Tuesday, December 30, 2008

Chemo Update

Just a quick update.  I have had chemo the last 4 days and my last day of the cycle is tomorrow.  Today was the second strongest hitter and tomorrow will be the strongest hitter at bat.  (So they say)  I will go into Seton for tomorrow afternoons treatment so that I am more comfortable.  It will probably take 7-8 hours.  

They say the next several days to a week is when most people notice most of their side effects.

So far I have been doing fairly well.  No significant nausea or temperature.  I still get some night sweats and have little cough.  Most of my main complaints have to do with lower extremity swelling which impacts sitting, standing and walking.  I can rarely sleep more than a hour or two at a time.  

I will have about 20 days to recover before I start the next cycle.  I plan to do my best to get my feet underneath me during this time and be a little more productive.  No further diagnostic tests are planned at MDA till early March unless needed.


Love,

Brian



Sunday, December 28, 2008

Thank You Report

I have to thank everyone sending me your positive prayers, thoughts, love, mojo, etc..  Bless you!

It is working!  I just have to report, to testify, that I felt better yesterday than I have in probably a month or more.

I really had no significant discomfort or pain the whole day or night, 

My appetite was better and I had no sign of nausea.

There was slight decrease in blood pressure and less shortness of breath.

I slept very well, with no meds and when I got up to go the bathroom, I was able to go right back to sleep.  I can't remember the last time I slept like that.

I also had decreased night sweats and fever.

I just wasn't in any real discomfort or pain the whole day or night  Amazing!  First time in months I can honestly say that.


We are overwhelmed by all your love and support!  Thanks so much!

Love,

Brian

Friday, December 26, 2008

Prayer & Visualization

As you know by now, I have had my my first two chemo treatments. So far so good!   I have treatments again Saturday thru Wednesday.  It has taken so long to get to this point.  While I am doing what I can, I am now asking you for coherent healing thoughts, intentive prayer and visualizations to assist me.  

I would like to share with you some thoughts I have read to optimize outcomes.  A lot of this I got from the "The Intention Experiment" by Lynne McTaggart.


There are many studies on prayer showing beneficial results, but there are just as many conflicting studies.  There are also many good studies on healing with intent.

Empathetic bond is important.  If you aren't really into it and are just going through the motions, then it is best not to participate.  Successful studies show that deliberate focused thought and peak attention on specific outcomes is important.

You have to believe that the thought or prayer will work. 

Healthy positive state of mind.  Your current state of mind will effect outcome.  So it is not good to shift from negative conscious or subconscious thoughts to try and provide a short lived positive prayer or intentive thought.

While positive thoughts are good, you also need to eliminate negative thoughts as well.  Even putting in a negative intention like “no complications” is not desirable.  A “return to natural order” thought works better than a destructive thought.

There are even some studies that suggest you can change the present by praying for the past. Pray now for that person, but back for five to ten years ago.  Pretty amazing, huh?

So, just saying the Lord’s prayer for someone, or to just say please heal this person, is not effective if it is not personalized.   Locking in the image of that person and using concentrated focus on exactly what expected outcome you want for that person works the best.


Visual imagery will also help me to fight the fight.

Successful visualization requires you to visualize vividly, with powerful images and symbols and lots of sensory detail.  Try and think of healing energy or divine white light.  Some like to think of good vs evil, epic battleground type of stuff.  I have thought of little pac men eating the mass, divine white light disintegrating the tumor and chemo pouring over cancer cells, just like acid and melting them.  I dreamed a few weird ones the other night but can't for the life of me remember them.  I would like to hear of some good visual images if you think of them.


I thought the clip below was cute.

  


I will post again when I can.  My battery feels like it needs some recharging and the next few days will be kind of rough.
Thanks for the Love!
Brian

Thursday, December 25, 2008

Chemo Has Started!

I hate to sound like a broken record, but I am getting tired of incompetence.  I don’t want to always find and write about the negative but it seems pervasive in my life right now.


I called Monday to get my new chemo schedule for Tuesday.  So I got the schedule, 11:45 lab and 1:30 treatment.  I repeated it back and confirmed it, then I asked if they would have the others days for me when I came in and they said they would.


They called Tuesday about 9:30 and asked where we were, that we had an 8:30 appointment. I said no, I was given 11:45.  Of course, we went round and round.  They said that schedule was for next Tuesday.  I asked why would they give me next weeks schedule when I asked about today.  Well, they said, you must have misunderstood and if you can't get in soon then we won't be able to treat you today.  

