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Life Unscripted

~ Living Life as I see it… or Don't

Life Unscripted

Tag Archives: videos

Do you See me with Vision?

26 Saturday Mar 2016

Posted by blindbeader in blindness

≈ 1 Comment

Tags

ambassadorship, blindness, comments, disability, perception, videos

Last week, the below video was shared in honor of World Down Syndrome Day. it is narrated by a young woman named AnnaRose, who has Down Syndrome, and the activities depicted are portrayed by an actress named Olivia Wilde, who does not. Only at the end of the video does one see AnnaRose herself, when she says |This is How I see myself. How do you see me?”

 

 

There seems to be two minds regarding this video, and in my opinion both are right. One is that it is important to look beyond the disability of Down Syndrome and embrace AnnaRose as a sister, daughter, or friend. On the Youtube video page, we learn that AnnaRose is a student, an employee, and an athlete. Her life is ordinary in many ways, so the hope is that you look beyond her disability and view her through the lens of humanity. She sees herself following her dreams, especially if they are impossible. She sees herself living an “important, meaningful, beautiful life”, and after all, isn’t that what we all want for ourselves?

 

The other train of thought is more about the visual depiction of AnnaRose’s life, her dreams and her goals. She says she wants to meet someone to share her life with, to be a sister, daughter, friend, to laugh until she can’t breathe, and to cry sometimes. But the video is acted by an actress who doesn’t live with Down Syndrome. This has left many disability activists with the sinking feeling that AnnaRose’s disability, and therefore a part of her identity, is being erased. In a world where disability is either fodder for inspirational feel-good stories or a means of discriminatory treatment, many people with disabilities want the public to see them openly living lives with Down Syndrome, or using a wheelchair, or accompanied by a service dog. Erasing disability is like erasing a part of one’s identity.

 

I first saw this video a week ago when it was first published, and honestly, it’s left me so conflicted. In my opinion, both schools of thought are absolutely right, and yet…

 

I am a woman with a disability. As such, I face many reactions from the general public. I’ve heard the sickly sweet tones of service staff talking to me like I’m a child. I’ve been told that it’s amazing and courageous that I’ve held over ten years of nearly continuous employment, heard the gasps of concerned protectiveness when I mention I enjoy running with my guide dog, or felt the need to fill the stunned silence when I mention that I have started up my own jewelry design business. Conversely, I’ve been told how sorry people are that I can’t see, that my husband is a good man for “taking care of me“, or that there’s no possible way that I can fit in in an office setting despite my work history proving otherwise. It would be a lie if I said these comments and impressions don’t affect me, because they do, no matter how I try and fight it. Not only do they affect how I see myself, they ultimately affect my livelihood and ability to be autonomous and self-sufficient. So, in a way, I want people to look past my disability, to allow me to make mistakes or succeed on my own merits as a woman, not just settle for “good enough” because of the perception that I can’t do any better because I have a proverbial scarlet D for Disabled tattooed on my forehead.

 

And yet, I have no desire to hide my disability. This is partly because it’s not possible for me, but it’s also because I feel like I need to live the best life I can – a vibrant, complex, nuanced, full life with blindness – in order to be happy and to embrace all of who I am. The comments and questions and seemingly constant advocacy aren’t ever going to go away, so as I see it, I have two choices: I can run and hide and let everyone else fight battles for me, or I can prove again and again that there is nothing shameful about being blind, and in fact it has its own advantages. To ignore my blindness completely is to ignore the one thing in my life that has made me as strong as I am while simultaneously bringing me to my knees. You wouldn’t expect a parent or spouse to hide the existance of their child or partner, and yet parenthood and committed relationships often change the lens in which we view the world. So why should anyone hide their disability just to make you more comfortable?

 

I want you to see more than just my blindness, to view me as a friend, an employee, an athlete, an entrepreneur, a customer… a human being. Talk to me, and anyone with a disability, as though your comments were directed back at yourself; realize that we are more than just people whose eyes don’t work or who don’t hear well or are unable to walk at all or without significant pain. We share your humanity, enjoy some of your hobbies, have opinions about religion or politics, have hopes and dreams and desires for our lives. But you don’t need to tiptoe around us, either. Don’t ignore our disability; it is still a part of who we are. In ignoring it, you are in effect not acknowledging the discrimination that we face and the pain and anger that engenders, and can’t truly get to know the completeness of our lives by truly celebrating our successes or picking us up when we’re feeling down.

