Tuesday, October 6, 2020

2020 10 06 Alexs Eyes

2020 10 06




This morning Alex opened his eyes. Yesterday morning both eyes were swollen shut. On Saturday night Alex had an unfortunate bedtime diaper change incident where he bumped his eyebrow/ forehead on the siderail of the hospital bed. An emergency ride by ambulance brought him back to the emergency room at Boston Childrens.  Here we are again three days into this stay under going MRIs and LUmbar Puncture and blood draws to confirm that the insane amount of swelling to this poor kids head is only a bump and not also a bump with infection.  Alex is on all of his original nine medications (original since surgery) and now two new antibiotics and a probiotic.

Last night he didnt sleep well. He was taken off one seizure medication and maybe the lack if it caused issue.  He however was able to open both eyes this morning. At four am When I opened my eyes from the short nap I heard him laugh, I leaned over and saw the white ans brown and cried tears of joy.  This poor kid had his eyes swollen shut and was swinging at his pillows with aggravation and frustration. I cant even imagine what was going through this poor kids mind. All the pain from the surgery, the inability to move, the inability to speak and now here he finds himself laid out flat and unable to see???? OMG!!!!!!  WTF???? 

How do I gain this kids trust again? Every day I wake and tell him that today is going to be a good day. Every day I go through the morning routine and tell him that everything is going to be alright..... This kid still holds my hand as if he is comforting me.  When things are about to happen he grabs my hand and I am blessed to have him do so. A few weeks ago he xouldnt grab anything. When he is about to be pinched bu a needle or touched by a nurse he turns, he tries to bury his head in the pillows. i tell him things are going to be alright and he straightens out. He trusts me. I am heart broken when so much uncontrollable crap happens. I hold his hand everynight before he goes to sleep. I tell him that tommorow will be a better day. Tonight he squeezes my hand. He squeezes tight as if to tell me he is alright, he slips his fingers under mine for the secret handshake and snaps as if to tell me that it is all good. We are all good.  We promise that things are going to be ok and we secret hand shake to seal the deal. This isnt good, this has been a roller coaster nightmare from hell, yet this kid can slip his little hands under mine to give me that secret handshake that lets me know that we still have a deal.  


2020 10 06 Ambulances

Eds Note Saturday October 3.

My intent was to leave quick enough to to get the parking lot sooner. It was late, it was dark, it was much colder now than it was only three hours ago. The outdoor temperature may have been the same, but my body felt and sensed it as if it were much cooler. I drove off and trusted that the dashboard gps would get me to where I needed to go. As the lady with the british accent spoke, I heard but couldnt always comprehend. I am tired, i am frustrated, nervous and annoyed. I take the next right sooner that the one thousand feet that the British lady had just mentioned. The GPS recalculates and I am back on route. As I sit at the red light I realize that the tips of my fingers are cold. I grip the steering wheel so hard that I stop the circulation to my finger tips. I loosen up and let the blood flow. I take a deep breadth and tell myself that this too shall pass.

A few lights later an ambulance approaches from behind me. I hate the sounds of the ambulances sirens.  

I flash back to when I was 13 years old, sitting behind a desk at St. Raphaels school. The smell of stale milk in the classroom because they didnt have a cafeteria and that strange smell of friday afternoons sweaty uniforms. Monday the class smelled like bleach and the kids smelled like various fabric softeners, friday the class smelled like stale milk and sweaty 13 year old body odor. Sitting behind our desk Sister Barbara, in her full head to toe dark black habit (that almost simulated the same scent schedule) would have us stand and say a prayer for the patient and the families as soon as we heard the ambulance sirens on the roads outside of our classrooms.  Ever since those classroom days, everytime that I hear a siren, I almost smell the milk and n.o. and I say a prayer.  i flash back to the times that I called the ambulance fir my father. I was young. I was nervous. I would call 911 with a tremble in my voice and my entire body would shiver uncontrollably. Ive ridden in several  with my father when he had strokes or heart attacks. I was scared then,  I was uncertain of the outcome and would just sit and pray. I hate the sound of sirens, even so, when I hear one...it brings back the memories and I can almost feel what the caregivers feel and so I say that prayer.

Sitting at the light, the sirens and lights get closer. I pull to the side and grip the steering wheel tighter than before. Im gripping the wheel so hard again that my finger tips are cold, Im clenching my teeth so hard that my jaw hurts. I ask the Lord to help who is in it and the family...how friggin Ironic.  The ambulance passes me on the left and I swallowed what I had, clenched my teeth and tried unsuccessfully to hold back a tear. I held back the rest of my tears because I still had to drive. The light remained red, the siren and the flashing lights disappeared slowly into the distance.  Here I am again, Im sitting in this car, at a red light as my kid gets further and further away from me.  Im so frustrated, annoyed, Lord......why?....one step forward and three steps back.  Lord, everything happens for a reason...right now I am confused.

