WEBVTT

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[ Music ]

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<v Anita> Hi guys.

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<v Group> Hey!

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<v Anita> How's it going?

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<v Group> Good!

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<v Anita> Hi, my name's Anita.

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I'm a college student and a
full-time wheelchair-user

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and today I'm at the UW campus
interviewing people with disabilities.

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[ Music ]

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<v Anita> Carl, what is it like
to be a wheelchair user?

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<v Carl> I don't really see it as
much different than walking,

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although I have to make sure
things are accessible

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before going to them

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and some people on the street might
look at me like I'm different,

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but I don't see
myself as different.

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<v Katelyn> I have Myotonic
Muscular Dystrophy.

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<v Anita> And how does that affect you
in your day to day life?

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<v Katelyn> I just can't walk far
as a "normal" person can

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or I can't lift up
heavy things

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or I can't talk as "normal".

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<v Eric> I have Stargardt's Disease,
which is macular degeneration,

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which affects my central vision.

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So I have a blind spot
in the middle of my vision,

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so I use the outside
of my eyes to see.

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<v Anita> Calleese, what is it like
to have a learning disability?

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<v Calleese> I mean, it's
not really "like" anything.

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I know I struggle
a lot in school,

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and I can get
extra help on things.

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But it's more of-I don't
really tell people about it,

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and so when I do, they're just like,
"but you seem so normal!"

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And I'm like,
"well, what is 'normal?'"

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in their sense.

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Because I like to believe
that no one is normal.

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Everyone is, like,
special in their own way.

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<v Anita> Carl, what are some
assumptions that people

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may make about you?

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<v Carl> Some people may think that
because I'm in a wheelchair,

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I have a mental disability
as well as a physical disability.

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But that's not true.

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<v Anita> When you tell people
about your disability,

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what are some common
reactions you get,

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or faces and looks you get

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as you're interacting
in your day-to-day life?

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<v Katelyn> They don't really ask.

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They usually try to avoid me
in some ways, and give a weird look,

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like "oh, she's weird"
or "she's not normal".

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<v Anita> What are some
common reactions

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you get from people when you
tell them about your disability?

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<v Eric> I get, "oh, you're so brave,
you're so inspirational" a lot.

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Just because I can't see
as well as other people,

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they think that me
doing things on my own,

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walking across the street
by myself,

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they think that's inspirational,

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whereas if anyone else
were to do it,

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it would just be a normal
everyday occurrence.

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<v Calleese> I just have
a challenge and I don't...

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it's just something
I have to face every day

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which isn't bad for me actually
because I can work my way around it,

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and it made me
the person I am today.

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<v Anita> How does this disability
affect your interactions

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in day-to-day life?

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<v Eric> I don't think,
personally-for me,

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it doesn't make my interactions
toward other people different,

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because I treat everyone the same
as if I had normal vision

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and I try to be as approachable
and normal as possible.

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I'm pretty open about my disability
because I think if people know,

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then they're more likely
to understand

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why I do things the way I do.

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<v Narrator> The students featured
in this video

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are participants in the
DO-IT Scholars program,

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where youth with disabilities
prepare for college and careers.

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For more information, consult the Disabilities,
Opportunities, Internetworking and Technology

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website at www.uw.edu/doit

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Copyright 2016 University of Washington.

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Permission is granted
to copy these materials

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for educational, non-commercial purposes,
provided the source is acknowledged.

