Doctors tell woman to abort, but her baby is born healthy

Linda Serrano, of Bakersfield, CA tells her story:

“I received a German measles shot two weeks before I got pregnant with my first child. I called three doctors, and none of them would accept me as a patient. They all wanted me to get an abortion. I went to a fourth doctor, and she also advised me to have an abortion, that my chance of having a healthy baby was 0%. When I told her no, she said, ‘Well then you will have a deformed baby, and you’d better tell your husband.’ I was in tears by this time. My husband said, ‘God loves all people the same. Then I asked God to have mercy on us, and heal my child. I told Jesus that if He didn’t, that would be okay, because I knew He would be in control. I would love my baby no matter what. “I’m very happy to say that my baby girl, Angela, is perfectly healthy! While the doctor was stitching me up, she said I still should have had an abortion!”

Melody Green “The Questions Most People Ask About Abortion” Last Days Ministries

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Doctors pressure mother to abort her child

Monique tells her story:

“My husband and I found out we were expecting our first baby and we were thrilled. The day came for our 20 week scan, but after the ultrasound we were just left to wait.

After several hours of delay, we were finally taken to see a doctor. They said outright – “There are issues with your baby’s head and heart; would you like to terminate the pregnancy?”

Just like that; no warning, no leading up to it, no more information than “issues” just “your baby’s not perfect, do you want to abort them?”

I was in shock, I couldn’t answer; this morning we were coming to find out what we were having and now you want to kill my baby? We didn’t even find out if it was a boy or a girl.

When I could speak again I said “No, we don’t want to do that” and we were given a referral to see a specialist.

When we saw the specialist, he also asked me straight up – “Do you want to terminate the pregnancy?” I answered “No! We told the doctor on Friday we don’t want to. That’s why we’re here.”

He completely ignored my ‘no’: “You can do it easily for the next four weeks so you have to decide before then. It gets a lot harder but don’t worry, we can still do it.” For a third time I said “No. We’ve already decided.”

He ignored me and said, “I can refer you to Brisbane but it will be stressful and expensive so are you sure you don’t want to terminate the pregnancy?”

By this point I was in tears. I sobbed “I want to do everything we can for our baby,” and after ignoring us 3 times, the nasty doctor finally rang the Mater Mothers Hospital in Brisbane.

We were squeezed in for an appointment that evening where we were told that our darling child had a perfect little heart and that we were having a baby girl.

A few weeks later we hit 24 weeks. I was so inexplicably glad now that it was “much harder” to kill my baby. She was loved from the moment I saw those two pink lines and to be asked 4 times in 4 days, with three of those being in a row, if I wanted to terminate my child was the worst thing that had happened to me up to that point in my life.”

Women’s Stories” Abortion Rethink

Visited October 3, 2018

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Woman says why she would abort child with down syndrome

Mary Ann Bailey, saying why she would have an abortion if her baby tested positive for down syndrome:

“Given a choice, I would rather my child did not have a disability. That’s all.”

Mary Ann Bailey “Why I Had Amniocentesis” in E Parens and A Asch (eds.) Prenatal Testing and Disability Rights (Washington, DC: Georgetown University Press, 2000) 68

Bailey also says that a child born with down syndrome will have “potentially significant limitations” (66) and that even though families with down syndrome children tend to function well, “life will still be more difficult” for her and her family (70).

Quoted in Chris Kaposy Choosing down Syndrome: Ethics and New Prenatal Testing Technology (Cambridge, Massachusetts: The MIT Press, 2018)

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Mother calls daughter with Down syndrome ‘closest thing to an angel’

Michele Harmon wrote about her child with Down syndrome in her essay, “The Most Beautiful Face on Earth.”

Ciarra attends a regular preschool program, she was potty trained before she was three, and is a very independent little kid. She is funny and spirited, stubborn and witty. She whistles little songs all day long. She idolizes her big brother. She loves to draw and can put all the details into a drawing of a face.

At five years old, this child they told me would be so unworthy of life, such a burden, has defied all predictions. She is in a mainstream kindergarten class where she holds her own nicely and is doing most things like any other child her age. Letters and words seem to be her strength.

She has so many friends that sometimes we get tired of dragging her to play dates and parties… All those worries I had about kids shying away from her have turned out to be the exact opposite. She is like a magnet.… Her teachers have fallen in love with her. Many of them were afraid of Down syndrome before… now they are like me, grateful for the opportunity to know her. She continues to touch people with her sweetness and surprise them with her ability. Ciarra is a little girl who has been the best teacher that I can ever imagine having. She is a joy like no other….

She seems to have a way with people that I have never seen before. I wonder if it is her cheerfulness or her simple joy in everything.…

Maybe someday it won’t be so scary to have a child with Down syndrome.Maybe someday 95% of her peers will not be eliminated.… I am blessed beyond words by this little girl. That blessing seems to know no end, it grows and grows and fills my heart daily. People may ask if it’s hard to have a kid like her. I wish they could know the truth. Sure, there are days I get tired. She asks a lot of questions, and she is in perpetual motion. But I wouldn’t trade her for the world…

She is the closest thing to an angel I will ever see.

Melinda Tankard Reist Defiant Birth: Women Who Resist Medical Eugenics (North Melbourne, Australia: Spinifex, 2006) 283 – 285

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Mother of daughter with down syndrome speaks out

Patricia E Bauer, whose daughter Margaret has down syndrome:

“Prenatal testing is making your right to abort a disabled child more like “your duty” to abort a disabled child.”

