{"id":58600,"date":"2015-08-03T17:47:32","date_gmt":"2015-08-03T21:47:32","guid":{"rendered":"https:\/\/rarediseases.org\/taking-rare-action-on-the-road\/"},"modified":"2015-08-03T17:47:32","modified_gmt":"2015-08-03T21:47:32","slug":"taking-rare-action-on-the-road","status":"publish","type":"post","link":"https:\/\/rarediseases.org\/es\/taking-rare-action-on-the-road\/","title":{"rendered":"Taking Rare Action\u2122 on the Road"},"content":{"rendered":"<p style=\"text-align: left;\">Over the next few weeks, I will be driving across the country to meet with NORD members and Rare Action Network\u2122 advocates in their community. All told, I will be traversing over 4,000 miles, and spending time in 10 different states (my full itinerary can be found below).<\/p>\n<p>In preparing for the trip, my colleagues and friends have all asked the same question: \u201cTim, why would you do this?\u201d It\u2019s a fair question, and truth be told there\u2019s nothing I\u2019d rather do than spend my summer driving through central Texas in 100 deg. heat (no offense, Texas).<\/p>\n<p>Bad jokes aside, the real answer is pretty straightforward. As a national organization representing patients and disease-specific groups, it is important for NORD to be more active in the areas where the rare community is doing great work every day.<\/p>\n<p>This idea is one of the founding principals behind the creation of NORD\u2019s Rare Action Network\u2122. With the ongoing implementation of the Affordable Care Act, now more than ever there are a host of health policy issues that can only be addressed at the state and local level. NORD wants to ensure that the needs of the rare disease community are being adequately addressed in these discussions. However, this cannot be achieved remotely from Washington, D.C.; it requires the expertise and passion of local advocates and local organizations.<\/p>\n<p>At the front lines of this grassroots effort will be NORD\u2019s State Ambassadors. These are local advocates (many of whom run their own organization) who will be the point people for NORD\u2019s grassroots activity in their state. Ambassadors will act as local NORD representatives, there to assist members and advocates in coordinating advocacy activities around key policy issues.<\/p>\n<p>Throughout this trip, I will be sharing the stories of our new Ambassadors and how local advocates can begin working with them. Feel free to reach out to them and share the experiences and goals of your community.<\/p>\n<p>The individuals I will be introducing you to on this blog are the tip of the iceberg. NORD has been thrilled by the outpouring of interest from individuals who are either signing up for the Rare Action Network\u2122 or expressing interest in becoming a State Ambassador themselves. Rest assured, there will be ample opportunities for you to get involved. This road trip is only the first step.<\/p>\n<p>Please continue to check back to this blog for updates on my trip and to meet the new Ambassadors. Also, if you see I\u2019ll be coming to your area, feel free to drop me a line and I\u2019d be happy to meet up.<\/p>\n<p><strong>Here\u2019s my itinerary for the next few weeks:<\/strong><\/p>\n<p>July 21-22: Atlanta, GA<\/p>\n<p>July 23: Tallahassee, FL<\/p>\n<p>July 24-25: Mobile, AL<\/p>\n<p>July 25-26, Houston, TX<\/p>\n<p>July 27-29: Oklahoma City, OK<\/p>\n<p>July 30-31: Denver, CO<\/p>\n<p>August 1-2: Salt Lake City, UT<\/p>\n<p>August 3-6: Seattle, WA<\/p>\n<p>August 7-9: Sacramento-San Francisco, CA<\/p>\n<p>August 9-12: Los Angeles\/Southern California<\/p>\n<p>&nbsp;<\/p>\n<p style=\"text-align: center;\"><strong>Join the road trip on twitter with #RareAction<\/strong><\/p>\n<p style=\"text-align: center;\"><em><strong>Want to learn more about the Rare Action Network\u2122 and how you can join? \u00a0Visit us on our\u00a0website\u00a0<a href=\"https:\/\/rarediseases.org\/advocate\/take-action-locally\/join-rare-action-network\/\" target=\"_blank\" rel=\"noopener\">here<\/a>.<\/strong><\/em><\/p>\n<p>&nbsp;<\/p>\n<p><em>About Tim Boyd<\/em><\/p>\n<p><em>Tim is NORD\u2019s Associate Director of State Policy. He lives and works in Washington, D.C. Feel free to reach out to Tim at <a href=\"mailto:tboyd@rarediseases.org\">tboyd@rarediseases.org<\/a><\/em><em> or at (202) 545-3830.<\/em><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Follow the cross-country road tour that introduces the NORD State Ambassadors and promotes the Rare Action Network\u2122.<\/p>\n","protected":false},"author":1,"featured_media":11900,"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],"tags":[659,526,658],"class_list":["post-58600","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-advocacy","category-featured-news","tag-rare-action","tag-rare-action-network","tag-rare-action-road-tour"],"acf":[],"_links":{"self":[{"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/posts\/58600","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=58600"}],"version-history":[{"count":0,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/posts\/58600\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/media\/11900"}],"wp:attachment":[{"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/media?parent=58600"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/categories?post=58600"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/tags?post=58600"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}