Waiting for another blog post…
Laura, add more pictures to the blog please..people want to
see more.....
How’s Larry?? – haven’t seen a post in awhile….
Taking a mental break is necessary. Whether you intend to or not. I will admit, I took one. I didn’t intend to, it just happened.
I set out to start
the blog to inform everyone on all things Larry Richard Matson and chronicle
his journey with colon cancer. What I
didn’t intend was for the blog to become ‘therapy’ for me. The weeks of and following my brother’s
diagnosis, I couldn’t sleep, I couldn’t eat, I could not turn my brain ‘off’
enough to relax. I tried everything with
no result. Then I discovered after I posted a blog and
put my computer to sleep, I found my mind more willing to shut off and
relax. So, I made it my nightly ritual –
come home from the hospital or from spending time with my brother, turn my
computer on, download pictures and blog. (some nights there might have been an
extra step of pouring a glass of wine-or 3)
I slowly started to sleep a couple of hours, which led to eating a
little bit more and then slowly started to venture out and have lunch or dinner
with a friend.
Then my brother recovered from his surgery, we met with the
oncologist and a chemo plan was set. He
started chemo and I started work. Again,
sleepless nights snuck up on me again, I HATED not being with him
everyday. But I had a new job with other
people depending on me and I quickly got into the routine of work. My brother made it easy on me because he
tolerated chemo so well. The day he
would go in for chemo was hard, but the days after and in between were easier –
he was working and feeling ‘normal’.
The normal routine felt good to me, it allowed me to think
of other things than the c word. It
allowed me to text my brother about other things than ‘how are you feeling
today? Did you poop? are you tired? Feel
nausesous? It felt good to Lar too.
I didn’t realize that the blog was not in my ‘normal’
routine. At first, I made the excuse
that I didn’t have time to update it and I consciously believed that. I met the initial task of informing everyone
– I updated the blog after every chemo treatment or event, but I realized that
I didn’t use it for therapy anymore. Larry
once yelled at me, “I’m not a fuck*ng charity case”. Part of that anger included this blog. If he didn’t have cancer there would be no
larrysoxcancer.blogspot.com. Although he
wanted his friends/family informed, the blog was a difficult concept for him-it
made his diagnosis real. As the blog
entries became less frequent, the more ‘normal’ he felt. My normal routine was enough to put me to
sleep, and to eat and to be social I didn’t need the blog, and neither did my
brother.
This realization came to me today. As we parked the car, walked on the pedway,
got off the elevator and entered Dr. Stein’s office for Larry’s 6th
and final chemo treatment. It ALL came
flooding back to me. We were on a
break. You know the famous Friend’s
episode when Ross and Rachel were on a break?
My brother and I (and I'm sure most of my family) were on a cancer break – a break from non-stop
cancer. I know he lives with it every
day of his life, but it was manageable, there were no variables, there was a
schedule in place, he tolerated the chemo with little effect. There were dinners, baseball games, parties,
a wedding, walks, everything that’s a part of a 'normal' life.
Twelve weeks of a reasonable break and routine.
I am so grateful for that mental break we were allowed to
take- grateful for Larry’s body tolerating the chemo so we could, grateful for
family and friends that allowed us to celebrate- the large and the small.
I am grateful for today-it made me stop, think and name this
mental break we have been on because folks, I am officially off that break and
ready to go! The break, although
unintended and unnamed for 12 weeks, has allowed me to charge up my mental
strength while we head into the next inning of the game -Larry’s cancer game.
Sitting in Dr. Stein’s office and listening to our next step
quickly snapped me out of this break and back into information gatherer,
questioner, protector and blogger! My brother has cancer dammit and I'm going to write about it.
So here is the game plan for the top of the 3rd –
Larry’s levels were good enough for him to have his 6th
chemo treatment. He will take the White
blood cell booster shot on Friday, along with the Clartin. There’s nothing new there.
In two weeks, he will go in for a CT scan that will scan his
entire body for tumors. We will then
meet with Dr. Stein the following day to go over the results.
If there are no tumors, we will go see Dr. Salti for a
surgical consult. He is the doctor that
will perform the ‘chemo bath’. That
would happen sometime between Thanksgiving and Christmas. I’ve talked about the chemo bath before- see
previous posts for an explanation.
If the scan shows tumor(s) one of two things could happen –
If the tumor can be reached with surgery than he will have
surgery to remove the tumor AND the chemo bath in one shot. If the tumor is not reachable, than he will
most likely start radiation and another round of chemo, before he goes through
the chemo bath.
Again, it all depends on the results of the CT scan. Both Dr. Stein and Dr. Salti will weigh in on
the decision for the next step. And as
always, we are very confident in any decision that those two will make.
Here are a few pictures from today. I wanted to REALLY celebrate his last
treatment and as many of you know I don’t do things small. I didn’t tell my brother that I took the day
off to join him at chemo. I wanted to
surprise him with a cake, and signs and maybe a balloon or two-but my mom said
absolutely not. I think my brother was
grateful for my mom’s decision. It was
hard enough for him to take these pictures.
Thank you to everyone for allowing us to take a mental break - sometimes you just need to...
Sox it to it Lar...
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