I’m a Real Girl!

A few months ago I was enjoying lunch at a pub with some friends. We were chatting idly about Lush Cosmetics, a particular weakness of mine, when the server approached to bring us drinks. Interrupting, she said, “Oh! I’ve heard of Lush, but don’t really know anything about it; I’m not a real girl.”. And this got me thinking…

 

What does it mean to be a “real” girl? Or, more appropriately, what does it mean to be a real woman? Some claim it’s motherhood—that the ultimate purpose and design of woman is to bear children. Our society has moved a little beyond such a primitive and restrictive view, but what hasn’t It moved beyond? Some say it’s about being “girly”. But what does that mean, exactly, and at what point aren’t you girly enough to be “real”?

 

When I was growing up, my lack of “girliness” was keenly felt. Not only was I a practical person who didn’t like to spend my precious free time jabbering constantly about makeup and boys, but I was also unable to fully appreciate many of the pursuits my girlfriends enjoyed. Sure, I could let someone give me a makeover, but I couldn’t look into the mirror and appreciate the full effect. I was not comfortable doing anyone else’s makeup either (though there are many blind women out there who do makeup, hair, and nails with confidence—I applaud their courage!). So, the common sleepover parties didn’t really appeal to me; they were filled with trying on each other’s clothes, giggling a lot, an drooling over “cute” boys I’d never even spoken to before.

 

There are many small things I have not and will never do for myself that would make me a more “real” girl. I didn’t get to pick my own grad dress; my sister and mom, both being possessed of excellent taste, did most of the “choosing”. All I could tell them was what I liked, and having been exposed to very few dresses of that grandeur, I really had no opinion. I soon realized It wasn’t about comfort or the feel of the fabric or any other element I could actually understand. It was all about the look. Similarly, I will not be able to independently choose my own wedding dress. While I’ll definitely have a say in the matter, I won’t be able to comprehend on a gut level how it flatters my body, or skin, or eye colour, or any of the rest of it. Even when I do occasionally let people do my makeup for me (it’s not something I bother with on a regular basis), I can’t say it’s a huge source of excitement. I appreciate the glow of being told I look beautiful, but that’s about as far as it goes in a lot of cases.

 

For a long time, I felt horribly ostracized. I worried that I wasn’t “real girl” material. I fretted that not being enthusiastic about fashion and general cosmetics made me inferior, somehow, even a step lower than someone who can see but who chooses not to get excited about such things. But that server in that pub got me thinking, and she made me realize something: I am as real as it gets. I love perfume, and fragrant tea, and artisan soap, and candles, and pretty dresses. I love picking out skirts and fancy high heeled shoes it’ll take me ages to learn to walk in at any speed. I like Lush Cosmetics, and The Body Shop, and Rocky Mountain Soap Company, and even Scentsy. So, I must be a real girl, right?

 

Hang on, though: if these are the measuring sticks by which we measure a “normal”, “real”, or even “successful” girl/woman, is that not just as primitive as the idea that it is motherhood which defines us? Some girls like things that smell and look pretty, but others don’t. Some girls plan to have children, but some can’t or won’t. Is there some arbitrary threshold past which you are an acceptably real girl and before which you’re straddling the line, not quite belonging? We should be past all that. We should be relating to each other as human beings who like the same things, not as “girls” and “guys”. If my male friend likes candles, then we’ll go candle shopping. It doesn’t mean he’s not a “real” boy.

 

It’s okay to generalize, but when you start pushing people out—especially for reasons they can’t control, like personal preference or in my case, visual impairment—that’s your cue to draw the line. We put people in neat little boxes enough as it is. Let’s all just focus on being real human beings, shall we?

Can You See Me?

A few years ago, I performed an informal little social experiment while in the grocery store: I began by walking just behind the cart (I was pushing, my sighted companion steering) with my cane out and plainly visible. After a few minutes, I folded the cane and put it in the cart so that it was out of sight. I have “normal” eyes, so I don’t look conspicuously blind; if the cane isn’t easy to see, people don’t always realize right away that I have any sort of disability at all. Since I was just pushing the cart, the blindness really wasn’t obvious. You may well ask what the point of such an experiment could be. Here is what I discovered: while my blindness was on display, as it were, I got pitying, fascinated, or outright terrified looks. Mothers instinctively pulled their children from my path, even when they were in no danger whatsoever of colliding with me. The elderly and the very young gazed at me as though I were some foreign creature they’d never seen before. It was clear that while everyone was looking at me, they weren’t seeing me, the human woman. They were seeing a blind person, and no more. When the cane was out of sight though, people either didn’t notice me at all, or (in the case of the young male population, anyway) looked at me with interest. (This is not vanity; my sighted companion was the one who told me of this!)

 

What have I learned from experiments such as these? Well, quite a few things. One is that people are inherently afraid of (or at least fascinated by) what they don’t understand. Another is that people will never be completely comfortable with difference, no matter how hard we work to encourage tolerance. A third thing is that those with disabilities are hypervisible and totally invisible at the same time. We are either the centre of attention (in a zoo-creature kind of way) or we don’t exist at all. We are either being asked to speak on behalf of all disabled people, or we’re being completely overlooked. We’re either being asked if we need help (or other more intrusive questions) or we’re being severely marginalized. Our canes, dogs, wheelchairs, cochlear implants, talking phones and computers…these all ensure that we are very visible to everyone and anyone who is curious, frightened, or hostile. Yet these things also make us totally invisible as human beings. We are not individuals. Instead, we are archetypes, or representatives, or ambassadors. If we’re not any of those things, we’re not anything at all.

