In Canada, you can drink at 19.
My friends and family forgot my 19th birthday. I bought a 6 pack of Coors light and drank it alone in our basement.
When I was 23, I was in love and had been dating the girl I fell for in high school. Although she could have stayed in town for my birthday, she left the day before because she didn't want to deal with holiday traffic.
I turned 40 the winter after I had my breakdown, choosing not to die, to struggle, to suffer because I realized I couldn't hurt my mother like that. On that birthday, I ordered myself a pizza and ate it in my bedroom.
I've gotten used to my birthday falling through the cracks. It's always just after new years and it seems everyone is done with celebrating.
I tried to put it aside this year. Despite still living on disability, I baked 5 types of cookies for family and neighbors, I took my mother out for Christmas eve, and blew over $100 so she could play some slot machines. I cooked Christmas dinner for all the family. I got my mom Ancestry DNA and spent money on my sister's family for gifts.
I got a pair of socks, a $3 bottle of sugar free mint coffee sweetner (I hate mint) and a box of egg replace so I could bake for myself if I wanted. My sister thanked my mother. For cooking dinner.
Today I found out my brother will be coming to town next week, two days after my birthday, staying with my sister and won't have time to even meet for a coffee.
One thing I learned in therapy was to speak out when you feel like your needs and emotions aren't being considered by those in your life. In 2017, after over 30 years of feeling like this I told friends and family that I felt neglected and unimportant. In Jan of this year, I went to the pub downstairs because they give you a free beer on your birthday.
Its hard to get through normal days. Five days from now, it wont be a normal day and I dont know how I'm going to make it through.
#anxiety #depression #bpd #borderlinepersonalitydisorder #mentalhealth #wellness
Saturday, December 29, 2018
Tuesday, November 6, 2018
Another Day in Paradise
March 24, 2016
6:30am
I am an
introvert with isolationist tendencies and darkness is a friend that gives me
hugs whenever I need one the most. At home, I never open my curtains unless I
have to and, if I had my way I’d open the door only when the pizza deliverer
brought my latest attempt to quell my pain. I am also seldom awake at this time
of the day unless I have been awake all night. So, the fact that it’s so bright
in here at 6:30 in the morning with not a window to be found is unsettling, to
say the least. Neither my body, nor my mind are, accustomed to this and I am
struggling to make sense of my surroundings. The word that comes to mind is “antiseptic”,
which I suppose is not a negative thing, especially as far as the staff is
concerned I suppose. That said, being up so early has made me wish I could see
the sunrise this morning. At the very least, it may give me a feeling of
change, rebirth, of hope.
They took
away all of my clothes when I was admitted to the hospital. A pair of light
pants was courteously, and laughably, offered but their meager size rendered
them useless to me. So, I am wearing two hospital gowns; one with the untied
opening to the back and the other with the opening to the front, like an untied
kimono. They are far too short and I seem to be constantly threatening to flash
anyone who walks past, even when I am lying on my gurney with a blanket over
me. It’s the closest I’ve gotten to wearing the kilt I’ve wanted to try on
since I first saw a video of the highland games.
As
uncomfortable as my outfit is making me, it’s the socks which are the most
frustrating. I am not a sock person and footwear of some sort is mandatory
here. I like my feet to be cold and these things are like little ovens for my
toes, so much so that my piggies are beginning to resemble bbq pulled pork, I’m
guessing. Sure, they aren’t cheap and even have a rubberized non-slip tread
complete with happy faces but they are making me quite uncomfortable.
I’ve been
up for three hours now and since no other patients are awake, the nurse on duty
has allowed me to sit in one of the interview rooms to write this. I am very
appreciative to her for the slight rule break. It’ gives me a small sense of
normalcy, something I didn’t realize I was missing until right this second.
Sitting in an uncomfortable, cheap office chair from 30 years ago is a comfort
I never thought I’d appreciate but considering the pain I deal with every day,
I suppose I should have gotten to this point before now.
I don’t
think that most people understand the irritating and embarrassing feelings that
psoriasis sufferers deal with on a daily basis, the flakes, the crusty skin
itch and the constant pain of arthritis. From a secondary point of view, it’s
hard to ignore the blatantly obvious flakes of skin but I have to wonder how
many actually understand the embarrassment which accompanies them. Of course,
those flakes come from plaques which often cover large percentages of our
bodies turning our skin into, at the best times, an itchy hive-like scab and at
the worst of times are akin to setting our skin aflame. What’s hidden from
everyone is the arthritis which often comes with the disease, as it has with
me, and has been a literal pain in my ass since my early twenties.
