{"id":7082,"date":"2021-04-23T07:45:05","date_gmt":"2021-04-23T07:45:05","guid":{"rendered":"https:\/\/sindromecharge.es\/index.php\/2021\/04\/23\/nos-sumamos-al-dia-nacional-de-la-dermatomiositis-juvenil\/"},"modified":"2021-04-23T07:45:05","modified_gmt":"2021-04-23T07:45:05","slug":"nos-sumamos-al-dia-nacional-de-la-dermatomiositis-juvenil","status":"publish","type":"post","link":"https:\/\/sindromecharge.es\/index.php\/2021\/04\/23\/nos-sumamos-al-dia-nacional-de-la-dermatomiositis-juvenil\/","title":{"rendered":"Nos sumamos al D\u00eda Nacional de la Dermatomiositis Juvenil"},"content":{"rendered":"<p>Leemos en FEDER la siguiente noticia que os reproducimos de forma \u00edntegra: <\/p>\n<p><p>Hoy se celebra el D\u00eda Nacional de la Dermatomiositis Juvenil para concienciar sobre esta enfermedad poco frecuente y desde FEDER nos queremos unir a esta jornada para trasladar todo nuestro apoyo al colectivo y al tejido asociativo. En esta jornada, la concienciaci\u00f3n es la protagonista y desde la Federaci\u00f3n Espa\u00f1ola de Enfermedades Raras (FEDER) se unen para mostrar su apoyo al colectivo y al tejido asociativo.<\/p>\n<p>La Dermatomiositis Juvenil es una enfermedad autoinmune. Las enfermedades autoinmunes se producen por una respuesta anormal de nuestro sistema de defensa que, sin que exista ninguna infecci\u00f3n, produce inflamaci\u00f3n de alg\u00fan \u00f3rgano del cuerpo.<\/p>\n<p>En la DMJ la inflamaci\u00f3n ocurre a nivel de los peque\u00f1os vasos sangu\u00edneos de la piel y del m\u00fasculo. Ello produce caracter\u00edsticamente erupciones cut\u00e1neas en la cara, p\u00e1rpados, nudillos, rodillas o codos , as\u00ed como dolor o debilidad muscular, sobre todo a nivel de los hombros y las caderas. La enfermedad puede afectar a ni\u00f1os y a adultos. Se considera que es la forma juvenil de dermatomiositis cuando los s\u00edntomas se producen antes de los 16 a\u00f1os.<\/p>\n<p>\u201cDesde FEDER nos unimos a esta jornada para impulsar la sensibilizaci\u00f3n social de la Dermatomiositis Juvenil, fomentando as\u00ed la transformaci\u00f3n social. Adem\u00e1s, en esta jornada, nos unimos para reconocer la labor de las entidades del movimiento asociativo que velan por el bienestar de las personas que conviven con alguna de estas patolog\u00edas y el de sus familiares\u201d afirma Juan Carri\u00f3n, presidente de FEDER y su Fundaci\u00f3n.<\/p>\n<p>El tejido asociativo trabaja diariamente con el objetivo de mejorar la calidad de vida del colectivo. Entidades como la Asociaci\u00f3n Nacional de Dermatomiositis Juvenil (ANADEJU) trabajan para mejorar la calidad de vida de los menores con esta enfermedad poco frecuente, as\u00ed como la de sus familias, brindando la informaci\u00f3n adecuada, sensibilizando sobre las necesidades espec\u00edficas que tiene el coelctivo, facilitando la integraci\u00f3n en los distintos \u00e1mbitos de su vida personal, educativa y social.<\/p>\n<p>Adem\u00e1s, con motivo de esta jornada, la Asociaci\u00f3n ANADEJU ha preparado una campa\u00f1a de sensibilizaci\u00f3n por esta jornada para impulsar la concienciaci\u00f3n sobre la realidad de las personas que conviven con esta enfermedad poco frecuente.<\/p>\n<p>\u00daltima actualizaci\u00f3n 23\/04\/2021<\/p>\n<\/p>\n<p>Fuente: FEDER <a href=\"https:\/\/enfermedades-raras.org\/index.php\/actualidad\/noticias-eventos\/2-feder\/15244-nos-sumamos-al-d%C3%ADa-nacional-de-la-dermatomiositis-juvenil\" target=\"_blank\" rel=\"noopener\">Nos sumamos al D\u00eda Nacional de la Dermatomiositis Juvenil<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Leemos en FEDER la siguiente noticia que os reproducimos de forma \u00edntegra: Hoy se celebra el D\u00eda Nacional de la Dermatomiositis Juvenil para concienciar sobre esta enfermedad poco frecuente y desde FEDER nos queremos unir a esta jornada para trasladar todo nuestro apoyo al colectivo y al tejido asociativo. En esta jornada, la concienciaci\u00f3n es [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[8],"tags":[36],"class_list":["post-7082","post","type-post","status-publish","format-standard","hentry","category-noticias","tag-enfermedades-raras"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.5 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Nos sumamos al D\u00eda Nacional de la Dermatomiositis Juvenil - Asociaci\u00f3n Espa\u00f1ola S\u00edndrome de Charge<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/sindromecharge.es\/index.php\/2021\/04\/23\/nos-sumamos-al-dia-nacional-de-la-dermatomiositis-juvenil\/\" \/>\n<meta property=\"og:locale\" content=\"es_ES\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Nos sumamos al D\u00eda Nacional de la Dermatomiositis Juvenil - Asociaci\u00f3n Espa\u00f1ola S\u00edndrome de Charge\" \/>\n<meta property=\"og:description\" content=\"Leemos en FEDER la siguiente noticia que os reproducimos de forma \u00edntegra: Hoy se celebra el D\u00eda Nacional de la Dermatomiositis Juvenil para concienciar sobre esta enfermedad poco frecuente y desde FEDER nos queremos unir a esta jornada para trasladar todo nuestro apoyo al colectivo y al tejido asociativo. 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