{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,1,14]],"date-time":"2026-01-14T16:22:50Z","timestamp":1768407770825,"version":"3.49.0"},"reference-count":30,"publisher":"Wiley","issue":"4","license":[{"start":{"date-parts":[[2010,10,8]],"date-time":"2010-10-08T00:00:00Z","timestamp":1286496000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Nursing &amp; Health Sciences"],"published-print":{"date-parts":[[2010,12]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>The aim of this study was to obtain descriptions of the experiences of fatigue of people with multiple sclerosis, including experiences related to their interpersonal relations and social life. We used a qualitative, exploratory, and descriptive design and conducted semistructured interviews with nine participants. Seven concepts emerged from the data analysis: \u201cfatigue as an individualized and novel sensation\u201d, \u201cself\u2010analysis of the factors that are associated with fatigue\u201d, \u201ceffects of fatigue on living and the self\u201d, \u201cunique measures for handling fatigue\u201d, \u201cinsufficient coping\u201d, \u201cliving with fatigue\u201d, and \u201cthe assumption of a lack of common understanding of fatigue.\u201d Based on these findings, fatigue was found to affect the lifestyle of people with MS and their ability to be true to themself. As a result, the participants devised their own way of coping with fatigue. However, the coping measures also created other dilemmas, which led to isolation. Nevertheless, the participants made efforts to live with fatigue on their own terms.<\/jats:p>","DOI":"10.1111\/j.1442-2018.2010.00554.x","type":"journal-article","created":{"date-parts":[[2010,10,8]],"date-time":"2010-10-08T06:56:24Z","timestamp":1286520984000},"page":"421-428","source":"Crossref","is-referenced-by-count":13,"title":["Fatigue in Japanese people with multiple sclerosis"],"prefix":"10.1111","volume":"12","author":[{"given":"Rika","family":"Moriya","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Masami","family":"Kutsumi","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2010,10,8]]},"reference":[{"key":"e_1_2_7_2_1","doi-asserted-by":"publisher","DOI":"10.1177\/135245850000600308"},{"key":"e_1_2_7_3_1","volume-title":"Multiple Sclerosis Theory and Practice for Nurses","author":"Burgess M","year":"2002"},{"key":"e_1_2_7_4_1","doi-asserted-by":"publisher","DOI":"10.1017\/S0317167100048691"},{"key":"e_1_2_7_5_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0020-7489(03)00010-5"},{"key":"e_1_2_7_6_1","volume-title":"[An Introduction to Qualitative Research: Methodology for Human Science.]","author":"Flick U","year":"2002"},{"key":"e_1_2_7_7_1","doi-asserted-by":"publisher","DOI":"10.4103\/0972-2327.44559"},{"key":"e_1_2_7_8_1","volume-title":"Advanced Concepts in Multiple Sclerosis Nursing Care","author":"Halper J","year":"2007"},{"key":"e_1_2_7_9_1","doi-asserted-by":"publisher","DOI":"10.1002\/j.2048-7940.1992.tb01542.x"},{"key":"e_1_2_7_10_1","doi-asserted-by":"crossref","first-page":"10","DOI":"10.1177\/135245859900500103","article-title":"The Fatigue Descriptive Scale (FDS): a useful tool to evaluate fatigue in multiple sclerosis","volume":"5","author":"Iriarts J","year":"1999","journal-title":"Mult. 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