Our lives are made up of events. Each moment in our history
has impacted who we are today, some insignificant and unknowingly and some
monumental and memorable. We never truly realize at that instance the impact
that those events will have on our future selves.
I have no idea how I ended up in the series of unfortunate events
that have plagued me through my 20’s. I stopped wondering “Why” a while ago. I
can’t figure it out, it makes no sense; and I realized the chaos in the
question was just never meant to be answered. The events of the past two weeks,
have left me withered and feeling defeated.
Monday had just started out bad. My Mom became sick and
couldn't watch Stephen so I could go to meet with the Radiation Oncologist. She sent my Dad over, which was great, but, it left me
to finish getting the girls ready for school by myself instead of being able to
rely on her to finish up. I was running late to get there. I hate being late.
I am not sure where the lines of communication get mixed up.
Different doctors interpret scans in unique ways. They type reports differently
and then there are the doctors that read the reports to their patients who analyze
the results in different ways. That leaves the patients with a small portion of
the actual results. It’s frustrating. It’s infuriating and there’s not a damned
thing you can really do about it unless you are staring at the actual scan. I
never asked for a copy of my scans, and never really had a doctor sit down and
show me what my scan looks like. That is, until Monday. Monday I sat down with
the Radiation Oncologist and he showed me the screen of my pelvic MRI. The
arrows pointed all over my pelvis to black dots. One, two, three, four, five,
six, seven, eight- I lost count. My pelvis is covered in cancer. I never
realized or was told how many lesions are in my pelvis. And just because it’s
news to me doesn't necessarily mean it is news to anyone else. It’s like
playing telephone and unfortunately I am at the last person to hear so it is a
bit garbled up by the time it reaches me. He explained that the lesions in my
upper pelvis, left to right, are small, but seem to be causing me the most
pain. As you move down my pelvis, they get larger. The ones along the bottom of
my pelvis are triple the size of the ones along the top. Apparently, in
not-so-technical radiation terms, your body is split into different sections.
You can only have one portion of your body radiated at one time. Your pelvis is
usually split into two sections. He wasn't sure if he would be able to radiate
my pelvis in one round (one round equals 10 sessions, 5 days a week for 2
weeks) or if it had to be done in two. I was to report back the following day
to have a special X-ray scan and a CT scan to measure my pelvis and then come
up with a treatment plan . . . a palliative treatment plan. Not one meant to
cure, just one meant to help improve the quality of my life.
I wasn't expecting to get a call that my sister and Dad had
called an ambulance for my Mom. She was rushed to the hospital for pretty
severe symptoms. I am pretty sure I had a mental breakdown later that day, one
of many to come over the course of the week. I was on the treadmill walking and
I looked out the window, only, I was back in the hospital. I was on the
hospital bed, just staring out the window. The doctor was sitting in a chair
across from me telling me how they found cancer all over my body. I looked at
her, in shock, and just asked “Am I going to die?” My very existence on this
planet was immediately threatened and I could no longer see my future, I couldn't
see my kids growing up, I couldn't see me growing old with my husband. I saw
black, I saw nothingness. I cried, like I have never cried before. I wasn't at
the hospital anymore; I was home, back on the treadmill and crying. My life is
still threatened. It doesn't move forward, I am stuck here, in Cancerland. I
feel like I am stuck in jail. The whole world moves on with their lives.
Friends are getting new jobs, new opportunities, finishing school; they are
buying houses, having more babies, and I am here. Just doing what I need to do
to live yet feeling like I am not getting to truly live my life. I am stuck
with the mundane activities of a terminal cancer patient. You know, just doing
what I can to improve the quality and time span of my life. I’m only 30.
Sheesh.
Then it just spirals out of control. I go back the next day for the scans and lay on this table. For. 45. Minutes.
Me. On this table. For 45 minutes. This table is flat and not cushioned- I cannot lay flat. It shoots pains in my hip down my leg. I swallow hard and
breathe heavy but the pain overwhelms me. Just when I think I cannot lay there
another second, the test is done. I don’t think the tech realized how disabled
I actually was laying there. See, I put on a good front and everyone sees it
because everyone tells me. I hear “If you didn't tell me you had cancer, I
wouldn't have known.” or “You don’t look sick” and the ever famous “But you
look great!” Well, I am not sure how a person with cancer is supposed to look?
