{"id":59025,"date":"2019-06-27T13:32:59","date_gmt":"2019-06-27T17:32:59","guid":{"rendered":"https:\/\/rarediseases.org\/nords-2019-living-rare-living-stronger-weekend-highlights\/"},"modified":"2019-06-27T13:32:59","modified_gmt":"2019-06-27T17:32:59","slug":"nords-2019-living-rare-living-stronger-weekend-highlights","status":"publish","type":"post","link":"https:\/\/rarediseases.org\/es\/nords-2019-living-rare-living-stronger-weekend-highlights\/","title":{"rendered":"NORD&#8217;s 2019 Living Rare, Living Stronger Weekend Highlights"},"content":{"rendered":"<p>We would like to extend our sincerest thanks to all those who joined us during the <a href=\"https:\/\/rarediseases.org\/living-rare-forum\/\" target=\"_blank\" rel=\"noopener noreferrer\">Living Rare, Living Stronger NORD Patient &amp; Family Forum<\/a>, June 21-23 in Houston. Over 500 individuals came out for a weekend filled with learning, sharing, bonding and fun. Our hope is that this event provided the tools, information and support needed for everyone to live their best rare life.<\/p>\n<p>We would not be able to present an event of this kind without the Living Rare Forum Advisory Committee, speakers, sponsors and media partners. Their hard work, insights and talent were integral to the success of this special event. We are truly grateful for their involvement in 2019.<\/p>\n<p>NORD\u2019s Living Rare Forum is a traveling event and we are looking forward to visiting a different city in 2020. We hope you will join us! Stay tuned for more details coming soon.<\/p>\n<hr \/>\n<h3 style=\"text-align: center;\"><span style=\"color: #0099bc;\">Weekend Highlights<\/span><\/h3>\n<p style=\"text-align: center;\"><a href=\"https:\/\/rarediseases.org\/living-rare-forum\/\" target=\"_blank\" rel=\"noopener noreferrer\"><em>Click here to view a selection of photos from the weekend<\/em><\/a><\/p>\n<p><span style=\"color: #fc4c02;\"><strong>Weekend-long learning<\/strong><\/span><\/p>\n<p><span style=\"color: #000000;\">Through educational programming on Saturday and Sunday, attendees were immersed in topics of their choosing. Caregivers came together to learn how to better support themselves and their rare loved ones, long-term survivors shared life hacks and resources, medical professionals and students spent their time better understanding the community for improved care and newly diagnosed patients got the tools needed to live their new normal.<\/span><\/p>\n<p><span style=\"color: #0099bc;\"><strong>Three days of fun<\/strong><\/span><\/p>\n<p>Hundreds of zebras kicked up their heels with a BBQ, Western line-dancing, selfie stations and the big event, NORD&#8217;s Rare Impact Awards. Retired NASA astronaut Colonel Kenneth Cameron welcomed us to Space Center Houston, emcee Mary Lou Retton energized the crowd with her spirit, and NORD honored 17 individuals and companies for the extraordinary work they&#8217;ve done to support people living with rare diseases.<\/p>\n<p><span style=\"color: #f2a900;\"><strong>#LivingRareForum online<\/strong><\/span><\/p>\n<p>Hundreds of tweets, snaps and posts were shared throughout the weekend, connecting not only 500 in-person attendees, but even more people online. NORD was honored to host select content from the Living Rare Forum and Rare Impact Awards on\u00a0<a href=\"https:\/\/www.facebook.com\/pg\/NationalOrganizationforRareDisorders\/videos\/?ref=page_internal\" target=\"_blank\" rel=\"noopener noreferrer nofollow\">Facebook Live<\/a>,\u00a0<strong>reaching over 5,000 individuals<\/strong>. Keep the conversations going! What was your favorite part of the weekend? Share using the hashtag #LivingRareForum.<\/p>\n<p><span style=\"color: #71cc98;\"><strong>Join us again!<\/strong><\/span><\/p>\n<p>We look forward to seeing you at a future NORD event! Save the date for our annual\u00a0<a href=\"https:\/\/rarediseases.org\/summit-overview\/\" target=\"_blank\" rel=\"noopener noreferrer\">Rare Diseases and Orphan Products Breakthrough Summit<\/a>, October 21-22 in Washington, DC. You can also check out NORD&#8217;s Rare Action Network site to find an\u00a0<a href=\"https:\/\/rareaction.org\/resources-for-advocates\/state-profiles\/\" target=\"_blank\" rel=\"noopener noreferrer nofollow\">event in your local community<\/a>.<\/p>\n<hr \/>\n<p><strong>Thanks to NORD\u2019s Living Rare, Living Stronger Advisory Board<\/strong><\/p>\n<p>NORD would like to extend our appreciation to the 2019 Living Rare, Living Stronger Advisory Board members who assisted with the program and its varied elements. Their dedication, time and insights help to assure a program that is timely, relevant and meaningful to all members of the rare disease community.<\/p>\n<p>Alice Chen, MD, National Center for Advancing Translational Sciences, NIH<br \/>\nXenia Chepa-Lotrea, NIH\/NHGRI Undiagnosed Diseases Program<br \/>\nSusan Fernbach, RN, Baylor College of Medicine<br \/>\nSusan Hedstrom, Foundation for Prader-Willi Research &amp; NORD Board of Directors<br \/>\nBrendan Lee, MD, PhD, Baylor College of Medicine<br \/>\nPilar Magoulas, MS, CGC, Baylor College of Medicine<br \/>\nMike Michaelis, OMS Life Foundation<br \/>\nDebra Regier, MD, PhD, Children\u2019s National Rare Disease Institute &amp; Children\u2019s National Health System<br \/>\nHarjot Singh Randhawa, MD, School of Medicine, American University of Integrative Sciences<br \/>\nDeborah Skolaski, NORD Rare Action Network Texas State Ambassador<br \/>\nReid Sutton, MD, Baylor College of Medicine &amp; Texas Children\u2019s Hospital<br \/>\nMonica Weldon, Bridge the Gap \u2013 SYNGAP \u2013 Education and Research Foundation<br \/>\nMarsha Zimmerman, Acid Maltase Deficiency Association<\/p>\n","protected":false},"excerpt":{"rendered":"<p>We would like to extend our sincerest thanks to all those who joined us during the Living Rare, Living Stronger NORD Patient &amp; Family Forum, June 21-23 in Houston. Over &hellip; <\/p>\n<p class=\"link-more\"><a href=\"https:\/\/rarediseases.org\/es\/nords-2019-living-rare-living-stronger-weekend-highlights\/\" class=\"more-link\">Continue reading<span class=\"screen-reader-text\"> &#8220;NORD&#8217;s 2019 Living Rare, Living Stronger Weekend Highlights&#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":[503,662,192],"tags":[1997,1363,1816,1908,1909],"class_list":["post-59025","post","type-post","status-publish","format-standard","hentry","category-events","category-get-involved","category-patients-members","tag-livingrareforum","tag-houston","tag-living-rare-living-stronger","tag-living-rare-living-stronger-nord-patient-family-forum","tag-patient-family-forum"],"acf":[],"_links":{"self":[{"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/posts\/59025","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=59025"}],"version-history":[{"count":0,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/posts\/59025\/revisions"}],"wp:attachment":[{"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/media?parent=59025"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/categories?post=59025"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/tags?post=59025"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}