World Down Syndrome Day 2013, RAISE YOUR FLAG

World Down Syndrome Day 2013, RAISE YOUR FLAG

AUTHOR

Today is World Down Syndrome Day 2013 …

And I have no idea what to write, let alone the message I want communicated in the words I type.

Why is this?

I’ve been advocating for my daughters with Down syndrome for seven years. Even in the beginning, after my daughter Polly was born, as I grieved the child I expected (mostly out of ignorance), I still picked up whatever flag I could and waved it vigorously for Down syndrome.

That first year, when my eyes were still rimmed red from crying, and my hands shook a bit when I talked because I couldn’t get this feeling of dread out of the pit of my stomach when I considered my daughter’s life and the effects of that extra chromosome, I still wrote a letter to the editor of a local newspaper about World Down Syndrome Awareness Day. I still joined my voice to countless others fighting to help the world see their children as they should: children. Normal children who may need a little extra help in certain areas, but who  have so much to offer, who are productive members of society if only those around them would take the time, and provide opportunities for them to display it.

I guess this year I’m just tired of convincing the world of my children’s worth.

As a special needs mom, my life is filled with advocacy, and fighting, and working to help my girls reach their God-given potential, and making sure they get fair shakes at life.

I’m tired.

My friend wrote this great post the other day about how Down syndrome must lead to action. To paraphrase (and you really should go read her post, because it puts much, much better), it is nice when kids with Down syndrome are acknowledged, and even appreciated. But what they need, what WE as their families need, is for society as a whole to pick up the flag of advocacy.

Yes.

If you are reading this post today on World Down Syndrome Day 2013, and you like, or love, or appreciate Polly and Evangeline, then I ask you to raise your flag. Appreciate my girls. Love my girls. And please, stand up and fight for my girls.

As my friend so eloquently put: 

I ask you to act on what you now know, what you are aware of. The next time you are in your child’s classroom, look around. Do you see any children with Down syndrome or other Neuro or physical differences there? No? Ask the teacher, ask the principal, “Where are they? Why are they not with my kids?” Tell them that you believe in the equality of all people, and the rights of children like mine to be educated in regular classrooms alongside their peers (your children).

What I love about my two daughters with Down syndrome, and what I want others to know about them is simple:

They are normal little girls, made of the stuff other little girls have, flesh, blood, love, laughter, selfishness, wonder, mischief, curiosity, impatience … When Polly was born I ignorantly assumed she would not be a typical little girl. I made the mistake of thinking she would not be the little girl I wanted. But her presence in my life and the God-ordained appearance of her sister Evangeline through international adoption from Ukraine daily eradicates my pre-conceived notions about individuals with disabilities. Sure, my girls have special needs. But they also have what I call “special powers,” the ability to love without limits, to smile at a new day without drudgery, and to teach this Mama over and over what really matters in life.

On World Down syndrome Day, I ask you to remember that regardless of a child’s ability or disability, she is a child first, and should be empowered and celebrated all the days of her life. If forced to point out differences about my girls, well then, they have ample supply of the good parts of the human heart, gifts from God himself to reveal his glory: joy, love, kindness, courage, endurance. Pay attention to my daughters, and to what they have to offer, because these are the things that most of us find wanting in ourselves.

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Want to read more about WORLD DOWN SYNDROME DAY? Here’s more:

Mothers share truths learned because of Down syndrome at NotAlone.com

3 for 21: A Bite Sized Blog Hop for Down syndrome and Change

Amy Julia Becker’s Down syndrome around the world series at Thin Places

International Down Syndrome Coalition: parents who blog about Down syndrome

10 things TO SAY when a baby is born with Down syndrome

10 things to say when a baby is born with Down syndrome

Here it is, day 31 of blogging for Down syndrome awareness the month of October. Phew. I’m tired!

A few weeks ago I posted 10 things not to say to a parent of a child with Down syndrome.

Someone emailed me a day or two later.

“My father and I were talking about your post about 10 things not to say to a parent of a child with Down syndrome, and we were wondering … What should we say?  … Please, help us. We really want to know.”

I was touched by this person’s desire to learn about such a delicate subject.

I’ve given this some thought. I know every parent is different, so not all of these on my list will resonate with everyone.

Here’s my list of 10 things to say to when a baby is born with Down syndrome

10. How are you doing?

After my daughter Polly’s birth and diagnosis of Down syndrome, I appreciated friends and family asking how I was doing. I realize not everyone would want to talk about their feelings but it meant a lot to me when people reached out and “went there.”

