Of course they never show up at the same time making
sleeping in the afternoons almost impossible as literally every 15 minutes
another DR or PA is showing up to examine you.
If I had a dollar for every time someone came in and put a stethoscope
on me I could likely pay most of my medical bills. The most interesting part is the lack of
coordination across the specialties. At
times Pam and I were coordinating treatments across DRs, treatments that often
conflicted with each other.
Which brings me to the nurses and techs (nurses aids). To call them angels is an
understatement. They were my daily
care givers, my lifeline to the DRs, my counselor when I needed to know what a
procedure entailed, my calendar keeper for tests and meds, my advocate when I needed help, and often late night conversationalist when I
couldn’t sleep. In addition to their
medical duties they made sure we were fed, cleared our food trays, emptied and
tracked bodily fluids, and tried their best to protect our sleep. They held my hand through the bone marrow
biopsy, entertained me by drawing a caricature of my best chemo look, encouraged
me as I walked the floor, and checked in to get the latest on the birth of our
newest grandchild (another boy). Ring
for a nurse and the majority of the time they were there faster than the best
concierge. Seldom in the course of the
last 30+ days did I feel like I was anything but the most important patient on
the floor.
The demons are the daily challenges that you face that eat
away at your confidence. Sometimes its
new challenges like determining what the volcano wounds on my back are (turns
out to be Sweets Syndrome), needing Heparin shots (which are given in the
stomach), dealing with spiking fevers (which in turn require tapping a new vein
for more blood), getting cardio problems under control (more EKGs,
Echocardiograms, and x-rays) and the biopsy the wounds as well as the bone. Some things you know are going to happen but
it’s still a blow when they do. Like
your feet swelling up from the fluids till they look like a uni-toe hoof. Or the day when my shower looked like it
was used by Chewbacca…didn’t need that hair anyway. In most cases it’s not one big thing that
gets you, it’s the constant barrage of body breakdowns and the resulting
treatments and their side effects.
Got to love MRIs.
Put somebody on a slab, tell them not to move for an hour put in ear
plugs, headphones (with music), stick them in a small metal container that
resembles a casket and then blast the sound of machine gun fire at them. Occasionally ask them how they are doing but
don’t listen to the answer. And what’s the
point of the music? You can’t really
hear it while the machine is pounding away, but if you happen to find yourself
tapping your toe to a tune you are abruptly asked to stop moving. Like going to a dance where the music is
great and you can dance all you want as long as you do it in your head.
And then there is the food.
After a while everything smells and taste like hospital. My daughter says it’s the chemo and she can
smell it coming off me. It makes
ordering food interesting….I’ll have the white fish cooked in the chemo sauce
and the bland brown rice with the hospital smell. And what is it with cooking everything
until it’s dried out, soggy or flavorless?
I guess if everything taste like nothing then you know exactly what you
are getting. It’s one area where there
were no surprises.
The hospital smell also making wearing a mask pretty interesting
since you end up recycling your own air.
Reminds me of being stuck in a cab in India without air and with a
driver who clearly had been working a 24 hour shift in 100 degree weather. Popping an Altoid (strong mint) before putting
on the mask can help.
I apologize, I know I’m whining a bit. I’m no hero, just a guy making it through
this phase so I can move on to the next phase of treatment with the goal that
somewhere down the road there will be a cure.
But there are heroes on the floor and I admire them greatly. The family members who come day after day and
sit by the bed of their loved one even when they are sound asleep. Who sleep on the couch in the room overnight
when a cancer patient is having a particularly hard night. Who take on the burdens of outside life so
the patient can focus on what they need to do to get better. And then there are the cancer patients
themselves. The ones that have been at
it for over 6 months, who are facing daunting odds to recover and who are in
significant pain yet they fight on, day after day. I’ve seen the determination on their faces,
heard the cries of despair in the night, and seen them work to make it easier
on their loved ones who come to visit. They
are the real heroes.
Angels, demons and heroes…it’s a strange combination but
then again a cancer ward is a strange world.
Next time…finishing up Phase 1 and preparing for Phase 2.
9 comments:
Dave you can do this! We am so sorry you have experienced so much pain and daily/hourly challenges and nightmares. We want you to know we have all crawled into that bed of yours with you and are right there cheering for you every step of the way! Thank you for being so incredibly courageous in sharing this very personal struggle with all of us. You couldn't be more loved or more surrounded by the power and strength of love and prayers. Strength to you sweetie, you can and will get through this! All our love and hugs The Bentleys xxxxooo
I am constantly amazed at how articulate you share this experience while going through so many treatments and discomforts! We are praying for you and hope with you that this phase passes soon. None of this is easy, but you and I are in this together...
Dave, I finish all your posts in tears. If anyone has a right to whine it's you and frankly you didn't sound like you were whining at all! Praying and thinking of you - stay strong!
<3
Cynthia
Don't ever apologize for for your feelings, you have a right to have them and it seems as though you are handling a terrible situation with dry humor. Keep up the fight and I am saying some special prayers for your complete recovery Dave.
Christine (Carlevale) McAllister
Dave-
It's funny that you are the only one who could possibly think you are whining. Your strength, humor and view of the strange world you have been thrust into are both amazing and admirable.
You are and will continue to do great and the party when this over will be a good one!
-Mike
Thank you for sharing your stories Dave. You continue to inspire by being "self-led" versus "symptom-led" - I'm convinced it's your mental attitude of having trained for a "few" marathons! Continue to fight and be present each day. You'll adjust to those headwinds, rain and hills and I'm convinced your inner determination will be your source of strength. Keep the faith.
One foot in front of the other...even if it's 21 laps. :)
Todd
Thank you for sharing your stories Dave. You continue to inspire by being "self-led" versus "symptom-led" - I'm convinced it's your mental attitude of having trained for a "few" marathons! Continue to fight and be present each day. You'll adjust to those headwinds, rain and hills and I'm convinced your inner determination will be your source of strength. Keep the faith.
One foot in front of the other...even if it's 21 laps. :)
Todd
Hey,Dave. Today's blog post on the Tortoise and the Hare is for you: http://bit.ly/1TTwrgA
Aline
Wow, Dave, for want of a better word, what a beautiful blog post. Absolutely harrowing what you have to go through. But how beautiful your ability to reflect and write about it; about the people around you and how they matter. In my previous life back in the Netherlands I worked in medical ethics and stories like yours, voices looks yours, were so necessary for patients to be heard and understood. That's why I can't help but say, what a beautiful blog boost. You make it so real.
Thank God you got through that first phase! And out of that lonely place! Thoughts, prayers and Boston strength for you! Inez
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