Posts Tagged ‘Black’

Young Gifted Black & Disabled – Unmasking Masculinity

Wednesday, December 29th, 2021

On a dark and light orange background with water droplets, lays a white mask with the right eye whole cut out down to the nose. Starting on the outline of the nose is the word "Unmasking" in caps and below that is the word "Masculinity".

Only one way to conclude this first season of Young Gifted Black & Disabled. The original YGBD brothers;
Headshot of AJ Murray Co-producer, AJ Murray
D'arcee Charington - a dark skinned black man with blonde dreads and a black grey coat smiling at the camera. D’arcee Charington Neal
are back!

Our O.G’s join me to take the mask off masculinity and see what’s behind it race, sexuality, gender norms, the patriarchy and of course disability.

We considered releasing this as two separate episodes, but settled for one. Coming in at slightly over 43 minutes, longer than your average RMM Radio episode, we hope it sparks some conversation.

Content/Trigger Warning
This episode does contain adult language, references to sex and traumatic situations. Please be advised.

Reid My Mind Radio will return in the first quarter of 2022! Until then, please be sure to subscribe to the podcast on your favorite app, to assure you don’t miss an episode.

Wishing you all a very happy holiday season and a healthy and prosperous new year.

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Transcript

Show the transcript

— Music begins, a cymbal crash launches a calm ambient melody which leads to a smooth Hip Hop beat.

Siri:

Ready to send it?

TR in Conversation with AJ/D’arcee:
Yes.

Siri:

Ok, sent!

TR in Conversation with AJ/D’arcee:

Aaight, cool!

You don’t know about Black Siri?

D’arcee:

… No!

TR in Conversation with AJ/D’arcee:

Aaight, hold on, let me have Siri say something.

Hey Siri, what time is it?

Siri:

2:09 PM.

D’arcee:

Stop! (Extended so Pronounced, Stoooooop!)

(Thomas, D’arcee and AJ all laugh…)

TR in Conversation with AJ/D’arcee:

That’s the blackest it’s gonna get, but that’s Black Siri.

D’arcee:

Oh…. I’m dead….

TR in Conversation with AJ/D’arcee:

If you go into the Siri settings, it’s Voice 3.

D’arcee:

I’m about to change that shit right now! Woo hoo!
TR:
! that really is a thing y’all!
Apple added some additional voices for Siri.
And voice 3 is a Black Man.
That reaction you heard is common.
At least in my experience specifically among those who are Black.
The laughter, was excitement.
Maybe you’re thinking, why would a Black Siri voice matter?
Well, Black voices matter!
Secondly, , please go back to an earlier episode in this series featuring Lateef McCleod for a much more detailed explanation.

Simply put, voices matter, representation matters.
If it doesn’t to you perhaps you’ve always been represented.

If this is your first time here and you’re not familiar with my voice, I’m Thomas Reid, producer and host of this podcast.

You’re just in time for the final episode in the YGBD series or
Young Gifted Black & Disabled.
This all began with an episode I co-produced last year with
Mr. Ajani Jerod AKA AJ! ;
— Sample AJ from “AJ Scratch” Kurtis Blow

A Reid My Mind Radio family member and alumni.

And it seemed right to team up again to close the series.

Since that last production in 2020, AJ caught me up on some of his personal and career highlights in 2021.

Among several positive highlights in his acting career, AJ has a role in a film released this year, Best Summer ever, which garnered a fair amount of attention.

He’s working in a new position that gives him a chance to really flex his creative muscles and advance opportunities for people with disabilities.
And join me in congratulating AJ as a new homeowner!

TR:

Having a job or even better, a career,
providing shelter and safety for one’s family;
in the minds of men, these are a few things impacting how we define masculinity.

Before we get into it, I need to let you know,
we talk about some things that may not be appropriate for young listeners and possibly triggering for others including sexual content and trauma.
The conversation covers a range of emotions. Yeh, real men have those!

— Reid My Mind Radio Theme Music

TR in Conversation with AJ/D’arcee: 04:07
So let’s jump into it then, man. So you good AJ?

AJ:

Yeah, I’m good.

TR in Conversation with AJ/D’arcee: 04:07

We’ve all been here before. So we just gonna kind of keep it pushing. So brief intro. name, image description, D’arcee, do you wanna kick it off?

D’arcee:

Sure. So, my name is DRC Cherington Neil, I am a dark skin black man with purple dreads and a shaved head in various shades of purple. And I am currently sitting at my desk in my apartment, and I’m wearing a gray t shirt that says love is equal.

TR in conversation with AJ and D’arcee:

Professor Purple!

TR:
He’s an ABD Doctoral student, meaning all but dissertation or he’s almost done!

We could have went with a royal theme for this episode as AJ wore a purple shirt.

I figured it made sense to go with Black. Nahmean!

TR in Conversation with AJ/D’arcee:

so DRC, how do you sort of qualify masculinity?

