{"id":2831,"date":"2025-02-07T14:02:00","date_gmt":"2025-02-07T13:02:00","guid":{"rendered":"https:\/\/prueba.esclerosismultiplegalicia.org\/?p=2831"},"modified":"2025-09-09T14:16:54","modified_gmt":"2025-09-09T12:16:54","slug":"consulta-publica-sobre-a-lei-ela-incluamos-a-esclerose-multiple","status":"publish","type":"post","link":"https:\/\/esclerosismultiplegalicia.org\/index.php\/2025\/02\/07\/consulta-publica-sobre-a-lei-ela-incluamos-a-esclerose-multiple\/","title":{"rendered":"Consulta p\u00fablica sobre a Lei ELA: incluamos a Esclerose M\u00faltiple"},"content":{"rendered":"\n<h3 class=\"wp-block-heading has-theme-palette-2-color has-text-color has-link-color wp-elements-0a00342f2aae6a7be14986051934e939\"><em>Dende FEGADEM pedimos a colaboraci\u00f3n de todas as persoas, asociaci\u00f3ns e organizaci\u00f3ns para inclu\u00edr a Esclerose M\u00faltiple no listado de enfermidades que desenvolver\u00e1 a Lei 3\/2024 (Lei ELA).<\/em><\/h3>\n\n\n\n<p>A&nbsp;<strong>Lei 3\/2024 (Lei ELA)<\/strong>&nbsp;\u00e9 un gran avance para as persoas con enfermidades neurodexenerativas, xa que busca&nbsp;<strong>axilizar tr\u00e1mites administrativos, garantir unha mellor atenci\u00f3n social e sanitaria e mellorar a calidade de vida<\/strong>&nbsp;de quen a precisa.<\/p>\n\n\n\n<p>Actualmente, o&nbsp;<strong>Ministerio de Sanidade abriu unha consulta p\u00fablica<\/strong>&nbsp;para definir que enfermidades se incluir\u00e1n no desenvolvemento desta lei. Dende&nbsp;<strong>FEGADEM e outras organizaci\u00f3ns de Esclerose M\u00faltiple a nivel nacional<\/strong>, estamos loitando para que a&nbsp;<a href=\"https:\/\/esclerosismultiplegalicia.org\/esclerose_multiple_ga.html\" target=\"_blank\" rel=\"noreferrer noopener\"><strong>Esclerose M\u00faltiple (EM)<\/strong><\/a>&nbsp;sexa unha das patolox\u00edas representadas.<\/p>\n\n\n\n<p>Participar \u00e9 sinxelo, polo que prec\u00edsase a colaboraci\u00f3n de todos e todas para logralo. Precisamos o teu apoio&nbsp;<strong>antes<\/strong>&nbsp;<strong>do domingo 9 de febreiro.<\/strong><\/p>\n\n\n\n<h3 class=\"wp-block-heading\"><strong>Por que \u00e9 importante que a Esclerose M\u00faltiple estea na Lei 3\/2024?<\/strong><\/h3>\n\n\n\n<p>Se a EM \u00e9 inclu\u00edda nesta lei, ser\u00eda posible mellorar aspectos clave como:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li><strong>Traballar polo reco\u00f1ecemento autom\u00e1tico do 33% de discapacidade<\/strong>\u00a0no momento do diagn\u00f3stico.<\/li>\n\n\n\n<li><strong>Axilizaci\u00f3n de tr\u00e1mites burocr\u00e1ticos<\/strong>\u00a0para o reco\u00f1ecemento de discapacidade e dependencia.<\/li>\n\n\n\n<li><strong>Maior acceso a coidados e axudas sociais e sanitarias.<\/strong><\/li>\n\n\n\n<li><strong>M\u00e1is apoio para os\/as coidadores\/as e familias.<\/strong><\/li>\n<\/ul>\n\n\n\n<p>\u00c9 unha oportunidade hist\u00f3rica para mellorar a vida das persoas con Esclerose M\u00faltiple.&nbsp;<strong>Pero para que isto ocurra, \u00e9 imprescindible que moitas persoas participen na consulta p\u00fablica.<\/strong><\/p>\n\n\n\n<h3 class=\"wp-block-heading\"><strong>Como participar na consulta p\u00fablica<\/strong><\/h3>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>Prazo<\/strong>:<\/h4>\n\n\n\n<p>Ata o&nbsp;<strong>domingo 9 de febreiro de 2025<\/strong>.<\/p>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>Quen pode participar<\/strong>:<\/h4>\n\n\n\n<p>Calquera persoa (pacientes, familiares, profesionais, asociaci\u00f3ns, empresas, cidadan\u00eda en xeral).<\/p>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>Como facelo<\/strong>:<\/h4>\n\n\n\n<p>Enviando un correo electr\u00f3nico ao buz\u00f3n habilitado polo&nbsp;<a href=\"https:\/\/www.sanidad.gob.es\/\" target=\"_blank\" rel=\"noreferrer noopener\"><strong>Ministerio de Sanidad<\/strong><\/a>e.