Skinnier maybe? Not happening. Tired? I wear makeup. Groaning in pain? Not a
chance. It’s called sucking it up, and that kids is what I do best. So I try to
sit up, and I physically cannot. I make a little noise and the tech comes over
to help me. I cannot even sit up myself so here he is actually lifting me, dead-weight, to sit up and I just start screaming and crying. The pain is
unbearable. And it only got worse as I went for the other scan. I should have
brought someone with me. Augh, stupid, stubborn me. They told me they would
call me in 2-3 days with a treatment plan. I’ll officially start radiation next
week. Side effects include but are not limited to: skin irritation on the area,
vomiting, diarrhea, trouble urinating, fatigue and a couple other
fun not-gonna-mention stuff. You’re jealous, aren't you?Then it just spirals out of control. I go back the next day for the scans and lay on this table. For. 45. Minutes.
The news on my Mom wasn't looking great. Not dead bad, but like need surgery bad. So it’s up to me and my other sister to make sure my Dad has food, and their dog is taken care of, and someone visits Mom and make sure Dad doesn't go ballistic on a nurse. The stress was mounting and absolutely no one, and I mean no one could understand. Not even the closest of friends could grasp how hard life is to juggle when shit literally hits the roof. I've gotten the most slack from people over my lack of ability to returns calls and texts, to get on Facebook every minute of every day, hang out or go out. I know for a fact that each one of my friends at one point or another has gotten annoyed with me over this. So, let’s add in that to this mountain of crap and I was headed straight for a mental ward. I’m not exactly sure what everyone wants from me? I am trying my best here. I am trying to not die while raising three little kids, be a wife, a daughter, a sister, an Aunt and a friend. Contrary to popular belief, it really isn't as simple as it seems.
Remember those events I talked about? A simple comment of an
Instagram picture of mine flashed me back to my childhood. I was where I loved
to be: the softball field. Nothing else in the world can touch me, can bother, or interrupt me. It’s just me and the game. It smelled of spring, the warm sun
on my skin, my adrenaline rushing just waiting for that line drive to come
straight to my glove. It’s one of those times, however oddly inconsequential it
may appear, is one that molded me to the person I am today. The innocence of
that little girl is something I will never have back, but her sheer persistence,
ingenuity and dedication is what followed me all through these many years
later. And it was in this moment that I realized that no matter what is thrown
my way, I got it.
My Mom was released from the hospital this weekend and really needs to start taking better care of herself (MOTHER! I KNOW YOU ARE READING THIS) or she will end up back in the hospital and next time it will probably require surgery. I will figure out the next weeks of my life with the same fortitude I learned playing softball. Radiation won’t be easy but it will help me, and even though I may not be able to buy a house, have more babies and start a new business, I will be able to move around easier and not have pain while checking things off of my Mommy Bucket List. And that is pretty much all I can ask for.
My Mom was released from the hospital this weekend and really needs to start taking better care of herself (MOTHER! I KNOW YOU ARE READING THIS) or she will end up back in the hospital and next time it will probably require surgery. I will figure out the next weeks of my life with the same fortitude I learned playing softball. Radiation won’t be easy but it will help me, and even though I may not be able to buy a house, have more babies and start a new business, I will be able to move around easier and not have pain while checking things off of my Mommy Bucket List. And that is pretty much all I can ask for.
Well my dear friend, I for one have not been annoyed with you in the least! Miss you and our one-on-one communications BUT so understand that life is busy and you are trying to survive. As for what your future holds - we honestly don't know. I am just so jelly of all the crazy symptoms you may have from radiation! So much so, asking to take some on for you! I for one sit back and admire your perseverance, fight and grace! Sending prayers and love!
ReplyDeleteDear Kate, you are amazing!! You have overcome, and overcome, and overcome!! Your sheer grit inspires me. It is my privilege to pray for you, and now, your mom, also. May God strengthen you inside and enable you to do what needs to be done. God bless you, Trece
ReplyDeleteKate, I will be looking for a post in a month or so that tells of the radiation shrinking the tumors and reducing your pain. My oncologist has never looked at my scans which I find odd. She only reads the report. I guess that is how things are done. I, too, was finally able to view my scans when I had a consultation with a radiologist. Yes, radiation won't be fun. But, the result will be smaller tumors!
ReplyDelete