{"id":39381,"date":"2015-10-01T16:51:46","date_gmt":"2015-10-01T14:51:46","guid":{"rendered":"http:\/\/www.arabtelegraph.com\/?p=39381"},"modified":"2015-10-01T16:51:46","modified_gmt":"2015-10-01T14:51:46","slug":"find-out-how-this-boy-has-survived-without-a-skull","status":"publish","type":"post","link":"https:\/\/www.arabtelegraph.com\/?p=39381","title":{"rendered":"Find Out How This Boy Has Survived Without a Skull"},"content":{"rendered":"<p>https:\/\/youtu.be\/T-zfV6ecSAQ<\/p>\n<p dir=\"ltr\"><strong>Jaxon Buell was born last August with Microhydranencephaly, an uncurable malformation of the brain. He is\u00a0missing most of his brain and skull. About one in 4,859 babies in the United States will be born with Anencephaly and the marjority die shortly after birth, according to the Center for Disease Control and Prevention.<\/strong><\/p>\n<div id=\"crtoTextBanner\" dir=\"ltr\"><\/div>\n<p dir=\"ltr\">Microhydranencephaly can cause microcephaly and scalp rugae which means Jaxon\u2019s head is smaller than normal\u00a0and his\u00a0scalp is ridged \u2013 but that doesn\u2019t stop Jaxon from laughing and playing like any other baby.<\/p>\n<p dir=\"ltr\">Brittany Buell, Jaxon\u2019s mom, has given up her job to care for this miracle baby and has since launched a crowdfunding page to help with Jaxon\u2019s medical bills.<\/p>\n<p dir=\"ltr\">On the page, she and husband Brandon<span style=\"color: #000000;\"> <a style=\"color: #000000;\" href=\"http:\/\/www.dailymail.co.uk\/news\/article-3251158\/Father-miracle-baby-Jaxon-just-turned-one-despite-missing-skull-opens-Internet-abuse-wife-received-letting-son-live.html?ito=social-facebook\" target=\"_blank\">wrote<\/a><\/span>: \u201cJaxon has already shown how strong, smart, and special he is, accomplishing feats that doctors doubted he\u2019d ever be able to do. He shows improvements each and every day, and just reached a miraculous milestone in celebrating his first birthday.\u00a0These funds help pay for our regular monthly expenses and Jaxon\u2019s continuous medical care, which changes frequently.\u201d<\/p>\n<p dir=\"ltr\">The family have so far raised an impressive $54,902 of their $70,000 target and\u00a0are now encouraging people to give them support for Jaxon\u2019s \u201cyear two.\u201d<\/p>\n<p dir=\"ltr\">Jaxon\u2019s father spoke out this past weekend\u00a0about the abuse he\u2019s received after their inspirational story went viral. Some have said that Brandon and his wife Brittany are selfish and should have aborted the child to avoid the pain he is\u00a0suffering. These\u00a0internet commenters also question\u00a0why the\u00a0couple\u00a0would bring Jaxon into a world where he will likely never be able to walk, talk, hear, see or know that he is hungry.<\/p>\n<p dir=\"ltr\">\u201cJaxon was our baby,\u201d Brandon<span style=\"color: #000000;\"> <a style=\"color: #000000;\" href=\"http:\/\/www.dailymail.co.uk\/news\/article-3251158\/Father-miracle-baby-Jaxon-just-turned-one-despite-missing-skull-opens-Internet-abuse-wife-received-letting-son-live.html?ito=social-facebook\" target=\"_blank\">explained<\/a>,<\/span> \u201cand we only had one shot to do everything we could for him.\u201d Brandon also added that he and Brittany didn\u2019t want to \u2018play God\u2019 by aborting Jaxon. Besides,\u00a0Jaxon is already showing the naysayers wrong: He\u2019s learned to say \u201cmama.\u201d<\/p>\n<p dir=\"ltr\">As rare as Jaxon\u2019s\u00a0long-term survival is, his parents are\u00a0determined to fight for their son\u2019s life. \u201cThere are cases of Microhydranencephaly children who have lived into their 30s,\u201d Brandon says. \u201cThey have lived relatively normal lives, can learn to swim, and have and can use their senses, as well.\u201d<\/p>\n<p dir=\"ltr\">As for\u00a0those who accuse the couple of exploiting the public with their <a href=\"https:\/\/www.gofundme.com\/eld1og\" target=\"_blank\"><span style=\"color: #000000;\">GoFundMe<\/span> <span style=\"color: #000000;\">page<\/span><\/a>,\u00a0Brandon explains: \u201cThe longer we can afford to keep Brittany home with Jaxon, the longer he can remain stimulated from that priceless mother-to-son relationship that no one else can give and is one of the main reasons we believe that Jaxon is still here with us and is doing as well as he is.\u201d<\/p>\n<p dir=\"ltr\">Despite the negativity surrounding them, the Buell family plans to keep working with top neurologists who may be able to help Jaxon live as long as possible. Also, there\u2019s so much that science can learn from Jaxon and\u00a0how\u00a0Anencephaly works. He truly is a miracle baby who may lessen the suffering of others like him.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>https:\/\/youtu.be\/T-zfV6ecSAQ Jaxon Buell was born last August with Microhydranencephaly, an uncurable malformation of the brain. He is\u00a0missing most of his brain and skull. About one in 4,859 babies in the United States will be born with Anencephaly and the marjority die shortly after birth, according to the Center for Disease Control and Prevention. Microhydranencephaly can &hellip;<\/p>\n","protected":false},"author":3,"featured_media":39384,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_monsterinsights_skip_tracking":false,"_monsterinsights_sitenote_active":false,"_monsterinsights_sitenote_note":"","_monsterinsights_sitenote_category":0,"_jetpack_memberships_contains_paid_content":false,"footnotes":""},"categories":[36],"tags":[],"class_list":["post-39381","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-te-public"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.4 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Find Out How This Boy Has Survived Without a Skull - Arab Telegraph<\/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.arabtelegraph.com\/?p=39381\" \/>\n<meta property=\"og:locale\" content=\"ar_AR\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Find Out How This Boy Has Survived Without a Skull - Arab Telegraph\" \/>\n<meta property=\"og:description\" content=\"https:\/\/youtu.be\/T-zfV6ecSAQ Jaxon Buell was born last August with Microhydranencephaly, an uncurable malformation of the brain. He is\u00a0missing most of his brain and skull. About one in 4,859 babies in the United States will be born with Anencephaly and the marjority die shortly after birth, according to the Center for Disease Control and Prevention. 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