Tuesday, September 29, 2020

2020 09 29 Rehab in these times

Tuesday September 29

Franciscans Childrens Day 01.

We were discharged from Boston Childrens Hospital this morning 1030ish.

Alex arrived at Franciscans 1100ish.

For the past fifty something days, I either stood or sat by Alexs bedside to provide support, care, playtime, med time, change time, etc. On the wall I had my notes of when, what and how.  For many normal people this may seem weird, awkward, like I am either ADHD or a straight up nut job. I kept these ever changing notes on long strips of paper towels.  The paper towel notes consisted of medicine schedule, feeding schedule, sleep schedule and the three or four therapy schedules. These were all important. Each of the schedules impacted each and every one of the others, yet no doctor, team, nor nurse would ever figure, nor begin to figure it out without daily noting.

His medicines make him drowsy therefore the drowsiness drives his sleep schedule. His sleep schedule interferes with his occupational, physical and speech therapies.

The goal here is to maximize and to take full advantage of his awake time. The goal is to utilize his awake time for the therapies therefore scheduling them appropriately. 

For the past twenty something days I kept these long paper towel lists, I've used them as a tool to talk with the teams every morning and during the day with the ever changing nursing staff. As a team we have made changes to medicines, their times thier doses etc. As a team we juggled scheduling of the therapies. We scheduled the time and the order of the therapies. We found with time and experience that less strenuous to most strenuous worked best.

Speech is less strenuous physically but most strenuous mentally and emotionally.  Ot (occupational therapy) may be less strenuous than the p.t. (physical therapy).

Almost every morning mom and I listened to what the teams had to say. Mom and I don't always agree with doctors or teams and we both ask questions from different perspectives. Mom and I dont always agree with each other,  but we always 100 percent of the time agrees that we do what we do and when we do for "what is best for Alex". It is teamwork between the doctors, nurses, therapists and parents. Both parents chiming in and coming to an agreement and a conclusion. This process of agreement is crucial, this process of agreement is important for Alexs health and for the sanity of a family that had a soccer ball kicking kid fifty something days ago.

Today that was stripped away from us. This morning we left Boston Childrens Hospital. Today we said...this is a new chapter, this is a new begining, today we start therapies in a new place. We are gonna get up and kick ass today.

We had a few issues with pick line dressing pain and Alex had notible anxieties about being transfered from his bed to the ambulance travel bed. Mom and I calmed him in our own way. We traveled out the door, hall, elevator and out the hospital back door entry / exit for the ambulance transport parking. Unbeknown to me,  Once he crossed the threshold of that ambulance door....that would be the last time that mom, I and Alex could be in the same place together until Alex is discharged from rehabilitation. Uhm....what the hell just happened?

Bela and Alex were transported to Franciscan Childrens. 

We considered it because of its name once we heard it, they have a chapel, we assumed that it had something to do with the Franciscan order, etc. Our insurance wouldnt cover the other options unless this option turned us down.  Most importantly we chose to stay here due to the short distance to the hospital if ever required. Physicians mentioned that rhe building is older but the therapists are outstanding.

I take the long lonely walk to the parking structure, get my self out of it and mapquest my way to the Franciscan Childrens. Generic  building, very blah, very sand toned brick from the seventees?, large, long half cylinder - laid flat bleeched over- the -years awning and confusing parking. The parking attendant seemed upset that I interrupted his lunch when i stopped to ask if I should park in visitor spots or long term spots. He answered while talking with his mouth full and Boston accent....so I understood almost nothing.  I parked where I think I understood it to be and made my way to the building. Im in the building and go through covid screening. I explained 3x that I was dad to the "Alex" that was just transported and transfered here. They asked me a few more questions, took my temp, made me swap my mask and asked if someone was with Alex...I said yes...his mom. The oriental lady taking my info and aiming the thermometer gun at my head said "ok...wait outside until your wife calls you."

Uhm what? What outside? Family room? Waiting room?

she said "No...outside building."

Confused I asked "Uhm what? Like parking lot outside?"

She said...."yes."

Ok so lalalalala, confusion, "what? Huh? Ok....so I am Alexs dad. He was just transfered here. Im going to be living here until he is better, I dont understand what misunderstanding we just had but you are asking me to go back outside? No waiting room?"

The oriental lady got nervous and made a phone call, a security guard was soon by my side and then some lady came over and without introduction starts the conversation with..."mom is with Alex and the nurses, they are settling in and our policy is only one visitor at a time". I was confused and said "that sucks, That wasnt expressed prior  and so what room do I sit in and wait in? She responded with "you need to leave the building".

That didnt go over very well in my stomach. Im currently writing this 3 hours later (after seeing Alex for a bit) I am writing this from a broken down... wood railroad tie wall in thier parking lot as it begins to rain.

I asked the lady to identify herself and she did, I told the lady that mom and I work as a team. I have Alexs schedules in my backpack. I have medicine schedules and doses, I have his schedule in writing that is crucial for all the nurses to be introduced to.  Not only that..."we could not be transfered here yesterday because you don't have epidiolex, a medication that Alex is on. Do you have it today?"...I knew the answer... The answer was no...."the answer is no because it was delivered to me in the hospital yesterday and is all in my backpack". Im thinking in my mind...I am Alexs rescue, mom and I work together at this and they are shutting us out over redtape bullshit.

We have to figure this out. At this moment as I sit on this broken down, half rotted broken down wall in the parking lot, my first impression of this place isnt a great first impression. From building, to parking attendant, to the crew that put up a wall between family and son. We understand 1 parent per night (we have organized arrangements elsewhere for that). We were prepared for that, but we weren't prepared to break up Alexs team during the day. This isnt something that a non verbal child who just lost half his brain function, mobility, and almost his life with in the past 50 days needs to go through. This isnt something that his family should go through. We understand the Covid requirements, we get it, we abide by and agree.  Ive been in quarantine in a hospital for over 50 days. I haven't left bedside other than to go to cafeteria for food. I left for 12 hours on the 12th of September and then right back to the bedside.  I dont leave, mom brings food. Mom gives Dad a break and vice versa. This Covid reg now just kicked our ass.  They have plans in place but they dont make sense. Ugh I have ten pages to vent on.

Prayer

We are here.. Lord... I believe in all things for a reason...we are here. I heard that this is the place for Alex to rehab and for Alex to get stronger.

Lord forgive me for the temper tantrum that I have just gone through.  I ask that you bring Alex the right people at the right time.

The outcome that I want and beg for Lord is a strong walking, kicking, fishing, rock throwing and talking Alex. If this is the place let it be...I will make whatever sacrifice and make this here ant infested wood wall my home.  I beg for his strength, his stamina and his recovery.

Our father. Hail Mary, Glory be.

Today is the feast of Holy Saint Michael the Arch Angel. 

Holy Michael, the Archangel, Defend us in battle. Be our safeguard against the wickedness and snares of the devil. May God rebuke him, we humbly pray; and do you, O Prince of the heavenly host, by the power of God cast into hell Satan and all the evil spirits who wander through the world seeking the ruin of souls.  Amen.


Monday, September 28, 2020

2020 09 28 Off to Rehab?

 2020 09 28 Monday Day 53?

This was to be our last day at Boston Childrens Hospital.  This morning at 545am we had Neurology rounds. During the visit nothing was said.7am Alex was awake and Alert. I turned on his tv and went to grab a few cups of coffee and a few of the cereal pods in the hall. 730 am the nurse stepped into our room and sang..."Youuuuu are leaving todayyyyyyyyy yeeeaahhhyyy."  My heart dropped. Huh???? Uhm I almost choked on my cheerios. OK.

I wasn't ready but can make myself ready pretty quickly. I travel light....but Bela and Alex require six trips to the parking structure a block away. Any..... way....long story short. I moved everything out of the hospital room and into Belas car.  Funny story short.....they couldn't get thier paperwork and medications aligned and prepared before the 3pm cut off....sooooo we stay the night and are to head out Tuesday 10am.

