{"id":2600,"date":"2024-01-15T07:44:04","date_gmt":"2024-02-09T10:38:44","guid":{"rendered":"https:\/\/002.chilluh.nl\/rare-disease-day-2024-uk\/"},"modified":"2024-01-15T07:44:04","modified_gmt":"2024-02-09T10:38:44","slug":"rare-disease-day-2024-uk","status":"publish","type":"post","link":"https:\/\/werelivingwell.com\/kncbw-rare-disease-day-2024-uk-yukjh-info\/","title":{"rendered":"Rare Disease Day 2024 Uk"},"content":{"rendered":"<div class=\"cd5c096581fd5fc23b44a4969c1e3c2e\" data-index=\"1\" style=\"float: none; margin:10px 0 10px 0; text-align:center;\">\n<div style='text-align: center;'>\r\n<script type=\"text\/javascript\">\r\n\tatOptions = {\r\n\t\t'key' : '0a1f35073c594f712b44ac459670782f',\r\n\t\t'format' : 'iframe',\r\n\t\t'height' : 250,\r\n\t\t'width' : 300,\r\n\t\t'params' : {}\r\n\t};\r\n\tdocument.write('<scr' + 'ipt type=\"text\/javascript\" src=\"\/\/www.profitablecreativeformat.com\/0a1f35073c594f712b44ac459670782f\/invoke.js\"><\/scr' + 'ipt>');\r\n<\/script>\r\n<\/div>\r\n\n<\/div>\n<p>\t\t\t\t<![CDATA[\n\n<p><b>Rare Disease Day 2024 Uk<\/b> &#8211; The research, published in Science Translational Medicine, found that messenger RNA (mRNA) could be used to correct a rare liver genetic disease known  Cancer Research UK, and the National  . A woman who thought her hands were shaking due to too much coffee was diagnosed with Motor Neurone Disease (MND) \u2014 and now she wants to raise awareness for the rare  it one day at a time. .<\/p>\n\n\n\n\n<h2>Rare Disease Day 2024 Uk<\/h2>\n\n\n\n\n<p align=\"center\"> <a title=\"Rare Disease Day 2024   Rare Disease UK\"><img decoding=\"async\" src=\"https:\/\/www.raredisease.org.uk\/wp-content\/uploads\/sites\/7\/2023\/12\/Website-banner-1920-%C3%97-650-px.png\" width=\"100%\" height=\"100%\"><\/a> <\/p>\n\n\nSource : <a href=\"https:\/\/www.raredisease.org.uk\">www.raredisease.org.uk<\/a>\n\n\n<h2>Rare Disease Day 2024 | Genetic Alliance UK<\/h2>\n\n\n\n\n<p align=\"center\"><a title=\"Rare Disease Day 2024 | Genetic Alliance UK\"><img decoding=\"async\" src=\"https:\/\/geneticalliance.org.uk\/wp-content\/uploads\/2023\/04\/RARE-DISEASE-DAY.png\" width=\"100%\" height=\"100%\"><\/a> <\/p>\n\n\nSource : <a href=\"https:\/\/geneticalliance.org.uk\" rel=\"nofollow\">geneticalliance.org.uk<\/a>\n\n\n<h2>RARE DISEASE DAY   FEBRUARY 29th 2024<\/h2>\n\n\n\n\n<p align=\"center\"><a title=\"RARE DISEASE DAY   FEBRUARY 29th 2024\"><img decoding=\"async\" src=\"https:\/\/itpsupport.org.uk\/wp-content\/uploads\/2023\/12\/RDD-2024_Support-Pledge-Strapline-1920x1080_ENGLISH.png\" width=\"100%\" height=\"100%\"><\/a> <\/p>\n\n\nSource : <a href=\"https:\/\/itpsupport.org.uk\" rel=\"nofollow\">itpsupport.org.uk<\/a>\n\n\n<h2>Downloads   Rare Disease Day 2024<\/h2>\n\n\n\n\n<p align=\"center\"> <a title=\"Downloads   Rare Disease Day 2024\"><img decoding=\"async\" src=\"https:\/\/www.rarediseaseday.org\/wp-content\/uploads\/Rare-Disease-Day-2024_Digital-poster.png\" width=\"100%\" height=\"100%\"><\/a> <\/p>\n\n\nSource : <a href=\"https:\/\/www.rarediseaseday.org\" rel=\"nofollow\">www.rarediseaseday.org<\/a>\n\n\n<h2>Get involved this Rare Disease Day 2024   Rare Disease UK<\/h2>\n\n\n\n\n<p align=\"center\"> <a title=\"Get involved this Rare Disease Day 2024   Rare Disease UK\"><img decoding=\"async\" src=\"https:\/\/www.raredisease.org.uk\/wp-content\/uploads\/sites\/7\/2023\/12\/RDD24-stats.png\" width=\"100%\" height=\"100%\"><\/a> <\/p>\n\n\nSource : <a href=\"https:\/\/www.raredisease.org.uk\" rel=\"nofollow\">www.raredisease.org.uk<\/a>\n\n\n<h2>Join the Countdown: Rare Disease Day 2024 Starts Now   Rare <\/h2>\n\n\n\n\n<p align=\"center\"> <a title=\"Join the Countdown: Rare