{"id":8292,"date":"2025-01-17T18:11:29","date_gmt":"2025-01-17T18:11:29","guid":{"rendered":"https:\/\/prrf.org\/?p=8292"},"modified":"2025-10-24T22:20:47","modified_gmt":"2025-10-24T22:20:47","slug":"turning-challenges-into-action","status":"publish","type":"post","link":"https:\/\/prrf.org\/zh\/turning-challenges-into-action\/","title":{"rendered":"Turning Challenges Into Action: The Walls Family Story"},"content":{"rendered":"<div id=\"fws_69e39a146696e\"  data-column-margin=\"default\" data-midnight=\"dark\"  class=\"wpb_row vc_row-fluid vc_row\"  style=\"padding-top: 0px; padding-bottom: 0px; \"><div class=\"row-bg-wrap\" data-bg-animation=\"none\" data-bg-animation-delay=\"\" data-bg-overlay=\"false\"><div class=\"inner-wrap row-bg-layer\" ><div class=\"row-bg viewport-desktop\"  style=\"\"><\/div><\/div><\/div><div class=\"row_col_wrap_12 col span_12 dark left\"><\/div><\/div>\n\t<div  class=\"vc_col-sm-12 wpb_column column_container vc_column_container col no-extra-padding inherit_tablet inherit_phone\"  data-padding-pos=\"all\" data-has-bg-color=\"false\" data-bg-color=\"\" data-bg-opacity=\"1\" data-animation=\"\" data-delay=\"0\" >\n\t\t<div class=\"vc_column-inner\" >\n\t\t\t<div class=\"wpb_wrapper\">\n\t\t\t\t\n\t\t\t<\/div> \n\t\t<\/div>\n\t<\/div> \n\n<div class=\"wpb_text_column wpb_content_element\" >\n\t<div class=\"wpb_wrapper\">\n\t\t\t<\/div>\n<\/div>\n\n\n\n\n<div class=\"sqs-html-content\">\n<h2 style=\"text-align: left\">Season 2 | Episode 32:<\/h2>\n<h4 style=\"text-align: left\">January 17, 2025<\/h4>\n<p class=\"\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-8293 size-medium alignright\" src=\"https:\/\/prrf.org\/wp-content\/uploads\/2025\/05\/Podcastepisode32-300x300.png\" alt=\"Graphic design of a teenage boy fixing a motorcycle with the title of the podcast on top.\" width=\"300\" height=\"300\" srcset=\"https:\/\/prrf.org\/wp-content\/uploads\/2025\/05\/Podcastepisode32-300x300.png 300w, https:\/\/prrf.org\/wp-content\/uploads\/2025\/05\/Podcastepisode32-150x150.png 150w, https:\/\/prrf.org\/wp-content\/uploads\/2025\/05\/Podcastepisode32-12x12.png 12w, https:\/\/prrf.org\/wp-content\/uploads\/2025\/05\/Podcastepisode32-140x140.png 140w, https:\/\/prrf.org\/wp-content\/uploads\/2025\/05\/Podcastepisode32-100x100.png 100w, https:\/\/prrf.org\/wp-content\/uploads\/2025\/05\/Podcastepisode32-500x500.png 500w, https:\/\/prrf.org\/wp-content\/uploads\/2025\/05\/Podcastepisode32-350x350.png 350w, https:\/\/prrf.org\/wp-content\/uploads\/2025\/05\/Podcastepisode32.png 750w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/p>\n<p>In this inspiring episode of\u00a0<em>Through Our Eyes<\/em>, we relaunch into a new season of the show with a powerful story of hope, resilience, and advocacy. Host Lisa Recchia welcomes Collin Walls and his father, Chuck, to share their journey navigating Collin\u2019s diagnosis of a rare retinal disease at just four years old. From early challenges and uncertainties to becoming advocates and champions for groundbreaking research, the Walls family\u2019s story offers valuable insights for anyone facing the unknown.<\/p>\n<p>Guided by our podcast assistant, Breyanna, the conversation dives into their experiences, the impact of the Pediatric Retinal Research Foundation, and Collin\u2019s inspiring determination to live a full and vibrant life. Whether it\u2019s overcoming challenges in education, finding joy in hobbies like working on cars, or embracing the power of advocacy, this episode is a must-listen.<\/p>\n<p>&nbsp;<\/p>\n<\/div>\n<p><iframe loading=\"lazy\" src=\"https:\/\/play.libsyn.com\/embed\/episode\/id\/34881760\/height\/192\/theme\/modern\/size\/large\/thumbnail\/no\/custom-color\/11B6F0\/time-start\/00:00:00\/hide-show\/yes\/hide-playlist\/yes\/hide-subscribe\/yes\/hide-share\/yes\/font-color\/FFFFFF?wmode=opaque\" width=\"100%\" height=\"192\" allowfullscreen=\"allowfullscreen\"><\/iframe><\/p>","protected":false},"excerpt":{"rendered":"<p>Season 2 | Episode 32: January 17, 2025 In this episode Collin Walls and his father, Chuck, share their journey navigating Collin\u2019s diagnosis of a rare retinal disease at just four years old.<\/p>","protected":false},"author":22,"featured_media":8293,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_coblocks_attr":"","_coblocks_dimensions":"","_coblocks_responsive_height":"","_coblocks_accordion_ie_support":"","om_disable_all_campaigns":false,"footnotes":""},"categories":[37],"tags":[],"class_list":{"0":"post-8292","1":"post","2":"type-post","3":"status-publish","4":"format-standard","5":"has-post-thumbnail","7":"category-podcast"},"_links":{"self":[{"href":"https:\/\/prrf.org\/zh\/wp-json\/wp\/v2\/posts\/8292","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/prrf.org\/zh\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/prrf.org\/zh\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/prrf.org\/zh\/wp-json\/wp\/v2\/users\/22"}],"replies":[{"embeddable":true,"href":"https:\/\/prrf.org\/zh\/wp-json\/wp\/v2\/comments?post=8292"}],"version-history":[{"count":10,"href":"https:\/\/prrf.org\/zh\/wp-json\/wp\/v2\/posts\/8292\/revisions"}],"predecessor-version":[{"id":8525,"href":"https:\/\/prrf.org\/zh\/wp-json\/wp\/v2\/posts\/8292\/revisions\/8525"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/prrf.org\/zh\/wp-json\/wp\/v2\/media\/8293"}],"wp:attachment":[{"href":"https:\/\/prrf.org\/zh\/wp-json\/wp\/v2\/media?parent=8292"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/prrf.org\/zh\/wp-json\/wp\/v2\/categories?post=8292"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/prrf.org\/zh\/wp-json\/wp\/v2\/tags?post=8292"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}