Psoriatic
skin flakes get into and onto everything. It doesn’t matter how often you
vacuum, how often you change the sheets or how often you clean your entire
home, there will always be flakes you missed. As a child, the flakes that my
mother would leave on the floor, especially in my parent’s bedroom fascinated
me. I would look for the big ones, often the size of dimes, and study them.
They were light yet thick. They were almost crispy, the way they would crack in
half when I applied pressure to their outside edges. Some kids pick their scabs
and are fascinated in this way. I had an almost unending supply to make me
wonder about the way the skin worked, growing and healing. It wasn’t until my
later teens that the flakes began to show up on me. Like dandruff, it was
coming off my scalp and suddenly high school became a battle against my own
body. How many 17 year olds do you know who carried around a lint roller in
their backpacks? At choir competitions, I would lend it out before just before
we performed ensuring that I was the last to use it because if I had used it
first, by the time I got it back only a couple minutes later I would need to
use it again.
I found myself
near constantly brushing my shoulders, pulling at my shirts and letting them
pop pack to my shape in hopes of forcing the flakes to release from the fabric.
The battle of the snowy shoulders is one that you can never win, so at some
point you just accept it and do the best you can. You begin to avoid dark and
solid coloured shirts. You accept that others are going to see the flakes and
immediately judge you with rather pity or disgust. When I turned 19 and began
going to dance clubs, my friend pulled me aside one night and pointed out my
shoulders. They were alight with little star-like sparkles, my psoriasis flakes
glowing in the black light that was popular back then. I was horrified because
even in the near complete darkness of cigarette smoke filled clubs, my
shoulders were shouting “I’m a gross slob!” to anyone I would meet. Women get
stared their chests stared at and to a degree I understood how they felt
because my shoulders were getting stared at. The difference is that one
attracts members of the opposite sex while the other repulses them.
As bad as
my scalp psoriasis was, my cousin had it far worse that the same age. At twelve
years old her head was covered in a layer half an inch thick over a four to six
inch diameter area. Her early teen life was an exercise in finding equilibrium
between the pressures of burgeoning womanhood and trying desperately to not
have her entire school know her secret. She was however lucky in that it
remained only on her scalp and was able to find medication which would control
it enough to keep it at bay until her body grew out of it. I was not so lucky.
Eventually,
parts of my body other than my scalp had breakouts, especially my back,
stomach, groin and shins. I began having to tuck in my shirts or avoiding black
pants as flakes began to appear on my hips if I was wearing my shirt loose. If
I had been wearing my shirt tucked in to contain them, the minute I untucked it
a blizzard would appear and it no longer mattered what I was wearing because
there were so many flakes that I would leave a patch on the floor below me.
What had once fascinated me as a kid exploring my parents’ bedroom had become
an embarrassment so bad that I refrained from going to pools, waterslides or
the beach. I was terrified of what strangers thought of me already due to my
anxiety but now I was actively turning down invitations out with friends
because I was worried what they would think of me.
My bedroom
was becoming uncontrollably dusty. Entering it was like going in search of the
home movies of your childhood, packed away years ago. On them were the images
of a carefree childhood, now so distant that you can’t recall the emotions
which made you smile at twenty four frames per second. Replacing them was a constant
reminder that I was different, judged, and, as far as I was concerned,
unlovable. While my friends were having relationships, I was the guy sitting in
the corner longing to be them but certain that I could never be. Looking back
now I can see that women were interested in me but I couldn’t conceive of that being
real so even when women threw themselves at me, I didn’t even respond. The girl
giving me a picture of her with her phone number on the back was just being
nice. The roommate climbing into bed with me one night was just being playful,
not wanting me to stroke her body. The girl in the bar standing two inches from
me with her hand on my chest and dragging her fingers across my skin was being
strange.
I had
gotten used to the assumption that I was different than everyone else. It isn’t
that this feeling was without merit for there were times when people would
ridicule me for the strange patch of skin on my forearms or my shins. I also
didn’t blame them for feeling this way. I can easily understand how a bad
patch, or plaque, would look like a communicable disease. People with eczema or
shingles are treated in a similar, despite general knowledge of these diseases
in the public being far more prevalent. We tend to fear of what we don’t understand.
This evolved response has protected us through the millennia but I have seen it
used far too often in today’s society, to justify prejudice, bigotry and willful
ignorance. The error I made was assuming that because one percent of people
were judging me like that, so was everyone else.
