I had been feeling somewhat better for a while, but I’ve had an
excess amount of anxiety for the past couple of weeks. I feel like my
attention and thoughts are unfocused, like a flat stone skipping
across the surface of the water. I’ve wanted to write, but I only
seem to think of a small amount of material before my brain moves on
to something else. It shouldn’t matter how much, or how little I
post, but lately it seems my output would be a number of posts, each
only about 3 or 4 sentences long.
It’s Snow-vembrrrr
here in Southern Onterrible. On Remembrance Day, the snow started
falling, and we ended up with a little more than 10cm on the ground.
Not too much, but it broke a record for that day, and it’s early
for this part of the country. It also got pretty cold – last night
it went down to -17°C. Not as cold as other parts of the country
get, but again, colder than normal for this part of the country at
this time of the year. Had to shovel, had to clean cars, and my
washer fluid froze a bit because I hadn’t yet put the winter one
in. A good long 1.5 hour sit on the 401 on the way home can do
wonders for warming up the engine & thawing things out.
E’s had a cold for
almost 8 weeks now. The poor little guy. He can’t catch a break.
His nose has been constantly running, but luckily, no fevers. He’s
dealing with a bit of a rash or eczema on his forehead, and we also
think in his hair. It’s chemo related, and not too bad, but it’s
noticeable, and it seems to bother him because we’ll see him
scratching at it. For now, we’re treating it with a calming,
moisturizing lotion recommended to us by our RN & nurse
practitioner. He’s been so tired lately. Recently, he fell asleep
at 4:30pm, and he’s had numerous nights of going to bed at 6:30pm.
He’s had a cough for a while, but over the last several days, it’s
developed into more of a wet sounding cough. I’ve been worried
about it. I’m often worrying about pneumonia, because it is a
somewhat common occurrence in cancer patients. We took him into
clinic today, and his counts were fine, and his lungs sound clear.
The lab seemed to have misplaced his blood sample today, because it
was about 2.5 hours waiting for the results to come back. Usually
it’s about 30 – 60 minutes. My wife & I were both starting to
worry that they had found something, or there was going to be bad
news which required them to test things more in-depth. All was fine
though.
Two weeks ago, I
sprung for some steelies & winter tires for my car. I had an oil
change done as well. About a day after the oil change, I noticed a
greasy/hot metal smell coming off the engine. I was worried, but I
looked on Google & spoke to a few people who are knowledgeable
about cars, and attributed it to some spilled oil during the change.
It would burn off after a couple of days. The smell didn’t go
completely away, but it diminished significantly, so I was in the
clear. Or so I thought... Last week, while driving J to his playgroup
in north Oshawa, a few electronic things in my car started randomly
turning off. The car lurched a couple of times, and then the engine
died. I coasted to the side of the road, pulling far onto the
shoulder, and called a tow. $750 in repair bills later, I found out
that what I was smelling was my alternator frying itself. I also
needed a new battery, but the it was covered under warranty. That
made it a little less painful.
A while back, E
figured out how to undo the seatbelt in his highchair & climb
out, so meals are a bit more difficult having a 3 year old perpetual
motion machine in the house. The stroller is made by the same company
as the highchair, so if we take him anywhere, he can get out and go
on a toddler rampage. Until about 3 weeks ago, I was bringing him
with me when I went grocery shopping. No more. I don’t know how he
does it, but he can Houdini himself out of the shopping cart when the
seatbelt is on tight enough so he shouldn’t be able to move. Then
he’ll be running up & down the aisles, putting everything in
the cart, trying to run away from me, or throwing himself on the
floor in a tantrum when he doesn’t want to listen. Taking him out
to visit is no better. When it’s time to leave he’ll shriek a
glass-shattering scream, throw himself on the ground, or pull your
hair/scratch your face/headbutt when you try to pick him up. These
are probably fairly common toddler things, but they pile up.
Especially with being under chronic stress.
With the early
snow/cold, I haven’t had a chance to get my wife’s snow tires on
her car. I’m thinking about that, and wanting to get it done. It’s
probably going to be a wait now to get it in, because I haven’t
been able to in the past couple of weeks. Not enough time in the day.
We also got E’s
flu shot done today at the POGO clinic, after we found out the counts
in his bloodwork were good. I went out to a local pharmacy after we
got home, and had mine done. My wife is planning on getting hers
tomorrow, and we’ll get J done on Friday or on the weekend.
