{"id":160401,"date":"2014-11-20T02:46:47","date_gmt":"2014-11-20T07:46:47","guid":{"rendered":"http:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/uncategorized\/rare-pairs-a-charity-dinner-for-orphan-disorders.php"},"modified":"2014-11-20T02:46:47","modified_gmt":"2014-11-20T07:46:47","slug":"rare-pairs-a-charity-dinner-for-orphan-disorders","status":"publish","type":"post","link":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/human-genetics\/rare-pairs-a-charity-dinner-for-orphan-disorders.php","title":{"rendered":"Rare Pairs: A charity dinner for orphan disorders"},"content":{"rendered":"<p><p>  'With the lack of support from the government, it is our  responsibility as private citizens to contribute and support this  ignored sector of our society'<\/p>\n<p>    MANILA, Philippines  In the Philippines, persons born with and    afflicted with rare disorders are a vulnerable and largely    unsupported population.  <\/p>\n<p>    A disease is considered rare if it affects 1 in 20,000    individuals or less, as defined by the Institute of Human    Genetics of the National Institute of Health. Pompe disease, Maple Syrup Urine disease,    Menkes syndrome, Lowe Syndrome are only a few of the registered    6,000-8,000 rare diseases globally. Because of the relatively    low number afflicted by these disorders, support from the Philippine government is    absent and access to basic health benefits such as    insurance coverage is unavailable to patients with rare    diseases.  <\/p>\n<\/p>\n<p>    Rare diseases in the Philippines  <\/p>\n<p>    Statistics show that 1 in 20,000 Filipinos are afflicted    with one of the 30 Rare diseases registered in the country, 75%    of which affect children.  <\/p>\n<p>    Without help from the government and private sector,    treatment and medication is elusive for these patients due to    their prohibitive cost and accessibility, most of which can    only be sourced from the United States.  <\/p>\n<p>    Formed with the help of the Institute of Human Genetics (IHG),    the Philippine Society for Orphan Disorders,    Inc. (PSOD), is a non-profit organization dedicated to be    the central network for the advocacy and effective    administration of sustainable support for the treatment and    medication for rare disease sufferers.  <\/p>\n<p>    Pairing up with Rare  <\/p>\n<p>    In support of PSOD's advocacy and efforts, Il Ponticello    Cucina Italiana will be holding RARE PAIRS, a Charity Dinner    and Wine Pairing fundraising event on November 22, 2014 to help    fund and contribute to the growing needs of the increasing    number Filipino patients afflicted with rare disorders.  <\/p>\n<p><!-- Auto Generated --><\/p>\n<p>Follow this link: <\/p>\n<p><a target=\"_blank\" href=\"http:\/\/www.rappler.com\/bulletin-board\/75468-rare-charity-dinner-philippines\/RK=0\/RS=SBYA41ab.sk__2CjBn0mQS3YKNM-\" title=\"Rare Pairs: A charity dinner for orphan disorders\">Rare Pairs: A charity dinner for orphan disorders<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p> 'With the lack of support from the government, it is our responsibility as private citizens to contribute and support this ignored sector of our society' MANILA, Philippines In the Philippines, persons born with and afflicted with rare disorders are a vulnerable and largely unsupported population.  <a href=\"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/human-genetics\/rare-pairs-a-charity-dinner-for-orphan-disorders.php\">Continue reading <span class=\"meta-nav\">&rarr;<\/span><\/a><\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"limit_modified_date":"","last_modified_date":"","_lmt_disableupdate":"","_lmt_disable":"","footnotes":""},"categories":[4],"tags":[],"class_list":["post-160401","post","type-post","status-publish","format-standard","hentry","category-human-genetics"],"modified_by":null,"_links":{"self":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts\/160401"}],"collection":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/comments?post=160401"}],"version-history":[{"count":0,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts\/160401\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/media?parent=160401"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/categories?post=160401"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/tags?post=160401"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}