{"id":58846,"date":"2017-03-15T15:36:09","date_gmt":"2017-03-15T19:36:09","guid":{"rendered":"https:\/\/rarediseases.org\/beth-nguyen-r-n-2017-rare-impact-award-honoree\/"},"modified":"2017-03-15T15:36:09","modified_gmt":"2017-03-15T19:36:09","slug":"beth-nguyen-r-n-2017-rare-impact-award-honoree","status":"publish","type":"post","link":"https:\/\/rarediseases.org\/es\/beth-nguyen-r-n-2017-rare-impact-award-honoree\/","title":{"rendered":"Beth Nguyen, R.N. &#8211; 2017 Rare Impact Award Honoree"},"content":{"rendered":"<p><b>2017 Honoree<\/b><b><br \/>\n<\/b><b>Rare Impact Awards<\/b><\/p>\n<p><a href=\"https:\/\/rarediseases.org\/wp-content\/uploads\/2017\/07\/bethpic-1-150x150.jpg\" data-rel=\"lightbox-image-0\" data-rl_title=\"\" data-rl_caption=\"\" title=\"\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-full wp-image-31487\" src=\"https:\/\/rarediseases.org\/wp-content\/uploads\/2017\/07\/bethpic-1-150x150.jpg\" alt=\"bethpic-1-150x150\" width=\"150\" height=\"150\" \/><\/a><\/p>\n<p><b>Beth Nguyen, R.N.<\/b><\/p>\n<p><span style=\"font-weight: 400;\">Mother, wife, nurse, patient, advocate, and leader; Beth Nguyen wears multiple hats, and not one loosely. <\/span><\/p>\n<p><span style=\"font-weight: 400;\">In 2007, before she began to experience health problems, Beth had a job she loved as an emergency room nurse and was highly-regarded by her colleagues, married to her high school sweetheart, and the mother of two young children.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">Then followed a 5-year battle with her health during which Beth could no longer work and doctors dismissed or incorrectly diagnosed her symptoms. \u00a0In 2012, Beth was finally given the diagnosis of Syringomyelia, a rare disease in which cysts form on the spinal cord and painfully destroy it from the inside out. \u00a0By then, she had unfortunately developed permanent damage. \u00a0She knew that she needed to do something to help others.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">She has since established a 501(c)(3) organization, the Worldwide Syringomyelia and Chiari Malformation Task Force (WSCTF), to increase understanding of the disease across all medical disciplines and to improve direct patient care. \u00a0She also started a patient registry to drive research, has organized support groups, and developed of the first-ever advocacy models of care for both Syringomyelia and Chiari Malformation. <\/span><\/p>\n<p><span style=\"font-weight: 400;\">Beth also became one of NORD\u2019s first Rare Action Network<\/span><span style=\"font-weight: 400;\">SM<\/span><span style=\"font-weight: 400;\"> State Ambassadors. In this role, she works with NORD to organize grassroots advocacy efforts in Georgia and serves as a mentor for rare disease advocates across the state. She has helped to establish a Rare Disease Advisory Council within the state government and has organized successful Rare Disease Day\u00ae events. <\/span><\/p>\n<p><span style=\"font-weight: 400;\">Why is Beth taking on so much while continuing to battle a health crisis of her own? \u00a0In response, she cites a favorite quote from Florence Nightingale, which reads, \u201cRather, ten times, die in the surf, heralding the way to a new world, than stand idly on the shore.\u201d Beth is passionate about using her experience as a way to prevent others\u2019 suffering.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">\u201cI worked in the emergency room and had no idea about disparities in rare diseases until I started my own journey and it opened my eyes,\u201d she says. \u00a0\u201cI felt terrible, and there was this whole other world of individuals who fought on a daily basis to survive\u2026 I\u2019m using my journey as a way to open doors for people who need help in the rare community. My heart is with the individuals who are suffering from this.\u201d <\/span><\/p>\n<p><span style=\"font-weight: 400;\">NORD is honored to present Beth Nguyen with a 2017 Rare Impact Award.<\/span><\/p>\n","protected":false},"excerpt":{"rendered":"<p>2017 Honoree Rare Impact Awards Beth Nguyen, R.N. Mother, wife, nurse, patient, advocate, and leader; Beth Nguyen wears multiple hats, and not one loosely. In 2007, before she began to &hellip; <\/p>\n<p class=\"link-more\"><a href=\"https:\/\/rarediseases.org\/es\/beth-nguyen-r-n-2017-rare-impact-award-honoree\/\" class=\"more-link\">Continue reading<span class=\"screen-reader-text\"> &#8220;Beth Nguyen, R.N. &#8211; 2017 Rare Impact Award Honoree&#8221;<\/span><\/a><\/p>\n","protected":false},"author":1,"featured_media":12412,"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":[232,191,505],"tags":[1313,1314,1315,526,1303,1302,930,652,651],"class_list":["post-58846","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-advocacy","category-medical","category-patient-stories","tag-beth-nguyen","tag-chiari-malformation","tag-ran-state-ambassador","tag-rare-action-network","tag-rare-impact-2017","tag-rare-impact-award-honoree","tag-rare-impact-awards","tag-syringomyelia","tag-wsctf"],"acf":[],"_links":{"self":[{"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/posts\/58846","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=58846"}],"version-history":[{"count":0,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/posts\/58846\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/media\/12412"}],"wp:attachment":[{"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/media?parent=58846"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/categories?post=58846"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/tags?post=58846"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}