{"id":23352,"date":"2026-02-24T09:34:59","date_gmt":"2026-02-24T08:34:59","guid":{"rendered":"https:\/\/sygeplejevidenskab.dk\/?p=23352"},"modified":"2026-02-24T09:34:59","modified_gmt":"2026-02-24T08:34:59","slug":"at-leve-med-multipel-sklerose-i-danmark-fra-de-foerste-symptomer-til-langvarig-haandtering","status":"publish","type":"post","link":"https:\/\/sygeplejevidenskab.dk\/index.php\/2026\/02\/24\/at-leve-med-multipel-sklerose-i-danmark-fra-de-foerste-symptomer-til-langvarig-haandtering\/","title":{"rendered":"At leve med multipel sklerose i Danmark: fra de f\u00f8rste symptomer til langvarig h\u00e5ndtering"},"content":{"rendered":"<p><img data-recalc-dims=\"1\" fetchpriority=\"high\" decoding=\"async\" class=\"alignnone wp-image-12780 size-full\" src=\"https:\/\/i0.wp.com\/sygeplejevidenskab.dk\/wp-content\/uploads\/2024\/06\/Neurologi.png?resize=690%2C204&#038;quality=80&#038;ssl=1\" alt=\"\" width=\"690\" height=\"204\" srcset=\"https:\/\/i0.wp.com\/sygeplejevidenskab.dk\/wp-content\/uploads\/2024\/06\/Neurologi.png?w=690&amp;quality=80&amp;ssl=1 690w, https:\/\/i0.wp.com\/sygeplejevidenskab.dk\/wp-content\/uploads\/2024\/06\/Neurologi.png?resize=300%2C89&amp;quality=80&amp;ssl=1 300w, https:\/\/i0.wp.com\/sygeplejevidenskab.dk\/wp-content\/uploads\/2024\/06\/Neurologi.png?resize=600%2C177&amp;quality=80&amp;ssl=1 600w\" sizes=\"(max-width: 690px) 100vw, 690px\" \/><\/p>\n<p><span class=\"a_GcMg font-feature-liga-off font-feature-clig-off font-feature-calt-off text-decoration-none text-strikethrough-none\">Parker Buch L, Midtgaard C, Noe Bj\u00f8rnshave B, Selb\u00e6k T, Mose Schlosser L; Navigating life with multiple sclerosis in Denmark: From First Symptoms to Long-Term Management. International Journal of MS Care. 2026, vol. 28. DOI:<\/span> <a class=\"a_GcMg font-feature-liga-off font-feature-clig-off font-feature-calt-off text-decoration-none text-strikethrough-none\" draggable=\"false\" href=\"https:\/\/doi.org\/10.7224\/1537-2073.2024-091\" target=\"_blank\" rel=\"noopener\">https:\/\/doi.org\/10.7224\/1537-2073.2024-091<\/a><\/p>\n<p><span class=\"a_GcMg font-feature-liga-off font-feature-clig-off font-feature-calt-off text-decoration-none text-strikethrough-none\"><em>Af Louise Parker Buch, sygeplejerske, ph.d.-studerende<\/em>. <\/span><a class=\"a_GcMg font-feature-liga-off font-feature-clig-off font-feature-calt-off text-decoration-none text-strikethrough-none\" draggable=\"false\" href=\"mailto:louise.parker.buch@rsyd.dk\" target=\"_blank\" rel=\"noopener\">louise.parker.buch@rsyd.dk<\/a><\/p>\n<p><a class=\"fasc-button fasc-size-medium fasc-type-flat fasc-rounded-medium\" style=\"background-color: #33809e; color: #ffffff;\" target=\"_blank\" href=\"https:\/\/sygeplejevidenskab.dk\/wp-content\/uploads\/2026\/02\/RESUME-1126-At-levemed-multiple-sclerose.pdf\">Download Resume som pdf<\/a><\/p>\n<p class=\"cvGsUA direction-ltr align-justify para-style-body\"><strong><span class=\"a_GcMg font-feature-liga-off font-feature-clig-off font-feature-calt-off text-decoration-none text-strikethrough-none\">Resum\u00e9<br \/>\n<\/span><span style=\"font-size: 16px;\">Introduktion<br \/>\n<\/span><\/strong><span class=\"a_GcMg font-feature-liga-off font-feature-clig-off font-feature-calt-off text-decoration-none text-strikethrough-none\">At f\u00e5 diagnosen multipel sklerose (MS) markerer et afg\u00f8rende vendepunkt i livet med stor betydning for livskvaliteten. Effektiv behandling afh\u00e6nger ikke alene af medicinsk intervention, men ogs\u00e5 af, hvordan mennesker med MS oplever omsorg, st\u00f8tte og inddragelse i behandlingsforl\u00f8bet. Der mangler fortsat viden om levede erfaringer med MS i en dansk sundhedskontekst, s\u00e6rligt i overgangene fra de f\u00f8rste symptomer til livet med en kronisk sygdom.<\/span><\/p>\n<p class=\"cvGsUA direction-ltr align-justify para-style-body\"><strong><span class=\"a_GcMg font-feature-liga-off font-feature-clig-off font-feature-calt-off text-decoration-none text-strikethrough-none\">Metode<br \/>\n<\/span><\/strong><span class=\"a_GcMg font-feature-liga-off font-feature-clig-off font-feature-calt-off text-decoration-none text-strikethrough-none\">Studiet er gennemf\u00f8rt med en f\u00e6nomenologisk-hermeneutisk tilgang. Der blev gennemf\u00f8rt 13 semi-strukturerede, individuelle interviews med personer diagnosticeret med MS inden for de seneste fem \u00e5r. Deltagerne blev rekrutteret fra tre danske MS-klinikker. Data blev analyseret ved hj\u00e6lp af refleksiv tematisk analyse.