 

Do you see me as a woman, with dreams for the future and hopes for tomorrow? A woman who likes watching hockey, loves running, and makes pretty beaded things? A woman who drinks too much coffee, loves the sound of a recent snowfall, and sings at the top of her lungs when no one’s around to hear her? That’s great! You see a big part of who I am. Do you see a woman whose eyes don’t work right, who puts labels on her canned goods in her pantry, who navigates the world with a guide dog by her side? A woman who is happy and content with her life, blindness and all, who wants to kick down doors and break down barriers? That’s another part of who I am. You can’t separate one from the other, and yet in a way I need you to. If all you can see is what doesn’t work (my eyes), then you’re missing out on a wicked Scrabble game, a loyal employee, or someone who will cause you to rethink your view of the world. And if you act like my blindness isn’t there, or is scary and uncomfortable, you’re ignoring a true reality of my existence. Put the pieces together, take them apart. See me completely, because I can’t envision myself as one person without the other keeping me company.

Not devoted to Blind Devotion

22 Saturday Aug 2015

Posted by blindbeader in blindness

≈ 6 Comments

Tags

blindness, independence, marriage, perception, relationships, trust, videos

I will be the first to admit that portrayals of blind people in books, movies, or articles tend to get my teeth on edge.  Contrary to what many might think I don’t expect a perfect portrayal of who we are, because we are all different, just like sighted people.  But perhaps even with the best of intentions, some of the worst stereotypes about blind people are perpetuated in these books, movies, or articles – that we are angelic inspirational beings for simply living our lives, that we require caretakers for everything from cooking to laundry to shopping, and if we do actually succeed at something it’s viewed as a miraculous feat tantamount to clearing tall buildings in a single bound.  These ideas are frustrating to those of us who live with blindness – and others’ perceptions of it – every day of our lives.

That having been said, few books, movie portrayals, or articles have concerned me quite as much as this video, largely because it’s been shared around the world as a “sweet tearjerker that shows what true love and “blind devotion” really is.

I’m leaving aside here the main character’s perception of what she can and cannot do as someone losing her vision; the anger and denial process are entirely normal, given a diagnosis like hers.  But the ending of the video infuriated me to no end.  It is viewed as sweet, and beautiful, and yet I find it ugly.  For those of you who cannot see (or just don’t feel like watching the video), this video ends with the husband following his blind wife to work every day without her knowledge.  We’re not talking about driving her to work, waiting in the car and watching her get in to a building before driving away; we are talking about physically following her on her walk to work every morning because (I presume based on the video) he doesn’t think of her as capable enough to do it on her own.  As a blind wife with a sighted husband, to me such behavior borders on stalking, and is not adorable and kind, but such a blatant abuse of trust that my blood is boiling even thinking about it.

Committed relationships (marriage in my case) are beautiful, messy and sweet and heart-breaking and restorative.  Relationships are not perfect, whether or not one partner has a disability.  Even if everyone disagrees on acceptable/unacceptable behaviors in any given relationship, I can think of no one who would disagree that trust is a foundation for any successful relationship.  It is one thing to stumble and fall, or be unintentionally hurtful, but to knowingly use your partner’s blindness or deafness to your own advantage – even while fooling yourself into believing it’s being done for their benefit – can shake a relationship to the core when your disabled partner finds out about it (and trust me, we’re not fools; we WILL find out).  Creating an admittedly fictional video as a feel-good look at what “true devotion” really is makes those of us living with blindness choke on the phony sweetness it’s meant to portray.  I have two questions for those who made, produced, and touted this video as sweet and romantic: How would you feel if your spouse went behind your back and, by their actions, showed the entire world – everyone but you – that they viewed you as incapable?  And what if you found out about it weeks, months, or years after the fact?  It isn’t so adorable and sweet now, is it…

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