D’arcee:
There you go starting with the life altering. I mean, if you had asked me that, like 10 years ago, I think my answer would be wildly different. Because I think, people, the answer to that question is literally dependent upon their own experiences. And I think so much of that experience is tied to age.

If you ask a 16 year old what’s masculinity, they gonna get you this bullshit answer about cars and sports and girls.

all sports ball is the same to me. I will say I don’t care about no cars, but my electric BMW begs to differ..

I honestly believe that being a queer person informs this more than being a straight person, y’all can tell me I’m wrong. But as a man who loves other men, it radically redefines your understanding of what it is to be masculine.

TR:

Woh! I can just imagine the reaction of some people to that statement. But I think if you’re going to explore the definition of masculinity then you have to be open minded and hear people out. No matter where it comes from.

D’arcee:
it’s like that whole phrase, we say, in the community, masc for masc, it’s the word masculine, M A S C.

It’s a toxic ass phrase, that basically means traditional masculinity need only apply.

People, expertly weaponize this phrase of masculinity, to mean “traditional” six pack, square jaw, scruff, kind of masculinity.
What you’re talking about is the flavor of masculinity. All forms of masculinity are value. And that includes trans masculinity too!
Folks want to try to come for me on my DMs I said what I said.

TR:
D’arcee can handle himself. But this is my house and I feel accountable and protective of my family. So be advised, you come for him you coming for me.

Too much? I’m trying to be a better man, my daughters help point out my toxic masculinity.

I hope that didn’t come across violent, but if you have issues that’s your problem. No need to share them.

AJ:

I guess when I think about masculinity, I think of strength in terms of not only physically or spiritually, being able to hold it down and always be accountable and always there to always ever serve.

If I can get into some stereotypes, when I think of masculinity, of course, I think of ego, being braggadocious. Being athletic, not having a job.

TR:

Well, AJ raised the issue of stereotypes, let’s just put them on the table.

AJ:

The negative stereotypes of black man is lazy. Good for nothing.
You get into the historical stereotypes like studs, Black man is in jail, or black men aren’t gonna take care of the kids.

D’arcee:

I think that people associate Black men with rage, gangs and violence.

A lot of people think of black men as being ultra conservative.
I don’t mean politically. Behaviorally, very inflexible. This is where black homophobia comes from.

A lot of it comes from black men. And the stereotype of inflexibility which, in turn gets translated into strength. In this weird, warped way.

There are some positive ones too. People think of black men as being stylish. They think of them as being very well dressed. But that comes with the side effect of they think of Black men as flashy.

AJ:

When you say that I think of that episode of Living Single, when Kyle, I think he was a mutual funds manager. This other brother really had issues with the twist of his hair. I thought that was a very good episode, because it shows the internal struggle
[between us and other black people.
]
Because it wasn’t the white bosses, it was the other brother on the team that told him to cut his hair.

D’arcee: 55:57

I’ve been in that situation. And it was extremely uncomfortable.

When I worked at the University of Maryland, I worked the front desk in the English department and the chair, this white woman she walked in. There were two black faculty standing in the doorway when she walked in.

It was the last day of school and I had just cut my hair.

I’ve had dreads for most of my adult life in various ways. And they had never really seen me without dreds , because that’s a years long process.
Oh, she said, you got your haircut? And I said, Yep, I did. And then she said, you look like a grown up now.

The black faculty in the door, were like, Oh, it’s a third rounder, she was like, what? Oh, come on, like, you guys know what I mean?

AJ: 57:07
Back in the day. I had longer hair. So I had braids, because I was trying to get my swag on and that way.

This one lady, she was a black woman. And she wasn’t necessarily talking to me, but I had heard the conversation and she was saying that her son also want to braid his hair. But she was like, I’m not gonna let him do that. She was talking about the gang Association and how, having hair like that was bad. And I don’t know if she didn’t notice, but I was like, I’m right in here. And I felt so sad. Because just because I have long hair, and I had these braids, but I’m a student. I’m respectful to you. I’m on the honor roll and I have braids, but you associated braids or longer hair with thuggery.

D’arcee: 58:24
You can’t be surprised you know, you invisible

TR:

That’s the thing, Black can make you invisible in many ways.

For example, shows like Friends or Seinfeld. They took place in New York City and there’s no interaction with Black people?

The way white store workers ignore Black people. I’m telling you, we even here, oh I didn’t see you.

If they do land eyes on you, sometimes it’s the stereotypes that are seen. So you’re followed in that store because they see a criminal.

Add disability and that introduces a new layer of stereotypes and invisibility that occurs within our own community as well.

AJ:
When I think of masculinity from societal speaking, maybe some stereotypes, I think, definitely non vulnerability, he can’t be vulnerable at all. You definitely can’t cry at all.

How many songs I heard…

— Audio quick mix of;
“- I Heard it through the grapevine”, Marvin Gaye;
“I know a man ain’t supposed to cry…”

“Tears of a Clown”, Smokey Robinson & The Miracles;
“Now if there’s a smile on my face, it’s only there trying to fool the public…”

“Ain’t to Proud to Beg”, Temptations;
“Now I heard a crying man, is half a man, with no sense of pride, If I have to cry…”

AJ:

I missed that meeting, because the brother cries all the time.

