{"id":3067,"date":"2017-11-14T10:41:22","date_gmt":"2017-11-14T18:41:22","guid":{"rendered":"http:\/\/blog.silviaskingdom.com\/?p=3067"},"modified":"2017-11-14T10:41:22","modified_gmt":"2017-11-14T18:41:22","slug":"help-nicky-raise-eb-awareness","status":"publish","type":"post","link":"https:\/\/blog.silviaskingdom.com\/?p=3067","title":{"rendered":"Help Nicky raise EB Awareness!"},"content":{"rendered":"<p><a href=\"http:\/\/blog.silviaskingdom.com\/?attachment_id=3068\" rel=\"attachment wp-att-3068\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-3068 aligncenter\" src=\"http:\/\/blog.silviaskingdom.com\/wp-content\/uploads\/2017\/11\/1229980_10151861361042174_1201642643_n-copy.jpg\" alt=\"\" width=\"500\" height=\"500\" srcset=\"https:\/\/blog.silviaskingdom.com\/wp-content\/uploads\/2017\/11\/1229980_10151861361042174_1201642643_n-copy.jpg 960w, https:\/\/blog.silviaskingdom.com\/wp-content\/uploads\/2017\/11\/1229980_10151861361042174_1201642643_n-copy-768x768.jpg 768w, https:\/\/blog.silviaskingdom.com\/wp-content\/uploads\/2017\/11\/1229980_10151861361042174_1201642643_n-copy-300x300.jpg 300w, https:\/\/blog.silviaskingdom.com\/wp-content\/uploads\/2017\/11\/1229980_10151861361042174_1201642643_n-copy-50x50.jpg 50w\" sizes=\"auto, (max-width: 500px) 100vw, 500px\" \/><\/a><\/p>\n<p style=\"text-align: center;\">Nicky was born on November 25th, 1996 and was diagnosed with Recessive Dystrophic Epidermolysis Bullosa (RDEB).<br \/>\nEB is a rare genetic skin disorder, his body does not produce a vital protein that glues the layers of his skin together, hence the slightest friction causes painful blisters and wounds. His body has to be covered with special wound products and bandages to allow his wounds to heal and protect his skin from further damage.<br \/>\nThere is no treatment or cure at this time.<br \/>\nYou can help Nicky and all the children like him by helping us raise awareness!<br \/>\nLike and share this image today.<br \/>\nFollow these links for more information:<br \/>\n<a href=\"http:\/\/www.debra.org\" target=\"_blank\" rel=\"noopener\">Debra of America<\/a><br \/>\n<a href=\"http:\/\/ebmrf.org\/\" target=\"_blank\" rel=\"noopener\">EB Medical Research Foundation<\/a><br \/>\n<a href=\"https:\/\/www.ebresearch.org\/\" target=\"_blank\" rel=\"noopener\">EB Research Partnership<\/a><\/p>\n<p style=\"text-align: center;\">Thank you!!!<\/p>\n<p style=\"text-align: center;\"><a href=\"http:\/\/blog.silviaskingdom.com\/?attachment_id=2414\" rel=\"attachment wp-att-2414\"><img loading=\"lazy\" decoding=\"async\" class=\"size-full wp-image-2414 aligncenter\" src=\"http:\/\/blog.silviaskingdom.com\/wp-content\/uploads\/2017\/01\/silviaeb.gif\" alt=\"\" width=\"176\" height=\"186\" \/><\/a><\/p>\n<div class=\"fb-background-color\">\n\t\t\t  <div \n\t\t\t  \tclass = \"fb-comments\" \n\t\t\t  \tdata-href = \"https:\/\/blog.silviaskingdom.com\/?p=3067\"\n\t\t\t  \tdata-numposts = \"20\"\n\t\t\t  \tdata-lazy = \"true\"\n\t\t\t\tdata-colorscheme = \"light\"\n\t\t\t\tdata-order-by = \"reverse_time\"\n\t\t\t\tdata-mobile=true>\n\t\t\t  <\/div><\/div>\n\t\t  <style>\n\t\t    .fb-background-color {\n\t\t\t\tbackground: #ffffff !important;\n\t\t\t}\n\t\t\t.fb_iframe_widget_fluid_desktop iframe {\n\t\t\t    width: 100% !important;\n\t\t\t}\n\t\t  <\/style>\n\t\t  ","protected":false},"excerpt":{"rendered":"<p>Nicky was born on November 25th, 1996 and was diagnosed with Recessive Dystrophic Epidermolysis Bullosa (RDEB). EB is a rare genetic skin disorder, his body does not produce a vital protein that glues the layers of his skin together, hence the slightest friction causes painful blisters and wounds. His body&#46;&#46;&#46;<\/p>\n","protected":false},"author":1,"featured_media":3068,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[4],"tags":[256,20,19],"class_list":["post-3067","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-blog","tag-ebawareness","tag-eb-awareness","tag-epidermolysis-bullosa"],"post_mailing_queue_ids":[],"_links":{"self":[{"href":"https:\/\/blog.silviaskingdom.com\/index.php?rest_route=\/wp\/v2\/posts\/3067","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/blog.silviaskingdom.com\/index.php?rest_route=\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/blog.silviaskingdom.com\/index.php?rest_route=\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/blog.silviaskingdom.com\/index.php?rest_route=\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/blog.silviaskingdom.com\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=3067"}],"version-history":[{"count":1,"href":"https:\/\/blog.silviaskingdom.com\/index.php?rest_route=\/wp\/v2\/posts\/3067\/revisions"}],"predecessor-version":[{"id":3069,"href":"https:\/\/blog.silviaskingdom.com\/index.php?rest_route=\/wp\/v2\/posts\/3067\/revisions\/3069"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/blog.silviaskingdom.com\/index.php?rest_route=\/wp\/v2\/media\/3068"}],"wp:attachment":[{"href":"https:\/\/blog.silviaskingdom.com\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=3067"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/blog.silviaskingdom.com\/index.php?rest_route=%2Fwp%2Fv2%2Fcategories&post=3067"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/blog.silviaskingdom.com\/index.php?rest_route=%2Fwp%2Fv2%2Ftags&post=3067"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}