My blood pressure is already way too high, so you can imagine where it is now.

I asked about lab and they said I didn’t need it.

I hustled Glenda from her work calls and we got there at 11:50  

I checked in and they said that I did need blood work before hand since this is my first treatment, but that they could do it back in the chemo dept.  I didn't even attempt to complain about the disorganization. 

I sat for about 10 minutes before they called me back.  They sat me down and got my chart.

"This is your first time for chemo?  We were told that you already had ...You need lab work before we can start"  They all looked pissed because lab work takes about an hour and they have another department that handles the blood work.  Hey!  Not my fault you can't get it together.


I hunkered down and read till they drew blood and hooked up my IV.  In an hour or so, they started the 15 minutes of premeds for nausea.  The chemo agent was adriamycin.  It was bright red and was given as a 15 minute push into the IV line.  They said my urine would probably turn red but not worry unless it lasted more than a day or two.  They flushed my lines, unhooked me and sent me on my way.  Not horrible, no immediate reaction, so I am good.


When I got home, I got to take my first shower in 6 days.  I got to peel off the chest tube dressing and get a look at my new battle wound.  Not bad but not good I guess.

I also started my oral chemo at dinner.  I did not have a good night.  A lot of pain, and could not sleep.


Chemo Day 2

Since the Oncologist's office closes early today, and the chemotherapy was going to take about 7 hours, I was scheduled to get it at Seton Central out patient. Check in was 12:30.

I was having some lower chest pain with inhalation before we left so I thought it might not be a bad idea to get another chest film in case it was related to the lung.  I had Glenda call the CV surgeons office to see if we could coincide the two.  They said no problem, they would coordinate it with the floor nurse.  Boy did we open up a can of worms.  They called back shortly and said we had to report to the ER and get cleared before out-patient would accept us.  Oh great!  This just got very complicated.  


We get to the ER and they do an EKG on the heart and shoot a couple of chest films.  Heart looks good other than high blood pressure.  I guess the left lung has still not fully inflated so the radiologist noted a pneumthorax on the left lung.  The ER doctor came and in said I had a deflated lung and I would have to get transferred to another room to get another chest tube.  They were not sure about chemo and would have to find the on call oncologists to see if we could still do chemo today.  

We are like, what?  Slow down.  Did you talk to the CV surgeons office or compare the films to last ones?

They said they would make some calls and get back to us.

They sweated us a bit and finally came back and said they got a hold of everyone and that they would go ahead and release us, but we would need to follow up with the CV surgeons office next week. 

Whew, Ok we can do that. They made we sign a release that I had a pneumothorax and that they recommended a chest tube and said we are free to go. 


We finally get to the chemo room and the floor nurse comes in and asks if I know that I have a pneumothorax?  I explain everything to her but her response is that they just administer chemo here and someone would have to OK treament.   I said ER talked to everyone and that they cleared us to come up.  Of course we went back and forth as I started to get hot again.  Well of course she has not heard that and will make some calls.  I am hold again.  We are already a couple hours past our scheduled start time.  Of course it finally gets worked out.


So here I am, sitting in a hospital room, 5:30 p.m. on Christmas Eve, documenting todays fun.  I am about to start the chemo.  I have had two hours of pre hydration and the anti nausea meds.


I am thinking of Glenda, who is currently out trying to take care of my needs as well as trying to make this some kind of Christmas for the kids.   She not only has to deal with her job responsibilities and her own frustrations with everything that is going on with me.  She has to deal with with all my emotions and moods.  I think that since my energy level is so high, and I am in constant pain, that I am even more demanding and short than usual.  I want things done right and I am hypervigilant.  If anything good comes out of this, maybe I will become less anal.  Bless her, she is stressed.  So many details, so much going on.  Please send her some love and appreciation. 


They finish up the chemo and post hydration and we walk out of Seton about 10:30 on Christmas Eve.


Glenda and I wish everyone a very Happy Christmas!  Please know how much all of you mean to us.  We Love You!

Wednesday, December 24, 2008

Having Faith

I don’t want to offend anyone with strict beliefs, or get into any big theological debates but I want you to know where my head is at.


I know many who believe in the personal God as a single entity encompassing the "Son and the Holy Spirit".  Some believe in the impersonal God, the “Universal Intelligence”. The American Indians in the “Great Spirit”, the Moslems in “Allah” and the Buddhist in “Dharmaka”.