 

These are general observations; do remember that. Before you indignantly point out that not all people treat us this way, please keep in mind that I’m aware of that. I am surrounded by wonderful friends, family, instructors, employers, and total strangers who treat me with dignity, respect, and courtesy. Most of the people I know think of me as an individual and not as a spectacle to be gawked at.

 

The trouble is, there are also many people who do treat me like a spectacle.

People watch me perform every little minor task, exclaiming over it and pestering me with endless questions. I am hypervisible.

People discuss me well within earshot, sometimes complimenting but often just speculating about what might be wrong with me. I’m invisible.

People stare openly at me while I enjoy a day at the mall, being careful not to actually interact with me in any way. I am hypervisible.

People confuse me with other blind people because they recognize the cane but don’t recognize my face. I am invisible.

 

My life is not a spectator sport. My identity is not simply made up of disability and the quest to overcome it. As I’ve said time and time again, there is far more to me than what I can’t do. I don’t want to be anyone’s representative. I don’t want to be “special” just because I’m the first person to take a certain course, or work at a certain organization. Many people with disabilities find themselves pioneering and paving the way (more on that in upcoming posts) but we seldom enjoy it. It’s just another reminder that we’re less an individual person and more a symbol.

 

I understand that you’re curious. I understand that you mean well (mostly). I also find that the open, discourteous way people often stare at me bothers the people who love me far more than it bothers me. Just ask my sister; she’ll tell you what she thinks of people who do that. (She has been known to smile and wave at them until they are shamed into looking away, because she’s gloriously protective. I’m very lucky.) I understand that difference will always be intriguing, and scary, and daunting. I get it. But…

 

Please don’t watch me eat. Please don’t comment on every little thing I do as though it were the most interesting thing you’ve ever seen. Please don’t observe me with an eagle’s eye, leaping to react to my every movement. Please don’t talk about me like I’m not in the room. Please don’t make fun of other people with disabilities (derisively) when I’m present…

 

Please try to see past my cane and get to know my face. Please get past the fact of my blindness and get to know me as Meagan—the professional communications student who loves cats and hates mosquitoes.

 

Can you see me?

I Apologize For The “Inconvenience”

I call you for the third time this week. I’m crying. I’m soaked with rain, and windswept, and utterly lost. There isn’t a soul around and I have no idea how I’m to get home. My phone is dying, my gps is no help, and I’m standing under a tree’s meager shelter while thunder explodes in the sky above. I feel like a complete failure. I’ve been getting lost so often lately, but then again this is a brand new neighbourhood. It’s the first time I’ve ever used transit in my life. I’ve lived here only two weeks, and barely have a handle on the route to and from work. I’m begging you to help me. And you do—but first, you tell me how inconvenient this is for you—that you’re getting awfully sick of it.

 

I sit hopelessly at my desk, explaining for the umpteenth time that the tactile diagram in front of me just doesn’t make sense. I’ve tried and tried to understand it, but it just doesn’t click for me. I am close to tears. I am failing this unit, and I know it’s not because I’m stupid, or bad at math, or lazy, or any other thing you care to name. I’m failing this because I’m unable to use the tactile diagrams that make so much sense to you. Hell, one of my sighted friends—a math whizz if ever there was one—can’t master circle geometry either. In a fit of frustration, I grab your hand and place it on the paper. “Feel this? Does this make any sense to you at all?”. You don’t speak. “Well? Does it?”. After a pause, you admit that it does not. You admit that this unit isn’t all that important anyway and that you’ll just have to waive it. But as you make this promise, you take special care to mention how inconvenient this is for you—that you really have no idea how to go about teaching me this material.

 

We’re having lunch, and you invite me out for drinks a few evenings from now. I casually mention that I’ll have to have a hunt for my ID; it fell out of my purse the other day and onto the floor of my suite. I still haven’t managed to find it. It’s probably off in a corner somewhere, but it will take a lot of scrabbling around for me to find it, and I just haven’t gotten around to it yet. It’s small, and easily buried or kicked or overlooked. You offer to come and help me look for it—something I’ve neither asked for nor welcomed, even—but first, you are sure to tell me how inconvenient this is, and how I’d better have a good search for it before you waste your time. I immediately lose my appetite and go home soon after. We never did go for those drinks.

 

I lean forward across the table separating us, entreating you to rethink your position. I lay out all the possible adaptations we could use to make this vital course accessible. I outline my hopes for the future and my goals for my degree. I assure you that if it really isn’t working, I’ll drop out and say no more about it. I am quite certain I probably sound pathetic and desperate, but I don’t much care. The truth is, I am desperate. I can do this course; I know I can. But you aren’t  so sure. You repeat that it’s nothing personal, that you’d love to help, really…but you only have so much time in the day. You only have so much energy to devote to one student, no matter how eager and dedicated. Really, it’s all very inconvenient for you…

 

I’m in the back seat of your car while you drive me to yet another engagement I can’t get to on my own. It’s a rural area. There are no buses, or cabs, or trains. It’s snowing, and bitterly cold. You didn’t want to go anywhere this evening. You’re grumpy and miserable about the whole thing. Of course, you give me a ride, because you know I don’t have an alternative, but you grumble to yourself about how inconvenient it is for you. I curl into myself and try to ignore it.

 

Every day, it’s something else. I never know what it will be today, but I know there will be something. You are displeased. You are ranting. You are telling me how frustrating it all is. You are cataloguing every way in which I am a burden. I create more work for you simply by existing–simply by being a flawed human being with, let’s be frank, special needs. Inconvenient needs. My eyes well up, because I am eight years old and all I want to do is please you—please everyone. You lash out, telling me to stop crying immediately. I put my head down, as it’s the next best thing. All the while, you continue, because I am ever so inconvenient. If my eight-year-old heart had the courage it ought to have, I would raise my head, tears and all, and remind you that while my blindness is awfully inconvenient for you, …it’s awfully inconvenient for me too. After all, I live with it. Every. Single. Day. I make it work, and usually I don’t mind much, but yes! It does make life a wee bit tough sometimes. I’m not unaware that it gets in people’s way, and I really am sorry about that. But as difficult as it is for you, it is ten times more so for me.