If you don’t have
a medical condition which prevents you from getting a flu shot, go
out and get one. Please. You might think that you don’t need one,
that you’re young & healthy, and can fight off germs. The flu
is a serious illness, and if you have a weapon to protect yourself
from it, you might as well use it. Plus, you’re contributing to
herd immunity to help protect the vulnerable population of people
with compromised immune systems, like my son. If you develop
immunity, you won’t catch it, and more importantly, you won’t
pass it on to someone else.
I don’t write
about it much, if at all, but work has me worried a bit lately. Not
the actual work, but potential changes down the road. Someone is
trying to impose a change management system where we’d spending
more time doing paperwork & red tape stuff than actually helping
the client. I spoke to my boss about it, he agrees with me, assures
me that it’s a ways off from being implemented, and insists
management will not let it be implemented as it is currently
proposed. It has me wondering what the point of everything is if
administrative tasks inhibit my ability to provide service to the
client. I mean, these people who approve the changes have no idea
about what they’re approving, nor do they have any idea about what
I actually do.
Our next SickKids
visit is quickly approaching. I always feel a bit on edge before
going. Whether it’s holding E, & trying to soothe him while
he’s frightened as the medical team is about to administer his
anaesthetic, waiting outside during the 5 – 10 minute procedure
that seems to take forever, or trying to calm him down when he wakes
up early. SickKids day gives you quite a bit to think about.
Halloween came &
went for another year. I don’t know what it is, but I wasn’t
feeling it this year. I love Halloween, but this year, I don’t
know. The boys had fun at least.
Things have been a
bit better for the past couple of weeks, but for a while in October,
little E was feeling a lot of nausea & had numerous vomit
sessions. He’ll tell us now “I feel sick”, or “tummy feel
yucky”, and when he says that, we can give him ondansetron for the
nausea. It’s difficult to see the nausea combined with his cough &
stuffy nose. That combination was particularly bad 3 – 4 weeks ago
when he’d start coughing to the point of making himself sick. This
would mostly occur in the middle of the night, or right about the
time we would wake up, and E would be asleep, or half-asleep. For the
most part we could tell & we’d whip him into the bathroom to
put him in the tub. It’s an awful feeling to rub your cancer
patient son’s back to try and comfort him while he brings up bile.
I had an... umm...
interesting? encounter this past weekend. I took J to his gymnastics
class. During said class, he somehow managed to knee himself in the
face, so he had a bruise under his eye. Already feeling anxious that
people are going to be thinking the worst when they see me with a
5y/o who has a bruise on his face, I took him to a doughnut shop for
a treat when the class was done. Long story short, some bible thumper
tried to recruit me into his church? cult?, and followed us out to
the car to give me his card. I’m sure he was harmless & there
was no nefarious intentions, but it was weird. No thanks.
Earlier this year,
there were some changes to E’s leukemia treatment protocol. I wrote
about it before, but it basically boils down to getting vincristine &
steroids once every twelve weeks instead of once every four weeks. I
am half-waiting for the other proverbial shoe to drop, which is the
extra year of treatment. Many hospitals are dropping the third year
of treatment for boys. Girls do ~2.5 years of treatment, boys do ~3.5
years because past studies have shown that leukemia can hide in the
testes, so they do an extra year to make sure they got it all. Now,
the thinking is that the research which supported an extra year for
boys was flawed & hospitals have been dropping the third year of
treatment. It would be good in a way that he wouldn’t be getting
more drugs that may be doing who-knows-what to him now, or setting
him up for late & long term effects down the line. We’re past
the 2.5 year mark, so if a decision is made, they could potentially
call us one day & tell us to stop the meds, E is done treatment.
There’s a whole bunch of thoughts/feelings about that: are they
correct?, why change the rules in the middle of the game?, are you
sure this won’t affect his outcome? Again, good if he has to take
less drugs. Bad because it makes me worry. This last thought might be
a bit selfish, but it would be anticlimactic. The whole
counting-down-until-the-last-chemo-dose-and-hospital-visit would be
taken away from us. Poof, you’re done. I feel like I might be a bad
person for thinking that.
We recently got the
ball rolling for E’s wish. He’ll get a wish from Make-A-Wish
Canada, we won’t have to choose between two options, because
Make-A-Wish Canada and The Children’s Wish Foundation Of Canada are
merging into a single organization: Make-A-Wish Canada. I’ll ask
him about what he wants for his wish, and he answers. 99 time out of
100 his reply is “Ummmm...dream come true”.
That’s a good
place to end it, goodnight!
No comments:
Post a Comment