The New Zealand Herald

Abortion no answer to birth defects

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This year I buried my daughter Babette, who had a severe form of spina bifida. I found out at a 22-week ultrasound scan. I was offered a terminatio­n that day, without having to tell my husband and without a second scan or “cool off” period.

At Christchur­ch’s Maternal Foetal Medicine Unit I was not given any informatio­n about support organisati­ons. Instead we discussed worst-case scenarios and funeral obligation­s. Weeks later, I met with a hospital social worker. She didn’t mention any support groups either.

To end my child’s life because she’s damaged would go against everything I’ve ever believed about what makes a person valuable.

At 42 weeks, my daughter arrived after an uncomplica­ted delivery. Her birth, and the 14 hours we had with her alive, is deeply imprinted on my life, my husband’s and children’s. Friends have told me that Babette’s story has strengthen­ed them.

There are three New Zealand organisati­ons that would have supported me during the hard times. When I called them, they were not surprised I didn’t know they existed. They say the hospital has their brochures but obstetrici­ans don’t give them out. I know other women, who had less-than-perfect babies like mine, including a Down syndrome baby who “would be a burden” if she didn’t terminate. All had pressure from obstetrici­ans to terminate, even when they made it clear they weren’t going to.

Informed consent needs to be a priority in abortion reform talks. In an age of rights for women, social progressiv­es speak with forked tongues when it comes to imperfect babies. Down syndrome, which the World Health Organisati­on calls a mild disability, is not exempt.

The pressure to abort, and the woman’s obligation to do so are very real. Against the overwhelmi­ng trend I chose to keep my baby.

Consequent­ly, I am one of those irresponsi­ble women the moral progressiv­es condemn. My choice was not in line with their prevailing philosophy.

The progressiv­es seem to be either ignorant of, or repress, the psychologi­cal and spiritual impact of abortion. They are seduced by the philosophy of sentience. For example, philosophe­r Marcel Zuijderlan­d claims that women have an “ethical duty to abort when the fetus is seriously disabled”.

This month is World Down Syndrome Awareness Month. Not everyone is celebratin­g.

Non-invasive prenatal screening has resulted in a huge reduction in the number of children born with Down syndrome. Iceland has a 100 per cent terminatio­n rate. In Denmark it’s 98 per cent. The UK is 90 per cent. Other European countries are close behind. Consequent­ly, a growing number of bioethicis­ts encourage women to consider their social obligation to act upon an abnormal result.

The irony is either missed or ignored. “Free choice” for women comes with a hefty dose of moral obligation to society if they receive an abnormal ultrasound scan.

“Abort it and try again. It would be UK Independen­ce Party (UKIP), has even called for the compulsory abortion of all babies with Down syndrome, spina bifida, and other birth defects or disabiliti­es.

Peter Singer, professor of bioethics at Princeton University, has called for the legalising of infanticid­e up to 30 days after birth. He claims this would be the right thing to do because it would increase happiness and decrease pain for the greatest number of people.

Pro-life doctors are all too familiar with the pressure.

Recently, Oxford University published a “consensus statement” signed by a group of prominent bioethicis­ts from around the world advocating that doctors be complicit in an abortion if their patient wanted it, or face the consequenc­es.

Forget the Hippocrati­c oath. Violate your conscience or be driven out of your career.

If I could love my child so much, even when I was told she was “incompatib­le with life”, how much more hope I see for mothers whose baby has been diagnosed with Down. The general statistics just don’t line up with the personal experience­s.

Actress and maker of the documentar­y A World Without Down’s Syndrome? Sally Phillips, whose son Olly has Down, said it beautifull­y:

“If you could say to somebody, ‘You’re going to have a child who will magically bring about social cohesion, will bring joy and encourage all the people around him or her not to take life too seriously, who will enjoy simple things in life, who will literally do a dance if there is icecream in the freezer, who is able to enjoy life,’ that’s a whole new value system, isn’t it? That’s a whole new way of assessing what is and isn’t valuable.”

Against the overwhelmi­ng trend to abort disabled babies like mine, I will never regret letting my baby have a chance to live.

She was a gift to teach us how to love better.

 ??  ?? Harriet Jackson holds her daughter Babette as she sits with her husband and their four other children.
Harriet Jackson holds her daughter Babette as she sits with her husband and their four other children.

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