I Still Need This Thing.

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Blood may be thicker than water,
but you can still drown in it.

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“Can’t you see I’m busy gettin’ high?”.
Bystander Grand Theft Auto: San Andreas.

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Salted Lithium is coming back…

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I still need this thing… because I’m not sane yet. So next week, maybe this weekend, I start posting here again.

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...thanks.

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Posted in Bipolar, Bipolar Disease, Bipolar Disorder, crazy people with no pants, Lithium, Living With Depression, Living With Manic Depression, Manic Depression, Mental Health, Ottawa, Poverty | 10 Comments

Just Something Funny I Wrote While Living On My Little Brothers Couch (1993)

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“There is no fucking ice cream
in your fucking future.”
Otis Driftwood, The Devils Rejects

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this was less than two minutes of ‘manic’:

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“If we could all erase the colour of our skin we would all die because we would have none and then what would hold our stomachs in and without stomachs we would go hungry and we would be so busy trying to hold our stomachs in place that we’d all starve and nobody wants to starve so we should leave our skin alone and maybe learn to live with different skins and be thankful we aren’t hungry or that we have to walk around without them because I don’t know about you but I hate to see blood. Or we could all wear Body Glove diving suits. Maybe the neon ones so nobody would dissapear in the night and get hit by a hippie driving a semi taking his fruit to market somewhere in Montreal because if you do get hit then the hippie is late with the fruit then it goes bad in the back of his truck then he’s out of a job and then he’ll blame the government and become a radical shit disturber and shoot his foot off during terrorist shooting practice and then he’ll go on welfare and go to college as a “mature student” and become a journalist and only make $9,000 a year and he’ll be really, really bitter and nobody will like him and he won’t get laid so he’ll become a yuppie but will remain bitter and nobody likes a bitter yuppie cause all they do is whine so keep your skin on stomachs in and wear neon otherwise the fruit will go bad and nobody likes a hostile fag but if it were possible to erase your skin and not create hungry bleeding hostile yuppie whining fags with one foot I’d like mine to be the colour of my couch so I could sleep all day and not have roommates hastle me about my dirty dishes or maybe the colours of a Chia Pet so people would pour warm water on me and rub green seeds all over my body. That would be cool.”

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When I was unmedicated I used to think that the pressure that built up in me was the inspiration welling up, I would scramble for a pen and some paper and furiously write until whatever was inside me calmed down. In 1992 I even wrote about how painful it was to be in one of those states: “Sometimes I’ll be writing and I’ll feel like I have to remove my socks, so I do, but then the feeling comes back so I remove my pants and then it’s my shirt and I’ll sit there naked in front of my page, pen in hand and I’ll still feel like I must remove something else, my skin, hair, blood, veins, muscle, everything — and I realize it’s my sould screaming to get out, so I lift my pen and put it to paper. God It Hurts”. I scrawled that in red pen across the torn and crumpled remnants of the last piece of paper I had in my little room. And I hate writing in red pen.

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When I was younger I thought my disease was what gave me my inspiration, and that everything else — the suicidal thoughts, the crippling depressions — were what had to be endured in order to keep that inspiration. I wasn’t the writer, I was the instrument for the disease to speak through me. But I was wrong. The disease wasn’t my inspiration, in fact my disease had taken my inspiration hostage and was keeping it in some previously abandoned barn a hundred miles north of here where, over a period of several years, my disease turned my inspiration into its Patty Hearst. In 1994, when I ended up in a College journalism program, I was also starting to experiment with Lithium. It’s remarkably easy to find a doctor willing to prescribe Lithium, and when I started school I thought the pills would give me the focus necessary to be able to attend class and be, bascially, normal. Which was a really, really good idea. But after two weeks of classes I became convinced that the pills were making me too normal, and were actually preventing inspiration from occuring. So I tossed the pills. And, of course, I was kicked out of the program. And still I didn’t take the pills. In fact I did everything except take the pills. I moved back to my little village so I could see my doctor, I tried a light lamp… actually, that was about it. Doctor appointments, the occasional handful of Lithium, and I stared into a stunningly bright lamp twice a day for a few weeks.

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And still, even though I wasn’t writing consistantly, I remained convinced that the only way I could be a writer was to be an Unmedicated Manic Depressive. I had spent close to four years one step away from being homeless, I had completed one semester of College before being asked to leave, the two most important relationships I had been in up to that point had been blown away, I had no job, no prospects of ever having a real job, most of my friendships had imploded and, for at least six years, I had the worst fucking haircuts this world has ever seen — I had a fucking “tail” for over a year. But I had a disease which had convinced me it was the only thing I needed. That it was the only thing I would ever need. I saw the world through the prism of mental illness for a very long time. It was never the disease offering me inspiration so powerful that I felt like tearing my skin off to find it. My inspiration had been so repressed by the disease that it had to fight through the disease to find me. I’m a writer who has a crippling mental illness.

