{"id":58884,"date":"2017-12-18T18:30:00","date_gmt":"2017-12-18T23:30:00","guid":{"rendered":"https:\/\/rarediseases.org\/nord-issues-statement-in-response-to-congressional-consideration-of-the-tax-cuts-and-jobs-act-conference-report\/"},"modified":"2017-12-18T18:30:00","modified_gmt":"2017-12-18T23:30:00","slug":"nord-issues-statement-in-response-to-congressional-consideration-of-the-tax-cuts-and-jobs-act-conference-report","status":"publish","type":"post","link":"https:\/\/rarediseases.org\/es\/nord-issues-statement-in-response-to-congressional-consideration-of-the-tax-cuts-and-jobs-act-conference-report\/","title":{"rendered":"NORD Issues Statement in Response to Congressional Consideration of the Tax Cuts and Jobs Act Conference Report"},"content":{"rendered":"<p><b>Washington, D.C., December 18, 2017<\/b><span style=\"font-weight: 400;\">\u2014The National Organization for Rare Disorders (NORD), the leading independent nonprofit organization representing the 30 million Americans with rare diseases, issued the following statement in response to the upcoming congressional consideration of the <\/span><i><span style=\"font-weight: 400;\">Tax Cuts and Jobs Act<\/span><\/i><span style=\"font-weight: 400;\"> Conference Report:<\/span><\/p>\n<p><span style=\"font-weight: 400;\">\u201cThis week, Congress will consider and potentially pass the <\/span><i><span style=\"font-weight: 400;\">Tax Cuts and Jobs Act<\/span><\/i><span style=\"font-weight: 400;\"> Conference Report. NORD does not support this legislation as it substantially diminishes the Orphan Drug Tax Credit and repeals the Affordable Care Act\u2019s (ACA) individual mandate.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">The Conference Report cuts the Orphan Drug Tax Credit in half by reducing the tax credit\u2019s value from 50 percent of qualified clinical testing expenses to 25 percent of qualified clinical testing expenses. This provision represents one of the most substantial rollbacks in incentives to develop orphan therapies.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">The Orphan Drug Tax Credit (ODTC) lowers the cost of developing and testing orphan therapies as they move through the clinical trial process. Without the ODTC, we estimate that one-third fewer orphan therapies would be developed going forward. The cost of conducting rare disease clinical trials could rise substantially enough to discourage some biopharmaceutical companies from developing orphan therapies altogether.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">We oppose this cut and have called on Congress to maintain the ODTC at every opportunity as tax reform has evolved. However, without the thousands of patients, family members, caregivers, patient advocacy groups, and advocates who voiced their concern, the ODTC may have been repealed entirely, as was proposed by the House of Representatives. We are extremely appreciative of the advocates who made their voices heard. <\/span><\/p>\n<p><span style=\"font-weight: 400;\">We are also appreciative of Senators Hatch and Roberts, Congresswoman McMorris Rodgers, and all Senators and Representatives who strongly supported the ODTC and contributed to ensuring its survival.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">While we are disappointed by this outcome, we are grateful for the efforts to preserve the ODTC from both inside and outside the rare disease community.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">In addition to cutting the ODTC, the Conference Report also repeals the ACA\u2019s individual mandate without replacing it with a comparable alternative. We oppose this provision as the individual mandate incentivizes healthy individuals to purchase health insurance, resulting in lower premiums for individuals with rare diseases. Without the individual mandate or a comparable alternative, we anticipate premiums to rise substantially for our patients and their families with incomes above 400% of the Federal Poverty Line, potentially pricing them out of the market. <\/span><\/p>\n<p><span style=\"font-weight: 400;\">We are supportive of the Conference Report\u2019s proposal to maintain the Medical Expense Deduction and lower the threshold of qualifying expenses to expenses above 7.5 percent of income for two years, rather than the current law\u2019s threshold of 10 percent. <\/span><\/p>\n<p><span style=\"font-weight: 400;\">While we support the expansion of the Medical Expense Deduction, the damage from cutting the Orphan Drug Tax Credit and repealing the individual mandate far outweighs any benefits. <\/span><\/p>\n<p><span style=\"font-weight: 400;\">For these reasons, we do not support the <\/span><i><span style=\"font-weight: 400;\">Tax Cuts and Jobs Act<\/span><\/i><span style=\"font-weight: 400;\"> Conference Report.\u201d<\/span><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Washington, D.C., December 18, 2017\u2014The National Organization for Rare Disorders (NORD), the leading independent nonprofit organization representing the 30 million Americans with rare diseases, issued the following statement in response &hellip; <\/p>\n<p class=\"link-more\"><a href=\"https:\/\/rarediseases.org\/es\/nord-issues-statement-in-response-to-congressional-consideration-of-the-tax-cuts-and-jobs-act-conference-report\/\" class=\"more-link\">Continue reading<span class=\"screen-reader-text\"> \u00abNORD Issues Statement in Response to Congressional Consideration of the Tax Cuts and Jobs Act Conference Report\u00bb<\/span><\/a><\/p>\n","protected":false},"author":47,"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],"tags":[1429,234,1425,1432,346,347,1430,1431,1402],"class_list":["post-58884","post","type-post","status-publish","format-standard","hentry","category-advocacy","category-featured-news","tag-aca-individual-mandate","tag-affordable-care-act","tag-conference-committee","tag-congresswoman-mcmorris-rodgers","tag-odtc","tag-orphan-drug-tax-credit","tag-senator-hatch","tag-senator-roberts","tag-tax-cuts-and-jobs-act"],"acf":[],"_links":{"self":[{"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/posts\/58884","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\/47"}],"replies":[{"embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/comments?post=58884"}],"version-history":[{"count":0,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/posts\/58884\/revisions"}],"wp:attachment":[{"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/media?parent=58884"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/categories?post=58884"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/tags?post=58884"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}