<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Email\u00a0ao que hai que escribir:\u00a0<strong>normativa-sgca@sanidad.gob.es<\/strong><\/li>\n\n\n\n<li><strong>Asunto\u00a0<\/strong>do correo:\u00a0&#8220;En referencia a la consulta p\u00fablica previa a la elaboraci\u00f3n del proyecto de Real Decreto que desarrollar\u00e1 la Ley 3\/2024 (Ley ELA) + [o teu nome e apelidos]&#8221;.<\/li>\n\n\n\n<li><strong>Mensaxe do correo:<\/strong>\n<ul class=\"wp-block-list\">\n<li><strong>Identif\u00edcate<\/strong>\u00a0co teu nome, apelidos, DNI\/CIF e correo electr\u00f3nico (<strong>IMPORTANTE<\/strong>. Se non te identificas correctamente, os teus comentarios non se ter\u00e1n en conta).<\/li>\n\n\n\n<li>Explica que &#8220;la remisi\u00f3n de comentarios al correo indicado es a efectos de la consulta p\u00fablica de la propuesta de Real Decreto referida&#8221;.<\/li>\n\n\n\n<li>Exp\u00f3n a t\u00faa opini\u00f3n sobre a inclusi\u00f3n da Esclerose M\u00faltiple na lei.<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n\n\n\n<h3 class=\"wp-block-heading\"><strong>Que podes dicir na t\u00faa aportaci\u00f3n?<\/strong><\/h3>\n\n\n\n<p>Podes basearte nestes puntos:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>A Esclerose M\u00faltiple \u00e9 unha enfermidade\u00a0<strong>neurodexenerativa, cr\u00f3nica e autoinmune<\/strong>, cunha reduci\u00f3n significativa da calidade de vida.<\/li>\n\n\n\n<li>Non existe unha cura e\u00a0<strong>os tratamentos actuais non sempre evitan a progresi\u00f3n da enfermidade.<\/strong><\/li>\n\n\n\n<li>A EM require\u00a0<strong>coidados complexos, tanto sanitarios como sociais<\/strong>, que supo\u00f1en un alto impacto na contorna da persoa.<\/li>\n\n\n\n<li>A progresi\u00f3n da EM \u00e9, moitas veces, r\u00e1pida e\u00a0<strong>fai imprescindible acelerar a valoraci\u00f3n de discapacidade e dependencia<\/strong>.<\/li>\n<\/ul>\n\n\n\n<p><strong>Cantas m\u00e1is persoas participen, m\u00e1is posibilidades teremos de lograr este avance.<\/strong><\/p>\n\n\n\n<h3 class=\"wp-block-heading\"><strong>Non deixes pasar esta oportunidade<\/strong><\/h3>\n\n\n\n<p>Dende FEGADEM instamos a todas as persoas con Esclerose M\u00faltiple, \u00e1s s\u00faas familias e \u00e1 cidadan\u00eda en xeral a participar nesta consulta p\u00fablica.&nbsp;<strong>\u00c9 un paso decisivo para mellorar a calidade de vida de quen convive coa EM.&nbsp;<\/strong>Se tes d\u00fabidas, contacta connosco. Xuntos\/as podemos logralo!<\/p>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>Prazo: ata o 9 de febreiro de 2025<\/strong><br><strong>Correo para participar:<\/strong>&nbsp;<a>normativa-sgca@sanidad.gob.es<\/a><\/h4>\n\n\n\n<p>Podes ver m\u00e1is informaci\u00f3n&nbsp;<a href=\"https:\/\/www.sanidad.gob.es\/gabinete\/notasPrensa.do?id=6605\" target=\"_blank\" rel=\"noreferrer noopener\">aqu\u00ed<\/a>.&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Dende FEGADEM pedimos a colaboraci\u00f3n de todas as persoas, asociaci\u00f3ns&hellip; <a class=\"continue\" href=\"https:\/\/esclerosismultiplegalicia.org\/index.php\/2025\/02\/07\/consulta-publica-sobre-a-lei-ela-incluamos-a-esclerose-multiple\/\">Ler m\u00e1is sobre<span> Consulta p\u00fablica sobre a Lei ELA: incluamos a Esclerose M\u00faltiple<\/span><\/a><\/p>\n","protected":false},"author":1,"featured_media":0,"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":[13,115],"class_list":["post-2831","post","type-post","status-publish","format-standard","hentry","category-novas","tag-fegadem","tag-reivindicacions"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v26.1.1 - 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