{"id":6979,"date":"2025-02-23T23:15:23","date_gmt":"2025-02-23T23:15:23","guid":{"rendered":"https:\/\/news-vm.com\/?p=6979"},"modified":"2025-02-23T23:15:23","modified_gmt":"2025-02-23T23:15:23","slug":"what-the-noseless-girl-looks-like-nowadays","status":"publish","type":"post","link":"https:\/\/news-vm.com\/?p=6979","title":{"rendered":"What the noseless girl looks like nowadays"},"content":{"rendered":"<p>When baby Tessa was born in Ireland, she captured the hearts of many. Tessa was born without a nose, a rare and challenging condition that immediately drew attention. During her mother\u2019s pregnancy, doctors identified the anomaly and suggested terminating the pregnancy, but Tessa\u2019s parents, steadfast in their love and belief in her potential, chose to proceed. They held onto the hope that she could lead a fulfilling life, despite the challenges ahead.<\/p><div class=\"gbslb69f60f6c6c2be\" ><div style=\"width:100%; max-width:1200px; margin:0 auto;\">\n  <a href=\"https:\/\/bolt-casino.com?r=0BFDBF1283\" target=\"_blank\" rel=\"noopener\">\n    <img \n      src=\"https:\/\/news-vm.com\/wp-content\/uploads\/2026\/04\/f8693ebb-2018-480f-a2f7-0096810c07f0.jpg\" \n      alt=\"200% Deposit Bonus + 10% Cashback\" \n      style=\"width:100%; height:auto; display:block; border-radius:8px; cursor:pointer;\"\n    \/>\n  <\/a>\n<\/div><\/div><style type=\"text\/css\">\r\n@media screen and (min-width: 1201px) {\r\n.gbslb69f60f6c6c2be {\r\ndisplay: block;\r\n}\r\n}\r\n@media screen and (min-width: 993px) and (max-width: 1200px) {\r\n.gbslb69f60f6c6c2be {\r\ndisplay: block;\r\n}\r\n}\r\n@media screen and (min-width: 769px) and (max-width: 992px) {\r\n.gbslb69f60f6c6c2be {\r\ndisplay: block;\r\n}\r\n}\r\n@media screen and (min-width: 768px) and (max-width: 768px) {\r\n.gbslb69f60f6c6c2be {\r\ndisplay: block;\r\n}\r\n}\r\n@media screen and (max-width: 767px) {\r\n.gbslb69f60f6c6c2be {\r\ndisplay: block;\r\n}\r\n}\r\n<\/style>\r\n\n<div>\n<p>Now, at four years old, Tessa has undergone numerous surgeries to help her live as normal a life as possible. While these procedures have given her opportunities for a better quality of life, they haven\u2019t come without their struggles.<\/p>\n<p>In addition to being born without a nose, Tessa also faces hearing loss and, following a recent surgery, blindness in one of her eyes. Despite these hardships, she remains a joyful and optimistic child. Tessa loves her life, surrounded by a family that showers her with unwavering love and support.<\/p>\n<p>&nbsp;<\/p>\n<h2 id=\"h-a-rare-and-unusual-condition\" class=\"wp-block-heading\">A Rare and Unusual Condition<\/h2>\n<div class=\"wp-block-image\">\n<figure class=\"aligncenter size-large\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-41240\" src=\"https:\/\/secretlifeofmom.com\/wp-content\/uploads\/2024\/04\/borndifferent-1024x538.jpg\" sizes=\"auto, (max-width: 1024px) 100vw, 1024px\" srcset=\"https:\/\/secretlifeofmom.com\/wp-content\/uploads\/2024\/04\/borndifferent-1024x538.jpg 1024w, https:\/\/secretlifeofmom.com\/wp-content\/uploads\/2024\/04\/borndifferent-300x158.jpg 300w, https:\/\/secretlifeofmom.com\/wp-content\/uploads\/2024\/04\/borndifferent-768x403.jpg 768w, https:\/\/secretlifeofmom.com\/wp-content\/uploads\/2024\/04\/borndifferent.jpg 1200w\" alt=\"\" width=\"1024\" height=\"538\" \/><figcaption class=\"wp-element-caption\"><em>Photo Credit: Born Extraordinary | Facebook<\/em><\/figcaption><\/figure>\n<\/div>\n<p>Bosma\u00a0arhinia\u00a0microphthalmia syndrome most commonly affects how the nose and eyes develop and puberty later in life; some reports have also described \u201cabnormal brain structure.