Disease Day 2024 Starts Now   Rare \"><img decoding=\"async\" src=\"https:\/\/www.rarediseaseday.org\/wp-content\/uploads\/Rare-Disease-Day-Official-Video-2024-thumbnail-1568x882.jpg\" width=\"100%\" height=\"100%\"><\/a> <\/p>\n\n\nSource : <a href=\"https:\/\/www.rarediseaseday.org\" rel=\"nofollow\">www.rarediseaseday.org<\/a>\n\n\n<h2>Rare Disease Day \u2013 looking to the future with hope   PMLiVE<\/h2>\n\n\n\n\n<p align=\"center\"> <a title=\"Rare Disease Day \u2013 looking to the future with hope   PMLiVE\"><img decoding=\"async\" src=\"https:\/\/www.pmlive.com\/__data\/assets\/image\/0006\/1388220\/Rare_disease_day_2022.jpg\" width=\"100%\" height=\"100%\"><\/a> <\/p>\n\n\nSource : <a href=\"https:\/\/www.pmlive.com\" rel=\"nofollow\">www.pmlive.com<\/a>\n\n\n<h2>LightUpForRare   Rare Disease Day 2024<\/h2>\n\n\n\n\n<p align=\"center\"> <a title=\"LightUpForRare   Rare Disease Day 2024\"><img decoding=\"async\" src=\"https:\/\/www.rarediseaseday.org\/wp-content\/uploads\/how_to_illuminate_RDD_2024_updated_Page_1-724x1024.png\" width=\"100%\" height=\"100%\"><\/a> <\/p>\n\n\nSource : <a href=\"https:\/\/www.rarediseaseday.org\" rel=\"nofollow\">www.rarediseaseday.org<\/a>\n\n\n<h2>aHUS Project for 2024 Rare Disease Day   aHUS Alliance Action<\/h2>\n\n\n\n\n<p align=\"center\"> <a title=\"aHUS Project for 2024 Rare Disease Day   aHUS Alliance Action\"><img decoding=\"async\" src=\"https:\/\/www.ahusallianceaction.org\/wp-content\/uploads\/2023\/12\/2024-RD-Day-general-29-FEB-1024x576.png\" width=\"100%\" height=\"100%\"><\/a> <\/p>\n\n\nSource : <a href=\"https:\/\/www.ahusallianceaction.org\" rel=\"nofollow\">www.ahusallianceaction.org<\/a>\n\n\n<h2>Rare Disease Day   Awareness Days Events Calendar 2024<\/h2>\n\n\n\n\n<p align=\"center\"> <a title=\"Rare Disease Day   Awareness Days Events Calendar 2024\"><img decoding=\"async\" src=\"https:\/\/www.awarenessdays.com\/wp-content\/uploads\/2018\/07\/rare.jpg\" width=\"100%\" height=\"100%\"><\/a> <\/p>\n\n\nSource : <a href=\"https:\/\/www.awarenessdays.com\" rel=\"nofollow\">www.awarenessdays.com<\/a>\n\n\n<p><b>Rare Disease Day 2024 Uk Rare Disease Day 2024   Rare Disease UK<\/b>:   Darius Hughes was a key figure in Pfizer\u2019s pioneering Covid vaccine drive. Now he has changed companies \u2013 and sees a big future for mRNA technology  . Moushmi Kapadia is an avid biker, trekker and a mom of two. Her older son Vedansh has Rigid Spine Muscular Dystrophy (RSMD) but has beaten all odds to travel the globe with his mom. This is her story  . <\/p>\n\n\n]]>\t\t<\/p>\n\n<div style=\"font-size: 0px; height: 0px; line-height: 0px; margin: 0; padding: 0; clear: both;\"><\/div>","protected":false},"excerpt":{"rendered":"<p>\t\t\t\t<![CDATA[]]>\t\t<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[57],"tags":[],"aioseo_notices":[],"_links":{"self":[{"href":"https:\/\/werelivingwell.com\/wp-json\/wp\/v2\/posts\/2600"}],"collection":[{"href":"https:\/\/werelivingwell.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/werelivingwell.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/werelivingwell.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/werelivingwell.com\/wp-json\/wp\/v2\/comments?post=2600"}],"version-history":[{"count":0,"href":"https:\/\/werelivingwell.com\/wp-json\/wp\/v2\/posts\/2600\/revisions"}],"wp:attachment":[{"href":"https:\/\/werelivingwell.com\/wp-json\/wp\/v2\/media?parent=2600"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/werelivingwell.com\/wp-json\/wp\/v2\/categories?post=2600"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/werelivingwell.com\/wp-json\/wp\/v2\/tags?post=2600"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}