{"id":16477,"date":"2024-11-14T09:48:12","date_gmt":"2024-11-14T14:48:12","guid":{"rendered":"https:\/\/www.ptcbio.com\/?p=16477"},"modified":"2024-11-14T09:48:12","modified_gmt":"2024-11-14T14:48:12","slug":"autumns-huntingtons-disease-diagnostic-journey","status":"publish","type":"post","link":"https:\/\/panel.ptcbio.com\/es\/2024\/11\/14\/autumns-huntingtons-disease-diagnostic-journey\/","title":{"rendered":"Autumn&#8217;s Huntington\u2019s Disease Diagnostic Journey"},"content":{"rendered":"\n<p class=\"wp-block-paragraph core-block core-paragraph\"><em>My VIBE<\/em> <em>Season 2, Episode 2: The Effects of Huntington\u2019s Disease, Part 2<\/em>\u00a0 <\/p>\n\n\n\n<p class=\"wp-block-paragraph core-block core-paragraph\">On this episode of My VIBE,\u202fLonden shares her story as the mother and caregiver of 17-year-old Autumn, who has juvenile\u202fHuntington\u2019s disease\u202f(HD). Listen as Londen describes Autumn&#8217;s diagnostic journey and more:<\/p>\n\n\n\n<center><iframe loading=\"lazy\" height=\"200px\" width=\"100%\" frameborder=\"no\" scrolling=\"no\" seamless src=\"https:\/\/player.simplecast.com\/a28d7a72-e605-483a-8dcb-c0100f9d3257?dark=false\"><\/iframe><\/center>\n\n\n\n<p class=\"wp-block-paragraph core-block core-paragraph\"><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Londen shares her story as the mother &#038; caregiver of Autumn, who has juvenile\u202fHuntington\u2019s disease. <\/p>\n","protected":false},"author":0,"featured_media":16476,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[5,6],"tags":[],"media-type":[20,21],"therapeutic-area":[34],"class_list":["post-16477","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-rare-disease-community","category-rare-journeys"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO Premium plugin v27.9 (Yoast SEO v27.9) - 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