Society of Genetic Counselors.

Entities:  

Keywords:  diagnostic odyssey; rare diseases; social media; undiagnosed diseases

Mesh:

Year:  2021        PMID: 34096130      PMCID: PMC8777467          DOI: 10.1002/jgc4.1438

Source DB:  PubMed          Journal:  J Genet Couns        ISSN: 1059-7700            Impact factor:   2.537


  24 in total

1.  Living without a diagnosis: the parental experience.

Authors:  Celine Lewis; Heather Skirton; Ray Jones
Journal:  Genet Test Mol Biomarkers       Date:  2010-10-12

2.  "Before Facebook and before social media…we did not know anybody else that had this": parent perspectives on internet and social media use during the pediatric clinical genetic testing process.

Authors:  Krysta S Barton; Andrew Wingerson; Julie R Barzilay; Holly K Tabor
Journal:  J Community Genet       Date:  2018-12-19

3.  Uncertainty and perceived personal control among parents of children with rare chromosome conditions: the role of genetic counseling.

Authors:  Shawn E Lipinski; Michael J Lipinski; Leslie G Biesecker; Barbara B Biesecker
Journal:  Am J Med Genet C Semin Med Genet       Date:  2006-11-15       Impact factor: 3.908

Review 4.  Ethics and Privacy in Social Media Research for Mental Health.

Authors:  Jennifer Nicholas; Sandersan Onie; Mark E Larsen
Journal:  Curr Psychiatry Rep       Date:  2020-11-23       Impact factor: 5.285

5.  How parents search, interpret, and evaluate genetic information obtained from the internet.

Authors:  Myra I Roche; Debra Skinner
Journal:  J Genet Couns       Date:  2008-10-21       Impact factor: 2.537

6.  A New Approach to Rare Diseases of Children: The Undiagnosed Diseases Network.

Authors:  Chloe M Reuter; Elise Brimble; Colette DeFilippo; Annika M Dries; Gregory M Enns; Euan A Ashley; Jonathan A Bernstein; Paul Graham Fisher; Matthew T Wheeler
Journal:  J Pediatr       Date:  2018-01-11       Impact factor: 4.406

7.  Benefit of social media on patient engagement and satisfaction: Results of a 9-month, qualitative pilot study using Facebook.

Authors:  Vikrom K Dhar; Young Kim; Justin T Graff; Andrew D Jung; Jennifer Garrett; Lauren E Dick; Jenifer Harris; Shimul A Shah
Journal:  Surgery       Date:  2017-11-29       Impact factor: 3.982

8.  Effect of Genetic Diagnosis on Patients with Previously Undiagnosed Disease.

Authors:  Kimberly Splinter; David R Adams; Carlos A Bacino; Hugo J Bellen; Jonathan A Bernstein; Alys M Cheatle-Jarvela; Christine M Eng; Cecilia Esteves; William A Gahl; Rizwan Hamid; Howard J Jacob; Bijal Kikani; David M Koeller; Isaac S Kohane; Brendan H Lee; Joseph Loscalzo; Xi Luo; Alexa T McCray; Thomas O Metz; John J Mulvihill; Stanley F Nelson; Christina G S Palmer; John A Phillips; Leslie Pick; John H Postlethwait; Chloe Reuter; Vandana Shashi; David A Sweetser; Cynthia J Tifft; Nicole M Walley; Michael F Wangler; Monte Westerfield; Matthew T Wheeler; Anastasia L Wise; Elizabeth A Worthey; Shinya Yamamoto; Euan A Ashley
Journal:  N Engl J Med       Date:  2018-10-10       Impact factor: 91.245

Review 9.  The Role of Online Social Support in Supporting and Educating Parents of Young Children With Special Health Care Needs in the United States: A Scoping Review.

Authors:  Beth A DeHoff; Lisa K Staten; Rylin Christine Rodgers; Scott C Denne
Journal:  J Med Internet Res       Date:  2016-12-22       Impact factor: 5.428

10.  Estimating cumulative point prevalence of rare diseases: analysis of the Orphanet database.

Authors:  Stéphanie Nguengang Wakap; Deborah M Lambert; Annie Olry; Charlotte Rodwell; Charlotte Gueydan; Valérie Lanneau; Daniel Murphy; Yann Le Cam; Ana Rath
Journal:  Eur J Hum Genet       Date:  2019-09-16       Impact factor: 4.246

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  3 in total

1.  Perceived utility and disutility of genomic sequencing for pediatric patients: Perspectives from parents with diverse sociodemographic characteristics.

Authors:  Meghan C Halley; Jennifer L Young; Liliana Fernandez; Jennefer N Kohler; Jonathan A Bernstein; Matthew T Wheeler; Holly K Tabor
Journal:  Am J Med Genet A       Date:  2022-01-03       Impact factor: 2.802

2.  Genome sequencing as a first-line diagnostic test for hospitalized infants.

Authors:  Kevin M Bowling; Michelle L Thompson; Candice R Finnila; Susan M Hiatt; Donald R Latner; Michelle D Amaral; James M J Lawlor; Kelly M East; Meagan E Cochran; Veronica Greve; Whitley V Kelley; David E Gray; Stephanie A Felker; Hannah Meddaugh; Ashley Cannon; Amanda Luedecke; Kelly E Jackson; Laura G Hendon; Hillary M Janani; Marla Johnston; Lee Ann Merin; Sarah L Deans; Carly Tuura; Heather Williams; Kelly Laborde; Matthew B Neu; Jessica Patrick-Esteve; Anna C E Hurst; Jegen Kandasamy; Wally Carlo; Kyle B Brothers; Brian M Kirmse; Renate Savich; Duane Superneau; Steven B Spedale; Sara J Knight; Gregory S Barsh; Bruce R Korf; Gregory M Cooper
Journal:  Genet Med       Date:  2021-11-27       Impact factor: 8.864

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
  3 in total

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