Existence versus Life

As I write this, my mind and heart is a jumble of myriad tangled feelings, thoughts, memories, and pain – each competing with the other and yet co-existing and draining my strength as they fight their constant battle. This battle? This war? This is grief. This is love when arms can no longer hold the loved one.

Less than 48 hours ago, my brother Ben passed away from septic shock combined with pneumonia that he developed from an infection in a tube-site for his gall bladder. The tube was initially inserted in February 2017 and his surgeon hesitated to remove both it and the gall bladder for fear of him experiencing a coronary on the table. He had atherosclerosis (with a total of 3 stents in various heart arteries, for which he was taking a blood-thinner since the last heart attack on February 14, 2019.)  He also had insulin-dependent diabetes, chronic obstructive pulmonary disease, nephrolithiasis, and chronic renal failure, and he was on dialysis three times a week.

In fact, that’s how I found out that he was in trouble. His dialysis nurse called me and said he didn’t show up for his Monday morning appointment. After trying to reach him, thinking he had overslept, I called a relative and asked them to go check to see if he was at home. His car was, but he didn’t answer. After that, I called 911 who patched me through to the RCMP. They went to his house, saw him awake on his bed through his (main floor) bedroom window, and he was unable to get up. They broke the door down and called the EMT people. That would have been around 3 pm or so. The EMTs came and got an IV started. They took him to the local hospital who assessed him and intubated him as he was having difficulty breathing. Then they ambulanced him to the hospital where he normally did his dialysis. They got him there around 7 p.m.  Three hours after he got there, he took a turn for the worse, and went into septic shock. The nurse called me and asked me or someone to come to the hospital right now. They tried to revive him three times but to no avail. At 10:15 pm, he was pronounced dead.

And that is what the doctor told me ten minutes later, over the phone, as I was getting my coat on to make the two-and-a-half-hour trip to see him. Such pain I had not felt in over six years since my youngest daughter died at the age of 21.

My night-time trip was cancelled, of course. I made plans to pack up the next day, and go to the homestead to assess the damage and the mess. I might have slept four hours that night. The next night, with the help of some Melatonin, I slept for six hours, although there was one interruption at five a.m. when Ben’s alarms went off to remind him to get up for dialysis. Hopefully, tonight will be better.

During my waking hours, I have been doing a lot of thinking about the difference between existing and living. For most of his life, Ben just existed. He grew up thinking that he was a nuisance to his parents. He bore the inner scars of physical and psychological abuse by his mom and abandonment by his dad who never stopped her, and the bruises of an older brother who criticized everything he did and regularly pounded on him. He bore other scars too: a marriage that lasted only 14 years before it ended in divorce, alienation from his sons, rejection from an endless string of women, as well as being used by women who befriended him only for his bank account. His was a lonely life. He battled the loneliness with his art: he could draw landscapes, animals, and people just by looking at pictures of things. He composed so many songs and sang them with me and with that older brother when we were all so young (I was 16 at the time, so he was 22 and the other brother was 26) – gospel songs that were so beautiful you could hear a pin drop when we were done.

Yet he suffered. I remember him coming home from senior high school and sobbing as he begged me never EVER to judge a man just on his appearance. I never EVER forgot his words. 

Yes, most of his life he was a melancholy man. He existed; he created beautiful things and appreciated beauty in nature and in people, but his existence was spent waiting for the next good thing to happen, and being disappointed time after time after time. 

After his divorce in the early 1990s, he moved in with Mom and Dad. He was there for Mom after Dad passed away, and he made sure he was there to look after things for her. Others would come in and see him lazing around, as they called it. He rested because he couldn’t breathe if he got up and moved around. He had so many ailments: his lungs, his kidneys, his heart, his gall bladder, his pancreas,… people didn’t understand and he felt a lot of condemnation come from them. Nobody understood him, he told me, except me. And sometimes even that wasn’t enough to tame the monsters of hatred and bullying that he experienced – whether real or imagined – from others.

Once, he even tried to commit suicide. He had finally learned how to love unconditionally, and his girlfriend stole from him and used the money to get high. 

A few months later that girl died … and it took him months to make peace with that.

