{"id":1045,"date":"2025-09-16T10:24:17","date_gmt":"2025-09-16T13:24:17","guid":{"rendered":"https:\/\/impactocastex.com.ar\/?p=1045"},"modified":"2025-09-16T10:24:18","modified_gmt":"2025-09-16T13:24:18","slug":"el-pedido-de-ayuda-de-una-adolescente-con-un-raro-tipo-de-cancer","status":"publish","type":"post","link":"https:\/\/impactocastex.com.ar\/?p=1045","title":{"rendered":"El pedido de ayuda de una adolescente con un raro tipo de c\u00e1ncer"},"content":{"rendered":"\n<p>Hace 3 minutos<\/p>\n\n\n\n<p><strong>Luana&nbsp;vive en San Antonio de Padua, Buenos Aires,&nbsp;tiene 17 a\u00f1os<\/strong>&nbsp;y este verano le diagnosticaron<strong>&nbsp;c\u00e1ncer de tiroides con met\u00e1stasis en los pulmones.<\/strong>&nbsp;Se trata de<strong>&nbsp;un tipo que solo tienen cinco personas en Argentina y 25 en Estados Unidos.<\/strong>&nbsp;Desde entonces su familia cubre la quimioterapia a trav\u00e9s de pastillas para controlar su situaci\u00f3n, pero la enfermedad avanz\u00f3 r\u00e1pidamente y&nbsp;ese tratamiento ya no es suficiente para su caso.<\/p>\n\n\n\n<p>El problema es que&nbsp;los medicamentos que necesita no ingresan al pa\u00eds&nbsp;y el precio en Estados Unidos es elevad\u00edsimo. Por eso, la adolescente difundi\u00f3 un video en el que pide colaboraci\u00f3n para poder costear el nuevo tratamiento que le mejorar\u00eda su calidad de vida.<\/p>\n\n\n\n<p>\u201cHola, soy Luana y ellas son mis amigas. Les vengo a contar un poco sobre mi situaci\u00f3n, necesito ayuda\u201d, comienza la grabaci\u00f3n que public\u00f3 en las redes sociales.<\/p>\n\n\n\n<p>La chica que asiste al Instituto Nicol\u00e1s Avellaneda,&nbsp;relat\u00f3 que el 1\u00b0 de enero los m\u00e9dicos detectaron el c\u00e1ncer y comenzaron con un tratamiento que le imposibilita llevar un ritmo de vida normal:<strong>&nbsp;\u201cLas pastillas serv\u00edan para que no avance, pero&nbsp;en este momento est\u00e1 avanzando de manera agresiva,&nbsp;por lo que no es efectivo y no es suficiente\u201d.<\/strong><\/p>\n\n\n\n<p>Y lament\u00f3: \u00abEstos efectos secundarios no me dejan vivir,&nbsp;<strong>me causan dolores musculares, n\u00e1useas y vomitos.&nbsp;<\/strong>Y el c\u00e1ncer en este momento est\u00e1 avanzando de manera agresiva\u00bb.<\/p>\n\n\n\n<p>En ese sentido, una de las amigas agreg\u00f3 que Luana no va al colegio desde que empezaron las clases por su malestar: \u201cTiene v\u00f3mitos, no puede comer sin sentirse mal.<strong>&nbsp;Tiene una dieta muy estricta y lleg\u00f3 a estar cinco horas en la guardia por haberle ca\u00eddo mal una comida<\/strong>. A veces,&nbsp;ni siquiera tiene fuerza para levantarse de la cama. Es muy grave\u201d.<\/p>\n\n\n\n<p>Seg\u00fan sus especialistas,&nbsp;<strong>el medicamento que actualmente requiere -el&nbsp;Selpercatinib- no ingresa a la Argentina.&nbsp;<\/strong>Est\u00e1 en Pa\u00edses Bajos y en Estados Unidos, donde&nbsp;la caja para un mes de tratamiento cuesta alrededor de<strong>&nbsp;20 mil d\u00f3lares.<\/strong><\/p>\n\n\n\n<p><strong>El 30 de septiembre Luana&nbsp;tendr\u00e1 su primera cirug\u00eda, pero&nbsp;la obra social no cubre los materiales necesarios<\/strong>&nbsp;y se suma a los gastos que a su familia le es imposible de costear.<\/p>\n\n\n\n<p>Entre l\u00e1grimas, la joven expres\u00f3: \u201cSin esos elementos no me pueden operar porque es una cirug\u00eda muy compleja y quieren que yo los pague. Y yo no tengo el dinero para pagarlo porque son millones de pesos.&nbsp;Soy muy chica para pasar por estas cosas.&nbsp;<strong>Quer\u00eda pedir un poco de ayuda, por m\u00e1s que me de verg\u00fcenza\u201d.<\/strong><\/p>\n\n\n\n<p>Luego de las emotivas palabras de Luana, su amiga reforz\u00f3 el pedido: \u201cNo es una situaci\u00f3n f\u00e1cil. Son millones y millones que se necesitan. La familia estuvo tratando de costear todo, pero se volvi\u00f3 cuesta arriba porque el hermano de Lu tambi\u00e9n tiene que operarse\u201d.<\/p>\n\n\n\n<p>\u201cPor favor si pueden colaborar y difundir, Luli&nbsp;nos necesita\u201d, cerr\u00f3 el posteo en redes y comparti\u00f3 el alias a donde se puede transferir para ayudar:&nbsp;<strong>TODOSXLULITA,&nbsp;que est\u00e1 a cargo de&nbsp;Valeria Mora, su mam\u00e1.<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-image\"><img decoding=\"async\" src=\"https:\/\/www.rosario3.com\/export\/sites\/rosario3\/img\/2025\/09\/16\/image_1.png_226096942.png\" alt=\"\" \/><\/figure>\n\n\n\n<figure class=\"wp-block-image\"><img decoding=\"async\" src=\"https:\/\/www.rosario3.com\/export\/sites\/rosario3\/img\/2025\/09\/16\/image_2.png_31177313.png\" alt=\"\" \/><\/figure>\n\n\n\n<h3 class=\"wp-block-heading\"><\/h3>\n","protected":false},"excerpt":{"rendered":"<p>Hace 3 minutos Luana&nbsp;vive en San Antonio de Padua, Buenos Aires,&nbsp;tiene 17 a\u00f1os&nbsp;y este verano&#8230;<\/p>\n","protected":false},"author":2,"featured_media":1046,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_jetpack_memberships_contains_paid_content":false,"footnotes":"","jetpack_publicize_message":"","jetpack_publicize_feature_enabled":true,"jetpack_social_post_already_shared":true,"jetpack_social_options":{"image_generator_settings":{"template":"highway","default_image_id":0,"font":"","enabled":false},"version":2}},"categories":[120],"tags":[],"class_list":["post-1045","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-salud"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.4 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>El pedido de ayuda de una adolescente con un raro tipo de c\u00e1ncer -<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, 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