One day at
work about ten years ago, while waiting on a table a child of about eight years
old pointed at the large plaque that had recently formed on my forearm and
asked me what was wrong with it. His mother immediately scolded him for being
so rude. Had I left the situation like that, the boy would have learned the
lesson that his innocent curiosity was something to be curtailed, that trying
to understand the world around him is not something to be embraced and encouraged.
Neil DeGrasse Tyson says that “We spend the first year of a child's life
teaching it to walk and talk and the rest of its life to shut up and sit down.
There’s something wrong there.”
To the
parent’s chagrin, I corrected them, getting down on my knees to be at his level
so as to minimize the trepidation on the child’s part. I softly explained that
I didn’t mind being asked and what the sore on my arm was, why he couldn’t
catch it and asked if he had any other questions about it. I find it very
important to speak to children about these types of things at their eye level
while talking to them as you would an adult. You don’t have to use big words
but there’s no point in dumbing it down either. It’s surprising how many
“mature” things you can talk to them about without upsetting or overwhelming
them. Unfortunately, the parents didn’t agree with me and lodged a complaint
for contradicting them to their child. I hope that boy learned something from
that interaction before his parents had the chance to drill it out of him.
One thing I
hadn’t counted on when the plaques first started to appear was how uncomfortable
they could be. At their best, they are best described as a slightly sensitive sunburn;
mildly itchy and painful at the same time. At worst, they are like poison ivy
rash covered in bee stings. And the things which can turn them from mild to
hellish are varied and seldom predictable. What does not affect them for 364
days will send them into a firestorm on that last day of the year. Eating a
tomato can do it. Being around a smoker. The wrong soap can set it off. A single
stressful moment at work or a bad night’s sleep. It’s virtually impossible to
nail down what single thing triggered the inflammation but it is not ambiguous
when a flare-up occurs. I have had nights where I lay in bed desperate to not
scratch, only to find myself unconsciously doing so to relieve the itch and
then discovering that my sheets and legs are covered in blood in the morning. I
once had a friend tell me that my scratching was making her uncomfortable
because I the sounds I would make as I relieved the itch were like “someone is
sucking on your dick”.
Trying over
the counter creams were a laughable attempt at stopping the plaques from
becoming so irritated often making things worse rather than being helpful. The
few topical choices which would work were by prescription only, difficult for
two reasons. Firstly, I could not afford the steroid sprays which worked the
best, over a hundred dollars for a two week supply for only my forearms and
scalp, and second because getting them would entail me paying for my medical
insurance and actually going to a doctor. I hadn’t been to a doctor since I cut
my hand after falling on and shattering a drinking glass when I was 13,
requiring emergency surgery, seventy stitches and two nights stay in the
hospital. Perhaps the only thing worse than my anxiety triggers of women was when
I was forced to deal with doctors and dentists. It didn’t matter that they were
professionals who had surely seen far worse. Opening my mouth wide or disrobing
in any manner was to be avoided at all costs, lest the other person in the room
voice their displeasure with my appearance.
As a
result, the psoriasis plaques spread over more and more of my skin, eventually
beginning to form on the backs of my hands, so long sleeve shirts no longer
covered them. The spots on my shins expanded from the tops of my feet to my
high on my thighs, wrapping around to the backs of my legs and knees, a particularly
painful and itch place to have them. They also began to show up on my face,
neck, eye lids and ears. The once small spot in my groin turned into a patch
which ram from the top of my bum crack all the way down and up again, reaching 3
inches above my genitals. The one half centimetre patch on the tip of my penis
was like the pièce de résistance. At one point in my early twenties, I had
begun a sexual relationship with a girl I had known since I was 14. She’d had a
crush on me since we were that age so I was able to accept that she would
consider a physical relationship. Unfortunately, her claim of a latex allergy
meant that our dalliances were done without protection, and the patch of
psoriasis made sex incredibly painful at times. One night it was even so
painful, as if there was an Exacto knife and a vat of battery acid in her
vagina, that I had to fake orgasm so that I could end it.
If I had
been able to keep the flakes at bay and hide the plaques under clothing I
would, at the very least, be far more comfortable going out in public but eventually
the patches began appearing on the backs of my hands, my now quite bald head
and even on my face. People had begun to stare at me, not like a man stares at
a woman in yoga pants or a dog makes eyes at a piece of pizza from across the
room. They were staring in wonder, fear and in some cases, revulsion. When I
had finally convinced Chrissy to go out with me, after years of trying, it
turned out to be a one date and gone situation. I found out through a mutual
friend a couple years later that her friends had convinced her that I wasn’t
”pretty” enough for her, confirming what I had always feared. I was being
judged by women, including the ones who were very attracted to me, the way I
had always feared except that now it wasn’t my weight or my looks. My skin and
immune system had conspired to keep me single and although it was something
that that I had always felt I deserved, to that point I had still had hope that
I could change it. That day I acquiesced. I was going to be alone. Forever.