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I wrote this next thing in a moment of clarity back in 1994. I had gone a few months relatively symptom free, and I could feel the disease coming back. The upper and lower case “I/i” was done on purpose… I can sort of remember why… since all upper case meant screaming, I thought all lower case could be whispering. So this is me whispering so I wouldn’t wake up the thing I was talking about. There’s also supposed to be an air of uncertainty to the whole thing, until the middle where I’m kind of standing up, but then I give in again. I know you didn’t ask. Back then, I would have been 24, I “saw” the diseased me, or the me that exhibited the symptoms of the disease, as almost a separate person — at least I did when I was writing poetry about the disease. And, in writing, I’ve always referred to the Disease as a “he”. Anyway… I wrote this, on a typewriter, back in early 1994 while living in Ottawa — so it would have been a few months before I tried College and a few months after I wrote that piece about erasing our skin. Basically this is my proof that I knew what was wrong, but I was lacking the awareness or knowledge — or even, possibly, the desire — to break away and get myself some help… maestro, in the key of weeping angels: 

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manic whispers

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i woke up this morning
and realized i had been asleep
for so long.
i had a friend once,
and now he’s back,
and i wished he’d stayed away.
because my friend is here
inside my head
and i’m starting to think maybe
he wasn’t so friendly afterall,
because he’s telling me things i had forgotten.
i woke up and the feeling was back and it scared me.
i had forgotten you see,
forgotten what the price was
for his friendship.
i can remember his name now,
because its the same as mine.
it is good to wish
but sometimes the price is too high.
i’ve lost all my friends but one,
it only makes sense that he would be the one to keep coming back
since i’ve known him the longest
and hated him the most.
i have this recurring nightmare.
in it i’m laughing.
that’s it.
in this nightmare, and i do have it,
i laugh.
sometimes i smile.
but always i’m happy.
it’s a nightmare because
when i wake up
i wish i were still
asleep.

i had a friend once.
and now he’s back.
i hate him.
when he comes,
he brings nightmares.
in them i laugh.
sometimes i smile.

i have this recurring nightmare.
in it i laugh.
that’s it.

The days I spent with you
were lonely and cold,
the nights I lay with you
were long and colder.
So why are you back?
I invited you I know.
But why me?
I never asked for a friend like you.
I never asked to hear your voices again.
By my actions maybe.
or my inactions.
But I didn’t know.
or maybe i did.
there were times i loved you i know.
but i never meant to.
i’ve always hated you.
so why are you here?
when i had dreams, you brought nightmares.
in them i would laugh.
sometimes i would smile.
that’s it.
my friends name is the same as mine.
and he’s back in his old room
here inside my head.

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…since november fourteenth, 2006.

“You burn things when there’s no going back. How much of
yourself have you had to burn away to be
the person you are today? Because baby, my body
is ash and my mind is still smoking.”

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Posted in Art & Depression, Bipolar, Canada, crazy people with no pants, Depression, Humor, Humour, Lithium, Living With Depression, Living With Manic Depression, Manic Depression, Memories, Ottawa, Poetry, Poverty, Punk, [redacted] | 8 Comments

This One’s For St. Michael And All The Memories In The Backrow


The Main Street of my little village; February 10, 2007 – Photo by Me.

The first cut is the deepest, Baby I know —
The first cut is the deepest
‘Cause when it comes to being lucky, she’s cursed
When it comes to lovin’ me, she’s worse
But when it comes to being loved, she’s first
That’s how I know.
Cat Stevens

“…I would cry if / I had been taught how. / But I don’t /
Because I wasn’t / Although / To speak a truth /
I wouldn’t even if / I could now / That I can /
Think. / My heart doesn’t / Scream / Any more /
And for that I / Thank / Someone /
I don’t know / Anymore.”
Excerpted From A Poem I Wrote A Few Months After Mary Left (1997)

We are stunted. There are pieces of ourselves, of our minds, that are stunted. Our disease keeps us from dealing rationally with events in our lives, so those events never grow. Those events never change. They don’t evolve. We are who we are, but who we could have been is changed for as long as we remain unmedicated and untreated. I have memories that have haunted me everyday for twenty years. Since I have started treatment for my disease I have started to manage these memories. I have started to deal with my Self. And I have learned that who I am is partially based on lies told to me by my disease. Lies I have told myself for twenty years because I thought they were truths because my disease convinced me I was moving forward when in fact my forward momentum was me falling.

