{"id":14953,"date":"2022-06-24T11:37:44","date_gmt":"2022-06-24T10:37:44","guid":{"rendered":"https:\/\/www.fundacionisabelgemio.com\/?p=14953"},"modified":"2022-06-24T11:39:54","modified_gmt":"2022-06-24T10:39:54","slug":"kick-off-meeting-of-the-erasmus-project-the-value-of-facing-school","status":"publish","type":"post","link":"https:\/\/www.fundacionisabelgemio.com\/en\/actual-en\/kick-off-meeting-of-the-erasmus-project-the-value-of-facing-school","title":{"rendered":"Kick-off meeting of the Erasmus+ project \u2018THE VALUE OF FACING SCHOOL&#8217;"},"content":{"rendered":"<p><a href=\"https:\/\/www.fundacionisabelgemio.com\/wp-content\/uploads\/2022\/06\/1.png\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-14949\" src=\"https:\/\/www.fundacionisabelgemio.com\/wp-content\/uploads\/2022\/06\/1.png\" alt=\"\" width=\"742\" height=\"337\" srcset=\"https:\/\/www.fundacionisabelgemio.com\/wp-content\/uploads\/2022\/06\/1.png 1911w, https:\/\/www.fundacionisabelgemio.com\/wp-content\/uploads\/2022\/06\/1-300x136.png 300w, https:\/\/www.fundacionisabelgemio.com\/wp-content\/uploads\/2022\/06\/1-768x348.png 768w, https:\/\/www.fundacionisabelgemio.com\/wp-content\/uploads\/2022\/06\/1-1030x467.png 1030w, https:\/\/www.fundacionisabelgemio.com\/wp-content\/uploads\/2022\/06\/1-1500x681.png 1500w, https:\/\/www.fundacionisabelgemio.com\/wp-content\/uploads\/2022\/06\/1-705x320.png 705w, https:\/\/www.fundacionisabelgemio.com\/wp-content\/uploads\/2022\/06\/1-600x272.png 600w\" sizes=\"auto, (max-width: 742px) 100vw, 742px\" \/><\/a><\/p>\n<p>The kick-off meeting of \u2018THE VALUE OF FACING SCHOOL: THE INCLUSION OF YOUTH WITH NEUROMUSCULAR DISEASES, MUSCULAR DYSTROPHIES AND OTHER RARE DISEASES IN EDUCATION\u2019 was hold last Wednesday, June 22<sup>nd<\/sup>, 2022. The online meeting, coordinated by Fundaci\u00f3n Isabel Gemio, was attended by representatives of all the partner organizations of the project:<\/p>\n<ul>\n<li>Universidade de \u00c9vora (Portugal), a center for the creation, transmission and diffusion of culture, science and technology, which, through the articulation of study, teaching and research, is integrated into the life of society.<\/li>\n<li>Fondation Maladies Rares (France), which has the French legal status of \u201cScientific Cooperation Foundation\u201d, a private non-profit legal person, promotes research projects and scientific excellence, as well as the sharing and dissemination of knowledge in the field of rare diseases.<\/li>\n<li>Federaci\u00f3n Espa\u00f1ola de Enfermedades Neuromusculares (Spain), a non-governmental organization that brings together associations and foundations for neuromuscular diseases. It currently represents more than 60,000 people affected throughout Spain.<\/li>\n<li>Parent Project per la Ricerca sulla Distrofa Muscolare (Italy), an association of patients and parents with children affected by Duchenne and Becker muscular dystrophy.<\/li>\n<li>Uniamo Federazione Italiana Malattie Rare (Italy), the representative body of the community of people with rare diseases. It has over 150 member associations, which are constantly growing.<\/li>\n<li>C.E.I.P. Clara Campoamor de M\u00e1laga (Spain), an early age and primary public school of bilingual education that uses research, experimentation and educational innovation as a fundamental element of teaching practice.<\/li>\n<\/ul>\n<p>The main objective of the project THE VALUE OF FACING SCHOOL is to create a partnership for cooperation, improving the quality of the work, activities and practices of the organizations and institutions involved. Besides, it should develop the capacity of the organizations to work transnationally and across different sectors, to address common priorities and needs, and to make a change in educational methods to students with muscular dystrophies.