 

Think about that. Then, come tell me how inconvenient it is for you.

Exhibit A: On Getting Past The Novelty Stage

It’s natural to be fascinated by someone new. Our brains love novelty; new things and people tend to seem more interesting and attractive by default. So it’s no surprise that many of my most cherished friendships were founded upon at least a little novelty. People are always curious about the blindness thing: they have questions, concerns, etc. While it’s not the most ideal way to make friends, I don’t mind too much. I might do the same if I made a friend who was deaf, or in a wheelchair; I have no doubt that I would have plenty of questions to ask, and wouldn’t always be successful in curbing my insatiable curiosity. All normal, all healthy, all good. But… (and there’s always a but)…

 

…there are some friendships (and I use the term loosely here) that seem to thrive upon the sheer novelty of disability. People really get into the whole sighted guide adventure. They love coming up with new questions to ask me long after I’ve answered all the usual ones. They want to help me with absolutely everything, just to see how “it all works”. This becomes a little off-putting after awhile, because I’m left wondering whether they’d be my friend at all if not for the blindness. Is that my only selling point? Is that what they’re into? Because if it is, then where exactly does that leave me? What if I eventually lose my intrigue? Will they go off and find some new disability to coo over?

 

I was once invited out for coffee by one of my instructors. I assumed we’d spend the time chatting about the course; I’d done quite well, and had more than a passing interest in it. Instead, it turned out to be an hour’s worth of Q and A. To his credit, once he figured out that there was more to me than spokesperson for all the blindies of the world, our conversations became far more interesting. Still, it was a rather disappointing experience.

 

There are even people who stick around after the novelty wears off because associating with me gives them the warm fuzzies. They think that helping me is the nicest, most Mother Teresa-like thing they could possibly do, and it reassures them that they are good people. (FYI, studies suggest that Mother Teresa was actually a little bit nuts, so maybe find a different role model.) I always appreciate magnanimity, but there’s such a thing as too damn much. People make me into a walking, talking source of validation, if you will. Beyond my need for help, I’m worth very little to them, even if they don’t consciously realize it. The more independent I am, (and I’d like to think I’m reasonably independent as people go), the less I matter to them. If I don’t need something, we don’t see each other, period. My value lies only in what they can do for me; beyond that, I’m not worth their time and energy, because they’re either out with more interesting friends, or busy saving other lost little souls. Invariably, the friendship ends when they become bored, and they move along to the next one. And there is always a next one.

 

Needless to say, I consider this type of friendship highly undesirable. I am fortunate in that I have had this happen to me only a very few times, but each time, it has hurt deeply. I befriend people because I like them; it’s as simple as that. To know that others befriend me because I’m some fascinating superfreak, or because I can help them feel good about themselves, is insulting, damaging, and depressing as all get-out. Friendship is supposed to be grounded in healthy, mutual interest and respect; I don’t want to be someone’s charity case or pet social experiment. I’m not a novelty object, and I’m not a living breathing pity party. If you want to be my friend, please do so because I make you laugh, or because you enjoy my company, or because I make delicious cookies (and I do), or because you think I’m a genuinely interesting person (you know, beyond the eye stuff). Don’t befriend me because you think it’s the “right” thing to do, or because you think you might be able to write a book about the experience later. You certainly shouldn’t befriend me solely because you want to blog about it; Blogging about my broken eyes is my job, damn it! PSA: Blogging/writing about me will not make you much money unless you’re good at embellishment; I’m not that interesting, just as a heads up.

 

In all seriousness, let me be a bit of a broken record and restate what I’ve been saying all along in these posts: disability in no way negates humanity. Treat us like people, not like objects, or circus freaks, or exhibits. We don’t exist for your personal validation. We love it when you help us, and if you are good friends to us we will adore you forever. Even if you’re not really friends with us, but you’re a naturally helpful person, we will still think you’re awesome. Just make sure that the friendship has a lot more to it than that, because on our end, it will be about way, way more than what you can do for us. If that does not prove true for you, find another friend, because no one deserves to be a walking support system.

 

For anyone who fears that a friendship is edging towards the danger zone, here are a few tips to nudge it back towards a healthier direction. I’ve used these for my own friendships, and I find them to be very effective.

 

Analyze the reasons you hang out with each other. If you find that the majority of your hangout time is devoted to helping your disabled friend, you may want to kill that pattern as quickly as you can. Feel free to be helpful to them, but ensure that you’re socializing with them just for the fun of it more often than not. The last thing you want (and probably the last thing your disabled friend wants), is a friendship built mostly upon your ability to be helpful.

 

Let your friend be of assistance to you in whatever ways they can. Everyone has something to offer; find out what your friend can help you with, so that you can break a potential cycle of mild parasitism. I’m not suggesting that you attempt to make your friend feel useful; I’m merely suggesting that you allow them to do for you what you do for them as a matter of course. Friendships in which one friend is of exponentially greater value to the other are destined for disaster, and can be enormously unfulfilling for both parties. Don’t assume that your disabled friend has nothing to bring to the table. I’ve been known to edit my friends’ essays, play counselor when they have profound issues they need to talk through, and make jokes when they’re sad. (You’ll have to check with them on the efficacy of that last, though.) It can’t be denied that I give fabulous hugs, as well, so there’s that. See? I’m positively brimming with perks!

