Truth!My take on this will be different than perhaps expected. Please bear with me.
Let me start by saying this – I do NOT fault the doctor, and I don’t think much of the mother.
The doctor who said the Downs Syndrome baby was “perfect” likely will get sued – perhaps many times over – by parents who will say, truthfully, “he said our baby was perfect but in fact the baby had a serious genetic abnormality.”
- First off, doctors today practice defensive medicine. The doctor who “advised her to have an abortion” was likely required to tell her that, by the hospital; his insurer; or both, or at least to offer it as an option. Sometimes the law requires it (see below). Basically any pregnancy like this one requires the doctor to say what he said. Sad, but it’s reality. Could he have said it more gently? There’s no good way to say it.
- These days, “wrongful life” suits – where parents sue for the cost of lifetime care where the parents were not offered the choice to abort their baby – are all the rage, and lawyers love them because the damages can be astronomical.
Sorry to be harsh but mom had no business posting her letter on facebook.
- Would the doctor have said the baby was “perfect” if the baby had been born with a hole in his heart; encephalopathy; zika virus; or a million other conditions? Do we want our doctors to just routinely say every baby is “perfect,” no matter how ill the child is?
- If mom really wanted “closure,” she’d mail the letter and close it. Did she do that? *No, she posted it on facebook. * Worse, she didn’t even post it on her own page (that probably no one reads); she posted it on a third party page to get it read by others. She wanted “closure?” BUNK – she’s some nameless mom who wanted to be a story and is getting her 15 minutes of fame. I’m sorry, I see mom as being a publicity hound, and no one will care who she is tomorrow.
+1. Antics like this look good to the crowd, but have absolutely zip to do with the true pro-life movement, or the genuine difficulties faced by the parents of children with disabilities.Truth!
I fully agree with you on a middle ground. There should be no requirement on the part of doctors to advice abortion, and even if there is, doctors should not be craven enough to bow to it without any resistance.I like the letter. I don’t know of any state where doctors are required to tell women that they recommend an abortion. They SHOULD tell women if their child has Downs, but that doesn’t require hammering into them the idea that their child will have no quality of life and is better off dead. I might be coming at this from another angle, but I know of two poor, single mothers who were encouraged to abort by doctors who were flat out lying about the child’s condition. In one case, the mother was told the child’s organs were outside her body and she couldn’t survive birth. This was the story until the child was too old to be legally aborted in our state and then she suddenly made a miraculous recovery and her organs osmosized their way back into her rib cage. The ought to be some sort of responsible middle ground between insisting a mother off her own baby and lying about her child’s condition!
you may have your opinions about facebook, but I have had positive experiencesI fully agree with you on a middle ground. There should be no requirement on the part of doctors to advice abortion, and even if there is, doctors should not be craven enough to bow to it without any resistance.
I also agree that mothers who defy secular values and carry such pregnancies to term are a valuable witness to the pro-life movement and the sanctity of life, and they deserve nothing but praise.
However: a letter on Facebook? Facebook, the shrine of Internet drama and petty “social justice” wars? If this letter had gone to, say, Priests for Life (or the Protestant equivalent), and they’d published the testimony, this would carry more weight. I doubt Jesus or the Apostles or Saints would want to take part in Facebook, Twitter or Tumblr drama. That’s where she lost me.![]()
What? I don’t understand what you mean.+1. Antics like this look good to the crowd, but have absolutely zip to do with the true pro-life movement, or the genuine difficulties faced by the parents of children with disabilities.
“And it’s a hollow rebellion,
Like rebellions mostly are
It’s just another raging tempest
In a jar…”
(Thank you, Don Henley.)
When I had my last baby I was almost 40, so higher risk for Downs. My doctor was a prolife doctor, and would never recommend abortion.I like the letter. I don’t know of any state where doctors are required to tell women that they recommend an abortion. They SHOULD tell women if their child has Downs, but that doesn’t require hammering into them the idea that their child will have no quality of life and is better off dead. I might be coming at this from another angle, but I know of two poor, single mothers who were encouraged to abort by doctors who were flat out lying about the child’s condition. In one case, the mother was told the child’s organs were outside her body and she couldn’t survive birth. This was the story until the child was too old to be legally aborted in our state and then she suddenly made a miraculous recovery and her organs osmosized their way back into her rib cage. The ought to be some sort of responsible middle ground between insisting a mother off her own baby and lying about her child’s condition!
One of my sons had a soft marker for Down Syndrome and so I had a couple additional scans. I had a meeting with a geneticist and one of the first things she told me was that it was too bad they caught it so late or I could have “done something.” It was recommended that in the future I do genetics testing and earlier sonograms.When I had my last baby I was almost 40, so higher risk for Downs. My doctor was a prolife doctor, and would never recommend abortion.
I know similar stories. My cousin’ baby was supposedly suffering from dwarfism. He’s 13 now, he’s not very tall, but both his parents are not tall either. Yet they were told to consider abortion due to too many issues.![]()
I was agreeing with you and pointing out that this woman’s taking the issue to Facebook was not constructive.What? I don’t understand what you mean.
Because being able to use those 6 months or so to look for a more flexible and/or higher paying job, move closer to family that can help, seek out resources for special needs babies and their parents, etc is extremely beneficial for families.Why do pregnant mothers have to take the syndrome test if they plan to have the child anyway?
But I heard the tests aren’t 100% accurate. What’s the use of feeling worried throughout the remaining days of pregnancy because of a test result that might not be true when the child is born? After moving and changing course, what if the child is born healthy? In the end, wouldn’t it be better make any decisions after the child is born?Because being able to use those 6 months or so to look for a more flexible and/or higher paying job, move closer to family that can help, seek out resources for special needs babies and their parents, etc is extremely beneficial for families.
Even if a woman doesn’t plan on aborting, there are things that can be done to ease the burden of what’s to come.
But I heard the tests aren’t 100% accurate. What’s the use of feeling worried throughout the remaining days of pregnancy because of a test result that might not be true when the child is born? After moving and changing course, what if the child is born healthy? In the end, wouldn’t it be better make any decisions after the child is born?
You don’t have to take the test, and in many cases it is incredibly expensive. Our insurance covered it if I was over the age of 35, but since I am not, the blood test would have cost us about $3000.Why do pregnant mothers have to take the syndrome test if they plan to have the child anyway?
Without going too far into banned “medical advice”; not all prenatal screening is the same. Many of the prenatal blood tests done in early pregnancy are indeed far from 100% accurate. But a karyotype from amniotic fluid showing an extra 21st chromosome, or an ultrasound showing a child is missing most of the brain, are far more accurate.But I heard the tests aren’t 100% accurate. What’s the use of feeling worried throughout the remaining days of pregnancy because of a test result that might not be true when the child is born? After moving and changing course, what if the child is born healthy? In the end, wouldn’t it be better make any decisions after the child is born?