Showing posts with label intubation. Show all posts
Showing posts with label intubation. Show all posts

Wednesday, July 10, 2013

Holding on to hope

I am positive that there are a few things in life that you can never be prepared for.

Seeing that tiny piece of you on a hospital bed with a machine pumping his lungs full of air, that air I admittedly take for granted all day, every day. Watching his body move and knowing its not being done by him is a strange realization. It takes some getting used to. You don't know what to expect. How much will he move, will he open his eyes, what is our new normal? It took me some time to adjust.. It was totally unreal. I needed a moment to gather my thoughts...We headed down to the lobby, grabbed a coffee and trekked to the parking garage. I opened the hatch to our trunk and just sat there letting it sink in. We didn't talk much, both kind of quietly picked our emotions up off the floor and gave them a good dusting. Pushed the negative out and let the positive settle back in. Out of the hospital room....just outside away from everything as I processed our "new". 

We ran into Hunters dad on the way out. I could tell he already knew what was going on. Our boys were neighbors again..only a sliding glass door to separate us. There isn't much that can happen around here without the other families noticing. As we walked out our eyes met miles before we did..there is something that happens when two scared souls suffering the same pains lock eyes. Its like all your thoughts and fears intertwine and there are hours of conversation had without the need for a single word..the connection in that gaze speaks about a level of pain few have ever experienced. A helpless pain. The pain of a parent that comes as they watch their child tiptoe on the very thin line of life and death. It's an understanding that can only be fathomed by someone in our situation. Truly An unforgettable moment. You share the same horrid life experience and you know the odds are someone has to lose...so when one of us teeters a little closer to stepping over that thin line, you feel sadness for them, not only because you have come to know and care for them but because you know it could easily in an instant be you. I'm sure a sorry and a sigh were exchanged somewhere in there...but there is nothing more memorable than the unspoken.

 We spent the rest of the day with Hud and our nurse Katy. I can't relay the importance of an awesome nurse during these stressful long term hospital stays. She is a complete match to our personalities. She loves to play with our daughter, she laughs at our jokes (probably the most important thing of all) and I'm always able to talk to her whether it be about my emotions, experiences or of course Hudson's medical issues.. Being completely comfortable with the person responsible for keeping your little one alive always makes it easier when you are on your way out for the night. I will always remain thankful for the days we have nurses like that.

When we arrived the next morning we were greeted with a rarely closed curtain in the first room. We entered Huds room and found the glass door joining us to Hunter unusually closed as well. I thought it odd, but sometimes during in room procedures or discussions they will close the partitions.  As I rotated around I caught sight of Hunters monitors. The screens were dark, my heart sank. That sweet boy was waiting for a transplant and no monitors could only mean one thing. His dad sat cradling him in his arms...then getting up to place him back on his bed. Instant grief washed over me. I wanted to run in and see what was going on...ask a million questions...hug them...cry for them. In the same sense I didn't want to intrude, I battled with myself as to what would be the most appropriate approach. I wanted to imagine it wasn't happening only feet away from us. I wanted to pretend the reality away. If I don't believe in it, it can't exist.  I caught glimpses of the hardest moments any parent can imagine play out. He exited the room...I seized the opportunity, stepped out of Huds room and as he was talking "y'all did everything you could" to his Dr. he began to break down. I instantly interrupted the conversation and wrapped my arms around him to comfort...I'd have done anything (seriously, anything) to make them feel better. I whispered "I am so very sorry" squeezed harder.....backed away, grabbed his arm and said the only thing I could offer..."if you need something, please don't hesitate"..I wish there was something more profound that I could have rattled off instead. Regretfully, that is all I had. There really are just no words. Shane and I were in total disbelief for the rest of the week. We still talk about Hunter and I doubt we will ever forget. So, to that sweet faced little man who always knew when to pull off his pulse ox and toss it out of his crib for attention, the soft little voice that always wanted yum yums, the 1 1/2 year old who touched so many lives....rest easy now, sweetheart.
Nothing around here is easy, nothing.


Friday, July 5, 2013

"Bagged"

  Walking into the waiting room to check on my boy's new set up in the PCICU..approaching the window my eyes were drawn just past the front desk clerk and instant fear smacked me in the face. I saw my son on a bed, arms wide to his side, his lifeless little pale body at the mercy of the Dr.'s. A bag being squeezed by (at the moment) the most important hands on the planet. My tiny little boy was being manually ventilated or "bagged". I was horrified and as I gasped the tears began to roll while I asked what was happening. It had been 5 hours since he was taken from me..way too long for a parent to wait without any updates, but we wanted to give them the time they needed.
 The receptionist completely lacking tact and compassion for the situation says "now don't you go doing that" in a tone as if my tears were annoying her. My heart began to thump hard in my chest as I turned my head and roared at her..."lady, that is my son and he is being bagged right in front of me..I NEED TO KNOW WHAT IS GOING ON?!". She got up and said someone would be with me as soon as possible.
  The worst was rolling around in my head, my son had just died...my son is dead...what am I going to do..my boy is gone. A fellow came out and greeted me at the door just moments later. She said Mrs. Moore, I am so sorry you had to see that, Hudson was having a really hard time with breathing and we decided the best option was to intubate him before it became a necessity. Holy shit. How can something so serious happen and Shane and I have no idea? I had a million questions but just wanted to get the gist of what was going on, so I held my tongue. Shane had popped in twice to check if he was ready before this and they said they were still getting him situated. We by no means expected a Dr. who had hands on our son to stop what they were doing and run to educate us...but there are a lot of nurses in there and someone....ANYONE..could have given me a minute of their time. We deserved that..we definitely didn't deserve what had just happened.
  I only caught a taste of the worst...and let me tell you, it is unbearable. It is everything you feel when that thought occasionally crosses your mind, for no good reason at times. Only 100 times worse, and I had a good reason. You know, the thoughts you would have as you read about other babies, or with no particular trigger you'd find yourself trying to imagine what it would be like if you were to lose your child. I'd be alone and a mess....but just like you, I could stop thinking about it..go to Emerson's room and watch her chest move up and down as she slept peacefully. I could stop thinking about it because it wasn't a reality. Now I face the thoughts everyday for my son, watch his chest move up and down only because a machine is forcing the air in, wishing it wasn't my reality.
I don't want to know what it's like...please don't let me have to find out. I'll ride this roller-coaster but I want to make sure we all get off when its over.

WARNING for my pics below, my son is intubated which may be disturbing to some.