{"id":4931,"date":"2025-01-12T13:50:42","date_gmt":"2025-01-12T11:50:42","guid":{"rendered":"https:\/\/lupusgalicia.org\/?p=4931"},"modified":"2025-01-12T13:50:45","modified_gmt":"2025-01-12T11:50:45","slug":"dia-mundial-do-lupus-2024","status":"publish","type":"post","link":"https:\/\/lupusgalicia.org\/?p=4931&lang=gl","title":{"rendered":"D\u00eda Mundial do Lupus 2024"},"content":{"rendered":"\n<figure class=\"wp-block-image size-large\"><img loading=\"lazy\" decoding=\"async\" width=\"1024\" height=\"768\" src=\"https:\/\/lupusgalicia.org\/wp-content\/uploads\/2024\/07\/HULA_quirofano-1024x768.jpg\" alt=\"\" class=\"wp-image-4734\" srcset=\"https:\/\/lupusgalicia.org\/wp-content\/uploads\/2024\/07\/HULA_quirofano-1024x768.jpg 1024w, https:\/\/lupusgalicia.org\/wp-content\/uploads\/2024\/07\/HULA_quirofano-300x225.jpg 300w, https:\/\/lupusgalicia.org\/wp-content\/uploads\/2024\/07\/HULA_quirofano-768x576.jpg 768w, https:\/\/lupusgalicia.org\/wp-content\/uploads\/2024\/07\/HULA_quirofano-1536x1152.jpg 1536w, https:\/\/lupusgalicia.org\/wp-content\/uploads\/2024\/07\/HULA_quirofano.jpg 2000w\" sizes=\"auto, (max-width: 1024px) 100vw, 1024px\" \/><\/figure>\n\n\n\n<h4 class=\"wp-block-heading\">Un D\u00eda para Facer Visible o Invisible<\/h4>\n\n\n\n<p class=\"wp-block-paragraph\">O pasado 10 de maio, a Asociaci\u00f3n Galega de Lupus (AGAL) uniuse \u00e1 conmemoraci\u00f3n do D\u00eda Mundial do Lupus, unha data crave para dar visibilidade a esta enfermidade autoinmune que afecta a mill\u00f3ns de persoas en todo o mundo. Este ano, esforz\u00e1monos por chegar a cada recuncho de Galicia cunha serie de actividades destinadas a aumentar a concienciaci\u00f3n e apoiar a quen convive co lupus.<\/p>\n\n\n\n<h4 class=\"wp-block-heading\">Mesas Informativas en Toda Galicia<\/h4>\n\n\n\n<p class=\"wp-block-paragraph\">Para educar ao p\u00fablico e proporcionar informaci\u00f3n valiosa sobre o lupus, AGAL instalou mesas informativas en diversas localidades ao longo do territorio galego. Estas mesas estiveron situadas en lugares estrat\u00e9xicos como prazas principais, centros comerciais e hospitais. Voluntarios e profesionais da sa\u00fade estiveron presentes para responder preguntas, distribu\u00edr folletos educativos e compartir recursos sobre o manexo e tratamento do lupus.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\"> A resposta da comunidade foi moi positiva, con moitas persoas acheg\u00e1ndose para aprender m\u00e1is sobre a enfermidade, compartir as s\u00faas experiencias persoais ou mostrar o seu apoio aos afectados. Esta actividade non s\u00f3 serviu para informar, sen\u00f3n tam\u00e9n para crear un espazo de di\u00e1logo e comprensi\u00f3n, fundamental para derrubar os estigmas asociados ao lupus.<\/p>\n\n\n\n<figure class=\"wp-block-image size-large\"><img loading=\"lazy\" decoding=\"async\" width=\"1024\" height=\"768\" src=\"https:\/\/lupusgalicia.org\/wp-content\/uploads\/2024\/07\/WhatsApp-Image-2024-05-10-at-20.40.54-1024x768.jpg\" alt=\"\" class=\"wp-image-4735\" srcset=\"https:\/\/lupusgalicia.org\/wp-content\/uploads\/2024\/07\/WhatsApp-Image-2024-05-10-at-20.40.54-1024x768.jpg 1024w, https:\/\/lupusgalicia.org\/wp-content\/uploads\/2024\/07\/WhatsApp-Image-2024-05-10-at-20.40.54-300x225.jpg 300w, https:\/\/lupusgalicia.org\/wp-content\/uploads\/2024\/07\/WhatsApp-Image-2024-05-10-at-20.40.54-768x576.jpg 768w, https:\/\/lupusgalicia.org\/wp-content\/uploads\/2024\/07\/WhatsApp-Image-2024-05-10-at-20.40.54-1536x1152.jpg 1536w, https:\/\/lupusgalicia.org\/wp-content\/uploads\/2024\/07\/WhatsApp-Image-2024-05-10-at-20.40.54.jpg 2048w\" sizes=\"auto, (max-width: 1024px) 100vw, 1024px\" \/><\/figure>\n\n\n\n<h4 class=\"wp-block-heading\">Iluminando Galicia de Morado<\/h4>\n\n\n\n<p class=\"wp-block-paragraph\">Como parte das iniciativas para dar visibilidade ao lupus, numerosos edificios e monumentos en Galicia ilumin\u00e1ronse de morado, a cor que simboliza a loita contra esta enfermidade. Desde a emblem\u00e1tica Fonte de Catro Cami\u00f1os na Coru\u00f1a ata o Tit\u00e1n do Hospital \u00c1lvaro Cunquiero en Vigo, pasando polo Concello de Santiago de Compostela, a rexi\u00f3n tinguiuse de morado nunha mostra de solidariedade e apoio. <\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Esta iluminaci\u00f3n especial captou a atenci\u00f3n dos residentes locais. A iniciativa axudou a sensibilizar a un p\u00fablico m\u00e1is amplo sobre a importancia da investigaci\u00f3n e o apoio continuo aos pacientes con lupus.