{"id":59237,"date":"2021-01-28T17:13:05","date_gmt":"2021-01-28T22:13:05","guid":{"rendered":"https:\/\/rarediseases.org\/how-will-you-show-your-stripes-in-30-days-join-nord-in-spreading-awareness-for-rare-disease-day-february-28\/"},"modified":"2021-01-28T17:13:05","modified_gmt":"2021-01-28T22:13:05","slug":"how-will-you-show-your-stripes-in-30-days-join-nord-in-spreading-awareness-for-rare-disease-day-february-28","status":"publish","type":"post","link":"https:\/\/rarediseases.org\/es\/how-will-you-show-your-stripes-in-30-days-join-nord-in-spreading-awareness-for-rare-disease-day-february-28\/","title":{"rendered":"How Will You Show Your Stripes in 30 Days? Join NORD in Spreading Awareness for Rare Disease Day\u00ae, February 28"},"content":{"rendered":"<p><b><span data-contrast=\"auto\">Washington, DC, January\u00a0<\/span><\/b><b><span data-contrast=\"auto\">28<\/span><\/b><b><span data-contrast=\"auto\">, 202<\/span><\/b><b><span data-contrast=\"auto\">1<\/span><\/b><span data-contrast=\"auto\">\u2014<\/span><span data-contrast=\"none\">\u00a0<\/span><span data-contrast=\"none\">Even with the world acutely aware of public health matters in light of the COVID-19 pandemic, there are millions in the United States and around the globe living with<\/span><span data-contrast=\"auto\">\u00a0<\/span><span data-contrast=\"auto\">ra<\/span><span data-contrast=\"auto\">re\u00a0<\/span><span data-contrast=\"auto\">diseases<\/span><span data-contrast=\"auto\">\u00a0and\u00a0<\/span><span data-contrast=\"auto\">accompanying<\/span><span data-contrast=\"auto\">\u00a0life-altering issues<\/span><span data-contrast=\"auto\">\u00a0<\/span><span data-contrast=\"auto\">that are\u00a0<\/span><span data-contrast=\"auto\">largely unknown to the\u00a0<\/span><span data-contrast=\"auto\">general\u00a0<\/span><span data-contrast=\"auto\">public<\/span><span data-contrast=\"auto\">.<\/span><span data-contrast=\"auto\">\u00a0<\/span><span data-contrast=\"auto\">R<\/span><span data-contrast=\"auto\">are Disease Day<\/span><span data-contrast=\"auto\">\u00a02021<\/span><span data-contrast=\"auto\">\u00a0is coming up in thirty days<\/span><span data-contrast=\"auto\">,\u00a0<\/span><span data-contrast=\"auto\">and\u00a0<\/span><span data-contrast=\"auto\">t<\/span><span data-contrast=\"auto\">he National Organization for Rare Disorders (N<\/span><span data-contrast=\"auto\">ORD<\/span><span data-contrast=\"auto\">\u00ae<\/span><span data-contrast=\"auto\">)<\/span><span data-contrast=\"auto\">\u00a0<\/span><span data-contrast=\"auto\">is inviting\u00a0<\/span><span data-contrast=\"auto\">all to join<\/span><span data-contrast=\"auto\">\u00a0<\/span><span data-contrast=\"auto\">in\u00a0<\/span><span data-contrast=\"auto\">shining a light on the\u00a0<\/span><span data-contrast=\"auto\">challenges<\/span><span data-contrast=\"auto\">\u00a0faced by<\/span><span data-contrast=\"auto\">\u00a0<\/span><span data-contrast=\"auto\">rare\u00a0<\/span><span data-contrast=\"auto\">patients and familie<\/span><span data-contrast=\"auto\">s<\/span><span data-contrast=\"auto\">, as well as those\u00a0<\/span><span data-contrast=\"auto\">still\u00a0<\/span><span data-contrast=\"auto\">without a diagnosis<\/span><span data-contrast=\"auto\">, and the need for research into treatments and cures<\/span><span data-contrast=\"auto\">.