What do Down Syndrome, Abortion, and Baby Girls Have to do with One Another?

Penny and William ride the subway on her 7th birthday

When I write posts for other sites, I generally avoid the comments sections. Some longtime readers might remember a post I wrote for Motherlode over two years ago in which I explained why I wasn’t screening my pregnancy for Down syndrome. Nearly 200 comments later, I was worn out as I realized how differently I see Penny and other individuals with Down syndrome in comparison to many readers. Still I counted it as a privilege to write for Motherlode about the topic, just as I count it as a privilege to write for The Atlantic, as I did yesterday (The Social Construction of Selective Abortion). I’m not going to chime in over there (though you are more than welcome to jump into that debate), but I did want to offer a few of the comments here.

My essay compares “gendercide” in some Asian countries to selective abortion of fetuses with Down syndrome in the United States. Statistics suggest that at least 100 million baby girls are “missing,” which is to say they were aborted because of their sex. Statistics also suggest that at least 50% of all fetuses with Down syndrome in the US are aborted. That rate becomes higher among women who have a prenatal diagnosis of DS (probably 70%) and higher still when talking about other Western nations (90%). So, while being born a girl in Asia is not exactly the same as being born with Down syndrome here, I wanted to suggest some parallels. I wrote:

 In India, daughters grow up with social stigma, a lack of educational opportunities and the prospect of becoming a burden to their parents. Substitute the words “America” and “children with Down syndrome” for “India” and “daughters,” and you get the picture.

I go on to describe some of the challenges faced by people with Down syndrome and then write:

… medical and social challenges seem fixed and unchanging. But as the past 40 years demonstrates, these challenges reflect social mores and choices as much as biologically-based reality or necessity. In 1975, Congress ensured all children’s rights to a free public education, including those with intellectual disabilities. Around that same time, parents on the whole stopped sending their kids with Down syndrome to institutions and availed themselves of “early intervention,” therapy services that target physical and brain development from very early on in a baby’s life. In 1980 the life expectancy for an infant with Down syndrome was 25. As a result of social change and medical advances, people with Down syndrome are now expected to live until at least 60. And people with Down syndrome overcome expectations every day. They read, they write, they go to work, they make friends. When given the opportunity, they lead lives of hope and promise.

Most of the commenters don’t seem to understand the argument. For example:

Having XX is not a disability… To pretend that DS is the same as having XX is stupid.

or:

To put it bluntly, there is no such thing as a shortage of DS people. Women are necessary for society in a very real and material fashion: if nothing else, they conceive and birth children. People with DS and other disabilities are not necessary in any culture. No society’s stability is dependent on accessible number of disabled people.

or

Penny reads one of her new books on Christmas Day

I think we can be pretty safe in assuming that the reasons for selective abortion of females reflect cultural gender distinctions, not biological differences between men and women. While Down Syndrome selective abortions may also partially reflect social constructions of disability, I think we can also agree that Down Syndrome involves real biological barriers.

or

Most Americans think there’s a difference between being female and having Down Syndrome. Many Americans think this kind of argument is just anti-abortion sentiment slipping in through the back door.

But some others offered counter-arguments:

First, in learning to care for and treat the disabled, we contribute to the body of medical and scientific knowledge that benefits the able as well. Second, we dramatically alter the character of our society by how we treat those perceived as “lesser”. The ramifications of eliminating most children with Downs, for example, is not really known.

and

Photo courtesy of Chris Cappozziello

The point is that in some countries, having a girl can be a significant financial burden to families and the girls/women themselves lead lives that are very limited. In effect, having XX is a type of disability, just one that is a construct of society instead of having a physiological basis.

and

People with Down syndrome are more aware than any commenter here is giving them credit for. 99 percent of people with DS questioned, refer to themselves as happy. Over 200 programs nationwide offered at University levels. NIH funding for Down syndrome research is around $20 million a year, that’s $40 per individual. Hardly a disproportionate drain on resources.

I could spend all day writing in response to these comments and the assumptions embedded within them, but I guess that’s why I wrote a (short) book about the topic. So if you’re interested in reading more or making your own comment, head on over to The Social Construction of Selective Abortion and consider purchasing What Every Woman Needs to Know About Prenatal Testing: Insights from a Mom Who Has Been There.

About Amy Julia Becker

Amy Julia Becker writes and speaks about family, faith, disability, and culture. A graduate of Princeton University and Princeton Theological Seminary, she is the author of Penelope Ayers: A Memoir, A Good and Perfect Gift (Bethany House), and Why I Am Both Spiritual and Religious (Patheos Press).

Comments

  1. I found this somewhat relevant quote while cleaning up my desk today: “Every Christian community must know that not only do the weak need the strong, but also that the strong cannot exist without the weak. The elimination of the weak is the death of the community.” – Dietrich Bonhoeffer, Life Together

  2. To me this is all very interesting & pertinent, and I’m going to try to follow up on your links.

    I see what you mean about being exhausted by comments, too — cf. your post of a few days ago. Just imagine: you open up your home to people because you’d like to share your thoughts about something. A few people respond respectfully — but then two people get in an argument about it. Others chime in, some quite nastily. The most persistent arguers come back to your house every day for the next week to try to one-up each other. Others who would like to share an opinion feel intimidated so they slip out quietly, maybe never to return. You’re tired so you go to bed — and the arguers are still there in your living room, having it out. It’s a strange, strange cyber world we live in.

    • Jeannie, As a blogger I’m probably not supposed to admit this but I have definitely started to ignore the argument going on in the living room right now! With that said, I really appreciated your comment about the Life of PI way back when, and I hope you’ll join the conversation about other topics here…

  3. Leticia Velasquez says:

    Amy Julia, I love having a book to hand people who want to know why you don’t want to test for Down syndrome, and your “Good and Perfect Gift” is a great one, however the very best advertisement for what our children give to society is the girls themselves.

    You can’t argue with charm!

  4. Thanks for your great post over at The Atlantic. It’s really good to see parents make a stand. Regarding the comments, I have seen worse, but really our words reflects our selves, so you are all good.

    I left this comment on the blog:

    The comparison is correct, both gender selective abortion and ability selective abortion are discrimination. Additionally, the use of genetic screening for selective abortions involving Down syndrome is eugenics, because it targets this particular group because of its identifiable biological difference. You will see by the comments above all the usual arguments to justify eugenics, it’s nothing new.

    • Thanks Mike for chiming in. I was fascinated by the way the comments themselves underscored the biases in our culture against individuals with Down syndrome, and I’m grateful to have some different voices chiming in.

  5. Thank you for a well-researched article in the Atlantic and your sharing of some of the comments here.

  6. The comments on the The Atlantic piece are hard to read. People really seem to have entirely missed the point of the piece, and that’s too bad. Instead of looking at the reality of eugenics plays through selective abortion in our culture and around the world, readers were wrongly distracted and took to insisting that being a woman is NOT a disability in our culture.

  7. Screening tests give parents opportunity to choose! Not everyone is capable of accepting disabled children, or giving them all they need. Eugenics is just a malicious excuse for ditching people who made their own choice, just as you did yours. I’m quite sick of sour grapes-sweet lemon as a result of frustrations.


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