Wednesday, 25 June 2008

The shadow of Monchberg

Here's another quote from Defiant Birth: Women Who Resist Medical Eugenics, that I wanted to share. It's from a mother with an interesting story. She grew up in Germany with a disabled brother who, if born 10 years earlier would have been sent to a concentration camp called Monchberg and killed in a gas chamber because of his disability. Years later, she moved to the US, studied, married and had children. When pregnant with her third child, she was told that her son would have Down Syndrome. She and her husband chose to proceed with the pregnancy against medical advice and much opposition from others around her. What really surprised her though, was the way people acted after she had given birth to her son, Peter:

I found, to my great surprise, that society still kept asking this question: Why did you have this baby? I have had people react with marked surprise when they hear that I knew Petey would have Down Syndrome before he was born. Though they do not ask aloud, you can see the question in their eyes: 'If you knew, why did you have the baby?' What's buried in the question, what's buried deep in their eyes as they ask it, is the perception of my son as 'a choice' -- specifically, my choice -- rather than as a unique human being, created in God's image, rather than as a fully fledged member of the human race.

What I see in their eyes is the lingering shadow of Monchberg that sometimes keeps me awake at night. I worry that the joint availability of tests and abortion seems to be eroding societal consensus about our collective responsibility for vulnerable people -- people with disabilities whose conditions were or could have been diagnosed prenatally, or even people born into difficult family situations or social structures. I am very frightened by the emerging attitude that if a woman exercises her 'choice' to have a child who can be identified in advance as 'vulnerable' for some reason, the woman herself bears the responsibility for dealing with that vulnerability. In other words, if the cost of a certain life is going to be more than its 'worth', someone has to make up the deficit. The assumption seems to be that if you 'choose' to impose that cost on society by having a baby you could so easily have aborted, you should pay the price.

6 comments:

janellehardy said...

Nicole,

Thank you for your comments on this book. The first post you did on was so relevant; I have a friend who discovered her baby was anencephalic (at about 28 weeks) and in the shock of it, with no time to think at all, went with the doctor's suggestion to induce labour. Afterwards, she was hurt by the hurried reaction of the medical staff and wished they'd advised her to think it over first. It was hardly an emergency!

She told me that it would have been a privilege to have had him growing the last couple of months inside her and they'd have had time as a family to get used to the inevitable after-effect of his birth.

I think I'd like to read this book. Have you finished it yet? (meaning can you tell me more? you mentioned emotionally harrowing...)

I'm going to put links to your quotes on my blog as my family/friends would be interested too. Thanks again.

Mrs. "M" said...

Nicole,

That's a powerful quote and a true one! We had people respond to us when our son was born and died as if "we did this to ourselves". We were isolated from certian people because we chose to torture ourselves....so we were told. We even had one person ask us why we would name our son if he was only going to die.
It is scarey where our society has come to in this regard. All these tests they offer have a hidden agenda. The scarey part is that many want the tests in the name of choice and not life. We are walking such a fine line with pre-natal testing.

Megan said...

We refused to have the test for down syndrome during all my pregnancies. Fortunately, my doctor was understanding of this choice. The first test doesn't risk the baby, but has a high false positive, and the next test which is more accurate has a chance of miscarriage, which we found unacceptable as we wouldn't consider aborting a child. I really find it hard to understand the attitude towards Down syndrome, who in my (admittedly not extensive) experience seem to be able to enjoy life and give and receive love and affection. What does it say that such babies are rountinely aborted? what makes a worthwhile person? I find it intensely troubling - where does the line get drawn? anyway, thanks for sharing the story!

Prue said...

I also chose not to have the nuchal translucencies for my pregnancies. It was not going to give me any information that would make me do anything - if God had placed those babies in my womb they were there for a reason. Even the one I miscarried was there for a reason.

Nicole said...

Yes, we made the same decision as you Prue and Megan (although the drs weren't impressed).

Mrs M - your story sounds a lot like the stories in this book - truly awful.

And Janelle, I have finished it and I'm about to write a 'review'. I am definitely going to recommend it.

MacCárthaigh Family said...

Very sad situations.. When it comes to what God sees, I think these children are an awful lot cleaner and holy in His sight than many of us...
Will put a link to my blog. Well done.
Ruth