This chapter closes and the next chapter will bring strength and healing.

Rehabilitation:

"Movement" is a medicine for "creating change" in a persons physical, emotional and mental states.....(by Carol Welch)


"Work out like your life depends on it because it does."  (unknown)


It will hurt. 
It will take time. 
It will require dedication.
It will require will power.
It requires sacrifice.
We will need to push your body to its max.
But I promise you, when WE reach OUR goal, it will all be worth it.   (unknown)



Prayer:

Lord God You are the Great Physician.Alex needs your healing touch Lord you are the healer of weakness,  viruses, chronic conditions, diseases, and You are the healer of our child Alex.  As we ask you to heal Alex, we will declare by faith that Alex IS receiving your abundant healing power right now and that Alexs' health IS steadily improving.We declare that we will not look at what our eyes see, but we will look at what our faith sees. We will feed our faith concerning the healing power that is bringing health to Alex.  We will stand strong by your biblical words: "By his stripes we are healed."  Thank you in advance Lord, for bringing your awesome healing power into Alex. Lord we praise you for healing Alex. In Jesus' name we pray.



St. Pio. Thank you for interceding for us and for making very clear to me the answer to my prayer. St. Padre Pio, please continue to intercede for Alex. We pray that the Sacred blood of Jesus wash and heal Alex from the top of his skull to the soles of his feet. The Lord has said...anything that we ask of the father through the intersession of Mary and in the name of Jesus...he would answer. We trust in his word ans that our prayers will be answered.  Our Father. Hail Mary. Glory be. 



Sunday, September 27, 2020

2020 09 27 Sunday

 2020 09 27 Sunday

Photo by mom

Photo by mom

Photo by mom

Photo by mom



Photo by mom

Alex slept well through the night.

It has been a very long and busy week with crazy anxiety ridden scheduling for surgeries, scans, etc. But this weekend he is doing better physically. He was able to get some sleep during the night as well as naps during the day.

Yesterday Alex sat up a few times showing us the beginnings of his core strength. He began to show leg strength on right leg and started showing little twitches on his left leg. Bedside we had music and dance time. We are able to get several minutes at a time.

Now....today...day 52 we begin a new chapter.  This chapter will focus on physical, occupational and speech therapies. We will review all therapies and see how the feeds and medications should be adjusted for their purpose, we will make the schedule adjustments and we will focus the feeding schedule around all therapies. We focus on what medicines to reduce, eliminate, or move on the daily schedule in order to maximize his potential and give him more awake time during therapies.  

It is taking a lot of planning, a lot of time, and a lot of energy. With that said...he is starting to do his work, currently  he requires equal amount of napping. This will be a long process, this may take months, but today we start. We take it slow and steady.

We had not yet seen him move his left arm or leg.  Today after completing our homework for occupational and physical therapies he was able to get stretched out, work range of motion and was then able to show slight movement of his left arm to touch his shoulder, touch his nose, mouth and chin. Within an hour he was shaking the maraca with his left hand.

This afternoon we worked on core, legs sitting upright and standing. Sitting and attempts at standing are a difficult and tiring thing. We were able to push up to standing position with our legs with assistance.  We are still not sitting nor standing alone, but we are working toward it.

Lord God thank you for the steps toward recovery. Thank you for laying your hand over us and for getting us through what we truly know was an extremely dangerous and desperate need of your assistance and your intersession. We truly know how dangerous the situation was and we truly know that we did receive a miracle. We thank all of the saints and all of the angels for the intercession. St. Pio thank you for the the very clear intercession and the extremely clear and direct answer to my prayer. St. Jude, St. Anthony, St. Michael,  St. Joseph, St. Lawrence, St. Gerard, St. Paregrine, Holy Mary, St. Therese etc. Thank you for your intercessions.  God I Thank you in advance for the upcoming energies and staminas. We ask for courage,  strength, stamina and progressive recovery.  We understand that we have a long road ahead of us, we thank you for this chance, this opportunity to be able to take the steps to recovery. Thank you for listening to the prayers of the hundreds of family and friends praying for our Alex.



Saturday, September 26, 2020

2020 09 26

2020 09 26 Day 50??? Will confirm.

We had mri Thursday night to see how things are progressing. I wrote a long description of the exhausting past couple of days. Because of Thursday night events, his Friday was very sluggish. Friday night he had Ambien to sleep, Saturday morning was a late start. 

Saturday he was to have a bedside procedure to remove his drain. They were to remove the drain placed in surgery.

Another day of waiting. Since the surgery we have had a drain to relieve pressure and to allow flow. Since Monday the amount of liquid per hour has reduced. This morning at 5:45 am the neurology team came in. The team did thier routine and said they would be back this morning to review the drain removal and stitching. At 10:30 the Neuro surgeon came in and said we will be back in half an hour to do the procedure. At 11:30 the nurse came in and said they were coming soon at 2:30 the nurse said they will be coming soon and that she would be giving morphine. At 3:00pm the nurse was in and the Neuro Surgery (Yassir) was in the room and ready.  The nurse stated that she hadnt sedated yet and morphine through pump would take 10 minutes. He mentioned reduce the amount and give via bolus direct with one minutes time. He mentioned that he just received emergency call to operating room. Yassir asked if I could glove up, mask on and help with supporting Alex for thr 5 minute bedside surgery.  I did as requested while Yassirs assistant stood by his side and updated him on the incoming emergency situation. 

The assistant updated him with age, transport situation, what the child was going through, what the child was feeling. She told him the medications that he is on and a little of the history. Yassir had asked only 2 questions about the incoming patient. What medications is he on? what event led to his current state? The assistant answered. When she answered with the medications I knew of or have heard of them. When she mentioned the event I opened my eyes wide and said wow...yeah...that is a tough sport...things happen...but you never want to hear about a kid who has a disability, yet does what he or she can to keep active and play a sport in order to pretend or to truly be a little closer to normal, get caught in the crossfire of the sport. "God we pray for the right people at the right time for that child. Give the child the strength and the opportunity to get back to his sport. Give the parents the strength, stamina and faith to get through it all." 

Alex was given morphine. Alex was very relaxed. Alexs hands were light, his head and neck were loose and his eyes were very glossy. His pupils were a very dark black. I was able to follow direction and hold Alexs head still while Alexs area was prepared, sterilized, drain removed, re sterilized and then stitched. Alex was a champ, he lay still, very still. Alex had a moment where he made an attempt to move. I said in a stern voice "Alex stay still" and he seemed to understand by the tone of my voice that this was not one if those times where he could disobey.

I held his head still, the surgeon pulled the last stitch and we were done. When I gave Alex the "ok we are done" he almost instantly made the attempt to roll to his left which is now his new sleeping position.

Never in my younger years did I imagine myself bedside holding my kids head still while a surgeon provide bedside procedure and stitching,  never did I think that I would have the courage to do so.  This kid has gone through so much, I hold him still so that he doesnt get hurt, Im not really certain if he understands. I know that I would be screaming or crying....but this little man looks around, he isnt looking right at me yet, but he hears me. He listens for me, he senses when Inor mom are there. He is a tough kid, he went through a lot of "stuff" he is small but he has been tossed into and has taken on and fought these large battles. He is young but had gone through more pain and suffering than many sixty, seventy or eighty year olds.

We pray that God give this little man the strength that he need to begin to recover. We pray that he recover as God leads his way. We ask that the Lord reward him with healing un exchange for all the suffering that he has withstood.  We pray for all of those around us in the hospitals that they heal and that vrow stonger daily.  May the Lord heal us and may the Lord give Alex strength and recovery so that we as a family may find a way to help others in avoiding the travel down this road.

