{"id":355,"date":"2024-12-23T17:38:02","date_gmt":"2024-12-23T16:38:02","guid":{"rendered":"https:\/\/afs-costello-cfc.asso.fr\/?page_id=355"},"modified":"2026-01-09T17:31:34","modified_gmt":"2026-01-09T16:31:34","slug":"a-propos-de-lassociation","status":"publish","type":"page","link":"https:\/\/afs-costello-cfc.asso.fr\/index.php\/a-propos-de-lassociation\/","title":{"rendered":"\u00c0 propos de l’association"},"content":{"rendered":"\n

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L\u2019association a pour objet d\u2019aider les personnes handicap\u00e9es atteintes du syndrome de Costello ; d\u00e9fendre leurs droits \u00e0 l\u2019\u00e9ducation et \u00e0 l\u2019int\u00e9gration ; promouvoir et soutenir les voies de recherches en cours et diffuser l\u2019information ; rechercher et mettre en \u0153uvre les moyens utiles \u00e0 la promotion de l\u2019\u00e9ducation des enfants et adolescents atteints de ce syndrome ; assurer les rencontres entre les parents.<\/em><\/p>\n\n\n\n

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Retrouvez tous les documents de l’Association Fran\u00e7aise des Syndromes de Costello et Cardio-Facio-Cutan\u00e9, class\u00e9s par ann\u00e9es : <\/strong><\/p>\n\n\n\n

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2024<\/strong><\/div><\/summary>
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Compte-Rendu
Assembl\u00e9e G\u00e9n\u00e9rale 2024<\/strong><\/span><\/a><\/div>\n<\/div>\n<\/div><\/details>\n\n\n\n
2023<\/strong><\/div><\/summary>
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Compte-Rendu
Assembl\u00e9e G\u00e9n\u00e9rale 2023<\/strong><\/span><\/a><\/div>\n\n\n\n
Le Petit Journal 2023<\/strong><\/span><\/a><\/div>\n<\/div>\n<\/div><\/details>\n\n\n\n
2022<\/strong><\/div><\/summary>
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Compte-Rendu
Assembl\u00e9e G\u00e9n\u00e9rale 2022<\/strong><\/span><\/a><\/div>\n\n\n\n
Le Petit Journal 2022 – FR<\/strong><\/span><\/a><\/div>\n\n\n\n
Le Petit Journal 2022 – EN<\/strong><\/span><\/a><\/div>\n<\/div>\n<\/div><\/details>\n\n\n\n
2021<\/strong><\/div><\/summary>
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Assembl\u00e9e G\u00e9n\u00e9rale 2021<\/strong><\/span><\/a><\/div>\n<\/div>\n<\/div><\/details>\n\n\n\n
2020<\/strong><\/div><\/summary>
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Assembl\u00e9e G\u00e9n\u00e9rale 2020<\/strong><\/span><\/a><\/div>\n<\/div>\n<\/div><\/details>\n\n\n\n
2019<\/strong><\/div><\/summary>
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Assembl\u00e9e G\u00e9n\u00e9rale 2019<\/strong><\/span><\/a><\/div>\n<\/div>\n<\/div><\/details>\n\n\n\n
2018<\/strong><\/div><\/summary>
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Assembl\u00e9e G\u00e9n\u00e9rale 2018<\/strong><\/span><\/a><\/div>\n\n\n\n
Le Petit Journal 2018<\/strong><\/span><\/a><\/div>\n<\/div>\n<\/div><\/details>\n\n\n\n
2017<\/strong><\/div><\/summary>
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Compte-Rendu
Assembl\u00e9e G\u00e9n\u00e9rale 2017<\/strong><\/span><\/a><\/div>\n\n\n\n
Le Petit Journal 2017<\/strong><\/span><\/a><\/div>\n<\/div>\n<\/div><\/details>\n\n\n\n
2016<\/strong><\/div><\/summary>
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Compte-Rendu
Assembl\u00e9e G\u00e9n\u00e9rale 2016<\/strong><\/span><\/a><\/div>\n\n\n\n
Le Petit Journal 2016<\/strong><\/span><\/a><\/div>\n<\/div>\n<\/div><\/details>\n\n\n\n
2015<\/strong><\/div><\/summary>
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Compte-Rendu
Assembl\u00e9e G\u00e9n\u00e9rale 2015<\/strong><\/span><\/a><\/div>\n\n\n\n
Le Petit Journal 2015<\/strong><\/span><\/a><\/div>\n<\/div>\n<\/div><\/details>\n\n\n\n
2014<\/strong><\/div><\/summary>
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Compte-Rendu
Assembl\u00e9e G\u00e9n\u00e9rale 2014<\/strong><\/span><\/a><\/div>\n\n\n\n
Le Petit Journal 2014<\/strong><\/span><\/a><\/div>\n<\/div>\n<\/div><\/details>\n\n\n\n
2013<\/strong><\/div><\/summary>
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Cliquez sur les boutons pour consulter les documents : <\/p>\n\n\n\n

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Le Petit Journal 2013<\/strong><\/span><\/a><\/div>\n<\/div>\n<\/div><\/details>\n\n\n\n
2012<\/strong><\/div><\/summary>
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Cliquez sur les boutons pour consulter les documents : <\/p>\n\n\n\n

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Compte-Rendu
Assembl\u00e9e G\u00e9n\u00e9rale 2012<\/strong><\/span><\/a><\/div>\n\n\n\n
Le Petit Journal 2012<\/strong><\/span><\/a><\/div>\n<\/div>\n<\/div><\/details>\n<\/div>\n\n\n\n

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L\u2019Association Syndromes de Costello et CFC<\/strong><\/h2>\n\n\n\n

Cr\u00e9\u00e9e en 2000 \u00e0 l\u2019initiative de 3 familles, elle compte actuellement 1000 adh\u00e9rents et 120 contacts avec des personnes atteintes du syndrome de Costello ou du syndrome CFC, un peu partout en France, en Europe et sur d\u2019autres continents.<\/p>\n\n\n\n

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En savoir plus sur l’association<\/strong><\/a><\/div>\n<\/div>\n<\/div>\n\n\n\n
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L\u2019association a pour objet d\u2019aider les personnes handicap\u00e9es atteintes du syndrome de Costello ; d\u00e9fendre leurs droits \u00e0 l\u2019\u00e9ducation et \u00e0 l\u2019int\u00e9gration ; promouvoir et soutenir les voies de recherches en cours et diffuser l\u2019information ; rechercher et mettre en \u0153uvre les moyens utiles \u00e0 la promotion de l\u2019\u00e9ducation des […]<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_themeisle_gutenberg_block_has_review":false,"footnotes":""},"class_list":["post-355","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/afs-costello-cfc.asso.fr\/index.php\/wp-json\/wp\/v2\/pages\/355","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/afs-costello-cfc.asso.fr\/index.php\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/afs-costello-cfc.asso.fr\/index.php\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/afs-costello-cfc.asso.fr\/index.php\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/afs-costello-cfc.asso.fr\/index.php\/wp-json\/wp\/v2\/comments?post=355"}],"version-history":[{"count":16,"href":"https:\/\/afs-costello-cfc.asso.fr\/index.php\/wp-json\/wp\/v2\/pages\/355\/revisions"}],"predecessor-version":[{"id":417,"href":"https:\/\/afs-costello-cfc.asso.fr\/index.php\/wp-json\/wp\/v2\/pages\/355\/revisions\/417"}],"wp:attachment":[{"href":"https:\/\/afs-costello-cfc.asso.fr\/index.php\/wp-json\/wp\/v2\/media?parent=355"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}