<\/span><span data-ccp-props=\"{&quot;201341983&quot;:0,&quot;335551550&quot;:1,&quot;335551620&quot;:1,&quot;335559739&quot;:160,&quot;335559740&quot;:240}\">\u00a0<\/span><\/p>\n<p><span data-contrast=\"auto\">Launched by EURORDIS-Rare Diseases Europe in 2008, Rare Disease Day is the\u00a0<\/span><span data-contrast=\"auto\">patient-led\u00a0<\/span><span data-contrast=\"auto\">international\u00a0<\/span><span data-contrast=\"auto\">awareness campaign that brings\u00a0<\/span><span data-contrast=\"auto\">people\u00a0<\/span><span data-contrast=\"auto\">together\u00a0<\/span><span data-contrast=\"auto\">in solidarity with the 300 million p<\/span><span data-contrast=\"auto\">atients<\/span><span data-contrast=\"auto\">\u00a0<\/span><span data-contrast=\"auto\">impacted by<\/span><span data-contrast=\"auto\">\u00a0rare disease<\/span><span data-contrast=\"auto\">s<\/span><span data-contrast=\"auto\">\u00a0worldwide.<\/span><span data-contrast=\"auto\">\u00a0In 2009,\u00a0<\/span><span data-contrast=\"auto\">Rare Disease Day became a\u00a0<\/span><span data-contrast=\"auto\">global event when\u00a0<\/span><span data-contrast=\"auto\">NORD\u00a0<\/span><span data-contrast=\"auto\">became<\/span><span data-contrast=\"auto\">\u00a0the official sponsor<\/span><span data-contrast=\"auto\">\u00a0<\/span><span data-contrast=\"auto\">of\u00a0<\/span><span data-contrast=\"auto\">the celebrat<\/span><span data-contrast=\"auto\">ion in the United States.<\/span><span data-ccp-props=\"{&quot;201341983&quot;:0,&quot;335551550&quot;:1,&quot;335551620&quot;:1,&quot;335559739&quot;:160,&quot;335559740&quot;:240}\">\u00a0<\/span><\/p>\n<p><span data-contrast=\"auto\">This year<\/span><span data-contrast=\"auto\">, NORD is asking individuals, organizations and<\/span><span data-contrast=\"auto\">\u00a0companie<\/span><span data-contrast=\"auto\">s in the US to<\/span><span data-contrast=\"auto\">\u00a0help\u00a0<\/span><span data-contrast=\"auto\">highlight<\/span><span data-contrast=\"auto\">\u00a0<\/span><span data-contrast=\"auto\">rare disease issues<\/span><span data-contrast=\"auto\">\u00a0and the need for\u00a0<\/span><span data-contrast=\"auto\">continued\u00a0<\/span><span data-contrast=\"auto\">progress in research and drug development<\/span><span data-contrast=\"auto\">.<\/span><span data-contrast=\"auto\">\u00a0<\/span><span data-contrast=\"auto\">Taking action\u00a0<\/span><span data-contrast=\"auto\">and \u201cshowing your stripes\u201d\u00a0<\/span><span data-contrast=\"auto\">to spread awareness<\/span><span data-contrast=\"auto\">\u00a0<\/span><span data-contrast=\"auto\">can\u00a0<\/span><span data-contrast=\"auto\">be done<\/span><span data-contrast=\"auto\">\u00a0in a variety of\u00a0<\/span><span data-contrast=\"auto\">ways<\/span><span data-contrast=\"auto\">, including<\/span><span data-contrast=\"auto\">\u00a0by<\/span><span data-contrast=\"auto\">:<\/span><span data-contrast=\"auto\">\u00a0<\/span><span data-ccp-props=\"{&quot;201341983&quot;:0,&quot;335551550&quot;:1,&quot;335551620&quot;:1,&quot;335559739&quot;:160,&quot;335559740&quot;:240}\">\u00a0<\/span><\/p>\n<ul>\n<li><span