{"id":1431,"date":"2024-10-06T22:56:59","date_gmt":"2024-10-06T22:56:59","guid":{"rendered":"https:\/\/buzzflash1.com\/?p=1431"},"modified":"2024-10-06T22:56:59","modified_gmt":"2024-10-06T22:56:59","slug":"parents-stunned-when-they-see-newborn-daughter-for-the-first-time-but-heres-what-she-looks-like-now","status":"publish","type":"post","link":"https:\/\/buzzflash1.com\/?p=1431","title":{"rendered":"Parents Stunned When They See Newborn Daughter For The First Time, But Here&#8217;s What She Looks Like Now"},"content":{"rendered":"<p><em>Note: we are republishing this story which originally made the news in March 2022.<\/em><\/p>\n<p>Nicole Hall, a determined mother, is on a mission to celebrate her daughter&#8217;s extraordinary beauty and individuality.<\/p>\n<p>Her 13-month-old daughter, Winry, was born with a rare congenital melanocytic nevi (CMN), a distinctive birthmark that sets her apart from other children. Initially, Nicole and her husband were taken aback by the birthmark&#8217;s appearance, with Nicole admitting, &#8220;When they first handed her to me, I thought it was a bruise, but it was quickly apparent that it was not. It resembled a mole.&#8221;<\/p>\n<aside class=\"m-in-content-ad-row l-inline not-size-b not-size-c not-size-d\" data-ad-group=\"outstream-0\">\n<div class=\"m-in-content-ad not-size-b not-size-c not-size-d is-empty not-filled\" data-ad-group=\"outstream-0\" data-zone-count=\"6\">\n<header class=\"m-ad-outstream--header\">\n<div class=\"m-ad-outstream--legend\"><\/div>\n<\/header>\n<div class=\"m-in-content-ad--slot not-size-b not-size-c not-size-d is-empty not-filled\">\n<div id=\"ad-outstream-9b03825b41184170843e0730b9749b9e\" class=\"m-ad-outstream--fallback is-filled\" data-outstream-slot-id=\"ad-outstream-outstream-04a3c27fe8ea490da950fc2302904d61\" data-google-query-id=\"COWz2prs-ogDFb8EvwQdY5YHpw\"><\/div>\n<\/div>\n<\/div>\n<\/aside>\n<div class=\"m-detail--body-item m-detail--body-item-inline\">\n<figure class=\"l-inline tml-image m-detail--tml-image--inline\"><a><picture class=\"is-loaded\"><source srcset=\"https:\/\/www.opposingviews.com\/.image\/c_limit%2Ccs_srgb%2Cq_auto:good%2Cw_380\/MjAxNTAyOTg2NTc1MjkxOTU3\/baby2.webp%20380w,%20https:\/\/www.opposingviews.com\/.image\/c_limit%2Ccs_srgb%2Cq_auto:good%2Cw_620\/MjAxNTAyOTg2NTc1MjkxOTU3\/baby2.webp%20620w,%20https:\/\/www.opposingviews.com\/.image\/c_limit%2Ccs_srgb%2Cq_auto:good%2Cw_700\/MjAxNTAyOTg2NTc1MjkxOTU3\/baby2.webp%20700w\" type=\"image\/webp\" sizes=\"(min-width: 1240px) 700px, (min-width: 675px) 620px, calc(100vw - 40px)\" \/><source srcset=\"https:\/\/www.opposingviews.com\/.image\/c_limit%2Ccs_srgb%2Cfl_progressive%2Cq_auto:good%2Cw_380\/MjAxNTAyOTg2NTc1MjkxOTU3\/baby2.jpg%20380w,%20https:\/\/www.opposingviews.com\/.image\/c_limit%2Ccs_srgb%2Cfl_progressive%2Cq_auto:good%2Cw_620\/MjAxNTAyOTg2NTc1MjkxOTU3\/baby2.jpg%20620w,%20https:\/\/www.opposingviews.com\/.image\/c_limit%2Ccs_srgb%2Cfl_progressive%2Cq_auto:good%2Cw_700\/MjAxNTAyOTg2NTc1MjkxOTU3\/baby2.jpg%20700w\" sizes=\"(min-width: 1240px) 700px, (min-width: 675px) 620px, calc(100vw - 40px)\" \/><\/picture><\/a><figcaption>\n<p class=\"tml-image--caption\"><em>Photo Credit: <\/em><a href=\"https:\/\/www.instagram.com\/p\/CLpz9_3Jfwj\/\" target=\"_blank\" rel=\"noopener\">nicolelucashall\/Instagram<\/a><\/p>\n<\/figcaption><\/figure>\n<\/div>\n<p>According to a report from the National Organization for Rare Diseases by Dr. Harper Price of Phoenix Children&#8217;s Hospital and Dr. Heather Etchevers of Marseille Medical Genetics, CMN can manifest as light brown to black patches and can cover various sizes and areas of the body.