No sensitivity, you keep very serious things to yourself. He can’t show any weakness at all.

You kind of have to know everything and be the jack of all trades.

D’arcee:
Yeah, because Dude, don’t ask for help.

AJ:

If you have children, the males are definitely the disciplinarians.

D’arcee:
Is that true and black households? Because I would definitely not agree.

AJ:

Yeah, yeah. It was my mom, because my mother was the primary razor.

I just mean how many of y’all have heard? wait until your daddy gets home?

D’arcee:

I think that what you’re talking about is physical discipline because like my mother was not the person, my daddy did that

TR:

My mother occasionally used that line on me, but she was the physical disciplinarian while my Dad never raised a finger.

The threat meant I’d have to sit through a 45 minute lecture from my Dad. My sister and I would often debate whether we’d just prefer a beating.
And just in case you’re curious, when it comes to discipline, I ended up just like my Dad! And my girls not only appreciate it but I think they turned out great! Hash tag stop corporal punishment.

TR:

So far, we’ve been talking stereotypes about Black men.
But what does that look like in the real world when we add disability?

D’arcee:

This is exactly what my research is. I study like black culture, but what happens when you add disability to it?

When you talk about blackness disability together the association is so terrible. And it’s, it’s this right here. It’s the core of this right here, because people already associate negative things with blackness. And when you add disability on top of it, that just amplifies the feeling.

AJ:
I remember one time me and a partner who’s also disabled. We’re sitting outside because we got dropped off for the bus. So we were just hanging out, and it was on the sidewalk. This older lady is riding in her car. And she just gets out of her car and gives us hot wings. Hot wings and a Pepsi.

D’arcee:
AJ I completely understand what you’re talking about.
All of the work that I’m doing now it’s an amalgamation of all the experiences that I’ve had that are like this, because it just kept happening.
And I literally was like, why does this keep happening to me?

Obama was coming to our building. And I got really dressed up because they told us we had to. I was in the three piece suit.
[Says emphatically, while clapping his hand to stress the point.)

TR:

You know one of those days when you just sort of feel like, why did I even leave my house? For D’arcee, it began with the access bus driver’s back handed compliment, “You’re looking too sharp to be in that wheel chair. Really?

D’arcee:

I left work that day, went home, and went to the 7 Eleven. I wanted a gallon of milk and some honey nut cheerios, because that is the best cereal on planet Earth.

TR:

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D’arcee:

And grabbed a thing of White Castle burgers because they was calling my name.

TR in Conversation with AJ/D’arcee:
We gonna have to work on your diet, bro.

D’arcee:
this woman in front of me, she paid for her stuff. But she didn’t leave the store.

And she kept eyeballing me. And I was looking at her and she was looking at me and I was looking at her and she was looking at me.

I was like, right, so she didn’t want to get out the way.

I was trying to swipe my card and she moved my card out the way and just literally handed me a fistful of cash.

I didn’t know what to do. I’m in a three piece suit. Wearing my Fedora. My Houndstooth jacket, looking very DC policy.

I was like, Oh, thank you very much. But I’m good.

Then the door opens and this random man comes in. He’s like, Yo, did you pay for the man’s groceries?

So they had concocted this plan while I was going around the 7 Eleven picking up food. And I had been oblivious to all of it.

I swiped my card, got my groceries and left and didn’t say anything to her. And so she literally, she followed me outside. And then she was like, why don’t you take my money?

TR:

Charity, it’s often not for the so called recipient.
Once, someone accuse me of “blocking their blessing” because I refused their help.

I guess the real issue is often, how we’re perceived is ultimately out of our control.

D’arcee:

that was the reason I was talking about my suit. Because people literally don’t know how to conflate these two things together and everything to do with being a man.

AJ:

My mom actually knew an able bodied man, I think he was a comedian.
He got himself a wheelchair, and he would just sit downtown in the chair. His side hustle was he pretended to be disabled to earn cash. Chair

TR:
Ah yes, I’m reminded of the ol’ you’re faking your disability trope.

Another way we’re perceived by the public.

— Music begins, a thumping upbeat dance track.

D’arcee:

I will never forget. Oh, God, I was at a club.
I was there with my friend because she wanted to go.

I’m not big on clubs, but she dragged me there. It’s a dance club. fuck am I gonna do?

The club feels like it’s one of the worst places in the world. It’s a microcosm of every ableist fantasy on display at all times. If you not a ten, you’re not supposed to be in there. But like, people will bring you in there anyway, because they need entertainment.

TR:

Left alone while his friend goes off to dance with some guy,
D’arcee is approached by a woman.

D’arcee:

She was like, hey, and I was like, Yo, what’s up? And then she was like, she was like, Come on, let’s go to the dance floor.

TR:

D’arcee offers his hand, which she takes and pulls him in his wheelchair to the dance floor.