Light changes and I make my way to the Boston Childrens Hospital parking structure. Mom is with Alex and must be a nervous wreck, which goes without saying. I am a wreck both inside and out but need to wipe my face off take a deep breadth and get into this emergency department.

Things just straight out SUCK. This little man has been at this for several months. It is enough already.

Bela and I are tired, Bela and I are on this crazy emotional roller coaster of happy...sad...annoyed...ok...happy... Really happy and then pissed.... aggravated ...etc.  I pray, we pray, we read comments and your supportive texts. We dont call because the tremble in our voice or our vulgarity of the moment may not be appropriate for conversation. We find support in what ever sign or reading or youtube video from different priests, pastors, motivational speakers etc. That we receive from you all.  We took a few steps forward and then again a few steps back. Everything happens for a reason...Lord....fix this.

Today as I sit in the vehicle wiping the tears from my eyes, I semi pray.  I semi pray because my anxieties dont let me focus on the words.  Im sitting in the car staring at the wall of the parking lot.  I recall a quote from....John Wayne.... I dont know why, but it is what comes to mind... "courage is being scared to death but saddling up anyway". Im scared about this situation, I dont want to walk through those doors again under these circumstances,  but no matter what I need to wipe off, toughen up and get in there. (I think john wayne kept a flask in his pocket for help...i dont right now...) I need to get in there hold the kid, move the kid, talk medicines, talk stuff and sit by this kids side yet again until he gets thru this.

Here we go again.

Monday, October 5, 2020

2020 10 05 Back to Boston Childrens Hospital

2020 10 05 Back to the Hospital

Alex was doing well Saturday Morning (I wrote about it in the last blog) and afternoon. Dad and mom switch for covid regs. He had a decent afternoon for mom.  Alex was working with mom on grip and grab, some OT, etc. 

Saturday night something happened and Alex now had a swollen right eye and forehead.  After nurse conferencing, after conferencing with all doctors up the ranks...We (mom and I...one of us on phone) requested that we move quickly and get Alex to Boston Childrens.  It didn't seem to sink into the team fast enough. I made clear that this was dangerous and dire and we needed to move asap.  At about 1030pm Alex was being transported by ambulance to Boston Childrens where we remain today Tuesday October 6th.  

Alex left eye is swollen shut and his right eye has swelling that changes through out the day. It is worse, then gets better, then fever spikes and then he feels crappy.  Alex has been looking horrible with the eye swollen shut and forehead swollen.  Alex is looking upset, angry and just rolls into a ball everytime a nurse comes near him. I don't blame him.

The Saturday night situation or episode may have caused a spiraling effect, but doctors are still confused and uncertain of what is going on. Maybe trauma bruise and maybe infection, so they are undergoing mri scans. Bloodwork. Spinal tap. Etc.  He is on fever reducing meds to keep him cool and he is on several antibiotics yet again just in case there are infections that are causing this swelling.

Lord. Our child has gone through so much in the past sixty something days. Thank you for the few days last weekend when Alex showed us his strength to begin recovery.  Give us that little man back. I sit in the corner of a hospital room watching my child as he lay yet again in a hospital bed.  Why Lord do you only allow us enough to get a few steps forward before we get sent several steps back? Why Lord do we fear you? Respect you? Pray to you for healing?  ask of you favors? ask that you pitty us? Beg that you forgive us? Request that you heal us?  Last week I asked that my family be together...here I am in a hospital emergency room with Alex and his mom.....this isnt what I meant...but it seams to me Lord that life for little man isnt fair right now.  Lord I am tired! Lord I am almost exhausted to the point that I just may not have the energy to pray....I beg you.  All who love and support Alex ask that you heal this boy. We ask that you you show us the healing and speedy recovery for this boy that we have beem praying for so that he and his family may rest through the night and have the strength to pray for others in need while rejoicing and praising you Lord for his healing. 



Saturday, October 3, 2020

2020 10 03 week review

 2020 10 03 Saturday Franciscans Day 5.



The photo is of today ... Saturday ... Day 5 of rehabilitation. The photo was taken by a hospital worker walking down the hall collecting the bags of used covid required gowns. It looked as if he pushed the button to take several photos. What It looked like and what truly happened were not the same. There was only one picture for what seemed to be a three minute event.

The photo however captures the true feeling of the place.  It is somewhat foggy and blurry, everything around us is blurry and almost colorless or colorblah. It is lonely. The two of us are here but we cant even see each other through these damned masks. I see myself here adjusting his mask, making sure it covers his nose so that tommorow they allow us in the hall again. When I was young my dads car didnt have seat belts. Alexs older brothers Dad "Ed" had seatbelts in his....now Alexs Dad "Ed" needs to have seat belts, a box of face masks, hand sanitizer, disinfectant wipes and a box of latex gloves at all times...

