Chad’s Story

Site created on December 27, 2020


I have cancer… 


It’s been three weeks since my diagnosis and those three words are still incredibly difficult to say. However, it’s our new normal…so, might as well embrace it. 


In November, I noticed a sore throat that I attributed to what has become the typical annual sinus infection. It persisted into December, and on the 20 th of December, I noticed a lump in my neck…a lump in my throat that is accompanied by pride in a family accomplishment, the Olympics, sharing utter joy with friends, etc., is expected…and this lump was out of place. When I asked Les about it, I got a cock-of-the-head, inquisitive look from an exceptional, highly accomplished nurse (I knew then it was
something to take to the doctor).


After a quick visit with my doctor the next day (and the same cock-of-the-head, inquisitive look – must be a thing with highly intelligent healthcare providers), I “earned” a CT. The next day, December 22 nd , I got a call and heard the words that no one ever expects, “Chad, I have really bad news.”


He wasn’t wrong, he did.


I have cancer…


Since that tsunami of overwhelming uncertainty and anxiety, I have been trying to comprehend what I, my family, and my career have ahead of me. And to be clear, you can’t imagine how many things race through your head at once. Seriously, it’s mind-numbing, the thoughts have included, but aren’t limited to the following:


WHAT THE FUCK?!
 There must be problem with the test.
 This really isn’t happening.
 How do I tell Leslie?
 How do I tell my kids?
 How do I tell my parents?
 Seriously, what the fuck?!
 Why me?


You get it…it’s a lot.


Thankfully, the first few days were full of distractions. Christmas – my family’s favorite holiday, New Year’s Eve, New Year’s Day, all provided a welcomed respite from my brain scrambling with unknowns, what-if’s, why’s and what-the-hells. It also affirmed what I always knew to be true.


I’m a blessed man. I have the most incredible, supportive, strong, and resilient family ever.


Leslie is an unwavering force of nature, who has kept my head up, feet moving forward and never allowed me to fall into a state of woe. My kids…damn…they inject me with strength and purpose that will allow me to lean into the tempest. They’re a daily reminder of who I am, and what I need to fight for.


I’m biased, of course, but it’s far more than I’ll ever deserve.


I have cancer…


My diagnosis is late stage-two/early stage-three cancer at the base of my tongue (primary), with spread to my lymph nodes (secondary). Thankfully, it hasn’t spread to my lungs, which is the organ it typically spreads to, so that’s great news. I’ll take it!


The past ten days have been a whirlwind of medical appointments, surgical procedures, reflection, and undergirding myself for the fight ahead. Each doctor’s visit brings another wave of daunting and sobering information, prognostications, potential side-effects, qualified-positivity, and otherwise the kind of shit you see on TV and say, “that’s great writing, and thankfully that won’t happen to me.”


This is a season in my life. Nothing more…less than baseball, hockey, or football season. It won’t be pleasant; my family knows this, it gives me pause, but we’re leaning into this season. We are steeled against it and ready to tackle/endure/shoulder into what lies ahead. My treatment will include at least 33 radiation treatments, with a parallel course of chemotherapy (cisplatin), or immunotherapy. Not the ideal way to shed those unwanted pounds, but I’ll take the silver linings wherever I can get them.


I have cancer…and it’s scary.


That said, this is but the beginning of 2021. It’s not the final chapter in a book with so much left to be written. Years (hopefully decades) await to be experienced, explored, lived to its fullest, and shared with all who have impacted my life in endless, wonderful ways. This fight couldn’t be won without every experience my life with family and friends have provided me…in this respect, my cup thankfully runs over.


My cancer…
Will not rob me of time with my family;
Will not take away my sense of humor;
Will not take away my sense of dignity;
Will deplete my strength, but will not rob me of my resolve;
Will make me sick, but I will flourish;
Will knock me down, but I will get back up;
Will win some battles, but I will win this war!


FUCK Cancer…We will beat you!

Newest Update

Journal entry by Leslie Linzy

Three Weeks In... the fight goes on.

 

Let me begin, as always, with gratitude.  Last week, I heard a phrase and it has been rolling about in my head ever since.  It was a thought waiting for a situation to bind itself to.  Simply put, it's "A community of neighbors."  At first glance, it could seem trite.  A cliché.  However, as I pondered it continuously, I realized how simply profound it is, and how perfectly it applies to me and my family...and how damned lucky we are to have our own Community of Neighbors.


This isn't, "It takes a village."  It's deeper, more meaningful.  A connection and sense of caring (wanting to care vs. feeling a compunction to care) that transcends typical community relationships.  

