{"id":14,"date":"2018-07-26T10:01:56","date_gmt":"2018-07-26T10:01:56","guid":{"rendered":"http:\/\/www.cln2family.com\/fr-fr\/?page_id=14"},"modified":"2018-07-26T14:25:54","modified_gmt":"2018-07-26T14:25:54","slug":"connecting-with-community","status":"publish","type":"page","link":"https:\/\/www.cln2family.com\/fr-fr\/connecting-with-community\/","title":{"rendered":"How can I connect with others?"},"content":{"rendered":"[mk_page_section bg_image=”https:\/\/www.cln2family.com\/fr-fr\/wp-content\/uploads\/sites\/6\/2018\/07\/banner-bg-new.png” el_class=”main-Hbanner” sidebar=”sidebar-1″][vc_column width=”2\/3″ el_class=”inner-banner-left”][vc_single_image image=”43″ img_size=”full” el_class=”inner-banner_img”][mk_fancy_title tag_name=”h1″ color=”#ffffff” size=”38″ force_font_size=”true” font_weight=”bold” margin_bottom=”30″ font_family=”Source+Sans+Pro” font_type=”google”]Comment puis-je communiquer avec d’autres personnes ?[\/mk_fancy_title][\/vc_column][vc_column width=”1\/3″ el_class=”header-callout”][\/vc_column][\/mk_page_section][mk_page_section el_class=”community_top” sidebar=”sidebar-1″][vc_column el_class=”community_heading”][vc_column_text]\r\n
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Rejoindre une communaut\u00e9 de soutien grandissante pour les personnes atteintes de CLN2<\/h3>\r\n<\/div>\r\nVous n’\u00eates pas seul(e) : il existe de nombreuses ressources pour soutenir les familles et les aidants d’enfants atteints de CLN2. S’occuper d’un enfant atteint de CLN2 peut \u00eatre \u00e9motionnellement et physiquement \u00e9prouvant. C’est pourquoi il peut \u00eatre plus facile de g\u00e9rer la maladie en \u00e9changeant avec d’autres parents et professionnels. Si vous avez un enfant atteint de la maladie de Batten, ces organisations sont l\u00e0 pour vous accueillir et r\u00e9pondre \u00e0 vos questions.[\/vc_column_text][\/vc_column][vc_column width=”3\/4″ el_class=”connect_row”][vc_row_inner][vc_column_inner el_class=”connect-img” width=”1\/3″][mk_image src=”https:\/\/www.cln2family.com\/fr-fr\/wp-content\/uploads\/sites\/6\/2018\/07\/batten-logo.png” image_size=”full” target=”_blank” title=”BDSRA logo” el_class=”community_btn”][\/vc_column_inner][vc_column_inner el_class=”connect_each” width=”2\/3″][vc_cta h2=”Batten Disease Family Association (BDFA)” shape=”square” style=”flat” color=”white” add_button=”bottom” btn_title=”Acc\u00e9der au site maintenant” btn_style=”flat” btn_shape=”square” use_custom_fonts_h4=”true” btn_el_class=”community_btn absarrow7″ css=”.vc_custom_1527938470504{background-color: #ffffff !important;}” el_class=”connect_box” btn_link=”||”]Cette organisation s’adresse aux familles, aux aidants et aux professionnels de sant\u00e9 qui s’occupent d’enfants, de jeunes gens et d’adultes atteints de la maladie de Batten. La BDFA a pour but d’offrir un soutien, de sensibiliser le public et de financer la recherche pour le d\u00e9veloppement de th\u00e9rapies potentielles et, \u00e0 terme, d’un rem\u00e8de \u00e0 la maladie.[\/vc_cta][\/vc_column_inner][\/vc_row_inner][\/vc_column][\/mk_page_section]","protected":false},"excerpt":{"rendered":"

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