What Goes Around
(Fall, 2013)
Last summer, as my mental illness pushed me over the edge, a defensive behavior of mine became uncontrollable and I pushed my friends out of my life at a shocking rate. I'm not saying that what they did and how I was being treated wasn't uncalled for but pretending what they had done didn't happen was, perhaps, the worst possible decision but it was also the only decision I could live with at the time. I hurt my friends greatly by doing so and after apologizing, some have forgiven me while others have completed what I tried to accomplish. I can't blame any of them for the decisions they have made. As my counselor used to say to me, "Most people are doing the best they can at any particular moment and we should remember the times when we hurt people by doing the best we could at the time."
Last summer, as my mental illness pushed me over the edge, a defensive behavior of mine became uncontrollable and I pushed my friends out of my life at a shocking rate. I'm not saying that what they did and how I was being treated wasn't uncalled for but pretending what they had done didn't happen was, perhaps, the worst possible decision but it was also the only decision I could live with at the time. I hurt my friends greatly by doing so and after apologizing, some have forgiven me while others have completed what I tried to accomplish. I can't blame any of them for the decisions they have made. As my counselor used to say to me, "Most people are doing the best they can at any particular moment and we should remember the times when we hurt people by doing the best we could at the time."
Now karma has come back to haunt me. Two of my oldest
friends, the ones I thought I could trust the most, have decided that the best
thing for our friendship right now is not to be friends and no matter how many
times I tell myself that they're doing the best they can, I still am pained a
great deal. I really didn't need an education of how much I had hurt them and
others in the past. Nights of tears and strained apologies with vicious
sobbing have scarred my heart, marking it for the rest of my life with a brand
that will always remind me of the pain I caused even after I am finally able to
forgive myself.
Five and a half years ago, a friend that I had found the
courage to tell me how some of the things I was doing had hurt her. They
weren't big things but they had bothered her and she was right to tell me but
in the mental place I was in I couldn't see how hard it had been for her to
tell me these things and instead I only saw how much it was hurting me to hear
it. I felt like I was being attacked and that she had lied to me for so long
rather than telling me the truth months before. I was self absorbed and had
been unable to see the courage it took for her to risk exposing a piece of
herself and jeopardize our friendship by bringing the conflict to the
forefront.
Today I think of a friend that has done the same to me.
After multiple occurrences of being treated like my time and emotions don't
matter and conversations about it I put my foot down and said that I thought she
needed to reexamine what her priorities were with our friendship. She replied
much like I had five years ago with my other friend, pushing me away but
throwing out another excuse like having reasons for her actions justified them.
As I look at where we are I see that I need to keep perspective and give her
the time to work through everything she's feeling. Knowing that I need to step
back isn't making it any easier to give her the space she says she needs but if
I make the mistake of pushing now I may never be able to speak to her again.
I also have another friend that trusted me with a serious
problem she was having necessitating a move out of her current living situation
right away. I did something that I would have never done in the past, throwing
my life to the side and making myself as available as she needed to help her
with the move. In the past I'd have found or created a reason to be too busy or
simply unavailable to help, avoiding actually making an effort of any kind. To
my surprise, my offer of help was returned with an accusation of having
ulterior motives and I was accused of trying to take advantage of her situation
to my advantage romantically. Despite a wordy explanation of everything
the accusations persisted and I was forced to withdraw the offer, fearful that
if I pushed her the depression she's been battling for years would do to her as
it had once done to me.
I was right to fear but too late in action to prevent her
pulling away. I don't know exactly what's going on in her mind but I only know
that I'm no longer welcome to be a part of her life and although that may
change in the future I have no control and having to allow her to step away is
rather difficult.
All I want right right now is a single friend I feel like I
can be honest with and will understand. I don't actually believe in karma
but if anyone wanted to make a case for it now might be the time because I feel
a little like the Universe is punishing me, trying to teach me a lesson that
I've already learned.
And I don't know if I'm strong enough to learn it a second
time.
Labels:
anxiety,
borderline,
bpd,
depression,
disorder,
friendship,
personality
Tuesday, October 23, 2018
A Disquiet Follows My Soul
Most days I spend 8-12 hours trying to reconcile two contradictory thoughts; that everyone in the world deserves a chance at a great, healthy, fulfilling life while I deserve to lie here and await my death. I logically know it's not logical but it doesn't make the process any easier.