<\/p>\n\n\n\n<h4 class=\"wp-block-heading\">Pegada de Carteis: Levando a Mensaxe a Cada Esquina<\/h4>\n\n\n\n<p class=\"wp-block-paragraph\">Ademais, AGAL organizou unha campa\u00f1a de pegada de carteis en farmacias, centros de sa\u00fade, escolas e outros espazos p\u00fablicos. Estes carteis inclu\u00edan informaci\u00f3n crave sobre o lupus, s\u00edntomas a ter en conta, e onde acudir para obter axuda e apoio. As farmacias, en particular, convert\u00e9ronse en puntos cruciais para esta campa\u00f1a, xa que son lugares frecuentemente visitados por persoas que buscan consello e produtos de sa\u00fade. <\/p>\n\n\n\n<p class=\"wp-block-paragraph\">A pegada de carteis foi unha estratexia efectiva para chegar a aqueles que talvez non te\u00f1en acceso \u00e1 informaci\u00f3n dixital ou que prefiren obter a s\u00faa informaci\u00f3n de fontes locais e confiables. Esta campa\u00f1a tam\u00e9n fomentou unha maior implicaci\u00f3n da comunidade, alentando \u00e1s persoas para participar activamente na sensibilizaci\u00f3n sobre o lupus.<\/p>\n\n\n\n<h4 class=\"wp-block-heading\">Compromiso Continuo coa Visibilidade e o Apoio<\/h4>\n\n\n\n<p class=\"wp-block-paragraph\">En AGAL, estamos profundamente comprometidos coa causa de mellorar a calidade de vida dos pacientes con lupus. A celebraci\u00f3n do D\u00eda Mundial do Lupus \u00e9 s\u00f3 una das moitas iniciativas que levamos a cabo para lograr este obxectivo. A trav\u00e9s da educaci\u00f3n, a concienciaci\u00f3n e o apoio comunitario, seguimos traballando para que o lupus sexa unha enfermidade cada vez m\u00e1is visible e comprendida. <\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Agradecemos a todos os voluntarios, colaboradores e \u00e1 comunidade galega polo seu incrible apoio nesta xornada. Xuntos, continuaremos loitando por unha mellor calidade de vida para os pacientes con lupus e seguiremos promovendo actividades que xeren un impacto positivo na nosa sociedade. V\u00e9monos nas pr\u00f3ximas acci\u00f3ns e grazas por ser parte deste esforzo colectivo!<\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Un D\u00eda para Facer Visible o Invisible O pasado 10 de maio, a Asociaci\u00f3n Galega de Lupus (AGAL) uniuse \u00e1 conmemoraci\u00f3n do D\u00eda Mundial do Lupus, unha data crave para dar visibilidade a esta enfermidade autoinmune que afecta a mill\u00f3ns de persoas en todo o mundo. Este ano, esforz\u00e1monos por chegar a cada recuncho de [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":4734,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","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":"","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 center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"tablet":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"mobile":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""}},"ast-content-background-meta":{"desktop":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"tablet":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"mobile":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""}},"footnotes":""},"categories":[103],"tags":[],"class_list":["post-4931","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-sin-categoria-gl"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.2 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\r\n<title>D\u00eda Mundial do Lupus 2024 - Asociaci\u00f3n Galega de Lupus<\/title>\r\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\r\n<link rel=\"canonical\" href=\"https:\/\/lupusgalicia.org\/?p=4931&lang=gl\" \/>\r\n<meta property=\"og:locale\" content=\"es_ES\" \/>\r\n<meta property=\"og:type\" content=\"article\" \/>\r\n<meta property=\"og:title\" content=\"D\u00eda Mundial do Lupus 2024 - Asociaci\u00f3n Galega de Lupus\" \/>\r\n<meta property=\"og:description\" content=\"Un D\u00eda para Facer Visible o Invisible O pasado 10 de maio, a Asociaci\u00f3n Galega de Lupus (AGAL) uniuse \u00e1 conmemoraci\u00f3n do D\u00eda Mundial do Lupus, unha data crave para dar visibilidade a esta enfermidade autoinmune que afecta a mill\u00f3ns de persoas en todo o mundo. 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