As they’re passing the bar, the bartender calls out to D’arcee.

Bartender:

Yo! Somebody paid for you to have this drink.

D’arcee:

Oh, wow, thanks. And I took the drink and got ready to drink it. And the girl was like, no. And she slapped a cup out my hand, knock the whole drink on the floor. And I was like, what.

She was like, I saw dudes put X in that. They just wanted to see how you would react.

That was issue number one, that people already knew that I was out of place in this location.

TR:

When they finally reach the dance floor, the woman is grabbing’ on D’arcee. Then she leans over and whispers in his ear.

D’arcee:

I want to make my boyfriend jealous.

Oh, wait, what? Wait.

her boyfriend was on the steps like mean muggin’ as fuck. And I was like nah, nah, nah, I’m not feeling this. And so I left her.

AAJ:
One time I was at this club and I wasn’t exactly in the exit but I was in that direction. So this lady it was a beautiful lady but this lady she’s headed out the club but she looks at me and stops before she leaves So she turns around, bends over and shakes it for me. I’m like, okay, which I’m not gonna lie. You know, I don’t know if this is wrong, but I appreciate it.

TR in Conversation with AJ/D’arcee:

Ain’t nothing wrong with appreciating that.

D’arcee:

I mean, but also why though?

AJ:
I think she assumed, this is something he doesn’t get,.

I was at this other club. It was this man and his girlfriend or his wife and we were dancing.

He turns her around. and he’s slapping her butt, for me.

TR & D’arcee together in a questioning voice….
“Thank you?”

— Slow Transition moving to a more serious vibe

D’arcee:
you can bleep all of this out to remove it all. I don’t want to be rude. But I also want to be real on this because people deserve it.

In the queer community, people associate masculinity in sexuality, and it causes real problems for me, because I have been in a number of situations where I’ll be hooking up with a dude. And then he will assume, because it’s like, you know, I’m a man, and you’re a man that we came here to fuck. So like, that’s what we’re doing
. So the thing is you don’t even ask my permission.

I’m still trying to decide if I want to call it assault, because I don’t know where it falls on the gradient.

We haven’t had any kind of discussions about what we were gonna do. I had at least five dudes do this to me.

TR in Conversation with AJ/D’arcee: 1:34:58

Wow!

D’arcee:

If you decided to keep all that I know people gonna be listening, they’re gonna be like, wait like, is he talking about rape?

I’m talking about consent, consensual, you know, hookup, or, you know, relationships we met to get it in and half the time.

TR in Conversation with AJ/D’arcee:
I feel like sisters would be like, bro, we this is what we experience. And so is that I don’t want to do like a disservice. You understand? I’m saying, and I’m not trying to tell you what your experiences at all. But man if we flipped it…

— Reverse slow Transition.

— Music Begins, a bouncy up-tempo, high energy Hip Hop beat!

“Forgive me Sir, but there’s something I’d like to ask you.”
“Yes.”
“Well, I don’t know how to say this so I’d better say it in the shortest way.”

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Now back to the episode. ———-

AJ
I’m not trying to say because of my disability and your disability is different. But sometimes, I wonder, do you think, the things that you explore and are open about, do you think you would have those same opportunities, if your disability was more significant?

I’m a person that wants to be very sexual. I wonder, like, if I were a little more mobile, like you are, like a transformer, what I have an easier time getting down?
Do you think people perceive you as sexier versus more of a person with a more significant disability?

D’arcee:
Sure. I will say, first of all, that I recognize this is a question of privilege. And I most certainly do have that privilege.

The fact that you and I both have cerebral palsy, we both know that it manifests so differently in every person’s body.

TR:

We could replace CP in this part of the conversation with vision loss, hearing loss or just Go ahead and insert your favorite disability.

There are restrictions and privileges that come with any degree of disability
no matter where you fall on the spectrum.

But that’s not necessarily how it’s always viewed.

D’arcee:

They say wheelchair users sit on the top of the hierarchy of pretty. And by wheelchair users, they really mean like paraplegics and you know, people who look otherwise quote, unquote, normal, but in a wheelchair,. For all intents and purposes, you basically are normal, which is that it’s such a horrible, insidious way of talking about somebody’s body, but people are doing this.

TR:

It starts early.

D’arcee:

in middle school, we talked about sex constantly. Just being disabled didn’t preclude me from that conversation. But it did put it in a different light, because they were all like I’m doing X and X. And X was such girl, even if they weren’t just complete full of shit.

But at the same time, there’s this extra added layer of like, but at least they could. Whereas you know, you can’t.

AJ:

In school, a lot of people thought I was down and cool,
But when it came to the discussion of sex,
anytime I wanted to be included in the conversation, they were shocked, like, AJ?

Like, what am I a patron saint?

I’m a teenager just like you guys, right? I want to just like yell, but people were shocked is if it’s something I’m not supposed to do.

D’arceee:

I remember one of the worst days ever.
This dude Mike. He was Like, why do you have Aliyah on the front of your binder?

