{"id":15671,"date":"2022-12-07T12:08:21","date_gmt":"2022-12-07T11:08:21","guid":{"rendered":"https:\/\/www.fundacionisabelgemio.com\/?p=15671"},"modified":"2022-12-07T12:51:19","modified_gmt":"2022-12-07T11:51:19","slug":"youth-with-courage-in-october-november","status":"publish","type":"post","link":"https:\/\/www.fundacionisabelgemio.com\/en\/actual\/youth-with-courage-in-october-november","title":{"rendered":"YOUTH WITH COURAGE in October-November"},"content":{"rendered":"<figure class=\"wp-block-embed is-type-video is-provider-youtube wp-block-embed-youtube wp-embed-aspect-16-9 wp-has-aspect-ratio\"><div class=\"wp-block-embed__wrapper\">\n<div class='avia-iframe-wrap'><iframe loading=\"lazy\" title=\"YOUTH WITH COURAGE: October - November\" width=\"1500\" height=\"844\" src=\"https:\/\/www.youtube.com\/embed\/j3txTT0ii40?wmode=transparent&amp;rel=0&amp;feature=oembed\" frameborder=\"0\" allow=\"accelerometer; autoplay; clipboard-write; encrypted-media; gyroscope; picture-in-picture\" allowfullscreen><\/iframe><\/div>\n<\/div><\/figure><p id=\"block-dbe18052-f11e-4050-a365-f522d83b54a4\">Get to know all the stories of October-November<\/p><ul class=\"wp-block-list\" id=\"block-9e9208e4-5a3b-4a8f-82fa-8cefd2b8ff80\"><li><a href=\"https:\/\/www.youtube.com\/watch?v=SZ3j-497Z_c&amp;t=401s\">Olivia <\/a>is 14 years old and she suffers the Charcot Marie Tooth degenerative disease. In the future she wants to study biomedicine.<\/li><li><a href=\"https:\/\/www.youtube.com\/watch?v=AdLLaboAHjo&amp;t=98s\">Davide <\/a>was diagnosed with Williams syndrome when he was a few months old. Sports have helped him to overcome several barriers.<\/li><li><a href=\"https:\/\/www.youtube.com\/watch?v=9vSANkrPOPk&amp;t=37s\">Andr\u00e9s <\/a>have Spastic Paraparesia. HE loves superheroes and his biggest dream is to become as fast as a lightning.<\/li><li><a href=\"https:\/\/www.youtube.com\/watch?v=7N4dKVdmmyE&amp;t=7s\">Cristina <\/a>suffers Phenylketonuria, a rare disease that can lead to intellectual and motor disorders. She encourages people to support people with rare diseases.<\/li><li><a href=\"https:\/\/www.youtube.com\/watch?v=oeLMWdktVPc&amp;t=2s\">Jacopo &amp; Matteo<\/a> are two friends from Italy affected by Duchenne Muscular Dystrophy (DMD). They ask people to treat them like any other person and to focus on their skills and possibilities.<\/li><\/ul><p id=\"block-4f45459c-bbce-4646-a285-fa2abf9cdf27\">The initiative, co-funded by the Erasmus+ Programme of the European Union, aims at the creation of a European network of European foundations, institutions, and entities in order to promote the exchange of experiences and good practices. The partners of the initiative are:<\/p><ul class=\"wp-block-list\" id=\"block-be2e4aa3-4393-4d1f-b74c-3265d264bcc9\"><li>Fundaci\u00f3n Isabel Gemio (Spain)<\/li><li>Federaci\u00f3n Espa\u00f1ola de Enfermedades Neuromusculares (Spain)<\/li><li>Parent Project APS per la Ricerca sulla Distrofa Muscolare (Italy)<\/li><li>Charcot-Marie-Tooth et Neuropathies Peripheriques (France)<\/li><li>Uniamo Federazione Italiana Malattie Rare (Italy)<\/li><\/ul><p>\ufeff<\/p>","protected":false},"excerpt":{"rendered":"<p>Get to know all the stories of October-November Olivia is 14 years old and she suffers the Charcot Marie Tooth [&hellip;]<\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_exactmetrics_skip_tracking":false,"_exactmetrics_sitenote_active":false,"_exactmetrics_sitenote_note":"","_exactmetrics_sitenote_category":0,"footnotes":""},"categories":[10,742],"tags":[],"class_list":["post-15671","post","type-post","status-publish","format-standard","hentry","category-actual","category-proyectos-europeos"],"_links":{"self":[{"href":"https:\/\/www.fundacionisabelgemio.com\/en\/wp-json\/wp\/v2\/posts\/15671","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.fundacionisabelgemio.com\/en\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.fundacionisabelgemio.com\/en\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.fundacionisabelgemio.com\/en\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/www.fundacionisabelgemio.com\/en\/wp-json\/wp\/v2\/comments?post=15671"}],"version-history":[{"count":1,"href":"https:\/\/www.fundacionisabelgemio.com\/en\/wp-json\/wp\/v2\/posts\/15671\/revisions"}],"predecessor-version":[{"id":15672,"href":"https:\/\/www.fundacionisabelgemio.com\/en\/wp-json\/wp\/v2\/posts\/15671\/revisions\/15672"}],"wp:attachment":[{"href":"https:\/\/www.fundacionisabelgemio.com\/en\/wp-json\/wp\/v2\/media?parent=15671"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.fundacionisabelgemio.com\/en\/wp-json\/wp\/v2\/categories?post=15671"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.fundacionisabelgemio.com\/en\/wp-json\/wp\/v2\/tags?post=15671"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}