Clara recently found this very cool post (with hilarious title) on Tumblr and knew I would love it (she was right, obviously). While the concept is pretty good and the photos are quite cool it’s actually the title of the post that caught my eye. No, not just because it has the word “porn” in it. In fact, you might be surprised to find out that stairs and pornography actually have something in common–you just have to consider the origin of stairs. Please note that there isn’t any pornographic content in this blog so if you came here looking for that, we’re sorry to disappoint.
Author: Jeffrey Preston
Born with a rare neuromuscular myopathy, Jeff has spent his life dedicated to advocating for himself and others with disabilities. With a PhD in Media Studies from Western University, Jeff's research focuses on the representation of disability in popular and digital culture. Jeff is currently an Assistant Professor of Disability Studies at King's University College @ Western University in London, ON.
Kanye West cares about seizures, people!
There has been some buzz around the Internets (like here and here) about the new Kanye West music video “All of the Lights” and the potential for it to cause seizures. I guess the outcry was so loud that West eventually produced a “less intense” version. But when the story first broke, many of his fans on social networking sites like Twitter explained it was just a cool video and didn’t see why it was such a big deal. Being someone who loves bright lights flashing at dangerously high speeds, I decided to do some investigation of my own. Lo and behold, the video is a little intense on the eyes. Here, the phrase “little intense” being the understatement of the century.
Doin’ what you can
From a young age, my parents always encouraged me to focus on my abilities and not dwelling on my disability–wise words I still cherish to this day. Looking back on it now, I’ve discovered my parents had ulterior motives to these sage words, aiming not just to make me feel better about disability but to inspire me to overcome it. You see, my parents figured out something very important out when I was just a little boy: they realized that slowly but surely I would grow up and, like all kids, there would come a time when they wouldn’t be there to support me anymore and I would be left to my own devices. Rather than dwelling on all the unfathomable barriers I would face in my life, my parents decided they would do whatever possible to give me the best opportunity to succeed and put me in a place where I could care for myself.
Signs of the Times (repost)
For your holiday pleasures, here is a rambly blog post from a few years ago that Jeff wrote about semiotics and disability. Enjoy!
Million Dollar Blunder (repost)
This is an old article Jeff wrote that was published in the London Free Press back in his Undergrad. He was just looking around the site and realized it hadn’t been ported over yet, so he decided to put it back up again for your enjoyment.
This article was published in the London Free Press on March 8th, 2005. Publication of the article resulted in a flood of email from pro-lifers (including the Bishop of London??) who apparently missed the point of the article a bit…
We talk a lot about disability and language in Cripz, so to help get you in the Holiday Spirit, here’s a short writing assignment Jeff did during his Masters Degree on Foucault, Discourse and Disability.
New Episode of Cripz — Starring Role
A lot has been made of the fact that most disabled characters on television and in movies are actually played by able-bodied actors. It’s a particularly tricky question because while you’d like to believe casting directors aren’t avoiding disabled actors simply because they don’t think they can perform, it’s been noted by many in the industry that there is a perception that disabled actors are more “expensive” than those without disabilities. This is because, rightfully so, it takes longer for these actors to do wardrobe changes and sets now need to be fully accessible to accomodate the actors needs.
The frustrating part though is that in an industry focused on “the right look and fit,” disabled actors are type casted into playing disabled character…except they can’t get those roles for reasons listed above.
That’s where this week’s episode of Cripz is coming from, in the first of a three part holiday series entitled “Starring Role.”
OT Class @ UWO
Yesterday I faced the snowpocolypse to deliver a guest lecture at Dr. Klinger’s 2nd year OT Class on Representations of Disability and Media Activism. I’m pretty sure this is my 4th year speaking to the class and I absolutely love it–the students are so engaged and determined to make a difference in the lives of people with disabilities.
Keep up the great work, together we can get people moving!
My Body is a Cage (repost)
For your enjoyment, here’s an old blog post Jeff wrote back in the summer of 2007. Post-script: that show Family Guy TOTALLY ripped him off on the creed at the end, just remember wrote it first.
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Over the past few weeks I have been struggling with the concept of language, specifically in relation to “disability”. To me, the word “disability” symbolizes everything I’m not–lacking ability. Sure, I’m not the greatest at math, cannot sing opera and will likely never dance like Ricky Martin, something my “Guide to being a Manly Man” tells me is probably not such a bad thing unless I truly am living “la vita loca,” but really, is this different than anyone else? Everyone has limitations, no one is perfect…especially not Ricky Martin.
But, irony raised its cruel and vengeful head this week when it came to be that time of the month. Yes, that period we all experience where we are force to suffer through obscene discomfort and frustration, which, we’re told is “only natural” and “ultimately for the best.”
