{"id":2559,"date":"2022-09-26T14:55:19","date_gmt":"2022-09-26T14:55:19","guid":{"rendered":"https:\/\/exciting-elbakyan.137-74-93-36.plesk.page\/index.php\/2022\/09\/26\/la-ataxia-telangiectasia-se-hace-visible-en-la-carreira-solidaria-de-lalin-pontevendra\/"},"modified":"2026-03-02T12:00:51","modified_gmt":"2026-03-02T12:00:51","slug":"la-ataxia-telangiectasia-se-hace-visible-en-la-carreira-solidaria-de-lalin-pontevendra","status":"publish","type":"post","link":"https:\/\/exciting-elbakyan.137-74-93-36.plesk.page\/index.php\/2022\/09\/26\/la-ataxia-telangiectasia-se-hace-visible-en-la-carreira-solidaria-de-lalin-pontevendra\/","title":{"rendered":"La ataxia telangiectasia se hace visible en la Carreira Nocturna de Lal\u00edn (Pontevedra)"},"content":{"rendered":"<p style=\"text-align: justify;\"><img fetchpriority=\"high\" decoding=\"async\" class=\" alignleft size-full wp-image-2558\" src=\"https:\/\/exciting-elbakyan.137-74-93-36.plesk.page\/wp-content\/uploads\/2022\/09\/Equipo_Aefat_en_Carreira_Nocturna_de_Lalin_23_sept_2022_llegada.jpeg\" alt=\"Equipo Aefat en Carreira Nocturna de Lal\u00edn 23 sept 2022 llegada\" width=\"500\" height=\"667\" style=\"margin: 10px; float: left;\" srcset=\"https:\/\/exciting-elbakyan.137-74-93-36.plesk.page\/wp-content\/uploads\/2022\/09\/Equipo_Aefat_en_Carreira_Nocturna_de_Lalin_23_sept_2022_llegada.jpeg 1200w, https:\/\/exciting-elbakyan.137-74-93-36.plesk.page\/wp-content\/uploads\/2022\/09\/Equipo_Aefat_en_Carreira_Nocturna_de_Lalin_23_sept_2022_llegada-225x300.jpeg 225w, https:\/\/exciting-elbakyan.137-74-93-36.plesk.page\/wp-content\/uploads\/2022\/09\/Equipo_Aefat_en_Carreira_Nocturna_de_Lalin_23_sept_2022_llegada-768x1024.jpeg 768w, https:\/\/exciting-elbakyan.137-74-93-36.plesk.page\/wp-content\/uploads\/2022\/09\/Equipo_Aefat_en_Carreira_Nocturna_de_Lalin_23_sept_2022_llegada-1152x1536.jpeg 1152w, https:\/\/exciting-elbakyan.137-74-93-36.plesk.page\/wp-content\/uploads\/2022\/09\/Equipo_Aefat_en_Carreira_Nocturna_de_Lalin_23_sept_2022_llegada-9x12.jpeg 9w\" sizes=\"(max-width: 500px) 100vw, 500px\" \/>Despu\u00e9s de so\u00f1arlo durante a\u00f1os, la lalinense Patricia Blanco, joven afectada con ataxia telangiectasia, pudo por fin el pasado viernes participar en una carrera en su pueblo natal, la Carreira Solidaria Nocturna de Lal\u00edn, junto a Sonia de Ferrol (\u00fanicas gallegas con la enfermedad declarada), y Sara, que vino a prop\u00f3sito desde Madrid para participar con sus compa\u00f1eras gallegas.&nbsp;<\/p>\n<p style=\"text-align: justify;\">Patricia lleva a\u00f1os participando con sus compa\u00f1eros (ni\u00f1os y j\u00f3venes con la misma enfermedad rara) de la asociaci\u00f3n Aefat en maratones, medio-maratones y carreras populares en los distintos puntos de la geograf\u00eda espa\u00f1ola\u2026&nbsp; Pero desde 2018 cuenta con un grupo de corredores solidarios coordinados por Centro ETP de Lal\u00edn para poder hacerlo en Galicia. Por ejemplo, m\u00e1s de 40 corredores le acompa\u00f1aron en la media marat\u00f3n \u00abVolta a r\u00eda: Memorial Adolfo Ros\u00bb en 2019, y tras la pandemia, el pasado 5 de junio, diez corredores participaron con ella y tres de sus compa\u00f1eros catalanes de la asociaci\u00f3n Aefat en la carrera Runki de A Coru\u00f1a.