{"id":55375,"date":"2024-06-21T09:13:09","date_gmt":"2024-06-21T07:13:09","guid":{"rendered":"https:\/\/www.rehagirona.com\/?p=55375"},"modified":"2024-06-21T09:40:59","modified_gmt":"2024-06-21T07:40:59","slug":"viure-europa-amb-ela-al-dia-internacional-de-lela","status":"publish","type":"post","link":"https:\/\/www.rehagirona.com\/ca\/dia-mundial-esclerosi-lateral-amiotrofica-2024\/","title":{"rendered":"Viure Europa amb Ela al Dia Internacional de l&#8217;ELA"},"content":{"rendered":"<p>Avui se celebra el <strong>Dia Mundial d&#8217;Esclerosi Lateral Amiotr\u00f2fica (ELA)<\/strong> que, amb el prop\u00f2sit de millorar i augmentar la qualitat i esperan\u00e7a de vida dels pacients amb ELA, promou la investigaci\u00f3 i la conscienciaci\u00f3 sobre aquesta malaltia.<\/p>\n<p>&nbsp;<\/p>\n<h2>ESDEVENIMENT VIURE EUROPA AMB ELA<\/h2>\n<p>L&#8217;<a href=\"https:\/\/adelaweb.org\/\" target=\"_blank\" rel=\"noopener\"><span style=\"color: #faaf08;\"><strong>Associaci\u00f3 Espanyola d&#8217;Esclerosi Lateral Amiotr\u00f2fica (ADELA)<\/strong><\/span><\/a> ha organitzat un esdeveniment, conjuntament amb l&#8217;Oficina del Parlament Europeu a Espanya, per visibilitzar i sensibilitzar sobre la situaci\u00f3 actual dels malalts d\u00b4ELA, els seus familiars i cuidadors a Espanya i Europa.<\/p>\n<p>Sota el nom <em><strong>Viure Europa amb ELA<\/strong><\/em>, avui a les 11 h t\u00e9 lloc a l&#8217;Oficina del Parlament Europeu a Espanya (Castellana, 46 \u2013 Madrid) aquest esdeveniment que t\u00e9 com a objectiu principal visibilitzar la realitat dels pacients d&#8217;ELA, els seus familiars i cuidadors a Europa, conscienciar sobre aquesta malaltia i fomentar la col\u00b7laboraci\u00f3 entre institucions, professionals de la salut i la societat civil.<\/p>\n<p>&nbsp;<\/p>\n<h2>QU\u00c8 \u00c9S L&#8217;ELA?<\/h2>\n<p>La malaltia afecta els m\u00fasculs del cos a poc a poc fins a arribar a una par\u00e0lisi total, per\u00f2 no afecta la ment, que es mant\u00e9 intacta. A Espanya estan diagnosticades amb ELA al voltant d&#8217;unes 4.000 persones. \u00c9s la tercera malaltia neurodegenerativa m\u00e9s freq\u00fcent despr\u00e9s de la dem\u00e8ncia i la malaltia de Parkinson.<\/p>\n<p>&nbsp;<\/p>\n<h2>ESPERAN\u00c7A DE VIDA<\/h2>\n<p>Actualment \u00e9s una malaltia que no t\u00e9 cura ni disposa d&#8217;un tractament que freni el seu aven\u00e7.<\/p>\n<p>L&#8217;esperan\u00e7a de vida dels afectats \u00e9s al voltant dels 3 anys, ja que nom\u00e9s un 20% sobreviu 5 anys i nom\u00e9s un 10% arriba a viure 10 anys despr\u00e9s del diagn\u00f2stic.<\/p>\n<p>&nbsp;<\/p>\n<h2>M\u00c9S INVESTIGACI\u00d3 PER A L&#8217;ELA<\/h2>\n<p>Des de Rehagirona ens sumem al clam per promoure la investigaci\u00f3 cient\u00edfica a l&#8217;ELA. Actualment s&#8217;estan duent a terme moltes investigacions a tot el m\u00f3n per descobrir qu\u00e8 \u00e9s el que origina l&#8217;Esclerosi Lateral Amiotr\u00f2fica i com aturar-ne l&#8217;aven\u00e7.<\/p>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Avui se celebra el Dia Mundial d&#8217;Esclerosi Lateral Amiotr\u00f2fica (ELA) que, amb el prop\u00f2sit de millorar i augmentar la qualitat [&hellip;]<\/p>\n","protected":false},"author":4,"featured_media":55372,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[6006],"tags":[3120,3119,1633],"class_list":["post-55375","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-dia-internacional-ca","tag-ela-ca","tag-esclerosi-lateral-amiotrofica","tag-rehagirona-2-ca"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v26.8 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Viure Europa amb Ela al Dia Internacional de l&#039;ELA - 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