Photo "Eye" by graur codrin at www.freedigitalphotos.net

But by that time, he had learned to live. To REALLY LIVE.

You see, in October 2016, Ben had been diagnosed with stage one colon cancer. And in January 2017, he underwent a six-hour procedure to remove the cancer along with a 5-inch section of bowel. And when he woke from that surgery, while he was still recovering in the hospital, he was listening to the radio and a singer Skip Ewing was singing, “How can he be a king? He’s just a kid.” And God spoke to him in his heart, and said, “Are you listening, son?”  And he responded, tears streaming down his face, “Yes, Father. I’m here. I hear You.”

From that moment on, Ben started to really LIVE. He had some setbacks and some heartaches (like the death of that girlfriend). And he was living on a very limited income, never knowing if he would need to starve in order to be warm, or to freeze in order to eat. It was hard. It was REALLY hard. But he was finally LIVING. We would talk on the phone – and I would let him listen to music that he liked – and he would cry tears of beauty and joy. He never forgot how God rescued him, miraculously let him live, and would look after his every need. Even if he misplaced his car keys. Or his needles. Or his wallet.

Last year, on Valentine’s Day 2019, he suffered a major heart attack. The paramedics found him and the emergency team had to put an intravenous shunt through his shin bone to give him liquids. He screamed in pain and then his heart went into atrial fibrillation. They had to use the paddles to get him back – and he was “gone” for a few seconds there.

He remembered those few seconds. He felt completely at peace. He couldn’t see anything, but he knew that he was loved, cared for, and safe. And from that time onward, he lost his fear of death. He lost his fear of living, too. And the living he had been doing up until then just intensified. He could not keep silent about God’s love for him. Anyone who knew him heard him talk about higher things, spiritual things, wonderful things like love and joy and peace and goodness. He touched so many people that way: people in dialysis, people in drug stores, people at church, in grocery store lineups, everywhere.

That’s not to say that he didn’t have questions. We would talk for hours at a time as he tried to understand some spiritual concept or other. We talked almost every day, for up to two or three hours at a time. (It’s a good thing I have such a good cell phone plan that includes free long distance!) But every time we talked, he would not hesitate to tell me what he had been learning, what God showed him or how He helped him find something he needed. Or met a need in his finances. Or let him talk to someone about his experiences in the Lord.

And now this week, I have been living in his house without him here. Memories galore. Yet it feels so surreal: not quite right, like he should be here laughing and joking with us, listening to YouTube videos, or talking about how wonderful Heaven is.

And yes, he could not let a conversation go by before he mentioned how deeply he longed to see his Master’s face, to walk the shores of Glory with Him, to hug Dad, and to jam with friends and family gone ahead.

And now he is there. And he is LIVING beyond his wildest imaginings – and he could imagine a LOT!!

Good night Ben. See you in the Morning. Keep a chair for me by the hearth, and say hi to Dad for me. I love you beyond measure. 

And … I will miss you. I’ll never forget what you taught me about how to live life in a positive way and not just exist expecting the worst.

Thank you. Thank you SO MUCH.

Part of your world

I've been taking some well-deserved time off from my studies to rest, reflect, and recharge. As I ponder the various facets of my life, I find myself thinking about the people in my life and what they mean to me. I try to put myself in their shoes to empathize better with them, and when I got to my mother, I found something quite distressful.

My mom's life sucks.

She has dementia. All of her life, she always looked at folks with dementia and told us, "If I ever get like that, take me out in the field and shoot me." And now she has dementia. And she is watched, twenty-four hours a day, seven days a week. And she is medicated if she gets unruly. And she feels like she is alone: even though people come to see her on a regular basis, she doesn't remember that. She only remembers the last fifteen seconds.

Image "Crying Old Lady" by
imagerymajestic at
www.freedigitalphotos.net

If ever anyone lived in the moment, it is a person with dementia. However, feelings - even if someone doesn't remember the reasons behind them - remain. The feelings affect mood, and can make a person with dementia profoundly depressed. Or anxious. Or angry.

