Thursday, October 20, 2011

Battle Hymn of a Dragon Mother

This post is a bit different than any other I have done.  Its not an update on Reagan's status or cute and cuddly pictures of our new little family.  Its a post about a really hard lesson that I have learned, and felt convicted to share.

We are nearing what would have been Reagan's due date.  It is hard to believe when I'm looking at my sweet girl that we would have had to wait 2 more months to get to know her!  I feel like I've cheated in a way, stolen 2 more months of getting to be her mom.

As a new mom of a NICU baby, you are so incredibly happy that your child is alive, breathing, healthy, and thriving. I spent my time in the NICU with Reagan looking toward the finish line of getting home, but soon after I came home I realize the race has just begun.  You've made it through her being "sick" and now she's not, so life goes on normally, right?!?  Wrong.

You take your newborn home, but she's not a newborn she's a 1 month old.  Its hard not to start comparing her to other kids her age.  In fact, there are kids that have been born well after her that are meeting milestones ahead of her.  The nurses in the NICU did a great job at managing our expectations as far as her development.  They discussed adjusted age and stressed the patience we should have in this next year.  However, the world (and my worldly self) hits you with something quite different.  Well meaning friends and family make casual comparisons that sit in your head and don't let go.  The first thing at her doctor's appointment is a barrage of questions about what she doing, what she's not, and while she was functioning like an average full term 1 month old, it was starting to stress me out.

Problem is, I was becoming anxious about it.

  I was baptized again at 25 which is a story all of its own, but it was then that I truly began the journey in becoming who I am to be in Christ.   Anxiety is something that I have found Satan can use as a stronghold in my life.  It causes me to become someone entirely unlike myself.  I become insecure and competitive and it gets in the way of my resting in His peace.  Its not pretty.

So I sat down for my morning quiet time (which is now about 4am...thanks Reagan) and started reading verses about casting our cares on the Lord.  After my prayer, I began researching additional info about preemie milestones (clearly I had not gotten the message) when I came across this article in the New York Times from a mother who's child has Tay-Sachs disease.  Now, while Reagan by no stretch of the imagination is or has ever been as ill as this precious angel, I found myself greatly inspired and convicted by her beautiful prospective and advice for parents.

Warning:  This is VERY hard to read.  Although the author never mentions God, He is certainly woven all throughout her testimony whether she realizes it now or not.  I LOVE it when he immediately answers prayers....even when its to give me a kick in the pants.

Warning #2:  I have had this kid home for 2 weeks and I've already failed as her mother....well now that that's out of the way....

I hope you are blessed by this as I was.