Since my access to proper therapy, counseling and psychoanalysis is limited to one, 15 minute session every three months, I have to try and challenge these thoughts on a daily basis. I try to write about them and find a reason for the latter not to be true but I have failed constantly since October 1st of 2012. Six years is a long time to doubt every thought in one's brain, especially the ones which I feel I should be certain of and those I am certain are destructive despite them feeling so correct.
Once I clean my living space, finish my book, and ensure my mom is taken care of until.she passes away, I simply don't see any other reason to be here I'm i have no evidence that will ever change, or that I deserve for it to do so.
I have been single for nearly 20 years, not for lack of trying. No one depends on or needs me in a romantic way and I see no reason to think that will change in the future. Being alone, in constant mental and physical pain is draining and I find myself searching in vain to find an reason for hope that things will stay the same, rather than deteriorate, which is my current prognosis.
I long to be drunk each day, ignoring the struggle for even a little while but even if I had the means to afford that, or the destructive will, i must put my mother first which only serves to elongate my suffering, like a rubber band being pulled ever tighter. The glue of my obligation to my mother's health is the bond keeping the elastic together and when that eventually breaks, the band will snap back. I refuse to allow myself to be pulled taught like that, ever again.
Thursday, October 11, 2018
Lists.
Once, I had a bucket list of things to do before I killed myself. I accomplished them all except for the last entry.
Today, I have a new one to remind me that even during my lowest days there are things that make the future a more appealing prospect.
the list
A
make love one more time
B
watch something launch into space
C
Choose 5 people that do not know
how you feel about them, tell them, good or bad
1) Heather's brother
2) Jaime Milligan
3) Gord Haid
4) kirstie's sister
5) Bob Hunt
D
Meet at least one of
1) Trevor Linden
2) Jamie Hubbard
3) Aaron Sorkin
4) Sarah McLachlan
5) Neil Degrasse Tyson
6) Anthony Bordain
E
try and outlive mom
F
Eat a taco Omlette
G
Buy a kilt
H
Meet Nicole face to face
I
Help those I love when they need it...
J
...without sacrificing myself.
K
Possess one of the following
1) A fossil
2) a meteorite
3) aerogel
4) A Klingon bat'leth
5)
L
Bands to see live:
1) Garbage
2) Pet Shop Boys - check
M
Go see a crater, such as Berringer crater
N
Hug an otter
Today, I have a new one to remind me that even during my lowest days there are things that make the future a more appealing prospect.
the list
A
make love one more time
B
watch something launch into space
C
Choose 5 people that do not know
how you feel about them, tell them, good or bad
1) Heather's brother
2) Jaime Milligan
3) Gord Haid
4) kirstie's sister
5) Bob Hunt
D
Meet at least one of
1) Trevor Linden
2) Jamie Hubbard
3) Aaron Sorkin
4) Sarah McLachlan
5) Neil Degrasse Tyson
6) Anthony Bordain
E
try and outlive mom
F
Eat a taco Omlette
G
Buy a kilt
H
Meet Nicole face to face
I
Help those I love when they need it...
J
...without sacrificing myself.
K
Possess one of the following
1) A fossil
2) a meteorite
3) aerogel
4) A Klingon bat'leth
5)
L
Bands to see live:
1) Garbage
2) Pet Shop Boys - check
M
Go see a crater, such as Berringer crater
N
Hug an otter
Wednesday, August 22, 2018
Morning in the Loony Bin – Part two
March 23, 2016
8:30am
I don’t think there is much I wouldn’t do for a couple pieces
of bacon or a thick slice of ham right now. Despite their knowledge of my
allergies I have been served two boiled eggs and a biscuit of some sort. The
nurses can’t tell me one way or another if there are eggs in it. At least the
tea is hot. I’m hoping to scam a fellow patient of two out of their fruit cups
so I can get more than a kiddie sized box of milk for my breakfast.
The TV is tuned to the news this morning, perhaps not the
greatest choice considering the state of the world right now. The refugee
situation in Europe has brought out the worst in some people resulting in three
bombings in Brussels last night. At least 31 are dead and over a hundred are
injured. I’m hoping they change the channel soon so that I don’t have to watch
those numbers tick up, like a telethon’s tote board. They will rise. They always
do. This is the earth after all and the human ability to hate and attack each
other seems boundless.
