{"id":377,"date":"2025-07-11T19:38:33","date_gmt":"2025-07-11T19:38:33","guid":{"rendered":"http:\/\/danielsfunddev.wpenginepowered.com\/?post_type=impact-stories&#038;p=377"},"modified":"2025-10-24T16:06:38","modified_gmt":"2025-10-24T16:06:38","slug":"whitney-ryan-petersen","status":"publish","type":"impact-stories","link":"https:\/\/danielsfund.org\/impact-stories\/whitney-ryan-petersen\/","title":{"rendered":"Whitney &amp; Ryan Petersen"},"content":{"rendered":"\n<p>At the Child Development Center in Casper, Wyoming, families like Otto\u2019s are finding hope and progress through early intervention and expert care. Born with arthrogryposis multiplex congenita, a rare genetic condition affecting joint movement, Otto faced an uncertain future. Thanks to the CDC\u2019s dedicated team, he\u2019s reaching milestones once thought impossible, including the potential to take his first steps. As one of Wyoming\u2019s leading organizations supporting children with disabilities, the CDC is helping make a normal childhood achievable for kids across the state. Their work is transforming lives and giving families the tools and support they need to thrive.<\/p>\n","protected":false},"featured_media":7605,"template":"","class_list":["post-377","impact-stories","type-impact-stories","status-publish","has-post-thumbnail","hentry"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.7 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Whitney &amp; Ryan Petersen - Daniels Fund<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/danielsfund.org\/impact-stories\/whitney-ryan-petersen\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Whitney &amp; Ryan Petersen - Daniels Fund\" \/>\n<meta property=\"og:description\" content=\"At the Child Development Center in Casper, Wyoming, families like Otto\u2019s are finding hope and progress through early intervention and expert care. Born with arthrogryposis multiplex congenita, a rare genetic condition affecting joint movement, Otto faced an uncertain future. 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