Notes From a Dragon Mom
MY son, Ronan, looks at me and raises one eyebrow. His eyes are bright and focused. Ronan means “little seal” in Irish and it suits him.
I want to stop here, before the dreadful hitch: my son is 18 months old and will likely die before his third birthday. Ronan was born with Tay-Sachs, a rare genetic disorder. He is slowly regressing into a vegetative state.  He’ll become paralyzed, experience seizures, lose all of his senses before he dies. There is no treatment and no cure.
How do you parent without a net, without a future, knowing that you will lose your child, bit by torturous bit?
Depressing? Sure. But not without wisdom, not without a profound understanding of the human experience or without hard-won lessons, forged through grief and helplessness and deeply committed love about how to be not just a mother or a father but how to be human.
Parenting advice is, by its nature, future-directed. I know. I read all the parenting magazines. During my pregnancy, I devoured every parenting guide I could find. My husband and I thought about a lot of questions they raised: will breast-feeding enhance his brain function? Will music class improve his cognitive skills? Will the right preschool help him get into the right college? I made lists. I planned and plotted and hoped. Future, future, future.
We never thought about how we might parent a child for whom there is no future.  The prenatal test I took for Tay-Sachs was negative; our genetic counselor didn’t think I needed the test, since I’m not Jewish and Tay-Sachs is thought to be a greater risk among Ashkenazi Jews. Being somewhat obsessive about such matters, I had it done anyway, twice.  Both times the results were negative.
Our parenting plans, our lists, the advice I read before Ronan’s birth make little sense now.  No matter what we do for Ronan — choose organic or non-organic food; cloth diapers or disposable; attachment parenting or sleep training — he will die. All the decisions that once mattered so much, don’t.
All parents want their children to prosper, to matter. We enroll our children in music class or take them to Mommy and Me swim class because we hope they will manifest some fabulous talent that will set them — and therefore us, the proud parents — apart. Traditional parenting naturally presumes a future where the child outlives the parent and ideally becomes successful, perhaps even achieves something spectacular. Amy Chua’s “Battle Hymn of the Tiger Mother” is only the latest handbook for parents hoping to guide their children along this path. It’s animated by the idea that good, careful investments in your children will pay off in the form of happy endings, rich futures.
But I have abandoned the future, and with it any visions of Ronan’s scoring a perfect SAT or sprinting across a stage with a Harvard diploma in his hand. We’re not waiting for Ronan to make us proud. We don’t expect future returns on our investment. We’ve chucked the graphs of developmental milestones and we avoid parenting magazines at the pediatrician’s office. Ronan has given us a terrible freedom from expectations, a magical world where there are no goals, no prizes to win, no outcomes to monitor, discuss, compare.
But the day-to-day is often peaceful, even blissful. This was my day with my son: cuddling, feedings, naps. He can watch television if he wants to; he can have pudding and cheesecake for every meal. We are a very permissive household. We do our best for our kid, feed him fresh food, brush his teeth, make sure he’s clean and warm and well rested and ... healthy? Well, no. The only task here is to love, and we tell him we love him, not caring that he doesn’t understand the words. We encourage him to do what he can, though unlike us he is without ego or ambition.
Ronan won’t prosper or succeed in the way we have come to understand this term in our culture; he will never walk or say “Mama,” and I will never be a tiger mom. The mothers and fathers of terminally ill children are something else entirely. Our goals are simple and terrible: to help our children live with minimal discomfort and maximum dignity. We will not launch our children into a bright and promising future, but see them into early graves. We will prepare to lose them and then, impossibly, to live on after that gutting loss. This requires a new ferocity, a new way of thinking, a new animal. We are dragon parents: fierce and loyal and loving as hell. Our experiences have taught us how to parent for the here and now, for the sake of parenting, for the humanity implicit in the act itself, though this runs counter to traditional wisdom and advice.
NOBODY asks dragon parents for advice; we’re too scary. Our grief is primal and unwieldy and embarrassing. The certainties that most parents face are irrelevant to us, and frankly, kind of silly. Our narratives are grisly, the stakes impossibly high. Conversations about which seizure medication is most effective or how to feed children who have trouble swallowing are tantamount to breathing fire at a dinner party or on the playground. Like Dr. Spock suddenly possessed by Al Gore, we offer inconvenient truths and foretell disaster.
And there’s this: parents who, particularly in this country, are expected to be superhuman, to raise children who outpace all their peers, don’t want to see what we see. The long truth about their children, about themselves: that none of it is forever.
I would walk through a tunnel of fire if it would save my son. I would take my chances on a stripped battlefield with a sling and a rock à la David and Goliath if it would make a difference. But it won’t. I can roar all I want about the unfairness of this ridiculous disease, but the facts remain. What I can do is protect my son from as much pain as possible, and then finally do the hardest thing of all, a thing most parents will thankfully never have to do: I will love him to the end of his life, and then I will let him go.
But today Ronan is alive and his breath smells like sweet rice. I can see my reflection in his greenish-gold eyes. I am a reflection of him and not the other way around, and this is, I believe, as it should be. This is a love story, and like all great love stories, it is a story of loss. Parenting, I’ve come to understand, is about loving my child today. Now. In fact, for any parent, anywhere, that’s all there is.

Was I anxious about Reagan hitting silly milestones for her or for me??  Was I trying to make her into what the world tells her she should be or what the world tells her that success is?? I wasn't happy with her just being ahead of the curve as far as preemies go and right on track for her age, I wanted her to be ahead of ANY curve....OUCH...I got it God.  You're probably going to have to teach me again, but for now, I got it. 

"And there’s this: parents who, particularly in this country, are expected to be superhuman, to raise children who outpace all their peers, don’t want to see what we see. The long truth about their children, about themselves: that none of it is forever."

What is forever is her relationship with Christ and who she is in Him.  That its more important than all the accolades and riches this world has to offer... its my Dragon Mother Battle Hymn

You have made her; and through Jesus you have made her perfect.  My job is clear and simple:  To love her as you love me, to teach her about you, to be on my knees every day to look to you as an example in being her mother.

Of course its fine to celebrate her successes and I will continue to be the proud mama that I have been since the moment I laid eyes on her.  My prayer is that I will remember this lesson and always be a Dragon Mother.
So I know I said no cute pictures, but I couldn't resist.  I love this little girl more than I could ever imagine and am so thankful God has entrusted her to me



Sunday, October 16, 2011

We're home!

