{"id":308140,"date":"2024-03-06T14:31:32","date_gmt":"2024-03-06T20:31:32","guid":{"rendered":"https:\/\/www.liveaction.org\/news\/?p=308140"},"modified":"2024-03-07T10:38:04","modified_gmt":"2024-03-07T16:38:04","slug":"killing-preborn-second-trimester-inspiring-state-union","status":"publish","type":"post","link":"https:\/\/archive.liveaction.org\/news\/killing-preborn-second-trimester-inspiring-state-union\/","title":{"rendered":"Killing second-trimester preborn babies to be presented as ‘inspiring’ at State of the Union"},"content":{"rendered":"
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Set to attend the State of the Union on Thursday is Kate Cox, upon the invitation<\/a> of First Lady Jill Biden. Cox sued the state of Texas for the right to kill her preborn child who was diagnosed with Trisomy 18 \u2014 a genetic condition that is considered<\/a> “life-limiting” but not fatal. She lost that legal challenge and ultimately had a D&E dismemberment abortion in New Mexico. Austin Dennard will reportedly also be present; she starred in a Biden campaign ad, and aborted a child with anencephaly<\/a>.<\/p>\n

Also set to attend upon the invitation<\/a> of U.S. Senator Patty Murray (D-Wash.) is Kayla Smith, a woman who traveled from Idaho to Washington to have a second-trimester abortion in 2022. Murray believes Smith has an “inspiring” story because of her determination to end her son’s life by abortion.<\/p>\n

Notably\u00a0not<\/em> invited to the State of the Union on Thursday are women who chose life for their babies after receiving a prenatal diagnosis, including Elisabeth Scott, whose daughter Brianna is four years old with Trisomy 18, and Alyse Schwartz-Mosca, whose son Ellis underwent heart surgery. These are the women who, when faced with a prenatal diagnosis, acted heroically to fight for the equal dignity and treatment of their children.<\/p>\n

Operable or inoperable?<\/strong><\/p>\n

In Kayla Smith’s case, she was expecting her second child with her husband James when they learned at a routine ultrasound at 18-20 weeks that their preborn son, Brooks, had two heart defects. The diagnosis came just two days after Idaho’s pro-life trigger law took effect. It is unclear if Brooks had additional diagnoses, though KTVB<\/a> reported he had “several fetal anomalies, including serious heart defects.” James told KTVB, “Based on what they were saying, it wasn’t going to be operable. So told it’s not operable, no choice is easy going forward.”<\/p>\n

But the two heart conditions the Smiths’ son had \u2014 based on those listed by Murray \u2014 are described as operable<\/em>.<\/p>\n

Murray claimed Brooks had critical aortic stenosis (CAS) and hypoplastic left heart syndrome (HLHS). According to The Mayo Clinic<\/a>, “Children with hypoplastic left heart syndrome will likely need several surgeries. … The procedures are done in three stages.” Live Action News recently<\/a> reported<\/a> on two young men<\/a>, Seth and Tate, who were born with HLHS and are now successful college students with promising futures.<\/p>\n

\"Credit:

Walter Joshua Fretz<\/a>, who was miscarried 19 weeks. Credit: Lexi Fretz & F2 Photography<\/p><\/div>\n

As for CAS, according to the National Institutes of Health<\/a>, “Among Symptomatic patients, the guidelines recommend aortic valve intervention prior to major non-cardiac surgery because of …. improved rates of long-term overall success.” According to Johns Hopkins<\/a>, in cases of congenital CAS, what’s known as the Ross procedure, can be carried out, in which the surgeon removes the abnormal aortic valve and replaces it with the child’s pulmonary valve. A donor valve is used to replace the pulmonary valve.”<\/p>\n

But this is not the only treatment option. Johns Hopkins reports that CAS is often present with other types of heart defects (as in Brooks’ case) but, “Most children do well with the Ross procedure.”<\/p>\n

Ellis Schwartz-Mosca also had aortic stenosis. Live Action News shared<\/a> his story recently, explaining that in 2019, Ellis was diagnosed at 20 weeks via ultrasound and underwent heart surgery at just a few days old. He became the recipient of the world’s smallest mechanical heart valve. Until a few years ago, that tiny valve hadn’t even been developed yet. \u201cHe\u2019s doing amazing. He\u2019s chatty all the time,\u201d said Ellis’s mother, Alyse.<\/p>\n

Willing to take the risk for a healthy baby?<\/strong><\/p>\n

Regardless of the available treatments, the Smiths moved forward with an abortion ultimately because, in addition to Brooks’ diagnoses, Smith had previously developed preeclampsia during her first pregnancy with their daughter, and was worried<\/em> she might develop it a second time. However, that concern always existed \u2014even when she believed Brooks to be “healthy.”<\/p>\n

It was only after his diagnosis that she ultimately decided the risk of possibly developing preeclampsia was not worth her son’s life.<\/p>\n

At 21 weeks, the youngest age at which children have survived preterm birth, the couple traveled (and eventually moved) from Idaho, where most preborn children are protected from abortion, to neighboring Washington state for an induction abortion. They claim they were “forced” to do so by Idaho’s pro-life law. Logic would dictate that no one was forced<\/em> to kill a yet-living child.<\/p>\n

During an induction abortion, a feticide is injected into the heart or head of the preborn child and he is then delivered prematurely. If he manages to survive the feticide, to ensure he does not survive long after birth, he may be denied medical care at the parents’ request \u2014 despite the fact that this is technically illegal. The goal<\/em> of the induction abortion was to ensure Brooks did not survive<\/em>.<\/p>\n

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