&nbsp;<\/p>\n<p style=\"text-align: justify;\">As\u00ed pues, tras volver a caer la coordinaci\u00f3n de la carrera de las fiestas de Lal\u00edn del viernes pasado en manos de <strong>Hern\u00e1n Garc\u00eda<\/strong>, speaker deportivo e instructor de actividades dirigidas de <strong>Centro ETP<\/strong>, el centro deportivo lalinense realiz\u00f3 las gestiones para que el Concello de Lal\u00edn (organizador del evento) pudiera incluir una salida especial para ellas.&nbsp;<\/p>\n<p style=\"text-align: justify;\">Los <strong>corredores solidarios<\/strong> que empujaron sus sillas durante esos 6 km fueron en esta ocasi\u00f3n los atletas Enrique Rojo (presidente de la Asociaci\u00f3n de familiares de enfermos de Alzheimer de Chantada), Andr\u00e9s Lareu, Leticia Vilar, B\u00e1rbara S\u00e1nchez, Emilio Fern\u00e1ndez, Jacobo Guerreiro, Jose Luis Cagide, Antonio Riera (fundador del club Atletismo Deza) y la entrenadora Vanesa Insaurralde. La Carreira Nocturna Solidaria estuvo repleta de emoci\u00f3n tras los aplausos del p\u00fablico presente y de corredores de la carrera absoluta que aguardaban su salida.<\/p>\n<p style=\"text-align: justify;\">El pueblo lalinense se mostr\u00f3 muy comprometido con la causa de Patricia y sus compa\u00f1eras de la asociaci\u00f3n Aefat, ya que el puesto de productos solidarios de la asociaci\u00f3n <strong>recaud\u00f3 m\u00e1s de mil euros<\/strong> en apenas dos horas, incluyendo un sorteo de una cesta de embutidos lalinenses (resultados publicados en nuestro canal de <a href=\"https:\/\/youtu.be\/su4_192EoNQ\">Youtube <\/a>y otras&nbsp;redes sociales de Aefat). Hern\u00e1n Garc\u00eda esta vez no pudo apoyar con sus piernas pero lo hizo poniendo emoci\u00f3n a cada palabra a trav\u00e9s del micr\u00f3fono, presentando la carrera y el preg\u00f3n de las fiestas.<\/p>\n<p style=\"text-align: justify;\">Aefat quiere <strong>agradecer enormemente el apoyo<\/strong> y gran esfuerzo demostrado por ETP, Hern\u00e1n Garc\u00eda, los corredores solidarios, el Concello y la gente de Lal\u00edn. Tambi\u00e9n a la empresa de transportes MRW por su inestimable colaboraci\u00f3n trasladando las sillas gratuitamente por toda la geograf\u00eda espa\u00f1ola, lo mismo que a la oficina de MRW Lal\u00edn por acercarlas hasta la zona de salida la propia tarde de la carrera.&nbsp;<\/p>\n<p style=\"text-align: justify;\">Patricia y su familia esperan poder volver a repetir su participaci\u00f3n el pr\u00f3ximo a\u00f1o. Mientras, ya se encuentran intentando coordinar su participaci\u00f3n en la nueva edici\u00f3n de la media marat\u00f3n \u00abVolta a R\u00eda\u00bb en diciembre de este a\u00f1o.<\/p>\n<p style=\"text-align: justify;\">Como algunos ya sab\u00e9is, la <strong>ataxia telangiectasia<\/strong> (AT o A-T) es uno de los 300 tipos de ataxia que existen. Es una enfermedad rara, gen\u00e9tica y neurodegenerativa que a\u00fan no tiene cura ni tratamiento, con dos afectadas en Galicia y casi 40 en todo el Estado. Provoca una discapacidad f\u00edsica progresiva y m\u00e1s riesgo de c\u00e1ncer, entre otras complicaciones.