{"id":156858,"date":"2016-11-20T09:32:03","date_gmt":"2016-11-20T14:32:03","guid":{"rendered":"\/news\/?p=156858"},"modified":"2016-11-17T13:47:41","modified_gmt":"2016-11-17T18:47:41","slug":"in-pursuit-of-perfection-will-we-sacrifice-what-it-means-to-love","status":"publish","type":"post","link":"https:\/\/archive.liveaction.org\/news\/in-pursuit-of-perfection-will-we-sacrifice-what-it-means-to-love\/","title":{"rendered":"In pursuit of perfection, will we sacrifice what it means to love?"},"content":{"rendered":"<div style=\"margin-top: 0px; margin-bottom: 0px;\" class=\"sharethis-inline-share-buttons\" ><\/div><p>(<a href=\"https:\/\/savethestorks.com\/2016\/11\/ethical-view-life\/?utm_source=Facebook\">Save the Storks<\/a>)\u00a0In April of 2003, Dr. Francis Collins announced the completion of the Human Genome Project. As a result, advances in science and healthcare have progressed with lightning speed.<\/p>\n<p><b>The promise of the genomic era is here, and with it comes a growing plethora of ethical challenges.<\/b><\/p>\n<p>Genetic tests are developing rapidly and are helping to identify gene mutations that increase the risk of hereditary diseases. Along with improvements in genetic testing and increased knowledge of the complexity of DNA, researchers are identifying ways to predict, prevent and individualize treatments for many individuals who test positive for high risk mutations. In my specialty of hematology\/oncology (cancer and diseases of the blood), we are able to identify individuals with hereditary hemochromatosis (a hereditary disorder that results in iron depositing in abnormal amounts that can lead to organ damage or diabetes), or individuals who are at high risk of developing breast cancer due to mutations in the\u00a0<i>BRCA1<\/i>\u00a0genes.<\/p>\n<p>In situations where hereditary disorders like these two are identified, healthcare providers can incorporate early screening, patient education, or, in some cases, initiate preventative interventions. For example, Angelina Jolie made headlines in 2015 when she decided to have surgery to reduce her chances of developing breast cancer. After losing her mother at a young age to ovarian cancer, Ms. Jolie found she carries a mutated copy of the\u00a0<i>BRCA1\u00a0<\/i>gene. Women who carry this mutation have a 60-90% chance of developing breast cancer, and a 40-60% chance of ovarian cancer.<\/p>\n<p><b>So what does this have to do with reproductive politics?\u00a0<\/b>A lot. You see, just as there are more advanced genetic tests in areas like blood disease and cancer, there are more advanced genetic screening panels in the prenatal setting as well. Genetic panels can detect not only Trisomy 21 (Down syndrome), but also Trisomy 18 (Edwards Syndrome), Trisomy 13 (Patau Syndrome), cystic fibrosis, fragile X, and a multitude of sex chromosome abnormalities.<\/p>\n<div class=\"ArticleAd1\">\n<p><!-- \/1011927\/LAN_300_by_250_top_article --><\/p>\n<div id=\"div-gpt-ad-1473179053567-0\" class=\"ArticleAd1a\"><script>\ngoogletag.cmd.push(function() { googletag.display('div-gpt-ad-1473179053567-0'); });\n<\/script><\/div>\n<\/div>\n<p><b>These issues are difficult, emotional, and are fueling the debate to once again liberalize abortion.\u00a0<\/b>Needless to say, Planned Parenthood is seizing this opportunity. And thus the issue of reproductive politics. How we as a society understand and respond to prenatal screening for potential genetic disorders or disabilities, will define our humanity (our compassion and dignity).<\/p>\n<p><a href=\"http:\/\/www.cnsnews.com\/news\/article\/eugenic-abortion-pre-natal-testing-9-10-down-syndrome-babies-aborted\">\u201cEugenic Abortion\u201d<\/a>\u00a0is a term used for justifying abortion rather than bringing children into the world with disabilities. Advocates would argue that life with a disability is not in the best interests of the newborn, the parents, or society. They would say abortion is the acceptable option (if not the only option) when social, emotional and health care costs are deemed too high. Genetic testing will also open the door for abortions based on race, gender, or other attributes the expectant parents deem less than desirable.<\/p>\n<p><i>\u201cOn the issue of abortion, the feminist and disability rights movement often come into uncomfortable conflict as they struggle to accommodate both the rights of a woman to control her own fertility and the rights of people with disabilities to exist.