<\/span><\/p>\n<p class=\"cvGsUA direction-ltr align-justify para-style-body\"><strong><span class=\"a_GcMg font-feature-liga-off font-feature-clig-off font-feature-calt-off text-decoration-none text-strikethrough-none\">Resultater<br \/>\n<\/span><\/strong><span class=\"a_GcMg font-feature-liga-off font-feature-clig-off font-feature-calt-off text-decoration-none text-strikethrough-none\">Overgangen fra at v\u00e6re rask til at leve med MS blev oplevet som en s\u00e6rlig s\u00e5rbar proces. Deltagerne beskrev betydelig f\u00f8lelsesm\u00e6ssig belastning i udrednings- og diagnosefasen samt oplevelser af at blive misforst\u00e5et og ikke taget alvorligt, n\u00e5r de fors\u00f8gte at forklare diffuse symptomer. Efter diagnosen tilpassede de sig gradvist nye livsvilk\u00e5r og udviste modstandskraft og tilpasningsevne i m\u00e5den at leve med sygdommen p\u00e5. <\/span><span class=\"a_GcMg font-feature-liga-off font-feature-clig-off font-feature-calt-off text-decoration-none text-strikethrough-none\">Analysen identificerede tre centrale temaer:<\/span><\/p>\n<ul>\n<li><span class=\"a_GcMg font-feature-liga-off font-feature-clig-off font-feature-calt-off text-decoration-none text-strikethrough-none\">At forst\u00e5 og skulle bevise sine symptomer<\/span><\/li>\n<li><span class=\"a_GcMg font-feature-liga-off font-feature-clig-off font-feature-calt-off text-decoration-none text-strikethrough-none\">Overvejelser om behandling og om hvorvidt og hvordan man skal fort\u00e6lle andre om sin diagnose<\/span><\/li>\n<li><span class=\"a_GcMg font-feature-liga-off font-feature-clig-off font-feature-calt-off text-decoration-none text-strikethrough-none\">At leve med h\u00e5b p\u00e5 trods af sygdommen.<\/span><\/li>\n<\/ul>\n<p class=\"cvGsUA direction-ltr align-justify para-style-body\"><strong><span class=\"a_GcMg font-feature-liga-off font-feature-clig-off font-feature-calt-off text-decoration-none text-strikethrough-none\">Diskussion<br \/>\n<\/span><\/strong><span class=\"a_GcMg font-feature-liga-off font-feature-clig-off font-feature-calt-off text-decoration-none text-strikethrough-none\">Fundene peger p\u00e5, at MS\u2019 ofte usynlige symptomer udfordrer b\u00e5de patienternes selvforst\u00e5else og kommunikationen med sundhedsv\u00e6senet. Manglende anerkendelse og tillid i den tidlige sygdomsfase kan forst\u00e6rke s\u00e5rbarhed og oplevelsen af at st\u00e5 alene i forl\u00f8bet.<\/span><\/p>\n<p class=\"cvGsUA direction-ltr align-justify para-style-body\"><strong><span class=\"a_GcMg font-feature-liga-off font-feature-clig-off font-feature-calt-off text-decoration-none text-strikethrough-none\">Konklusion<br \/>\n<\/span><\/strong><span class=\"a_GcMg font-feature-liga-off font-feature-clig-off font-feature-calt-off text-decoration-none text-strikethrough-none\">Mennesker med MS i Danmark oplever ofte et f\u00f8lelsesm\u00e6ssigt belastende sygdoms- og diagnoseforl\u00f8b. For sundhedsprofessionelle er det afg\u00f8rende at forst\u00e5 patienternes oplevelser fra de f\u00f8rste symptomer til behandling og opf\u00f8lgning.<\/span><\/p>\n<p class=\"cvGsUA direction-ltr align-justify para-style-body\"><strong><span class=\"a_GcMg font-feature-liga-off font-feature-clig-off font-feature-calt-off text-decoration-none text-strikethrough-none\">Implikationer for praksis<br \/>\n<\/span><\/strong><span class=\"a_GcMg font-feature-liga-off font-feature-clig-off font-feature-calt-off text-decoration-none text-strikethrough-none\">Sygeplejersker og \u00f8vrige sundhedsprofessionelle har en central rolle i at st\u00f8tte patienter i den tidlige sygdomsfase og underst\u00f8tte mestring, h\u00e5b og patientinddragelse gennem hele sygdomsforl\u00f8bet.<\/span><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Parker Buch L, Midtgaard C, Noe Bj\u00f8rnshave B, Selb\u00e6k T, Mose Schlosser L; Navigating life with multiple sclerosis in Denmark: [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":12782,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"_ppp_document_settings_meta":"","site-sidebar-layout":"default","site-content-layout":"","ast-site-content-layout":"default","site-content-style":"default","site-sidebar-style":"default","ast-global-header-display":"","ast-banner-title-visibility":"","ast-main-header-display":"","ast-hfb-above-header-display":"","ast-hfb-below-header-display":"","ast-hfb-mobile-header-display":"","site-post-title":"","ast-breadcrumbs-content":"","ast-featured-img":"","footer-sml-layout":"","ast-disable-related-posts":"","theme-transparent-header-meta":"default","adv-header-id-meta":"","stick-header-meta":"","header-above-stick-meta":"","header-main-stick-meta":"","header-below-stick-meta":"","astra-migrate-meta-layouts":"set","ast-page-background-enabled":"default","ast-page-background-meta":{"desktop":{"background-color":"var(--ast-global-color-4)","background-image":"","background-repeat":"repeat","background-position":"center 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