{"id":59082,"date":"2019-12-04T17:41:11","date_gmt":"2019-12-04T22:41:11","guid":{"rendered":"https:\/\/rarediseases.org\/nordinthenews-nord-summit-content-featured-in-two-new-articles\/"},"modified":"2019-12-04T17:41:11","modified_gmt":"2019-12-04T22:41:11","slug":"nordinthenews-nord-summit-content-featured-in-two-new-articles","status":"publish","type":"post","link":"https:\/\/rarediseases.org\/es\/nordinthenews-nord-summit-content-featured-in-two-new-articles\/","title":{"rendered":"#NORDinthenews: NORD Summit content featured in two new articles"},"content":{"rendered":"<p>BioNews Service reporter Larry Luxner attended the 2019 NORD <a href=\"https:\/\/www.nordsummit.org\" rel=\"nofollow noopener\" target=\"_blank\">Rare Diseases and Orphan Products Breakthrough Summit<\/a> in Washington, DC in October, and has since written two articles based on Summit content.<\/p>\n<p>Sickle Cell Disease News published the following article, centered on HHS Secretary Alex Azar&#8217;s Summit speech and comments regarding progress on the sickle cell disease front, on December 3:<\/p>\n<blockquote class=\"wp-embedded-content\" data-secret=\"IQlRZGSpgZ\"><p><a href=\"https:\/\/sicklecellanemianews.com\/news\/hhs-secretary-alex-azar-touts-white-house-efforts-fight-sickle-cell-disease\/\" rel=\"nofollow noopener\" target=\"_blank\">HHS Secretary Alex Azar Touts White House Efforts to Fight Sickle Cell Disease<\/a><\/p><\/blockquote>\n<p><iframe loading=\"lazy\" class=\"wp-embedded-content\" sandbox=\"allow-scripts\" security=\"restricted\" style=\"position: absolute; clip: rect(1px, 1px, 1px, 1px);\" title=\"&#8220;HHS Secretary Alex Azar Touts White House Efforts to Fight Sickle Cell Disease&#8221; &#8212; Sickle Cell Disease News\" src=\"https:\/\/sicklecellanemianews.com\/news\/hhs-secretary-alex-azar-touts-white-house-efforts-fight-sickle-cell-disease\/embed\/#?secret=V4nKJjePbx#?secret=IQlRZGSpgZ\" data-secret=\"IQlRZGSpgZ\" width=\"600\" height=\"338\" frameborder=\"0\" marginwidth=\"0\" marginheight=\"0\" scrolling=\"no\"><\/iframe><\/p>\n<p>&nbsp;<\/p>\n<p>Angelman Syndrome News published the following article, featuring Angelman advocate and Tennessee Rare Action Network Ambassador Terry Jo Bichell, on December 3:<\/p>\n<blockquote class=\"wp-embedded-content\" data-secret=\"QeiN9qIgM6\"><p><a href=\"https:\/\/angelmansyndromenews.com\/news\/angelman-advocate-launches-combined-brain-rare-disease-consortium\/\" rel=\"nofollow noopener\" target=\"_blank\">Angelman Advocate Launches \u2018Combined Brain\u2019 Rare Disease Consortium<\/a><\/p><\/blockquote>\n<p><iframe loading=\"lazy\" class=\"wp-embedded-content\" sandbox=\"allow-scripts\" security=\"restricted\" style=\"position: absolute; clip: rect(1px, 1px, 1px, 1px);\" title=\"&#8220;Angelman Advocate Launches \u2018Combined Brain\u2019 Rare Disease Consortium&#8221; &#8212; Angelman Syndrome News\" src=\"https:\/\/angelmansyndromenews.com\/news\/angelman-advocate-launches-combined-brain-rare-disease-consortium\/embed\/#?secret=vuc1MHviRd#?secret=QeiN9qIgM6\" data-secret=\"QeiN9qIgM6\" width=\"600\" height=\"338\" frameborder=\"0\" marginwidth=\"0\" marginheight=\"0\" scrolling=\"no\"><\/iframe><\/p>\n","protected":false},"excerpt":{"rendered":"<p>BioNews Service reporter Larry Luxner attended the 2019 NORD Rare Diseases and Orphan Products Breakthrough Summit in Washington, DC in October, and has since written two articles based on Summit &hellip; <\/p>\n<p class=\"link-more\"><a href=\"https:\/\/rarediseases.org\/es\/nordinthenews-nord-summit-content-featured-in-two-new-articles\/\" class=\"more-link\">Continue reading<span class=\"screen-reader-text\"> \u00ab#NORDinthenews: NORD Summit content featured in two new articles\u00bb<\/span><\/a><\/p>\n","protected":false},"author":47,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"_relevanssi_hide_post":"","_relevanssi_hide_content":"","_relevanssi_pin_for_all":"","_relevanssi_pin_keywords":"","_relevanssi_unpin_keywords":"","_relevanssi_related_keywords":"","_relevanssi_related_include_ids":"","_relevanssi_related_exclude_ids":"","_relevanssi_related_no_append":"","_relevanssi_related_not_related":"","_relevanssi_related_posts":"","_relevanssi_noindex_reason":"","_price":"","_stock":"","_tribe_ticket_header":"","_tribe_default_ticket_provider":"","_tribe_ticket_capacity":"","_ticket_start_date":"","_ticket_end_date":"","_tribe_ticket_show_description":"","_tribe_ticket_show_not_going":false,"_tribe_ticket_use_global_stock":"","_tribe_ticket_global_stock_level":"","_global_stock_mode":"","_global_stock_cap":"","_tribe_rsvp_for_event":"","_tribe_ticket_going_count":"","_tribe_ticket_not_going_count":"","_tribe_tickets_list":"[]","_tribe_ticket_has_attendee_info_fields":false,"footnotes":""},"categories":[1],"tags":[],"class_list":["post-59082","post","type-post","status-publish","format-standard","hentry","category-uncategorized"],"acf":[],"_links":{"self":[{"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/posts\/59082","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/users\/47"}],"replies":[{"embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/comments?post=59082"}],"version-history":[{"count":0,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/posts\/59082\/revisions"}],"wp:attachment":[{"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/media?parent=59082"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/categories?post=59082"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/tags?post=59082"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}