Most of us
have had those times in our lives when we have so much going on that we start
to become forgetful. The signs are
usually things like…Where are my car keys?
Oh crap, I was supposed to be at the dentist a half hour ago? I can’t find where I put the TV remote? One of my favorites is when you are asked “have you seen my glasses?” and you
can see them sitting on the person’s head.
Yup, been there, done that…both sides of that situation.
These are
typically followed by statements like…”If I had a half a brain I’d be
dangerous” or “If brains were dynamite mine couldn’t blow out a candle”. In our multitasking, always connected, fast
paced lives sometimes we are just trying to do too much at the same time. And
sometimes it’s chemo brain.
Nurses and
doctors have warned me that a side effect of the treatments can be muddled
thinking, forgetfulness and general brain lapses. Big deal, those are challenges I’ve been
facing for the last 10 years. But as
the treatments have progressed it’s pretty clear that the chemo does have a
negative effect on your cognitive abilities.
It also appears that the stress of the illness can spread the effects to
the immediate care givers as well (at least that is what Pam claims).
Much like
the 5 stages of grief we were initially in denial. We blamed the misplaced items, almost missed
meetings, and multiple trips to the grocery store to buy the same item as just
the stress of the illness and hectic nature of all the activities we needed to
coordinate. The frequency made it clear
it was more than that. It was time to
move from denial to the next stage…anger.
Situations now resulted in muttering expletives under our breath (or in
some cases out loud) and blaming secret government agencies for following us
around and hiding our cell phones or moving our car while we were in shopping.
Misplaced
cell phones were a common occurrence and we were in the habit of using one
mobile phone to call the lost one.
Until the day we lost both of them.
The immediate reaction was to have a friend or family member call one of
the phones but of course that would require having a phone to ask them to
initiate the call (we don’t have a land line).
While laughing hysterically about the situation a fortuitous call from a
friend allowed us to find one of them.
We decided we were skipping right over the bargaining and depression
stages of grief and moving right on to acceptance. That’s when we decided it was time to put the
fun into our dysfunction.
First up was
Grocery Store Roulette. Much like
normal people we would have a list of what we needed before we headed to the
store(s) but for some reason key items always seem to fall off the list (or
never made it on). The goal is to bet on how many trips we will
end up making before we get everything we need.
Then there is the take off on Where’s Waldo
that we call Where’s Cell Phone. The
goal is to see who can guess/remember where they last saw the phone before
running around looking for it (or calling it). This is equally fun for car keys, wallets,
purses and TV remotes as well.
Keeping
track of my medical stats like when was my last transfusion or what were my
white blood cell counts two days ago can be a challenge with chemo brain. Often times the nurses are asking you these
questions or other more personal ones like when was your last bowel movement
(it can range from “so long ago I can’t remember” to “excuse me…got to
go”). At first I tried to keep a
folder of all the questions they might ask so I could look it up but either I
couldn’t find the answer in the folder or they would ask something I had no
idea they needed to know. After I
fumble around for a while they would infuriatingly say “don’t worry, I can look
it up in the computer”. I just want to
scream “I have chemo brain, couldn’t you just have looked it up first”? Instead I’ve decided to deploy the “dumber
than a rock” approach. The goal is to
see how long I can keep them waiting for an answer before they give up and go
to the computer. Thumbing through a
folder with no relevant information in it for minutes is usually the quickest
way to get them to move on but I like the approach of thinking out loud as I
try to track back to an answer.
Nurse…“What were your platelet counts last Tuesday and when was your
last transfusion”. Me out loud…”Last
Tuesday, last Tuesday. Let me see I know
Monday morning I was at the Doctor’s office and Weds we were shopping at
Wegmans…I had to get that special salad dressing that only Wegman’s carries,
what a great store. Did you know they
have one of the highest customer satisfaction ratings? So the transfusion couldn’t have been on
Wed. Could have been Monday afternoon
or Tuesday but I know I had something going on Monday afternoon so it was likely
Tuesday. But it couldn’t have been
Tuesday afternoon because I think that was the day we went for a Rita’s. Do you like Rita’s?
It usually
doesn’t take too much past a discussion of Rita’s menu for them to give up and
accept that I have a bad case of chemo brain and it is best if they just stopped
asking questions.
Then there is Insurance Company Jeopardy. The insurance company loves to send statements that give you the answers on how much you owe but leave you guessing at what the service was that resulted in this bill. If it were on Jeopardy it would sound something like this “I’ll pick Unknown Medical Services for $500. The answer is Diagnostic lab test on 3/25.” We then have to come up with the question identifying the service provided….in this case, “What was a bone marrow biopsy?” Actually this game is much more frustrating than it is fun. I guess the fun part is nobody is getting paid till we get some answers.
No need to
ask if my brain is fried, this blog says it all. The second round of consolidation chemo
ended last Sunday and as promised the effects were faster and nastier than last
time. Within 5 days I had gone neutropenic
(no infection fighting white blood cells) and have needed transfusions of both
blood and platelets this week. Frankly,
other the usual nausea, plumbing challenges and fatigue I’m actually doing
pretty well. All the prayers and words
of support really help.
Now if I
could just find my cell phone….
6 comments:
Dave, you are such an entertaining writer! You find humor in the grimness of times. You are my inspiration! Karen
When someone stares at you while you are wearing the mask just ask if they would like to be your next patient.
Keep putting the "fun" in "dysfunctional" and I love the game of just rambling on when answering questions until they just look on line. I may even try that with my sales team!
Take care
What a fantastic blog post Dave. I really had to laugh out loud. 'I usually end with a cough'. Awesome. Yes to the fun back into the dysfunctional! :-) It's probably the only way.
I loved reading the other posts before this one too, btw. Especially the 'Life is messy' one. 'No more plans, but wishes'. How true! Let me add our wish here, that this cycle may be as light as it possibly can be. And that you both, and all of you, manage to keep the strength to laugh and joke whenever you can. All the best, love and prayers for you, from far too chilly Amsterdam and Nova Scotia, Stephen and Inez.
Way to keep up with the humor Dave. You certainly made me chuckle on this round. Keep up the spirits and keep improving.
Eric
This is not a comment to this blog post, but just a way to reach out.
Far too quiet on your blog, Dave. I so hope you are okay. It's been 2 weeks since the second round of chemo ended, so you must be in the midst of the roughest time, battling through....
We're thinking of you. Thoughts & prayers.
Stephen and Inez
Hey nice post man! Thanks for incredible info.
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