Illness Experiences and Attitudes towards Medication in Online Communities for People with Fibromyalgia

Fibromyalgia is a chronic disabling syndrome, and the legitimacy of its diagnosis is still debated. Internet and online communities may become a relevant resource for affected people. This present study aims to understand the role of online communities relating to fibromyalgia syndrome (FMS) patients' illness experiences and their attitudes towards medication. A qualitative content analysis based on the grounded theory approach was conducted on 19 conversations from an online forum, and 14 online interviews. Illness experience, lack of reference points, online communities, personal role and attitude towards medication were the five categories identified, with the search for recognition as the core category. The study highlighted that online communities represent a resource that allows users to express and share their needs, especially in terms of legitimacy and recognition.

Medienart:

E-Artikel

Erscheinungsjahr:

2020

Erschienen:

2020

Enthalten in:

Zur Gesamtaufnahme - volume:17

Enthalten in:

International journal of environmental research and public health - 17(2020), 22 vom: 23. Nov.

Sprache:

Englisch

Beteiligte Personen:

Cipolletta, Sabrina [VerfasserIn]
Tomaino, Silvia Caterina Maria [VerfasserIn]
Lo Magno, Eliana [VerfasserIn]
Faccio, Elena [VerfasserIn]

Links:

Volltext

Themen:

E-health
Fibromyalgia
Illness experience
Journal Article
Medication
Online communities

Anmerkungen:

Date Completed 28.01.2021

Date Revised 28.01.2021

published: Electronic

Citation Status MEDLINE

doi:

10.3390/ijerph17228683

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM318050870