{"id":58842,"date":"2017-03-15T15:23:42","date_gmt":"2017-03-15T19:23:42","guid":{"rendered":"https:\/\/rarediseases.org\/brandon-hudgins-2017-rare-impact-award-honoree\/"},"modified":"2017-03-15T15:23:42","modified_gmt":"2017-03-15T19:23:42","slug":"brandon-hudgins-2017-rare-impact-award-honoree","status":"publish","type":"post","link":"https:\/\/rarediseases.org\/es\/brandon-hudgins-2017-rare-impact-award-honoree\/","title":{"rendered":"Brandon Hudgins &#8211; 2017 Rare Impact Award Honoree"},"content":{"rendered":"<p><b>2017 Honoree<\/b><b><br \/>\n<\/b><b>Rare Impact Award<\/b><\/p>\n<p><a href=\"https:\/\/rarediseases.org\/wp-content\/uploads\/2017\/07\/Brandon-Hudgins.jpg\" data-rel=\"lightbox-image-0\" data-rl_title=\"\" data-rl_caption=\"\" title=\"\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-31473\" src=\"https:\/\/rarediseases.org\/wp-content\/uploads\/2017\/07\/Brandon-Hudgins-300x200.jpg\" alt=\"Brandon Hudgins\" width=\"300\" height=\"200\" \/><\/a><\/p>\n<p><b>Brandon Hudgins<\/b><\/p>\n<p><span style=\"font-weight: 400;\">For 20 years, Brandon Hudgins has chased his dreams of being an elite athlete and has put the demanding sport of competitive running at the center of his life. \u00a0Yet in September 2007, as a Division I college athlete attending Winthrop University, running became difficult when he began to experience health issues, breathing trouble, and a lack of energy. \u00a0He suddenly went from being one of the fastest runners on the team to the slowest, and remembers needing to drag himself between bed and class. He also experienced a 70 percent hearing loss in one ear and a 90 percent loss in the other.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">Several months later, in April 2008, Brandon was diagnosed with a type of vasculitis, a rare condition that involves inflammation of blood vessels, cutting off vital blood supply to tissues and organs. \u00a0As he received treatment, he continuously told himself that he would get back to running. \u00a0Finally, after being cleared by his doctor that December, Brandon picked himself up and resumed training. <\/span><\/p>\n<p><span style=\"font-weight: 400;\">After this health scare, Brandon saw considerable success in his running. \u00a0He became one of only 449 Americans to race a mile in under four minutes and earned a spot in the 2016 Olympic Trials. \u00a0It was at this point, upon reaching the pinnacle of his sport, that he seized the spotlight as an opportunity to stand up and give others with vasculitis a voice.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">\u201cI didn\u2019t talk about it for the longest time,\u201d Brandon remembers. \u00a0\u201cVasculitis is so personal. \u00a0It gets ugly at times.\u201d<\/span><\/p>\n<p><span style=\"font-weight: 400;\">Brandon now leads a campaign called \u201cVictory over Vasculitis\u201d to inspire others to feel larger than their disease diagnosis and to create more awareness. The campaign has been successful in filling a void that the community needed, Brandon says, and \u201cthe response is overwhelming sometimes. I get a lot of messages from other patients\u2026people pouring their hearts out. \u00a0That means a lot, which is why I can\u2019t stop now.\u201d<\/span><\/p>\n<p><span style=\"font-weight: 400;\">While Brandon is not sure of what will come next because he does not know what his health will bring, he knows that he will not stop raising awareness and trying to reach more and more people. He add, \u201cThis isn\u2019t just me; this is all of us. I challenge all of us, all of the time, to inspire each other, and challenge each other to live the life that we want to live.\u201d<\/span><\/p>\n<p><span style=\"font-weight: 400;\">NORD is honored to present Brandon Hudgins with a 2017 Rare Impact Award.<\/span><\/p>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>2017 Honoree Rare Impact Award Brandon Hudgins For 20 years, Brandon Hudgins has chased his dreams of being an elite athlete and has put the demanding sport of competitive running &hellip; <\/p>\n<p class=\"link-more\"><a href=\"https:\/\/rarediseases.org\/es\/brandon-hudgins-2017-rare-impact-award-honoree\/\" class=\"more-link\">Continue reading<span class=\"screen-reader-text\"> &#8220;Brandon Hudgins &#8211; 2017 Rare Impact Award Honoree&#8221;<\/span><\/a><\/p>\n","protected":false},"author":1,"featured_media":12404,"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":[232,505],"tags":[1305,1303,1302,930,1306],"class_list":["post-58842","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-advocacy","category-patient-stories","tag-brandon-hudgins","tag-rare-impact-2017","tag-rare-impact-award-honoree","tag-rare-impact-awards","tag-vasculitis"],"acf":[],"_links":{"self":[{"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/posts\/58842","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=58842"}],"version-history":[{"count":0,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/posts\/58842\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/media\/12404"}],"wp:attachment":[{"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/media?parent=58842"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/categories?post=58842"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/tags?post=58842"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}