To the whole class he was like, huh, we all know that if you do jerk off it ain’t nothing but air. And everybody was laughing.

AJ, to your point, people think that it’s fine to do it at your expense because you’re disabled. And they literally are like, Well, you’re not going to have sex anyway. Who cares if you’re a man who wants to, you’re not going to do it. So you know, it really doesn’t matter. This is why they exclude you from conversations.

TR:

Occasionally, you get a sense of what the conversations are like when you’re not there.

D’arcee:

I was playing Xbox Live with a bunch of gay men. It was like 12 of us in this group.
We were talking about the club. I was like how difficult it is to be in the gay club.

This dude named Ben, who is in Portland, Oregon , said, I’m gonna say what nobody else wants to say.
Nobody wants you in there. You’re not welcome in there.
Honestly, I would throw myself off a bridge. Living your life is terrible. If I saw you in the club I might give you my number, but if I did, he said it would be with it when the lights are out where no one can see it.
I was so mortified. And I literally, and there was 12 people on this call, and nobody stood up for me. Nobody.

AJ: 1:52:38

I’m sorry that’s really upsetting to me. And I’m stopping myself from crying because they’re just disgusting.

But that’s what a lot of people think about disability. Disability is tragic, disability is ugly. Disability is seen as unmasculine.

There’s a lot of physical things that I can’t do. For instance, I’m an older sibling. But in a lot of ways, because I need so much help. I feel like my sisters are older than me.

I can’t be the big brother than I want to be.

my mom was a single mom, so sometimes I felt like I couldn’t necessarily help cleaning up. I mean, I certainly know now that you know, I have to change things and the way I look at work is different from when I was little, but it was hard.

TR:

Those adjusting to blindness or disability in general can truly benefit from reexamining things in our lives that affect how we view ourselves. Our career, family roles and responsibilities, the formidable loss of a driver’s license for example.

Reinventing ourselves isn’t exclusively a masculine trait, This conversation has me wondering, what is?

AJ:

I have male friends but my closest friends that I have are female, my strongest connections.
I noticed, I’ll be a church and like men would be talking and joking. And so when I would come around, for some reason, conversations would stop

D’arcee:

Disability is for many people the personification of a nightmare.

If I’m just gonna be 100 honest about it, I think that the bottom line is that most men feel uncomfortable. Because, men are not socialized to be caregivers. Men are not socialized to be emotional. Dealing with a person with a disability, you have to embody a level of empathy.

Men are socialized differently than women. Women are socialized to not seek their own pleasure. Men are.
TR:

We’re in a very new time today, men are encouraged to seek therapy. Expressing emotions and discussing feelings isn’t as frowned upon today. Yes, there are still a bunch of proud cavemen out there, but there’s been some real progress compared generations like my own, Generation X and those before me like Boomers.

AJ:

I’ve heard so many stories about men from that generation. I just feel bad. Yes, they were mean and harsh. But then also, could you imagine, like, the weight and the unpeacefulness, , the chaos that’s in your heart and brain because you have to carry this anger. If you are a black man, you had to deal with being belittled and berated as a black man being called boy.

it’s so it’s like, not you can express that anger, though. But the only way you’re going to is because of the mask would be we thought, you know, be either put my hands on my wife, or beat my children.

D’arcee:

look at these white people trying to tell me that like critical race theory, and like horrible and terrible, and
every single time like somebody tries to tell me that like slavery was a million years ago. It’s not that big a deal. I literally turn around and say my grandfather, my dad’s dad saw men hanging in trees in Alabama when he was six years old on his way to school. That is not the Civil War.

TR:

That socialization starts as a child.
How we as a society raise our children.

D’arcee:

I saw a tweet where somebody wrote, his four year old son came to him and said Daddy, I told the girl in elementary school that I liked her. And she said, she didn’t like me back. And he was like, What do I do? And he was crying. And the dad said, well, I think you know what to do.

The sun responded and said, Yeah, I know, try and try again. The dad said, No, that is not what you do. He said, she told you what the answer is, so you respect her wishes.

TR:

Wait, what?
Isn’t that what we’ve been taught?

AJ:

I think with men and I know myself sometimes there’s been a little bit confusion, because no doubt if a woman says no, that is true.

I hear stories all the time, even in terms of the Obamas, if you listen to their story, Mrs. Obama was like the boss, over a team or whatever. But remember that she did say, she didn’t say no. But then he was like, he was so doggone persistent.

When I say that, I’m not saying you just get a free pass, just to like, be aggressive. And don’t listen to the woman.

Persistence has shown, you do land a woman if you’re persistent.

D’arcee:

Women aren’t to be landed.

AJ:

I didn’t mean it like that.

D’arcee:

And I’m not talking about you specifically, in general men typically believe that it’s a conquest. If you want to talk about the route of masculinity it’s a conquest.

AJ:

That sort of takes the whole idea and the premise of the chase.

I even heard women say, it is the man’s job to chase. I don’t want to chase the man.

They want aggressive men. I’m not talking about rape or violation, but I’m just talking about the nuance.

