{"id":59000,"date":"2019-03-28T13:26:05","date_gmt":"2019-03-28T17:26:05","guid":{"rendered":"https:\/\/rarediseases.org\/nord-video-provides-advice-for-the-newly-diagnosed\/"},"modified":"2019-03-28T13:26:05","modified_gmt":"2019-03-28T17:26:05","slug":"nord-video-provides-advice-for-the-newly-diagnosed","status":"publish","type":"post","link":"https:\/\/rarediseases.org\/es\/nord-video-provides-advice-for-the-newly-diagnosed\/","title":{"rendered":"NORD Video Provides Advice for the Newly Diagnosed"},"content":{"rendered":"<p><span style=\"font-weight: 400;\">A rare diagnosis can be a frightening and isolating experience, whether you are the patient or a caregiver for a loved one. However, NORD has created a <a href=\"https:\/\/youtu.be\/wZX9HABjT4Q\" target=\"_blank\" rel=\"noopener nofollow\">video providing tips for newly diagnosed<\/a> patients and families as they begin their journey down this new road. One of the key messages is that you are not alone. <\/span><\/p>\n<p><span style=\"font-weight: 400;\">\u201cWorking with NORD and our nearly 300 member organizations, you can learn how to connect with others, find a medical expert, get involved in research and gain the power that comes with knowledge,\u201d the narrator begins. <\/span><\/p>\n<p><span style=\"font-weight: 400;\">Advice provided in the video is based on NORD\u2019s more than 35 years of leadership in the rare disease community. Since 1983, millions of patients and caregivers \u2013 many of whom are coping with a new diagnosis \u2013 have turned to NORD for information and advice.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">Building upon that history as well as input from leading patient advocates and medical experts, NORD\u2019s Educational Initiatives staff compiled 10 tips to help those newly diagnosed with rare diseases take positive steps to become their own best advocates and participate as active partners in their care. <\/span><\/p>\n<p><span style=\"font-weight: 400;\">These tips include links to resources from NORD and others to support networking, learning about medical research, and joining the broader rare disease community in advocacy and education. <\/span><\/p>\n<p><span style=\"font-weight: 400;\">As always, one of the primary themes is NORD\u2019s key message: Alone we are rare. Together we are strong.\u00ae<\/span><\/p>\n<p><span style=\"font-weight: 400;\">This video is just one of many resources provided by NORD\u2019s Educational Initiatives Department, which include webinars, videos, fact sheets and databases created specifically for patients and caregivers. For an overview, visit NORD\u2019s <\/span><a href=\"https:\/\/rarediseases.org\/for-patients-and-families\/information-resources\/patient-and-caregiver-resource-center\/\"><span style=\"font-weight: 400;\">Patient and Caregiver Resource Center<\/span><\/a><span style=\"font-weight: 400;\"> to find resources such as:<\/span><\/p>\n<ul>\n<li style=\"font-weight: 400;\"><a href=\"https:\/\/www.youtube.com\/watch?v=5ChXI6cSQs0&amp;index=2&amp;list=PLMmYBWQscoiG1OLjxb0hHtXJ4kTuPbLId&amp;t=\" rel=\"nofollow noopener\" target=\"_blank\"><span style=\"font-weight: 400;\">Gene Therapy: Your Questions Answered<\/span><\/a><span style=\"font-weight: 400;\"> video <\/span><\/li>\n<li style=\"font-weight: 400;\"><a href=\"https:\/\/www.youtube.com\/watch?v=cZEmt4eyaHQ&amp;index=7&amp;list=PLMmYBWQscoiH3t2SzSP1gYjP2q8sZxCo9\" rel=\"nofollow noopener\" target=\"_blank\"><span style=\"font-weight: 400;\">How to Make Your Health Insurance Work For You<\/span><\/a><span style=\"font-weight: 400;\"> webinar<\/span><\/li>\n<li style=\"font-weight: 400;\"><a href=\"https:\/\/www.youtube.com\/watch?v=eEdV2vwz160&amp;index=6&amp;list=PLMmYBWQscoiH3t2SzSP1gYjP2q8sZxCo9&amp;t=0s\" rel=\"nofollow noopener\" target=\"_blank\"><span style=\"font-weight: 400;\">Genetic Testing 101 for People with Rare Diseases<\/span><\/a><span style=\"font-weight: 400;\"> webinar<\/span><\/li>\n<li style=\"font-weight: 400;\"><span style=\"font-weight: 400;\">NORD\u2019s <\/span><a href=\"https:\/\/rarediseases.org\/for-patients-and-families\/information-resources\/rare-disease-information\/\"><span style=\"font-weight: 400;\">Rare Disease Database<\/span><\/a><\/li>\n<li style=\"font-weight: 400;\"><a href=\"https:\/\/rarediseases.org\/wp-content\/uploads\/2018\/05\/NRD-1123-5_OD_Myths_Infographic_FNL2.pdf\"><span style=\"font-weight: 400;\">5 Myths About Orphan Drugs and the Orphan Drug Act<\/span><\/a><\/li>\n<\/ul>\n","protected":false},"excerpt":{"rendered":"<p>A rare diagnosis can be a frightening and isolating experience, whether you are the patient or a caregiver for a loved one. However, NORD has created a video providing tips &hellip; <\/p>\n<p class=\"link-more\"><a href=\"https:\/\/rarediseases.org\/es\/nord-video-provides-advice-for-the-newly-diagnosed\/\" class=\"more-link\">Continue reading<span class=\"screen-reader-text\"> &#8220;NORD Video Provides Advice for the Newly Diagnosed&#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":[190,192],"tags":[1906,1907,315,228],"class_list":["post-59000","post","type-post","status-publish","format-standard","hentry","category-featured-news","category-patients-members","tag-newly-diagnosed","tag-patient-and-caregiver-resource-center","tag-rare-disease","tag-rare-diseases"],"acf":[],"_links":{"self":[{"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/posts\/59000","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=59000"}],"version-history":[{"count":0,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/posts\/59000\/revisions"}],"wp:attachment":[{"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/media?parent=59000"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/categories?post=59000"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/tags?post=59000"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}