\u201d<\/i>\u00a0\u00a0<a href=\"http:\/\/www.huffingtonpost.com\/entry\/zika-virus-us-abortion-disability_us_56b2601be4b04f9b57d83192\">Chloe Angyal<\/a><\/p>\n<p><i>\u201c\u2026as prenatal tests become available for a range of other perceived genetic imperfections, they may also be heralding a broader cultural skirmish over where to draw the line between preventing disability and accepting human diversity\u201d. \u00a0<\/i><a href=\"http:\/\/www.nytimes.com\/2007\/05\/09\/us\/09down.html\">Amy Harmon<\/a><\/p>\n<p><b>If we purge society of those who do not meet our standards, weed out the imperfect to design a perfect human race, we will sacrifice what it means to love, we will place compassion on life-support, and in the end we will sacrifice freedom.<\/b><\/p>\n<p><img decoding=\"async\" loading=\"lazy\" class=\"aligncenter size-large wp-image-97649\" src=\"\/news\/wp-content\/uploads\/2016\/07\/down-syndrome-3-700x467.jpg\" alt=\"down-syndrome-3\" width=\"700\" height=\"467\" srcset=\"https:\/\/archive.liveaction.org\/news\/wp-content\/uploads\/2016\/07\/down-syndrome-3-700x467.jpg 700w, https:\/\/archive.liveaction.org\/news\/wp-content\/uploads\/2016\/07\/down-syndrome-3-300x200.jpg 300w, https:\/\/archive.liveaction.org\/news\/wp-content\/uploads\/2016\/07\/down-syndrome-3-768x512.jpg 768w, https:\/\/archive.liveaction.org\/news\/wp-content\/uploads\/2016\/07\/down-syndrome-3.jpg 1000w\" sizes=\"(max-width: 700px) 100vw, 700px\" \/><\/p>\n<p>Already in Oregon, where Physician Assisted Suicide is legal, Medicaid does not cover a variety of important treatments, but will pay for assisted suicide. It is not unperceivable that at some point Medicaid or insurance companies may decline to cover health care for those diagnosed with disabilities in utero, but instead will cover Eugenic abortions.<\/p>\n<p><b>So, now what? \u00a0How should we respond?\u00a0<\/b><\/p>\n<p><b>First,<\/b>\u00a0we must educate ourselves to understand the issues and speak truth into our culture, with wisdom, conviction, compassion, and insight. We must be the voice to frame the issues and the force to prevent further societal harm.<\/p>\n<p><b>Second,<\/b>\u00a0we must not let Planned Parenthood take the lead in these situations. In cases where deformity is suspected, an abortionist should be required to refer the woman to an OB-GYN physician, or a High-Risk pregnancy OB-GYN specialist. The abortionist should not be the one to decide or recommend an abortion.<\/p>\n<p>Planned Parenthood should never be the one to offer genetic testing.\u00a0These tests should be ordered by an OB-GYN specialist, or in some cases by her primary provider, in collaboration with a Genetic Counselor. Planned Parenthood has already shown their \u201cinformed consent\u201d was used to coerce women to have an abortion and that they have a profit motive. OB-GYN specialists, especially those who care for High-risk pregnancies, are equipped to offer early diagnosis and support. They are also equipped to have honest candid conversations, while often other healthcare providers or abortionists tend to present information as \u201cbad news\u201d and be biased to abortion as the only option.<\/p>\n<p><b>Third,<\/b>\u00a0the Genetic Information Act of 2008 (GINA) and the Americans with Disabilities Act (ADA) offer protection for those with genetic mutations and\/or disabilities; however, there is yet to be any protection for the unborn. We should support efforts to protect the unborn with disabilities.<\/p>\n<p>Finally,\u00a0the Pro-life community needs to work to ensure that there are resources to help expectant parents, whose unborn child has tested positive for a genetic mutation or disability, have the community support they need, including: support groups, counseling, insurance or financial assistance. We need to be there for them, to partner with disability support organizations to<br \/>\nadvocate for them. Otherwise we fail them during one of the most difficult times in their life.<\/p>\n<p>This is what it means to love.<\/p>\n<div class=\"ArticleAd2\">\n<p><!-- \/1011927\/LAN_300_BY_250_mid_article --><\/p>\n<div id=\"div-gpt-ad-1473179101244-0\" class=\"ArticleAd2a\"><script>\ngoogletag.cmd.push(function() { googletag.display('div-gpt-ad-1473179101244-0'); });\n<\/script><\/div>\n<\/div>\n<p>I close with a quote from Chuck Colson (former presidential aide to Richard Nixon, founder of Prison Fellowship and the Colson Center for Christian Worldview) whose grandson, Max, has autism.<\/p>\n<blockquote><p>\u201cMax forces us to raise the most important question of our age. What does it mean to be human? \u00a0If the geneticists and \u2018science for science\u2019s sake\u2019 crowd were to have their way, we would weed out the unfit and create the perfect human race by infanticide, euthanasia, or, eventually, genetic engineering.