Whatever your belief or non - belief, at this time in my life, I need to focus on the personal God and ask you to substitute your personal version.  I will try not to go off the deep end on all this, but I need to have the faith and belief that there is a higher healing power.  It as been so easy to just go through the motions over the years with periodic prayers and intentive thought when needed for myself or someone else.  


Now that my life is on the line, I need to really focus and have faith that I will be healed and the single entity God works the best for me.  That if I believe, I will receive.  So I have given my sickness to God.  That it is "His" will that I be healed and restore my health.


One night several weeks ago, I had a profound sense of peace and absolutely no pain.  I forgot what it was like to not be in constant pain.  I thought I had been touched by God, that he was with me.  It only lasted a few moments but it is not something I have not forgotten.


I thought some of you might like this poem I came across in some of my Dad’s things.

Many of this guy’s love poetry I have sent to Glenda just like my Father must have done to my Mom.


A James Metcalfe Prayer


I MUST BELIEVE


I must believe in God because

There is no other way

That I am able to explain

Why I am here today


There is no reason for

The mystery of me

The mind that plans, the heart that loves

The soul of memory


There is no answer in a book

Or in the changing sky

Except that God created me

And only He knows why


I must believe in God because

I see so many signs

that indicate my life is just

A part of His designs


So many signs that point the way

To choose the right from wrong

And how to walk in faith and hope

And keep my courage strong


Lot's of Love to all

Brian

Monday, December 22, 2008

You Wont Believe This - Part II

This a continuation of "You Won't Believe This"

Thursday night - 

As I rolled down the hallways, the light panels flashing by overhead, I thought of reality moments.  This was definitely one of them.  Like something you would see in a movie but without the suspense music.  I made a mental note to try and record all my reality moments over the last few months. 


As I was rolled up to my room a little after 7 p.m.  I was instructed that I absolutely could not move my right leg or raise my head, for the next 6 hours.  Of course, I am uncomfortable and squirming about and the nurse has already reprimanded me several times. 

The nurse was looking at me in frustration and telling me to keep my leg still once again.  We got to my room and after a bit of line and apparatus hookup, they transferred me over to my hospital bed.  I kept raising my head and moving my legs to get comfortable.  There was a pile of sheets and stuff under me, but they decided they would move all that stuff later.


Bop!   The nurse just bopped me on the forehead.  “Sir, you need to keep you head down and your leg flat for the next 6 hours.”  

I had heard that before.  I can’t believe he just thumped me on the head!

“When can I eat?”   He was going over instructions with the night nurse.

“What about eating?”  I asked again.

“Not until you can sit up.”  They said together.

Unbelievable, that would make it about 30 hours since my last meal.  Refusing all those pain meds throughout  the day seemed like a really stupid idea in retrospect.  So now, I can’t have anything substantial till about 1:30 in the morning.  Great!

Just then, Glenda walked in with chicken lasagna from the Brick Oven.  Oh what torture!

After a few hours, I raised the head of the bed just a bit and Glenda was able to give me water and juices.  She also fed me a few bananas, some yams and a little of the lasagna.  I finally let Glenda doze off and tried myself.  


I had the nurses coming in every couple of  hours to give me pain meds,  They had me on 2 Norcor (5/325) every 4 hours.  I was taking one every two hours and it wasn’t cutting it.


At exactly 1:20 a.m. I raised my bed, tried to get comfy, and proceeded to eat.  Pretty much anything that was around.  Yams, chicken Lasagna, crackers, bananas.

About 3 in the morning, the nerve block wore off and the dull pain became brighter, more intense.  Kind of like turning the treble up on your car stereo.  I really couldn’t move and stayed in one spot. Not a good night but my chest tightness was mostly gone.


On Friday morning. Radiology came in and took two chest films  They messed up the first one.  It was very hard to sit up or get comfortable.  The day was pretty much, pain discomfort, pain and discomfort.  I should have asked for the morphine and just knocked myself out.   It wasn’t awlful if I kept still, but I wanted to get out of there so that meant I had to move around, stand and try to walk.  I was pretty much confined to the bed area because of the chest tube suction device.  I wasn’t really sleeping and I couldn’t stay comfortable.  I would raise and lower the bed as needed to eat and urinate and then try to breathe whenever there were spasms.  I had one of those beds that prevent bed ulcers and it would constantly puff up here and there, and I would constantly have to readjust my position.


