{"id":58664,"date":"2015-12-02T19:43:54","date_gmt":"2015-12-03T00:43:54","guid":{"rendered":"https:\/\/rarediseases.org\/be-a-hero-help-nord-educate-current-and-future-medical-professionals\/"},"modified":"2015-12-02T19:43:54","modified_gmt":"2015-12-03T00:43:54","slug":"be-a-hero-help-nord-educate-current-and-future-medical-professionals","status":"publish","type":"post","link":"https:\/\/rarediseases.org\/es\/be-a-hero-help-nord-educate-current-and-future-medical-professionals\/","title":{"rendered":"Be a Hero: Help NORD Educate Current and Future Medical Professionals"},"content":{"rendered":"<figure id=\"attachment_22915\" aria-describedby=\"caption-attachment-22915\" style=\"width: 300px\" class=\"wp-caption alignleft\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-22915 size-medium\" src=\"https:\/\/rarediseases.org\/wp-content\/uploads\/2015\/12\/KG-StudentGroup-300x202.png\" alt=\"KG-StudentGroup\" width=\"300\" height=\"202\" \/><figcaption id=\"caption-attachment-22915\" class=\"wp-caption-text\">Keck Graduate Institute Students giving a presentation on Rett Syndrome, a rare disease.<\/figcaption><\/figure>\n<p>Education has always been a key component of NORD\u2019s mission and this year we expanded our outreach to two vitally important audiences \u2013 medical professionals and students preparing for health-related careers.<\/p>\n<p>Today\u2019s healthcare professionals are aware that they will encounter patients with rare diseases, and they are eager for information and resources to help them provide the best possible care. In a survey published last year, Frontline Medical Communications reported that 88% of more than 1,600 HCPs expressed a need for more rare disease information.<\/p>\n<p>NORD\u2019s approach to addressing this need is threefold:<\/p>\n<ul>\n<li>Harnessing the power of our nearly 250 member organizations and their medical experts to educate about specific rare diseases and the patient\/family experience;<\/li>\n<li>Establishing innovative partnerships and collaborations with medical publishers and professional societies; and<\/li>\n<li>Conducting outreach to medical students and others preparing for healthcare careers.<\/li>\n<\/ul>\n<p><strong>What Have We Accomplished this Year?<\/strong><\/p>\n<figure id=\"attachment_21881\" aria-describedby=\"caption-attachment-21881\" style=\"width: 300px\" class=\"wp-caption alignright\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-21881 size-medium\" src=\"https:\/\/rarediseases.org\/wp-content\/uploads\/2015\/09\/NORD-AMSA-meeting-sign-up-for-student-membership-photo-300x225.jpg\" alt=\"NORD-AMSA meeting-sign up for student membership-photo\" width=\"300\" height=\"225\" \/><figcaption id=\"caption-attachment-21881\" class=\"wp-caption-text\">NORD at the 2015 AMSA meeting<\/figcaption><\/figure>\n<p>During 2015, NORD\u2019s Department of Educational Initiatives partnered with Frontline Medical Communications, Medscape, and Rare Disease Report to reach millions of healthcare professionals with targeted information. We now have opportunities to create CME resources, and we are exploring innovative ways to use video, podcasts, telemedicine, and other media to convey the patient experience and connect rare disease experts with community physicians.<\/p>\n<p>Our outreach to students included hosting a \u201cMeet the Patients\u201d event at the 2015 American Medical Student Association (AMSA) annual conference. We established a new free student membership and worked with rare disease clubs at Keck Graduate Institute and the University of Notre Dame. Through a new collaboration with the University of Connecticut, advanced science students will learn about rare diseases and sharpen their writing skills by working with NORD\u2019s editorial team.<\/p>\n<p>&nbsp;<\/p>\n<p><strong>What\u2019s Ahead for 2016?<\/strong><\/p>\n<p>With your help, we want to build on this momentum with expanded outreach to professionals and students. Specific opportunities include:<\/p>\n<p><u>Patient\/Caregiver Speakers Bureau<\/u><\/p>\n<p>NORD has developed a Speakers Bureau of patients and caregivers with powerful stories that they are eager to share. We want to bring these speakers to classrooms across the US to educate and motivate future healthcare professionals. The intent is not to try to teach students about all 7,000 rare diseases but rather to encourage a different way of thinking that will promote earlier diagnosis and greater understanding of rare disease challenges.<\/p>\n<p><u>Rare Disease Grand Rounds<\/u><\/p>\n<p>NORD hopes to launch a pilot Grand Rounds program in 2016 to bring rare disease medical experts to hospitals across the US with the ultimate goal of reducing time to diagnosis and improving patient care.<\/p>\n<p>While these new initiatives are exciting, our team will also continue to update and expand NORD\u2019s longstanding educational services such as our Rare Disease Database, which provides patient-friendly information to millions of people through NORD\u2019s website and others, including WebMD.<\/p>\n<p>NORD\u2019s Online Physician Guide platform, launched in 2013, will be expanded to cover additional topics. These guides are free, written by medical experts, and had 57,409 page views during 2015 with 24,615 visits from 164 countries.<\/p>\n<p>With your help, NORD can continue to refine and expand its longstanding educational services while also launching exciting new ones at this moment in time when students and health professionals are eager to hear from us!<\/p>\n<p>&nbsp;<\/p>\n<p style=\"text-align: center;\"><em>Your donations will support NORD&#8217;s efforts in continuing outreach to current and future medical professionals. <\/em><\/p>\n<p style=\"text-align: center;\"><em>If you&#8217;re interested in making a donation, please <a href=\"https:\/\/salsa3.salsalabs.com\/o\/51076\/donate_page\/donate-now?track=Blog_Mary\" target=\"_blank\" rel=\"noopener nofollow\">click here.<\/a><\/em><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Education has always been a key component of NORD\u2019s mission and this year we expanded our outreach to two vitally important audiences \u2013 medical professionals and students preparing for health-related &hellip; <\/p>\n<p class=\"link-more\"><a href=\"https:\/\/rarediseases.org\/es\/be-a-hero-help-nord-educate-current-and-future-medical-professionals\/\" class=\"more-link\">Continue reading<span class=\"screen-reader-text\"> &#8220;Be a Hero: Help NORD Educate Current and Future Medical Professionals&#8221;<\/span><\/a><\/p>\n","protected":false},"author":1,"featured_media":12065,"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":[190,662,210,191,192,193],"tags":[870,873,715,869,871,872,801],"class_list":["post-58664","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-featured-news","category-get-involved","category-industry","category-medical","category-patients-members","category-research","tag-american-medical-students-association","tag-be-a-hero","tag-donate","tag-educational-initiatives","tag-keck-graduate-institute","tag-rare-disease-club","tag-rett-syndrome"],"acf":[],"_links":{"self":[{"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/posts\/58664","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=58664"}],"version-history":[{"count":0,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/posts\/58664\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/media\/12065"}],"wp:attachment":[{"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/media?parent=58664"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/categories?post=58664"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/tags?post=58664"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}