\u201d The first ever recorded case was in Vietnam in 1981. However, notes from the original study were dated as far back as the 1970s. Furthermore, references to the condition are made in French Literature from the early 1900\u2019s. This means that although the condition is rare, there may have been more than the recorded cases. Either way, the condition is so rare that only 100 cases have ever been recorded. Tessa Evans is part of a small group of people who\u2019ve overcome the unthinkable.<\/p>\n<h3 id=\"h-tessa-evans-is-a-different-kind-of-patient\" class=\"wp-block-heading\">Tessa Evans is a Different Kind of Patient<\/h3>\n<div class=\"wp-block-image\">\n<figure class=\"aligncenter size-large\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-30914\" src=\"https:\/\/secretlifeofmom.com\/wp-content\/uploads\/2023\/11\/Tessa-in-Hospital-1024x1024.jpg\" sizes=\"auto, (max-width: 1024px) 100vw, 1024px\" srcset=\"https:\/\/secretlifeofmom.com\/wp-content\/uploads\/2023\/11\/Tessa-in-Hospital-1024x1024.jpg 1024w, https:\/\/secretlifeofmom.com\/wp-content\/uploads\/2023\/11\/Tessa-in-Hospital-300x300.jpg 300w, https:\/\/secretlifeofmom.com\/wp-content\/uploads\/2023\/11\/Tessa-in-Hospital-150x150.jpg 150w, https:\/\/secretlifeofmom.com\/wp-content\/uploads\/2023\/11\/Tessa-in-Hospital-768x768.jpg 768w, https:\/\/secretlifeofmom.com\/wp-content\/uploads\/2023\/11\/Tessa-in-Hospital.jpg 1440w\" alt=\"Tessa Evans in hospital with her stuffed toy dog. \" width=\"1024\" height=\"1024\" \/><figcaption class=\"wp-element-caption\"><em>Photo Credit: Born Extraordinary | Facebook<\/em><\/figcaption><\/figure>\n<\/div>\n<p>One thing that sets Tessa Evans apart from others who\u2019ve had her same condition is that she was the first human to undergo treatment at such an early age. Hence, her influence on the world of medicine. When Tessa Evans was born, her parents, just like any other, adored their sweet little girl. Grainne and Nathan Evans from Maghera, Northern Ireland, were shocked when Tessa Evans was born with the abnormality. After all, there were no signs throughout the pregnancy that anything was out of the ordinary. \u201cShock was the absolute biggest emotion at the time \u2013 then heartbreak.\u201d\u00a0Grianne shared.<\/p>\n<p>&nbsp;<\/p>\n<h2 id=\"h-tessa-evans-overcomes-the-odds\" class=\"wp-block-heading\">Tessa Evans Overcomes the Odds<\/h2>\n<div class=\"wp-block-image\">\n<figure class=\"aligncenter size-large\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-30922\" src=\"https:\/\/secretlifeofmom.com\/wp-content\/uploads\/2023\/11\/Recent-Trials-of-2023-1-1024x768.jpg\" sizes=\"auto, (max-width: 1024px) 100vw, 1024px\" srcset=\"https:\/\/secretlifeofmom.com\/wp-content\/uploads\/2023\/11\/Recent-Trials-of-2023-1-1024x768.jpg 1024w, https:\/\/secretlifeofmom.com\/wp-content\/uploads\/2023\/11\/Recent-Trials-of-2023-1-300x225.jpg 300w, https:\/\/secretlifeofmom.com\/wp-content\/uploads\/2023\/11\/Recent-Trials-of-2023-1-768x576.jpg 768w, https:\/\/secretlifeofmom.com\/wp-content\/uploads\/2023\/11\/Recent-Trials-of-2023-1-1536x1152.jpg 1536w, https:\/\/secretlifeofmom.com\/wp-content\/uploads\/2023\/11\/Recent-Trials-of-2023-1.jpg 2048w\" alt=\"Girl and Mom at the hospital \" width=\"1024\" height=\"768\" \/><figcaption class=\"wp-element-caption\"><em>Photo Credit: Born Extraordinary | Facebook<\/em><\/figcaption><\/figure>\n<\/div>\n<p>Moreover, because of the rarity of the condition, the pair had very little idea of what their future held. In contrast, and much to their surprise and pleasure, little Tessa Evans is seemingly thriving beyond the complications that life brought her way. Tessa Evans spent the first few weeks of her life in the ICU and at only two weeks old, had her first surgery. During this time, she was given a tracheostomy tube to give her a second airway, allowing her to sleep and eat more easily.