{"id":13567,"date":"2021-06-03T18:40:24","date_gmt":"2021-06-03T22:40:24","guid":{"rendered":"https:\/\/www.myface.org\/?p=13567"},"modified":"2021-06-03T18:40:24","modified_gmt":"2021-06-03T22:40:24","slug":"my-brother-kyle-sibling-perspective","status":"publish","type":"post","link":"https:\/\/www.myface.org\/es\/my-brother-kyle-sibling-perspective\/","title":{"rendered":"My Brother, Kyle: A Sibling Perspective"},"content":{"rendered":"<p><span style=\"font-weight: 400;\">My brother, Kyle, was born with a very rare condition called Nablus Syndrome. There are less than 15 documented cases in the world. It is a microdeletion of the chromosome 8q22 and is characterized as a mask-like facial appearance along with other distinct malformations of the body.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">As Kyle\u2019s older sister, I\u2019ve watched him overcome so many medical and emotional challenges throughout his youth and develop into a remarkable young man. I may be the elder sister, yet he has taught me so much. I watched Kyle grow up dependent on his trach and vent to breathe, endure countless surgeries, undergo hours of doctors and specialists visits, and deal with the emotional stress of life that comes with having a facial difference. It has all given me a unique perspective on life. And an unwavering admiration for my brother.<\/span><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignleft wp-image-13568\" src=\"https:\/\/www.myface.org\/wp-content\/uploads\/2021\/06\/Erin-Kevin-jr-Kyle-OReilly-225x300.jpeg\" alt=\"\" width=\"301\" height=\"401\" srcset=\"https:\/\/www.myface.org\/wp-content\/uploads\/2021\/06\/Erin-Kevin-jr-Kyle-OReilly-225x300.jpeg 225w, https:\/\/www.myface.org\/wp-content\/uploads\/2021\/06\/Erin-Kevin-jr-Kyle-OReilly-768x1024.jpeg 768w, https:\/\/www.myface.org\/wp-content\/uploads\/2021\/06\/Erin-Kevin-jr-Kyle-OReilly-1152x1536.jpeg 1152w, https:\/\/www.myface.org\/wp-content\/uploads\/2021\/06\/Erin-Kevin-jr-Kyle-OReilly-1536x2048.jpeg 1536w, https:\/\/www.myface.org\/wp-content\/uploads\/2021\/06\/Erin-Kevin-jr-Kyle-OReilly-9x12.jpeg 9w, https:\/\/www.myface.org\/wp-content\/uploads\/2021\/06\/Erin-Kevin-jr-Kyle-OReilly-scaled.jpeg 1920w\" sizes=\"auto, (max-width: 301px) 100vw, 301px\" \/><\/p>\n<p><span style=\"font-weight: 400;\">Kyle has taught me that, no matter what you look like on the outside, it\u2019s what\u2019s on the inside that matters. The strength Kyle has and the confidence he exudes, despite his unique look, is truly amazing. He shows me every day that anything is possible.\u00a0<\/span><\/p>\n<p><span style=\"font-weight: 400;\">There are times when kids &#8211; and adults &#8211; have shied away from Kyle, or simply stare at him incessantly, because of the way he looks. It\u2019s their loss not getting to know him, because, once you do, you realize just how smart he is and fun to be around. Not to mention how passionate he is about sports!<\/span><\/p>\n<p><span style=\"font-weight: 400;\">Kyle is an inspiration to me and so many others. I see firsthand the impact he has had on our own family and the positive impact he has had &#8211; and continues to have &#8211; on every person he meets.<\/span><\/p>\n<h3><b><i>\u201cKyle shows me every day that anything is possible.\u201d &#8211; Erin<\/i><\/b><\/h3>\n<p><span style=\"font-weight: 400;\">If you are a craniofacial patient or a family member and wish to join a <\/span><b><i>Virtual Support Group<\/i><\/b><span style=\"font-weight: 400;\">, please email Dina Zuckerberg, Director of Family Programs, at Dina@myFace.org.<\/span><\/p>","protected":false},"excerpt":{"rendered":"<p>My brother, Kyle, was born with a very rare condition called Nablus Syndrome. There are less than 15 documented cases in the world. It is a microdeletion of the chromosome 8q22 and is characterized as a mask-like facial appearance along with other distinct malformations of the body. As Kyle\u2019s older<\/p>\n<p><a class=\"sd-more sd-all-trans\" href=\"https:\/\/www.myface.org\/es\/my-brother-kyle-sibling-perspective\/#more-13567\">Leer m\u00e1s<\/a><\/p>","protected":false},"author":15,"featured_media":13527,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[30],"tags":[241,45,320,182,322,321],"class_list":["post-13567","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-spotlights","tag-community","tag-craniofacial","tag-naomi","tag-patient-spotlight","tag-patient-stories","tag-van-der-woude-syndrome"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.2 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>My Brother, Kyle: A Sibling Perspective - myFace<\/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.myface.org\/es\/my-brother-kyle-sibling-perspective\/\" \/>\n<meta property=\"og:locale\" content=\"es_ES\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"My Brother, Kyle: A Sibling Perspective - myFace\" \/>\n<meta property=\"og:description\" content=\"My brother, Kyle, was born with a very rare condition called Nablus Syndrome. There are less than 15 documented cases in the world. It is a microdeletion of the chromosome 8q22 and is characterized as a mask-like facial appearance along with other distinct malformations of the body. 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