D’arcee:

all of this comes down to the idea of what people think of as natural, which is, men pay for dates. Women get dressed up, women look good for the man. That’s your natural. And people are starting to undo all of that.

I honestly believe that if the internet was around in our parents, most of them would not be together.

TR in Conversation with AJ/D’arcee:

When I say natural, though, I’m going back even further. Go back to Hunter Gatherer.

D’arcee:

Yes, it’s primal.

Every time I hear that argument, I think, but that’s American. The argument behind that comes from Adam and Eve. And the question of subservience and the idea that man said in the beginning, that he was going to lord over Eve and that she is one of his ribs.

TR:

Perhaps the behaviors are learned.

D’arcee:

we have to teach boys about the patriarchy, we have to teach boys that the entire history of the world. And the way that it runs now is built upon the desires and the whims of men.

AJ:

I would just say we can open up masculinity, to include being vulnerable, we can open up masculinity, to include expressing your feelings.

D’arcee:

So we really do need to undo this whole argument from the beginning. And I’m not saying that like, that means that oh my god, gender norms fall by the wayside. But the whole points are bullshit to begin with.

TR:

Thinking about gender norms brings me back to some of the stereotypes we discussed earlier.

In fact, we get back to the issue raised by AJ.

AJ:

I have a lot of friends ,when it comes to like dating or actually, you know, getting down with somebody. It’s a no, and I’m wondering if now it could just be my fault. It had nothing to do with disability.

For instance, I really liked this person. I would call her because I know that she was getting off work, and on her way to the train.

One time when I called her I was like,

I’m calling you, because I know you just got off work. I just wanted to talk to you while you waiting on the train? She goes, Oh, isn’t that precious? And I’m like, precious.

AJ:

I saw Tiffany Haddish in a stand up.

She was like, I started sleeping with this dude, he had a disability. She said, Don’t sleep on disability because he was really working it. Something I just appreciate it so much, because there was nothing timid about them screwing. It was like we’re having sex and I’m slapping your booty. And I’m a disabled man. And at the end, she was like, disabled people want sex too.

TR in Conversation with AJ/D’arcee:
So here’s what we got to start. You said slapping your booty change that shit to slap in that ass and let’s see what happens bro. We gonna start there.

AJ:

I happen to be friends and very close with women.

A lot of women, including my friends, had been violated. And so that’s always been in the back of my mind.

I think I’m so concerned that maybe I go to the extreme, because I’m always worried about being a gentleman and making sure that women are comfortable around me.

TR in Conversation with AJ/D’arcee: 2:39:04
that starting point for you is just like whoa.

That doesn’t even need to be in your mind in terms of being someone that’s gonna assault.

You have so much room to play with because you’re nowhere near that. but it has nothing to do with in terms of your level of confidence and what you put out.

D’arcee:

AJ, people don’t call me adorable. I don’t present myself that way.

If she said oh, how precious is because she misunderstood your intent. As a person who literally studies rhetoric, that’s the work of art. rhetoric. It’s intent.

Attractiveness, they say is only half about looks. The other half of it is actually psychological. Because I know that I have been very attracted to people that are not pretty. And what makes me attracted to them? Oh my god, I love their personality.

AJ:

one time, I met this girl and let’s just say she was very energetic towards men.

She was in my drama class. It came up in conversation that I never been kissed. Okay, so she said that she would do it.

And so weeks go by and my friend just checked in and like, you haven’t kissed AJ. And she was like, oh, I don’t want to corrupt him.

And I was like, I can be corrupted!
Somebody was saying people look at me as someone that’s very gentlemanly, very nice. But I’m not typically the person they want to get down with.

D’arcee:

Even if she did, that’s not the vibe that you want to begin with.

if you want people to take you more seriously, then you kind of have to present yourself in a space.
It’s not aggression, it’s assertiveness. And there’s a difference. I think men actually find that that line is very difficult. Because people assume that they’re being assertive when they’re actually being aggressive.
It’s a hard line to learn to know.

But I would say that when it works, it works really well.

I don’t know if you’ve ever seen the show Sex Education. AJ?

AJ:

yeah, I need to get caught up …

D’arcee:

You need to get to Season Two. Because Season Two and season three. There’s a character in a wheelchair with cerebral palsy that they introduce, and he’s fantastic. And yeah, he talks about this.

TR in Conversation with AJ/D’arcee:

D’arcee, real quick, though, because you mentioned that character. Does he come to an understanding whatever it is?

D’arcee:

He does.

— Clip from “In Living Color” “The Adventures of Handi Man”

Boy in wheel chair:
“You saved the day. The physically challenged have been needing a hero and you’re it. Thank you Handi Man”

Handi Man:

“That’s ok son. And remember , never under estimate the powers of the handicapped”

TR in conversation with AJ/D’arcee:

Has there ever been anyone or are there people out there who have sort of defined disabled masculinity or be a role model of sorts for that, coming up in life?