9. He/she has your eyes/nose/hair etc…

One of the things I worried about after Polly’s birth was that she wouldn’t look like the rest of our family. Of course, she does. Sure, it’s noticeable that Polly has Down syndrome. Her eyes are almond shaped. Her nose is a bit flat. But she also has blonde hair like her sisters. She has my smile.

At first, I just wanted to know that although she had Down syndrome, she was my baby.

8. How’s her health?

Most people are aware that an extra chromosome on the 21st pair brings with it added medical concerns. I was fine when people asked about Polly’s health. It provided common ground, something to talk about during awkward pauses. And of course, friends and family asked so that they could pray for her health.

7. You are going to be a great parent.

I needed to hear these words. I was afraid. Down syndrome was new. I would have loved the reassurance.

6. We brought the baby a present.

Our daughter was sick right after her birth for three weeks. We went from having a baby to having a sick child. Polly didn’t get gifts, and we didn’t get cards with hearty congratulations on the birth of our child.

Hear me, you guys. If you are going to see a family after their baby is born with Down syndrome, bring a cute outfit, or balloons, or a stuffed animal.

In other words, celebrate new life.

5. I am bringing you a meal Tuesday at six o’clock.

Offer practical help. And don’t say, “what can I do?” or “let me know if I can help.” Parents are too out of it to ask. Just tell them you are bringing a meal. And be specific. Give the day and the time. The parent will check it off her list. Being concrete will put her mind at ease.

4. Can I hold him/her?

Pay attention to the new baby. Hold him. Cuddle him. Love on him. Pray for him. Your tangible, bodily acceptance will have a great, positive effect on the family.

3. We’d like to take the other kids out to a movie Saturday and then have them over for pizza.

Once again, tangible help. If there are other children in the family, chances are they are getting lost in the shuffle. Schedule a time to take the kids out to do something fun. Again, tell the parents when, where, and for how long.

Another tip: take them for a full afternoon or for the day. Parents need time together and with the baby, and they need to know their other kids are attended to.

2. You make beautiful children.

I always say this to a new parent and I always get a huge smile in return. Parents crave assurance that they did well, because trust me, in the beginning they aren’t sure when Down syndrome is in the picture. Compliment the baby. Fuss over her. And compliment the parents on a job well done.

1. Congratulations on the birth of your baby!

I don’t recall getting congratulated. Those first days are squiggly in my mind, but oh how I’d love a story to pop up of someone embracing me and congratulating me on this new little life that with God’s help, I produced.

Make a big deal over the baby. It’s a baby! And she/he and the parents deserve all the love, attention, and excitement that comes with new life.

Parents, what would you add?

An unusual story of a Down syndrome diagnosis

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An unusual story of a Down syndrome diagnosis

(This is another excerpt from my book KRASATA, a memoir of motherhood, Down syndrome, and surprising beauty. It takes place in Kiev, Ukraine, after the birth of our third daughter while living there as missionaries.)

***

On the sixth morning of Polina’s life, I stood next to her incubator in Kiev, Ukraine. My hand pushed through the plastic window and rested on her ankle. My fingers cupped her heel. She opened her eyes. It made me smile.

I got up that morning and came to check on Polly first thing like usual since we had been in the hospital after my emergency C-section. Nurses rushed around changing babies and fitting clean sheets on cribs in the two adjoining rooms. Their movement made me weary. Sensing someone behind me, I turned. It was Polly’s doctor.

“Dobroye Utro,” I said, greeting her in Russian with a smile. The Doctor stood staring down at her white shoes. She sighed, looked up, and fixed her eyes past me.

I am afraid of heights. My fear is shared with others in my family; my father, my oldest daughter. In middle school I was the kid who wouldn’t go on rides at the amusement park. I pretended to prefer the carousel, but everyone in my class knew I was scared. I’m even a little jumpy in elevators.

The doctor started to speak. Her Russian was hurried, making it difficult for me to follow her. “K Sashaleneeoo, Gillian, ooh vashoo dochkee syndromom Downa.” No good morning, how are you today. No, will your husband be here soon because there is something I’d like to discuss with you.

Her only words were, “With disappointment, Gillian, your daughter has Down syndrome.”

I let go of Polina’s heel and pulled my hand out of the incubator. I took a step back, like I was stepping off a cliff.