data-ccp-props=\"{&quot;201341983&quot;:0,&quot;335551550&quot;:1,&quot;335551620&quot;:1,&quot;335559739&quot;:160,&quot;335559740&quot;:240}\">\u00a0<\/span><b><span data-contrast=\"auto\">Joining\u00a0<\/span><\/b><span data-contrast=\"auto\">the Show Your Stripes movement\u00a0<\/span><span data-contrast=\"auto\">and<\/span><span data-contrast=\"auto\">\u00a0wearing stripes on Rare Disease Day, taking a photograph and posting it with a message of support on social media, using the hashtags #ShowYourStripes and #RareDiseaseDay. Discover more ways to Show Your Stripes\u00a0<\/span><a href=\"https:\/\/rarediseases.org\/rare-disease-day\/get-involved\/\"><span data-contrast=\"auto\">here<\/span><\/a><span data-contrast=\"auto\">\u00a0(<\/span><a href=\"https:\/\/bit.ly\/RDD21-Get-Involved\" rel=\"nofollow noopener\" target=\"_blank\"><span data-contrast=\"none\">https:\/\/bit.ly\/RDD21-Get-Involved<\/span><\/a><span data-contrast=\"auto\">)<\/span><span data-contrast=\"auto\">.<\/span><span data-ccp-props=\"{&quot;134233279&quot;:true,&quot;201341983&quot;:0,&quot;335551550&quot;:1,&quot;335551620&quot;:1,&quot;335559739&quot;:160,&quot;335559740&quot;:240}\">\u00a0<\/span><\/li>\n<li><span data-ccp-props=\"{&quot;201341983&quot;:0,&quot;335551550&quot;:1,&quot;335551620&quot;:1,&quot;335559739&quot;:160,&quot;335559740&quot;:240}\">\u00a0<\/span><b><span data-contrast=\"auto\">Advocating<\/span><\/b><span data-contrast=\"auto\">\u00a0for more than 25 million Americans impacted by rare diseases through\u00a0 participating in a NORD Rare Action Network\u2122 (RAN) virtual Rare Disease Day event, in which key state policies affecting rare patients and families will be discussed. Register to take part in a RAN virtual Rare Disease Day event<\/span><span data-contrast=\"auto\">\u00a0<\/span><a href=\"https:\/\/rarediseases.org\/rare-disease-day\/events\/\"><span data-contrast=\"auto\">here<\/span><\/a><span data-contrast=\"auto\">\u00a0(<\/span><a href=\"https:\/\/bit.ly\/RDD21-Events\" rel=\"nofollow noopener\" target=\"_blank\"><span data-contrast=\"none\">https:\/\/bit.ly\/RDD21-Events<\/span><\/a><span data-contrast=\"auto\">)<\/span><span data-contrast=\"auto\">.<\/span><span data-ccp-props=\"{&quot;134233279&quot;:true,&quot;201341983&quot;:0,&quot;335551550&quot;:1,&quot;335551620&quot;:1,&quot;335559739&quot;:160,&quot;335559740&quot;:240}\">\u00a0<\/span><\/li>\n<li><b><span data-contrast=\"auto\">Pledg<\/span><\/b><b><span data-contrast=\"auto\">ing<\/span><\/b><span data-contrast=\"auto\">\u00a0to\u00a0<\/span><span data-contrast=\"auto\">help<\/span><span data-contrast=\"none\">\u00a0our\u00a0<\/span><span data-contrast=\"none\">rare\u00a0<\/span><span data-contrast=\"none\">community light up as many buildings and landmarks as possible in Rare Disease Day colors<\/span><span data-contrast=\"none\">\u00a0(blue, green, pink and purple)<\/span><span data-contrast=\"none\">\u00a0on or around February 28.