{"id":289823,"date":"2023-04-27T06:44:18","date_gmt":"2023-04-27T11:44:18","guid":{"rendered":"https:\/\/www.liveaction.org\/news\/?p=289823"},"modified":"2023-04-25T16:03:13","modified_gmt":"2023-04-25T21:03:13","slug":"rejected-abortion-edmund-blessing-inspiration","status":"publish","type":"post","link":"https:\/\/archive.liveaction.org\/news\/rejected-abortion-edmund-blessing-inspiration\/","title":{"rendered":"We rejected abortion, and our son Edmund has been a blessing and an inspiration"},"content":{"rendered":"<div style=\"margin-top: 0px; margin-bottom: 0px;\" class=\"sharethis-inline-share-buttons\" ><\/div><p><em>Disclaimer: The views and opinions expressed in this article are those of the guest author and not necessarily of Live Action or Live Action News.<\/em><\/p>\n<p><span style=\"font-weight: 400;\">On February 10, 2022, my husband and I were told that our 13-week old baby had a 5% chance of survival due to a cystic hygroma, a build-up of fluid most often found on the back of a baby\u2019s neck in-utero. <\/span><\/p>\n<p><span style=\"font-weight: 400;\">Cystic hygromas are frequently associated with chromosomal abnormalities, and since we lost a baby with a cystic hygroma back in 2019, it felt like a horrible nightmare all over again. We were given a very grim prognosis and were immediately told abortion was an option, but we knew this baby had infinite value regardless of possible abnormalities.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">We were sent to a high-risk doctor who was an absolute light throughout my entire pregnancy. With 12 children of his own, he understood the value of our baby and never once treated our situation as a lost cause. He scheduled constant ultrasounds to check on our baby\u2019s well-being, and always let us know that he was available at all times for us.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">We soon found out that our 3 girls were going to have a little brother, but we also found out that our little guy had a congenital heart defect called double-outlet right ventricle, as well as some possible brain malformations. Since we opted-out of an amniocentesis or any invasive genetic testing, we weren\u2019t quite sure what kind of diagnosis our baby Edmund would have or whether he would survive the pregnancy, let alone the birth itself.<\/span><\/p>\n<div id=\"attachment_289826\" style=\"width: 410px\" class=\"wp-caption aligncenter\"><img aria-describedby=\"caption-attachment-289826\" decoding=\"async\" loading=\"lazy\" class=\"wp-image-289826 \" src=\"https:\/\/archive.liveaction.org\/news\/wp-content\/uploads\/2023\/04\/IMG_7892-Edmund-525x700.jpg\" alt=\"\" width=\"400\" height=\"533\" srcset=\"https:\/\/archive.liveaction.org\/news\/wp-content\/uploads\/2023\/04\/IMG_7892-Edmund-525x700.jpg 525w, https:\/\/archive.liveaction.org\/news\/wp-content\/uploads\/2023\/04\/IMG_7892-Edmund-225x300.jpg 225w, https:\/\/archive.liveaction.org\/news\/wp-content\/uploads\/2023\/04\/IMG_7892-Edmund-768x1024.jpg 768w, https:\/\/archive.liveaction.org\/news\/wp-content\/uploads\/2023\/04\/IMG_7892-Edmund-500x667.jpg 500w, https:\/\/archive.liveaction.org\/news\/wp-content\/uploads\/2023\/04\/IMG_7892-Edmund.jpg 1200w\" sizes=\"(max-width: 400px) 100vw, 400px\" \/><p id=\"caption-attachment-289826\" class=\"wp-caption-text\">Photo courtesy of Anna Denny<\/p><\/div>\n<p><span style=\"font-weight: 400;\">On July 26, 2022, we welcomed Edmund David to the world at 4lbs 10oz, tiny but mighty, with an entire team of doctors and nurses there ready to do whatever they could for him. <\/span><\/p>\n<p><span style=\"font-weight: 400;\">After an emergency baptism given by my husband, the NICU team whisked Edmund off to stabilize him. He needed some assistance with breathing and was given an NG tube for feedings. Thankfully, his heart was stable despite his double outlet right ventricle, and the brain malformation that they were afraid of in-utero was not as severe as they had originally thought. <\/span><\/p>\n<p><span style=\"font-weight: 400;\">Three days after birth, he was diagnosed with Hirschsprung\u2019s disease, an intestinal disorder, and had colostomy surgery at one week old to correct it. Due to the number of complexities that he had, we had some genetic testing done and found out that Edmund has an unbalanced translocation; he has an extra portion chromosome 7 and a partial deletion of chromosome 10. These unbalanced translocations, especially ones with a larger deletion like Edmund\u2019s, are very rare and usually quite severe. Even his geneticist was surprised at how well he was doing given his specific chromosomal condition. <\/span><\/p>\n<p><span style=\"font-weight: 400;\">And while Edmund definitely has some obstacles, he came home after a month in the NICU on absolutely zero medications.