I was able to sit on the edge of the bed a couple of times and stand in place a couple of times till back spasms took me down.  The stupid chest tube sticking in my side not only creates a vacuum with the lung, but the end also wobbles between the rib cage.  Both of those send all kinds of weird sensations into my organs, nerves and muscles.  Every time I would move, the hose would move and send pressure waves into my chest and wobble the tube that would irritate the muscles and nerves between the ribs.  My chest and back muscles would then start to spasm, I would get as still as possible and breathe my way through it until it would pass.  

That usually created more discharge  They had a 150 cc’s (I guess it was cc’s) or lower 24 hour level before going home.  Discharge increased first thing in the morning, whenever I sat up, or when I stood.  The discharge hadn’t stopped coming out since I got there.  I think I had put out another 250 cc’s.


The Oncologist stopped by and we all decided we would start the chemotherapy on Tuesday.

All the "on call 'doc’s that needed to, would come by through out the day, checking incision sites, etc.

They gave me a spirometry device to measure lung inflation and instructed me on exercises to improve lung function.  I could barely make 1000ml on the scale.  The nurse said that for my age, I should be above 3000 and had I better get on it.  They said it would also help keep my lung inflated


Friday evening, someone from the C-V surgeons office came in and said that lung inflation looked good and there was no more collapse and that the chest was clearing nicely,   They unplugged the vacuum line and decided to allow the tube to drain on its own.  They said we would still need to wait another 24 hours from this point.  This was good news.  I had more freedom to move about and our stay looked shorter.

The Nurses were taking vitals every 4 hours.  Unfortunately, my blood pressure has remained in the high stage I-II area the last several days.  150’s/100, this is not good.  One of the reasons I need to get the chemo started right away.

Friday night they changed the meds and I got a few good hours of sleep and a significant decrease in pain.  


Saturday- morning another x-ray, washed hair and rest of body, changed sheets and gown.  I felt so much better.  Still occasional spasms from chest tube, but less frequent.  The

drainage had slowed down but I could still hear gurgling and squishy noises in my upper chest. 

We were feeling optimistic that we would be out there soon.  I was doing remarkably well considering.


A C-V surgeon came back and told me the the last x-ray showed that the lung had partially deflated and I would have to go back on the vacuum line.  Oh, major let down!

We were very disappointed that we would have to stay longer.  They told us that this is a serious condition, if we had not already been told.  That, no, we could not go home till maybe Monday. 

Nurse said that she has seen these things take a couple of weeks and she could not believe how little I was taking in pain medication. She said most people with chest tubes want morphine constantly.


Glenda was very angry and frustrated.  She was looking for some ones head to bite off.  I could feel her energy and impatience.  She was ready to go and resented being told something different each time someone came in the room.  

I was pretty much confined to bed again,  I could stand near the bed, but the suction irritated the tube more and I would get more spasms.


That afternoon, they came in and took another x-ray


I woke up at 5:30 Sunday morning.  I had slept almost 5 hours.  The first time in months I had slept for more than 2-3 hours at a time.  Oh how glorious that was.  I could feel the pain but wanted to delay the meds until when I was up and about doing things.  Another bad idea.

I cranked the bed back down and kind of dozed off and on till 7:30.  I really felt the need for the meds so I pushed the nurse call button and they said they would send my nurse. 


I was getting settled, eating a banana, when the C-V surgeons PA came in and said she was going to take out the tube and discharge us.  What?  Glenda, popped up off of her cot.  Yeah the last x-ray showed there was no change in the space on the upper lung with suction and they thought it had more to do with the tube placement.  They said it should resolve on its own but I would probably have some chest crackles for a while.

We were in shock.  What great news!  

“So then how long till we can be discharged?”  i asked

“Probably in an hour or two.’ The PA said

Glenda was so happy she was almost giddy and on the verge of tears.  She was bouncing around like a little kid at Christmas.  I do believe she was even happier than me.  My big concern now, was that I had not taken any pain meds since 12:30 that night, and I knew as sensitive as the chest tube area was, this was going to be an event. 


I asked for a pain med ASAP and got to take one just as the PA started to snip the sutures.  Oh man, not enough time to for this to kick in.  Grin and bear it time I guess.  Not the most fun thing to do shortly after waking up. 

