{"id":4742,"date":"2025-12-18T14:13:04","date_gmt":"2025-12-18T13:13:04","guid":{"rendered":"https:\/\/esclerosismultiplegalicia.org\/?p=4742"},"modified":"2025-12-18T14:50:20","modified_gmt":"2025-12-18T13:50:20","slug":"dia-nacional-da-esclerose-multiple-2025","status":"publish","type":"post","link":"https:\/\/esclerosismultiplegalicia.org\/index.php\/2025\/12\/18\/dia-nacional-da-esclerose-multiple-2025\/","title":{"rendered":"D\u00eda Nacional da Esclerose M\u00faltiple 2025"},"content":{"rendered":"\n<p class=\"wp-block-paragraph\">Con motivo do <strong>D\u00eda Nacional da Esclerose M\u00faltiple<\/strong>, as entidades que representamos \u00e1s persoas con EM e \u00e1s s\u00faas familias pedimos m\u00e1is compromiso institucional, social e pol\u00edtico. A Esclerose M\u00faltiple \u00e9 unha enfermidade neurodexenerativa cr\u00f3nica que impacta na calidade de vida de <strong>arredor de 68.000 persoas en Espa\u00f1a e 4.500 en Galicia<\/strong>. Atender \u00e1s necesidades de cada unha destas persoas requiere respostas coordinadas, sostidas no tempo e equitativas.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Este manifesto de <a href=\"https:\/\/aedem.org\/\">AEDEM <\/a>recolle un <strong><a href=\"https:\/\/aedem.org\/en-el-dia-nacional-de-la-esclerosis-multiple-aedem-cocemfe-reclama-financiacion-publica-estable-y-lanza-la-iii-edicion-de-contemos-historias-2\/\">Dec\u00e1logo de Reivindicaci\u00f3ns<\/a> <\/strong>que se centra nos dereitos, a dignidade e a igualdade de oportunidades das persoas con EM e as familias, independentemente do seu lugar de residencia.<\/p>\n\n\n\n<h3 class=\"wp-block-heading\">Financiaci\u00f3n, diagn\u00f3stico temper\u00e1n e investigaci\u00f3n<\/h3>\n\n\n\n<p class=\"wp-block-paragraph\">Garantir unha <strong>financiaci\u00f3n xusta, adecuada e sostible<\/strong> serve para asegurar o futuro das asociaci\u00f3ns de EM. Estas entidades desempe\u00f1amos un papel esencial dende o diagn\u00f3stico. Ofrecemos servizos de rehabilitaci\u00f3n, apoio psicosocial e recursos que melloran de forma directa a calidade de vida das persoas con EM e as s\u00faas familias.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">O <strong>diagn\u00f3stico temper\u00e1n da Esclerose M\u00faltiple<\/strong> \u00e9 outro eixo fundamental. Detectar a enfermidade a tempo permite un acceso precoz a tratamentos farmacol\u00f3xicos e rehabilitadores. Tam\u00e9n a medidas de protecci\u00f3n social que reducen o impacto da discapacidade e a incertidume dende as primeiras fases.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Xunto a isto, resulta imprescindible <strong>incrementar os recursos destinados \u00e1 investigaci\u00f3n<\/strong>, co obxectivo de avanzar cara tratamentos m\u00e1is eficaces e, a longo prazo, cara unha cura definitiva da EM.<\/p>\n\n\n\n<h3 class=\"wp-block-heading\">Atenci\u00f3n integral<\/h3>\n\n\n\n<p class=\"wp-block-paragraph\">Reivindicamos o acceso a un <strong>tratamento rehabilitador integral, personalizado, gratuito e continuado<\/strong>. Igual en todos os territorios, urbano e rural, reforzando o papel das asociaci\u00f3ns de pacientes como axentes de apoio do sistema de atenci\u00f3n.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">A <strong>equidade no acceso aos tratamentos farmacol\u00f3xicos<\/strong> segue sendo unha materia pendente. Non poden existir desigualdades entre territorios nin entre centros hospitalarios. E menos cando se trata de garantir a mellor atenci\u00f3n posible para cada persoa con EM.<\/p>\n\n\n\n<h3 class=\"wp-block-heading\">Emprego, familias e corresponsabilidade social<\/h3>\n\n\n\n<p class=\"wp-block-paragraph\">A inclusi\u00f3n laboral \u00e9 un dereito. Por iso, reclamamos un maior compromiso do tecido empresarial na <strong>adaptaci\u00f3n dos postos de traballo<\/strong>. Tam\u00e9n no cumprimento da normativa vixente sobre contrataci\u00f3n de persoas con discapacidade.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Ademais, \u00e9 imprescindible <strong>reforzar o apoio das administraci\u00f3ns p\u00fablicas \u00e1s familias<\/strong>, que en moitos casos asumen o rol de coidadoras principais. Isto sup\u00f3n un impacto persoal, laboral e econ\u00f3mico.<\/p>\n\n\n\n<h3 class=\"wp-block-heading\">Progresi\u00f3n silenciosa e apoio econ\u00f3mico estable<\/h3>\n\n\n\n<p class=\"wp-block-paragraph\">Estas reivindicaci\u00f3ns al\u00ed\u00f1anse coas mensaxes trasladadas recentemente no Congreso dos Deputados, durante a xornada <em>\u201cEsclerosis m\u00faltiple y progresi\u00f3n de la discapacidad: retos para un abordaje \u00f3ptimo\u201d<\/em>, celebrada no Congreso dos Deputados.