 

  • A special thank you to my mom, who came to care for and generously support me and the family.  It was wonderful to have her here, thanks Mom.   
  • Thank you to Keith and Diane (our literal neighbors), who have provided a seemingly never-ending stream of wonderful meals, words of encouragement, lifting of spirits (faithful and liquid), and a ramrod determination to see us through this difficult journey.
  • To Dot, Charles and Stacy, who's messages of support, dinners, and visits with needed hugs are wonderful.

 

And, to all of you who have become my Band of Brothers and Sisters, my community neighbors...thank you so much for reaching out with words of encouragement, prayers, delicious meals (I'm now living vicariously through my family, watching them enjoy the tantalizing food), wine and drink, and everything in between.  The support has been beyond anything we, as a family, ever expected and has touched us to the bottom of our hearts.  It will be a genuine privilege and honor to reply in-kind and beyond, with every one of you.

 

Some suggestions I've received, gathering everyone together to run a 5K, throw a blow-out Kansas City barbecue party (all keys to be turned in at the door/ and any tattoos received during the party cannot be blamed on the host).  Whatever we decide, please allow for my taste to return.  I ask for this grace for your benefit - you see, after getting COVID last year, I lost my sense of taste.  When I began cooking again, I was asked in no uncertain terms to let others handle the responsibility of seasoning, especially the salt.  Apparently, I was overdoing everything.  So, I am learning from previous mistakes and beg your kind patience.  Salt licks should never appear on any menu.

 

Yesterday, Monday, February 22, marks my second (and last) chemotherapy treatment.  It also marks three weeks of radiation treatments completed, the halfway point.  This is great news!  The treatment chain is shrinking!  These thoughts were running through my head throughout the day...then I met with my Radiation Oncologist.  To be clear, I think the world of my doctor.  He's a great physician, one hell of a supportive advocate, and he's curing me of cancer.  However, his direct approach of the next three-and-a-half weeks certainly gave me pause.  He celebrated my positive labs, keeping my weight loss to limited proportions, and overall approach to the first half of treatment.  Then he said, "you're half way there, but that was the easy half.  The hard half is here."

 

Well, as Hugh Grant said so eloquently in Four Weddings and a Funeral, "fuckadoodledoo."

 

On the way home, I tried to come up with a way of explaining this to my kids.  Something they can easily understand, and not scare the edge of hell out of them.  They want and deserve to know what's on the horizon, just sans the startling details.  Here's how we shared this with the kids.

 

"How's it?" to my Hawaiian ohana, Ke Kaua Maika'i

 

For those of you have ever braved a surfing board, you'll immediately get the references.  If you haven't, the references are just as easily understood if you've seen the 90’s preeminent film, Point Break.  As someone who has experienced surging, let me set the stage.  After paddling out into the surf, you typically sit or lay on your board waiting for your ride.  The waves are barely perceptible.  Then you see it.  The wave.  Your wave.  You hear Patrick Swayze in the back of your mind, "This looks like your wave Johnnie.  It's got your number."  Even if your name isn't Johnnie, you hear it.  

 

That's how I view the first three weeks.  Paddling out and waiting for a hell of a ride.  Now comes your wave...it grows bigger as you near the break, it builds before it crests, and now you're in it...no getting off now.  The effects of the second half of treatment don't diminish, but rather continue to build on themselves, the ride is going to continue all the way to the shore.  This ride will include vastly increased throat pain, damage to my voice, and fatigue.  There will be others, but no need to share the delightful details.  It's time to kau lewalewa e hakaka i ka hakaka maika'i - hang loose and fight the good fight.

 

Lastly, I've had some questions about the side effects, so a brief update on the prominent ones:

 

I'm getting closer to a reunion with my jaw line, and my abdominal muscles (I keep reminding myself that you can't have a six pack before you have a two pack).  I feel like being at the airport, eagerly awaiting Les' return, watching as each plane nears the landing strip, growing more impatient with each plane.  

 

In the "every challenge has a silver lining" category, my voice is nearly gone.  I'm down to sounding like a really bad Clint Eastwood impersonation.  Imagine Clint in his full-on western persona, but without the cinematic charm.

  

When I started this journey, a nurse told me that treatment will be like, "giving you a very nasty sunburn inside your throat on a daily basis."  They are achieving this goal with supreme gusto. See above side effect.

 

Fatigue continues to be a growing issue.  I'm not yet like a narcoleptic who did a weekend long binge on sedatives, which I take as a positive note.  That said, I feel slightly concerned that my family has created a warning sign that reads, “Caution: cancer patient with narcoleptic-type tendencies nearby, watch your step.” 

 

Thank you again one and all for your support.  It keeps me going!

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