2020 09 25 past couple days

Friday September 25th



Last night Alex went for an mri. This was a short scan of his brain to get a quick look at what was just done, his healing progress and to see if there were any new issues. We were scheduled for this exact mri on Wednesday morning. Alex was transfered out of the ICU on Tuesday night / Wednesday morning at 2:00am. This poor kid had the craziest week (schedule-wise). Very little sleep Sunday night, Monday night and Tuesday night. Wednesday night they were prepared to put us through the waiting game anxiety torture again but I begged for a break. They agreed to give us a break Wednesday night and agreed to do the scan on Thursday during the day. Alex then had the ability to sleep through Wednesday night into  Thursday morning with the assistance of a sleepy time medication.  Thursday during the day they attempted the mri early in the morning. They attempted to do the mri without sedation and Alex didnt cooperate. Alexs lack of cooperation on Thursday cost us

A waiting game for the rest of the day and into the night.

Monday.We were scheduled for Monday morning surgery. Through the early morning blood work was drawn, he was cut off from feeds at Sundays midnight. We were told that we would be in que and therefore anesthesia and surgeons would come with consent forms. Through the night knocks and consent forms were delivered by thier corre- sponding providers.  During the night, knocks and the night nurse delivered his medicines, during the night, knocks and the CA (which is the night nurses assistant) would come in and do Alex's vitals and neuro check...The blood pressure, temperature, bright light in the eyes etc. The door would close and almost instantaneously one of the machines would start to beep. The iv machine pushing fluid or iv medication is the machine that beeps the most. It beeps when almost done, when done, or when the line has a kink it it from movement, etc.

As a patient or parent there is no rest. There is no piece, the minute you as a parent sit on the hard plastic cover of the single pull out  couch bed and so much as reach for the pillow or hospital blanket, another beep or another knock at the door.  I gaze over at the large round clock on the wall and count the time that I have for potential sleep before the first rounds of doctors come in the morning. The first rounds which are neuro surgery rounds come early.  The neuro surgery team consistently walks into the room somewhere between 5:45am and 6:00am. They "need to do what they need to do" and waking Alex up and pissing him off at 545am seems to be "what they need to do".  So I look at the big round clock and count the hour and one half before nuero surgery bust in the room.  At 6:00am Neuro Surgeons come in and followed through with thier normal routine as I antcipated..at least I was ready. Once they  were done, I asked if they had a time slot for Alexs procedure. They said Alex was third in line, the first two were short cases so we should be ready to receive the call.

The entire day was a blur. The entire day was A blur of aggrevation for me. I recall that we were told several times that we were waiting on the call to go to surgery but not sure if it could be in one half an hour or not. As an anxious parent I waited. No breakfast, no lunch and then no dinner. Who has?...what parent has the stomach to go to subway and order the spicy italian with cheese, toasted and "run it through the garden with mayo and oil and vinegar" at a time like this? The furthest thing from my mind right now was nutrition. I couldnt get myself to drink coffee at the moment because I know how I get after my 5th cup. 


During the day I sit to pray. I am not certain of wether I am praying as a meditation, as a release, as a method to remove myself from the situation, as a request for healing, a request to heal Alex, A request to heal me, his mom, his brother, his grandparents and all that pray for him. I am certain that as quickly as I sit down to pray, meditate or get away from the situation for a bit.... is as quickly as I get interrupted by beeps, dings, knocks, questions, a briefing, my own anxieties or exhaustion. In between it all, I put my hand in my right pocket and grasp and move my Rosary into the palm of my hand.  I have enough time and energy to start the Hail Mary but find myself then thumbing through the beads backwards to find the cross with the true, whole hearted intention to start from the begining. With my fingers I find the cross, I start the Apostles Creed and midway draw a blurr, my anxieties hit me even more now because I realize that I can not remember the order of the words within the prayer. I realize why, I know why, "God forgive me,  forgive me so that my prayers can be heard. Right now Im trying to focus, I am trying to be strong, trying to pray the right prayer, but I cant remember the words" I reach for my phone and scroll to the picture that I took of the prayer years ago. I find myself reading the prayer about 3 or 4 times. I repeat my reading because by the time I get to the middle of the prayer... my mind wanders and I catch myself. I tell myself that If I am in this prayer, then I need to know exactly what I am saying and exactly what I just read, exactly what I just said. I feel guilty about my mind wandering and I force myself to start again. I dont know why I start again. I dont know if It is truly about me feeling guilty, I dont know if I do it as punishment or if I do it out of respect and expect to give one hundred and ten percent or nothing at all. I finish reading the Apostles Creed from the screen on my phone, I was in it with one hundred and ten percent. I shut off my phone. I can now lean back on the couch, cover my eyes with a rolled up t shirt to mimic darkness, put my hand in my pocket, hold my rosary beads between my thumb and pointer finger and make yet another attempt at saying a few more Hail Marys.  True story... we waited...No joke..we waited...we waited some more...we waited forever...we waited all day long...If it were not for the interruptions, the anxieties, the mental and physical exhaustion, one may have been able to pray one hundred rosaries, but I did not, I could not, the anxiety brain fried me. We were finally called for surgery at 330pm for 400pm roll in..

(I wrote about the surgery in a separate blog)

Late Late Late in the night We finally get to see Alex. We get to see him somewhere about 1030pm. The anxiety over night last night was noted, but I truly do not have the ability to express the true intense feeling of that anxiety, the sounds of all the dings and bings that save his life while waking him, annoying him and raising his own anxieties that in turn may end up producing more sounds. It is ironic that it may be a vicious circle. The smell of the place, the sterile stuff has a weird very bad tequila scent, the cold temperatures, the cold lighting and the voices of the professionals. The professionals that walk through the door, do what they need to do and then all say "ok we are done, we will not bother you anymore....try and get some rest!" They have no idea that once they leave, the next team is right behind them. I can note it, but the anxieties and feelings during these moments are so much stronger, so much more overwhelming than I have ability to express. All day long the anxieties peak and drop. The anxiety levels are like a first time rollercoaster ride with the unexpected highs the unexpected drops the crazy assed unexpected turns, etc...the days and nights when things are not going well are truly unexplainable. Several times through out the day I try to close my eyes but not always able to get more than 15 -20 minutes at a time.

Now...here WE were in the ICU  again, 1030pm, We are exhausted and he is just now coming off of sedation. Here we are exhausted and this has only just begun.  I know where we have been and it has not been fun. Right here, right now, we are tired and have no idea what to expect.

This time we walked into the ICU and it was was different. This time Alex was awake, this time Alexs eyes were moving around the room. Alex was sitting up, there were only 2 nurses in the room and they were calm.  The room was cold, the smell was unexplainable. It smelled like some kind of sterilization smell, maybe the bad tequila that i mentioned earlier. The room was small, tight in width. The bed and the nurse occupied the majority of the width. Behind his bed were the emergency movable towers that contain dozens of power switches,  several oxygen hookups, several vacuum hook ups and many vertical bars that hold the pumps, and many high hooks to support iv bags, transfusion bags, etc. The lighting was cool white, alexs color was pale. The first impression was...he is awake! That was a great sign. The bandages cover a large portion of his head but he looked ok. He is still no where near the Alex that came through the doors forty something days ago, but he was sitting upright was awake and looking around.

The last several times that we walked into an ICU room after surgeries Alex was asleep and had so many wires, so many machines. The last several times Alex had life saving respirators and a dozen IV lines into him. The first time we walked into the ICU room forty something days ago, several nurses moved around feverishly pushing a dozen meds, several nurses in panic mode watched the vital signs on various monitors while several other nurses pulled us into the hall and asked us questions. That visualization in my head was then, this is now...So many thoughts went through my mind and so much strength was required to make the attempt to stay in the "right here right now" moment and focus on where we were now. While walking toward the ICU room just minutes ago, these flashbacks of the first night had hit me. In my mind I began to recall the nurses, the doctors, the fast movement, the number of people involved. On day one, forty something days ago, I walked into a hallway that was busy and in panic.