The news is talking to people jumping to assign blame to the
refugees themselves, not even considering the possibility that it was right
wing radicals trying to make their point, and this brings to mind two thoughts.
The 9/11 attacks were perpetrated by sixteen non-refugee
men. In the fifteen subsequent years, how many attacks have been on American
soil have been carried out by Muslim extremists? One, perhaps two (what I wouldn’t
give for access to the internet right now so I could find out for sure) and
neither of those were carried out by refugees. Instead, it was men and women
living in the country by completely legal means.
I am trying to focus on something of consequence rather than
the minutiae of life but my brain has other ideas. Did the Canucks win last
night? #teamtank My blood pressure was way down this morning. 131/81 is almost
normal and far less terrifying than the artery bursting 171/104 reading that I
got last night while being admitted. It makes me wonder what meds they gave me
last night. While my heart beats are better, I have heart burn. I really do
need more than milk. Dry toast is even appealing at this point.
I know I had a second point to make about the bombings but
it has left my mind. My brain is often like this and it’s why Dr Jahmeel tried
me on Ritalin when I first got my depression diagnosis. Even as a small child,
I remember my mind being four or five steps ahead of where I was. Every possibility
opened before me like a branching tree, reaching skyward for the sun. Early in
grade school, this meant that I was not only ahead of where the class was in
whatever lesson we were doing, I was often ahead of the teacher. When we were
doing addition, I could already see how subtraction worked. I was reading at t
third or fourth grade level while the concept of “sun”, “fun”, and “bun”
rhyming was just becoming apparent to the rest of the class.
This skill had its advantages but, while I didn’t know it at
the time, it had far more disadvantages. I was so far ahead in my assignments
that I was often extremely bored and would get myself in trouble while trying
to occupy my mind. I often found something in my bag to surreptitiously damage
my desk, just to see what was under the next layer of fake wood. I got good at
it. In the third grade, I drilled a hole into the front edge of my desk that
was deep enough to fit an entire crayon in it, lengthwise. My chairs were a
monument to scratching with makeshift shivs and extreme boredom. It’s hard to
convince an 8 year old to do the lessons being assigned when he’s read six chapters
ahead in the textbook and could teach the class if necessary, so the habit of
not bothering with homework was well established, following me into high school.
It was never that I was lazy but rather I was quite bored with most of school
and what few topics and subjects which interested me never challenged me in any
way. I really don’t like this about myself and it is something I have fought
against nearly constantly since my diagnoses.
It is why going back to school and getting my high school
diploma meant so much to me. It was the first time in decades then I had set a
goal and followed through on it. It’s also why writing down these thoughts are
important to me right now. I don’t know if they’ll be useful in the future but,
at least for now, they are something I’m working on which has no specific
purpose and is also a means to try and slow my mind down. Right now, in this
place it doesn’t seem to be working.
My bed is in a specified area, my very own five by five
space, separated from the person on my right by a curtain and a wall to my
left. Halfway up the wall are stains in the paint looking suspiciously like a splatter
of some bodily fluid. There are five or six of these of these spaces in a row,
making privacy flexible and important but a complete illusion at the same time.
However intrinsic and flawed the uncomfortableness of this situation is to me,
I am one of the lucky ones. Just outside this are three gurneys lined up along
the wall with no privacy whatsoever. I wonder if I get a curtain because I am
not likely to need emergent care or if it’s because I just happened to get here
first. There are also patients to whom a bed is an unattainable luxury for they
await a better situation sitting in a hospital style recliner chair. About a
half a dozen people have been in those all night. For them, I’m sure a
goodnight’s sleep must have been a fantasy, unless of course the nurses were
able to knock them out with a cocktail of meds. The only one I’m sure slept
well in those chairs is the young man with the mark on his face. He seems to
have been comfortably asleep throughout the night, his hat pulled over his eyes
as a shade from the pulsating fluorescent lights above that I doubt are ever
turned off.
There is one thing about the curtain beside me that I have
not mentioned. I have been reluctant to do so for it is a reminder of why I’m
here, more than the bed situation, or the bracelet on my right wrist. I could
have easily deluded myself, created a delusion as to why those things are
present. The curtain is of a cheap artificial fabric of some source, although I
doubt it’s nylon as it has a tendency to go up in flames like a flamethrower.
It must be thirty or forty years old, perhaps even the surplus from Super 8
motels from across North America bathrooms. I am in a section of the hospital
where clean, new and soothing is not a concern because those states are reached
through the use of Thorazine, Xanax and Valium. I am not meant to be
comfortable. I am meant to be alive.
