Woman describes trauma and nightmares after aborting disabled baby

Nancy Kreuzer from Illinois talks about her abortion and its aftermath:

“My baby was 22 weeks, I was five and a half months pregnant, when I was told that she had water on the brain (hydrocephalus) and was advised by my doctor to “terminate the pregnancy.”

It was explained that the abortion would be a simple procedure. My husband and I were told we could leave this behind us, get on with our lives and try for another baby…

It was not, as the doctor described, “simple.” At the abortion clinic no one asked how I was or explained what was happening to me. I felt alone, afraid and devastated. While I sat, waiting for the doctor to arrive, many nurses and workers in the abortion clinic casually walked by me. I sat there for hours. Tears streamed down my face but no one talked to me, no one acknowledged my pain.”

After the abortion, she says:

“The day after my abortion, I felt numb. I left the abortion clinic with no baby to bury, no doll-size casket, no funeral service, no grave to adorn with flowers. I vomited in the parking lot and rode home in silence.

No one brought meals, no one sent cards, no one called, because I had been too ashamed to tell anyone what I had agreed to do. In the weeks that followed, I tried to bury the memory of the abortion and not look back.

In the months and years afterward, there were clear signs that the scars of my abortion existed, but I didn’t recognize them at the time. Interestingly, I assumed I was doing just fine. But below the surface, I was unusually fearful.

As time went on, I often had the sense that I wanted to run and I had repeated nightmares of running from something horrible. I would awaken panicked, unable to sleep the rest of the night. There was an internal sadness, not visible to the world.”

Quoted in Janet Morana Everything You Need to Know about Abortion – For Teens (Gastonia, North Carolina: TAN Books, 2021) 82 – 83

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Politician: better to abort “mentally defective” children

While advocating for legalized abortion, British politician Renee Short stated:

“We must consider what happens to some of the unfortunate unwanted children born into inadequate homes, disabled children, mentally defective children. They come into the care of the local authority.

A research project has been carried out by a Birmingham University social worker, who shows that it is not uncommon for a child of this kind to have up to 10 different homes in five years…

He believes the children coming into care in this way are often more difficult and more disturbed, and that they are the delinquent adolescents. The delinquent adolescents become the parents of more unwanted delinquent adolescent children in the next generation, generating another cycle of cruelty and neglect.”

Fran Amery Beyond Pro-Life and Pro-Choice: The Changing Politics of Abortion in Britain (Bristol: Bristol University Press, 2020) 59

This politician seems to think that because the foster care system is inadequate, so-called “unwanted” children are better off dead.

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Woman describes pressure to accept fetal testing

One mother spoke about how a doctor tried to pressure her into having tests done on her preborn baby to see if the child was disabled. The implication is that disabled babies will be aborted. She didn’t want to abort her baby and would’ve accepted a disabled child:

“I don’t think that the test for disability in the unborn child is presented as a choice. When I said I didn’t want to be tested, the doctor was shocked, and she tried to talk me into it because it’s an easy test. Everybody gets it done nowadays. It’s simple.

But I don’t think there is a choice. I think that we’re pressurized into taking as many of these tests as are available.”

T Shakespeare, “Choices and rights: eugenics, genetics and disability equality” Disability & Society, 13:665 – 681

 

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Lawyer who argued Roe v. Wade calls disabled children “defective”

In her oral arguments before the Supreme Court, lawyer Sarah Weddington said:

“If the pregnancy would result in the birth of a deformed or defective child, [preborn baby’s mother] has no relief.”

Sarah Weddington, arguing in favor of striking down laws against abortion, on December 13, 1971

Quoted in NEH Hull, Williamjames Hoffer and Peter Charles Hoffer, eds. The Abortion Rights Controversy in America (Chapel Hill: The University Of North Carolina Press, 2004)

This dehumanizing language about disabled people is appalling and the fact that getting rid of “defective” children (and the “relief” caused by eliminating them) was an argument used to legalize abortion shows the ableism inherent in the pro-abortion position.

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Insurance company demands couple abort baby with cystic fibrosis, refuses coverage

An article in the Christian Century tells of the following:

“CAN WE FORECAST a connection between genetic discrimination and selective abortion? Yes. A couple in Louisiana had a child with cystic fibrosis, a genetic disorder leading to chronic lung infections and excruciating discomfort.

When the wife became pregnant with the second child, a prenatal genetic test revealed that the fetus carried the mutant gene for cystic fibrosis.

The couple’s health maintenance organization demanded that they abort. If they refused to abort, the HMO would withdraw coverage from both the newborn and the first child. Only when the couple threatened to sue did the HMO back down and grant coverage for the second child.”

