Artist Statement
I
have had Tourette's syndrome since I was about 3 years old. My tics started off with me grabbing handfuls
of rocks in my backyard, sifting them through my fingers, then returning to
whatever activity I was doing. Now, my
tics mostly include finger twitching and making strange noises with my
mouth. Fiddling with string is often
involved. I have become so accustomed to
my tics that I sometimes forget how strange it actually is. I have met very few people who have
Tourette's Syndrome, even though it is a surprisingly common disorder. Reading the Cracked.com article "5 Ways Life
with Tourette's is Way Weirder than in Movies" helped me to see that not
only do other people suffer with the same things that I do, but others have
even worse symptoms, including self-inflicted pain and painful body
spasms. In creating my game, I wanted to
give players an idea of what it is like to live with Tourette's. I wanted to emphasize the involuntary nature
of my condition. Most people seem to
grasp the strange nature of my condition, but many have a hard time
understanding that a person with Tourette's syndrome is not consciously
choosing to say strange things and move their bodies in strange ways. In fact, I have had several strange arguments
about this very subject, and I included some of these conversations within my
game. Most of the situations in my game are based on my own personal
experiences or the experiences of other people with Tourette's Syndrome.
As
stated in Chimamanda Adichie's TED talk, if we continue to hear
the same stories over and over again, we start to believe them, and we inevitably have a harder time telling different
stories. She experienced this when a
critic claimed that her book wasn't "authentically African" because
the characters drove cars, ate food, and lived middle class lifestyles. I have a similar experience growing up with
Tourette's syndrome. Tourette's Syndrome
is constantly portrayed in the media as a disorder that causes you to swear
involuntarily. This is only one of many
different symptoms for Tourette's, but the media keeps returning to this
portrayal because this makes for easy comedy.
It completely ignores the majority of what people with Tourette's
syndrome actually experience. By telling
the same story over and over about Tourette's, most people begin to believe
that this is the only possible portrayal of Tourette's, and it makes it
difficult to change their minds. We need
to remember that there are multiple angles to approach a story, and there are
many stories that haven't been told yet.
If we're willing to empathize with someone and put ourselves in their
shoes, we will be able to learn so much more and break through existing
stereotypes and limited, one-dimensional stories.
Sources:
"I have Tourette's but Tourette's Doesn't Have Me", Ellen Goosenberg Kent, HBO, 2005.
Mannen, Amanda, et. all, "5 Ways Live With Tourette's is Way Weirder Than in Movies", Cracked.com, August 14, 2014,
"Research." Centers for Disease Control and Prevention. Centers for Disease Control and Prevention, 11 Mar. 2015. Web. 31 Mar. 2015.
Sources:
"I have Tourette's but Tourette's Doesn't Have Me", Ellen Goosenberg Kent, HBO, 2005.
Mannen, Amanda, et. all, "5 Ways Live With Tourette's is Way Weirder Than in Movies", Cracked.com, August 14, 2014,
"Research." Centers for Disease Control and Prevention. Centers for Disease Control and Prevention, 11 Mar. 2015. Web. 31 Mar. 2015.
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