The nurse has taken pity on my empty stomach and found me a
fruit cup and grabbed me a tea from her private stash. I don’t have the heart
to tell her that I wish it was decaf. It
makes me feel completely uncomfortable because I feel like I’m getting special treatment
as it is so to but in a special request is completely out of the question.
The mental image of me being on a fat camp reality TV show
has jumped into my brain. I feel like I’m getting ready to do my
last-chance-workout, all the contestants sleeping in the same room but I won my
bed and curtain space in this week’s reward challenge. The state of curtain
betrays that thought.
As I turn and lean on my left shoulder to hide these
thoughts, I am faced by the discoloured wall. Twisting to keep my legs on the
bed I am face to face with the one foot square section of wall which is now
clearly a stain from arterial spray. I am currently both glad and upset at
having seen so many episodes of CSI over the years. I can falsely speculate on
speed and directionality based on the size and shape of the droplets. I think I
can discern a void in the stain, as if there used to be something in the way; a
person perhaps.
This is the beginning of page twelve in my notebook, which
means I’ve written more in the last 16 hours than I have in a very long time,
perhaps ever. Doing it curled up on a hospital gurney is very uncomfortable and
my back is beginning to get sore. I only hope that, if not today, it helps me
at some point. Otherwise, I’m just spinning my wheels again, distracted by my
seething mind, destined to end up in the same place I began.
Friday, August 17, 2018
Morning in the Loony Bin - part one
March 23, 2016
7:30am
Morning has come, far too early for my liking. While snoring
is rampant here, my little corner is full of people very much awake and yet
somehow making less noise than those sleeping. In the hall are two people
sleeping on the thinly mattressed gurneys they put you on in here. Presumably,
mobility can become unexpectedly important, even in the psych ward. I'm curious
if there are leather straps stowed under these but I'm just too nervous about
the truth to try and find out. The small size could explain why I am curled
into a ball, hugging my chest, trying to keep my bulky front from spilling over
the side of the gurney. It's more likely that my extreme mental discomfort has
me craving the fetal position. It also explains why my back and hip are killing
me, although not literally. A large, vocal part of me is sad about that
literally thing.
Close to me is a new recruit to our little encampment.
Sitting up, he is talking to himself, embodying the lostness I feel inside. He
is mumbling in Punjab or Farsi, I can't tell the difference. His face is frozen
in a mask of concentration, as if spending all his energy trying to comprehend
what is happening to him. In this matter he is a kindred spirit and I feel a
little less alone.
Two curtains over is a young girl talking in her sleep. Her
words alternate between those expressing terror and bliss, like a scene from
Fifty Shades of Grey, unable even in her sleep to escape whatever it is that
put her in this place. Before I had realized she was asleep, I found myself wondering
if she was masturbating but although I am quite sure that is not uncommon thing
to happen here, I am now leaning to her being a scared little girl trapped in a
no longer naive young woman's body. She's in pain, likely both physical and
mental, her dreams desperate to understand anything that is going on, whether
that be out here or in her mind. I doubt her perception of reality can tell the
difference anymore. After all, they are both prisons.
I haven't eaten in over 14 hours, getting down only water
and extremely unconcentrated orange juice. I don't find myself overly hungry
but the bottle of Ensure I was offered a couple of hours ago is beginning to
sound appealing, despite my distaste for them. I know a headache from not
eating will be coming on soon, along with the stress and mindlessness which
will accompany it. I am the person in the Snickers candy bar commercial who is
"not himself" when he's hangry.
Mindlessness. In a world that seems to be pushing the
concept of mindfulness on everyone, the idea of existing in an exact opposite
manner sounds appealing right now. It is the premise behind self-medication,
which I have done many times. The tears live just below the surface, held back
now only by the paper I am writing on. They are a pressure bomb in my chest and
I'm terrified of looking weak in here. I'm terrified of the meds the nurse will
give me. I'm terrified of the others here seeing me as a target. I'm terrified
of having to acknowledge that right now, this is where I belong.
~
The Ensure is like a mouthful of Buckley's Mixture cough
syrup mixed with a pound of chalk dust. Buckley's was my mother's go to cough
treatment and I half suspected that it's terrible flavour was her way of
determining if we were truly sick and deserving of a day off from school. Over
the years I had learned to tolerate it, even looking forward to the soothing
feel of it running down my throat. I find it exceedingly doubtful that I should
ever expect to get to the point of respect with Ensure like I am with
Buckley's.