<\/p>\n<p style=\"text-align: justify;\"><strong>Aefat<\/strong> es una asociaci\u00f3n sin \u00e1nimo de lucro creada en 2009 y declarada de utilidad p\u00fablica desde 2014. Pertenece a FEDER (Federaci\u00f3n Espa\u00f1ola de Enfermedades Raras), FEDAES (Federaci\u00f3n de Ataxias de Espa\u00f1a) y la entidad internacional A-T Global Alliance (<a href=\"http:\/\/www.cureat.org\/\">www.cureat.org<\/a>).<\/p>\n","protected":false},"excerpt":{"rendered":"<p style=\"text-align: justify;\"><img fetchpriority=\"high\" decoding=\"async\" class=\" alignleft size-full wp-image-2558\" src=\"https:\/\/exciting-elbakyan.137-74-93-36.plesk.page\/wp-content\/uploads\/2022\/09\/Equipo_Aefat_en_Carreira_Nocturna_de_Lalin_23_sept_2022_llegada.jpeg\" alt=\"Equipo Aefat en Carreira Nocturna de Lal\u00edn 23 sept 2022 llegada\" width=\"500\" height=\"667\" style=\"margin: 10px; float: left;\" srcset=\"https:\/\/exciting-elbakyan.137-74-93-36.plesk.page\/wp-content\/uploads\/2022\/09\/Equipo_Aefat_en_Carreira_Nocturna_de_Lalin_23_sept_2022_llegada.jpeg 1200w, https:\/\/exciting-elbakyan.137-74-93-36.plesk.page\/wp-content\/uploads\/2022\/09\/Equipo_Aefat_en_Carreira_Nocturna_de_Lalin_23_sept_2022_llegada-225x300.jpeg 225w, https:\/\/exciting-elbakyan.137-74-93-36.plesk.page\/wp-content\/uploads\/2022\/09\/Equipo_Aefat_en_Carreira_Nocturna_de_Lalin_23_sept_2022_llegada-768x1024.jpeg 768w, https:\/\/exciting-elbakyan.137-74-93-36.plesk.page\/wp-content\/uploads\/2022\/09\/Equipo_Aefat_en_Carreira_Nocturna_de_Lalin_23_sept_2022_llegada-1152x1536.jpeg 1152w, https:\/\/exciting-elbakyan.137-74-93-36.plesk.page\/wp-content\/uploads\/2022\/09\/Equipo_Aefat_en_Carreira_Nocturna_de_Lalin_23_sept_2022_llegada-9x12.jpeg 9w\" sizes=\"(max-width: 500px) 100vw, 500px\" \/>Despu\u00e9s de so\u00f1arlo durante a\u00f1os, la lalinense Patricia Blanco, joven afectada con ataxia telangiectasia, pudo por fin el pasado viernes participar en una carrera en su pueblo natal, la Carreira Solidaria Nocturna de Lal\u00edn, junto a Sonia de Ferrol (\u00fanicas gallegas con la enfermedad declarada), y Sara, que vino a prop\u00f3sito desde Madrid para participar con sus compa\u00f1eras gallegas.&nbsp;<\/p>\n","protected":false},"author":1,"featured_media":2558,"comment_status":"closed","ping_status":"open","sticky":true,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[51],"tags":[],"class_list":["post-2559","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-actividades-solidarias"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.2 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>La ataxia telangiectasia se hace visible en la Carreira Nocturna de Lal\u00edn (Pontevedra) - Aefat<\/title>\n<meta name=\"robots\" content=\"noindex, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<meta property=\"og:locale\" content=\"es_ES\" \/>\n<meta property=\"og:type\" content=\"article\" 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