{"id":376,"date":"2018-07-09T14:21:57","date_gmt":"2018-07-09T20:21:57","guid":{"rendered":"https:\/\/scda.dojiggyengage.com\/?page_id=376"},"modified":"2022-01-14T21:05:27","modified_gmt":"2022-01-14T21:05:27","slug":"london-knight","status":"publish","type":"page","link":"https:\/\/www.sicklecelldisease.org\/advocacy\/ambassadors-celebrity-champions\/london-knight\/","title":{"rendered":"London Knight"},"content":{"rendered":"<div id=\"attachment_869\" style=\"width: 210px\" class=\"wp-caption alignleft\"><img loading=\"lazy\" decoding=\"async\" aria-describedby=\"caption-attachment-869\" class=\"size-medium wp-image-869\" src=\"https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2018\/12\/rsz_8c5faa26-e90c-4b79-996d-8b5f2f694d75-200x300.jpg\" alt=\"\" width=\"200\" height=\"300\" srcset=\"https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2018\/12\/rsz_8c5faa26-e90c-4b79-996d-8b5f2f694d75-200x300.jpg 200w, https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2018\/12\/rsz_8c5faa26-e90c-4b79-996d-8b5f2f694d75-scaled-600x899.jpg 600w, https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2018\/12\/rsz_8c5faa26-e90c-4b79-996d-8b5f2f694d75-684x1024.jpg 684w, https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2018\/12\/rsz_8c5faa26-e90c-4b79-996d-8b5f2f694d75-768x1150.jpg 768w, https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2018\/12\/rsz_8c5faa26-e90c-4b79-996d-8b5f2f694d75-1025x1536.jpg 1025w, https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2018\/12\/rsz_8c5faa26-e90c-4b79-996d-8b5f2f694d75-1367x2048.jpg 1367w, https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2018\/12\/rsz_8c5faa26-e90c-4b79-996d-8b5f2f694d75-1568x2349.jpg 1568w, https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2018\/12\/rsz_8c5faa26-e90c-4b79-996d-8b5f2f694d75-scaled.jpg 1709w\" sizes=\"auto, (max-width: 200px) 100vw, 200px\" \/><p id=\"caption-attachment-869\" class=\"wp-caption-text\">London Knight<\/p><\/div>\n<h2 style=\"text-align: left;\">\u201cKeep going, don\u2019t ever give up. Everything you dream of will come to you.\u201d<\/h2>\n<p style=\"text-align: left;\">\u2013LONDON<\/p>\n<p>London Knight was born June 16 in San Diego, California, and she was diagnosed with sickle cell SC at the age of 3 months. Ever since she understood what sickle cell was she knew it was very important to follow her dreams as a model. Now she\u2019s successfully modeling and traveling all over the world, seen in magazines such as Elle, Cosmopolitan, Glamour, Marie Claire. She is also gracing runways in New York\u2019s and Johannesburg\u2019s Mercedes Benz Fashion Week. London has also appeared in commercials and movies.<\/p>\n<p>\u201cKeep going don\u2019t ever give up,\u201d says London. \u201cEverything you dream of will come to you.\u201d One of London\u2019s passions is volunteering in children\u2019s hospitals. It is something that is close to her heart, as she is an advocate for young sickle cell warriors, preaching that no matter your trials and tribulations it is important to follow your dreams.<\/p>\n<p>London says the difficulties she has experienced with having sickle cell directly relates to her mental health. \u201cI think its important to keep a positive outlook on dealing with sickle cell disease,\u201d she says. \u201cOnly those of us living with sickle cell disease know the true pain and mental strengths it takes to be a sickle cell warrior.\u201d<\/p>\n\n\t\t<style type=\"text\/css\">\n\t\t\t#gallery-1 {\n\t\t\t\tmargin: auto;\n\t\t\t}\n\t\t\t#gallery-1 .gallery-item {\n\t\t\t\tfloat: left;\n\t\t\t\tmargin-top: 10px;\n\t\t\t\ttext-align: center;\n\t\t\t\twidth: 25%;\n\t\t\t}\n\t\t\t#gallery-1 img {\n\t\t\t\tborder: 2px solid #cfcfcf;\n\t\t\t}\n\t\t\t#gallery-1 .gallery-caption {\n\t\t\t\tmargin-left: 0;\n\t\t\t}\n\t\t\t\/* see gallery_shortcode() in wp-includes\/media.php *\/\n\t\t<\/style>\n\t\t<div id='gallery-1' class='gallery galleryid-376 gallery-columns-4 gallery-size-thumbnail'><dl class='gallery-item'>\n\t\t\t<dt class='gallery-icon landscape'>\n\t\t\t\t<a href='https:\/\/www.sicklecelldisease.org\/dsc01397-982-of-1325\/'><img loading=\"lazy\" decoding=\"async\" width=\"150\" height=\"150\" src=\"https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2019\/01\/DSC01397-982-of-1325-150x150.jpg\" class=\"attachment-thumbnail size-thumbnail\" alt=\"\" srcset=\"https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2019\/01\/DSC01397-982-of-1325-150x150.jpg 150w, https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2019\/01\/DSC01397-982-of-1325-scaled-300x300.jpg 300w, https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2019\/01\/DSC01397-982-of-1325-scaled-100x100.jpg 