And what makes the feelings? Thoughts lead to feelings, even though the thoughts are no longer remembered. And words - whether spoken by the person or by those around them - create the thoughts. Combined with core beliefs about oneself - things one tells the self through decades of habit - a person who has dementia cannot reason themselves out of those feelings. Reasoning is useless. For someone (like my mom) who has prefronto-temporal dementia, the ability to reason and to make decisions and carry them out is absolutely GONE.  All that is left is the lizard-brain ... the limbic system ... the one that lives totally in the present, that is influenced by words and thoughts but that doesn't remember them; it just feels what it feels. 

So for those who think that it doesn't matter what they say when they visit a dementia patient because "they won't remember what i say anyway", think again. Their MIND may not remember, but their FEELINGS remember. So trying to convince them of the rightness of something about which they have believed all their life is wrong will serve only to frustrate and upset them without knowing why. And after the visitor leaves, it is the staff who have to deal with the fallout: the patient becomes agitated, distressed, depressed, anxious, or whatever, and needs to be medicated more just to make them "manageable." 

So - dear readers - leave your arguments and your opinions home when you visit a person who has dementia. Learn to enter their world - the world of the continual present - and even when they bring up your pet topic, refrain from discussing it. Distract the person toward the positive (not YOUR idea of positive, but THEIRS). If that means lying to them and telling them that it won't be long before they will be going home, then do that rather than tell them that they're going to a nursing home.  To many, including my mom, a nursing home is a horrible, torturous place where people go to be forgotten and to die alone. You can't convince her otherwise; it's too deeply ingrained. Don't even try. 

Phone them. Talk to them, let THEM talk. If you can't physically be there, phone them, send them cards and letters (happy ones!) and little gifts.  Do it often. The hospital / nursing home can be a lonely place. Don't forget them.

If you can be there, then BE there for THEM.  Play cards or board games with them. Watch TV with them. Encourage them, compliment them in every way possible. They are no longer part of your world; accept that. Be part of their world. Enter THEIR reality, the reality of seconds. Not days, not hours, not even minutes, but seconds. Leave your preconceptions and your grief at what they have already lost, and what you have lost with it, at the door. You are there for that person, not for yourself. You are not there to talk anyone else down or to win any arguments.  You are there to brighten their outlook. You are there to make it easier for that person (and for the staff who look after that person) to live a little more pleasantly. 

That is the way you visit those who are infirm, who live inside the prison of their own mind. Don't judge them. Don't judge those they love. Talk only of pleasant things, things that are pleasant for THEM.

Just be there for them, whether in person or not. Just BE.

The View from Behind the Mask

I don't know if it's that people are just tired of winter and want something to pick them up emotionally, or whether they are wearing less bulky clothing on some days and are wanting to celebrate, but lately I have been wearing my mask a lot more. Those of you who follow my blog know that I have multiple chemical sensitivities (MCS) and that my sensitivities (not allergies: worse) are to the kinds of petrochemicals that exist in all sorts of scented products from shampoo to antiperspirant to laundry detergent to room deodorizers. I could go on and on about what scent is, and repeat myself (ad nauseum) that it's not the "smell" but the "chemical" that I am sensitive to ... but I'll spare you that rant today.

Today, I am just pondering and interpreting the looks I have been receiving just because I refuse to be made sick any more by the invisible clouds left behind by people who have no clue of the havoc their cleaning / cleansing / moisturizing products cause. 

For example, I went to a meeting yesterday with a bunch of people, most of whom respect the scent-free policy at work.  Then this one person walked in and sat across from me.  Within seconds, the tissues in my eyes started to swell up, I started to get a headache and lose concentration, and I would have had disorientation and memory loss if things had continued. So, I reached into my pocket and pulled out my trusty mask and put it on, fitting the upper metal band to the bridge of my nose. I had to sit for the entire meeting (over 30 minutes) breathing through this thing, which filtered most (but not all) of the chemical out. It was rather amusing (but not really) when I saw the looks on people's faces. 

My manager was there, and since she and I had talked about this problem before, she just minded her own business.  But others were rather unprepared and most averted their eyes, as if I had some sort of big zit on my face and people were too polite to point it out.  A couple of people were shocked; however, nobody said a word or asked me why.  The lady whose chemicals had made it necessary for me to use the mask did not offer to move, but looked decidedly uncomfortable. But instead of leaving to go to my desk and phone into the teleconference, I persisted in this overt display of self-care, and at the first opportunity to leave after the meeting was done, I left. Once across the hall, I could remove the mask and all was well. Well, sort of.  I was "off" - feeling not quite myself - for the rest of the day, so much so that one of my team members told me four hours later that I looked like I wasn't feeling well. (Sighh.)

