{"id":58856,"date":"2017-08-15T13:49:59","date_gmt":"2017-08-15T17:49:59","guid":{"rendered":"https:\/\/rarediseases.org\/advance-the-dialogue-at-the-nord-rare-summit\/"},"modified":"2017-08-15T13:49:59","modified_gmt":"2017-08-15T17:49:59","slug":"advance-the-dialogue-at-the-nord-rare-summit","status":"publish","type":"post","link":"https:\/\/rarediseases.org\/es\/advance-the-dialogue-at-the-nord-rare-summit\/","title":{"rendered":"Advance the Dialogue at the NORD Rare Summit"},"content":{"rendered":"<p>It has been an interesting year for healthcare reform and the Orphan Drug Act, and as I\u2019m sure you are aware; the conversation isn\u2019t over yet.\u00a0Major changes to healthcare and tax reform continue to be discussed and that is why it is so important that now, more than ever, rare disease stakeholders come together to advance the\u00a0<span class=\"il\">dialogue<\/span>\u00a0on these and other emerging issues, policies and strategies that will affect the environment for rare diseases and orphan products.<\/p>\n<p>That is why I am urging you to attend NORD\u2019s 2017\u00a0<a href=\"https:\/\/r20.rs6.net\/tn.jsp?f=001Bn1rUzeCiSHZdz_T-8YE8Nw73aIuLD-ODckgPReeWJp5zFYHdGSYxCig7v7PT9eYm3ajbuGB7TmJHLLM4k6pmfc7Cxp3lUd1T__i9dAvyNMQvvckezF5oyE-OACNK611D29c2w0xUdocburk-mQrKA==&amp;c=hG8m8MKrbaatJT69aZhPMAxRCL5psmPEn9GjdyIRhfpk1dyVYWtmuA==&amp;ch=Q4hwEIFHMvDNBibOmPJFk2_tCf9Hq2e2he03_g7M6aNc9rmq6OvUkg==\" target=\"_blank\" data-saferedirecturl=\"https:\/\/www.google.com\/url?hl=en&amp;q=https:\/\/r20.rs6.net\/tn.jsp?f%3D001Bn1rUzeCiSHZdz_T-8YE8Nw73aIuLD-ODckgPReeWJp5zFYHdGSYxCig7v7PT9eYm3ajbuGB7TmJHLLM4k6pmfc7Cxp3lUd1T__i9dAvyNMQvvckezF5oyE-OACNK611D29c2w0xUdocburk-mQrKA%3D%3D%26c%3DhG8m8MKrbaatJT69aZhPMAxRCL5psmPEn9GjdyIRhfpk1dyVYWtmuA%3D%3D%26ch%3DQ4hwEIFHMvDNBibOmPJFk2_tCf9Hq2e2he03_g7M6aNc9rmq6OvUkg%3D%3D&amp;source=gmail&amp;ust=1502890632291000&amp;usg=AFQjCNHW4GrYsU2nKkmiwRgPevdF7ujIuw\" rel=\"noopener nofollow\">Rare Diseases and Orphan Products Breakthrough Summit<\/a>\u00a0this\u00a0<span class=\"aBn\" tabindex=\"0\" data-term=\"goog_1667949336\"><span class=\"aQJ\">October 16-17<\/span><\/span>\u00a0in Washington, D.C.<br \/>\n<b>Why attend?<br \/>\n<\/b>Creating a culture of conversation, education, and engagement around the debate in our nation&#8217;s healthcare system, the NORD Rare Summit is the place for YOU to interact with leaders from the FDA, NIH, patient advocacy groups, medical professionals, the orphan product industry and your colleagues. At NORD, we value your personal and professional insights and participation to help establish an inclusive environment of meaningful inspiration and collaboration.<br \/>\n<b>The keynotes<br \/>\n<\/b>As you may have read, this year\u2019s event will feature parent advocate, award-winning journalist, and founder\/CEO of\u00a0<i>The Mighty<\/i>, Mike Porath; and the new Commissioner of the Food and Drug Administration, Dr. Scott Gottlieb. The keynotes are a pinnacle example of the viewpoints and topics that will be discussed at the summit this year.<br \/>\n<b>What else can you expect?<br \/>\n<\/b>NORD, our members, our sponsors and you continue to play an integral role in advocating for the rare disease patient community. In support of our mutual commitment, we are proud to present:<\/p>\n<ul>\n<li>Over 20 roundtable topics each day<\/li>\n<li>Six breakout tracks<\/li>\n<li>96\u00a0speakers discussing topics from guidelines to next-generation treatments to\u00a0<span class=\"il\">advancing<\/span>\u00a0global collaboration<\/li>\n<li>Poster sessions highlighting groundbreaking innovation and emerging research<\/li>\n<li>Countless networking opportunities available through our networking app, Converve<\/li>\n<\/ul>\n<p>I urge you to be part of the conversation and debates as we work together to drive improvement and progress. As an incentive, we are pleased to offer advanced pricing until\u00a0<span class=\"aBn\" tabindex=\"0\" data-term=\"goog_1667949337\"><span class=\"aQJ\">August 25<\/span><\/span>.