"Aren’t you going to unplug the suction before you pull it out." I asked

"No , don’t need to."  "Here we go"  She pulled on it and heard/felt the squishy plop and fluid running down my side.  I was hyperventilating again.  They put a compression dressing on it and told me I could shower on Tuesday.

Glenda commented that she didn't think the tube would be that long inside of me.  I didn't get to see it.

We packed up, cleaned up and headed home in about an hour.

Hooray - home sweet home.

I am doing well but pretty beat up.  I still have some upper chest gurgling and crackling in my chest in certain positions.


Chemo starts Tuesday afternoon so, I need to get my head around that once again.

Wish me luck!  Thanks for reading and all your support.

Love,

Brian





Sunday, December 21, 2008

You Won't Believe This!

Please read the ‘Wednesday at the Oncologist’ blog before you read this one so that you are up to speed.


I am writing the bulk of this on Friday and Saturday, in a groggy state of mind, but I did do some editing.


Thursday Morning


I had Ryan pick me up at the house at 9:30 so I could be at Seton central by 10.  Of course, I had to fast the night before with no fluids after 7 a.m.  and I was already parched.  Maybe it was from the mexican food the night before.


We got there on time, but the front entrances were blocked by big construction trucks for paving.  I guess 10 a.m. is better than 10 p.m. for that sort of thing.  He dropped me off at the back and I told him I would call him when I was ready to be picked up.  


I walked through Seton to the front where Day Surgery is located.  They were quite busy and I painfully waited in line for about an hour.  I was told that they could not accept the diagnosis as written and they had to contact the Doctor’s office.  I guess someone had written or relayed an incomplete diagnosis.  So I waited another  20 minutes till that was straightened out.  At least I got to sit as I was having a lot of trouble standing for so long.


They called my name and took me back to a pre-op room and told me to change.  I waited about 45 minutes before any one even acknowledged I was there.  I waited about another 25 minutes before I saw the next person.    

I needed to do some Qi - Gong centering in my head, along with entrainment breathing to get settled and balanced.  I felt pretty wound up.  I don’t think that it was just that I was being neglected.


They took my vitals, did all the paperwork, took my possessions and started the IV.  I had to count my cash and sign for my valuables.  Those would go into a safe as opposed to the clothes locker. 


I found out that recovery would only take an hour instead of 2-3 hours so I would still be able to do chemo before the oncologists office closed.  I think that helped lower much of the stress I was feeling.  I was thinking that my stress threshold must be getting lower since I was feeling more anxious than normal.  Maybe it was the realization that I was about to start chemotherapy after all this time and this was the start of what Glenda and I had been mentally and emotionally preparing ourselves for.  


I was rolled back to OR and the incision site was prepped.  I was sliding off into La La land, so I guess the anesthesiologist was doing her thing. 

I woke to them pressing gauze and band aids into both sides of my clavicle.  My initial thought was, hmmm.... that’s odd, but I was still a little groggy.  


The surgeon leaned over just before they wheeled me to recovery and said that he could not place the P-o-C  at the original site because of weight loss and proximity of the vessels to the clavicle.  So they had to place it over on the right side.   He said that the right side worked out good and was ready to go.  He said that during the procedure, the left subclavian artery had been was nicked and there might be a hematoma over the site because of some of the blood loss.


They rolled me back to recovery.  Overall, that wasn’t so bad, other than the mishap.  It seemed quick and painless.  The first thing I did was ask for something to drink.  It is amazing how good, even tap water can taste, when you are so thirsty.  I usually ask for half juice with water.  Every time I saw the nurse I asked her for another drink.  I was so dehydrated.


I had a few new aches and pains in recovery.  I noticed some left sided lower chest pain and some lower mid back pain.  Not unusual I guess when laying on OR tables.  I felt pretty good in recovery.  I wasn’t nauseous, my vital signs were all good, I could take a good  breath and I was able to drink fluids.  


The nurse said that an x-ray was ordered and they could not release me until the x-ray was taken and read but it shouldn't take more than an hour.


Somehow, during this time, the bathroom toilet between the adjoining rooms became stuck. The nurse said that maintenance was called but he had two other stops before this.  Talk about loud and obnoxious.  Even with the door closed, it sounded like a 747 ready to take off.  I hate to think what all they can flush down those things.


So now I am playing the waiting game with Radiology.  I am listening to the water wailing next door and starting to worry about making chemo on time again.  I can feel my chest tightening.  I started my calming exercises again.


In about half an hour, mobile radiology came down to shoot the x-ray.  Good, still have an hour to spare.