\u00a0<\/span><\/p>\n<p><span style=\"font-weight: 400;\">Edmund continued to thrive after coming home from the NICU for those next two months, but in November 2022, when he was around 4 months old, he came down with RSV, respiratory syncytial virus, and took a turn for the worse very quickly. He was hospitalized for three weeks in the PICU, spending two of those weeks on a ventilator because his lungs were so sick. On his worst day we were preparing ourselves with the possibility of saying goodbye to him when he spontaneously made a miraculous recovery and once again defeated the odds that were given to him. He came back home with us on December 8<\/span><span style=\"font-weight: 400;\">th<\/span><span style=\"font-weight: 400;\"> and has continued to thrive ever since.<\/span><\/p>\n<div id=\"attachment_289825\" style=\"width: 410px\" class=\"wp-caption aligncenter\"><img aria-describedby=\"caption-attachment-289825\" decoding=\"async\" loading=\"lazy\" class=\" wp-image-289825\" src=\"https:\/\/archive.liveaction.org\/news\/wp-content\/uploads\/2023\/04\/IMG_7372-525x700.jpeg\" alt=\"\" width=\"400\" height=\"533\" srcset=\"https:\/\/archive.liveaction.org\/news\/wp-content\/uploads\/2023\/04\/IMG_7372-525x700.jpeg 525w, https:\/\/archive.liveaction.org\/news\/wp-content\/uploads\/2023\/04\/IMG_7372-225x300.jpeg 225w, https:\/\/archive.liveaction.org\/news\/wp-content\/uploads\/2023\/04\/IMG_7372-768x1024.jpeg 768w, https:\/\/archive.liveaction.org\/news\/wp-content\/uploads\/2023\/04\/IMG_7372-500x667.jpeg 500w, https:\/\/archive.liveaction.org\/news\/wp-content\/uploads\/2023\/04\/IMG_7372.jpeg 1138w\" sizes=\"(max-width: 400px) 100vw, 400px\" \/><p id=\"caption-attachment-289825\" class=\"wp-caption-text\">Photo courtesy of Anna Denny<\/p><\/div>\n<p><span style=\"font-weight: 400;\">This past March, Edmund underwent mandibular distraction surgery to move his jaw forward and help with his breathing, and now we are preparing for his heart surgery this coming summer.\u00a0<\/span><\/p>\n<p><span style=\"font-weight: 400;\">And here we are at 9 months old and Edmund continues to be such a fighter! Through all of the trials that he has endured, he never fails to have a smile on his face and find joy in even the smallest things in life. <\/span><\/p>\n<p><span style=\"font-weight: 400;\">I feel blessed that God instilled in my husband and me the value of life no matter what sacrifices may come with it, and I\u2019m so thankful that we were not scared into thinking that abortion was our only option. God has allowed Edmund to be a source of inspiration to not only us, but also to his medical team and all of those who have followed on his journey. <\/span><\/p>\n<p><span style=\"font-weight: 400;\">I hope that Edmund\u2019s beautiful smile will show others that medical conditions do not mean \u201csorrow\u201d and that joy can be found in <\/span><span style=\"font-weight: 400;\">all<\/span><span style=\"font-weight: 400;\"> life, whether \u201chealthy\u201d or not.\u00a0<\/span><\/p>\n<p style=\"text-align: center;\"><strong><a href=\"https:\/\/give.liveaction.org\/general-donation\/?utm_source=lan&amp;utm_medium=display&amp;utm_campaign=monthly&amp;utm_content=article\"><i>Did you know that as little as $10 a month is enough to reach more than 3,000 people with the truth about abortion that no one else is telling them? Click here to start saving lives 365 days a year.<\/i><\/a><\/strong><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Disclaimer: The views and opinions expressed in this article are those of the guest author and not necessarily of Live Action or Live Action News. On February 10, 2022, my husband and I were told that our 13-week old baby had a 5% chance of survival due to a cystic hygroma, a build-up of fluid [&hellip;]<\/p>\n","protected":false},"author":934,"featured_media":289824,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"om_disable_all_campaigns":false},"categories":[7077,9455],"tags":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v20.7 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>We rejected abortion, and our son Edmund has been a blessing and an inspiration<\/title>\n<meta name=\"description\" content=\"We were given a very grim prognosis and were told abortion was an option, but we knew this baby had infinite value regardless of possible abnormalities.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" 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