Patricia Bauer “The Abortion Debate No One Wants to Have” Washington Post October 18, 2005

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Woman who aborted down syndrome baby: “The psychological pain is enormous”

Rayna Rapp, who aborted her baby because the child had down syndrome:

“The psychological pain is enormous. Deciding to end the life of a fetus you wanted and carried for most of five months is no easy matter. The number of relatively late second trimester abortions performed for genetic reasons is very small. It seems an almost inconsequential number, unless you happen to be one of them.”

Quoted in Anna Bonavoglia The Choices We Made: 25 Women and Men Speak out about Abortion (New York: Random House, 1991) 160

5 months
5 months
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Father of down syndrome child speaks

Chris Kaposy, who is pro-choice but has written a book on why parents shouldn’t choose to abort babies after finding out they have down syndrome, talks about his own son, Aaron:

“At seven, Aaron is a happy little kid who enjoys playing ball hockey, watching YouTube videos, playing with his train set, and learning how to read. Aaron is especially devoted to his older sister, Elizabeth, and his younger brother, Ty. He looks forward to visits from his grandparents, and he misses them when they are not around. I put him to bed at night and get him ready for school in the morning. When I leave the house with him or walk him into school, Aaron dutifully holds my hand. At midday, Aaron eats lunch with his friends at school. To our surprise, he has learned his letters and the alphabet about as quickly as Elizabeth did, though he takes longer to learn other things, such as how to drink milk from an open cup without spilling it all over himself. In all these respects, Aaron is very much like most other children who do not have a disability. He is good at some things and not so good at others. Our lives are better with him here with us. Our feelings toward Aaron are very similar to feelings that parents and siblings have to any child who does not have a disability. I know this because I feel the same way about Elizabeth and Ty.”

Chris Kaposy Choosing down Syndrome: Ethics and New Prenatal Testing Technology (Cambridge, Massachusetts: The MIT Press, 2018) X – Xi

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Worldwide, 90% of down syndrome pregnancies are aborted

Termination rates of around 90% after prenatal diagnosis of Down syndrome are documented in a systemic review of International studies.

C Mansfield et al “Termination Rates after Prenatal Diagnosis of Down Syndrome, Spina Bifida, Anencephaly, and Turner and Klinefelter Syndromes: A Systematic Literature Review” Prenatal Diagnosis, 19 (1999) 808 – 813

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Woman pressured to abort allegedly unhealthy twin

A woman named Mary in Melbourne had a 10 week ultrasound that showed one of the twins in her womb was smaller than the other. The doctor suspected that the little boy was badly disabled. She writes:

“This meant the baby was likely to have gross abnormalities because although it’s normal for twins to differ in size late in pregnancy and after birth, in early pregnancy they should be exactly the same size to be normal.

The doctor immediately recommended that I should ‘terminate that fetus’.

‘You mean kill the baby?’ I replied, at which he got a bit upset with me and asked me not to use such language!”

The doctor preferred the term “selective reduction”…..

One or more babies in the womb are injected in the head with saline, which kills them, and they are then left dead in the womb until the healthy baby or babies are delivered.

This is sometimes done because of abnormalities, but is also routinely done for mothers who simply don’t want twins, triplets or quads.

How parents of healthy babies choose which will live and which will die, and how a mother lies on a table while a saline needle is inserted in her stomach to kill one of her babies is beyond me, but apparently this is normal.

My main memory of all of this is the doctor’s incredible nonchalance.

He was not only blase about what he proposed to do, he was even eager to do it – and he was quite forthright about his belief that any baby with even a suspicion of abnormality, or indeed any baby the parents simply did not want, should be dispatched forthwith.

He was keen to perform this procedure on me as soon as possible, without any further testing of any kind.

I even remember him reminding me that I was not being fair to my other larger twin if I did not allow him to kill the smaller one. This was because I was already at risk of premature birth.

I’m university educated and am a pretty strong woman with a good marriage – so together, my husband and I found the strength (although it wasn’t easy at the time in an emotional state) to resist the doctor’s recommendations and stall for time…

How do single women, or women intimidated by the medical profession, or emotionally fragile women, or women with poor family support resist the eagerness that some in the medical profession have to solve what they simply see as a ‘problem

I still remember lying on the table waiting to have this test, arguing with the doctor as he stood over me, huge needle in hand, as he tried to convince me to have the amnio test done on both babies rather than just one – ‘because you may as well now that you’re here’.

This from a man who knew that the risk of miscarriage after an amniocentesis is about 1 per cent for a single pregnancy and up to 5 per cent for twins. He still wanted to double the risk – to ensure that we didn’t bring any handicapped babies into the world.

We managed to resist this pressure and only had the amnio on the smaller baby, although I will regret until the day I die even agreeing to this, as I nearly miscarried the following day.

I have a result sheet issued by the doctor from my 10-week ultrasound on which are written the words, ‘fetus 2 not viable’.

I like to compare this document with the child it refers to – now an 11-year-old, funny, sensitive, gifted, football-playing, blues-guitar-addicted, satin-skinned and perfect little boy, our son.

It turned out that the only explanation there was for the boys’ different sizes early in pregnancy was that they must have been conceived a week or two apart . . .

I was not told that this could be a possible explanation until well after I was meant to have made a decision to inject my son Paul in the head with saline.”

Andrew Bolt “Born in defianceHerald Sun 10th March 2006

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Parents call children with down syndrome “gifts from God”

The parents of a child with down syndrome wrote a newspaper editorial about how valuable children with down syndrome are. Here is an excerpt:

“There are no more giving, joyful, happy or precious children then Downs children. They are a genuine gift from God. Our son teaches us the meaning of patience and love and faith – just by his very existence. He has touched the lives of so many of our relatives and friends, adding dimensions they had not known existed. And he has helped us grow as a couple and as parents.”

Randall J Hekman Justice for the Unborn (Ann Arbor, Michigan: Servant Books, 1984) 55

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