<\/p>\n<p>But what would happen to our humanity? Gone would be many of the problems and ailments \u2013 that\u2019s true. \u00a0But also gone would be the trials that shape our character \u2013 and inevitably our freedom would disappear. \u00a0For to be perfect and live problem-free in a fallen world is to be a slave to whomever makes you that way. \u00a0And if we, as creatures, were perfectly programmed by our genes, we would be stripped of the capacity for genuine love, which by its very definition must be an act of free will. \u00a0Love goes to the very essence of being a Christian, indeed of being human\u2026Real love is refined through pain and suffering.\u201d<\/p><\/blockquote>\n<p><em>Editor&#8217;s Note: This article was originally published at <a href=\"https:\/\/savethestorks.com\/2016\/11\/ethical-view-life\/\">Save the Storks<\/a> on November 11, 2016, and is reprinted here with permission.<\/em><\/p>\n","protected":false},"excerpt":{"rendered":"<p>(Save the Storks)\u00a0In April of 2003, Dr. Francis Collins announced the completion of the Human Genome Project. As a result, advances in science and healthcare have progressed with lightning speed. The promise of the genomic era is here, and with it comes a growing plethora of ethical challenges. Genetic tests are developing rapidly and are [&hellip;]<\/p>\n","protected":false},"author":440,"featured_media":98721,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"om_disable_all_campaigns":false},"categories":[7],"tags":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v20.7 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>In pursuit of perfection, will we sacrifice what it means to love?<\/title>\n<meta name=\"description\" content=\"If we purge society of those who do not meet our standards, weed out the imperfect to design a perfect human race... in the end we will sacrifice freedom.\" \/>\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\/in-pursuit-of-perfection-will-we-sacrifice-what-it-means-to-love\/\" \/>\n<meta property=\"og:locale\" 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Smith, RN, MSN, ACNP, AOCN, has worked in the medical field for over 30 years, specializing in hematology\/oncology. She has published within her profession in both text and peer reviewed journals. She has also been a speaker on the state and national level addressing issues pertinent to hematology\/oncology nursing, and advocacy for her patients and profession. Through advances in genetics, cellular\/molecular and imaging technology (e.g. ultrasound, MRI, CT scanning) in treating cancer, Wendy has gained knowledge and insight into life from stem cells, conception, the embryo and throughout the trajectory of life. Over the years Wendy has volunteered with pregnancy centers, the Navigators, and Prison Fellowship. She has a passion to address pro-life issues from the perspective of a health care provider and science. She understands that \u201cScience is on the side of life\u201d. Wendy is married to her best friend, Fred. Fred and Wendy enjoy living in Colorado Springs close to their daughter, Sarah, son-in- law, John, and three granddaughters, Abigail, Anna, and Ali Stonestreet. Psalms 71:18 \u201cEven when I am old and gray, do not forsake me, my God, till I declare your power to the next generation, your mighty acts to all who are to come.\u201d (NIV)","url":"https:\/\/archive.liveaction.org\/news\/author\/wendy-smith\/"}]}},"_links":{"self":[{"href":"https:\/\/archive.liveaction.org\/news\/wp-json\/wp\/v2\/posts\/156858"}],"collection":[{"href":"https:\/\/archive.liveaction.org\/news\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/archive.liveaction.org\/news\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/archive.liveaction.org\/news\/wp-json\/wp\/v2\/users\/440"}],"replies":[{"embeddable":true,"href":"https:\/\/archive.liveaction.org\/news\/wp-json\/wp\/v2\/comments?post=156858"}],"version-history":[{"count":2,"href":"https:\/\/archive.liveaction.org\/news\/wp-json\/wp\/v2\/posts\/156858\/revisions"}],"predecessor-version":[{"id":156860,"href":"https:\/\/archive.liveaction.org\/news\/wp-json\/wp\/v2\/posts\/156858\/revisions\/156860"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/archive.liveaction.org\/news\/wp-json\/wp\/v2\/media\/98721"}],"wp:attachment":[{"href":"https:\/\/archive.liveaction.org\/news\/wp-json\/wp\/v2\/media?parent=156858"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/archive.liveaction.org\/news\/wp-json\/wp\/v2\/categories?post=156858"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/archive.liveaction.org\/news\/wp-json\/wp\/v2\/tags?post=156858"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}