 

Resist bringing disability into every conversation. It’s okay to be open about it, and if it comes up, then it comes up. However, there is such a thing as making it into something bigger than it needs to be. It shouldn’t be an integral part of everything you discuss, and it shouldn’t be the centre of attention at all times. Chances are, your friend is sick to death of talking about it anyway, and would love to chat about almost anything else. I admit that it can be cathartic to vent about my disability to friends sometimes, but it’s definitely not something I’d want to do every day. As an experiment, try spending a whole day with your friend without mentioning it beyond what necessity might dictate. If it’s hard to find things to talk about, you know you’re in trouble. On the flip side, if you catch yourself completely forgetting that your friend has a disability at all, pat yourself on the back: you’re doing just fine.

 

When introducing your friend to others, don’t dwell on the disability; make sure you mention cool stuff about them, like what they’re really good at, or what they’re interested in. Establish common ground, so that the focus can shift away from the novelty of their existence and toward things they might actually want to be known for. If you set the tone, others will follow your lead.

 

Assess your friend’s attitude towards their disability, particularly in the ways that affect your relationship with them. If you find that they are focused only on what you can help them with, not to mention how utterly tragic their lot is, it’s time to say your farewells. As I mentioned earlier, no one deserves to be regarded as little more than a source of help and comfort. Don’t let yourself be used, no matter how guilty you might feel. The majority of us would never do that to you, so don’t let the few of us who would get away with it.

 

Finally, reassure your friend that you appreciate them for more than their disability. I have actually caught myself making blind jokes because I felt like that was all the other person wanted to hear. I even found myself going out of my way to discuss it, because it was guaranteed to peek their interest in a way that nothing else could. As soon as I realized what I was doing, I felt almost self-exploitative, and was ashamed of both myself and the state of the friendship. Never let things get as bad as that, if you can help it. Even if it feels a bit awkward, make sure they know that you value them for themselves most of all. It may seem obvious to you, but it may not be obvious to them. For all you know, they’ve been spending hours trying to think of a delicate way to bring it up. I know I have..

Don’t Get Grabby: Respect The Personal Bubble

I’ll be the first to admit that my personal space is quite small as they go. I’m apt to hug strangers (assuming they’re okay with it, obviously), I love handshakes, and I have no trouble taking someone’s arm in order to be guided—or just to be companionable, because why not? That said, one of the things I have to be hyper-aware of is the personal space of other people. Just because I’m comfortable with casual touch doesn’t mean that everyone is. So, out of simple respect, I refrain from touching, grabbing, or manhandling people without their permission. Seems obvious, right? Not really.

Ever since I can remember, I have been casually touched and/or grabbed by complete strangers, usually without any kind of warning or preamble. Sometimes, it’s justified enough: I’m headed straight for a pole, and someone panics and grabs me to keep me safe. I can understand that, even though I’m often aware of exactly where I’m going, and know that my cane will strike the pole before my face will. I can forgive that kind of protective instinct. It gets a little problematic when people decide to grab or otherwise touch me for very flimsy reasons, the most common of which is because they seem to think that people with disabilities—especially blind people—don’t have a personal bubble in need of respecting.

I’m not the only one who has noticed this, either. Just about every blind person I’ve ever spoken to at any length has mentioned that they’ve been frequently grabbed, touched, or otherwise physically manipulated either against their will, or at least without permission. This might start out sounding a little silly: what’s the big deal, right? So someone grabs you to keep you out of the way of some obstacle? What could possibly be wrong with that, in this otherwise apathetic society?

Here’s what’s wrong with it: many of us have a large personal space, and we don’t appreciate being grabbed, nudged, or prodded without warning, especially if the reason is anything less than “I thought you were going to get yourself killed”. Here are just a few scenarios (because I like lists, sue me), in which I’ve been grabbed or otherwise touched in a way I disliked, with explanations as to why I object. In all cases, speaking to me first would have been the best option. Perhaps, by the end of this little post, people will be a bit more willing to keep their hands to themselves unless the circumstances are especially dire. Here goes …

In my first year of university, quite early in the term, I was headed for one of my classes. Just as I was nearing the door, I felt an arm wrap tightly around my waist, and I was steered bodily towards a hallway I had no intention of going down. I was so shocked I couldn’t say a thing; I just turned my head towards the person who had hold of me, and gaped. Eventually, after a few awkward steps, I was given an explanation of sorts: “The hallway is this way”. “I don’t want to go down the hallway.”

“You were about to run into a door.”

“No no, I was headed towards the door on purpose so I could open it…”

“Look, where are you trying to go?”

“Room 6-262!”

“Oh!” he cried, sounding indulgently exasperated, “it’s right here!”

Where do you suppose he led me? Back up the hallway, and right to the door I’d originally been heading for. He then acted as though I should have been grateful for the guiding. Think again, buddy. You do not just grab a strange woman, especially when she can’t see you, and lead her off somewhere. Didn’t your mother teach you anything?

In the same university, I was heading past a staircase, intending to go down a different path. Suddenly, a woman appeared at my shoulder and locked my left arm in a death grip, locking both my elbow and wrist so that I couldn’t disengage without considerable effort. “Where you want to go?” she demanded, in a frighteningly strident voice. “Um…where I was headed…” was all I could mutter. “Stairs?” she asked, ushering me towards the staircase. “No, no! I’m okay, thank you!” … It took a long time to get my arm back, and I booked it away from her as quickly as I could. I understand that she meant well, but having my arm immobilized by someone so determined to take me down the stairs to some unknown fate was a little on the unnerving side.