<\/p>\n<aside class=\"m-in-content-ad-row l-inline mm-in-content-ad-row--in-content not-size-b not-size-c not-size-d\" data-ad-group=\"in_content-0\">\n<div class=\"m-in-content-ad not-size-b not-size-c not-size-d\" data-ad-group=\"in_content-0\" data-zone-count=\"6\">\n<div class=\"not-size-b not-size-c not-size-d m-in-content-ad is-empty not-filled\">\n<div id=\"ad-in_content-71def662f81d461c88306f5937b19d96\" data-google-query-id=\"COiM1Jns-ogDFe4EVQgdjYME6A\"><\/div>\n<\/div>\n<\/div>\n<\/aside>\n<p>Instead of succumbing to sadness about her daughter&#8217;s condition, Nicole turned to the power of social media to raise awareness about CMN and send an essential message: &#8220;Being different is your superpower.&#8221; She aims to enlighten those who have not previously come across such a birthmark and to offer support and representation to children and parents facing comparable challenges<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/buzzflash1.com\/wp-content\/uploads\/2024\/10\/IMG_3917-240x300.webp\" alt=\"\" width=\"240\" height=\"300\" class=\"alignnone size-medium wp-image-1432\" srcset=\"https:\/\/buzzflash1.com\/wp-content\/uploads\/2024\/10\/IMG_3917-240x300.webp 240w, https:\/\/buzzflash1.com\/wp-content\/uploads\/2024\/10\/IMG_3917.webp 700w\" sizes=\"auto, (max-width: 240px) 100vw, 240px\" \/><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Note: we are republishing this story which originally made the news in March 2022. Nicole Hall, a determined mother, is on a mission to celebrate her daughter&#8217;s extraordinary beauty and individuality. Her 13-month-old daughter, Winry, was born with a rare congenital melanocytic nevi (CMN), a distinctive birthmark that sets her apart from other children. Initially,&#8230;<\/p>\n","protected":false},"author":2,"featured_media":1432,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_kad_post_transparent":"default","_kad_post_title":"default","_kad_post_layout":"default","_kad_post_sidebar_id":"","_kad_post_content_style":"default","_kad_post_vertical_padding":"default","_kad_post_feature":"","_kad_post_feature_position":"","_kad_post_header":false,"_kad_post_footer":false,"_kad_post_classname":"","footnotes":""},"categories":[1],"tags":[],"class_list":["post-1431","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-uncategorized"],"_links":{"self":[{"href":"https:\/\/buzzflash1.com\/index.php?rest_route=\/wp\/v2\/posts\/1431","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/buzzflash1.com\/index.php?rest_route=\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/buzzflash1.com\/index.php?rest_route=\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/buzzflash1.com\/index.php?rest_route=\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/buzzflash1.com\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=1431"}],"version-history":[{"count":1,"href":"https:\/\/buzzflash1.com\/index.php?rest_route=\/wp\/v2\/posts\/1431\/revisions"}],"predecessor-version":[{"id":1433,"href":"https:\/\/buzzflash1.com\/index.php?rest_route=\/wp\/v2\/posts\/1431\/revisions\/1433"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/buzzflash1.com\/index.php?rest_route=\/wp\/v2\/media\/1432"}],"wp:attachment":[{"href":"https:\/\/buzzflash1.com\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=1431"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/buzzflash1.com\/index.php?rest_route=%2Fwp%2Fv2%2Fcategories&post=1431"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/buzzflash1.com\/index.php?rest_route=%2Fwp%2Fv2%2Ftags&post=1431"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}