{"id":58957,"date":"2018-09-20T14:36:50","date_gmt":"2018-09-20T18:36:50","guid":{"rendered":"https:\/\/rarediseases.org\/chat-chew-and-be-challenged-lunchtime-learning-at-the-nord-rare-summit\/"},"modified":"2022-12-02T08:11:55","modified_gmt":"2022-12-02T13:11:55","slug":"chat-chew-and-be-challenged-lunchtime-learning-at-the-nord-rare-summit","status":"publish","type":"post","link":"https:\/\/rarediseases.org\/es\/chat-chew-and-be-challenged-lunchtime-learning-at-the-nord-rare-summit\/","title":{"rendered":"Chat, Chew, and Be Challenged! Lunchtime Learning at the NORD Rare Summit"},"content":{"rendered":"<p>Make your choice from this menu of thought-provoking, informative Lunch &amp; Learn sessions available for attendees of the 2018 NORD Rare Summit. With only 25 days to go, be sure to save your seat at the table by registering for the Summit and choosing your lunch option now! <em>Lunch &amp; Learn sessions have limited seating and will be first-come, <\/em>first-served<em>.<\/em><\/p>\n<p style=\"text-align: center;\"><a href=\"https:\/\/nord.cvent.com\/events\/rare-diseases-and-orphan-products-breakthrough-summit-2018\/event-summary-434d756f95fc43cfa2a4ac02dc9b4a90.aspx\" target=\"_blank\" rel=\"noopener nofollow\"><strong>Register for the NORD Rare Summit Here<\/strong><\/a><\/p>\n<div class=\"gl-contains-divider\">\n<table class=\"editor-divider\" border=\"0\" width=\"100%\" cellspacing=\"0\" cellpadding=\"0\">\n<tbody>\n<tr>\n<td class=\"\" align=\"center\" valign=\"top\">\n<table class=\"galileo-ap-content-editor\" style=\"height: 29px;\" width=\"1369\">\n<tbody>\n<tr>\n<td class=\"divider-base divider-solid\" align=\"center\" valign=\"top\" width=\"100%\"><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<\/div>\n<table class=\"galileo-ap-layout-editor\" border=\"0\" width=\"100%\" cellspacing=\"0\" cellpadding=\"0\">\n<tbody>\n<tr>\n<td class=\"split-layout-margin\" align=\"left\" valign=\"top\" bgcolor=\"#ffffff\">\n<table class=\"feature-split-container\" border=\"0\" width=\"100%\" cellspacing=\"0\" cellpadding=\"0\">\n<tbody>\n<tr>\n<td class=\"mobile-hidden layout-container\" align=\"center\" valign=\"top\" bgcolor=\"#ffffff\" width=\"5\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/imgssl.constantcontact.com\/letters\/images\/sys\/S.gif\" alt=\"\" width=\"5\" height=\"5\" border=\"0\" hspace=\"0\" vspace=\"0\" \/><\/td>\n<td class=\"split feature editor-col OneColumnMobile\" align=\"left\" valign=\"top\" bgcolor=\"#ECF0F1\" width=\"50%\">\n<div>\n<div class=\"column-resize-bar\"><\/div>\n<\/div>\n<div class=\"gl-contains-image\">\n<table class=\"editor-image content-image editor-image-vspace-on editor-image-hspace-on\" border=\"0\" width=\"100%\" cellspacing=\"0\" cellpadding=\"0\">\n<tbody>\n<tr>\n<td align=\"left\" valign=\"top\">\n<div class=\"publish-container\"><img decoding=\"async\" class=\"aligncenter\" src=\"https:\/\/files.constantcontact.com\/e0ab2096501\/b83cebd9-d303-4319-9efd-1d105eece882.jpg\" alt=\"\" width=\"235\" border=\"0\" hspace=\"0\" vspace=\"0\" \/><\/div>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<\/div>\n<div class=\"gl-contains-text\">\n<table border=\"0\" width=\"100%\" cellspacing=\"0\" cellpadding=\"0\">\n<tbody>\n<tr>\n<td class=\"editor-text feature-text\" align=\"left\" valign=\"top\">\n<div><\/div>\n<div class=\"text-container galileo-ap-content-editor\">\n<div>\n<div>Monday, October 15<\/div>\n<div><\/div>\n<ul>\n<li>Cannabinoid Treatments &amp; Rare Diseases<\/li>\n<\/ul>\n<div><\/div>\n<ul>\n<li>Caring for an Adult Rare Disease Patient<\/li>\n<\/ul>\n<div><\/div>\n<ul>\n<li>How Genetic Testing Can Guide Treatment<\/li>\n<\/ul>\n<div><\/div>\n<ul>\n<li>Legal Considerations and Strategies for Non-Profit and For-Profit Joint Ventures<\/li>\n<\/ul>\n<div><\/div>\n<ul>\n<li>The Next Generation of Rare Disease Advocates<\/li>\n<\/ul>\n<div><\/div>\n<ul>\n<li>NIH Resources for Rare Disease Research and Information<\/li>\n<\/ul>\n<div><\/div>\n<ul>\n<li>Rare Diseases and ICD Codes<\/li>\n<\/ul>\n<\/div>\n<\/div>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<\/div>\n<\/td>\n<td class=\"mobile-hidden layout-container\" align=\"center\" valign=\"top\" bgcolor=\"#ffffff\" width=\"5\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/imgssl.constantcontact.com\/letters\/images\/sys\/S.gif\" alt=\"\" width=\"5\" height=\"10\" border=\"0\" hspace=\"0\" vspace=\"0\" \/><\/td>\n<td