{"id":58728,"date":"2016-05-31T17:18:11","date_gmt":"2016-05-31T21:18:11","guid":{"rendered":"https:\/\/rarediseases.org\/rareaction-network%e2%84%a0-releases-may-june-state-policy-legislative-tracker\/"},"modified":"2016-05-31T17:18:11","modified_gmt":"2016-05-31T21:18:11","slug":"rareaction-network%e2%84%a0-releases-may-june-state-policy-legislative-tracker","status":"publish","type":"post","link":"https:\/\/rarediseases.org\/es\/rareaction-network%e2%84%a0-releases-may-june-state-policy-legislative-tracker\/","title":{"rendered":"RareAction Network\u2120 Releases May\/June State Policy Legislative Tracker"},"content":{"rendered":"<div style=\"text-align: center;\"><em><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-26375  aligncenter\" src=\"https:\/\/rarediseases.org\/wp-content\/uploads\/2016\/05\/RAN_USA_States_MayJune2016.jpg\" alt=\"RAN_USA_States_MayJune2016\" width=\"600\" height=\"493\" \/>RareAction continues to make strides around the country for the 1 in 10 Americans with rare diseases.<\/em><\/div>\n<div style=\"text-align: center;\"><\/div>\n<div style=\"text-align: center;\">In this version of the <a href=\"https:\/\/rarediseases.org\/wp-content\/uploads\/2016\/05\/NORD-May_June-Leg-Tracker.pdf\" data-link-type=\"web\">State Policy Legislative Tracker<\/a>, there is an increase in the bills being supported in both Massachusetts and Tennessee. <a href=\"https:\/\/rarediseases.org\/wp-content\/uploads\/2016\/05\/NORD-May_June-Leg-Tracker.pdf\" data-link-type=\"web\">Learn more<\/a> about the bills that RareAction\u00a0is tracking and supporting to improve the lives of people and families in the rare disease community.<\/div>\n<div style=\"text-align: center;\"><\/div>\n<div style=\"text-align: center;\">\n<div>GET\u00a0<em>YOUR STATE<\/em> ON THE LIST!<\/div>\n<div><\/div>\n<div>Contact NORD to get the issues that you are facing added to this list. The<a href=\"https:\/\/rarediseases.org\/advocate\/take-action-locally\/join-rare-action-network\/\" target=\"_blank\" rel=\"noopener\"> RareAction Network\u2120<\/a> increases the awareness of those issues to key decision-makers and\u00a0elected\u00a0officials in the\u00a0states or regions that can take action to make essential changes.<\/div>\n<\/div>\n<div style=\"text-align: center;\"><\/div>\n<div style=\"text-align: center;\"><i>If you&#8217;re interested in taking action in your state, contact Tim Boyd at t<\/i>im.boyd@rareaction.org<\/div>\n<div style=\"text-align: center;\"><em>Join the conversation online by using #RareAction<\/em><\/div>\n","protected":false},"excerpt":{"rendered":"<p>RareAction continues to make strides around the country for the 1 in 10 Americans with rare diseases. In this version of the State Policy Legislative Tracker, there is an increase &hellip; <\/p>\n<p class=\"link-more\"><a href=\"https:\/\/rarediseases.org\/es\/rareaction-network%e2%84%a0-releases-may-june-state-policy-legislative-tracker\/\" class=\"more-link\">Continue reading<span class=\"screen-reader-text\"> &#8220;RareAction Network\u2120 Releases May\/June State Policy Legislative Tracker&#8221;<\/span><\/a><\/p>\n","protected":false},"author":1,"featured_media":12208,"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":[232,662,192],"tags":[967,663,1145,1144,1146],"class_list":["post-58728","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-advocacy","category-get-involved","category-patients-members","tag-advocate","tag-rare-disease-advocacy","tag-rareaction","tag-rareaction-network","tag-state-policy-legislative-tracker"],"acf":[],"_links":{"self":[{"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/posts\/58728","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=58728"}],"version-history":[{"count":0,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/posts\/58728\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/media\/12208"}],"wp:attachment":[{"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/media?parent=58728"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/categories?post=58728"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/tags?post=58728"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}