After the second and third surgeries, Alex had a breathing tube and was heavily sedated. We had walked into the room and sat by his side with the "God please help us! God help Alex and get us through this". It is almost like we prayed alot harder...did we have a lot more energy to pray or was the situation different?  Tonight I walked into a room that did not present panic. There were not a lot of nurses nor doctors moving around frantically. Alex was awake and showing signs of waking up more than he already was, showing signs of confusion, aggrevation, discomfort and pain. He squinted his eyes as if he were about to cry.y heart broke for him, I could almost feel his pain and his confusion but I couldnt let him nor anyone else know that deep down inside I was hurting with him. Alex had just gone through a 6 hour procedure. Alex just had a crazy amount of stitching....something has to hurt!!!  

I have had stitches before and they hurt! I have also had minor stitching to my finger and oh my goodness...that hurt.  I can only imagine the pain and discomfort that this poor child was going through.  What hit me the hardest was his fascial color and the bright red blood stream that ran down his forehead. The nurses asked questions, I couldnt hear anything at the moment. I had not seen my kid all afternoon, now I see him and he has a slow steady stream of blood flowing down his forehead and I stop it before it hits his eyebrow. The nurse is still asking me questions. All I hear is blah blah blah blah..."Nurse. Get some more bandaides, stop this blood from flowing and then maybe I may be able to hear you...at this moment I can not take the focus off of my bleeding kid to look your way".  The nurses gave me a couple of boxes of gauze and stepped out of the room in search for large enough bandaids.

Within a few minutes Alex had three large bandages over his scars and blood ran down through the bandage on his left side as he laid his head that way, the blood was now being absorbed by the bandage and no longer flowing down his forehead and toward his eyes. My son was awake but he was bleeding. The bright red was very bright red in contrast with the bright white bandage and the greenish gray color of his skin.

Alex was stable. He needed blood because he lost a lot of it. He wasn't able to get any rest In the ICU Monday night. While in the ICU the nurses have to poke him every hour. Temperature, blood pressure, heart rate, oxygen levels, listen to lungs, listen to belly, shine bright light into eyes, etc.  Monday was now another no sleep kind of night with all of this going on and with all of the nurses asking us hourly if this was baseline or if we see anything of concern. Midnight through 9am Tuesday was a blur. Alex was given medication to sleep and relax....they wouldn't give me any.

Tuesday was a blur during the day. The ICU, the family room, the halls, the dings, we want out of here. I was exhausted and as soon as mom could relieve me for a bit, I went over to the parent sleep room to make an attempt at sleeping. I was able to get a little sleep between 9am and 12pm with only 3 knocks on the door about room cleaning, a turn in your key reminder and some little sibling looking for his parents room after taking a quick visit to the public hall bathroom and all doors looking exactly alike.

By 130pm I was back to Alex bedside. Alexs drain was draining a lot of blood. The team was reviewing his status and his schedule as to when to transition to the floor. My first impression of Alex right now was that he looked pale, I mentioned it and the team decided to draw some blood and check it all.  An hour later the lead nurse came by and said "you guys arent going anywhere....Alex needs a transfusion, He lost blood and we will get him back to himself in 4 to 5 hours".  We waited on the delivery of the transfusion.  Once we received the bag...somewhere around 6pm the nurse began her set up of the machines. The iv machine was to pump the blood into Alex via his pick line. Over the first hour the machine kept beeping occlusion on patient side. The nurse would flush the line and the flush went fine but the blood would not. The nurse changed several pumps, changed several iv lines and then made decision to swap from pic line to another iv that was in his left arm. 7pm a nurse came in and said..."as soon as the infusion is complete you can go to the floor". A few minutes later another nurse came in and said "no...it doesnt make sense to go up now, you stay the night". I set up my window seat nesting area and lay my head on my backpack. I placed my hand in my pocket and had enough energy to hold the beads and ask for forgiveness so that my prayers could be answered. Im uncertain if I even closed my eyes before the night nurse came in and said "I hate to do this to you but....we were just told that there is a big influx of children in need of ICU beds. Alex is pretty stable and can be moved to the floor".  I was annoyed about the uncertainty, I was annoyed that this poor kid had to keep getting woken up after all the crap that he has gone through. On the other hand I was excited, blessed and fortunate that they considered him safe enough to travel. Thirty days ago Alex was so fragile that everything came to him. Thirty days ago Alex could not be moved up nor down nor side to side.

Right now she was telling me that he just had surgery yesterday, but right now less than 24 hours later there were a lot of kids in the hospital that needed ICU care more than Alex. Alex was stable and could rest peacefully upstairs. Right here, right now, there were a few kids that were going to be in desperate need of the equipment. We waited, I waited, I was annoyed, but I understood. It sucked to be moved but it was a relief to only need ICU for one night.

At 2am we rolled out. We arrived back onto the same floor and same exact room that I emptied out three nights ago.

It was now Wednesday morning. 230am and I was turning his lights of, I was making attempts to get myself ready for sleep because it was 230am and we know who wakes us at 5:45am. It is 230 and knocks at the door. The nurse in charge of the floor needs to come in, introduce herself, check Alexs tags, ask questions, ask about concerns, etc. It is 2:50am and knocks at the door, two or three people walk in, they are neurology, they introduce themselves, they need to do a neuro check and they ask me about his seizures and ask if I have any concerns. It is 330am and knocks on the door, the night nurse checking in on us, do we need anything? She lets us know that she will be back at 4am to hook up his antibiotic to the iv and then at 6am for vitals and his 6am medication.  We review the medications, I ask if she needs me or if I can shut my eyes....I do not even remember the answer.

Wednesday morning at 545am the neuro team came through. They let  us know that they anticipated the mri this morning. We waited. Same story as surgery. We waited all day, there were anxieties. We waited all day and we kept getting told that we were in que. It was a long day, but a recovery day. Alex slept on and off through out most if the day. We met the different teams, all said that he is doing very well compared to 40 something days ago and compared to the direction that they thought he was going to take. He received his 6pm meds, he received his 8pm meds and at some point this night nurse came in to say tbat he was in que and brought me the consent form. I was confused, upset, annoyed, frustrated, you name it.

I asked if I could refuse. Nurse said I had the authority to refuse, accept, reschedule, etc.  I didnt even take a split second. I straight out said "Nope...not tonight....last night was an anxiety attack all night till 3am in the morning. Alex may have slept, but I havent. Its 9pm bring Alex an ambien to help him sleep and lets turn these lights off until Neuro surgeon turn them on at 5:45am Thursday morning.  It was a long day, sleep is good, I couldnt stay up late.  Even then knocks on the door, teams come in to tell me that I made the right decision and that tomorrow is another day.

Thursday 545am. Neuro surgery came in, did thier bedside exam and again stated mri this morning. We waited. We received a time slot for early morning. We rolled down to the floor for the procedure. My anxieties were through roof again. Everyone let me know that this was fast, didnt require sedation and that it is done all of the time. This was to be a fast maybe 10 minute scan. I was trying to picture it. Ive done stuff with him...he doesnt keep his head still how is rhis going to happen.  We get down to the mri room ans they wouldnt let me in. Now I was mire confused. They said you need to change out of all your clothes ans into scrubs, they said they can do the scan faster that I can disrobe and robe and to trust them. I was confused, but this was in Gods hands.  They told me where I could stand and so I stood. Alex was rolled through 2 doors with the two nurses that brought us all down from the floor. They didnt need to disrobe nor robe and i am pretty certain that thier scrubs came from home, so I didnt truly understand the difference.  15 minutes later I heard and saw them come through the doors. He looked exactly the way he did when he was rolled in through the doors. The nurses shook thier heads and said that he didnt cooperate. They laid him down but he didnt keep his head still. The lead nurse said...our RN will need to come up with a plan and revisit.  His not cooperating this morning cost me the day if anxiety all iver again.  We waited and waited and waited....he had his 6pm meds, he was about to have his 8pm meds and at that moment I told the nurse. If we dont roll out by 930 so that he is back by 10pm, they will need to reschedule for another day. She looked upset and frustrated about what I had just said.  Well...I get it...it was her 2nd 12 hour shift and she is juggling three patients, it isnt easy to organize and coordinate transport and mri room and mri techs, etc...but damn....im on my 48th or 49th straight 24 hour shift.  At 9pm they gave Alex a dose of Ativan. He fell asleep and was able to be rolled out, transported to the mri room, shifted off of beds, had the loud mri in his ears and didnt move. He was transported back to the room by ten. Alex remained asleep until 545 when neuro surgery came in for thier review.