<\/span><span data-contrast=\"none\">\u00a0<\/span><span data-contrast=\"auto\">This concept originated in 2019 when the Empire State Building in New York City was striped in Rare Disease Day colors thanks to the work of\u00a0<\/span><span data-contrast=\"auto\">RocketPharma<\/span><span data-contrast=\"auto\">, a member of NORD\u2019s Corporate Council. F<\/span><span data-contrast=\"auto\">ind out more about<\/span><span data-contrast=\"auto\">\u00a0NORD\u2019s<\/span><span data-contrast=\"auto\">\u00a0<\/span><a href=\"https:\/\/rarediseases.org\/wp-content\/uploads\/2021\/01\/NRD-2096-RDD-Monuments-Toolkit_FNL-2-light-up-for-rare.pdf\"><span data-contrast=\"none\">Light up for Rare<\/span><\/a><span data-contrast=\"auto\">\u00a0<\/span><span data-contrast=\"auto\">(<\/span><a href=\"https:\/\/bit.ly\/Light-Up-For-Rare\" rel=\"nofollow noopener\" target=\"_blank\"><span data-contrast=\"none\">https:\/\/bit.ly\/Light-Up-For-Rare<\/span><\/a><span data-contrast=\"auto\">)\u00a0<\/span><span data-contrast=\"auto\">campaign<\/span><span data-contrast=\"auto\">\u00a0and how you can<\/span><span data-contrast=\"auto\">\u00a0<\/span><span data-contrast=\"auto\">participate<\/span><span data-contrast=\"auto\">.<\/span><span data-ccp-props=\"{&quot;134233279&quot;:true,&quot;201341983&quot;:0,&quot;335551550&quot;:1,&quot;335551620&quot;:1,&quot;335559739&quot;:160,&quot;335559740&quot;:240}\">\u00a0<\/span><\/li>\n<li><span data-ccp-props=\"{&quot;201341983&quot;:0,&quot;335551550&quot;:1,&quot;335551620&quot;:1,&quot;335559739&quot;:160,&quot;335559740&quot;:240}\">\u00a0<\/span><b><span data-contrast=\"auto\">Watching<\/span><\/b><span data-contrast=\"auto\">\u00a0<\/span><span data-contrast=\"none\">Behind the Mystery: Rare and Genetic, the recurring rare disease series on the award-winning morning show The Balancing Act, airing on Lifetime Television. Premiering February 24 at 7:30am ET<\/span><span data-contrast=\"none\">\u00a0<\/span><span data-contrast=\"auto\">then streaming online at\u00a0<\/span><a href=\"https:\/\/www.TheBalancingAct.com\/Rare\" rel=\"nofollow noopener\" target=\"_blank\"><span data-contrast=\"auto\">TheBalancingAct.com\/Rare<\/span><\/a><span data-contrast=\"none\">,\u00a0<\/span><span data-contrast=\"none\">the\u00a0<\/span><span data-contrast=\"none\">Rare Disease Day\u00a0<\/span><span data-contrast=\"none\">Sp<\/span><span data-contrast=\"none\">ecial will feature\u00a0<\/span><span data-contrast=\"none\">NORD\u2019s\u00a0<\/span><span data-contrast=\"none\">Lisa Sarfaty<\/span><span data-contrast=\"none\">\u00a0<\/span><span data-contrast=\"none\">presenting facts on rare disease and how to get involved with the awareness day, and\u00a0<\/span><span data-contrast=\"none\">three<\/span><span data-contrast=\"none\">\u00a0patients sharing their\u00a0<\/span><span data-contrast=\"none\">inspiring\u00a0<\/span><span data-contrast=\"none\">stories<\/span><span data-contrast=\"none\">:\u00a0<\/span><span data-contrast=\"auto\">William<\/span><span data-contrast=\"auto\">\u00a0Yank, a\u00a0<\/span><span data-contrast=\"auto\">t<\/span><span data-contrast=\"auto\">hree-time leukemia survivor with his own podcast, clothing line<\/span><span data-contrast=\"auto\">\u00a0and<\/span><span data-contrast=\"auto\">\u00a0over 90,000 followers on\u00a0<\/span><span data-contrast=\"auto\">TikTok<\/span><span data-contrast=\"auto\">; Kelly Barendt, a blogger and YouTuber with over 300,000\u00a0<\/span><span data-contrast=\"auto\">TikTok<\/span><span