I’ve found myself in the
center of a squall this past week. A squall of my own making. When I wrote
about my choice not to screen the baby in my womb for Down syndrome, I didn’t
expect it to draw any attention other than readers of this blog. But Lisa Belkin,
of the New York Times’ Motherlode, was willing to post it, and just a few more
people read her blog than mine. So far, there are 180 comments and counting. And
then there was the second post, “Is it Harder to Have a Child With Down
Syndrome?“, published Tuesday, which has brought with it a comment stream of
its own.

While many of the comments
have been incredibly encouraging, supportive, wonderful testimonies to life
with disabilities or life in general, I’m focusing for the purposes of this
post on the other side. Here’s a sampling from
the first post:

“I’m tired of people painting
crippling disabilities in a rosy light, claiming that it’s all the same and
“just another way of being. Choosing to bring a child into the world,
knowing that s/he will be doomed for
life with such a condition, isn’t something that every woman is ready to
do, or should be obliged to do.” (#11)

“But I think deliberately choosing to bring a child into the
world knowing that they will never live
a full, independent, healthy life is strange and selfish in a way.” (#52)

“The bottom line is that Down’s
Syndrome children are also a burden to society.” (#73)

“It’s bizarre to me to see statements that these children enrich
their parents lives or bring joy, but
luckily we all get to choose.” (#78)

“The ones who
suffer? The SMART kids. Only a deeply
self-destructive society dumps all of its resources into a population that,
frankly, isn’t going to show a return on the investment.” (#96)

From the second post:

“Yes, some disabled kids live in
blissful ignorance and enjoy the dance classes of life. But others suffer with
the knowledge and the despair. Which kind you’re gonna get, nobody knows, but
I’m not willing to take the risk.” (#3)

“Unfortunately, the real challenge
may come when the child grows up. Raising a Down’s child is nothing compared to
managing a Down’s adult.” (#24)

“What we have a difficult time
understanding is when a person has FORESIGHT into a situation, particularly
concerning disability and prenatal screening, why someone would CHOOSE to have
a child that has a disability like Down Syndrome, when we KNOW the hardships
(for everyone) that are involved.” (#85)

And these are just the
ones that lend themselves to quick quotations.

A number of you have asked
me how I feel about all this. Not
just how I think about it, but how I
feel about it.

I wasn’t feeling very
emotionally engaged until Sunday morning. But then I found myself sitting in
church next to Penny. She had taken a Bible from the chair in front of her and
opened it on her lap. Her fingers were tracing the words and she was “reading”
(which means she was narrating the page as if she knew what the words said).
And as I saw her there–with her soft brown hair cradling her face, her glasses
slipping to the end of her nose, her long eyelashes–absorbing some sense of God’s
love for her, all I could think was, There
are people in this world who think you shouldn’t exist. Like an arrow to my
heart.

So, the comments sting.
The ignorant ones provoke anger. The stories of family members of people with
disabilities who say they think their sibling/child/mother/etc. should never
have existed provoke sorrow and confusion and compassion. The mean ones make me
want to protect my daughter and never write a word about her again. But my
overriding sense in the midst of it all is of gratitude. When I write on this
blog, or at Bloom (a blog specifically for parents of kids with disabilities), I’m writing to a pretty sympathetic audience. So the
opportunity to write for people who think my life makes no sense whatsoever,
well, really, it’s a privilege.

I’ve shed some tears this
week. I’ve endured some sleepless nights. I’ve hugged Penny tight and kissed
her head and wished that everyone in the world had a chance to meet her. And I
plan to keep telling her story, in spite of the hurt and the anger and the
sadness, in hopes that hers might be a narrative of love and hope and embracing
the fragility, complexity, and beauty that every human life has to offer.