I was able to rest now. I was anxious now about the result of the test that we could only hear about Friday. I had to block that from my mind.  Its ten oclock thats 2 hours till midnight meds, thats 6 hours till his antibiotics and eight hours until neuro surgery wakes us. I hope that I can get somwe sleep. Mom is in the room tonight, i set up my camp cott, lay myself down. I dont even have enough energy to put my hand in my pocket to reach for my rosary. I make the attempt to pray using my fingers as the digits for the beads.  Alex is sleeping, within this room things are quiet, things are not as cold as they have been. Within this room we plan on staying and resting. Alex is asleep, Alex is stable, I fall asleep without praying and ironically my prayer of the moment for restful sleep is answered.



Thursday, September 24, 2020

2020 09 24 Alex Spoke!


On Wednesday Alex spoke...who would have ever guessed what his first words would be. All my life Ive heard the words, shared them, used them in jokes or fugure of speech.  Alex and I goof around, mom hated it, but now fell in love with it.  Figo just reminded me via The portuguese kids videos and coincidentally on the same day, the pork-chop in Alex that wore off from Dad came out in a time that was so desperately necessary.


 2020 09 19 Saturday

There were no scheduled therapies today. Last week while I was away for Ride Closer to Free with Jordan, the Weekend Physical Therapist didn't disconnect Alexs' G and J tube and they both got caught on something and got pulled out of his body. Alex then required emergency surgery to have the g tube replaced and the J tube rethreaded with use of xray technology in the operating room. I believe that this weekend the weekend PT was staying away from Alex and I and rightfully so.

Today Alex was awake alert and enthusiastic. We had to do something, so we worked on our range of motion and stretching.  By the afternoon I gathered up enough courage and energy to sit Alex up alongside his bed. Alex gave me that look of..."Dad...you better know what the F@#& your doing". I hadn't even yet grabbed for his hand and he already had it in the air and his right leg up as if he were trying to do it all himself.   Several times I brought him up into the seated position. He wanted to get up, but once up he was up he had that look in his eyes as if he were in pain. His body swayed from side to side when his head was up and then when tired his chin was buried in his chest. He sat and was able to tolerate for a minute or two before he buried his chin in his chest. I then lay him down for a break. We repeated this several times with hopes of strengthening his core and neck.

2020 09 20 Sunday

Today Alex was alert. Awake and was able to sit bedside with my assistance. His torso and core was a little stronger than yesterdays attempts. He was lifting his head up on command.  He sat bedside, his legs dangling off of the side of the bed and his feet dangling. He kicked hard with his right but nothing from his left. It felt as though he was using his right leg for balance or to make an attempt at moving. His head was not stable. He looked around, opened his mouth and moved his eyes as if he was getting some type of stimulation with all if this movement. He is moving his right arm a lot. If the rattle is in his hand he is shaking it like crazy. He listens to command. If I tell him to stop, he does. As he sits bedside I am on my knees in front of him. I have my hands at his sides and I support his waste from going to far to the left, right, front or back. Today is Sunday, I took it upon myself to give it a go without the physical therapist. The therapist requires two professionals, a nurse, a helmut, a big chair and a lot of pillows.

Bedside it is Dad and Alex. We sit, we sway, we listen to music. We sway a little to left and right (supported) and we work our core.  Alex has not done much in the past forty something days so this is a big step.  His head moves left to right, front to back. He works real hard to keep his head up and then gravity brings his chin right back down into his chest. I give him a few minutes and then tell him to lift his head and he does. When he lifts his head, I can almost feel his sense of accomplishment. I tell him that I am so proud of him and I can see right away that he lifts his head higher, his shoulders straighter and the tallness of his core reduces the load on my two hands that support his waist. He seems to be able to hold it for about 2 minutes before gravity drops his chin right back into his chest again.  He rocks his head from left to right, his chin buried in his chest, his eyes look upward, he isn't looking straight at me, but it appears as though he is looking up and waiting for my direction or my praise.  I tell him..."ok buddy, one more time...chin up lets count to 10..."and he does. He lifts his head up and begins that stimming thing again.

He is working hard. He is trying harder. He is definitely trying to focus, but he us having trouble.

When his head is up, his eyes are heavy, he looks like and reminds me of the drunken state Party nights when I was sober but everyone around me was blitzed. The heavy eyes, the attempt to focus but the see right past people and weird breathing and drooling that came with it.  Alex is trying, but the meds that are helping him are also kicking his ass.

Even though the process is slow, these past couple days have been better than any of the other forty something. He is awake. He is alert. He is draining my energy and I love it.  Sitting and core strength are a big step in his recovery.  I see that as we work the core, he is begining to come out if his shell. These past couple of days have been better than the past forty something.

2020 09 21 Monday

Today Alex goes for surgery. We sit up bedside like we did yesterday right now so that mom can see the progress that we are making. He sits bedside, I support his trunk, he lifts his head higher and taller today than he did Saturday and Sunday. I am pleased to see that he is gaining strength. We have a long way to go, but we are definitely showing slow progress. Mom stands behind me and calls for Alex. He lifts his head and looks in that direction but does not yet focus. She tries hard to get his attention and he tries hard to give it. We will get there, we are not there yet but we will het there.

2020 09 22 Tuesday

No sleep, had surgery yesterday, today was a big blurr, recovery day.

Back in ICU. It is cold, loud, the nurses poke and check Q1 which means every hour. No break, no rest, they need to assure that all is well and that they do not miss any issue.

All day long the teams teetered on whether ir not we were to leave ICU to go to the floor. All day long we were given conflicting information. At 2am we were packing up to move to the floor.

2020 09 23 Wednesday

Today alex spoke!!!

Mom was trying very hard to get Alexs' attention. Alex was not able to focus nor make eye contact yet, but he was trying.  I went on with my type of talkin "you need to wait...like a hunter you need to wait all day for that very small moment in time that will save your life. The moment that will provide you with the food that you need as the nutrition, energy, etc." Mom responded with something blah blah blah tired, blah blah blah back hurts. I responded with " It is like fishing...you wait all day for the fish to bite, they will come, the school will pass, you need to be ready and time it correctly. When the time is right....things happen...you just have to wait, you need to be patient but most of all you need to pay attention and not let your guard down."  I relate this right back to fishing. Anyone can fish all day long but only the one who studies the tide or river flow, the temperature, the sunrise, the sunset  the barometric pressures and moons can have better success rate.  I can usually work with Alex and succeed but I know that he wont do anything when tired, sleepy, post ictal or heavily medicated. I look for his body language, I wait for his demeanor, his energy, his sign to me that he is ready.  It doesnt come often but like the sportsman I wait, I am patient and take full advantage when that time comes.


I was sitting bedside singing one of Jorge Ferrieras' songs for the umpeenth time. The song I was singing was one that mom hated, but a song that Alex and I love. I drive Alex around town, we have the top down, windows open and the radio blaring...We bob our heads and repeat the phrase "E Pa" and "Vira Maria". Alex responds to it, we make noise, he is engaged and we pass our time searching for stop signs, counting fire hydrants and reprating the phrases.  While on the hospital bed we were listening to the music via youtube on the tv.  As we listened I said "E Pa" real loud along with the beat of the song...I looked down to Alex and asked him "Alex YOU say it". You wouldnt believe my surprise when I looked down toward his lips and saw the movement and heard the soft sound of his breath mimicking the words "E PA"!!!!!!. I damned near fell right off the bedside.  I called Bela right over as I said..."This is exactly what I am talking about..."Alex....say "E Pa"" and in a silent voice he breathed out the words yet again. They were sift but they were clear, they were meaningful and they were on command!!!!!. I was so happy. Bela was so happy...It couldnt have come at a better moment in following the lecture that I was preaching...lol. Bela hated the song, she hated that we sang it over and over....today...at this moment what she hated then was her favorite now!.