\u00a0<a href=\"https:\/\/r20.rs6.net\/tn.jsp?f=001Bn1rUzeCiSHZdz_T-8YE8Nw73aIuLD-ODckgPReeWJp5zFYHdGSYxP5jsr5YxuvBCk-VkUuvvkS0lRy7Swuk_WPCIJOIezKQrSuqhxa-8WW6kRaaEeJuGCGl0-irAjE61UtGOGLTNKG1zCaykimICsCGa8crgx7VKvZt6IyRlj0=&amp;c=hG8m8MKrbaatJT69aZhPMAxRCL5psmPEn9GjdyIRhfpk1dyVYWtmuA==&amp;ch=Q4hwEIFHMvDNBibOmPJFk2_tCf9Hq2e2he03_g7M6aNc9rmq6OvUkg==\" target=\"_blank\" data-saferedirecturl=\"https:\/\/www.google.com\/url?hl=en&amp;q=https:\/\/r20.rs6.net\/tn.jsp?f%3D001Bn1rUzeCiSHZdz_T-8YE8Nw73aIuLD-ODckgPReeWJp5zFYHdGSYxP5jsr5YxuvBCk-VkUuvvkS0lRy7Swuk_WPCIJOIezKQrSuqhxa-8WW6kRaaEeJuGCGl0-irAjE61UtGOGLTNKG1zCaykimICsCGa8crgx7VKvZt6IyRlj0%3D%26c%3DhG8m8MKrbaatJT69aZhPMAxRCL5psmPEn9GjdyIRhfpk1dyVYWtmuA%3D%3D%26ch%3DQ4hwEIFHMvDNBibOmPJFk2_tCf9Hq2e2he03_g7M6aNc9rmq6OvUkg%3D%3D&amp;source=gmail&amp;ust=1502890632291000&amp;usg=AFQjCNF9EdvxHQFo5-ZIz1NIXe_bNupocA\" rel=\"noopener nofollow\">View the agenda<\/a>\u00a0and start planning today!<br \/>\nI look forward to greeting you in person.<br \/>\nPeter L. Saltonstall<br \/>\nPresident and CEO<br \/>\nNational Organization for Rare Disorders (NORD)<\/p>\n<hr \/>\n<p style=\"text-align: center;\"><em><strong>NORD&#8217;s Rare Diseases and Orphan Products Breakthrough Summit is the largest multi-stakeholder event in rare diseases.<br \/>\nThe NORD Rare Summit takes place in Washington, D.C. October 16 -17.\u00a0<\/strong><\/em><\/p>\n<p style=\"text-align: center;\"><em><strong>We hope you can join us! <a href=\"https:\/\/rarediseases.org\/summit-overview\/\" target=\"_blank\" rel=\"noopener\">Learn more<\/a> and <a href=\"https:\/\/www.cvent.com\/events\/rare-diseases-and-orphan-products-breakthrough-summit-2017\/event-summary-15d59fdbbde14f23b22306f23328ccb9.aspx\" target=\"_blank\" rel=\"noopener nofollow\">register today<\/a>. <\/strong><\/em><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Register now for the NORD Rare Summit to advance the dialogue on issues of unprecedented importance to the rare disease community.<\/p>\n","protected":false},"author":1,"featured_media":12199,"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":[232,503,190,662,210,191,192],"tags":[1274,244,1088,317,1333,1496,200,262,199,1075,228,1497,1127,1334],"class_list":["post-58856","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-advocacy","category-events","category-featured-news","category-get-involved","category-industry","category-medical","category-patients-members","tag-dr-scott-gottlieb","tag-fda","tag-healthcare","tag-healthcare-reform","tag-mike-porath","tag-nord-rare-summit","tag-nord-summit","tag-orphan-drug-act","tag-orphan-products","tag-policy","tag-rare-diseases","tag-rare-diseases-and-orphan-products-brekathrough-summit","tag-rare-summit","tag-the-mighty"],"acf":[],"_links":{"self":[{"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/posts\/58856","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=58856"}],"version-history":[{"count":0,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/posts\/58856\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/media\/12199"}],"wp:attachment":[{"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/media?parent=58856"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/categories?post=58856"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/tags?post=58856"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}