There have been many things missing in my life. Some things I had no control over, some things I could have taken control over but was too sick to realize. When I was a child I lived in a home with ten adults. Sometimes more, sometimes less. When I was a child I called no one mother and no one father. I grew up in a Collective, a political commune based on goodwill, then Lenin, then Stalin, then Mao and finally Insanity. For the first five years of my life my mother was sick and hospitalized more than not. My father placed my care into the Hands of The Collective because he was sick. He was mentally ill. And he was In Charge. And I became a Chore, placed on the corkboard along with grocery lists and Items to be Accomplished. But I didn’t know this. I had a bike. I had some friends. I had school. And I had to pack, often, because every six months The Collective had to move because people were watching.

Who teaches a child about life? “Give me a child when he is seven and I will show you the man.” What happens when a child has been left on his own inside a larger group of adults who are trying to create a revolution for most of his first seven years? What happens when he is eight and, when his mother is healthy enough, she escapes from the Insanity and he is taken along and away from everything he has known? What happens when, from the age of nine that child only sees his father for two hours? What happens when half of his entire biological family stays away, and the child is told horror stories about them by his relatives? What happens when you take a child, who lived in a full-to-bursting, hectic household in a small city and place him, the very next day, into an apartment in a small town 500 miles away?

What happens when none of this is explained to him? No one taught me about life. Everything I learned I learned from observation and trial and error. And that included love. Especially love. I have had people in my head since I was a teenager. Now I have some clarity afforded to me now by medications and therepy, and memories that have never been dealt with are coming back with a ferocity that takes my breath away.

I was never told about love or sex or relationships. And I never asked because those constant childhood moves, and The Final Move away from my family and friends, left me numb and insecure and embarrassed and an introvert and Clinically Depressed and by 16 I was rapidly moving into full blown Manic Depression. And then, in October, 1987, when I was 17 and a year before being diagnosed, the man my mother was going to marry, the man who had become my first substitute father, died. And right at this time, right at this time in my life, I was dating Illona. A beautiful, special, unique, fantastic girl. There are people in our lives who become memories that do not leave us. Illona is one of mine.

We had been dating for a few months and Illona surprised me on a Friday afternoon. Her parents were away and I should spend the weekend with her. So I’m freaked out, but I’m too embarrassed to say no. So I call my mom and tell her I’m leaving school to go hang out with friends for the weekend. With no clothes, no money and I don’t even have a family name for my fictional-friend to give her so I make one up and it just happens to be the name of her boyfriends cousin. So now I am terrified, freaked out, nervous and embarrassed. The bus ride to Illona’s place was an hour long.

Then we’re both naked, in the spare bedroom of her parents home, and I have no idea what’s going on because I still had never actually been in this situation before and all I can feel is my heart banging and I’m touching things I’ve never touched before and I’m wondering what the fuck am I supposed to do now and I’m just so incredibly terrified of what’s happening and I’m so damned embarrassed and I freeze. I shut down. And I roll over and I pick up my clothes, and get dressed and head for the door and I can’t say a fucking word. And the whole time she was begging me to say something to explain to her what she had done wrong and what was wrong with me… and I walked outside and I was 20miles from home in the middle of a field in the middle of the night and I was wearing a light jacket over a light shirt and it was late fall and I walked home. And I yelled at Orion the whole way. But I never said another word to her…

Since I wrote that post about Infected Memories I’ve considered that some of my memories about Illona, Melanie, Mary and a couple of others might have been blown out of proportion. And some of them, I think, have been. Specifically the memories I have about Mary. We dated for close to three years. She broke up with me because I was sick and she wasn’t a nurse, and I have the clarity necessary to respect and understand that now. Even Melanie… I know why we broke up, I know why I broke up with her. I know exactly why I broke up with her. Part of it was the disease, the first time we broke up was because I was going into the hospital because I was suicidal and needed to have my medications monitored. But there was also a lot of pressure from “others”.

Melanie and I were in love and I still believe I’m in love with her. But what’s frustrating is I’m not sure anymore if those feelings are me or remnants of the disease. We broke up because when we started dating I was eighteen and she was fifteen and my mother was sixteen when she met my biological-father, who was then about 25. Every chance my mom had, and I believe she was doing it subconsciously, she was passive aggressively pushing a wedge between Melanie and myself (I watched my mother do the same thing to my youngest brother about eight years later for similar reasons). Until, for completely irrational reasons, I broke down and told Melanie we were through. And, again, that image of Melanie asking me what the fuck she had done wrong has stayed with me for almost eighteen years.

