Sunday, March 17, 2013

A Thursday in September...

At 4:13 p.m. on a random Thursday in September 2002, the woman I was exchanged places with the one I had to become. It was not a heroic decision; it was not a decision at all-I was jolted.  Alarms and guttural fear heralded the event and an overwhelming desire to will survival into another human being overtook any pain I experienced.  Quickly followed by the murky realization that I was secondary to the existence of a six pound baby struggling, grasping and clutching to remain in this world, jarred me from a past where I believed in white picket fences. 
     My son, Quinn’s, birth  was not one of gentle memories and swaddled joy.  It was one of rushing and flailing.  He entered the world without a sound; he could not announce his arrival with the typical cries of a newborn; he was drowning in his own fluid.  Before that day, I did not even know he was a boy and I did not know his birth and death had the chance of being closely entwined.  He started life troubled, not thriving, and I was unprepared.  Unprepared for my thoughts to immediately turn to “take me instead of him”; thoughts I had for a child I would never see until many hours later.  I did not need to see or hold him; I was a mom and I wanted to breathe life into him.  Medical personnel ripped my baby from me and rushed him to Pic lines, chest tubes and ventilators before I even got the chance to touch his cheek and revel in the miracle.  He was somewhere fighting without even drawing his own breath; I could not share mine because I left it in the operating room.  As I lay on the table in the recovery room, people spoke and I heard pieces of muffled conversations referencing priests, baptisms, and last rites.  “He can’t go before I meet him,” I wanted to scream but I could not find my voice.  I knew that I could not leap from the bed because I just had a Cesarean Section and doctors roughly converged on my recovery room trying to regulate my temperature. As I lie on my bed, flashes of light and memories interrupted me while I continued searching my mind for comfort.  Words would not come and the unfamiliar faces that entered and exited my room offered no information.  I wanted to crawl to Quinn; I wanted to grasp my baby from the clutches of death and run- run with him to a place where I could cradle him from the harsh entrance and struggles of his first minutes.  
 I made it to my room later that evening in a blur of familial tears and embraces.  Standing up from the confines of my hospital bed while grasping the IV pole, I willed myself to take steps.   In those first dark, hazy hours, I raged at the unfolding drama.  My anger and disbelief flowed outward and I wished for others to feel my pain.  These moments still wrack my memory at times; moments when my soul showed a capability to turn evil.  As I listened to nurses wheeling the white-picket-fence babies to the waiting arms of exultant parents, I wanted to extinguish their joy.  The sound of those squeaky wheels on the freshly waxed linoleum served as a constant reminder that my son would never make an appearance in my doorway and I wanted them silenced.  Those parents did not deserve these gentle moments more than I did and I yearned for what I rightly deserved.  During those hours, I questioned any faith that remained, I cursed god and demanded deliverance from the dark.  Finally, the nurse agreed to wheel me to the Neonatal Intensive Care Unit and once again I was unprepared; unprepared for the intensity of my love for this baby boy covered in wires, tape and tubes.  That was the beginning of the journey of building our white picket fence.  At 2:33 a.m. on the day after my son’s birth, I touched his small, swollen and bruised hand and found my new builder.  The next morning brought our first obstacle; I had to mourn the child that would never be.       
In a suffocating and institutionalized room beside the NICU, a Genetic Counselor opened her chart of chromosomes and announced in a cold and matter-of-fact manner that my son had Down syndrome.  That is when I hit the floor, literally and figuratively.  Familiar hands cradled my splintered mind and body and gently placed me back in my wheelchair. Watching the counselor’s mouth moving, I heard nothing as every corner of my mind filled with the “never and what-ifs”.  As family members stared motionless at the news, the invasion of thoughts included, “He will never attend a prom, go to college or get married….I am not this mother.  I am not this strong.  I am defeated….”  I did not know until years later why I projected so far into the future; I now know that it was the beginning of the mourning.   My son would never be the baby I hoped to welcome.  My support system offered kindness and comfort, but ultimately nobody helps someone with that realization; I had to go straight through the grief.  The intensity of the emotions in that small room almost broke me.  Because of those frozen minutes, I understand the insurmountable weight that sorrow can bring.  Those moments I spent under the poundage of lost dreams smothered me; I climbed and thrashed back to the faces staring at me.  My son had Down syndrome.  Down syndrome.  I repeated the words to myself over and over trying to digest my new reality.  Focusing on the dim lights and stained walls, I strained to stay with the conversation.  When the Genetic Counselor entered the room from the hallway,  the air left the room and I found myself searching for oxygen.  Then I realized that in the next room my son wrestled in the same way and I woke up.   That moment was the beginning of collecting splintered dreams and starting to build a new version of a white picket fence. Quinn was on the other side of the wall and I inched through the tangles of medical terminology and uncomfortable change.   I do not remember who followed me, but I remember sitting and gazing into the face of a baby that could not yet open his eyes, could not support his own breath and could not reach for me, and I changed.  The change occurred forcefully and within seconds.  Without doubt, I determined that I would find strength because this boy deserved a mother that believed in his possibilities before he could do it for himself.  Over the endless hours of that second day, I sat.  I sat and spoke softly, stroked his beaten arm and solidified a bond.  I connected with my son; it was differently than expected, but it was our way.    
Over the next days that turned into weeks, the most important moments of my life became watching numbers on machines.  I monitored oxygen levels and heart rates while reading, studying and asking questions about medical terms and situations I never wanted to know. I spoke with doctors, counselors and experts in order to piece all of the information together and learned how to keep building our fence.  On Quinn’s fifth day, I left the hospital and Quinn stayed where he would for many weeks.  The chill invaded my lungs as I walked out of the revolving door and the endless tears started.  In the car ride on the way home, I stared at the passing cars and the nonchalant people going about everyday tasks and the anger made it back to my thoughts.    But, Quinn’s face flashed before me and the anger subsided; as has occurred countless times since his first day, he calmed my restlessness.  His face stayed in my mind during those dense and dismal moments in the deepest part of the nights when the phone calls from the NICU shattered the silence.  The nurses with updates; some depressing and some encouraging, the communication carried me through the night.  Every day I rose and made my way to that face.  My son.  My reason.  
The building of our new fence required that I learn the gentle ebb and flow of Quinn’s timeframe.  Many days he and I took steps back only to step forward the next day.  I learned significant lessons about myself and those around me.  Previously I always searched for the next goal or step, but with Quinn, I learned how to exist in the moment and savor every success.  Quinn’s presence in my life gave me perspective on the importance of working on my fears and weaknesses while developing into the mom Quinn deserved.   Above all, I learned that strength grows when life destroys old dreams.  I spent countless hours over the years in hospital rooms, in therapists’ offices and in improvised places of prayer.  Additional diagnoses and health concerns arrived and at times, questions of fairness and faith clouded choices and blurred our vision.  This never lasted long; Quinn kept me focused and we kept building.  The many nights spent sitting and watching Quinn sleep carried me when life gutted my hopes and flung me to my knees. His tender presence in my life softened the blows and healed my wounds.  People close to me shattered my spirit and walked out; however, those of stronger character and resolve entered my life. The baby that I mourned in those first days traded places with a boy full of infinite possibilities that could accomplish all the things that I foolishly dismissed in my mind as not possible.   Quinn created everything I am, everything I strive to accomplish, and everything pure and compassionate in my spirit.
Ten years ago and fallen with fear, I yearned for a “white-picket-fence life”; if I could go back and hold the woman I was then, I would tenderly whisper in her ear…”Quinn will be a fighter, a giver of unconditional love, a stubborn force, a singer of Jingle Bells in the middle of July and a savior.  The trials will come, but so will a childhood that lingers a bit longer.”  If I could go back to those first tumultuous minutes, I would not silence the sirens or dim the fear because those moments are the ones that proved a catalyst for my transformation.  Within frightening and frenzied moments exist opportunities for priceless gifts.  People often say to me, “God gave you Quinn because you are strong enough to be his mother.” The reality is that Quinn gifted himself to me because I needed direction and purpose.  He is my teacher and guide.   I am better because he reaches for my hand and holds it while he walks beside me. Quinn teaches me every day the importance of living a life of vibrant color and enthusiastic existence and that white picket fences belong on other people’s lawns. 