Well after 27 days in the NICU we heard the words that we have been waiting for since they day Reagan arrived..."You are going home in the morning."  As excited as we were, I immediately started worrying if it was too soon.  You become so dependent on the monitors to tell you that everything is ok, that your baby is breathing and all is well.  Fortunately they allow parents to "room in" the night before you go home.  They take the baby off all monitors but you still have nurses close by if you need anything or worry about how she's doing.  

Let me just say that neither Larry or I slept a wink.

We were a lot more confident after that night about her continuing to do well at home.  The previous few days she really seemed to turn the corner.  She was quickly emerging from what felt like a fragile preemie baby, into the stable, much more tolerant newborn infant...who just happens to be nearing her 1 month mark.  Her breathing was much more rhythmic and we hadn't seen her drop her heartrate in days.  When she would choke while feeding, instead of de-satting and dropping her heartrate to below 80 her vital signs would remain much more normal and she would rebound quicker.

All of these things were very reassuring, plus we had looked up epidemiology articles about the recurrance of apnea and bradycardia after 5 days without an episode....Yes Reagan, your parents are nerds, but well informed nerds.

Still, all rationale, facts and figures go completely out of the window when its your baby.  I think all new moms must go through this, but it hit especially hard for me, as I have witnessed first hand, on multiple occasions, my baby stop breathing and her heart drop to a level that would not sustain her.  So needless to say we were a little nervous.

But we all made it through the night with flying colors.





Going home was rather sureal.  I never got the chance to be "ready" for Reagan to come home.  I was extremely blessed by wonderful friends and family who got her room together, clothes and blankets washed, and baby gifts organized.   For ALL of you who have not yet received a thank you card, I'm so so sorry....hopefully you will get them soon!

I can't thank Dana, Sheila and Rachel enough for driving all the way from Houston to hang pictures and refinish my dresser for me.  Those are true friends right there.  Larry and I really got the benefit of seeing how many wonderful friends we have and how blessed by the body of Christ we are.  We had so many people that prayed for us, brought us food or giftcards to local restaurants, brought food to the nurses, and other odds and ends that we needed.  Your care for us not only blessed us, but was a ministry to the hospital staff as well.  We had several comments about "where did we go to church" and "I don't really do church, but that one I'd go to."  Such a blessing to see the many ways the Lord uses a situation for His glory!

I'm not really sure how Larry and I made it through that month.  Have you ever gone through something really tough in life, work, school, or maybe athletically that you just do what you have to do to make it through, and then when you look back, realize how truly difficult it was?  Well that's how we feel about this experience.  There is not a thing I would change though.  I loved being able to work to save my maternity leave and be able to help take care of Reagan around the clock, but it really wore me down.  Larry was staying at the house to take care of our dogs and actually get some sleep so that he could work.  I missed my partner.

Home has been the polar opposite experience.  Reagan and I haven't stopped snuggling since she's been home.   Our schedule is pleasantly flexible and Larry is here to help with feedings so I can sleep through one or two and nap.  Its amazing!

We love you so much Reagan!  Life is so much better with you in it!

Friday, October 7, 2011

Reagan is 1 month old!

Reagan came home shortly before her 1 month mark so her newborn and 1 month doctor's visit were all rolled into one!  Its hard to think of my baby as a one month old, because she just came home she feels more like a newborn to me.

As a preemie you are supposed to go by her "adjusted age" rather than her chronological age as far as milestones go.  That makes her negative 1 month old, so basically she has a a couple of months before we stress about what she's doing other than eating and sleeping well.

The kid sleeps like a champ!  I joke that she has a solid 30 minutes of awake time in a 24 hour period, but its absolutely true.  When she is awake she's doing all the things a one month old should be doing, its just hard to catch her awake!

Her first walk
 Holding on to her Grandmama
Pretty sleepy...Cricket wanted to be in the picture

Her 1 month stats:
Weight: 5lbs 7oz (not even on the charts)
Height: 19.5 inches (5th percentile)

What she's doing:
Eating and sleeping like a champ
Lifting her head and turning it side to side during tummy time
Making brief eye contact
Briefly tracking an object
Making lots of grunts and coos....her fav is one that sounds a lot like a baby goat....we love it!
Quickly growing out of preemie clothes in length not in weight

What she loves:
Her bath!
Snuggling/Kangaroo care time

Being swaddled - wont sleep unless you can control those arms and legs!
Her paci

She also got to meet her cousins!


BFFs
Love these three!