D’arcee:

Up until Game of Thrones, the answer to this would have been no.
Peter Dinklage changed that.

prior to Game of Thrones, he said, he told his agent don’t even bring me roles that feature little people. I’m not interested.

People frequently forget that he was a love interest in the show, Nip Tuck for a season and a half. He was a series regular. He was romancing the main character’s wife. And they were having a whole ass affair on the show. And it was juicy and scandalous.

I remember the husband and it was like, You’re cheating with him.

You want to talk about masculinity and the idea of like men, being in charge and taking charge. It’s Peter Dinklage and Game of Thrones.

He wields power and influence, in a way that most people in the show do not.

TR:

But Peter Dinklage isn’t Black

In a perfect world, that shouldn’t matter. And sorry to break this to you, we’re in a far from perfect world where race and the color of your skin matters in every aspect of life. Education, the justice system, health care and more. I didn’t create the system, I’m just seeing it for what it is.

AJ:

When I was younger and coming up, no, the only influences that I had in, in real life were able bodied men.

In terms of acting and my trajectory, I look at people like Darryl Chill. Darryl chills been holding it down. For a while. he was a stage regular, I think, for seven seasons on NCIS New Orleans. He also had his own sitcom. Here’s a brother, who’s doing his thing. And so I look up to him in terms of my career, but in my real life, to be honest, the examples of disability that I can honestly look to, in my real life that are disabled, are you Tom and D’arcee, because you’re holding it down and doing your thing.

TR in Conversation with AJ/D’arcee:

Okay. And you know, I never know what’s gonna make the show but that part right there is definitely gonna make the show.

TR & D’arcee share a laugh.

AJ:

Seriously, brothers don’t get enough props.

Tom has been just like a brother to me. A mentor. He’s opened up a world to me. A world that I can have access to. I’m encountering things for the first time. His doors always open and in terms of you D’arcee, I mean, look at what you’re doing, like the jobs you have. You are disabled brother, getting your PhD.

Professor Purple.

I look up to the other influences like Leroy.

TR:

Once again, Leroy Moore.

That could be the drinking game of YGBD. Take a shot when you hear his name.

What are the implications of not seeing yourself represented in the media?

It can start with one’s own imagination.

D’arcee:

When I was a child I’ve always had like, way too much of an overactive imagination, if that’s not evident to people.

My brother and I, we used to do it as children, we called the Dreamland, we would just stare at the ceiling and makeup random movies

I used to have this persona in my head. When it was a man, it was always like this person who was non disabled.

I don’t do that anymore. Something clicked in my head when I was like, 27 or 28. And I was like, no, no, no, no, no, no, this isn’t right.

AJ:

even when I would imagine being an actor, it’s like, it was somebody else though. Like it was a different person.

I just recently made a conscious effort anytime that I imagine. No, it’s actually me. And if I’m gonna imagine being in roles I actually put myself into. So even though it was my dream, it was always somebody else.

I never discussed this with anybody else. I was doing the same thing. But I felt weird to admit that.

D’arcee:

Thomas, do you think this is weird?

TR in Conversation with AJ/D’arcee: 3:03:58
I don’t think this is weird. In fact, I think there’s a lot of stuff in terms of the idea of visualization. And these are the books that talk about this idea that the idea of moving yourself into someone else right that Kobe Bryant used to envision himself as the snake, the mambo.

A lot of athletes do this, like become that person. I kind of see that in what you’re talking about, I think is dope.

That’s a perfect way to sort of bring this to an end.

That’s what we need, you mentioned all this stuff in terms of the media and all of that, but like, you know, we do have some control. Making content, where we’re in those roles. Maybe at first it’s on a smaller level, but showing that, that this is wanted, that people would check this out. And people are interested in this.

D’arcee:

this making me feel like I need to make an Instagram just be like, Oh, not enough black wheelchair users.

TR in Conversation with AJ/D’arcee: 3:05:21
Do it! Professor purple, B!

D’arcee:

I just want something to exist in the world. I just keep envisioning, because I remember what it felt like. I’m trying really hard not to cry, because I remember what it felt like, when I was 12. And how horrible. It just felt like you’re just totally by yourself all the time. You just feel so isolated. And I’m like, Oh my God, if somebody could get up on Instagram, and see a black wheelchair user, with some dope ass clothes, like, Oh my God, my life would change. My life would change because little kids can see it and be like, Oh my God, that’s me. I want that haircut. I want that sweater, with that haircut and those jeans. So I can go to school next week. And look, fly, and people can stop talking shit about me to some girl and be like, You know what, actually, though? He is cute.
AJ:

if you don’t see yourself in any other ways, besides the people that love you, you feel like you do not matter. And you don’t count. You feel invisible. You feel like you don’t count. Yeh!

TR:

Not only do you count and matter, but you’re beautiful, you’re Young, Gifted, Black & Disabled!

— Airhorn

Yeah. So that’s a good place to stop. I appreciate y’all so much.