2020 09 21 surgery


 2020 09 21 Monday Day 46

Monday morning (Monday) Alex was able to sit up along the side of the bed as he had done Saturday and Sunday. He still requires a lot of assistance, but he appears to look forward to sitting up. Saturday we sat up 3 or 4 times for about 4 minutes each time. Sunday he sat up 10 times for 5 minutes or longwr per sitting. Sunday I would ask him if he wanted to sit up, he heard me and he would then bring his head and chin to his chest and lift his right leg as if he was making the attempt to get up. Sunday he was up and at his bedside well over ten times.  He was able to sit upright at the edge of the bed while I held his waist with both of my hands, one on each side.  He would tire quickly, his chin would drop to his chest. I would ask him to lift his head and he would. He would raise his head up and move his head left to right as if he were trying to look around the room. He was making the attempts to look around the room but had no focus. I had music in the background on the tv and the bedside hand held speaker.  The music appeared to be the distraction and he appeared to be able to hold his head up a little while longer with the distraction.  If I counted, he anticipated the numbers and would drop his head exactly 1 number before the number that we spoke of.

Monday afternoon (4pm) Alex went into surgery and Monday night 10pm Alex was out of surgery and back into the Intensive Care Unit for recovery. At 10pm when the surgeon came to talk to us all that I wanted to hear was that Alex was ok and that things went well and without complications. The surgeon sat down and said that all went well and that Alex was in the ICU room. He stated that the piece of area that was to be replaced had to be done in three sections due to its size. It required more plates, screws and adjustment time than they had previously anticipated. The surgeons took longer to stitch him closed due to the amount of stitching, they chose a specific stitch over the conventional... and.... blah blah blah....all I wanted to hear at that moment in time was that my kid was safe, had his skull back on and was going to be alright.  The surgeon continued to speak and I now have his notes written down elsewhere....but then at that moment I just wanted to hear "Alex is alright and you can see him now".

The surgery prep and holding room


Was cold, there was this ridiculous draft that blew the curtains several feet in different directions when the doors where open. Alexs space was directly next to the doors and so the curtains kept slapping against my body as I stood bedside. I held Alexs hand while the sedation team came, spoke, had me sign the dotted line and waited for questions. The neuro surgery team came in and did same, the nursing team came in and did same. I knew almost everyone on the surgery team, They had done the initial surgery and had visited our room every morning at 6am for the past forty something days. The surgery team spoke and hung around. The surgery team now felt a connection, they knew Alex before, after and had seen him everyday fir the past forty something days. The team had seen my fear before, had seen my frustration, have heard my comments about not waking Alex up every morning at 6am to piss him off and then walk away. They heard me say "there are 10 of you here. You wake him...and one of you WILL be held hostage to watch him while I sleep!". They hung around and I could feel that they were searching for words to console me. Almost all if them came iver to me one by one and gave me an eye to eye and let me know that he was in good hands and that they were going to do thier best.  I wished them all good luck and begged God to bless them. The surgeons walked away and anesthesia crew was bedside. They gave Alex a little sedation and he was sleepy. I gave him a kiss on the forehead and told him I would see him upstairs.  The room was cold, windy and monotone color wise in my eyes.  It may have had color, but then and there I saw no color.  I was upset, I was worried, I was nervous, I was anxious...but all I could do is pray for the right people at the right time and ask God to give them all courage, knowledge, stamina and steady hands. I begged God to look over it all.  I had been here forty something days ago..."please lord make this time different than the last". I watched him being rolled away again this time like I watched him forty something days ago. It hurt to watch, it broke my heart to watch, my hand let go seconds ago but my heart and eyes couldnt. Some nurse kept talking to it...something about her showing me the way out, the way to the parent station blah blah blah. My eyes and heart were on my kid as he was being pushed away, my inner voice and conscience was talking to God. As the doors closed between Alex and I the voice if the nurse became audible but didn't yet make sense. I nodded to whatever she said and followed her out of the cold, windy, blurry, colorless room.

While Alex was in surgery, Mom and I waited in Surgery Parent holding areas until we were the only ones there.  While Alex and I were in the cold, windy, blurry, colorless room, Bela and a chaplain had sat in a corner covid 19 space and waited on me. I took a little longer than expected so she must have had to get somewhere else. At this pont in time I couldnt be in any corner, I skipped over my designated spot and searched for one with window natural light and sky view.  I sat and prayed the rosary. At times like these one cant focus much, I kept getting the flashbacks of Alex rolling away and the doors closing between us. As time went by and as the hours past the areas that mom and I were waiting in became dark, cold and lonely. As time went by other families left one by one. It became somewhat frightening and nerve racking as employees, nurses and liaisons left one by one until there were none. By 7pm Everyone was gone, there was no one around for us to ask or request updates from. We felt as though we missed the call about going up to the ICU to greet our son. I left my covid 19 space and walked the halls while peeking into other rooms other spaces in search of other families, other parents, anybody.... any sign of others in equal anxiety would have reduced mine . As I am walking I am thinking to myself.  "Here we were again....last in line..." I was feeling all alone...in this large emptied out lonely place that was now feeling  darker, colder, scarier and dungeon like. In someone elses eyes they would see that in fact there were bright lights, there were windows, it was very well lit and through the windows anyone could see the street, the traffic, the surrounding buildings, the weather, but even so, right here, right now, This was the "oh crap moment". This was the moment when the sitting in our designated parent recovery covid 19 space in quiet prayer turned into "anxiety driven mind torture". We waited for the hours that felt like days. "What is taking so long? This can't be good. Why haven't they come out to talk to us? Something must have gone wrong". Ugh the damned questions!!!!! We all know that when in doubt...well...yup...people think the worse case and they ask the questions. As a parent whos anxiety and blood pressure is through the roof I turn to the paintings on the wall, the size and shape of the floor tile, the pattern on the carpet....anything...anything to take my mind off of the "anxiety driven mind torture". I try to pray, but find myself babbling in my head.

Alot of time went by...8pm and no one around.


Mom went up to the floor while I waited within the covid 19 wait bubble that I was assigned to. Forty minutes later mom texted that Alex wasnt on the floor yet but on the way. So I headed up. As I was leaving the lower level the chaplain was arriving. She followed me up in search of Bela and in search for Alex answers.


Wednesday, September 23, 2020

2020 09 23 Surgery Recovery

2020 09 23 Surgery Recovery.

Quick summary (will write detail in sep post)

Alex was doing well Saturday and Sunday. Monday morning he was sitting up bedside.

Monday afternoon Alex went into 2 hour surgery that lasted 6 hours.  The replaced his scalp and put him back together with titanium plates, screws and stitches.

Monday and Tuesday Alex stayed in the Intensive Care Unit for hourly monitoring.  They claim that all went well. today (Wednesday) we wait on his turn to go into the MRI scan to check all and make sure (via imaging) that all went well.

We are back on the main hospital room floor and waiting our turn for the mri. We are unable to do any therapies until all teams approve them. Alex is in pain amd very figity. He is on pain management medication every 4 hours and on back onto his routine AED medicines that also happen on a four hour interval.

Alex is back together, still in pain, but now in the position to move forward with aggressive rehabilitation.

Tuesday, September 22, 2020

2020 09 22 email scam

2020 09 22 Email and text Scammer

Some low life took advantage of a situation.

Please do not send any funding nor moneys nor respond to any solicitation emails for Ed, Bela or Alex. Some low life scammer has hacked into our emails and is scamming our family and friends for money.