Image "Female Doctor Wearing Surgical Mask"
courtesy of stockimages at
www.freedigitalphotos.net

The mask is a stop-gap measure until I can leave whatever situation is causing me distress. It is not a perfect solution.  A perfect solution would be for people to educate themselves about fragrance-free options ... but I digress.

I thought about people's perceptions to my mask again this morning as I sat in a walk-in clinic waiting room, waiting to have some blood work done.  Someone was in the lineup with me who was "using product" as I call it, leaving behind pockets of scent. Out came the mask.  Once I had my turn and sat down, every patient who came around the corner into the waiting room saw me wearing the mask.  The reactions were anything from alarm (she has H1N1 or something), to pity, to double-takes and then confusion when I turned out to NOT be Asian. (Where I live, many Asians wear masks in public to protect themselves from others' germs.)  The best reaction, though, was from a little girl.  She was perhaps 5 years old, and came in with her mother, standing in line beside her to see the receptionist.  She caught sight of me, and stared at my face, unashamed, curious, with a questioning look on her face.  I met her gaze and smiled under my mask, and she could see my eyes crinkle.  She relaxed, gave a little half-smile back to me, and amused herself with other things.  

She could see the humanity behind the mask.  Many others could not.  If we had been alone, with nobody else around, she probably would have asked me why I was wearing a mask.  I don't mind that question; I welcome it.  What bothers me is the fear and the ignorance combined with suspicion and sometimes even disgust. That is uncomfortable for me (and no doubt for others too!) 

I wish I could tell or show people what it is like to have MCS.  I don't like having to wear my mask.  I don't like being a public spectacle.  I don't like the moist, sweaty feeling inside the mask when I am forced to wear it just to be able to breathe without getting sick.  But I like being sick even less.  And maybe, someday, that mask will open a discussion with someone who will finally understand how debilitating this disease is and who will be motivated to do whatever is necessary to allow me to NOT wear it. 

I have been given a lot of advice about this illness. Go to this naturopath. Take that allergy medication.  Allergy medications do no good; in fact, they open my nasal passages so that more toxin enters my bloodstream and causes neurological symptoms (headache / migraine, brain fog, disorientation, dizziness, muscle weakness, even an inability to speak more than a couple of words at a time, etc.)  And while I understand that naturopathic doctors can help, I am taking a supplement, prescribed by a specialist, that acts as a bounty hunter in my bloodstream, taking those free radicals captive and delivering them to my bladder to be eliminated.  The only problem is, they keep getting put into my bloodstream by those chemicals people use to make themselves (or their clothes or their houses) smell good or to keep themselves from smelling bad.  And it's not like there aren't fragrance-free options out there.  (Hint: choose "fragrance free" and NOT "unscented." It's not the "smell", it's the CHEMICAL. Plus, not everything that says it is "pure" is fragrance-free. Just saying.)

The view from behind the mask sucks, really.  I would love nothing better than to be rid of the need to wear it.  However, I know people who are way worse off than I am, people whose symptoms are far more severe than mine, who suffer from MCS.  If my mask helps to raise awareness so that even one person refrains from wearing or using chemically-scented products, then I'll wear it ... because it will have all been worth it.

The right to take up space

Some time ago, I was watching a comedian on television do his routine.  Comedians are sometimes the only people who can get away with telling truth because they tell it in a funny way (they hope). This comedian's name was Greg Rogell, and the line I remember most is when he started talking about golf and golf caddies. "Golf is the only sport that comes with a slave." He then started to demonstrate. He held his microphone like it was a golf club, made the classic golf swing with it, and then dropped the mike on the floor and walked away.

While that was funny, Mr. Rogell was also highlighting an attitude that exists not only in golf, but in everyday life.  Some people, for reasons that still mystify me, have a really hard time with the simple concepts of saying Please and Thank you.  If someone puts themselves out to help them, especially if that putting out is physically or psychologically hard for them, you'd think that "thank you" might be on the list of things to say.  Treating people with courtesy, respecting their personhood, would seem to be a basic skill.