class=\"mobile-hidden layout-container\" align=\"center\" valign=\"top\" bgcolor=\"#ffffff\" width=\"5\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/imgssl.constantcontact.com\/letters\/images\/sys\/S.gif\" alt=\"\" width=\"5\" height=\"5\" border=\"0\" hspace=\"0\" vspace=\"0\" \/><\/td>\n<td class=\"split feature editor-col OneColumnMobile\" align=\"left\" valign=\"top\" bgcolor=\"#ECF0F1\" width=\"50%\">\n<div class=\"gl-contains-image\">\n<table class=\"editor-image content-image editor-image-vspace-on editor-image-hspace-on\" border=\"0\" width=\"100%\" cellspacing=\"0\" cellpadding=\"0\">\n<tbody>\n<tr>\n<td align=\"right\" valign=\"top\">\n<div class=\"publish-container\"><img decoding=\"async\" class=\"aligncenter\" src=\"https:\/\/files.constantcontact.com\/e0ab2096501\/46feb8f0-8e43-41ac-9ab2-333b917eab46.jpg\" alt=\"\" width=\"235\" border=\"0\" hspace=\"0\" vspace=\"0\" \/><\/div>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<\/div>\n<div class=\"gl-contains-text\">\n<table border=\"0\" width=\"100%\" cellspacing=\"0\" cellpadding=\"0\">\n<tbody>\n<tr>\n<td class=\"editor-text feature-text\" align=\"left\" valign=\"top\">\n<div><\/div>\n<div class=\"text-container galileo-ap-content-editor\">\n<div>\n<div>Tuesday, October 16<\/div>\n<div><\/div>\n<ul>\n<li>Caring for Someone with a Chronic Disease<\/li>\n<\/ul>\n<div><\/div>\n<ul>\n<li>How to Start a Patient Registry<\/li>\n<\/ul>\n<div><\/div>\n<ul>\n<li>NIH Resources for Rare Disease Research and Information<\/li>\n<\/ul>\n<div><\/div>\n<ul>\n<li>Patient-Informed Drug Development<\/li>\n<\/ul>\n<div><\/div>\n<ul>\n<li>Patient Perspectives on Gene Therapy<\/li>\n<\/ul>\n<div><\/div>\n<ul>\n<li>Rare Diseases and Emergency Situations<\/li>\n<\/ul>\n<div><\/div>\n<ul>\n<li>Regulatory Considerations and Strategies for Gene Therapy<\/li>\n<\/ul>\n<\/div>\n<\/div>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<\/div>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><em><strong><br \/>\nDon&#8217;t forget the party!\u00a0<\/strong><\/em><\/p>\n<div>NORD Rare Summit registrants are invited to \u201cCocktails and Conversation with Children\u2019s National Rare Disease Institute\u201d on Tuesday, October 16 at 6:15 pm, hosted by\u00a0Marshall Summar, MD and members of the Children\u2019s National Rare Disease Institute.<\/div>\n<div><\/div>\n<div>The registration link for the reception is:\u00a0https:\/\/childrensnational.org\/NORD2018<\/div>\n","protected":false},"excerpt":{"rendered":"<p>Make your choice from this menu of thought-provoking, informative Lunch &amp; Learn sessions available for attendees of the 2018 NORD Rare Summit. With only 25 days to go, be sure &hellip; <\/p>\n<p class=\"link-more\"><a href=\"https:\/\/rarediseases.org\/es\/chat-chew-and-be-challenged-lunchtime-learning-at-the-nord-rare-summit\/\" class=\"more-link\">Continue reading<span class=\"screen-reader-text\"> &#8220;Chat, Chew, and Be Challenged! Lunchtime Learning at the NORD Rare Summit&#8221;<\/span><\/a><\/p>\n","protected":false},"author":1,"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":[503,190,662],"tags":[1755,1697,270,212,277,1758,1757,1496,200,1754,1756,643,893],"class_list":["post-58957","post","type-post","status-publish","format-standard","hentry","category-events","category-featured-news","category-get-involved","tag-adult-rare-disease-patient","tag-chronic-disease","tag-drug-development","tag-gene-therapy","tag-genetic-testing","tag-icd-codes","tag-nih-resources","tag-nord-rare-summit","tag-nord-summit","tag-patient-registry","tag-rare-disease-advocates","tag-rare-diseases-and-orphan-products-breakthrough-summit","tag-washington-d-c"],"acf":[],"_links":{"self":[{"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/posts\/58957","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\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/comments?post=58957"}],"version-history":[{"count":0,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/posts\/58957\/revisions"}],"wp:attachment":[{"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/media?parent=58957"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/categories?post=58957"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/tags?post=58957"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}