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Aborting Imperfection

Modern technology brings diagnoses earlier–even in the womb. In the U.S., that means that 90% of children with Down’s Syndrom are aborted thanks to amniocentesis. In this UK example, a child diagnosed via ultrasound with Spina Bifida was aborted [WARNING: this is very disturbing]. His mother’s experience is what follows:

Yet if making that choice was hard, the physical ordeal was only just beginning. At 18 weeks pregnant, I was too far gone for a surgical termination and would have to go through a labour and delivery, under the care of midwives at our local hospital.

The first step was to take the drug Mifepristone to block progesterone, a hormone vital to pregnancy. I swallowed the pill in a side room on the labour ward — the same room where I’d given birth to our younger daughter two years previously.

Over the two days that followed, I fought the urge to put my hands on my stomach when I felt the baby move. Knowing that he was slowly dying inside me was the very definition of hell.

After two days, I returned to the same room to take a second drug to induce labour.

What followed were the worst 16 hours of my life. They passed in a morphine-induced haze, but there was no dulling what was happening.

My baby was being forced into the world long before he could survive in it, and it felt unnatural — completely at odds with my instincts as a mother. My body seemed to be doing all it could to hold onto him, and the labour went on and on.

At one point, in the grips of what felt like a panic attack, I became hysterical. Gasping for breath and screaming, I demanded that Andrew tell me why we were doing this and why it was the right thing for our son.

What follows is her husband’s, her doctor’s, her family’s rationalization for aborting a baby that would have a difficult life.

Reading this sickens me. My own son was born severely premature and ended up with the diagnosis of autism. He was on medications, oxygen, etc. when he came home from the hospital four months later after surgeries and fears including blindness, palsy, mental retardation. We didn’t know what we’d end up with. For that matter, we still don’t know our son’s ultimate path.

You might think that makes me condemn this family for their decision to abort their baby. No. I’m too crushed to cast stones.

Their decision to abort is utterly, completely, and frightfully hopeless. There is no room for God. There is no room for hope. There is no room for the expansion of human frailty. And by frailty, I’m not talking about the disabled child, I’m talking about the parents–their selfishness, weakness, limitations of spirit. By aborting him, they’ll never fully know what they’re capable of as people.

I think about my own walk–parenting my son. The limitations, I can assure you, are mine, not his. My humor, my patience, my vision, my work-ethic are non-stop challenged and unfortunately, I fall short embarrassingly often.

Just when I think I’m going to lose it, there’s a break-through. I’ve had to expand beyond my pathetic, small, inwardness. My judgmental nature? Well, it’s still there, but the wings have been clipped. Cavalier condemnation, so easy for someone who has had the bramble-free path, that’s gone by the wayside, mostly. Thankfully.

My son loves professional wrestling. This family who aborted their son–what loves did they extinguish? What unique personality and hopes and dreams were killed when he died? And really, who are they to decide that this child’s future, as different as their own might be, is unworthy?

Parents who are able-bodied and minded project their own expectations for life on a disabled child. And while all parents do that with all their children, kids turn out to be their own people. They end up having their own hopes, dreams and ideas. The same is true for a disabled child.

How is it fair to take away that will from a child?

When we get pregnant, as ironic as it is, we relinquish control over our own lives and submit to the hopes and desires of this other life force. We spend the rest of our days negotiating this paradox. We expand our own world by making room for another person’s world. And we often do that by pruning parts of our world that we thought we needed to survive. We die a little so another can live and in the process, we live more.

As this family sees their able-bodied children grow up, they’ll see the fallacy of their thinking. I hope. It might be painful to see. Still, in front of them, if they have the eyes to see, they’ll witness a unique being straining to be his or her own person. They’ll realize how little control they have. They’ll realize that their own decision at the start most certainly began something that is now not theirs.

And for all their careful planning and protection, tragedy will strike. Evil befalls us all.

In some ways, I think abortion, just like the technology that prompted this family to abort their child, foists the illusion of control over life. As if by aborting the baby, the parent now has perfect control over her life. Life will be good, easier, better, more pleasant…guaranteed.

What if one of their children becomes paralyzed in a car accident (heaven forbid), for example? Is this child better off dead? And what do they tell this survivor about the worth and meaning of his life? How about people who sacrifice a limb for their brothers on the battlefield? Another meaningless life? How about the elderly parent with full faculties but incapacitated due to ALS or some other degenerative disease?

What life is worth living and who gets to decide this for someone else? Do these parents feel comfortable with their children making the decision to “abort” them when they reach an age where they’re no longer deemed useful…to the children? Maybe their children will project their ideas about living with deafness or blindness or incontinence or immobility or pain or paralysis and decide, prematurely, to end mom or dad’s life. Is their reasoning any different?

This callous disregard for the imperfect life rests on the premise that there’s a perfect life. Anyone who has done much living knows that’s not true. There are many shades of gray on the scale of life and value.

That’s why life, all life, must be honored and protected. That’s why we’re so careful about meting out justice. Life is valuable. To snuff it out is to end a potentiality and no one can know where a life will go or what an individual’s purpose on this earth is.

The family that aborted their eighteen-week gestated baby were surrounded by friends, family, doctors who all advised them to abort. This wasn’t just an individual or family decision, it was a societal one.

What have we become that this decision was encouraged?

That’s a question for another post. Today, it’s enough to grieve for the life of a boy with Spina Bifada who was killed inside the womb “for his own good.” It is a tragedy of epic and personal proportions. Who knows who the world is missing because he’s not here.