But no. Instead, such people are more likely to find fault with something else that same person is NOT doing, but which they never said they expected. Since different people have different priorities, it is impossible to read minds; expectations need to be stated at the outset, even if it might seem like a no-brainer.  For example, I'm more of a sit-and-visit kind of person; the housework can wait.  For others, housework is this huge thing and they can't sit and visit until it's out of the way. So my sitting and visiting is like laziness to them, perhaps even inconsideration. Yet their refusal to sit and visit until the housework is done tells me that things and appearances are more important to them than friendship and spending time with people. Dishes don't have feelings. People do.  

And yet, who is it that apologizes when the topic comes up? Typically it has been me - because no matter which way you slice it, for whatever reason, I usually end up looking like the one in the wrong... and I have been cow-towing to guilt trips my whole life.

All of my life, I have been fighting for the right - taken for granted by most - to take up space in the world, to be appreciated, and to own my own feelings and opinions without being told (verbally or non-verbally) that they are insignificant. Or wrong.  Or whatever other negative adjective you might want to use.  I'm uncomfortable with confrontation, and my natural response is to withdraw or feel bad for friction existing between people - even if I'm not one of those people. The fact that it exists makes me feel and act guilty.  I lose sleep. I get far more upset for far longer than I need to. Often, I feel like if I screamed at the top of my lungs to be heard, nobody would listen anyway; even if I have something important to say, a large part of me doesn't believe anyone will pay attention to it. 

Photo "Businesswoman Asking To Stop" by imagerymajestic at
www.freedigitalphotos.net

Maybe (and I know that this is a rather big logical jump for some) maybe a big part of it has to do with the fact that I'm under five feet tall. Not being taken seriously because of my height, not having my short legs taken into consideration when doing tasks that take an average-sized person about half the number of steps it takes me, and being twitted (or laughed at) for something over which I have no control, is one of those sore spots with me, because I've had to put up with it all of my life.  

People do it without thinking of the consequences, and they think that by doing so they are funny, or somehow superior.  As if it is by some accomplishment of theirs that things are easier for them (when it is simply a fluke of DNA), they criticize (or laugh) and tell me to keep up. (By the way, these are the people who treat me like a slave without saying thank you...)  Or they laugh and tell me to stand up (when I'm already standing.) Or they worry out loud (like someone did once), when I drop a few pounds, that I'll "disappear."  One person even looked past me and asked where I was ... pretended he couldn't see me.

Ouch!  That behavior and those kinds of statements convey dismissal of my existence and (knowingly or not) they are an attack on my worth.  They reduce all that I am down to what I look like on the outside, and they fail to acknowledge accomplishments that a regular-sized person would be proud of and never would expect to have called into question. Yet it happens to me all the time! Because of that patronizing "I'm better than you, and you don't even have the right to exist" mentality, this kind of belittlement (no pun intended) really hurts. 

In the past, I wouldn't say anything when people treated me this way (or worse yet, I would try to laugh it off), but all that succeeded in doing was (a) send the message that I was okay with it, and (b) make my resentment grow and grow so that finally, I would explode - and not in a nice way.  Someone would invariably get hurt.  And then I would end up looking like the bad guy.  After all, they were "only having fun." Or worse yet, they considered their fun-loving nature (read here: cruelty) to be part of their personality, and took my affront to their unthinking behavior as a personal attack against them.  Suddenly they were the injured party.

Wow. What is worse, I would beat myself up for weeks, months, sometimes even years, for something that at the source, had more to do with someone else's thoughtlessness and insecurity than it did about my reaction to it. It's what kept me in abusive relationships with some people for far too long.

So I'm looking at things a little differently now.  I am telling myself that I have a right to take up space, that my feelings and opinions matter and are valid, and that I have the right to tell someone who is behaving like a jerk toward me that they're behaving like a jerk.  I have the right to expect an apology from them, (not the other way around) and I have the right to require them to be accountable for their actions, to realize that they can't just say any old thing they want to and to blazes with the consequences.  I have the right to be angry when that happens, to work through that anger and to take the time that I need to do that fully before moving past it and on with my life, with - or without - them.  