The only solicitation that we do as a family or team will always always always go directly to a foundation or organized event. We will never ask for any personal funding over any social platform, email, text, etc.

We do not know this low life but we do intend to follow all links and press all charges allowable by law.



Monday, September 21, 2020

2020 09 21

 2020 09 21. Mom and daughter on Bridge


As I carried Alexs belongings into the parking lot I watched the people before me. We are going into surgery so we have to store our belongings in the car until we know where we are going later tonight after surgery.

Before me a little girl and an adult woman held hands as they walked in the same direction. The girl was about 3ft tall maybe 6 or 7 years old. Her beautiful long blond hair was visible through the bottom and sides of the head stocking. Her little legs and her tiny sneakers skipped on the bridge. Her tiny legs jumped over the shadows created by the skylights above. Her voice was like that of a little angel so I will refer to her as the little angel. The little angel kept speaking. She kept telling the adult something about something. The adult women had the same long blonde hair. The adults long blonde hair was visible through the bottom and sides of her stocking cap.  (The stocking cap is all too familiar to Alex and I. I can recall almost every visit to get and to remove tue stocking cap...we did it here several times, Yale several times, Columbia Presbyterian several times). My mind starts to search for the memories and I have to force myself to stay in this moment and not recall the past events.

The little girl appeared to have the type of eeg that is the short term eeg. These are leads set up and hooked to a backpack that you carry around for 24 to 48 hours. The cap started on her forehead and went all the way to her backpack that is used to support and house the eeg recorder. The stocking cap (brown stocking) is used to cover and support the leads. Getting them put on and having them taken off is a process. It is a stressful process, an ordeal for a child and therefore also an ordeal for the parent to witness the child going through it.  Once on, the leads are uncomfortable. There are probably 30 little metal circles glued and taped to the scalp with wires that run between the metal circles (leads) and the recorder that is housed in the backpack.

The little girl had the leads, the stocking cap that held it all and the backpack to support the recorder. The stocking cap is a long stocking, it is about 5 or 6 feet long and it strectches at the head and is tight between the neck and the backpack. The stocking then runs consistent from head to backpack so that no wires are visible.  As I watched the little girl jump over the shadows she did so while talking. She was calm. She did not seem nervous nor anxious, nor bothered by the fact that these annoying metal circles were glued and taped to her head. I could hear her little voice ask the adult. "Will you keep yours on for 21 days?" The adult answered, "No....I will take mine off when you take yours off...we will do it for the same time..". The voice of the little angel kept talking, I could no longer make out the conversation, nor was it my place to listen...I had heard enough. This adult was the little angels twin, the little angels comforter. Somehow the adult managed to find her way and her strength to get through this with her little one.  These two touched me. I saw the calm, I saw the peace, I saw the attempt to keep it all together, I felt the love, I understood the pain.  These two werent wearing these eeg stockings on thier heads as a fashion statement. With these stockings, we who go through and experience them understand the reason for getting one. The stockings cover the pain that both the child and the parent go through. The stockings cover the technology that is to bring the news...the news that may be good or may be bad. The stockings cover the technology that may bring hope if the technologies assist in finding proper medication for the episodes recorded. 

The stockings are traumitizing to both child and parent so it is only fitting to see both adult and child wear them.  This little angel and her very own angel had matching stocking eeg caps. Both had matching backpacks. Both were going through this together.  Together they both crossed that bridge. Together they held hands, talked, absorbed the daylight from above and beside. Together they worked as a team. The adult angel had a lot of work to do, the adult had to hold herself together and stand tall, strong and present herself as equal so that the little angel could see her adult as if she was looking in a mirror. They matched, they had same cap, same backpack, same hair color, same attitude.

It was a simple walk over the bridge. It was less than a 2 minute passing, yet a lifelong process and lesson to learn from.

Both look the same. Both ease each others anxieties, but neither of them know what the other is truly feeling.

They both ease each others anxieties. The mom wears the cap to express to the little angel that it is ok. You have one...i have one just like it...you go through it....i go through it with you. This all eases a little of the anxieties for both of them but neither expresses the truth in what either of them are feeling mentally, emotionally nor physically.

For the little angel to be going through this cap wearing eeg cover, there must be seizure like activity. If there is seizure like activity this poor little angel is going through "stuff".  If she goes through "stuff", then the parents must be going through the same hell like torture that I too go through.  The little angel can look at her mom...but she will never know what her mom feels when she sees her little angel go through "stuff", nor will mom ever, ever, know exactly how her little angel feels when she goes through her episodes...her "stuff".  As a stranger walks by them, as a stranger sees that they both match, the first thing that comes to mind is "cute...look at them, they match", until you start to think about it. This is a couple....these are two two people going through a hard time, neither know exactly what the other is going through but they both do what they do to ease each others anxieties.


Saturday, September 19, 2020

2020 09 19

 2020 09 19 Saturday Day 44



"The real enemies of our life are the "oughts" and the "ifs". They pull us backward into the unalterable past and forward into the unpredictable future, but real life takes place in the here and now". Henri Nouwen 1932-1936

As parents we have a lot of regrets. Seeing our child in a hospital for this amount of time is truly beyond words. We regret taking a step in this direction that had the intention of healing. Our Feelings, Emotions, Stresses, Exhaustion beat us up. They all beat us up mentally, physically, emotionally.  Friends and family ask how one can do it or say things like "I dont know how you do it".  I cant look back to revisit these past forty something days or it will break me to pieces. Somehow I had the strength to do it once, but I do not have the strength to look back and re-live it. I do not have the ability to go back and change it, so I should not waste any energies on the past. I need energies for the "Now".  Teams come in and ask what I / We  am/are going to do when we get home. I keep responding with..."I don't know...I need to see what he will do NOW, Today, Tomorrow before I can talk about 3 or 4 weeks from now." My hope is that he gets to walking so that We do not have to worry about ramps or lifts. My hope is that he walks and walks tall so that we dont have to rebuild bathrooms. I cant think about the future right Now. I havent seen my kid in 40 something days....I need to focus on the "Now".

2 days ago I met a chaplain. I like and need different perspectives on obtaining and keeping faith and energies, so I request to speak to different people. The Chaplain asked me to look into "Henri Nouwen", I did, I found many quotes. One of which I added at the top of this note. The quote above resonated with me. In the "here and now" one needs to feed off of positive energies. In the "here and now" we can not look nor fix the "back" we truly can not predict the upcoming events nor future so....we need to live in the "right now". The right now is "the moment". If we are to make a change or a difference....it has to be "right Now".....

As a parent I Now sit bedside. While he sleeps Now, I sleep Now. I may not sleep as much Now because I need to also be his door guard Now. While he sleeps Now, I want and need him to have solid sleep so I give every nurse, doctor, cleaning crew the evil look when they walk through the door. They get the..."YOU WAKE UP MY KID NOW FROM THIS PEACEFUL SLEEP....SO HELP YOU GOD...He better help you roght Now!!!!". I know they need to do stuff Now....but if my kid sleeps Now....they need do thier stuff Not Now!.

When he wakes Now, I frantically make all crazy attempts to get him to move around Now or I make all types of crazy, silly sounds while touching every single toy that we have brought Now. I touch everything with the hope that something will spark his interest Now, something will excite him Now, something will make him track with his eyes Now, something will make him smile or laugh Now. It has been forty something days...he is Now finally tracking a little with his eyes but I have not heard his voice yet.

When will I hear his voice? When will he sit alone? When will he stand alone? When will he greet me as I walk in the door or say God Bless You daddy when I sneeze?  As a guy thing we burped or made our noises from the opposite end....when will he remind me to say excuse me again? He isnt doing so Now...I wait.