<\/p>\n<p><a href=\"https:\/\/www.fundacionisabelgemio.com\/wp-content\/uploads\/2022\/06\/2.png\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-14950\" src=\"https:\/\/www.fundacionisabelgemio.com\/wp-content\/uploads\/2022\/06\/2.png\" alt=\"\" width=\"769\" height=\"408\" srcset=\"https:\/\/www.fundacionisabelgemio.com\/wp-content\/uploads\/2022\/06\/2.png 1916w, https:\/\/www.fundacionisabelgemio.com\/wp-content\/uploads\/2022\/06\/2-300x159.png 300w, https:\/\/www.fundacionisabelgemio.com\/wp-content\/uploads\/2022\/06\/2-768x408.png 768w, https:\/\/www.fundacionisabelgemio.com\/wp-content\/uploads\/2022\/06\/2-1030x547.png 1030w, https:\/\/www.fundacionisabelgemio.com\/wp-content\/uploads\/2022\/06\/2-1500x796.png 1500w, https:\/\/www.fundacionisabelgemio.com\/wp-content\/uploads\/2022\/06\/2-705x374.png 705w, https:\/\/www.fundacionisabelgemio.com\/wp-content\/uploads\/2022\/06\/2-600x318.png 600w\" sizes=\"auto, (max-width: 769px) 100vw, 769px\" \/><\/a><\/p>\n<p>During the meeting, Fundaci\u00f3n Isabel Gemio explained the different phases of management and implementation of the project. The partnership will develop two main intellectual outputs: a DIGITAL METHODOLOGICAL GUIDE that will decisively help the school and the teachers to meet the educational needs of students with muscular dystrophy and other rare diseases; and a set of DIGITAL OPEN EDUCATIONAL RESOURCES (OERs) adapted to the beneficiaries and developed by experts, that really contribute to developing the educational competences of students with muscular dystrophy and other rare diseases. The project will end with the celebration of a MULTIPLIER EVENT in which the main results of the initiative will be presented to the beneficiaries themselves, and to social entities, policy makers, and scientific experts, as well.<\/p>\n<p>The first face to face meeting of the consortium is planned to be held on October, in Madrid, Spain.<\/p>\n<p>&nbsp;<\/p>\n<p><a href=\"https:\/\/www.fundacionisabelgemio.com\/wp-content\/uploads\/2022\/06\/Co-funded-by-the-European-Union.jpg\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-14954\" src=\"https:\/\/www.fundacionisabelgemio.com\/wp-content\/uploads\/2022\/06\/Co-funded-by-the-European-Union.jpg\" alt=\"\" width=\"366\" height=\"77\" srcset=\"https:\/\/www.fundacionisabelgemio.com\/wp-content\/uploads\/2022\/06\/Co-funded-by-the-European-Union.jpg 1085w, https:\/\/www.fundacionisabelgemio.com\/wp-content\/uploads\/2022\/06\/Co-funded-by-the-European-Union-300x63.jpg 300w, https:\/\/www.fundacionisabelgemio.com\/wp-content\/uploads\/2022\/06\/Co-funded-by-the-European-Union-768x161.jpg 768w, https:\/\/www.fundacionisabelgemio.com\/wp-content\/uploads\/2022\/06\/Co-funded-by-the-European-Union-1030x216.jpg 1030w, https:\/\/www.fundacionisabelgemio.com\/wp-content\/uploads\/2022\/06\/Co-funded-by-the-European-Union-705x148.jpg 705w, https:\/\/www.fundacionisabelgemio.com\/wp-content\/uploads\/2022\/06\/Co-funded-by-the-European-Union-600x126.jpg 600w\" sizes=\"auto, (max-width: 366px) 100vw, 366px\" \/><\/a><\/p>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>The kick-off meeting of \u2018THE VALUE OF FACING SCHOOL: THE INCLUSION OF YOUTH WITH NEUROMUSCULAR DISEASES, MUSCULAR DYSTROPHIES AND OTHER [&hellip;]<\/p>\n","protected":false},"author":2,"featured_media":14949,"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":[719,743],"tags":[],"class_list":["post-14953","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-actual-en","category-proyectos-europeos-en"],"_links":{"self":[{"href":"https:\/\/www.fundacionisabelgemio.com\/en\/wp-json\/wp\/v2\/posts\/14953","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=14953"}],"version-history":[{"count":4,"href":"https:\/\/www.fundacionisabelgemio.com\/en\/wp-json\/wp\/v2\/posts\/14953\/revisions"}],"predecessor-version":[{"id":14962,"href":"https:\/\/www.fundacionisabelgemio.com\/en\/wp-json\/wp\/v2\/posts\/14953\/revisions\/14962"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/www.fundacionisabelgemio.com\/en\/wp-json\/wp\/v2\/media\/14949"}],"wp:attachment":[{"href":"https:\/\/www.fundacionisabelgemio.com\/en\/wp-json\/wp\/v2\/media?parent=14953"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.fundacionisabelgemio.com\/en\/wp-json\/wp\/v2\/categories?post=14953"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.fundacionisabelgemio.com\/en\/wp-json\/wp\/v2\/tags?post=14953"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}