Literature DB >> 29130143

Incorporating Social Media into your Support Tool Box: Points to Consider from Genetics-Based Communities.

Heather Mae Rocha1, Juliann M Savatt2,3, Erin Rooney Riggs3, Jennifer K Wagner4, W Andrew Faucett2, Christa Lese Martin2,3.   

Abstract

Patients with newly-described or rare genetic findings are turning to social media to find and connect with others. Blogs, Facebook groups, and Twitter have all been reported as tools for patients to connect with one another. However, the preferences for social media use and privacy among patients, their families, and these communities have not been well characterized. To explore preferences about privacy and membership guidelines, an online survey was administered to two web-based patient registries, Simons Variation in Individuals Project ( www.simonsvipconnect.org ) and GenomeConnect ( www.genomeconnect.org ). Over a three-month period, invitations were sent to 2524 individuals and 103 responses (4%) were received and analyzed. Responses indicate that Facebook is the most popular resource accessed within this sample population (99%). Participants used social media to look for information about their diagnosis or test results (83%), read posts from rare disease groups or organizations (73%), participate in conversations about their diagnosis (67%), and connect with others to find support (58%). Focusing on privacy issues in social media, respondents indicate that membership and access impact the level of comfort in sharing personal or medical information. Nearly 60% of respondents felt uncomfortable sharing photos or medical information within a public Facebook group, whereas only 12% of respondents felt uncomfortable sharing in private group targeted to families alone. Using this preliminary data concerning social media use and privacy, we developed points for genetic counselors to incorporate when discussing available support resources for patients with a new, or rare, genetic diagnosis or genetic test result. Genetic counselors are trained to provide anticipatory guidance to families adapting to new genetic information, and are well-equipped to help patients consider their preferences about using social media as a source of information and support.

Entities:  

Keywords:  Facebook; Genetic Counseling; Rare Disease; Social Media; Support

Mesh:

Year:  2017        PMID: 29130143     DOI: 10.1007/s10897-017-0170-z

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


  10 in total

1.  Introduction to the "Technology in Practice" Special Issue.

Authors:  Vickie Venne; Megan Doerr
Journal:  J Genet Couns       Date:  2018-03-01       Impact factor: 2.537

2.  An in-depth exploration of the post-test informational needs of BRCA1 and BRCA2 pathogenic variant carriers in Asia.

Authors:  Jeanette Yuen; Si Ming Fung; Chin Leong Sia; Mallika Venkatramani; Tarryn Shaw; Eliza Courtney; Shao-Tzu Li; Jianbang Chiang; Veronique Kiak-Mien Tan; Benita Kiat-Tee Tan; Joanne Ngeow
Journal:  Hered Cancer Clin Pract       Date:  2020-10-23       Impact factor: 2.857

3.  Concerns of Thalassemia Patients, Carriers, and their Caregivers in Malaysia: Text Mining Information Shared on Social Media.

Authors:  Yuen Chi Phang; Azleena Mohd Kassim; Ernest Mangantig
Journal:  Healthc Inform Res       Date:  2021-07-31

4.  Facebook Support Groups for Pediatric Rare Diseases: Cross-Sectional Study to Investigate Opportunities, Limitations, and Privacy Concerns.

Authors:  Sarah Catrin Titgemeyer; Christian P Schaaf
Journal:  JMIR Pediatr Parent       Date:  2022-01-06

Review 5.  Using Social Media to Engage Knowledge Users in Health Research Priority Setting: Scoping Review.

Authors:  Surabhi Sivaratnam; Kyobin Hwang; Alyssandra Chee-A-Tow; Lily Ren; Geoffrey Fang; Lindsay Jibb
Journal:  J Med Internet Res       Date:  2022-02-21       Impact factor: 7.076

6.  Understanding the #longCOVID and #longhaulers Conversation on Twitter: Multimethod Study.

Authors:  Sara Santarossa; Ashley Rapp; Saily Sardinas; Janine Hussein; Alex Ramirez; Andrea E Cassidy-Bushrow; Philip Cheng; Eunice Yu
Journal:  JMIR Infodemiology       Date:  2022-02-22

Review 7.  Genetic Counseling in Neurodevelopmental Disorders.

Authors:  Alyssa Blesson; Julie S Cohen
Journal:  Cold Spring Harb Perspect Med       Date:  2020-04-01       Impact factor: 6.915

8.  Profiling trial burden and patients' attitudes to improve clinical research in epidermolysis bullosa.

Authors:  Christine Prodinger; Anja Diem; Katherina Ude-Schoder; Josefina Piñón-Hofbauer; Sophie Kitzmueller; Johann W Bauer; Martin Laimer
Journal:  Orphanet J Rare Dis       Date:  2020-07-10       Impact factor: 4.123

9.  Communication Needs for Individuals With Rare Diseases Within and Around the Healthcare System of Northern Ireland.

Authors:  Ashleen L Crowe; Amy Jayne McKnight; Helen McAneney
Journal:  Front Public Health       Date:  2019-08-21

10.  Role for Social Media in Pediatric Liver Disease: Caregiver and Provider Perspectives.

Authors:  Douglas B Mogul; Mary Grace Bowring; Jennifer Lau; Erin Babin; John F P Bridges; Sanjiv Harpavat; Tamir Miloh
Journal:  Pediatr Gastroenterol Hepatol Nutr       Date:  2020-11-05
  10 in total

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