10 comments:

  1. Wow...a lot of love in this blog. Good stuff Kelly. Very inspirational.

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  2. That was great....We all have moments of doubts in ourselves, in our children, in our family or friends but in the end we realize these doubts are because we love our life, our children, our family and friends. This is not only inspirational but also a testimony of how hard the first moments of a child's life can be wether or not there is something genetically wrong. Thank you for this post Ms. Jones.

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  3. This has brought tears to my eyes Kelly!! You are a strong woman and Quinn has a wonderful mother. You are his strength as well. I have always said God only gives what we can handle and he knew you would be one hell of a mother!!!

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  4. Your story hits very close to home. I only wish I was as strong as you are. I am 7 years in to my new life...and every day is a struggle.

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  5. Wow... You took me right back to the birth of my Mya! I had forgotten a few of the details you mentioned. After, 3 long months in the hospital, conquering infections and open heart surgery we came home to more IV antibiotics and the start of in house therapy. Wouldn't change it for the world. Would relive it a thousand times over. What miracles we are blessed with. How I learn everyday about more blessings... Going on 7 years of daily blessings! Take care and thank you for reminding me about the beginning days!

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  6. Thank you. I read this, weeping, reliving our own initial days after our son's diagnosis. Thank you for sharing your story, for finding a way to put that all into words!

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  7. I love this blog and I can relate in a thousand ways!! My son was diagnosed with Down's when I was 4 months along but a specialized ultrasound proved that Nicholas had none of the several markers for Downs. When I was 7+ months along they found out that he had a Duodenal Atrsia which means that his small intestines were almost completely closed up and that he definitely had Downs. He was born c-section in Pittsburgh after a 3 hour ambulance ride and taken almost immediately to have tubes and whatnot inserted into his poor small body. When I finally got to see him after they had him loaded into a carrier to transport him to the Children's hospital a block away so full of tubes and wires it was so heartbreaking. I could only barely touch him through the carrier. Then he was whisked away and left me sad and alone without my baby to cradle to my chest. I also felt the feelings of malevolence toward the other happy parents that got to hold their babies. Nicholas had to have surgery the next day because his pancreas had grown around his small intestines and they had to cut above and below and stitch it back together. Which also involved a 5+ week stay in Children's, as well as several visits since for various other medical problems. I spend more time in hospitals and with therapists then I do with my son most days. But I wouldn't give him up for anything, he is my world!!!

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  8. Kelly, isn't that the thing, to allow us as parents to watch and marvel at how wonderful our children have been made by our loving Father. My husband and I are getting ready for our wee girl's first birthday and your post took us back to the beginning of our journey. Thank you for sharing your heart with us. We are rejoicing with you in the lives of our dearest children.

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  9. Wow...u hit every detail of our daughters birth on the nail...and just like you...I didnt believe I was strong. When they said the words "down syndrome"...it was as if I was sitting on the birthing table stiff as a board and the rest of the world was spinning around me and I could see all the blurry sides spinning. Then u see your baby...and you know why...because you needed her first.

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  10. I absolutely LOVE this! Thank you for sharing, you took the words right out of my heart!

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