Sometimes I dream I am falling. It’s said that if you hit bottom in your dream you are dead in real life. But I wasn’t asleep. I was very much awake.

I stared at the doctor, blinking. Maybe I misunderstood her? The test results were positive? Polly had Down syndrome? I hit bottom. My hope that Polly wouldn’t have had Down syndrome died.

No! I don’t want this. I don’t want to have a disabled child! I don’t want to be the old mom in Wal-Mart with the adult child shuffling behind her. Scanning the nursery, I was alone in the midst of a group of nurses going about their routine. A regular work day for them. The last regular day of my life. Where was Sergei? I wanted to hide but there wasn’t any place to go.

The doctor stared at me. “So, what do we do now?” I asked, feeling like I needed to say something. She started talking, but I could not understand a word she was saying. Not wanting to fall, I stood with my feet planted on the white tile. My legs pushed my shoulders upward while gravity pulled me down to the ground. I wanted to fling myself on the floor, bang my fists and tear my clothes, but I didn’t dare move for fear of crumbling.

The doctor paused. Say something, Gillian, I told myself. “Spaseeba.” I choked out. Thank you? That’s it. I was just told my baby had Down syndrome and all I could say was thank you. A better mother, I thought, would have probably bent down and drawn close to her child. She would meet her baby’s sleepy eyes and vow to protect her, to treasure her.

I, instead, separated myself from Polly. My feet were at once unstuck and I darted out of the room without even a glance back at the baby. I couldn’t look at her. If I did, I feared I could have turned to salt, like Lot’s wife in the Old Testament when she glanced back to her city while fleeing.

I was like a woman on a television show who dies, and then watches people fuss around her dead body. I watched her run to her room. She flung herself down on the hospital bed and howled. I hovered above her, willing her to stop crying. At that moment, that woman was not a person with faith in God. She was someone abandoned.

I had already believed in Jesus for over half of my life. I attended church. I read scripture. I went to Bible College and became a missionary and then later a pastor’s wife.

My faith was more than a career. I believed in Jesus. I believed in him like John Lennon believed in giving peace a chance. I believed in him like Democrats believed Obama during his Yes We Can speech after winning the presidency. I believed in Jesus. And yet, when told that Polly had Down syndrome, my faith buckled with my legs.

C.S. Lewis writes about the loss of his wife, Joy, in A Grief Observed:

“I thought I trusted the rope until it mattered to me whether it would bear me. Now it matters, and I find I didn’t.” – page 37

While waiting for the test results for six days, assorted scenarios played out in my mind. I talked to my mom and Sergei both about the possibility of Polly having Down syndrome. If she did, we’d move back to America for her care. Or maybe we’d stay in Kiev. I’d research services provided here for families with disabled kids. I’d find a way to make it work. I made plans and weeded through logistics. I put together a list of things to do once we got out of the hospital: apply for an American passport for Polly in case we wanted to go to the States, get her in to see the American pediatrician that lived in Kiev.

But not for a second, did I consider how it would feel to hear that my baby had Down syndrome.

In my room across the hall from Polly, nurses surrounded me as I sobbed on my bed. One patted my arm. Another handed me a plastic cup filled with purple liquid. It looked like a communion cup from church.

Russian mutterings swirled above me, “neecheevo, pearestine krechat,” –it’s nothing, stop crying. I once again found myself deaf and dumb. Dazed, I gulped down the thick liquid. Polly’s doctor stood closest to my head on the left side of the bed.

“Stop crying!” she said. “Yes, it’s terrible that your daughter has Down syndrome, but you have options. You can terminate your parenting rights or take her to live in the village. Take her some place quiet. She’ll play. Life is slow there. Now, stop crying!” Everyone around me nodded and patted me, muttering again, “neecheevo, Gillian, neechevo.” It’s nothing, Gillian, it’s nothing.

I came back to myself and thought about Sergei and Elaina and Zoya. What have I done? What were we going to do?

Sleep, God whispered to me. Sleep.

I closed my eyes.

***

I’m Polly & I don’t want to talk about Down syndrome, I want to talk about my loose tooth

 

I’m Polly Marchenko and I don’t want to talk about the fact that I have Down syndrome, I want to talk about my loose tooth.