My final scenario is one which, while the most benign, terrified me the most. It is illustrative of exactly why you should treat blind people like normal people and respect their personal spaces. I was walking along, quite lost in profound thought (probably imagining what I’d have for dinner or something) when I was grabbed out of nowhere. I could immediately tell that it wasn’t the typical “you’re about to walk over a cliff edge” grab, and it wasn’t the “I want to guide you somewhere” grab either. It was more of a “stop walking” grab, and while I didn’t tell him so at the time, I was absolutely terrified for a split second. Luckily for me, it turned out to be a good friend, and I was very pleased to see him. He’d just wanted to get my attention, and I guess he decided that he really really wanted me to join him over by the wall. Instead of calling my name, though, he chose to simply grab me and move me towards where he wanted me to stand. While I understand why he did it, I still think calling my name would have been far more polite. He really scared me for a second there.

If this comes off sort of bitchy, please try to understand me when I say that this is a very common complaint. It is mostly just annoying, but it can be dangerous at times. Many of the blind people I know have recommended that I take self-defense classes, not just to fend off those who mean harm, but also to free myself from well-meaning strangers who decide to get grabby. I once heard that one poor blind girl was grabbed by a stranger who was absolutely convinced that she wanted to go down the escalator. Escalators are a bit dangerous at the best of times; they’re made even more so when you can’t see where you’re going and have a stranger dragging you alongside them. I have heard of blind people being pulled into streets they didn’t want to cross because someone was trying to be helpful. I have heard of blind people being dragged off somewhere because people decided they wanted them to go there. I have had people grab my hands and been made to feel things, because it was assumed that being blind means you want to touch everything in sight. I have even been hugged and kissed by people who knew me, but who didn’t think to introduce themselves first or even warm me that they were nearby. It’s not okay.

You would never ever dream of touching the average person in this way, so why on Earth would you think it’s okay to randomly grab a blind person? Disability makes us no less human, and we have boundaries, just like you do. Please, for the safety of us all if nothing else, respect them.

Things That Go Buzz In The Night

Summer is drawing to a close, and to make myself feel a little better about the autumn chill in the air, I’m going to take this opportunity to discuss creepy crawly buzzy creatures you only find during the otherwise idyllic summer months.  Who knows? It might just make you feel better about the impending cold, too!

 

 

Insect phobia, also called entomophobia, is one of the most common phobias worldwide. Its effects can range from irritating to crippling. Some people won’t even leave their houses for fear of encountering even the most inoffensive of insects.

 

I didn’t always identify as insect phobic, reasoning that my fears did not impede my life enough to qualify as bona fide phobias. I’ve since changed my mind, and use the label quite freely. I am irrationally afraid of many different types of insects, and being blind can add a further dimension to this fear, making it harder to cope with and more severe.

 

Sometimes, coping with insects when you’re blind is no more difficult than it would be for a sighted person: as you’re lying in bed, drifting off, the insidious whine snaps you back to alertness. Then, you search vainly for the mosquito, intent upon murdering the insolent little nasty before sleep is possible. Turning on the light doesn’t help; the mosquito usually vanishes until darkness returns. Mosquitoes are easy enough for blind people to kill. They’re usually too stupid or too slow to escape a swat once they’ve landed. (I’m not yet at an emotional point where I’m fully capable of letting mosquitoes get near enough to land on me at all, but I’m working on it.)

 

Unfortunately, it’s another matter altogether where bees, wasps, hornets, and other bugs are concerned. There are generally several tasks that blindness makes more challenging. First, you have to identify the insect. What are you dealing with? Is it a mellow bumblebee, high on nectar and enjoying life? Is it a slightly more threatening honeybee, looking for a snack but not unwilling to attack if frightened? Or is it—horror of horrors—an evil little wasp, just waiting to launch its vile assault?

 

Second, where is it? Sometimes, insects that make especially loud noise can seem closer than they actually are. Is the bug near enough that any sudden movement will disturb it, or is it far enough away that escape is possible? And do you dare find out?

 

Third, how should you go about eliminating the threat? I’m as big a bleeding heart as anyone I know, so my first instinct is usually to put a harmless spider or lady bug outside rather than ending its little wee life. I’m not near as philosophical when it comes to creatures that buzz, however. My fear of insects is sometimes so acute that the mere sound of an insect—even a house fly—will set me so on edge that most thought processes simply stop. I want to either escape, or see the creepy-crawly slaughtered (hopefully by someone who isn’t me).

 

I’m not alone, either. Alicia tells me that she finds the mere idea of being trapped in an enclosed space with an unidentified insect terrifying in itself. If there’s an insect in her house, she’ll avoid it rather than trying to kill it or put it out. Even worse, she hates the knowledge that she may not know a bug is around until it crawls on her, at which point she has no warning, no sense of what the bug might be, and virtually no time to evade it.

 

Once, while alone in a car, I noticed that there was an awful lot of buzzing going on directly behind my head, right against the back window. I knew there had to be at least four or five different insects there, but I wasn’t entirely sure what they might be. They sounded like they could be flies, but they also could be bees or wasps for all I knew. Positively quaking with fear, I hunched down, put my head between my knees, and stayed curled like that until my friend turned up. “Oh my God!” he exclaimed, opening the car door, “There are about six bumble bees in here!”. … I still shudder at the thought.

 

I’ve been by turns laughed at, scoffed at, sympathized with, and coddled because of my all-consuming fear of big buzzy things. While a lot of the fear is quite normal and part of being human, some of it is directly related to being blind, and I wanted people to understand that feeling as much as possible. It starts to make a tad more sense once you step into my shoes for a moment. Keeping in mind that not all blind people react this way (my boyfriend, for instance, feels little more than irritation with most bugs), I beg my readers to cut me some slack when it comes to things that go buzz in the night.