George. His name is George.

COMMENTS

  • bcochran1981

    5′s across the board, but I just can’t. Not on this topic. A splendidly written article. But just absolutely crushing and horrifying.

  • earlgrey

    affect how she parents her living children?

    What kind of after care do the pro-aborts give to women that have had their babies killed inside of them?

    • bassethound

      other than telling her to post cute little “angel baby” justifications of her aborted child, free from his imperfections, playing in Heaven.

      Or worse, they might tell her to suck it up and move on with her life.

  • Jim Tomasik

  • Uma Richie

    Your response to a mother killing her beautiful fetus is good judgment. Pro-abortion forces want to make us feel judgmental and censor ourselves, because its not nice to be judgmental; however, exercising good judgment and offering counsel to those in error may be the most merciful thing a person can do.

    Thank you for this diary.

  • momma

    This baby was killed for the parents’ own good, as they perceived it at the time. I’m sorry for them, because they have no idea of the regret they will carry in their hearts for the rest of their lives, whether or not they acknowledge it. I’m sorry for their remaining children, their extended family, and their community.

    Thanks for writing this.

  • http://theminorityreportblog.com Repair_Man_Jack

    No one is ever quite perfect, unless they are exactly like me…

  • http://www.sunshinestatesarah.com SunshineStateSarah

    “George. His name is George.”

  • phlogiston

    … that this decision was encouraged?”

    That’s simple.

    We have become a people willing to countenance unspeakable evil in the name of creating “perfect” people.

    We have become the people the “greatest generation” fought against.

    We have become Nazis.

  • TopGun

    We have become a nation who has allowed the Communists [Progressives] to demonize Christians who worship God to the point to where it is looked at as not

  • melissatx

    becuase at 38 I was pregnant and too old. Hey, don’t think we tried and tried and tried, but gave up, at 38 when it happened and was totally unplanned there was NO way I was going to allow the insurance company or any one else to mess with it. After the genetics testing and the “could be this could be that” song and dance I told the gentecists that all they could do was guess while God knew what the real deal was. I was baking on God being smarter than them all.

    I am happy to report that my 6 year old has no problems, but even if she did God’s will would have superseded anything they had to say about it. My husband was scared, however, my feeling is that whatever will be will be and your character is formed when deal with adversity head on. I didn’t hide from it, but I was not about to allow someone else to frame my life, our my daughters.

    This is the same tact we should take with those who invoke the ghoulish spirit of Margaret Sanger and/or propose eugenics as “sound policy.”

    In the meantime, if eugenics was in play, I would not get to have that good horse laugh with Dad, who has ALS, after testing out his new ALS mobility chair and he ran THROUGH the wall.

  • rogershru2

    When they say [insert govt healthcare program] will not cover abortions. “medically necessary” now includes those with known or suspected birth defects if they are bothersome to the mother. Also, if the mother simply does not want the baby, they may have “clinical depression” that makes the abortion “medically necessary.”

  • rightwingmom52

    I daresay her hours pale in comparison to George’s.

    I grieve for a world that will never meet George or the millions of other aborted babies, but not for George for he has a glorious and eternal life in heaven.

    Thank you for another well-written diary and for sharing some of your personal trials with us. May God bless you and your family.

  • mkozikowski

    since 1970.

    That is THE Human Tragedy.

  • Jewels

    try to talk you into something that your gut is telling you is morally wrong, than maybe that’s because you’re doing the wrong thing.

    Good decisions never require a committee to convince you. You know already what is right.

  • dmacleo

    and I am teared up over george.

  • danielsmum

    My little boy has Spina Bifida and like the mother above, we
    found out at 20 weeks gestation. Was I upset, confused,
    thrown into a world where medical expectations and prognosis
    were all extremely negative, absolutely yes but we carried
    on and what a gift we have been given. He is the apple of
    our families eye, bright, happy always into mischief. Will
    he use a wheelchair for mobilty, potentially yes, but what
    is the big deal about this – its just a tool, no more or
    less than a car is for me. Will he have control of his
    bladder and bowels, maybe, too early to tell, but whether he
    does or not doesn’t diminish who he is, or who he will be. A
    Spina bifida diagnosis is just the beginning of a wonderful
    journey and opportunity to learn more than you ever thought
    you might about something different, meet some wonderful
    caring people that you otherwise might not meet and in doing
    so make lifelong friends and contacts. Have there been times
    in the last two years when I have reached the end of myself,
    absolutely yes, I would be untruthful if I said this was an
    easy journey. Having a special needs child demands more from
    us all, love, goodness, patience, self control, advocacy,
    growth. Are we better off for the experience – absolutely
    yes and I would encourage any mother (or family for that
    matter) faced with a Spina bifida diagnosis to give
    themselves room – room for growth, potential and for
    achieving more than they ever thought possible. Do I love my
    little boy with Spina bifida – absolutely yes. He is my
    heart expanded.

  • bassethound

    of callous disregard for the disabled, a British “advice columnist” advocated that suffocating a “suffering” infant is an act of “kindness”. Disabililty rights activists were appalled.

    After all, what is “suffering”? A disability diagnosed after birth, such as autism? A high fever infants sometimes spike for no good reason? Or the fact that maybe the woman finds that motherhood isn’t all about gaining unlimited attention from a cute little goo-goo doll, and objects to the demands caring for a dependent human being places on her lifestyle.