Thursday, February 26, 2015

How to Outswim a Shark Without a Snorkel


This is for all the moms out there who are with me on this journey.  The journey of having a child who has a rare chronic illness. 
 
 
I would not consider myself a movie buff.  When I do watch movies they are generally comedies I have seen a hundred times before or classics I watched with my mommom.  But I remember watching the movie Men of Honor.  It was not the best movie I have ever seen, it did not set my heart on fire but the scene in which Cuba Gooding Junior had to walk across a courtroom in that scuba suit got me.  Watching him take each slow, painful step made you yearn for him to be able to take just one more.  You cannot stop watching, waiting, hanging on to see what was going to happen next.  Having a child with a rare chronic illness means that every day feels like walking across that courtroom in that damn scuba suit, that movie is now my life.  The thing is I am not just living this for a few days or a few weeks.  The suit never comes off.  I carry that suit around all day every day and it is never coming off.  My baby is sick.  She is in pain at some point every day and she is never going to get better.  This is a realization I come to over and over again.  Just when I think I have accepted it, normalcy reigns in some benign way for a short period of time and then the beastly disease rears its ugly head again.  
 
 
My dive suit is my prison.  I never take it off because I never know when I will need it.  When you live with a rare chronically ill child, you have to be ready at a moment's notice to jump into the depths of the dark ocean, terrifying in its unfamiliarity.  Each dive is new terrain that you must navigate... in the complete and utter lack of light.  You do not know how far down you will have to go until you are on your way.  You pray, on your way, that your suit will withstand the pressure.  "It has to, it just has to," you say to yourself.  There is a house to keep up, laundry to do, bills to pay, a husband to love and siblings to nurture and probably a job, hopefully some friends who have loved you enough to stay.  Remember though that this suit never comes off so the weight is constant but the dive just adds to the pressure, the never ending strain.  You go down, down, down until you find the bottom, feel around for a bit and start to come up.  Only to wait for a bit for the next dive.  Is the wait easy?  Is your suit lighter in the interim?  No.  Why?  Because you have been to the depths and the memory clings to you like so much seaweed and sand.  It takes awhile to brush off.  Sometimes it is not even gone before you are diving again. 
 
 
While on the surface, the weight of the suit is something you just carry with you.  Sometimes it is lighter and sometimes it feels like all you can do is lift one foot and put it in front of the other just like good old Cuba.  And  there is the guilt.  The things you have done to her.  The pain you have caused him.  The frustration you have felt.  You have shoved tubes in them.  You have held them down while doctors and nurses have done things most adults could not even fathom.  You have stuck them with needles, over and over.  And then the siblings, the guilt over the siblings.  You have ignored them.  Forgotten their school projects.  How many nights have they showered and eaten at the hospital?  How many hours of TV have they watched because you are dealing with vomit?  The list goes on and on.  
 
The biggest reason to feel guilty?  Sometimes the only thing that lifts the weight of that suit is when she reaches over a takes your hand from her hospital bed.  Or when he splashes around in his bath.  You should feel that way about the other kids too.  What about your husband?  But no, it is only her.  You could have just held her down for two hours while doctors pulled bandages off of open wounds and she will still reach for you... Mommy.  It lifts that suit away and gives your tired, bone-tired, body a small break.  You feel free for just a moment.  Until he coughs or adjusts his body from pain and the suit comes crashes back down onto you as you remember your baby is sick.  Your baby is in pain.  Your baby will always have pain.  And you, you, will always be Mom.  You will always wear this suit. 
 
The suit can be a comfort some days.  It is dark and quiet inside.  It is all yours.  No one can reach you.  No one can hurt you.  You can scream.  You can cry.  No one can hear.  You can scratch and claw and fight.  And when the guilt gets to be too much you can punish.  Punish yourself that is. The inside of that suit is awful rough and it is quite sharp.  Forgot that homework assignment?  A little rub on the ankle will take care of that.  Did not remember the medicine tonight?  A scratch to the shoulder for that.  Can't take the pain away?  Can't save her?  What is the price for that?
 
Someday you know that they might wear their own suit.  They might have their own worries.  They might make their own decisions about which medicine to take: the one that causes cancer or the one that eats away their intestines.  For now you make those decisions and it is ok.  You almost revel in it.  You almost love every minute of it.  The vomit, the hospital, the stress, the deep sea dives, the needles, days spent on the couch, the crying and the fussing, the sleepless nights.  You think that sounds crazy?  Let me explain very simply.  There are some parts of the ocean that have no bottom.  When you have a child with a rare chronic illness you never know, is this going to be the dive where you do not find a bottom?  Most of us do not know how long we have with our babies.  So yes, I will hold her all night. Yes I will wipe those beautiful lips even if it is disgusting vomit I am wiping away.  Yes I will sacrifice my own body so she can have what she needs, what she wants.  People are always telling us 'you have to take care of yourself so you can take care of her' or him.  They do not know.  They cannot possibly understand, unless of course they have lived it.  Of course if they have lived it they would not say that.  When you are taking care of your sick baby, whether you are 3 months in or 5 years in, when you do not know where the bottom is or when it you are going to hit it, you will do anything, sacrifice anything.  It is not dramatic, it is not a scene from a movie, it is so simple.  There is no question.  It is not hard.  Walking around in the murky depths it is just you and your baby after all.  Where it is dark and scary you still have those sweet arms, that forgiving hug and that heartbreaking laugh.  You do not need food and sleep, you don't even want it.
 
So what do you need?  Some of us may say we need our babies to be better but most of us know that our babies are following their paths as they are intended.  You hate it.  It breaks your soul but it is theirs.  So what do you need? You need understanding. You need lack of judgment.  You need kindness.  And people come through.  Thank God, people come through.
 
Tonight my baby hurt.  She hurt a lot.  She cried for me, Mommy, and I held her until she stopped.  I am diving this week.  I don't know how far down I will be going.  I am scared.  My cumbersome suit surrounds me.  It is shadowy, dank and unwieldy.  My vigilant suit protects me but the cost is great.  I do not know who the person is who is going to come out in the end... if there ever is an end.  But this is my life.  This is what we learn to accept.  We accept it in waves because you could never just accept that this is the rest of your life. Worrying about things we will never have answers to and loving babies we don't know the futures of.  Thank you for traveling this journey with us and thank you for trying to understand...  
 
 


2 comments:

  1. Gina,my heart and prayers are with you as always.I wish I had a magi wan that could take all of her pain and disease she endures away. That they get to the bottom of this horrible disease and Lillyanna can run and play. Wishing so much joy for you and Chris and family. God,please hear my plea. Make a miracle and let Lillyanna be cured of this horrible disease. I love all of you. from Maryellen Strohm. Take care and God bless.

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