I have become one of those individuals who requires the
little green man in order to cross the road. I depend on him. I am the woman
standing at a set of traffic lights on an empty suburban four way intersection,
eyes fixed intensely, focusing on the little red man, waiting for him to stride
off in little green man fashion thus making my road crossing decision for me.
Then I realise I have never pressed the button; the little red man is
permanently stationary. And so I push the button, slump against the traffic
light pole for support and wait some more. Should the intersection be uncontrolled
a detailed six step plan of attack is required before I can even approach the
curb. What is the intersection type? T, ok. Which direction is the initial
traffic coming from? From the right, that is normal, good. Can I see past that
parked white van? Sigh, those white vans are always too wide, and they always
seem to be double parked, and they drive just far too quickly; I wonder what is
inside those white vans…… HEY! This is no time for mind deviation. Back to the
task at hand young lady. Now, I’ll ask again, can you see past that parked
white van? Yes. Good. Is there a chance of any traffic coming from the T? Not
really, the road is almost overrun with rolling dust balls. Alright then, look
right, is there any traffic? No. Ok, look left, is there any traffic? No. OK,
look right again, remember how we went over this at primary school? Little
field trips to practice crossing the road? So, look right again, take a step to
the curb, off the curb, scanning left and right as you cross, in case you got
something wrong. Phew, centre island. Now begin again, only left, right, left
this time. Things get a little more complicated, a little more panicked, if there happens to be traffic. Don't worry, I am not driving.
It was not until I was slaughtered by indefatigable
exhaustion that I realised quite how many subconscious decisions I make in a
day. I have never before been so grateful for little green crossing men. I have
never before been emotionally distressed at the lack of little green crossing
women. I know I have referred to fatigue in the past. I was wrong. Compared to
what I am feeling now I was hyperactive before. I have a permanent prostration
slap across my face; a burning red strip running along my cheekbones, ashen
rings arching upwards towards my bloodshot eyes. My own little facial scrub
fire; the mark of irrepressible tiredness. I went to bed on Saturday night,
around nine pm. I did not really rise until six am Monday morning; my rest occasionally
interrupted for feeding. It is not only my body but my mind also. I was lying
in bed Sunday, distraught, because I could not focus on any books, any
articles, any words. It is a dark day when I cannot read. It did not even cross my mind to use this novel invention
called TV. I am not sure if you have heard of it. Laying around, trying to find
a way to pass the time, and I did not even think of TV. That is how tired my
mind is. Presently, I cannot cope with modern day branding, advertising or newspapers. Any changes in font, incorrect or unexpected
capitalisations, erratic bolded words, underlined sentences, images and colours
thrown in for good measure; my brain freezes then shatters. I cannot read this
material. It is like an optical sensory overload, my cerebral lobes cannot
convert the data from my eyes into logical thought. If the start of each
word is capitalised and there is a picture nearby, my brain will be unable to
decide which direction the text runs in. I start to read things downwards, or
miss out words, or infer meanings because of the pictures, but the
interpretations are distorted; jumbled; incorrect. I finally understand why tabloid newspapers adopt this method of 'reporting'.
I am acutely aware that the ABVD chemotherapy regime is far
from the most potent. Granted the doses are more frequent and longer than other regimes,
but the side effects have nothing on say a breast cancer regime. Three months
ago I started writing of my fatigue. That youthful, inexperienced, past Liv had
no idea. And the condition of others will be more severe; that poor cancer
patient who has small children, say. How do I describe my current level of enervation
if, in two weeks, the level will again plunge? The worst I feel is only a
perception, not a reality. The truth is I can always feel much worse. Others are feeling much worse. This
sounds rather doom and gloom but it is not really the case. The contrast on how
I felt two weeks ago and how I feel now is blatant. I imagine there is a high
possibility that my condition could further deteriorate significantly next
fortnight. Therefore I should enjoy the now, in case of steeper decline. This
is an easier attitude to adopt with the (unlikely) prospect of further chemo.
Whatever I am feeling now will not cast a shadow on what is (unlikely) to come.
For someone else that unlikely has happened. I know this. I know am lucky. I am not
trying to sympathise with myself here, purely document my persisting
degradation.
I believe it will surprise no one to learn that work has
beaten me. Three weeks from the finish line and I have pulled up lame. Lamer
than a photo slide evening of Uncle Bob’s 1967 holiday to Twizel. A few weeks
back, when I first started contemplating returning to sick leave, I was
disappointed in myself; stubbornly persisting with work each day. Currently, I
am just too tired to care. Here are the facts: Liv, you cannot continue to
work. Take a big gulp of your pride, the little you have after that
haemorrhoids post, and move on. Plus, we do not want your sexy bald patches
causing a distraction in the mixed gender laboratory now do we? It is the
mental exhaustion that has sealed my fate. The physical exhaustion I can
handle, with a many complaints of course, but mentally if I cannot cross the
road without electronic aid, well, I am not fit for work. Plus, in my current
emotional state, I will definitely cry if criticised.
I shall cease my fatigue complaints for now and describe
some physical ailments. Yay for you. Ever since my 0.2 neutrophil scare I have
been prescribed regular G-CSF injections; five days after each chemo for three
concurrent days. I confess that I find the number three arbitrary. Quite often
three turns into two. It is difficult when I can feel every bone in my body,
even bones I swear are not large enough to contain the marrow required for leucopoiesis,
to again inject myself on the third day. I can close my eyes and picture my
skull, its osteo outline a map of bone pain. Even my teeth ache, which is
either referred pain or imaginary, certainly not scientific. The bones in my
ankles, my fingers, my wrist; all are doing their part to keep my immune
response intact. My ribs resonate pain like a musical scale; deep persisting
aches in the bottom gradually moving with rib to small high pitched stabs at the top. My spleen is working hard once again. Honestly when all this is over I will nominate my
spleen as the union rep for my body. “Look, look, look at what I am doing here!
Hey, pay attention! All your blood cells are passing through me regularly. That
is only some of what I am doing, thanklessly, and without pay.” I have been
doing quite a bit of blood film morphology at work of late, a physically sedentary task so
it fits in with my capabilities. Plus I get a little excited over morphology, intermittently
distracting my male colleagues. I have found that sometimes I suffer
sympathetic spleen pain; in a CLL patient for example. Occasionally my spleen
mourns a fellow comrade with a little kick of agony if I chance upon a
Howell-Jolly body in a hyposplenic blood picture. I myself display the same
oversensitive attributes as my spleen, so I can sympathise, but after seven months
of unrelenting reminders I am ready to part with this mighty little organ.
Hopefully little organ.
And that is me for now. It hurts to breathe, but I think the
sharp pang on inhalation is muscular. Three months of awkwardly sleeping on my
PICC line arm has contributed to some wicked muscle changes, and I don’t have
the strength for pectoral exercises. Although I ought to find it because I have
heard that failing to breathe can be fatal. I have had a gum infection for seven weeks now. It is superficial, so no chance of sepsis, but unmovable and
uncomfortable. Tongue ulcers make eating a bit of a drag, my taste buds are
erratic and confusing. I am rehashing multi-syllabic words incorrectly; a fine
display of my mental capacity. I am well aware that the quality of my writing
has languished. Significantly. I am sorry about that. I am over this chemo business.
No comments:
Post a Comment
Note: only a member of this blog may post a comment.