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Neste foro, subli\u00f1ouse que<strong> a EM tam\u00e9n progresa cando non hai brotes visibles<\/strong>. A progresi\u00f3n silenciosa esixe unha atenci\u00f3n m\u00e1is coordinada, unha visi\u00f3n a longo prazo e pol\u00edticas sanitarias e sociais que non se limiten tan s\u00f3 aos momentos m\u00e1is evidentes da enfermidade.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Pedro Cuesta Aguilar, Presidente de AEDEM-COCEMFE, afirmou nesta xornada:<\/p>\n\n\n\n<blockquote class=\"wp-block-quote is-layout-flow wp-block-quote-is-layout-flow\">\n<p class=\"wp-block-paragraph\">&#8220;O traballo das nosas asociaci\u00f3ns \u00e9 imprescindible e evita que moitas persoas queden desatendidas. Pero esta labor non pode sosterse sen un apoio econ\u00f3mico estable e suficiente. Reclamamos un compromiso firme das administraci\u00f3ns p\u00fablicas que garanta un financiamento regular e cun pago puntual das subvenci\u00f3ns, que permita manter a nosa estrutura e desenvolver os nosos proxectos e servizos&#8221;.<\/p>\n<\/blockquote>\n\n\n\n<p class=\"wp-block-paragraph\">Este mesmo, continuou no mesmo discurso:<\/p>\n\n\n\n<blockquote class=\"wp-block-quote is-layout-flow wp-block-quote-is-layout-flow\">\n<p class=\"wp-block-paragraph\">&#8220;Sen un financiamento adecuado \u00e9 imposible levar a cabo estas obrigas sen po\u00f1er en risco a superviviencia das asociaci\u00f3ns&#8221;.<\/p>\n<\/blockquote>\n\n\n\n<figure class=\"wp-block-video\"><video height=\"360\" style=\"aspect-ratio: 640 \/ 360;\" width=\"640\" controls src=\"https:\/\/esclerosismultiplegalicia.org\/wp-content\/uploads\/2025\/12\/WhatsApp-Video-2025-12-18-at-11.55.40.mp4\"><\/video><\/figure>\n\n\n\n<h3 class=\"wp-block-heading\">Informaci\u00f3n, accesibilidade e sensibilizaci\u00f3n social<\/h3>\n\n\n\n<p class=\"wp-block-paragraph\">Garantir a <strong>accesibilidade universal e fomentar unha maior sensibilizaci\u00f3n<\/strong> social son condici\u00f3ns indispensables para unha inclusi\u00f3n real. Neste sentido, resulta fundamental o impulso de campa\u00f1as de informaci\u00f3n e educaci\u00f3n sobre a Esclerose M\u00faltiple, promovidas polos Gobernos central e auton\u00f3micos, apoiadas en materiais educativos rigorosos e accesibles. Non s\u00f3 para nenos e nenas nas escolas, sen\u00f3n tam\u00e9n para o persoal profesional da sa\u00fade que atende a persoas con EM e familiares no desenvolvemento do seu traballo.<\/p>\n\n\n\n<h3 class=\"wp-block-heading\">A Esclerose M\u00faltiple non agarda<\/h3>\n\n\n\n<p class=\"wp-block-paragraph\">A Esclerose M\u00faltiple<strong> non sempre se ve a simple vista, pero est\u00e1.<\/strong> Avanza, condiciona e esixe respostas acertadas, r\u00e1pidas e claras. Coordinarse e traballar en conxunto \u00e9 moi importante para avanzar cara un modelo m\u00e1is xusto, equitativo e humano, centrado nas necesidades de cada persoa.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Garantir estes dereitos hoxe, significa construir unha mellor calidade de vida para todos e todas o d\u00eda de ma\u00f1\u00e1. <strong>Porque a Esclerose M\u00faltiple non agarda. Porque o cambio ten que vir xa.<\/strong><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Con motivo do D\u00eda Nacional da Esclerose M\u00faltiple, as entidades&hellip; <a class=\"continue\" href=\"https:\/\/esclerosismultiplegalicia.org\/index.php\/2025\/12\/18\/dia-nacional-da-esclerose-multiple-2025\/\">Ler m\u00e1is sobre<span> D\u00eda Nacional da Esclerose M\u00faltiple 2025<\/span><\/a><\/p>\n","protected":false},"author":1,"featured_media":4360,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_kad_post_transparent":"","_kad_post_title":"","_kad_post_layout":"","_kad_post_sidebar_id":"","_kad_post_content_style":"","_kad_post_vertical_padding":"","_kad_post_feature":"","_kad_post_feature_position":"","_kad_post_header":false,"_kad_post_footer":false,"footnotes":""},"categories":[103],"tags":[154,13],"class_list":["post-4742","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-novas","tag-dia-nacional-em","tag-fegadem"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v26.1.1 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>D\u00eda Nacional da Esclerose M\u00faltiple 2025 - FEGADEM<\/title>\n<meta name=\"description\" content=\"Con motivo do D\u00eda Nacional da EM, as entidades pedimos m\u00e1is compromiso institucional, 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