Maybe someday soon, I might even act on those new ways of thinking. 

Stranger things have happened.

Never again

“Evil begins when you begin to treat people as things.”

– Terry Pratchett

When we think of the atrocities of WWII - the concentration camps, Hiroshima, Nagasaki, the internment camps where Japanese North Americans were imprisoned - two words come to mind: NEVER AGAIN. I was reading yesterday of an atrocity that spanned several decades in our own country, in the words of those who had survived it: the First Nations people. In the residential school system, generations of First Nations children were ripped from their parents (some of them without the parents' knowledge or consent, some at the threat of their parents going to jail) and treated shamefully, in an effort to assimilate them ... to make them into white people.

What if some military or political power were to give police the authority to come into your home, take you and the things you hold dear from it, and give you to prison wardens who stripped you down, called you filthy, washed your hair with kerosene, shaved your head, took your clothes and gave you ill-fitting shoes, burned all of your sports equipment, took your phone, your musical instruments, your credit cards, your jewelry, everything that distinguished you as a person, gave you a number and called you by nothing but that number, fed you substandard food and made you eat it, and beat you if you spoke your mother tongue? What if this went on for years before you were allowed to return to your family? The equivalent of that is only the beginning of what happened to these wonderful, peaceful people.

Reading the accounts of what happened in the victims' own words powerfully reminded me of reading Viktor Frankl's book, Man's Search for Meaning (you can look it up and read it free online) where he described what he went through in the Nazi death camps upon arrival, and then on a daily basis.  He spoke for millions who could not, whose voices were silenced.  He helped to expose the atrocities motivated by fear and hatred.

Isn't that what racism is: fear and hatred gone wild?  That it happened here ... that the spirits of those children were sucked out of them - their way of life and even their own language called demonic - this is Canada's shame. 

I'm sorry, folks, but an official apology from the government, nearly a hundred years after the fact, just does not make up for the thousands of lives, families and communities that were destroyed, the very fabric of their way of life (family, connection with nature, traditions) unraveled.  It does not give the stolen spirits of those people back to them.  It does not restore their lost heritage, nor the way of life they were brainwashed into rejecting. 

 

Photo "Dreamcatcher" courtesy
of Serge Bertasius Photography at
www.freedigitalphotos.net

The nightmare isn't over for First Nations people just because some white man in a three-piece suit said, "Sorry." The way we silence the monsters is to let people know how horrific those attitudes are: the ones that led to daily spiritual and cultural atrocities. The attitude that "white makes right." The attitude that "Christian values are the only ones worth espousing" and "these people are savages."  And oh, my favourite (not): "It's for their own good." It was wrong. It was wrong then and it's still wrong now.

There, I've said it.  I'm a white, Christian, "civilized" (whatever that means) person and I KNOW that what happened was wrong.  I KNOW that every day for multiple generations, there are adults who wake in cold sweats from nightmares about "that place." There are grown men who question every move they make: am I allowed to sit here, am I allowed to go to that place, am I allowed to talk to this person?

Knowledge is power.  I freely admit that I was ignorant.  I didn't know that I didn't know.  And although it was painful, I had to educate myself.  I went to the Truth and Reconciliation Commission of Canada website and I started reading one of the many documents available there  (link).  I confess that I was only able to get through half of it - it was very emotional for me.  The language is easy enough to understand, but the stories themselves - first of how life used to be, and then of how life changed forever - broke my heart. 

Perhaps the reason that some Canadians have a hard time with immigrants coming into our country is because our own ancestors carried out the very thing that they fear the newcomers will do: destroy our way of life, take over our land and make us into second-class citizens.  The difference is that we whites hold a position of privilege ... and we therefore have a responsibility to use our power for good.  Not evil.

Never again.

Acceptance - the royal road

I learned a new word this week: "microagressions." These are tiny, almost subconscious ways in which aggressors mistreat those they target, based on a belief that the other person is 'wrong', 'misguided', 'stupid', 'lazy', 'over-sensitive', or whatever. This is usually the case when aggressors have prejudged someone on the basis of his or her race, religious belief, lifestyle, appearance, gender identity, etc. These microaggressions can come out in the workplace as increased scrutiny (careful examination) of the quality of someone's work (over and above what would be done to another person in the same job), a dismissive attitude of what someone says or contributes, or even just a raised eyebrow (indicating the aggressor doesn't believe what the person is saying). 

