{"id":10,"date":"2017-02-03T05:54:04","date_gmt":"2017-02-03T05:54:04","guid":{"rendered":"http:\/\/www.cln2family.com\/en-uk\/?page_id=10"},"modified":"2017-03-14T11:02:59","modified_gmt":"2017-03-14T11:02:59","slug":"connecting-with-community","status":"publish","type":"page","link":"https:\/\/www.cln2family.com\/en-uk\/connecting-with-community\/","title":{"rendered":"How can I connect with others?"},"content":{"rendered":"[mk_page_section bg_image=&#8221;http:\/\/www.cln2family.com\/en-uk\/wp-content\/uploads\/sites\/2\/2017\/02\/banner-bg-new.png&#8221; el_class=&#8221;main-Hbanner&#8221; sidebar=&#8221;sidebar-1&#8243;][vc_column width=&#8221;2\/3&#8243; el_class=&#8221;inner-banner-left&#8221;][vc_single_image image=&#8221;38&#8243; img_size=&#8221;full&#8221; el_class=&#8221;inner-banner_img&#8221;][mk_fancy_title tag_name=&#8221;h1&#8243; color=&#8221;#ffffff&#8221; size=&#8221;38&#8243; force_font_size=&#8221;true&#8221; font_weight=&#8221;bold&#8221; margin_bottom=&#8221;30&#8243; font_family=&#8221;Source+Sans+Pro&#8221; font_type=&#8221;google&#8221;]How can I connect with others?[\/mk_fancy_title][\/vc_column][vc_column width=&#8221;1\/3&#8243; el_class=&#8221;header-callout&#8221;][\/vc_column][\/mk_page_section][mk_page_section el_class=&#8221;community_top&#8221; sidebar=&#8221;sidebar-1&#8243;][vc_column el_class=&#8221;community_heading&#8221;][vc_column_text]\r\n<div class=\"commuhead\">\r\n<h3>Connect with a growing community of support for CLN2 disease<\/h3>\r\n<\/div>\r\nYou are not alone \u2014 there are many support resources for families and caregivers of children with CLN2 disease. Caring for a child who has CLN2 disease can be emotionally and physically demanding. That\u2019s why finding other parents and professionals to talk to can make the disease easier to manage. If you have a child with Batten disease, these organisations welcome you and want to answer your questions.[\/vc_column_text][\/vc_column][vc_column width=&#8221;3\/4&#8243; el_class=&#8221;connect_row&#8221;][vc_row_inner][vc_column_inner el_class=&#8221;connect-img&#8221; width=&#8221;1\/3&#8243;][mk_image src=&#8221;http:\/\/www.cln2family.com\/en-uk\/wp-content\/uploads\/sites\/2\/2017\/02\/batten-logo.png&#8221; image_size=&#8221;full&#8221; target=&#8221;_blank&#8221; title=&#8221;BDSRA logo&#8221; el_class=&#8221;community_btn&#8221;][\/vc_column_inner][vc_column_inner el_class=&#8221;connect_each&#8221; width=&#8221;2\/3&#8243;][vc_cta h2=&#8221;Batten Disease Family Association (BDFA)&#8221; shape=&#8221;square&#8221; style=&#8221;flat&#8221; color=&#8221;white&#8221; add_button=&#8221;bottom&#8221; btn_title=&#8221;Connect today&#8221; btn_style=&#8221;flat&#8221; btn_shape=&#8221;square&#8221; use_custom_fonts_h4=&#8221;true&#8221; btn_el_class=&#8221;community_btn absarrow7&#8243; css=&#8221;.vc_custom_1481117833394{background-color: #ffffff !important;}&#8221; el_class=&#8221;connect_box&#8221; btn_link=&#8221;||&#8221;]An organisation for families, caregivers and healthcare professionals supporting children, young people and adults living with Batten disease. The BDFA aims to provide support, raise awareness and fund research into potential therapies and ultimately a cure.[\/vc_cta][\/vc_column_inner][\/vc_row_inner][\/vc_column][\/mk_page_section]","protected":false},"excerpt":{"rendered":"<p>[mk_page_section bg_image=&#8221;http:\/\/www.cln2family.com\/en-uk\/wp-content\/uploads\/sites\/2\/2017\/02\/banner-bg-new.png&#8221; el_class=&#8221;main-Hbanner&#8221; sidebar=&#8221;sidebar-1&#8243;][vc_column width=&#8221;2\/3&#8243; el_class=&#8221;inner-banner-left&#8221;][vc_single_image image=&#8221;38&#8243; img_size=&#8221;full&#8221; el_class=&#8221;inner-banner_img&#8221;][mk_fancy_title tag_name=&#8221;h1&#8243; color=&#8221;#ffffff&#8221; size=&#8221;38&#8243; force_font_size=&#8221;true&#8221; font_weight=&#8221;bold&#8221; margin_bottom=&#8221;30&#8243; font_family=&#8221;Source+Sans+Pro&#8221; font_type=&#8221;google&#8221;]How can I connect with others?[\/mk_fancy_title][\/vc_column][vc_column width=&#8221;1\/3&#8243; el_class=&#8221;header-callout&#8221;][\/vc_column][\/mk_page_section][mk_page_section el_class=&#8221;community_top&#8221; sidebar=&#8221;sidebar-1&#8243;][vc_column el_class=&#8221;community_heading&#8221;][vc_column_text] Connect with a growing community of support for CLN2 disease You are not alone \u2014 there are many support resources for families and caregivers of children with CLN2 [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-10","page","type-page","status-publish","hentry"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v24.5 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Connect with the CLN2 community<\/title>\n<meta name=\"description\" content=\"Find out how you can connect with a growing community of support for families and caregivers of children with CLN2 disease.\" \/>\n<meta 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