data-contrast=\"auto\">\u00a0followers<\/span><span data-contrast=\"auto\">,<\/span><span data-contrast=\"auto\">\u00a0<\/span><span data-contrast=\"auto\">relating<\/span><span data-contrast=\"auto\">\u00a0her journey with Friedreich\u2019s ataxia<\/span><span data-contrast=\"auto\">; and Travis Flores, a cystic fibrosis survivor and recipient of a very rare third double-lung transplant, sharing<\/span><span data-contrast=\"auto\">\u00a0what he has learned from<\/span><span data-contrast=\"auto\">\u00a0living with his condition<\/span><span data-contrast=\"none\">.\u00a0<\/span><span data-ccp-props=\"{&quot;134233279&quot;:true,&quot;201341983&quot;:0,&quot;335551550&quot;:1,&quot;335551620&quot;:1,&quot;335559739&quot;:160,&quot;335559740&quot;:240}\">\u00a0<\/span><\/li>\n<\/ul>\n<p><span data-ccp-props=\"{&quot;201341983&quot;:0,&quot;335551550&quot;:1,&quot;335551620&quot;:1,&quot;335559739&quot;:160,&quot;335559740&quot;:240}\">\u00a0<\/span><span data-contrast=\"auto\">\u201c<\/span><span data-contrast=\"auto\">Rare Disease Day<\/span><span data-contrast=\"auto\">\u00a0<\/span><span data-contrast=\"auto\">is<\/span><span data-contrast=\"auto\">\u00a0a<\/span><span data-contrast=\"auto\">n<\/span><span data-contrast=\"auto\">\u00a0opportunity to\u00a0<\/span><span data-contrast=\"auto\">enlighten\u00a0<\/span><span data-contrast=\"auto\">t<\/span><span data-contrast=\"auto\">he public<\/span><span data-contrast=\"auto\">\u00a0<\/span><span data-contrast=\"auto\">about<\/span><span data-contrast=\"auto\">\u00a0<\/span><span data-contrast=\"auto\">issues<\/span><span data-contrast=\"auto\">\u00a0<\/span><span data-contrast=\"auto\">affecting rare disease patients\u00a0<\/span><span data-contrast=\"auto\">such as\u00a0<\/span><span data-contrast=\"auto\">overcoming health inequities<\/span><span data-contrast=\"auto\">\u00a0&#8211;<\/span><span data-contrast=\"auto\">\u00a0including\u00a0<\/span><span data-contrast=\"auto\">the<\/span><span data-contrast=\"auto\">\u00a0lack of understanding\u00a0<\/span><span data-contrast=\"auto\">around\u00a0<\/span><span data-contrast=\"auto\">rare conditions<\/span><span data-contrast=\"auto\">\u00a0and challenges patients\u00a0<\/span><span data-contrast=\"auto\">must\u00a0<\/span><span data-contrast=\"auto\">face to even get an accurate diagnosis<\/span><span data-contrast=\"auto\">,<\/span><span data-contrast=\"auto\">\u201d said Peter L. Saltonstall, President and CEO of NORD.\u00a0<\/span><span data-contrast=\"auto\">\u201c<\/span><span data-contrast=\"auto\">NORD\u2019s mission is<\/span><span data-contrast=\"auto\">\u00a0to<\/span><span data-contrast=\"auto\">\u00a0<\/span><span data-contrast=\"auto\">ensure that all rare\u00a0<\/span><span data-contrast=\"auto\">diseases\u00a0<\/span><span data-contrast=\"auto\">have a<\/span><span data-contrast=\"auto\">n accessible<\/span><span data-contrast=\"auto\">\u00a0treatment or cure<\/span><span data-contrast=\"auto\">. Only then will\u00a0<\/span><span data-contrast=\"auto\">our<\/span><span data-contrast=\"auto\">\u00a0community<\/span><span data-contrast=\"auto\">\u00a0have the equity\u00a0<\/span><span data-contrast=\"auto\">it<\/span><span data-contrast=\"auto\">\u00a0deserve<\/span><span data-contrast=\"auto\">s<\/span><span data-contrast=\"auto\">.