I cant imagine what Jordans kids will witness.


Tuesday:

we were transfered by ambulance type vehicle to Franciscans for Rehabilitation.

Alex needs rehabilitation in order get all of his functions back.

as of Monday he is unable to sit, stand, move his left arm or leg, Walk, talk, nor focus.  He began to show signs of it all, but has not had the strength nor ability to do any of it alone.

We spent Tuesday settling in. We spent Tuesday in the shock of change and in the shock of the place that we have just entered into.

We came from state of the art facilities and are now in a building that is definitely "not". We do our best to put place aside and focus on the people and the teams.  It is extremely tough to do though...but we need to see what these teams are about.. We pray that it is all about the people here....because the building definitely needs help.


Wednesday:

We met all the teams. Bela meets half, I meet the other have. The goals are promising

..we hope to work hard and get things done. Alex is stable, he is hot and sweaty which is a big big problem, but he lays on the bed hoping that mom and dad have made the right decision in coming here. While here the goals are to fine tune his feeding, reduce his medicines, transfer all foods and medicines from J to G to finally some real meals that can be chewed and swallowed, and all types of therapies. The goal is to see him walk, kick, throw and ride his bike again. The goal is to hear him talk amd sing again. Wednesday was all about getting to know Alex.

His stiching is still not healed, they think a month or two, we cover every now and then because he scratches at them.


Thursday:

Alex worked with Dad and the PT and the OT. We made the attempt at getting him comfortable with them. With me Alex sat bedside several times. He looked like he was in pain and he hit the pillow really hard with his right hand. I think that Alex is showing his aggression by hitting the pillow. Alex ia not yet talking but he is laughing at mom amd silly stuff that I do. The therapies are starting slow with intent to progress as time goes. Currently Alex is being a hard ass and stuffs his head in the pillows when he sees the therapists coming.


Friday.

Last night was tough. The walls are paper thon and we can hear everything around us. Alex woke several times through the night. He is medicated and tube fed throughout the day and night, so nurses come in and out of his space often.  We have a schedule and a weekly plan of reducing and eliminating medicines and reducing and shifting feeding so that we can get closer to normal.  Today Alex had PT and OT with the therapists. I stayed back to see if they would succeed alone, but they are not there yet. Alex gave them all a hard time and didnt want to cooperate.

Im the afternoon the therapists brough a wheel chair and took him for a ride. Bela and Alex shared some laughs up and down the hall.

Alex was happy in the afternoon and toward the evening. He and mom had a successful afternoon.  By the time that I got to Alex at 830pm he had his night medication and was ready for sleep. I was able to get him to laugh at a few toys and play a few sillys before he fell asleep.

Saturday.

It was a good morning. Alex woke up less cranky than yesterday. We increased feeding and he seems to be tolerating it.

We had our routine morning "Portuguese Shower" (bedside towel wash). We brushed our teeth and put Jorge Ferieras "Tiro Liro" on the cell phone and got to bedside stretching. We worked OT

..the arms and hands, lifting, hitting, touching our nose and grasping with both hands. We worked these for about 1 hour 15 minutes...with the music he didnt even know.

After OT he had his noon medication that puts him to sleep for an hour. Once awake...i stretched his legs a little, sat him up bedside 3x for a few minutes at a time with lay down breaks in between. We attempted several hugs and then 3x standing hug for about 15 seconds each time. The standing works him so hard that his legs shake and he looks uncomfortable.

After about half hour of hard work he was able to get pushed around in his wheel chair.  He was all happy until he had to put the mask on. Learning is tough...changes suck...learning or relearning in a changed or different environment sucks even more.


2020 10 02 Covid and Invisible Walls

 2020 10 02 Friday Franciscans Day 4


Our lives during Covid Rules and Regulations. The invisible walls

Note from Friday Evening.

I have a knot on my stomach. I want and need to sleep but the anxieties dont allow for the restful, peaceful sleep that one needs. I have a knot in my stomach. I want and need to eat but my teeth clench down so hard that they wont allow me to.