"What am I going to do now?" has popped into my
mind and the tears I have been holding back are moistening the pillow beneath
my head. I am reminded of the scene from Terminator 2, when right before
leaving the group to kill the engineer Dyson, Sarah Connors carved the words
"No future" into the top of the picnic table where she had been
sleeping. I am that lost as to what will become of me. Do I have a future? What
niche will I fill in the world if I even find an opportunity for another chance
and a new direction? People have told me to be like Dory, the fish Ellen
DeGeneres voiced in Finding Nemo. "Just keep swimming" they would
tell me but keep swimming in what? If you drop a fish into a vat of Sulfuric
acid should it just keep swimming or is it logical for it to panic? Where can
it go? Even if it ends up in plain water, what would swimming accomplish? Is a
life of simply being enough? Existence for the sake of existence? Without a
destination, there is no journey to learn from unless you account for a final
destination.
It's hardly a new idea or question. Is life's journey
towards death a sufficient reason for continuing life? Is life for its own sake
reason enough to keep moving from one moment to the next? While I don't have an
answer for that question it is something worthy of further exploration.
As a bit of a hobby, I dabble in religious
counter-apologetics; the examination and refutation of religious reasoning and
justifications of believers' views. There is a concept within this sphere of
study which deals with the sufficient and necessary. Specifically, is the
concept of a god sufficient to account, not only for the universe we
experience, but the entire universe we could ever experience? Can god
completely explain the 5% of matter and energy we have an understanding of as
well as the other 95% which we know is there but have virtually no
understanding of, AND any materialistic or non-materialistic reality of which
we may have no concept, imagination or ability to experience.
Further, it must also be shown that god is a necessity, that
there is and could never be any other proposition which would account for
existence. If anyone can propose a logically and rational concept which would
account for our local presentation of the universe, then the idea of necessity
is immediately falsified.
While I have opinions on these questions, I have neither the
intelligence nor the education to take them on when dealing with the
massiveness of our universe, let alone the possibility of the multiverse which
has popped out of current attempts at super-unification. I can, however, apply
these ideas to the question, "Do I have an obligation to live? “As I am an
experimental materialist, I have no belief in a god, an afterlife or an
immortal soul so the question of necessity can only apply to the universe I can
experience and account for. To whom or what would a necessity of life be
related to? When it comes to the nonliving world, it couldn't care less if I
was alive. Further, when my eventual end comes, microbes and insects will
likely be very glad to fulfill their destiny and consume my non-animated flesh.
When considering the living world, I have no pets, no children, and no
dependents of any kind. I hold no financial obligation to anyone. No one will
end up on the street starving if I cease to be.
The emotional stability of those in my life, as far as I can
see, is the only consideration which may satisfy necessity. I have few close
friends, most of whom struggle with these same thoughts. Those who do not
understand from experience have done well to understand by talking to me and
have come to accept how hard my struggle has been. So, if my life were to end,
by any means, it is safe to say that my friends would be able to move on with
an understanding, and while it would in no way completely relieve the resulting
emotions, they would be minimized with the knowledge that I had likely
struggled as much as I possibly could. Their lives would move on without me.
Obviously my family adds another level of thought which must
be considered. My brother and sister have attempted to help me in the best way
they can. Both of them being in the medical field give them an uncommon
perspective on how my thoughts work and I have been very lucky to have them
around. My Nephew has struggled with depression as well, including stints on anti-depressants
over the years. My nieces are teens and have been brought up in the social
media age where open discussion of topics once taboo are now commonplace. LGBTQ
rights are a comfortable topic for them. So is personal sexual responsibility.
Mental health is also a topic of which they are well versed and although I'm
sure they want the best for me, they understand that the best for me may be
ending my life someday.
My mother is, perhaps, the only trump card which I have to
deal with. We have lived together since my first collapse in late 2012 and it
has become obvious that she is uncomfortable with my illnesses in every way.
She wants to listen, to be the one I can talk to but it is awkward and
distressing for her, so I try to keep it to a minimum such as when things
directly affect her or our relationship. I suspect that the anxiety issues hit
far too close to home and that she's been dealing with many of the same
relationship problems and thoughts as I do throughout her life. It just hasn't
been acceptable acknowledge them personally, let alone discus them with others,
until very recently. I'm guessing that watching so many people discuss so many
personal issues without shame is off-putting, to say the least. While it is the
one final thing that saved my life, is it necessary to remain alive because of
the emotional turmoil that my suicide would cause to my mother.
I know she would do almost anything to want my suffering to
end but does that list include accepting my death. I simply don't know.
Subscribe to:
Posts (Atom)