There are other names. Other memories. Other horrors. Julie. Anji. Wendy. Lynne. Debbie. It’s like every relationship I was in before I was… not a virgin I guess… I just bailed out of right when I was either falling into love or we were getting ready to fall into bed. I know the causes of the breaks of those relationships had something to do with Clinical Depression, and possibly they were happening around when the Manic Depression was kicking in, but they had so much more to do with the Nurture role… no father; no parental sex talk; I was an introvert; an overbearing mother trying to cover over eight years of Insanity; confused family roles… but the disease never allowed me to see those reasons. The only reasons I was allowed to see were in the mirror.

When I think about Mary I feel regret at the lost opportunities. When I think about Melanie I think she was my Love. But… when I think about Illona all I see is her holding onto my arm as I tried to put my fucking shirt on. All I can see when my mind holds up Illona to me, every fucking day, is her pain in that moment.

Manic depression stunts our emotional and mental growth. We’re permanently locked in to a certain time and a certain age. It doesn’t allow us to deal with shit so the shit stays fresh for as long as we’re unmedicated. I’ve thought about Illona and Melanie and Mary and Debbie everyday for almost twenty years. And most of those times it feels like my heart wants to stop. I don’t know if I was in love with Illona. I probably should have been. There are reasons for what happened between us. For what I did to her. But there are always reasons. How much do I trivialize her pain if I list my reasons? I’m not even sure it’s a matter of pain anymore… I don’t know what this did to her, how it changed her. If she thinks about it. If she’s haunted. But I know I am. Fuck. All I want to do is beg these people to stop being in my head and that just isn’t possible yet.

While I was writing this post I had an email conversation with a friend about Illona and Debbie and Melanie and Mary. And I told her that I was trying to write this thing but I kept getting this fucking image of Illona in my mind. And if it wasn’t her it was Debbie. My friend told me to remember that I was seventeen, a confused and messed up kid. That I shouldn’t hold this kind of thing as an example of who I am or even who I was. And that’s my point. There is a normal amount of regret. We do horrible things and naturally spend the next ten years fixing them. Maybe what I did was a relatively normal, albeit horrible, part of being a young person. But the disease wouldn’t let me react rationally. This isn’t me. At least not who I think I’ve become anyway.

This is the very first time I’ve written about any of this. Anytime I’d start in the past it would end with torn paper and broken pens. I think what’s happening is this: this post and the past few weeks and months, is the pills and therepy giving me the clarity necessary to start dealing with these twenty year old and thirty year old memories. So, yeah, take the fucking pills and kill some ghosts, and understand that the disease has always lied to you and kept you from knowing who you are.

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Posted in Bipolar, crazy people with no pants, Depression, General Tao's Chicken, Health, Lithium, Living With Depression, Living With Manic Depression, Manic Depression, Memories, Ottawa, Poetry, Poverty, Publishing, Punk, [redacted] | 5 Comments

Seeing What People Never See Unless Someone They Love Films It

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“Sometimes Mommy laughs when she has her
medicine. Mommy says the medicine makes the pain
better, and makes her want to eat more.
Boy, does Mommy ever eat.”
“Mommy’s Funny Medicine”
Written By Russell & Christine Lowe,
Illustrations By Christine Lowe

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“Mommy’s Funny Medicine is the story of a girl named Heather, whose mother uses medicinal cannabis. Arguably, it is the world’s first children’s book about this subject.
Book Review, Crosstown Traffic

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“I wanna be sedated
Just put me in a wheelchair, get me on a plane
Hurry hurry hurry, before I go insane
I can’t control my fingers, I can’t control my brain
Oh no oh oh oh oh”
“Ramones; ‘I Wanna Be Sedated’, “Ramones”

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This one’s not about me, it’s about epilepsy and how my friends are dealing with the disease. My long, long-time good friend Russell and his wife Christine made a movie a few years ago… Christine has severe epilepsy and that morning she had a really bad seizure. Afterwards she asked Russell to tape the next one. A few hours later she had another major seizure. Russell, and Dave Van S. — another friend — filmed the seizure… the intention was to have graphic evidence of what a real seizure looks like, so they could show people what people like Christine go through nearly every day. So they could show how crippling epilepsy really is. Russell and Christine have become two of the more — I want to say “infamous” but I’ll say ‘known’ — medical marijuana activists in Canada. They have both been issued medical marijuana licenses from Health Canada (our federal Government) so they, along with about 1400 others, are federally recognized users of medical MaryJane. Ruddell uses marijuana for pain management. Christine uses The Reefer to control her exceptionally severe epilepsy. Since this filmed seizure, Christine’s use of medical marijuana has decreased the severity and amount of seizures from a few hundred per year to almost zero.