Google maps says that there are dozens of places to eat near me, but I lay here in the back of Belas car and have no desire to take a step in any direction other than the direction that leads me to my kids bedside. Unfortunately I cant (by law) take those steps yet because its not yet my turn (I count the hours before I can relieve Bela). I have several bags full of snacks, microwavable meals, water, coffee, tea and sports drinks, but no desire to have any of it...I usually enjoy food, real food of course...not the kind of food that I can pull from a target bag, but right now I have no desire to eat nor drink. I know that I have to, and I will force myself to, but I have no desire to. It is not for lack of having stuff...it is lack of having the desire.  I lay in the back of this car as if I am homeless, but I am not... I am very far from it. Materialistically I have everything that I need and too much more. I lay in the back of this car as if I am alone, but I am not...I have a huge loving family and a very large circle of friends that are at my side in spirit and would be at my side in person at the drop of a hat. I am blessed. I am. Very very blessed to have all that I have. I am blessed to have the love and the support of so many. I am so blessed to have all of the stuff...but all of it right now feels so useless.  What good is all the "stuff"?  What good is all of my cool, solid stuff when these invisible walls keep me from holding my childs hand or receiving that hug that at the same time is his physical therapy homework for sitting and standing ...but he doesnt know it.  At this moment none of the stuff nor family nor friends can change the situation that I and my family are in.. Stuff is useless...friends and family however keep my hopes up and encourage me, lift me, keep me focused on the long term picture...yet the Invisible walls continue to keep me from being by my kids side to help and see him progress. We currently have these invisible walls set in place by the very important covid 19 CDC guidelines.I inderstand the rules, the regulations, the guidelines....they kist now make a truly truly fucked up situation so so so much worse.  We have a health situation. My sons health is in need of medicine, physical therapy, occupational therapy, speech therapy, music therapy, professional care and most of all the love and the support of his mom, his dad, his brother, and family. Currently the rules say only 1 parent at a time and we can swap out 1x im the day. Only one parent can stay the night. We can have all types of cleaning crew, doctors, nurses, janitors, etc. But 2 parents cant be in the building at the same time. If moms in the room, Dads out in the parking lot and vice versa.  It is such a tough time. I can handle Alex physically and his mom can handle him mentally. I could get him to work and cooperate, but moms the one with all the book smart degrees in all the schooling and special needs stuff.  At all tomes now, one of us is stuck in a room with Alex independently, frustrated about how to help our child because the other cant be there at the same time to assist with normal day activities.  The simple activity of bathing my son who currently cant do it for himself is now daddy and some stranger nurse who hides behind mask, goggles and full body gowns. This was a mom and dad thing, yet "from here on out" during this "forced stay", my autistic, special needs son, who just had traumatic brain injury due to unforseen, unpredicted issues in surgery and that was in a medically induced comma for well over thirty days, this is now how he will relearn life. He will begin to wake, he will again learn to sit, learn to walk, learn to talk, he will begin to see these walls that we are within as his new normal and this weird mommy and some face masked people or daddy and some face masked people will be this kids new normal. Well....in my mind, in my heart, in my soul. THIS BULLSHIT IS NOT NORMAL!!!!!!

They have psychologists on his team, the psychologists cant see that this goes against everything ever written?? studied?? researched??

I havent seen my sons soul nor charecter since before his surgery almost sixty something days ago. Today I lay in the back of a car (one of my stuff...so I guess that I miswrote earlier...this is one piece of materialism that is pretty damned important right now, if it wasnt for this car ide be sitting on the broken down rottwd wood, carpenter ant infested rail road tie wall with an umbrella unable to type this note on my phone because i need two thumbs to type, but one would be holding the umbrella). I lay here listening to the rain and praying harder than ever for my sons recovery, Im praying for his strength, praying for his courage. I need him to sit up, get up, walk, talk so that we can get out of this place. 

I mean no disrespect to this place. I mean no disrespect to the people here, and I want nothing more than for us to all succeed together as a team. But right now this fucking place is just so dark and so lonely...It doesnt have to be...but it is.

There is that saying that "home is where the heart is".  Anything or any place can be a house or a shelter. I am studied in Architecture and studied as an Architect. My business and  profession was to make the spaces...the spaces are all great if you have a healthy happy heart, a healthy happy family. Try this...sit at your dining room table with your happy family, eat drink, tell stories...feel the space? It is a happy space. Now sit in that dining room alone...sit in silence...feel the emptiness...that space means nothing without the healthy happy family to fill it. When the room is filled with family the colors are brighter. Pull the families apart and the colors seem to fade. 

I live for my boys. For me to be well, they need to be well.  If They dont eat? I dont eat. If they hurt, I hurt. If they laugh....I laugh...

We are in a place. Due to covid there are invisible barriers. Invisible walls, social distancing, these guidelines force the businesses to follow CDC guidelines. The people here state that only 1 parent can be with the child and that a visitor may visit but

Only once a day and when visitor comes the parent needs to leave the building. They state that never can 2 parents be in the same room at rhe same time. Mom and I need to share time, swap out when convenient and communicate through notes on a bulletin board or by phone.

Right now Alex needs to make this place a home. When he is happy, I am happy. He isnt doing well with all of the strangers that come at him with masks, goggles and safety gowns, he is a kid, a scared kid, a kid in pain and know all this adds visual fear and trauma.

Alex needs to get better. We need to make things work.  We are now pulling all stops and coming at this from every direction but need to wait. I lay here in this car, praying, begging for the answers that will make him what he needs to be.

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.