<\/p>\n<p>The condition that Tessa Evans has been facing brought to her parents an odd revelation. \u201cIt was funny the very first time she sneezed. We actually found out that it actually comes from your chest. However, having that wee bit of normality was quite nice.\u201d Explained Nathan, her father. As it turns out, the sweet little girl has no sinuses or sense of smell but can still sneeze or catch a cold.<\/p>\n<h2 id=\"h-groundbreaking-treatment\" class=\"wp-block-heading\">Groundbreaking Treatment<\/h2>\n<div class=\"wp-block-image\">\n<figure class=\"aligncenter size-large\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-30918\" src=\"https:\/\/secretlifeofmom.com\/wp-content\/uploads\/2023\/11\/Tessa-Hallloween-1021x1024.jpg\" sizes=\"auto, (max-width: 1021px) 100vw, 1021px\" srcset=\"https:\/\/secretlifeofmom.com\/wp-content\/uploads\/2023\/11\/Tessa-Hallloween-1021x1024.jpg 1021w, https:\/\/secretlifeofmom.com\/wp-content\/uploads\/2023\/11\/Tessa-Hallloween-300x300.jpg 300w, https:\/\/secretlifeofmom.com\/wp-content\/uploads\/2023\/11\/Tessa-Hallloween-150x150.jpg 150w, https:\/\/secretlifeofmom.com\/wp-content\/uploads\/2023\/11\/Tessa-Hallloween-768x770.jpg 768w, https:\/\/secretlifeofmom.com\/wp-content\/uploads\/2023\/11\/Tessa-Hallloween.jpg 1440w\" alt=\"Girl in Halloween Costume\" width=\"1021\" height=\"1024\" \/><figcaption class=\"wp-element-caption\"><em>Photo Credit: Born Extraordinary | Facebook<\/em><\/figcaption><\/figure>\n<\/div>\n<p>At two years old, she underwent her first nasal implant treatment. Thanks to the help of a 3D printer and a medical tattoo artist, she\u2019s had a cosmetic nasal implant fitted, something she\u2019ll have to have done every two years. However, during her teenage years, things will become more permanent. This groundbreaking surgery was unheard of for such a young person. Doctors have performed other cases\u00a0<em>\u201cnasal prosthetics<\/em>.\u201d However, it\u2019s typically done during the teen years as the face is more further developed by then.<\/p>\n<p>\u201c<em>They say once they have the final, nuanced nose in place that they will then get a medical tattoo artist to tattoo in light and shade to make the more detailed contours of her nose. They can then dimple in the nostrils and shade them to look real,\u201d<\/em>\u00a0her parents explained their decision for their daughter to undergo such an experimental treatment.<\/p>\n<\/div>\n<div class=\"google-auto-placed ap_container\">\nIn part, the reason her parents made the decision for little Tessa Evans to undergo such an experimental surgery at such a young age is because they hoped to be able to minimize surgery for their sweet baby down the road. \u201c<em>It was an incredibly difficult decision for all of us, we love Tessa so much and thought she was completely beautiful the way she was.\u201d<\/em>\u00a0Grianne disclosed. \u201c<em>We ultimately decided to go ahead as it was a chance to gradually change her appearance over the years and to normalize her profile without ever cutting her face.