The post op nurse apologized about the noise while she gave me something more to drink.  She took out the IV and I was able to change into my street clothes.  She said she would call Ryan to pick me up, and as soon as Radiology cleared me, I could go.


As I was changing clothes, I noted that I had more chest and rib pain as well as trouble standing straight, almost to the point of being doubled over.  Since I hadn’t been standing for a while, I thought I was really stiff and sore. I finished dressing and sat back down.  The back pain had now moved around more to the side and front of chest.  It was getting harder to breathe.


The surgeon walked around the corner.

“Where’s your better half”

“She had depositions today that were scheduled months ago.  My son is going to pick me up and take me to chemo.” 

“OK - Well, the chest x-ray showed a lot of fluid build up in the chest cavity.  I think we need ... what is all that noise?”  He turned around to look at the bathroom door.  

“The toilet is stuck”  I stated.  “ I have been dealing with it for an hour now.”

“Jeez, I don’t know how.”  He said shaking his head.  “Thirty seconds is about all I can handle.”


I had a hunch what was coming.  My chest pain was getting worse.


He continued.  “We need to get a chest CT to see how bad the fluid accumulation is and try and see if the vessel is still losing blood.”  


I looked at the clock, twenty minutes to chemo.  Frustration time again.  “Chemo isn’t happening today is it?”  


“I’m so sorry Brian but I can’t let you leave to go home or go to chemo before this is all checked out.  This hospital is exactly where you want to be, and not at home, if there is still some blood leakage.”


I knew he was right.  “OK”  I said.  Tears of frustration started welling in my eyes.

“ I know, this has been a tough few days” he stated

“Tough few months.”  I lamented 

He stood up  ‘Let me get this scheduled STAT and I will be back to talk with you.”

Don’t drink anything!


Luckily, I got some fluids in. But I was still so dehydrated.  I had not eaten in about 21 hours at this time.


Thoughts were flying through my head.  The realization of what happened burned through the anesthesia.

They punctured my subclavian artery!  Oh my God!  I don’t believe they friggin punctured the subclavian artery.  

Well luckily, my current condition did not feel unmanageable so I am thinking, lets get this over with so I can get the hell out of here.


As I sat there, listening to that damn water, I thought about all the time and energy Glenda and I had put into getting chemotherapy started as quickly as we could.  All the frustration with the time lost in testing and diagnostics at MDA.  I thought about how all of our mental/emotional energy has been directed to this moment and now there was another setback.

I am usually a pretty tough guy emotionally, but I started to cry.  I also started thinking about the potential seriousness of a slow bleeder and how my father had pretty much died from complications of a similar thing.  

What if.....


I got more emotional and began to sob.  I just couldn’t help it.  It would have been so easy to really let the dam burst, and I probably should have.  Sitting alone in the room, I guess I started feeling sorry for myself.  I reined myself in and sought out support.  Glenda was in Depositions, so I tried her sister, Sandi.  I was choking back sobs and couldn’t talk. 

Like usual, she answered cheerfully  “Hi Darling”  How are you?”

“...............Sandi..............I...........uh.............need ..................huhuhuhu...........................”

“I’ll be right there”

I know there was a little more said, but that was about it.  The nurses looking in on me were very compassionate once they saw I was crying but obviously did not know why. 


Some how I sucked it up and called my son and told him he didn’t need to pick me up, that I had to stay a bit longer.  Shortly there after, Glenda called to say that she was done, heard the tone in my voice as I tried to get her up to speed and said she would be there as quick as possible.  


A nurse came down to draw blood.  I said I had blood drawn earlier but she said they needed a creatinine level prior to the CT.  She did not get the stick on the first try.


The surgeon reappeared and said everything was set to go and that they would get me in a bit.  He said he would be with me during my CT.

  

The pain was starting to get worse now.  It felt like a heart attack must feel like. I  was having trouble breathing like some one was giving a bear hug.  

“My chest hurts and is really squeezing me.”  I told him.  

The Surgeon said  “Yeah, that’s what it feels like. It can be very painful.”   “We have all kinds of pain medication.  Do you want something for your pain?”  

“No, I want to be able to eat afterwards”  I had decided to tough it out for a while longer.  (big mistake)

“OK, then, just let me know.”  “I’ll be back when they come for you.”  


He left and Glenda arrived shortly there after.  She walked over to hold my hand.  We tried to talk over the water noise.