It’s graphic, but not abusive. It is very, very real. There is only one semi-controversial bit to this project. In the captioning Russell refers to himself as “her meat puppet”, in a nationally reported story in the Canadian “Sun” chain of newspapers the reporter screwed up and thought Russell was referring to the woman he loves as a “Meat Puppet”. The reporter then went to the Ontario Epilepsy Group and asked the spokesperson about Russell’s use of the ‘Meat Puppet’ terminology. The spokesperson was duly horrified and confused. I don’t know if a correction was published, but there should have been… you can find the article here [link is dead]. Russell has a tendency to get a little… emotional when he’s being interviewed, and gets a little flustered (justifiably so), you can find a video of Russell being interviewed regarding medical marijuana on local Ottawa television news here.

One other thing… Christine has no memory of this event, or any of her other hundreds and hundreds of seizures. And now you’re all caught up, so push play and see what Christine saw for the first time.

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Russell and Christine are both fantastic artists and wonderful people, and they have both sacrificed a lot for the things they believe in. And now, this is Russell’s tribute to the glory that is Christine.

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fucking hippies.

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Posted in Art & Depression, Artists With Depression, Bipolar, crazy people with no pants, Depression, Friends, Health, Lithium, Living With Depression, Living With Manic Depression, Manic Depression, Medical Marijuana, Ottawa, Politics, Poverty, Publishing | 23 Comments

A Perfect World Would Start With An Intervention

“Today I am off the medication and all of this is useless. I need help. My sleeping pattern is completely reversed: I am sleeping from 6am to 6pm, I never know when to take my medication anymore so I usually don’t bother… I have my rent money but cannot take a bus across town to pay the landlord… I have a cheque for the phonebill but cannot motivate to get to their office. I am a BiPolar Manic Depressive and I am off my medication, I need help.”
Gabriel [saltedlithium].
May 9, 1992, Age 22

“I am a Manic Depressive (bi-polar) and I still don’t know what that means. I know it’s supposed to be genetic, which only means I can blame somebody else for it. I know that Lithium helps, but the “Why Bother Syndrome” takes hold if I miss one dose. I really don’t like lying awake until 6am every night, sleeping until the afternoon everyday, the suicide fantasies I dream up when I’m alone, the writing I produce — yet it all lends itself to an air of mystery, an addiction to the depth of character. Do I feed off the disease or vice-versa? Why don’t I want to heal?”
Gabriel.
November, 1992.

“A depressive phase is a sign for [people with BiPolar Disease] and people around them to look at what is causing them to worry, boost emotional support and get help to get the emotional needs met. This is so obvious but is incredibly important and can’t be said enough times.”
The MindFields College Blog

“More than one in three Canadians treated in hospital for some form of mental illness are back in hospital within a year of their discharge, says a report that raises questions as to whether patients with psychiatric disorders are getting appropriate care.
About 37 per cent of people with mental illness were readmitted within a year, and that compares to just over 25 per cent that were readmitted following admission for other types of disease or conditions,” [said Ian] Joiner [manager for rehabilitation and mental health at the Canadian Institute for Health Information].”
Canadian Institute for Health Information Press Release, Nov. 29, 2006.

“Don’t let me die while I’m
living in my mothers basement.”
One Star Cop, Grand Theft Auto: San Andreas

We can spend so many years trying to convince people of how sick we are then, when we’re finally diagnosed, we’re left by the health care system to fend for ourselves as if our family and friends network was fully formed and operational, as though we have a working understanding of what the disease is doing to our minds and bodies, as though we should know and understand what the medications will do to our minds and bodies.

It’s not just Manic Depression, it’s every mental illness. Obsessive Compulsives, Panic and Phobia Disorders, Attention Deficit Disease, Bulimia, Anorexia. We spend, on average, years trying to break into the Mental Health System. The only time we’re taken seriously and pushed into “hyper-care” is if we’re chronic: a teenage girl with Anorexia slips below 90lbs and the symptoms become too extreme to not notice anymore gets placed into a special home or is hospitalized. A young man is taken over by his Manic Depression and is found with slashed wrists is hospitalized and entered into an Out-Patient Program. A young woman gives into the schizophrenic voices and hurts her children and is immediately medicated into a coma which she’s unlikely to ever be allowed to come out of.

