{"id":91296,"date":"2016-04-06T16:32:35","date_gmt":"2016-04-06T20:32:35","guid":{"rendered":"\/news\/?p=91296"},"modified":"2016-04-06T20:47:07","modified_gmt":"2016-04-07T00:47:07","slug":"families-chose-life-faced-fetal-abnormalities","status":"publish","type":"post","link":"https:\/\/archive.liveaction.org\/news\/families-chose-life-faced-fetal-abnormalities\/","title":{"rendered":"These families chose life when faced with fetal abnormalities"},"content":{"rendered":"<div style=\"margin-top: 0px; margin-bottom: 0px;\" class=\"sharethis-inline-share-buttons\" ><\/div><p>No parent wants to hear that their child has been\u00a0diagnosed with a fetal abnormality. \u00a0But some families compound the tragedy, aborting their children rather than giving them a shot at life. Some are convinced to have the abortion\u00a0&#8211; and\u00a0<a href=\"\/news\/mother-testifies-she-aborted-son-at-22-weeks-out-of-love\/\">others even claim<\/a> that they are aborting\u00a0out of love.<\/p>\n<p>But the\u00a0truth is that\u00a0abortion, by its very nature, can never be a loving act, because it has one objective: to kill the child.\u00a0Some children have been aborted, only to later find\u00a0that\u00a0<a href=\"http:\/\/www.dailymail.co.uk\/news\/article-3123078\/New-blood-test-blamed-women-choosing-abort-babies-s-syndrome-disabilities-soars-34-three-years.html\">the doctors were wrong<\/a>. Fortunately, other babies\u00a0<a href=\"http:\/\/christiannews.net\/2014\/10\/20\/baby-born-healthy-after-couple-refuses-abortion-despite-doctors-fetal-abnormalities-claim\/\">were allowed to live<\/a>\u00a0after being misdiagnosed. Following are four families who chose life for their children in the face of death&#8230;<\/p>\n<p><!--more--><span style=\"text-decoration: underline\"><strong>The Dennis Family<\/strong><\/span><\/p>\n<p>In 2013, Florida couple Lindsey and Kevin Dennis received a prenatal diagnosis of anencephaly for their 20-week-old daughter, Sophie.\u00a0Rather than choose abortion like their doctor suggested, Sophie was born and lived for 10 hours, where loving friends and family stood by her side.<\/p>\n<p>Lindsey <a href=\"https:\/\/vaporandmist.wordpress.com\/2013\/07\/23\/why-we-chose-to-carry-sophie\/\">spoke about<\/a> how people asked why she was still carrying her daughter, but she also spoke of faith in God and wrote:<\/p>\n<blockquote><p>So though sadness and grief surround us always\u2026 there is a beauty of the Joy and Celebration of her life mixed in the sadness. Joy and sadness can be a beautiful thing.<\/p><\/blockquote>\n<p>In 2014, the Dennis couple also carried to term their daughter, Dasah, who <a href=\"https:\/\/vaporandmist.wordpress.com\/dasah-brielles-story-a-journey-with-acrania-carrying-to-term-twice-and-holding-on-to-hope\/\">was diagnosed with<\/a>\u00a0acrania, a similar condition at 12-weeks. Dasah lived for 12 hours, and has likewise been celebrated and remembered by her family in <a href=\"https:\/\/vaporandmist.wordpress.com\/2014\/12\/11\/the-day-you-were-born-dasah\/\">a blog post<\/a> and the video below.<\/p>\n<p>About the day Dasah was born, Lindsey wrote:<\/p>\n<blockquote><p>Loving you that day brought joy, praise, laughter, tears and sorrow. \u00a0Joy as we delighted in the life and breath God was giving you for those 12 hours and sorrow as we knew \u201cgood-bye\u201d would come far too soon. \u00a0But this is Love. \u00a0And this is why we chose to carry you to term, to walk through a loss we knew all too well a second time\u2026 for love. \u00a0For the love of you, our second born daughter. \u00a0Loving you meant we would embrace joy and also sorrow. \u00a0That we would willingly step into the heartache of loss because we knew it was worth it to give you life.