(A little context: Polly is six years old. She has three sisters, one dog, two parents, and one extra chromosome, also known as Down syndrome. Polly knows she has Down syndrome and she doesn’t care. She’s more interested in talking about her loose tooth, the tooth fairy, her sister Evie, and yelling at her cousin Ben to go into the other room b/c he is laughing during the video.)

For new parents of children with Down syndrome, the news can be scary. Hopefully Polly can help you feel a bit better.

I also want to say that our other daughter Evangeline, six months younger than Polly is non-verbal and mostly non-communicative. It can be hard to have two kids so close in age so differently, but that’s kids for you. Each is their own. Doesn’t always make it easy.

(Oh, and she wants comments, so don’t forget to say “Hi” to Polly :) ).

To the new mother of a baby with Down syndrome

To the new mother of a baby with Down syndrome

Meeting Her

I remember the feeling.

That first meeting with another family farther along the path of Down syndrome after the birth of our child with the same diagnosis.

I remember fear and fascination.

Fear of the child four or five years old who’s eyes mirrored my baby’s. She shouldn’t have looked like him. I birthed her. She should have resembled me.

Fascination, as I watched his sister play with him; he hit her, she cried, mother reprimanded. So common, so usual, so family. Things I thought we may have lost with the appearance of an extra chromosome.

I cried quietly for two hours while visiting this dear little boy and his family. They loved him. They cherished him. He played games, and communicated with his hands and with his voice. He chowed down on his lunch.

But still, I cried, because this path wasn’t my choice. At my point of weakness his mother appeared strong. I was an anthill. She, a mountain. I clutched my baby to my chest, each second teetering between relief and uncertainty.

His mother was gracious, tender. We whispered to each other as her children played nearby. ”I love him. Our life is good. Really. It is.”

Her smiling eyes met mine.

I looked away.

I loved my baby.

But that day I did not love Down syndrome. It was too big, too unknown.

Meeting You

Your husband contacted us last week. We scheduled dinner. The following days you kept popping up in my mind. A mother forced to move from a typical parenting landscape to some place new, a place everyone claimed was special. If you are anything like me, shocked by a culture wildly unknown and unsolicited.

“Mom, why are you cleaning up around the house, and making us all put on fresh shirts and brush our hair?” Elaina asked as I set the table. “You usually don’t make such a big deal out of dinner guests.”

Several responses queued on my tongue. Instead, in a brief moment of clarity, understanding that Elaina would learn more from the truth, I responded.

“Because, this family had a baby a few months ago with Down syndrome and I want them to feel welcome. I want them to see that we are happy, and that Papa and I treasure all four of our girls. I want them to see that we are OK.”

Your family arrived. We cooed over both of your children. I held your new baby in my arms. He smelled like sunshine.

His eyes mirrored my daughter’s.

I held your little one to my chest as our children played close by. Polly hit Zoya. Zoya cried which made Evie cry, and Elaina played on the floor with your son.

You probably aren’t excited to be a part of our special needs club. I have to tell you, though, welcoming you into my home was like welcoming family.

You teared up as you talked about your love for your son. “Down syndrome is something different. It’s a lot to take in.”

Oh, how I know.

I am a bit farther down your new path. Give yourself time to fall in love with your son, and to get used to Down syndrome. Breathe in his baby smell. Watch how his brother kisses the top of his head, how your husband gently puts him down to sleep, how your baby locks eyes with you when he eats. The weight of the world is in those eyes.

Today, you don’t have to love Down syndrome. Just love your son.

And know that we, other parents in this very special club, are here when you need us and that someday, you will be the one looking a new mother in the eye saying,

“Our life is good. Really. It is.”

(This is a post from the archives that is part of the Disability Series Blog Hope: A Favorite Post. Be sure to go to With A Little Moxie to check out other fabulous posts about disability.)

10 SPECIAL NEEDS OF SPECIAL NEEDS PARENTS FREE PDF

Here’s the 10 special needs of special needs parents free PDF download available for personal use!

I wrote a post about 10 special needs of special needs parents that was well received.

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One day at a time

 

One of the biggest lessons I’ve learned in parenting is this:

Take life one day at a time.

That’s it.

You don’t have to have everything figured out today.

Today I am overwhelmed. I am worried.

Worry doesn’t help. It just robs us of the here and now.

What I have to do today: love my family, maybe take a shower, do some laundry, and pray and ask God to meet me here where I am at.

What about you? Are you struggling? Worrying? Something heavy on your heart?

One day at a time, friend.

One day at a time.