100w\" sizes=\"auto, (max-width: 150px) 100vw, 150px\" \/><\/a>\n\t\t\t<\/dt><\/dl><dl class='gallery-item'>\n\t\t\t<dt class='gallery-icon portrait'>\n\t\t\t\t<a href='https:\/\/www.sicklecelldisease.org\/77236aa6-f6fe-4282-bdff-afc17b94a196\/'><img loading=\"lazy\" decoding=\"async\" width=\"150\" height=\"150\" src=\"https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2018\/12\/77236AA6-F6FE-4282-BDFF-AFC17B94A196-150x150.jpeg\" class=\"attachment-thumbnail size-thumbnail\" alt=\"\" srcset=\"https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2018\/12\/77236AA6-F6FE-4282-BDFF-AFC17B94A196-150x150.jpeg 150w, https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2018\/12\/77236AA6-F6FE-4282-BDFF-AFC17B94A196-300x300.jpeg 300w, https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2018\/12\/77236AA6-F6FE-4282-BDFF-AFC17B94A196-100x100.jpeg 100w\" sizes=\"auto, (max-width: 150px) 100vw, 150px\" \/><\/a>\n\t\t\t<\/dt><\/dl><dl class='gallery-item'>\n\t\t\t<dt class='gallery-icon portrait'>\n\t\t\t\t<a href='https:\/\/www.sicklecelldisease.org\/8e1ba63b-25ef-439d-9ee0-c16b024b3ed5\/'><img loading=\"lazy\" decoding=\"async\" width=\"150\" height=\"150\" src=\"https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2018\/12\/8E1BA63B-25EF-439D-9EE0-C16B024B3ED5-150x150.jpeg\" class=\"attachment-thumbnail size-thumbnail\" alt=\"\" srcset=\"https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2018\/12\/8E1BA63B-25EF-439D-9EE0-C16B024B3ED5-150x150.jpeg 150w, https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2018\/12\/8E1BA63B-25EF-439D-9EE0-C16B024B3ED5-300x300.jpeg 300w, https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2018\/12\/8E1BA63B-25EF-439D-9EE0-C16B024B3ED5-100x100.jpeg 100w\" sizes=\"auto, (max-width: 150px) 100vw, 150px\" \/><\/a>\n\t\t\t<\/dt><\/dl><dl class='gallery-item'>\n\t\t\t<dt class='gallery-icon portrait'>\n\t\t\t\t<a href='https:\/\/www.sicklecelldisease.org\/8d1405d2-9205-4ae8-8f52-203212067f41\/'><img loading=\"lazy\" decoding=\"async\" width=\"150\" height=\"150\" src=\"https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2018\/12\/8D1405D2-9205-4AE8-8F52-203212067F41-150x150.jpeg\" class=\"attachment-thumbnail size-thumbnail\" alt=\"\" srcset=\"https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2018\/12\/8D1405D2-9205-4AE8-8F52-203212067F41-150x150.jpeg 150w, https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2018\/12\/8D1405D2-9205-4AE8-8F52-203212067F41-300x300.jpeg 300w, https:\/\/www.sicklecelldisease.org\/wp-content\/uploads\/2018\/12\/8D1405D2-9205-4AE8-8F52-203212067F41-100x100.jpeg 100w\" sizes=\"auto, (max-width: 150px) 100vw, 150px\" \/><\/a>\n\t\t\t<\/dt><\/dl><br style=\"clear: both\" \/>\n\t\t<\/div>\n\n<p>As a SCDAA Celebrity Ambassador, London is committed to increasing awareness about sickle cell disease and to giving kids and young adults, just like her, a voice. \u201cGod has a plan for you,\u201d she says. \u201cAnd having sickle cell shouldn\u2019t give you doubt. It should be the thing that drives you. God has chosen you as one of the stronger soldiers to teach compassion and love because you never know what other people are going through!\u201d<\/p>\n<p>SCDAA thanks London for all that she has done for the sickle cell community in increasing awareness about sickle cell disease as one of our Celebrity Ambassadors. We appreciate her continued support of our work, and we look forward to collaborating on new awareness initiatives.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>\u201cKeep going, don\u2019t ever give up. Everything you dream of will come to you.\u201d \u2013LONDON London Knight was born June 16 in San Diego, California, and she was diagnosed with sickle cell SC at the age of 3 months. Ever since she understood what sickle cell was she knew it was very important to follow [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":2319,"parent":368,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-376","page","type-page","status-publish","has-post-thumbnail","hentry"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v24.0 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>London Knight - Sickle Cell Disease Association of America Inc.<\/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:\/\/www.sicklecelldisease.org\/advocacy\/ambassadors-celebrity-champions\/london-knight\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"London Knight - Sickle Cell Disease Association of America Inc.\" \/>\n<meta property=\"og:description\" content=\"\u201cKeep going, don\u2019t ever give up. 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