<\/p><\/blockquote>\n<div class=\"video-container\"><iframe loading=\"lazy\" src=\"https:\/\/player.vimeo.com\/video\/114488846\" width=\"640\" height=\"360\" frameborder=\"0\" title=\"Celebrating Dasah\" webkitallowfullscreen mozallowfullscreen allowfullscreen><\/iframe><\/div>\n<p><span style=\"text-decoration: underline\"><strong>The Deibert Family<\/strong><\/span><\/p>\n<p>In Washington in 2005, Jeanne and Steve Deibert were told their son would have Trisomy 18. Instead of an aborting him, <a href=\"http:\/\/www.nbcnews.com\/id\/23682263\/#.VK6WUCvF8T8\">Jeanne had Robbie<\/a>, and\u00a0got to see, hold, and take in every detail of him. He\u00a0lived for 29 days and received\u00a0hospital perinatal hospice care. Robbie and his parents were visited by friends, family and a priest. His mother Jeanne described the experience as &#8220;serene.&#8221;<\/p>\n<p style=\"font-size: 11px;font-family: Arial, Helvetica, sans-serif;color: #999;margin-top: 5px;background: transparent;text-align: center;width: 420px\">Visit NBCNews.com for <a style=\"text-decoration: none !important;border-bottom: 1px dotted #999 !important;font-weight: normal !important;height: 13px;color: #5799db !important\" href=\"http:\/\/www.nbcnews.com\">breaking news<\/a>, <a style=\"text-decoration: none !important;border-bottom: 1px dotted #999 !important;font-weight: normal !important;height: 13px;color: #5799db !important\" href=\"http:\/\/www.nbcnews.com\/id\/3032507\">world news<\/a>, and <a style=\"text-decoration: none !important;border-bottom: 1px dotted #999 !important;font-weight: normal !important;height: 13px;color: #5799db !important\" href=\"http:\/\/www.nbcnews.com\/id\/3032072\">news about the economy<\/a><\/p>\n<p>While Robbie was one of the 90 percent of babies who do not live past their first birthday when diagnosed with Trisomy 18, others have defied the odds. Former Senator and presidential candidate Rick Santorum (R-PA) has often spoken of his daughter Bella, who was born with such an abnormality. She will be turning eight in May.<\/p>\n<p><span style=\"text-decoration: underline\"><strong>The Hebron Family<\/strong><\/span><\/p>\n<div id=\"attachment_91882\" style=\"width: 330px\" class=\"wp-caption aligncenter\"><img aria-describedby=\"caption-attachment-91882\" decoding=\"async\" loading=\"lazy\" class=\"size-full wp-image-91882\" src=\"https:\/\/www.liveactionnews.org\/wp-content\/uploads\/2016\/04\/neonatology-patient-savaughn-16x9.jpg\" alt=\"The Hebron family (via chop.edu)\" width=\"320\" height=\"180\" srcset=\"https:\/\/archive.liveaction.org\/news\/wp-content\/uploads\/2016\/04\/neonatology-patient-savaughn-16x9.jpg 320w, https:\/\/archive.liveaction.org\/news\/wp-content\/uploads\/2016\/04\/neonatology-patient-savaughn-16x9-300x169.jpg 300w\" sizes=\"(max-width: 320px) 100vw, 320px\" \/><p id=\"caption-attachment-91882\" class=\"wp-caption-text\">The Hebron family (via chop.edu)<\/p><\/div>\n<p>In 2000, retired Philadelphia player Vaughn Hebron and his wife Kim were told at five months that <a href=\"http:\/\/www.chop.edu\/stories\/twin-twin-transfusion-syndrome-savaughn-and-savions-story#.VwVOJsfFoTU\">their twins<\/a> had the life-threatening condition of twin-twin transfusion. Doctors told them that there was a 70 percent chance one or both would die, but both twins survived and are healthy teenagers.<\/p>\n<p><span style=\"text-decoration: underline\"><strong>The Rodriguez Family<\/strong><\/span><\/p>\n<div id=\"attachment_91887\" style=\"width: 484px\" class=\"wp-caption aligncenter\"><img aria-describedby=\"caption-attachment-91887\" decoding=\"async\" loading=\"lazy\" class=\"wp-image-91887 size-large\" src=\"https:\/\/www.liveactionnews.org\/wp-content\/uploads\/2016\/04\/12241499_196705390662479_5745313414401468007_n-e1459969001198-700x463.jpg\" alt=\"Evan, Olivia, and Layla Rodriguez (via Facebook)\" width=\"474\" height=\"314\" srcset=\"https:\/\/archive.liveaction.org\/news\/wp-content\/uploads\/2016\/04\/12241499_196705390662479_5745313414401468007_n-e1459969001198-700x463.jpg 