Thursday, September 4, 2008

some mothers get babies with something more...

A friend recently passed along this newspaper column to me and I wanted to share it with all the amazing mothers I have met along our journey of special needs. I am filled with respect, love and admiration for all that you are and all that you do.

My friend is expecting her first child. People keep asking what she wants. She smiles demurely, shakes her head and gives the answer mothers have given throughout the ages of time. She says it doesn't matter whether it's a boy or a girl. She just wants it to have ten fingers and ten toes. Of course, that's what she says. That's what mothers have always said.

Mothers lie. Truth be told, every mother wants a whole lot more. Every mother wants a perfectly healthy baby with a round head, rosebud lips, button nose, beautiful eyes and satin skin. Every mother wants a baby so gorgeous that people will pity the Gerber baby for being flat-out ugly. Every mother wants a baby that will roll over, sit up and take those first steps right on schedule. Every mother wants a baby that can see, hear, run, jump and fire neurons by the billions. She wants a kid that can smack the ball out of the park and do toe points that are the envy of the entire ballet class. Call it greed if you want, but we mothers want what we want.

Some mothers get babies with something more. Some mothers get babies with conditions they can't pronounce, a spine that didn't fuse, a missing chromosome
or a palette that didn't close. Most of those mothers can remember the time, the
place, the shoes they were wearing and the color of the walls in the small, suffocating room where the doctor uttered the words that took their breath away.
It felt like recess in the fourth grade when you didn't see the kick ball coming and it knocked the wind clean out of you.

Some mothers leave the hospital with a healthy bundle, then, months, even years later, take him in for a routine visit, or schedule her for a well check, and crash head first into a brick wall as they bear the brunt of devastating news. It can't be possible! That doesn't run in our family. Can this really be happening in our lifetime?

I am a woman who watches the Olympics for the sheer thrill of seeing finely sculpted bodies. It's not a lust thing; it's a wondrous thing. The athletes appear as specimens without flaw - rippling muscles with nary an ounce of flab or fat, virtual powerhouses of strength with lungs and limbs working in perfect harmony. Then the athlete walks over to a tote bag, rustles through the contents and pulls out an inhaler.

As I've told my own kids, be it on the way to physical therapy after a third knee surgery, or on a trip home from an echo cardiogram, there's no such thing as a perfect body. Everybody will bear something at some time or another. Maybe the affliction will be apparent to curious eyes, or maybe it will be unseen, quietly treated with trips to the doctor, medication or surgery.

The health problems our children have experienced have been minimal and manageable, so I watch with keen interest and great admiration the mothers of
children with serious disabilities, and wonder how they do it. Frankly, sometimes you mothers scare me. How you lift that child in and out of a wheelchair 20 times a day. How you monitor tests, track medications, regulate diet and serve as the gatekeeper to a hundred specialists yammering in your ear. I wonder how you endure the praise and the platitudes, well-intentioned souls explaining how God is at work when you've occasionally questioned if God is on strike.

I even wonder how you endure schmaltzy pieces like this one saluting you, painting you as hero and saint, when you know you’re ordinary. You snap, you bark, you bite. You didn't volunteer for this. You didn't jump up and down in the motherhood line yelling, "Choose me, God! Choose me! I've got what it takes."

You're a woman who doesn't have time to step back and put things in perspective, so, please, let me do it for you.

From where I sit, you're way ahead of the pack. You've developed the strength of a draft horse while holding onto the delicacy of a daffodil. You have a heart that melts like chocolate in a glove box in July, carefully counter-balanced against the stubbornness of an Ozark mule. You can be warm and tender one minute, and when circumstances require, intense and aggressive the next. You are the mother, advocate and protector of a child with a disability. You're a neighbor, a friend, a stranger I pass at the mall. You're the woman I sit next to at church, my cousin and my sister-in-law. You're a woman who wanted ten fingers and ten toes, and got something more. You're a wonder.

(Lori Borgman is a newspaper columnist and author)

7 comments:

Lynden Jen said...

Wow - tears and hugs, Amy, tears and hugs. That writing pretty much says it all.

Eva and her 'rents said...

That's right. We DO feel ordinary and didn't volunteer to have a child with needs, but shouldn't fail to give ourselves credit for the amazing things we do with and for our children. I'm grateful Eva was born to me because I really feel that no one else could raise her as well as I can.

Melissa said...

So that article basically says everything I've wanted to say. Awesome and I hope, Amy, that you took it to heart to because that's exactly how I feel about you! Amazing my friend.

Cheryl said...

Oh Amy! Thank you for sharing this wonderful essay. It touched my heart so deeply, expressing just what I was feeling about my daughter and the process of letting her go, as she is now living in Seattle. It also is an almost perfect picture of you my friend and I hope you keep a copy close for those many days when you need to be remined of how blessed Max is and how blessed you are to be Max's Mama.

Unknown said...

a great story i jsut so love that

~Kimberly said...

Well that just brings tears to my eyes! All so true.

Kim

hannah m said...

Thank you for sharing this (as the tears stream down my face!).