{"id":59080,"date":"2019-12-02T13:05:34","date_gmt":"2019-12-02T18:05:34","guid":{"rendered":"https:\/\/rarediseases.org\/what-questions-would-you-ask-about-gene-editing\/"},"modified":"2019-12-02T13:05:34","modified_gmt":"2019-12-02T18:05:34","slug":"what-questions-would-you-ask-about-gene-editing","status":"publish","type":"post","link":"https:\/\/rarediseases.org\/es\/what-questions-would-you-ask-about-gene-editing\/","title":{"rendered":"What Questions Would You Ask About Gene Editing?"},"content":{"rendered":"<p><span style=\"font-weight: 400;\">Do you have questions about gene editing and how it may advance the treatment of people with rare diseases? Much has been written lately about the promise of CRISPR and other gene-editing tools as future treatments for many rare diseases.\u00a0<\/span><\/p>\n<p><span style=\"font-weight: 400;\">NORD is creating a new educational video on this topic, and we want to be sure it addresses the questions that are most important to patients and caregivers across the rare disease community.\u00a0 For that reason, we are asking patients, caregivers and leaders of patient organizations to share their thoughts with us.\u00a0<\/span><\/p>\n<p><span style=\"font-weight: 400;\">Since gene editing is potentially helpful in treating many different rare diseases, we invite everyone across the spectrum of rare diseases to share their questions, hopes and concerns about this approach to treatment. You can do this quickly and easily on a special form we\u2019ve created for the NORD website. All responses will be confidential.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">For more than 35 years, NORD has been the primary provider of information about rare diseases and related topics to patients and caregivers across the spectrum of the 7,000+ rare diseases. In fact, when the patient advocates who established NORD discussed next steps \u2013 after their successful advocacy for the <\/span><i><span style=\"font-weight: 400;\">Orphan Drug Act<\/span><\/i><span style=\"font-weight: 400;\"> \u2013 they all agreed that education should always be one of NORD\u2019s top priorities.\u00a0<\/span><\/p>\n<p><span style=\"font-weight: 400;\">As a result, providing educational resources that are accurate, relevant and truly helpful to the intended audience is an important part of NORD\u2019s mission.\u00a0<\/span><\/p>\n<p><span style=\"font-weight: 400;\">You can help to ensure that the information NORD provides about gene editing addresses the most timely, relevant and frequently asked questions. Please take a minute today to fill out this brief form. NORD will aggregate the responses to identify the questions most frequently asked by patients and caregivers across the community.\u00a0\u00a0\u00a0<\/span><\/p>\n<p><span style=\"font-weight: 400;\"><a href=\"https:\/\/rarediseases.org\/your-questions-about-gene-editing\/\">SHARE YOUR QUESTIONS HERE<\/a>\u00a0\u00a0\u00a0<\/span><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Do you have questions about gene editing and how it may advance the treatment of people with rare diseases? Much has been written lately about the promise of CRISPR and &hellip; <\/p>\n<p class=\"link-more\"><a href=\"https:\/\/rarediseases.org\/es\/what-questions-would-you-ask-about-gene-editing\/\" class=\"more-link\">Continue reading<span class=\"screen-reader-text\"> &#8220;What Questions Would You Ask About Gene Editing?&#8221;<\/span><\/a><\/p>\n","protected":false},"author":1,"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":[190,662],"tags":[319,2129,2128,262],"class_list":["post-59080","post","type-post","status-publish","format-standard","hentry","category-featured-news","category-get-involved","tag-crispr","tag-educational-video","tag-gene-editing","tag-orphan-drug-act"],"acf":[],"_links":{"self":[{"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/posts\/59080","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=59080"}],"version-history":[{"count":0,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/posts\/59080\/revisions"}],"wp:attachment":[{"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/media?parent=59080"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/categories?post=59080"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/tags?post=59080"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}