I finally had enough of the water and asked the nurse to move us.  We moved next door and could barely hear the water now.  I told Glenda that I did not think this was good and that I had a suspicion I might need to have my chest area drained.


The guy doing the CT showed up with a wheelchair.  I climbed in, kissed Glenda bye, and we headed off.  The Surgeon rounded the corner and said he wanted to talk to Glenda and that he would meet me in CT. 


I couldn’t sit straight during the wheelchair ride.  Every little bump on the way sent pain through my chest causing me to contract into myself even more, if that was possible.  I could barey breathe. I was in my warm street clothes but could not stop from shivering in the cold hallways between all the big diagnostic equipment.  


We got into the room, and they wanted me to change into a gown.   At this point I had trouble standing and sitting from the pain.  I could barely raise my arms from the two incisions on my clavicle.  I couldn’t straighten from the shivering and muscle contractions.  Somehow, I got into a gown and laid out on the tray.  

Of course it was a contrast CT, so he hooked me up to the auto injector.  (Here we go again)  I had to try keep my arms above my head for the imaging.  They rolled the tray into the doughnut hole and asked me to take a deep breath and hold a few times.  That was laughable since I was hyperventilating.   I could barely breathe in but I could kind of hold my breath for like a second or two.  A few passes and it was over.  I barely even felt the rectal flush until I sat me up.


The surgeon came out and said  “The images show there is a substantial amount of fluid accumulation and blood that has perfused into the chest cavity.  It is creating tremendous pressure that we need to get off your lungs and heart.”

I frowned and shook my head.

"There is too much accumulation for your body to absorb and deal with on it’s own.  He continued.  If we leave that blood in there, it will congeal and form a big scar tissue mass around everything.  We are going to need to drain the area.”  

I knew this was coming.   I have been in medicine long enough to know how things happen and progress.  Yet, I was still so overwhelmed by the negative turn of events in such a short period, I had another little sob spell.  

“Yeah, I figured as much”  I nodded.

He continued.  “There just so happens to be an outstanding Cardio-Vascular surgeon who has done hundreds of drainage tubes. He is currently performing surgery at this hospital and I have asked him to do the tube for you and he said he would.” 

Well, that sounded good!  "Sounds good to me."


“They will take you to surgery recovery to do this.  I will go tell Glenda what is happening and meet you up there.”

I nodded OK and he was off.


The CT guy rolled my wheel chair up to recovery.  It was a big rectangular room with a dozen or so partitioned areas containing beds and patients.  Most of the partitions were open to the inside of the room but several were open between the patients.  I was in excrutiating pain at this point and most have looked quite odd.  I had a hospital gown on over my street pants and shoes.  I guess I was white as a sheet.   

I don’t know how or why I even noticed, maybe because I was under medicated and alert, but I got this eerie, deja vu, kind of feeling as I entered this large room.  So many of them were watching me, following me with their eyes, as I was wheeled in.  I of course, was checking them out as well.  It was almost like a modified dark corridor dream with people I did not know.  


The CT guy rolled me around the room, as if on parade, looking for a place to park me.  He found an open space with out a bed and one of the recovery nurses came over looking confused.  I don’t think they were expecting me.


The CT guy told her that the C-V surgeon wanted me up here.  About that time, the C-V surgeon walked up and introduced himself and told the nurse that he needed a bed.  

He quickly explained the procedure to me as I sat in the wheelchair.  He said that he has done a thousand of them and promised it would be quick and painless.  I asked a few questions about the procedure so that I was fully informed.  I was in so much pain and discomfort that I probably did not make a lot of sense.  I think I asked the same thing more than once. 

“You don’t have to be a cowboy on the pain.”  The C-V surgeon said.  “We can give you what ever you need.”  

“No.”  I said. “I want to eat afterwards”.  (what a dumb ass I can be)  They must have thought my focus on eating was strange at a time like this.  I really didn’t comprehend how serious this all was.   I just knew that I wanted to eat afterward and by God, I was going to eat!  

I kept asking them for an IV since I was so dehydrated.  My surgeon told one of the nurses to start an IV, one saline and a Ringers after that.


All of a sudden, a half dozen nurses in scrubs rolled in with carts with trays and a bed.  They quickly got me on the table and undressed. (Me, not them)  They started prepping the incision site and discussing what percentage of Marcaine they were going to use. They surrounded the table and worked very efficiently.  I presume they must have been his OR staff.  


