{"id":59010,"date":"2019-05-20T17:18:52","date_gmt":"2019-05-20T21:18:52","guid":{"rendered":"https:\/\/rarediseases.org\/dr-debra-regier-2019-rare-impact-award-honoree\/"},"modified":"2019-05-20T17:18:52","modified_gmt":"2019-05-20T21:18:52","slug":"dr-debra-regier-2019-rare-impact-award-honoree","status":"publish","type":"post","link":"https:\/\/rarediseases.org\/es\/dr-debra-regier-2019-rare-impact-award-honoree\/","title":{"rendered":"Dr. Debra Regier: 2019 Rare Impact Award Honoree"},"content":{"rendered":"<p><span style=\"font-weight: 400;\">Debra Regier, M.D., Ph.D. is the Director of Genetic and Genomic Education at Washington, DC\u2019s Children&#8217;s National Medical Center, attending physician in genetics and metabolism and Primary Investigator (PI) for the Rare Disease Clinical Research Scholars Program. <span style=\"font-weight: 400;\">A graduate of the University of Utah School of Medicine in 2009 as Primary Investigator, Dr. Regier now leads a\u00a0<\/span>program that offers early career rare disease researchers with a curriculum designed to address their specific needs. Currently, her research is focused on assessing outcomes in genetic and genomic education at multiple levels of training.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">\u201cWhen I began my career, I quickly learned that I alone could not see all of the patients or ensure their optimal care. But I could help to ensure that there are rare disease doctors to care for the unique needs of this group of patients,\u201d says Dr. Regier.<\/span><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignright wp-image-39245\" src=\"https:\/\/rarediseases.org\/wp-content\/uploads\/2019\/05\/Trinity_Hall_GSD1a-Debra-Regier-1-225x300.jpg\" alt=\"\" width=\"179\" height=\"239\" \/><\/p>\n<p><span style=\"font-weight: 400;\">Named Clinical Educator of the Year by the National Human Genome Research Institute of NIH in 2018, Dr. Regier has served as a valued mentor to NORD\u2019s Education team, donating her time as a resource. In addition to her role as NORD\u2019s Education Committee Chairperson, Dr. Regier volunteers as the genetics and rare disease expert for the Make-A-Wish Foundation\u2019s national medical advisory council and on the Society for Inborn Errors of Metabolism board of directors. Her work with Make-A-Wish has helped to significantly increase the number of rare disease patients who have been granted wishes.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">Reflecting on her work in continuing rare disease education, Dr. Regier says, \u201cFamilies have impacted me more than I have them. I&#8217;ve been honored to \u2018live life\u2019 with amazing families who have allowed me to know them, care for them and be a part of their journey.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">NORD is honored to present Dr. Debra Regier with a 2019 Rare Impact Award.<\/span><\/p>\n<p>&nbsp;<\/p>\n<hr \/>\n<p style=\"text-align: center;\"><em><strong><a href=\"https:\/\/rarediseases.org\/living-rare-forum\/\" target=\"_blank\" rel=\"noopener\">Join us<\/a> <\/strong>during NORD&#8217;s annual Rare Impact Awards ceremony, presented as part <\/em><br \/>\n<em>of the 2019 Living Rare, Living Stronger Patient &amp; Family Forum in Houston, TX.\u00a0<\/em><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Debra Regier, M.D., Ph.D. is the Director of Genetic and Genomic Education at Washington, DC\u2019s Children&#8217;s National Medical Center, attending physician in genetics and metabolism and Primary Investigator (PI) for &hellip; <\/p>\n<p class=\"link-more\"><a href=\"https:\/\/rarediseases.org\/es\/dr-debra-regier-2019-rare-impact-award-honoree\/\" class=\"more-link\">Continue reading<span class=\"screen-reader-text\"> &#8220;Dr. Debra Regier: 2019 Rare Impact Award Honoree&#8221;<\/span><\/a><\/p>\n","protected":false},"author":1,"featured_media":12659,"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":[232,190,662],"tags":[1942,1953,1950,720,1952,1951,932,1627,1089],"class_list":["post-59010","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-advocacy","category-featured-news","category-get-involved","tag-2019-rare-impact-award-honoree","tag-childrens-national-medical-center","tag-living-rare-living-stronger-patient-and-family-forum","tag-make-a-wish-foundation","tag-nih-clinical-educator-of-the-year","tag-nord-education-team","tag-rare-impact","tag-rare-impact-award","tag-rare-impact-award-honorees"],"acf":[],"_links":{"self":[{"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/posts\/59010","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=59010"}],"version-history":[{"count":0,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/posts\/59010\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/media\/12659"}],"wp:attachment":[{"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/media?parent=59010"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/categories?post=59010"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/tags?post=59010"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}