 

 

Running In Circles: Superblinks And The Quest For “Normalcy”

Today, Gregg and I have teamed up to address a topic which troubles us both. We hope that this offers some insight, even if you do not agree with our general stance. Enjoy!

 

Anyone reading this article is apt to have seen at least one so-called “supermom”. She’s the sort of woman who’s involved in everything her kids do, while still managing to cook, keep house, balance the family accounts and take time for herself to pursue a hobby or three. Many of these women are wonderful people, but the worst among them can be frustrating, condescending and infuriating by turns if others don’t do as they do. This particular phenomenon isn’t limited to mothers, however. A small group of blind people are guilty of much the same thing, and we commonly refer to them as “superblinks”.

 

Being good at a lot of things doesn’t make you a superblink. Trying to help other blind people get better at things you can already do quite well doesn’t make you a superblink either. There’s nothing wrong with either one of these things, as long as you exercise caution with the latter so as to avoid coming across as a know-it-all. Superblinks are defined by a rather strange paradox. They do as much as they possibly can, in as “normal” a manner as they can manage, to stop people from thinking they’re inept; being blind, however, means they’re going to stand out sometimes no matter what they do, and since relatively few superblinks exist, they end up seeming more abnormal than ever. Their desire to blend in makes them stand out. Central to the idea of the superblink, as well, is the insistence, to any and all around them, that their way is best. This often manifests even if the superblink in question has trouble with the task at hand or cannot fully understand why they need to do something a specific way. Many superblinks are excellent at the things they do, but some are not; for those latter individuals, doing something well becomes secondary to doing something normally.

 

Most of the time, it’s easy enough to let “superblinks” be. True, they can sometimes be irritating, just like supermoms who drive everyone else crazy with their insistence upon being the very best at absolutely everything. Unfortunately, there is a certain subset of superblinks who can be downright damaging to themselves and to other blind people.

 

It can be very taxing to associate with someone who tries with all their might to seem “normal”. They are so unwilling to accept their blindness as part of them that they do everything in their power to behave as much like a sighted person as possible. For these people, appearing “blind” in any way is undesirable. I’ve even met some people who refuse to carry canes because they don’t want to “look blind”. These people are a danger to themselves and occasionally, to others. These are the superblinks who march out into traffic without caution, explore new routes without a clue where they’re going, and refuse to acknowledge that they are different in any way. Needless to say, this lifestyle is absurd at best and dangerous at worst.  No matter how hard you try, your blindness will never go away. We’re not suggesting that one has to embrace their blindness with open arms and adore that part of themselves; it’s perfectly normal to feel a little subpar sometimes. But to ignore it completely? That’s wrong on so many levels. To value normality above all other things is a grievous mistake, considering that no one really knows what normal means.

 

Those who dismiss their blindness can be trying enough, but still worse are the superblinks who define themselves by their disability. These are the types of people who are inordinately proud of their accomplishments in the context of their blindness. For example, someone might be very proud of their cooking skills, employment-related skills, etc. That’s perfectly fine. Being proud of one’s accomplishments is sometimes underrated. What isn’t so nice is when someone is proud of these things because they are blind and still manage to do them. Sighted people do this to us all the time: “Look! This guy is a singer/skier/teacher/lawyer … and he’s blind! Isn’t that just amazing? What a hero!”. There are people who defy the odds and take on tasks that are difficult for the blind to do. This is admirable, certainly, but there is really no need to go around singing one’s own praises. Be proud, by all means, of what you have achieved, but don’t contextualize it all the time.

 

I’ve known blind people who are so intent on defining themselves by their blindness that it’s almost as if they think they have “blindy” superpowers. “Look at me go! I’m blind but I can do this, this, this, and that!”. It sends the message that we’re special or heroic or worthy of adulation simply because we do what sighted people do anyway with particular skill. Certainly sighted people might admire us, and that’s not in itself a horrible thing, but we should know better than to adopt the practice ourselves. In fact, for someone who is so intent on seeming “normal”, defining all of one’s accomplishments by the difficulties caused by blindness is awfully counterproductive.

 

The main reason that these types of superblinks are a problem, though, is the judgmental behaviour they often exhibit towards other blind people. They assume that, just because they can do certain things well, every blind person should be able to do them equally well. “What’s wrong with you? Why can’t you do this? I can. There must be something the matter with you.”. I’ve already discussed the dangers of comparing blind people to one another, and superblinks really should know better. There’s a difference between being supportive (“You can do this!”) and being judgmental (“Why can’t you do this?”). Call me a dreamer, but I think the world would be a much better place if people spent less time judging and comparing, and more time supporting and encouraging.

“I’m Right Here!”: On Treating Us Like People

Before I begin the meat of my post today, I’d like to stress a few things: one is that I understand that not everyone knows how to behave around people with disabilities, so they do whatever they can think of at the time. The second is that generally, people mean well, even if they do things that make me angry or hurt my feelings. Third, despite the somewhat ranty nature of the following, I accept that not everyone gets it right the first time. I’m here to help you get it right in the future. Of course, “getting it right” is subject to my views; other blind people may have opposite opinions. Try and read this with an open mind, and understand that while I feel strongly about this matter, the last thing I mean to do is offend.

 

I literally cannot count the times I’ve gone into a restaurant, store, or other public place, and been treated more or less like a child. If I’m with a friend, for instance, servers will sometimes ask what “she’d like to order”, as if either I can’t decide for myself, or I can’t hear the conversation at all. Other times, people will talk about me at great length, sometimes when I’m just a few feet away; it’s as if they believe that deafness (or at least lack of awareness) inevitably accompanies blindness. This is, of course, true in some cases, but my ears are in excellent working order, and I hear everything going on around me most of the time. Just recently, I went into a Starbucks with some friends, only to find that the group at the next table were having a loud conversation about how nice it is that people help “the poor blind people of the world”. I chose to laugh the whole thing off, but it bothered me. Why do people insist on talking about me when I’m right there, just because I can’t see them? Do they think I’m deaf, or do they honestly fail to consider that I might overhear (and care about) what they’re saying?