T Peters “In search of the perfect child: Genetic testing and selective abortion” The Christian Century Oct 30, 1996

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Couple chooses life for dying baby, donates her organs

Bishop Kevin Vann from the diocese of Orange in California, telling the story of a couple whose baby, Rylei was diagnosed with severe disabilities in the womb:

“Given the choice to abort, the parents, Krysta and Derek, decided instead that their daughter Rylei should be born and that her organs would be donated upon her natural death. She lived for only a few days. But she transformed the lives of her parents – who were forever changed by knowing her – and the lives of all the infants who received her donated organs, not to mention their families, friends and so on.

These infants will go on to have lives like the rest of us, full of dreams and joys among the disappointments and sadness. Such is the human experience… But all of this is made possible because of the life of this one child who only lived for a few days outside her mother’s womb.”

Rick Garrett The Duping of America (Maitland, Florida: Liberty Hill Press, 2021) 134 – 135

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Parents of surgeon born with club foot are horrified late-term abortions are done for that reason

The parent of a child who was born with a club foot and is now a surgeon wrote a letter to the editor to express their shock at laws in England allowing abortion up to birth for the condition:

“We were surprised to see that club foot (talipes) was mentioned in connection with late abortions…

Our son was born with severe talipes in 1979. He was described as handicapped and mixed race when we adopted him as a baby…

His legs are still thin, but his mobility has been only slightly limited. His two children do not have the condition.

We suspect that because of his childhood experience he was determined to be a surgeon, an ambition that he has achieved: he is now a very successful senior consultant surgeon in Australia. Thank goodness his birth mother did not opt for a termination.”

Dr and Mrs C Mackay “Late abortion could have claimed our brilliant boy” The Times July 11 2021

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Severely disabled child had life “full of joy”

Pro-life activist and abortion survivor Claire Culwell wrote about a little girl she took care of who had severe disabilities.

In her book, Culwell wrote about four-year-old Riley–Jane and her mother Gayle. She says of Riley – Jane:

“… Her muscles didn’t function normally; her bones were soft; she had a tracheotomy; she was on oxygen and had a feeding tube.

Gayle said that the doctors didn’t think she could experience a good quality of life. However, despite all her challenges, Riley-Jane’s life seemed full of joy. Her parents wanted to nurture that apparent joyfulness and enable her to live as well as she could. They decided to ask me to be her caregiver as much as my schedule would allow. I was eager to help. Riley- Jane could do nothing for herself. I fed her, bathed her, dressed her, and just tried to help her feel loved and accepted.

Right away I saw the joy that her mother had talked about. As I rocked Riley- Jane, she would grin up at me, communicating without needing to say one word. I wasn’t sure whether she could really see me, but something inside Riley- Jane generated a spirit of happiness that was awe-inspiring. Her vulnerability and trust fulfilled and blessed me more than I could have ever imagined. I saw beauty that radiated from her soul, surpassing the usual physical definition of beauty.

Riley- Jane passed away a few years ago. It wasn’t surprising to see so many people who had been touched by her life – and the lives of her parents – gathered to celebrate her… Her quality of life here on earth defied what the doctors had said, and I am grateful for the opportunity to have been blessed by Riley- Jane.”

Claire Culwell, Lois and Steve Rabey Survivor: An Abortion Survivor’s Surprising Story of Choosing Forgiveness and Finding Redemption (WaterBrook, 2021) 35 – 36

All human life is valuable, even lives lived with a severe disability.

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Tests to detect down syndrome lead to two miscarriages for every three Down syndrome babies aborted

An article in The Telegraph said the following:

“Two healthy babies are miscarried for every three Down’s Syndrome babies that are detected and prevented from being born, research has suggested.

The losses are down to the invasive methods used to test for the condition…

The NHS [National Health Service] cites a miscarriage rate of between one and two per cent following the tests, but the researchers, from the charity Down’s Syndrome Education International, point out that only the number of Down’s babies terminated, miscarried or born are recorded, not the number of healthy babies lost….

Although they admit that their ratio is only an estimate, they are backed by a number of independent experts who fear inexperienced practitioners may also be to blame.”

The article also said:

“Professor Kypros Nicolaides, head of the Harris Birthright Centre at King’s College Hospital in south London, said the loss of healthy babies was “completely unacceptable.”

The deaths of babies with Down syndrome through abortion, however, are perfectly acceptable to this doctor.

Aislinn Simpson “Two healthy babies miscarried for every three Down’s Sydrome babies detectedThe Telegraph 16 September 2008

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Disability rights activist speaks out against aborting disabled babies

Disabled woman and activist Marsha Saxton:

“The message at the heart of widespread selective abortion on the basis of prenatal diagnosis is the greatest insult: some of us are “too flawed” in our very DNA to exist; we are unworthy of being born… Fighting for this issue, our right and worthiness to be born, is the fundamental challenge to disability oppression; it underpins our most basic claim to justice and equality – we are indeed worthy of being born, worth the help and expense, and we know it!”

Marsha Saxton “Disability Rights and Selective Abortion” Ricky Solinger, ed. Abortion Wars: A Half Century of Struggle, 1950 – 2000 (Berkeley and Los Angeles: University Of California Press, 1997) 391

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