I keep hearing and reading about “Perfect World” responses. In a perfect world someone with manic depression would have understanding parents, a group of witty friends who look and act like Emma Thompson and Hugh Grant, a doctor who is available on a moments notice, medications which work the first time exactly the way the available literature says they’re supposed to work. Well, what the fuck? What other disease, or group of diseases has to rely on a Perfect World scenario to get the patient through their initial treatment phase? And when — just when — just one fucking time has it ever happened that a person with Manic Depression has ever had a “Perfect World” scenario? Why are we, the mentally ill, left to the vaguaries of the Perfect Scenario? Why are our doctors, once THEY’VE made the diagnosis, not making sure our families are in the room so the explanation can be made by THE DOCTOR as to why we’ve been such shitty fucking children over these many years? Why are our doctors not bringing dietitians into our appointment if diet is so important to our recovery? Why are we not being handed massive amounts of Vitamin D along with our Lithium? Why, if sleep is so all fucking important to our recovery, are we not being handed a sleep aid along with our Lithium and Vitamin D? Why does it take so fucking long for people to tell us that, “yes, in fact, your bizarre sleeping patterns are, in fact, quite abnormal and, yes, in fact, there are ways to manage your sleep with medications, in fact”? Why, with a disease that fucks with OUR MINDS, is it assumed that we have an understanding of the disease on par with that of the doctor? Why is it left to us to inform family, friends, co-workers, bosses about the effects of the disease as though we had written the DSM-IV?

In the minds of the people around us, as soon as we’re diagnosed our problems are over. Parents have something they can tell friends when they’re embarrassed “Oh, don’t mind little Bobby, he’s got the manic. Yes, it was going around his class last year and he hasn’t managed to shake it yet. Apparently you treat it with salt.” All you have to do now is take the fucking pills and everything will be Norman Rockwell. As if your brain was no longer working against you which, until this very fucking morning when you had that twenty minute suicide fantasy, it was. But, hey, the doctor says everything should be fine now, right? Because that’s how it works with cancer, or diabetes, or genital warts, or the Bird Flu. You get diagnosed, the doctor says here, and you do what he says because, obviously, any right thinking person would want to get better. When you get the Bird Flu your brain, obviously, says “hey, we should get that taken care of.” When you “get” Manic Depression your brain tells you “hey, you’re worthless, lets crawl into a corner and I can show you thirty different ways you can kill yourself.” Where’s the “Perfect World” scenerio there?

There’s a program on A&E, an American television station, it’s called “Intervention” and it is the most gut wrenching, tragic program you will ever see: “Each documentary follows the lives of these addicts, taking an unflinching look at the impact of their addictions on their everyday lives, all the while the addicts are unaware that an intervention is being planned. (A&E)” These things will tear your fucking heart out. The addicts are at their very bottom, they are young women selling themselves for a bottle of whiskey, they are young men bleeding crack from their eyes. The thing is, these addicts remind me of mentally ill people* who have been fighting to get into the health care system for so long that they’ve given up… like the non-addicted mentally ill they’ve had all of the hope sucked out of their bodies, there is nothing left but the body and the drug / disease.

When the intervention happens the addicts are led into hotel rooms where a counselor and their remaining friends and family are waiting. What happens next is the amazing part… the last loved ones in the addicts life tell them about all the crap the addict had caused through their addiction, and what the bottom-line consequences are to not getting better. About 60% of the addicts agree to go to a centre where they can receive help, but it’s the hope… their eyes just open right up as they realize there are people left who care for them. And the promises the family makes, the friends make, to learn about their addiction, to attend AA, NA, AL-Anon, to read the pamphlets, you can see the addict just melting, giving in “everything, from this day forward, gets better and finally they will understand me”. So off they go to get help. And the ones who come back reunite with their families and friends… who have done nothing. Not a fucking thing. Not a pamphlet, not a meeting, nothing. There is no understanding beyond “Well, Jimmy was a raging crack addict, but now he’s fine. Sure, he’s hanging out with some of the same people, but what are you gonnna do?”

I was Clinically Depressed before I was Manically Depressed. When I was finally diagnosed in 1988/89 as having Manic Depression there were no explanations, there were no pamphlets, I walked around for years thinking I could, after forgetting for a week, just start popping the Lithium again and everything would be fine. If I missed a dose, I’d just double, triple or quadruple it up. When I tried to take control over the disease, and get back into the health care system I’d run into doctors who insisted on psychoanalysis, insisting on delving into the minutiae of my childhood, as if my Clinical Depression had any relation to my Manic Depression. These people were looking at a 20-year old kid, who had already been diagnosed with Manic Depression, who was on welfare, eating from food banks, sharing rooming houses with alcoholics, drug dealers and prostitutes and they insisted that my salvation from Mental Illness lay in my understanding of family events and breathing techniques rather than in medication and diet.