<\/span><span data-contrast=\"auto\">\u201d<\/span><span data-contrast=\"auto\">\u00a0<\/span><span data-ccp-props=\"{&quot;201341983&quot;:0,&quot;335551550&quot;:1,&quot;335551620&quot;:1,&quot;335559739&quot;:160,&quot;335559740&quot;:240}\">\u00a0<\/span><\/p>\n<p><span data-contrast=\"none\">For more information on #ShowYourStripes<\/span><span data-contrast=\"none\">,<\/span><span data-contrast=\"none\">\u00a0to download materials including a social media toolkit, media outreach templates, infographics and printable stickers,\u00a0<\/span><span data-contrast=\"none\">and to stay abreast of Rare Disease Day\u00a0<\/span><span data-contrast=\"none\">virtual\u00a0<\/span><span data-contrast=\"none\">events in the United States,\u00a0<\/span><span data-contrast=\"none\">be sure to\u00a0<\/span><span data-contrast=\"none\">visit\u00a0<\/span><a href=\"https:\/\/rarediseases.org\/rare-disease-day\/\"><span data-contrast=\"none\">rarediseaseday.us<\/span><\/a><span data-contrast=\"none\">.\u00a0<\/span><br \/>\n<span data-ccp-props=\"{&quot;201341983&quot;:0,&quot;335559739&quot;:160,&quot;335559740&quot;:240}\">\u00a0<\/span><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Washington, DC, January\u00a028, 2021\u2014\u00a0Even with the world acutely aware of public health matters in light of the COVID-19 pandemic, there are millions in the United States and around the globe &hellip; <\/p>\n<p class=\"link-more\"><a href=\"https:\/\/rarediseases.org\/es\/how-will-you-show-your-stripes-in-30-days-join-nord-in-spreading-awareness-for-rare-disease-day-february-28\/\" class=\"more-link\">Continue reading<span class=\"screen-reader-text\"> &#8220;How Will You Show Your Stripes in 30 Days? Join NORD in Spreading Awareness for Rare Disease Day\u00ae, February 28&#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":[232,190,192,504,1827],"tags":[2629,2229,729,2408,2634,2632,2635,2628,2630,1278,225,243,525,526,219,2636,1833,2627,2633,2631],"class_list":["post-59237","post","type-post","status-publish","format-standard","hentry","category-advocacy","category-featured-news","category-patients-members","category-press-releases","category-rare-disease-day","tag-behind-the-mystery","tag-covid-19","tag-cystic-fibrosis","tag-eurordis-rare-diseases-europe","tag-friedreichs-ataxia","tag-kelly-barendt","tag-leukemia","tag-lifetime-television","tag-lisa-sarfaty","tag-national-organization-for-rare-disorders","tag-nord","tag-peter-l-saltonstall","tag-ran","tag-rare-action-network","tag-rare-disease-day","tag-rocketpharma","tag-show-your-stripes","tag-the-balancing-act","tag-travis-flores","tag-william-yank"],"acf":[],"_links":{"self":[{"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/posts\/59237","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=59237"}],"version-history":[{"count":0,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/posts\/59237\/revisions"}],"wp:attachment":[{"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/media?parent=59237"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/categories?post=59237"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/tags?post=59237"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}