 

The thing is, I’m a human being—a highly functional one who can hear and understand things. The other common mistake people make is assuming that, while I may be able to hear them, I won’t understand. I have had many people talk to me in excessively loud voices, speaking slowly and clearly as though to one who barely speaks English. Worse still, some people will speak to me in a high-pitched, sickly sweet voice, as though addressing a child. A few years ago, I went into a salon to get my hair cut. The hairdresser, who couldn’t have been more than a year or two older than I was, said “What can I do for you today, sweetie?” in a singsong, overly motherly tone. This would have been okay if she talked to every customer this way, but I soon discovered that she only spoke this way to me. It was infuriating. I have seen people do this to blind people who are much older than them, and I simply don’t get it.

 

Then there are those who try to speak for me. I’ll go somewhere with them, and when I’m asked what I’d like, they answer for me right away, as if I can’t do it for myself. This is often done by family members who used to do it when I was very young, but who haven’t grown out of the habit over the years. It’s easy, I suppose, to do this without thinking, but it’s really not necessary. You wouldn’t speak for any other nineteen-year-old, so why speak for me? I have command of the English language, and I certainly have the autonomy to decide things for myself.

 

Don’t believe me? Try watching an elderly person with a walker sometime. They’ll be patronized; they’ll be called “sweetie” by people half their age; they’ll be spoken to in slow, singsong tones; they won’t be taken seriously, or they’ll be treated like children. They’re just old, and they have a walker. This does not automatically transform them into someone completely subhuman (or inhuman). Unless they have some form of serious dementia or similar condition, speak to them as the capable adults that they are.

 

I can both hear and understand what’s being said to and about me. I am an adult who is capable of speaking for myself, making my own decisions, and having normal conversations with people. There is no need to speak for me, or to speak to me like a child (or worse, act like I’m not even there). While I realize that most of this is entirely unintentional, I want people to realize how it feels, and understand why they should try not to speak this way. It’s patronizing, and even hurtful at times. I’m used to it, so I tend to let it roll off me, but it saddens me that I even have to. There are enough barriers, real or perceived, separating blind people from the “rest of the world”. There is no need to add another one. People with physical disabilities are still people, and they ought to be treated as such.

Small Injustices

Last summer, while I was riding the bus home from work, an older man with a walker boarded the bus, explained to the exceptionally grumpy driver that he had vision and hearing problems, and asked to have his stop announced. He wanted to be dropped off on 152nd street, I believe. When my stop on 149th street came along, I rose to leave, but was blocked by the man with the walker.
“Is this my stop, driver?” he asked in strongly accented English.
“What?” the driver demanded, sounding irritated.
“My stop? Is this 152nd street?”
“No, this is 149th street. Now move, this lady needs to pass by.”
“But…but I need to get off on 152nd…”
“Look,” the driver snapped, in quite possibly the most discourteous tone I’ve ever heard a bus driver use with anyone, “I announced your stop and you didn’t get off, so it’s your problem, not mine. Now get out of this lady’s way, it’s her stop!”. I was about to interject—I knew for a fact the stop had not been announced at all—but I seemed to be frozen in place. I was shocked at the driver’s rudeness, upset on behalf of this poor, confused passenger, and thus unable to do much other than stand there and gape. I’ve always had great respect for bus drivers, and didn’t feel quite prepared to begin questioning his authority on his own bus. As it turned out, my passivity was a mistake.
“I did not hear you announce it; I told you I have hearing problems. Could you guide me across the street, so I can catch a different bus?”
“No, I can’t, now move!”
“How long will it be till we are at Westmount station?”
“Not for another hour.”
“I can’t wait that long…what should I do…”
“Look, just. Sit. Down. I don’t really care what you do, as long as you stop holding us up. . You’ll just have to wait until we get back to the station; you can figure out your own way from there. Now, get the hell out of this lady’s way.”
The man sat back down with a forlorn sigh, and I moved slowly towards the door of the bus. My head was full of possibilities: should I call the man a cab? Should I offer to guide him across the street myself? No, bad idea. What if I messed up and got us both lost? The blind leading the blind isn’t always the best option, even though I did know the area quite well. So what on earth could I do? And, more importantly, did I dare?

Apparently not. Even if I’d dared to speak out, I was so choked with tears that I couldn’t have said much anyhow. I knew and understood that the driver couldn’t do much to help, but did he have to be so heartless? . I remember standing on the corner, waiting to cross, tears continuing to pour down my cheeks. I’d never felt so helpless, ashamed, and angry all at once. I was angry with the world, for having such harshness in it. I was angry with the bus driver, who’d handled the entire situation so roughly. Most of all, though, I was angry with myself. True, I could have done little more than give the driver the rough side of my tongue, but surely anything would have been better than standing by and watching it all happen right under my nose?

I remain frustrated with my utter powerlessness against small injustices which too often go unnoticed. I am, of course, especially hurt by those injustices which I myself could easily face in place of another. Watching someone with vision problems, among others, being treated so shabbily is beyond description. As separate as we often are from each other, many of the blind people I know feel a small measure of protective solidarity with each other, especially when mistreatment is involved. Watching someone being mistreated the way I have been, (and will be), is painful beyond words.