The first time anyone explained to me that Manic Depression fucked with your sleep was when I read “An Unquiet Mind” in 2000. The only book anyone in my family ever bought for me which dealt with depression was a memoir of an aged former journalist who suffered from clinical depression because he grew up gay in a community that didn’t appreciate homosexuals — even though I’ve never been gay, at that point reporting was not my profession, I’ve never been sixty and I was not raised in rural America. My mother has been to three doctor appointments with me since 1988, after each one she insists that I blame her for everything and that all of my childhood memories are suspect. After being on the pills and 99% sober for three years my family still asks me why I’m not drinking alcohol with our meal. None of my family have read any literature on depression, and my mother insists to this day that she knows all about the disease simply from having to deal with me.

To a slightly lesser degree, when I was diagnosed, I was that addict walking into his Intervention. All of those same promises, explicit and implied, were laid out for me: “We know what’s causing the shit in your life now, Gabriel. It will take hard work, and we’ll all do our part, but things will get better from here.” After surviving eighteen years with the glories of manic depression it was coincidence that finally got me into treatment: my mother was home to take my suicide call. Things are only easier in my family now because I’m not insane anymore. No more 4am suicide phone calls, no more “230lb Dark Gabriel sitting on the couch using the TV to drown out his depressions”. Now it’s “easy to get along with 238lb Light Gabriel” so everything must be better. “See,” they say, “that wasn’t so hard. Obviously you were doing something wrong before because all you had to do was take your pills.”

We fight so hard to get into that room and when we leave we’re convinced that, finally, everyone who is important to us, everyone who loves us and who we love, is going to ‘get us’, but they don’t. And that’s a crime. We need more than we’re getting, especially those right at the beginning of the process, and especially from a “mental health” system that has been leaving too much responsibility for too long in the hands of people who — for most of our diseased lives — want nothing more than to slide a fucking razor across our collective wrists.

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[*without a doubt addicts are mentally ill…]

...thanks.

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Posted in Bipolar, Bipolar Disease, Bipolar Disorder, Classic, Clinical Depression, crazy people with no pants, Health, Intervention, Living With Depression, Living With Manic Depression, Manic Depression, Mental Health, Poverty, Psychiatry | 27 Comments

America May Be The Trigger But Europe Is The Finger


This was originally published on a blog I’ve since taken down called “Fear The Seeds”.

Congress shall make no law respecting an establishment of religion, or prohibiting the free exercise thereof; or abridging the freedom of speech, or of the press; or the right of the people peaceably to assemble, and to petition the government for a redress of grievances.
First Amendment of The Constitution of The United States of America

Everyone has the following fundamental freedoms:
a) freedom of conscience and religion;
b) freedom of thought, belief, opinion and expression,
including freedom of the press and other media of communication;
c) freedom of peaceful assembly; and
d) freedom of association.

The “Fundamental Freedoms” of
The Canadian Charter of Rights And Freedoms

France is an indivisible, secular, democratic, and social Republic. It ensures the equality of all citizens before the law, without distinction as to origin, race, or religion.
It respects all beliefs.

Article 2 of The Constitution of The Republic of France

Ten years of growing nationalism and a crackdown on immigration may seem like the beginning of a trend in European politics, but really it has been the continuation of policies in place for centuries. What started out as religious persecution of one tribe of Christianity over other Christian religious groups, has evolved into secular persecution of “Other” groups, be they Hindu, Sikh or, especially, Muslim.

The Paris riots of 2005 where disaffected Muslim youth burned cars and engaged French police in minor street skirmishes, were just the latest in European religious persecution dating back to the initial religious settlement of America, and even further back into the Crusades. But modern Europe has discarded Christianity so now instead of the sects of Christianity fighting each other internally or slipping across the Mediterranean to fight against Jews and Muslims the latest conflict is being fought by Secular Europe against Islamic immigrants fleeing to Europe from wars started by the European imperialism of the 18th, 19th and 20th centuries.

Swedish International Radio recently [Fall 2006] spent half an hour discussing whether Islam poses a threat to Swedish Secularism. Nearly 4% of the population of Sweden is Muslim, which works out to approximately 300,000 people. These people are predominantly from Iran, Turkey and Bosnia and some are beginning to demand the right to practise their religion in the open, including prayer breaks at work. A Swedish mosque, one of only five in Sweden, was recently burned to the ground.

This follows two tumultuous years of clashes between the Muslim community in France and French lawmakers. France has banned religious symbols from schools, and over half of all German states now have laws banning Muslim teachers from wearing the hijab. In large parts of Germany it is also now illegal to wear Muslim head-dresses to work and prayer in public has also been banned. And now Sweden is considering a similar or greater ban, including a potential ban on Halal foods.