The curtain to my right was closed but the curtain to my left was open and the lady sitting up in her bed, had a bird’s eye view.


The CV surgeon started off gently enough while numbing the area, but each needle insertion was progressively harder and deeper.  If he felt me flinch he would work the area some more.  I was shaking the whole time he worked on me.

He kept jabbing and jabbing and jabbing me.  I could feel him push into the area and then squeeze down to inject the Marcaine.   I don’t know how many syringes he went through. There were dozens of sticks.

“You have enough Marcaine in you to keep you numb for 12 hours.” He commented

 I knew he was making the incision even though I didn’t look.  I could feel pressure as he would cut, wipe, cut, dab explore, cut.  I did feel the tube being inserted and the sutures tightening it in place.  They then hooked the tube up to suction.  A lot of fluid came out.  I guess about 700 cc’s to start.


He said I should start to feel some relief.  I wasn’t really feeling any different.  My whole chest felt like it was in a vise and I could barely breathe.  But, I didn’t say a thing since I had refused the pain meds.  ( Can we say dumbass, again?)


They still hadn’t hung an IV.  My lips and mouth felt like hot sand paper.  Two of the recovery room nurses were debating back and forth during the procedure who was going to do the IV and what vein would be best for what gauge needle and so on.  I again asked for an IV.


I finally asked for some pain meds and they said I would soon be gettig the same thing I had in the original surgery when they do the Arteriogram.


“Arteriogram?  What arteriogram?”  I asked.  

Oh God, not another procedure I thought.  I felt like I was on a roller coaster of nightmares that would not end.

It was explained to me that an arteriogram still needed to be performed. That it was important to make sure that the nicked blood vessel was not still leaking.

“I thought that the CT showed it wasn’t leaking”  I asked

My surgeon explained the the arteriogram was a better test.  They would thread a catheter up through my groin into the area of the damaged blood vessel by my clavicle, spray some dark dye, and then see if it is still leaking.

I asked about risks and if there was a chance of re-injury to the area and he said no to re-injury.  He said the usual risks outlined on the consent form.  That caused a stir.  

"Oh yeah, we better get some consent forms signed."  I heard someone say.  


He said he found a doctor who could do the procedure right away.

“If we have to, then we have to.”  I sighed.  I must have said this with a tremendous amount of resignation, because he kind of stopped and looked at me compassionately.  At this point I was a whooped puppy and I was wondering if this nightmare would ever end.

“ I know that this has been a long day and has not turned out as planned.  We are almost done.” 

“ I need to go talk to Glenda and get this set up.  They will draw some blood for the test and be down to get you shortly.”   He took off once more.

More blood?  Oh come on!

By this time, I already had several consent forms lined up to be signed by a vigilant nurse I spied in the background.

The two recovery room nurses finally decided who would get the blood and from where.  Most of the C-V surgeons staff was gone by now.  The nurses missed on their first stick.  I think I see how easily torture can break ones will.


I signed several consent forms and luckily this nurse from the arteriogram place took over.  He hooked up the IV, discussed with me everything that was going to happen, covered me in warm blankets, loaded up my tube suction device and wheeled me out of there.  Wow, he seemed like a guardian angel.  


Once I got into the room, several people slid me over onto the table under the imaging devices. The covers had come off and I was shivering once again.  I couldn't really feel the chest tube and hose sticking out of my side but I could hear it running.  They located some more warm blankets and covered me up.  Wow, did that feel good.


The doctor performing the procedure told me this was a search and repair procedure.  If he found a leak he would repair it with a stent although it would be a temporary fix and would most likely have to be repaired surgically in the future.  They had me initial the consent form after they added the stent part.  My vitals were still stable from what I could gather, and I figured that the artery had stopped leaking, but could not be sure.

"OK, let's do it"  I said.

I told them I had to pee really bad and they got me a plastic urinal.  I had to roll to the side a bit and actually didn't make a mess of things.  Ahh, warm blankets and a pee.  Much better.

They uncovered me and prepped both of my groins.  They shaved me and washed me with a cold wet dye.  I don't remember anything after that but I recall waking to the doctor showing me the pictures on the screen and the blood vessels with dye in them.  He said everything looked fine and they would take me to my room now. 

It was a little after 7 p.m.


In my next blog, I will tell you about that night and the next few days.

I hope this is not too much detail.  So much happened that I tried to capture.

Love,

Brian