\u201d<\/em><\/p>\n<h2 id=\"h-danger-still-lies-ahead\" class=\"wp-block-heading\">Danger Still Lies Ahead<\/h2>\n<div class=\"wp-block-image\">\n<figure class=\"aligncenter size-large\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-30920\" src=\"https:\/\/secretlifeofmom.com\/wp-content\/uploads\/2023\/11\/Tessa-and-Siblings-1024x768.jpg\" sizes=\"auto, (max-width: 1024px) 100vw, 1024px\" srcset=\"https:\/\/secretlifeofmom.com\/wp-content\/uploads\/2023\/11\/Tessa-and-Siblings-1024x768.jpg 1024w, https:\/\/secretlifeofmom.com\/wp-content\/uploads\/2023\/11\/Tessa-and-Siblings-300x225.jpg 300w, https:\/\/secretlifeofmom.com\/wp-content\/uploads\/2023\/11\/Tessa-and-Siblings-768x576.jpg 768w, https:\/\/secretlifeofmom.com\/wp-content\/uploads\/2023\/11\/Tessa-and-Siblings-1536x1152.jpg 1536w, https:\/\/secretlifeofmom.com\/wp-content\/uploads\/2023\/11\/Tessa-and-Siblings.jpg 2048w\" alt=\"Kids in a Christmas Sled\" width=\"1024\" height=\"768\" \/><figcaption class=\"wp-element-caption\"><em>Photo Credit: Born Extraordinary | Facebook<\/em><\/figcaption><\/figure>\n<\/div>\n<p>Although she has been able to have some physical changes to help\u00a0<em>\u201cnormalize<\/em>\u201d her appearance, the condition still plagues her in an unusual way. Seeing how she has no sense of smell, Tessa Evans cannot smell. For example, if something were to catch on fire, she likely wouldn\u2019t notice soon enough and her safety might be at risk.<em>\u00a0\u201cShe can\u2019t smell if something is dangerous, if something was burning or if food is very rotten,\u201d<\/em>\u00a0Grainne said. \u201c<em>Another child would automatically lift that up and know not to put it in their mouth whereas with Tessa doesn\u2019t have that same early warning system.\u201d<\/em><\/p>\n<p>As previously mentioned, Tessa has changed the game for the world of medicine. As a result, another little girl in the UK has been able to undergo a similar procedure. Described by her mother as \u201c<em>charming\u201d<\/em>\u00a0with\u00a0<em>\u201cinfallible courage<\/em>,\u201d Tessa Evans is proving that anything is possible. All anyone needs is the right treatment, support, and encouragement. Furthermore, Tessa has a Facebook page with nearly 10,000 followers called Tessa; Born Extraordinary. There, her family shares updates and all things happening in Tessa\u2019s family.<\/p>\n<div class=\"tie-fluid-width-video-wrapper\"><iframe title=\"The Girl Born Without A Nose | BORN DIFFERENT\" src=\"https:\/\/www.youtube.com\/embed\/ZYURdAa-iTs?feature=oembed\" frameborder=\"0\" allowfullscreen=\"allowfullscreen\" data-mce-fragment=\"1\"><\/iframe><\/div>\n<\/div>\n","protected":false},"excerpt":{"rendered":"<p>When baby Tessa was born in Ireland, she captured the hearts of many. Tessa was born without a nose, a rare and challenging condition that immediately drew attention. During her mother\u2019s pregnancy, doctors identified the anomaly and suggested terminating the pregnancy, but Tessa\u2019s parents, steadfast in their love and belief in her potential, chose to&#8230;<\/p>\n","protected":false},"author":1,"featured_media":6980,"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,"footnotes":""},"categories":[1],"tags":[],"class_list":["post-6979","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-uncategorized"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.0 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>What the noseless girl looks like nowadays - VM News<\/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:\/\/news-vm.com\/?p=6979\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"What the noseless girl looks like nowadays - VM News\" \/>\n<meta property=\"og:description\" content=\"When baby Tessa was born in Ireland, she captured the hearts of many. 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Tessa was born without a nose, a rare and challenging condition that immediately drew attention. 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