The Socioeconomic and Psychological Impact of the COVID-19 Pandemic on People with Multiple Sclerosis in Turkey

dc.contributor.authorGunduz, Tuncay
dc.contributor.authorUzunkopru, Cihat
dc.contributor.authorDemir, Serkan
dc.contributor.authorTutuncu, Melih
dc.contributor.authorSeferoglu, Meral
dc.contributor.authorGumus, Haluk
dc.contributor.authorSen, Sedat
dc.contributor.authorGungor Dogan, Ipek
dc.contributor.authorTutuncu, Mesude
dc.contributor.authorSolak Calikoglu, Yasemin
dc.contributor.authorBeckmann, Yesim
dc.contributor.authorSagduyu Kocaman, Ayse
dc.contributor.authorSiva, Aksel
dc.date.accessioned2023-02-21T12:40:50Z
dc.date.available2023-02-21T12:40:50Z
dc.date.issued2022-01-01
dc.description.abstractIntroduction: Various restrictions due to the coronavirus infection have affected working life globally. People with multiple sclerosis (pwMS) have several difficulties in social life, patient follow-up, and receiving treatments. In this study, we aimed to evaluate the experiences of pwMS during the COVID-19 pandemic. Method: We developed a 50-question survey aiming to determine fears, anxieties, and the problems experienced by patients regarding their diseases and social lives during the COVID-19 pandemic. The questionnaire was released online via the Turkish MS Society website, local MS societies websites, and social media accounts. Only the answers of the patients who filled out the questionnaire completely were evaluated. Results: In total, 6008 patients took the survey, and 3255 of them completed the questionnaire. Among all, 378 patients (11.6\%) were positive for COVID-19. The most common COVID-19-related symptom was fatigue (48.4\%). The routine medical follow-up was interrupted in 61.4\% and the medication was discontinued in 14\% of the patients. Approximately 25\% of the patients reported different symptoms related to relapse activity. The main concern of the patients related to the COVID-19 pandemic was the disruption of the health of the ones they loved. Among all the patients, 4.4\% lost their jobs. Conclusion: Our data showed that the COVID-19 pandemic strongly affected the working lives of pwMS. Also, the pandemic changed the attitudes of patients and neurologists. Therefore, the long-term effects of the COVID-19 pandemic on disease approach, patient follow-up, social conditions, and working life should be monitored.
dc.description.issue3
dc.description.issueSEP
dc.description.pages226-231
dc.description.volume59
dc.identifier.doi10.29399/npa.28189
dc.identifier.urihttps://hdl.handle.net/11443/2657
dc.identifier.urihttp://dx.doi.org/10.29399/npa.28189
dc.identifier.wosWOS:000852623200011
dc.publisherTURKISH NEUROPSYCHIATRY ASSOC-TURK NOROPSIKIYATRI DERNEGI
dc.relation.ispartofNOROPSIKIYATRI ARSIVI-ARCHIVES OF NEUROPSYCHIATRY
dc.subjectMultiple sclerosis
dc.subjectpandemic
dc.subjectpsychological effects
dc.subjectsocioeconomic effects
dc.titleThe Socioeconomic and Psychological Impact of the COVID-19 Pandemic on People with Multiple Sclerosis in Turkey
dc.typeArticle

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