Those who feel subjugated as a result of microaggressions lose motivation (they're going to find fault with what I do anyway, so why even try?) and may even succumb to physical illness more frequently as a result of significantly increased stress.

Microagressions are particularly problematic in the helping professions, where there is an inherent imbalance of power. Counsellors, pastors, doctors, and nurses (among others) are held to a higher ethical standard and yet ... abuses occur every day. Patients are not believed, their legitimate symptoms "gas-lighted". People in pain because of a specific problem are turned away (or worse yet, turned into a personal project to "convert") when they reveal a totally unrelated lifestyle not considered acceptable by the helper. It happens every day!

The more I study counselling, the more I realize that the key to becoming a good counsellor - indeed, the key to becoming a better person - is acceptance of other people, regardless of how different they are from me, my thoughts, and my beliefs.  This is much more than just "love the sinner, hate the sin." It goes WAY beyond that fallacy.  It involves a deep-seated belief that every single person has the right to be who they are and feel what they feel. That belief is HARD to cultivate... but it is crucial.  If it is not there, I could turn into (or perhaps continue to be) a microaggressor. 

People who habitually commit microaggressions rarely see their behaviour as aggressive or prejudicial.  They usually consider themselves to be wonderful, caring people ... and they may be in some contexts ... but there is this huge blind spot that obstructs their ability to accept that the other person has just as much right to be there as they do.

I have been the target of microaggressions.  The perpetrators were simply acting on their core beliefs, based on their own chosen lifestyles, that (for example) all short people never become adults and should not be taken seriously, that all fat people are lazy, ugly and stupid, that all Christians are crazy bigoted right-wingnuts, that all depressed people are suicidal, that all civilians (or non-professionals) are ignorant, and so forth. It's probably not obvious to anyone watching, and certainly not to those who have acted on those beliefs, because they cover it up with a veneer of civility and respectability.  Yet ... it exists.

Photo "Conflict In The Office" courtesy of
franky242 at  www.freedigitalphotos.net

I've also watched people commit microaggressions against others without them even realizing it, and I have seen the results in their victims ... who feel as though they have just been bullied, but can't quite put their finger on how.   All they know is that they feel belittled, condescended to / patronized, and made to feel powerless .... like the person who makes a mistake at work (due to a misunderstanding) and is not called into the supervisor's office to chat one-on-one, but is confronted about the mistake in front of his or her co-workers.  The co-workers (not being the ones under attack) can easily identify the conversation as one that should have been conducted in private. Why wasn't it?  The microaggressor (for whatever reason) believes that the person in question does not merit that kind of consideration ... whether that belief is on a conscious or subconscious level.  Often the victim's feelings don't happen during the encounter but afterward, after the shock of the (usually verbal) assault wears off.  This is how bullies get away with bullying.  Talk about feeling ambushed!  Not to mention vulnerable, helpless, trapped, and a whole host of other unpleasant things. 

Those feelings (though unpleasant) are VALUABLE because they are the brain's early warning system: danger, danger, danger!  They can lead you and me to recognize when such things are happening and to speak out against them, so as to do something to stop them from happening again.  Nobody has the right to be treated like a disposable person, a worthless piece of junk.  NOBODY. 

And truly, acceptance (valuing the other person as a person, with the same rights as anyone else) is the key.  It is the royal road to creating a safe place where non-judgmental, non-aggressive conversations can happen.  It is much easier to create that safe place when two people are on a par with each other, where one does not hold power over another, where one is not more qualified than another.  However, it becomes far more difficult (yet still equally as important, if not more so) when there is an imbalance of power. 

Raising awareness is only the first step in addressing this problem.  I've used the example here of a co-worker with a supervisor, but this could apply to pretty much every arena where there is a perceived difference in the level of power two people hold.  People in positions of power or influence MUST learn that the fact that they hold more power makes them more accountable for the way they treat those who have less ... or none.