Sadly, I hear stories like this all the time. Stories like these are not the aberrations we’d like them to be. They are common, widespread, and indiscriminate. Most of the time, I only hear about them after they’ve happened (if I hear about them at all) and am forced to nurse my rage and frustration in silence and impotence. If you have any type of noticeable disability, it’s not if you will be mistreated, but when and how and by whom. Even if your disability is a result of normal aging, you’re very likely to face this kind of treatment at some point, no matter how lucky you are.

People commonly believe—whether they know it or not—that disability is a state of complete otherness. Those who don’t have noticeable disabilities tend to think that they are both separate from and invulnerable to disability of any meaningful sort. Unfortunately, none of us are invulnerable. Many of us have latent disabilities (like chronic pain, or mental illness, for example), and a few of us, like myself, have more noticeable disabilities. This noticeability encourages the idea that disability is some kind of obscure shroud that drapes itself around certain people, (never you, of course). That bus driver was probably thinking of the time he was losing because of that disabled gentleman, but perhaps he should also have been thinking of how he might be when he reaches that passenger’s advanced age. I hope that that bus driver is treated with more kindness than he has given; if he isn’t, it will be a harsh road for him.

When you see these small injustices, (and you will see them), I urge you not to choose the path of least resistance like I did. Do what you can to help, even if it doesn’t seem like you can do much at all. If you don’t do it for me, or for anyone else, at least do it for yourself: you, too, may become disabled someday. Last year, it was an anonymous old man. Today, it’s me. Tomorrow, it could be you. So if altruism isn’t enough, (and it’s okay if it isn’t), fight these small injustices, in the hope that someday, someone will be willing to fight for you.

The Delicate Art of “Blind Jokes”

We’re all guilty of making the odd insensitive joke, even when we know better. Most of the time, this is perfectly harmless, and the subject of the joke may even join in with relish. I’m one of these people: in general, I’m happy to laugh at (and tell) blind jokes, especially when I know they’ll be well-received. I have unintentionally shocked many an unsuspecting sighted person with the many blind jokes I make. I have heard everything from “Don’t talk about yourself like that!” to “I thought you were serious!”. Last year, a professor asked if anyone had described a particular object to me, and I replied, “No. I live in darkness.”. I, (silly me), thought that it would be obvious that I was kidding around. Apparently, I was just a little too good at the straight-faced thing, and he took me seriously. He seemed shocked that I’d ever joke about myself this way, but I’ve always found the odd joke to be very healthy. After all, the best way to rob hardship of its power is to reduce it to something you can laugh at. It’s how I get through life, most of the time anyway. Sometimes, (like when I run headlong into a wall or nearly get killed crossing the street), it’s a choice between laughing and crying. I’d rather laugh.

 

As with all good things, though, there are right ways and wrong ways to go about making blind jokes—at least if you’re dealing with me. Again, other blind people may not echo my views, so please keep that in mind. Today, I’d like to talk about the types of jokes I consider acceptable, and the ones I consider potentially harmful (with explanations, of course). This is a rough guide, so keep an open mind and a light heart as you read through this post.

 

The practical joke: I’m really, really not a fan of these. I suppose there are some that are relatively harmless, but I haven’t yet found one I found truly funny. These can range from the benign (stealing a plate of food out from under my nose), to the moderately irritating (disguising one’s voice to make me think you’re someone else—it never works, by the way), to the downright dangerous (warning me of obstacles that aren’t really there). Some say that intention is everything, and I subscribe to this when dealing with inappropriate practical jokes. I realize that many of these jokes were meant in fun, with no malice at all behind them. The line between bullying and joking around isn’t all that fine. Still, as I said, few to none of these jokes are really funny, and many of them are potentially dangerous. Think, for example, of what would happen if someone stole my cane and ran off with it: I’d be stuck without the tool which allows me to travel independently and safely, with no real way to get it back without chasing, which is in itself dangerous. Also consider how I feel when people try to disguise their voices to trick me: as I mentioned, this never works, and it’s more irritating than anything else. Amazingly enough, being told to watch out for a hole or tree that isn’t there isn’t what I consider a good laugh. In short, I’d advise against practical jokes, unless you are certain that the blind person you’re dealing with is okay with them. There is a big difference between tolerating them and enjoying them; pay attention to that difference.

 

Wordplay: This usually takes the form of, say, “blind stupidity”, or “See what I did there?” or “Did you *watch* that movie last night?”. These are silly, but not really harmful unless they’re being made constantly. I don’t often make them, (unless I’m deliberately trying to make people groan), but I don’t mind it when they’re made about me. They’re not very effective, but they’re definitely tolerable. Just watch (ha ha) that you don’t use them too often; anyone would get tired of that after a while.

 

Personal barbs: If ever there was a landmine in the world of blind jokes, this would be it. These jokes are usually tailored to the type of person who is their subject. Say, for example, that there is a blind person out there who has a lot of trouble with cooking on the stove; the heat frightens them, and they’re really insecure about it. Joking about this insecurity, especially if you aren’t all that close to this person, might be dangerous at best and downright mean at worst. Chances are that blind person is acutely aware of, and unhappy with, their inability to use a stove properly, so joking about it may only hurt them. Messing with a person’s confidence—sighted or blind—is always risky and seldom funny. If you’re going to make jokes like that, be damn sure that the subject is comfortable with it.

 

So, to sum up, be kind, and be careful when joking around. Jokes are meant to be enjoyable for everyone, not just the one telling them, so as I’ve said in previous posts, always act with respect. Get to know the blind person you’re joking with, and pay attention to their comfort level. Most of us are happy to set you straight if you’re open to that, but it’s always easier to learn first and tell jokes later, rather than extracting your foot from your mouth and apologizing. I’m a lighthearted person with a wicked sense of humour. There is very little that I don’t take well. Don’t feel like you have to tread on eggshells. Just be nice, and you should be fine.