700w, https:\/\/archive.liveaction.org\/news\/wp-content\/uploads\/2016\/04\/12241499_196705390662479_5745313414401468007_n-e1459969001198-300x198.jpg 300w, https:\/\/archive.liveaction.org\/news\/wp-content\/uploads\/2016\/04\/12241499_196705390662479_5745313414401468007_n-e1459969001198.jpg 765w\" sizes=\"(max-width: 474px) 100vw, 474px\" \/><p id=\"caption-attachment-91887\" class=\"wp-caption-text\">Evan, Olivia, and Layla Rodriguez (via Facebook)<\/p><\/div>\n<p><a href=\"\/news\/couple-expecting-baby-anencephaly-peace\/\">Evan and Olivia Rodriguez&#8217;s<\/a>\u00a0daughter Layla Sky was\u00a0diagnosed with anencephaly, but they chose life, with their faith as a big part of that decision, and said &#8220;we&#8217;re\u00a0at peace.&#8221;\u00a0The Rodriguez family\u00a0beautifully communicates the pro-life view:<\/p>\n<blockquote>\n<p style=\"padding-left: 30px\">Layla\u2019s parents won\u2019t have any regrets, no matter how long they have with their daughter, but if they had chosen to abort, they know they would have had a life of regret.<\/p>\n<p style=\"padding-left: 30px\">\u201cLife is compatible with us,\u201d said Mrs. Rodriguez. \u201cWhether you get 10 minutes with your child, months, or hours, you don\u2019t have that regret of \u2018what if\u2019.\u201d<\/p>\n<\/blockquote>\n<p>After Layla Sky was <a href=\"https:\/\/www.facebook.com\/TheFightForLaylaSky\/photos\/a.168847983448220.1073741829.146439995689019\/209556312710720\/?type=3&amp;theater\">born on November 13, 2015<\/a>, her parents spent\u00a040 minutes with her until her passing and then\u00a0spent the entire night holding her. Family and friends <a href=\"https:\/\/www.facebook.com\/TheFightForLaylaSky\/videos\/vb.146439995689019\/210998942566457\/?type=2&amp;theater\">gathered some time later<\/a> for a burial.\u00a0This year on\u00a0February 29, Olivia announced that she and Evan <a href=\"https:\/\/www.facebook.com\/TheFightForLaylaSky\/photos\/a.168847983448220.1073741829.146439995689019\/237906423209042\/?type=3&amp;theater\">are expecting<\/a> their second child. You can follow their journey <a href=\"https:\/\/www.facebook.com\/TheFightForLaylaSky\/timeline\">here<\/a>.<\/p>\n<p>The Charlotte Lozier Institute has put forth an\u00a0<a href=\"https:\/\/lozierinstitute.org\/stories-of-premature-births-lethalnon-lethal-anomalies-with-fetal-surgery-and-perinatal-hospice\/\">inspiring compilation<\/a>\u00a0of other families who have chosen life when they were given &#8220;incompatible with life&#8221; diagnoses.<\/p>\n<p>By being given a chance at life, children receive the dignity they deserve, and a chance to\u00a0have an impact on their parents and the world.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>No parent wants to hear that their child has been\u00a0diagnosed with a fetal abnormality. \u00a0But some families compound the tragedy, aborting their children rather than giving them a shot at life. Some are convinced to have the abortion\u00a0&#8211; and\u00a0others even claim that they are aborting\u00a0out of love. But the\u00a0truth is that\u00a0abortion, by its very nature, [&hellip;]<\/p>\n","protected":false},"author":205,"featured_media":60491,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"om_disable_all_campaigns":false},"categories":[4],"tags":[1779,56,4761,3233,7925,8241,8240,5464,8242,8243,8244,3944,892],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v20.7 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>These families chose life when faced with fetal abnormalities<\/title>\n<meta name=\"description\" content=\"By being given a chance at life, children receive the dignity they deserve, and a chance to have an impact on their parents and the world.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/archive.liveaction.org\/news\/families-chose-life-faced-fetal-abnormalities\/\" \/>\n<meta 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