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Nobody Told Me!

Emily Ladau: ...that my disability does not make me any less worthy as a human being

Nobody Told Me!

Nobody Told Me!

Business, Entrepreneurship

4.2671 Ratings

🗓️ 3 December 2022

⏱️ 33 minutes

🧾️ Download transcript

Summary

Many of us are fearful, confused and unsure of what to say and how to act around someone with a disability. On this episode, we’ll “demystify disabilities” with our guest, well-known disability rights activist, blogger and speaker Emily Ladau. She is passionate about getting nondisabled people to stop treating disabled people as a weird cross between precious gems and alien creatures.  She’s the author of the book, "DEMYSTIFYING DISABILITY: What to Know, What to Say, and How to Be an Ally".  Her website is https://emilyladau.com/
 
Note: This episode was previously aired.
 
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Transcript

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0:00.0

Welcome to Nobody Told Me.

0:13.0

I'm Laura Owens, and I'm Jan Black.

0:15.6

You may not realize it, but more than one billion people around the world are disabled.

0:22.1

Yet there are a lot of misconceptions about what it means to be disabled. Many of us are fearful, confused, and unsure about

0:27.7

what to say and how to act around someone with a disability. On this episode, we'll demystify

0:33.2

disabilities with our guest, well-known disability rights activist, blogger, and speaker, Emily LaDow.

0:40.0

Emily's work has been featured by the New York Times, CNN, and U.S. News and World Report, to name

0:45.8

just a few. She is, in her words, getting non-disabled people to stop treating disabled people

0:52.0

as a weird cross between precious gems and alien creatures.

0:56.9

She is the author of a new book called Demystifying Disability, What to Know, What to Say, and How to Be an

1:03.6

Ally.

1:04.5

Emily, we thank you so much for joining us.

1:06.9

Thanks for having me.

1:08.0

I am so excited to talk with both of you.

1:10.4

Well, we feel the same, and we what if you can tell us about your story and why it is that you're so dedicated to demystifying disability?

1:19.5

Absolutely. So I have a physical disability called Larson Syndrome. It's a genetic joint and muscle disorder and I was born with it.

1:29.8

My mother and my uncle, her younger brother, also have the same disability.

1:34.8

And you might think, oh, that's such a tragedy.

1:38.0

But for me, it's just a part of my life and part of what makes me who I am.

1:43.0

And because I have this part of my identity,

1:46.4

I am, as you mentioned, incredibly passionate about educating people, about the disability experience

1:53.2

and letting everybody know that it's part of what makes humanity so beautiful and diverse.

...

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