This is all pretty exhausting. Time goes bye, he sleeps, I sleep. He wakes, I wake. I wake up tired. I wonder if he feels tired or bored. I wake up tired.... is he? "Alex Buddy!. You awake already? Arent you tired???" then he smiles or he has some crazy laugh as if he just had a really funny dream.  The kid laughs and the parent then receives that boost of energy equivalent to about 3 or 4 espressos.  We get to it Now and start the hospital day routine all over again right Now...

Now Slowly waking. Now Slowly recovering. Now Vital signs have been stable. Now Slowly removing some medicines while Now slowly adding Physical, Occupational and Speech therapies.  In the past few days we were not seeing progress with the therapies due to the scheduling of the medicines in relation to the times of therapy services. Alex has been very slow at gaining his physical and mental strength but I feel and believe that it has a lot to do with the amounts and the scheduling of his medications.  After this upcoming Mondays surgery we intend to get Alex back to a normal schedule. Currently Alex requires 9 visits from the nurse to provide medicines and 3 visits to reload feeding. Alex is currently requiring 12 nurse visits in a 24 hour period for medications alone. this kid is consistently being messed with for meds. In the afternoon there is a 6 hour window where he has a medication break, but gets " his work on". His therapies are scheduled between 1 and 5.

Right before medicines are Alexs "Good Times". At the tail end of meds Alex laughs and plays. As soon as meds are given he seems to slow down and becomes more serious facially. 

It is Now a balancing act between medication scheduling and his therapies. Right at this moments "Now" he is a little better than he was at yesterdays "Now".  We cant go back to fix anything about yesterday and we can not predict what will happen tomorrow we just hope that tomorrows "Now" is a little better and stronger than todays.


Wednesday, September 16, 2020

2020 09 16

 2020 09 16 Wednesday Day 41


Sunrise through our window

I sit bedside and hold Alexs hand. Alex gives me the beginnings of our secret handshake. His hand trembles, his hand is weak, but he gives me an all out effort to go through the motion that we call our "Snap". I hold his hand and make funny sounds, he likes the "ducks quack", the "swish" and the "splat". Alex hears the sounds and he laughs. Alex doesnt seem to get tired of hearing the same damned sounds over and over and over again. For as long as he can tolerate the silly sounds, for as long as he continues to smile and laugh at the silly sounds, I will continue to provide the silly sounds. Currently my silly sounds and his correlating laughs seem to be the only communication that we currently have between us...so at this moment I live for and I love every minute of it.  I know where we have been in the past forty something days. I know the pain that we suffered and the agony that we lived through in the past forty something days.  Today I sit bedside, I hold his hand, I make thes sounds and realize how fortunate I am to have been given the opportunity to sit bedside and make these silly sounds that make my kid laugh. I am blessed to have the opportunity to witness, to see, to hear my kid laugh.  Alex isnt the same kid that walked through these doors forty something days ago but I have faith that with time he will be. It is impossible for me to truly express what I felt in the past forty something days. It has been a nightmare that I can not and will not ever wish on anyone. Life as I once knew, as WE once knew it will never - ever be the same...that I know. Now....with that being said....I have time... WE have time...We definitely can not dwell on the HELL that we just went through. The dedication, the energy and the focus must now be on making this little man...."THE MAN". The focus is now on strength and recovery.

This is where all of the prayers, the positive thoughts, positive energies, the Lord, all of the angels and all of the saints need to lend us thier hands. With many hands make lite work. When he lays..may the hands of the Lord cradle him so that he may rest peacefully, when he sits... may the hands of the Lord support his back and neck so that he sit steadily, when he stands...may the hands of the Lord lift him so that he may stand strong and tall.  in the past forty something days we have gone through a time that we termed "HELL", this poor kid has gone through a lot! We beg for better days.


2020 09 15 Tuesday Day 40

Alex is recovering on a normal floor of the hospital. Slowly we are removing medicines by decreasing doses on a schedule and slowly we are transitioning his nutrition from the "IV" line and the "J tube" and into his stomach via his "G tube".  It is a slow process but the safest process. We have taken a few steps forward and we have taken a few steps backward. I say a few steps back, for example, Over the weekend a physical therapy session cost him an accidental pull or tug on his feeding tubes that then required emergency surgical room visit and an emergency procedure to rethread and replace what had been accidentally and mist likely painfully tugged out out of him.

Yesterday we made the first attempt at feeding via his G tube which is how he obtains 50 to 60 percent of his nutrition at home. After meeting with several teams throughout the day a plan was set and a flow rate was determined. Once determined, mom and I asked that they cut the rate in half so that he would get less per hour to avoid upset stomach and vomiting.  Teams, Doctors and nurses followed through.

Yesterday Alex had a tough time with his Occupational therapist Melody which works his hands, arms, shoulders, neck, upper body, etc. Alex appeared exhausted from not yet having slept an entire night.

Alex was showing signs of discomfort on and off. He has times where he laughs and other times where he looks pretty darned miserable.

Yesterday Alex had a tough time with his Physical therapist Jessica. Alex was tired and not giving her his undivided attention. Jess, Mom and

I worked together to get little man to sit and to stand (assisted) alongside his bed.  It was great to see how tall he was, but he didnt look comfortable at all. Alex stood up 3x (assisted) and was able to sit at the edge of his bed for a little while. At the edge of his bed he was able to make an effort to kick a volley ball that we have in the room. The required helmet is still a little heavier than he can support, so he is having a tough time lifting his head.

Yesterday Alex had a tough time with the speech therapist, but not as tough a time as with the other therapists. Alex is not yet speaking nor making sounds. Speech is working with his visual movements and attempting to get him to make choices with his eyes.  If he begins to make choices with his eyes, then they can format a computer program that will assist him in communicating with us.  Mom and the speech therapist worked together and claim that they made progress.

Last night Alex was very agitated. It was very difficult to calm him down. Alex was rapidly moving his head from left to right continuously between 6pm and 10pm. The poor kid looked so uncomfortable, yet I feared allowing the doctors to give pain meds (morphine) or sleeping meds (ambien) that each had reverse effects when given in the Intensive Care Unit. Last night at 945pm (I state the time because it was the same for several nights in a row. It was the same Friday, Saturday, Sunday, ) he fell asleep and slept very well until midnight.

At midnight he woke and was aggitated and wouldnt fall asleep again. 2 hours past, my energy level diminished and I gave into the nurse and doctors recommendation of giving Alex Ambien. 

The nurse gave him Ambien and Alex vomited within 5 minutes. He shook or trembled for 10 to 15 minutes after meds where given. Alex Vomited and appeared very agitated for several minutes. After several minutes he appeared as if he were a different kid. He was then calm, focused and relaxed.

He then slept from 3am to 6am. Over night Alex got a total of 5 hours.  It was no where near enough sleep for this little guy, but it was better than nothing.

Sleep or no sleep the surgeons and thier teams, doctors and thier fellows, the nurse and thier C.A.s still keep coming.  The cleaning crew still enters, the laundry crew still retrieves. The alarms in our room still ding on and off, but luckily only for completion of meds or nutrition.  Alexs sleep schedule is off, he is unable to rest or focus. We all work toward giving him the most rest possible, but we cant let him lay for to long. We all want him to rest, but we also need to visit, poke, test, lift, lay, touch, feel, and recheck in order to assure his safety. Day by day we do less of each which is a sign of recovery.


Alex is not yet anywhere near the same child that walked through these doors forty something days ago. At this moment he is still unable to speak, track with his eyes, grip or kick with his right and unable to move his left.  He lays in bed and we work with him to sit , grip, move.  We have made strides in range of motion with everything except his left arm. Today we will receive a hand brace and by end of week we will do botox injections with hopes to get his range of motion back.


This week we work toward Mondays surgery. Monday they replace the bone that they removed. After Monday he will be safer to work with and will not require a helmut. After Mondays surgery recovery we hope to aggressively target Physical, Occupational and Speech therapies.


Today I sit bedside.


Sunday, September 13, 2020

2020 09 13 #AlexStrong



Enough Said.....Thank you Uncle Manny!



        Retro 5am training early birds!!!!