Now usually I don’t loathe the standard wheelchair tune-up, but this month proved to be particularly bothersome as my chair required some extra special attention after it had a minor run in with a certain form of transportation that is not the most…accepting…of “differently abled” individuals. I don’t want to name names or point fingers because that’s not the point of this entry, but, lets just say if the powers that be wanted me to fly they likely wouldn’t have put me in a wheelchair…or at least would have provided me some wings…or a rocket pack.
So because this was gonna be a day or two to deal with, Shoppers Home Health Care offered me a loaner chair so that I wouldn’t be completely immobilized for an entire day, left to the whim of gentle strangers and friends who may be around to graciously transport my little crippled body around the apartment.
While it was a nice gesture, don’t get me wrong, this loaner chair turned out to be a little bit of a disaster. This shouldn’t be too surprising, as it is just a loaner chair after all, but the experience I had while using this loaner chair was something pretty remarkable.
For one of the first times in my life…I felt disabled. It was almost like my brain had been scooped out of my body and plopped down into the body of a perfect stranger…a stranger who walked funny and had about 150lbs of extra junk located inside their trunk. Navigation was nearly impossible as the loaner chair drove differently than mine along with being significantly wider and longer. The results were humorous, albeit regrettable for my apartment walls and door frames. Truly, for that day my substitute body was a cage and contrary to what The Arcade Fire may tell you, my mind certainly did not hold the key. No matter how hard I concentrated I just couldn’t get the hang of it–instead I just looked like I was drunk…which I guess is okay, it helped me blend in with the other University of Western Ontario students.
No, instead of figuring out how to drive the chair, my mind spent a majority of the day yearning for that warm, comfortable consistency of my old body, my old chair. I felt like an amputee, mourning the loss of his favourite limb or like a junkie craving just one more ride on the white pony. I needed my fix and I needed it bad! What I realized is that my chair, which I’m comfortably lounging in as we speak, has truly penetrated me deeper than I could have ever imagined. It has become an intimate part of my life, a part so deeply intertwined with my identity that I don’t feel quite complete without it and actually yearn for it when it’s taken away from me!
I know I shouldn’t be saying this and disability theorists everywhere are probably pulling out their hair screaming “PEOPLE FIRST! PEOPLE FIRST LANGUAGE! THE MACHINE DOES NO MAKE THE MAN! I’M GOING TO KILL YOU PRESTON, I’M GOING TO KILL YOU DEAD! AHHHHHHHH!”, but I think there is really some validity to the statement that my wheelchair has had a profound affect on me over the past few years that I have used it, in the same way that I have had a profound affect on it. Oh yes, this is not a one way street and I think that’s where the power of it all comes from. No, the chair does not make me who I am, however, it is a part of who I am, possibly one of the best parts, and I don’t think there is anything wrong with that. In fact, I urge all you adaptive technology users out there to proudly show and respect your equipment!
So sing it loud and sing it proud. The Marine Corp wrote this little ditty to train killers, but with a bit of modification I think it becomes a nice little ode:
This is my wheelchair. There are many like it, but this one is mine.
My wheelchair is my best friend. It is my life. I must master it as I must master my life. My wheelchair, without me, is useless. Without my wheelchair, I am useless. I must drive my wheelchair true. I WILL…
My wheelchair and myself know that what counts in this life is not the batteries we fry, the noise of our burnouts, nor the tire tracks we make.
My wheelchair is human, even as I, because it is my life. Thus, I will learn it as a brother. I will learn its weaknesses, its strength, its parts, its accessories, its controls and its tires. I will ever guard it against the ravages of weather and damage as I will ever guard my legs, my arms, my eyes and my heart against damage. I will keep my wheelchair clean and ready. We will become part of each other. WE WILL…
Before God, I swear this creed. My wheelchair and myself are the defenders of independence. We are the masters over immobilization. WE ARE THE SAVIORS OF MY LIFE.
New Episode of Cripz — Harry Potter
Another fresh offering over at Cripz: A Webcomic, this week featuring a parody of the recently released movie, Harry Potter. I have to admit, I was never a real fan of the Harry Potter series, struggling to make it through the first 3 books before ditching them to re-read Lord of the Rings. Having said that, I understand why people love them so much and the movies are definitely well done and, above all, entertaining.
While the series is, of course, based in fantasy, I’ve always been left wondering where all the disabled wizards are? None of Harry’s classmates have physical disabilities and, aside from perhaps Luna, don’t appear to have social or intellectual limitations either. I guess it’s for the best though, considering all those stairways at Hogwarts. This week’s comic is really about that, the lack of access in schools, because it’s not a problem that just affects the fantasy world of Harry Potter. Right now in Ontario, there are tons of schools that don’t provide access for students with disabilities and school boards that relegate all students with disabilities, regardless of their intellectual abilities, to Developmental Learning Classes.
We need to do better and one of the easiest ways we can help the disabled population right now is by empowering our youth to get educated. Now is the time to make education accessible to everyone!