Forced assimilation is becoming the policy of Europe, their argument: Without secularism there cannot be democracy. None of this is new, but what is amazing in these recent discussions is, with the same breath these politicians who are setting policies calling for the forced integration of Muslims into European’s various Secular Societies, they then condemn America for having “racist” tendencies.

It’s easy to understand why the Europeans are doing this, they’ve always been xenophobic. There are not a whole lot of coloured people in Sweden, so when those populations start to grow (due to the migration of people suckered in by the advertised tolerance) and those migrants bring with them their religions and customs, Swedes get freaked. Same for Norway, Finland and so on. Now throw in the growth potential for religious militants (as they see happening in The World in general), be they Sikhs, Hindu’s or Muslims, and the Swede Freak Meter goes into the red. There are three countries on this planet who have managed to become multicultural: Canada, America and India. Japan, China, Taiwan, Singapore, Hong Kong, South Korea and the rest of South East Asia restrict immigration to the point where it just doesn’t happen, and citizenship is limited to those with long and deep roots in those countries. If you’re a recent or even third of fourth generation immigrant to Europe, Russia and Australia you’re marginalized — your religion and customs are quaint as long as they don’t grow or gain momentum, then they’re dangerous and the laws start getting passed.

But if you listen closely to what’s happening in Europe, France especially, you’ll find Secularism is finally being acknowledged as their True Religion. France’s constitution guarantees a Secular State, therefore there can be no religion. The new European Union constitution will, when it has been written, make sure no religion will have influence over the state or over the citizens of the state. This is why Catholic Poland, Italy and Spain are taking so long to ratify the constitution, these three countries may inevitably get some concessions based solely on the “historical relevancy” of Christianity, but if you’re a Sikh living in Europe and you want your kids wearing their head dresses at school you might want to start pricing overseas moving companies.

Secular States are more likely to become fascist, that’s the problem. Take France as an example. Right now it is illegal for a student in a public school to wear a religious headdress, as a penalty the child will be sent home until they’re willing to come to school without it. But what if the child refuses? Does that child get suspended? Expelled? Lose their right to a state sponsored education? How far does it have to go before that child, or their parents, is jailed? Not far at all. What if all Muslim children refuse to acknowledge the law? How long before the state ups the penalty? If there is civil disobedience, how long before the majority demand the laws and penalties be expanded beyond the classroom?

Or, conversely, if the public school version of the law is successful, how long before it’s applied to areas outside the schools? If children inside schools are so uncomfortable having religious clothing and symbols in their classrooms that laws must be passed to protect them, how long before enough people complain about religious symbols outside of school until laws are passed to protect them?

In India you are free to worship, and that freedom is protected by The State. There are some recurring tensions between specific groups, but India is quickly moving beyond the murderous strife of the past and is now allowing The State to settle disputes. To a certain extent Canada and the Americans are on the same road as Europe. In Canada and in the United States there can be no mention in Public Schools of Christianity at Christmas, the Ten Commandments cannot be posted in court houses, even though they form the basis for all of the Western legal systems. But we haven’t made Secularism our State Religion yet. What we have done, or are on the road to doing, is creating a Multicultural Society in which the dominant culture is the one least revered. But still, if an American or Canadian child wants to wear a Cross, so be it, same with a Sikh’s head wrap, a Muslim’s Hijab or the Jewish Skullcap.

It’s widely misunderstood that the American Constitution protects the State from Religion, when it’s actually the other way round. The American Constitution protects Religion from the State. When the Great Thinkers wrote the American Constitution they were remembering the religious persecution which drove them away from Europe in the first place, so they created a legal document protecting All Religions from State persecution. Here in Canada we have a document — the Charter of Rights and Freedoms — which guarantees our Right to practise any religion we wish. [aside: seeing that our country has only had a constitution and a Charter since 1982 we’re still trying to figure out exactly what all of this multiculturalism thing means…].

But those types of documents are missing in Europe. They don’t understand the persecution suffered by the Jews, Muslims, Sikh’s and the rest are running from, because for the past 1500 years it has been Europe doing the persecuting so they still see nothing wrong with a few more laws limiting the ability of these peoples to worship their Gods inside Europe.

Ultimately it seems that while America claims to be spreading democracy across the Middle East in an effort to protect itself, Europe is limiting the role of democratic freedom inside its borders in an effort to save Europeans from the rest of the world.

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...thanks.

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Posted in crazy people with no pants, Fear The Seeds, Uncategorized | 53 Comments