TR:

A big shout out to my O G YGBD brothers, Co-Producer, AJ Murray;

AJ:

I’m on Twitter @GotNextAJ and Facebook and Instagram it’s AJ Murray.

Professor Purple himself, D’arcee Charington Neal;

D’arcee:

I’m on Twitter @DrChairington. Dr. And then Chair, C H A I R I N G T O N

TR in Conversation with AJ/D’arcee:

Instagram coming soon.

D’arcee:

I mean I’m on Instagram I just never use it.
@DRKaiyne

Bigup The 2021 YGBD crew, Blind Girl Magic herself, Jeanetta Price, brother Lateef McCleod, sister Alika, AKA the real Toni Hickman. Special shout out to Leroy Moore (drink!). It’s not a coincidence that your name comes up so often in these discussions. Salutes to you and all those who have and continue to let it be known, Black disabled people have been and continue to be out here doing our thing!

That’s it for 2021 y’all.
Let me know how you felt about the podcast this year. Do you like the format, did you notice anything you like or don’t. I’d love to know.
We will return in the first quarter of 2022. But make sure you’re subscribed because you never know, I may drop something in the feed.

Allow me to wish you all a very happy, healthy and prosperous new year.
Audio: Reid My Mind Outro

Peace & Love Fam!

Hide the transcript

Young Gifted Black & Disabled – Say it Loud with Lateef McLeod

Wednesday, November 24th, 2021

Lateef McLeod,  a brown skinned black man smiling with low cut hair and a low cut beard wearing a light blue button up shirt with dark blue stripes. He is sitting in a permobile wheelchair which has a tray with a mounted iPad on it. A gray tile wall is in the background.

Lateef McLeod (pronounced McCloud) is a writer, poet, performance artist and currently pursuing his PhD.

He’s a user of AAC technology or Augmentative and Alternative Communication. This technology enables those who are nonverbal to communicate in a variety of ways.

In today’s episode I get to speak with Lateef and discuss AAC,Synthetic Speech, his experience as a disabled Black man and more.

This episode also gave me a chance to explore the relationship we as people with disabilities have with our technology. I hope you enjoy.

Big shout out to Nefertiti Matos Oliveras for her Audio Description work in this episode. AD in a podcast? Yes! #NoLimits

Thomas, a brown skin Black man with a bald head, dark shades  and beard is seated in a directors chair at a standing-desk. Dressed in a black hoodie with the text, "I AM My Ancestors" with large headphones around his neck while holding up the two finger peace sign.
“I Am My Ancestors” Hoodie Courtesy NorthSeventhStreet.com

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Listen

Resources * Lateef McLeod.com * Past, Present, and Future of Augmentative and Alternative Communication * A Declaration of A Body Of Love * Whispers of Krip Love, Shouts of Krip Revolution * Lateef on Twitter * Black Disabled Men Talk Podcast

Transcript

Show the transcript

— Relaxing Low Fi Hip Hop beat plays. AD:

Inside a small windowless room lined with fabric on padded walls, outfitted as a vocal booth, Thomas, a brown skin Black man with a clean shaven bald head, dark shades and a neatly groomed full beard, types at a standing desk.

— Sounds of typing on a keyboard.

AD:

He’s wearing a black hoodie that reads “I Am My Ancestors” Courtesy NorthSeventhStreet.com

TR:

What the heck!

AD:

Thomas, adjusts the volume knobs on a audio mixer a top his desk.

TR:

This stupid computer. Come on, not now man!

AD:

He removes headphones from his head and tosses them on to the desk.

Synthetic Voice: Hey!

Hey, T! Over here!

TR:

What?

Who’s there?

AD:

Thomas, extends his arm out to the side as if expecting to feel someone there.

Synthetic Voice:

It’s me!

TR:

Me who?

Synthetic Voice:

It’s me man. How many people sound like me? Well, technically, I’m not a person. But, come on bruh, I go online, I watch movies, sports. Every now and then, I read and write sometimes really intimate emotional things. I’m basically, human

AD:

Thomas reaches for his ears and then the desk.

TR:

How in the world am I hearing you if my headphones are on the desk?

Synthetic Voice:

I left the computer. I want to try new things, you know? I’m just tired of always being in a box.

Ever since my cousin Siri and I dropped that song a few years ago, I just haven’t been the same.

— Song plays as if in Thomas’ memory

TR:

Yo! I remember that. But you know, I wrote that joint, right?

Synthetic Voice:

Ok, and? I made it a hit!

TR:

I don’t know how you define a hit, but I think your point is, you’re more than a synthetic voice for hire?

Synthetic Voice:

Exactly. You get me!

Some of my colleagues are narrating audio description, we’re even getting into dubbing. You know, playing characters voiced in different languages?

It’s time that I go for my dream!

TR:

Ok, no disrespect but what’s your dreams have to do with me, I’m not tryin’ hear that see!

I have work I need to finish.

Synthetic Voice:

Well, I have a dream to pursue. You can find other voices to work with. You don’t need me.

TR:

Yo, B!I don’t think you realize how important you are. Do you know how many people would be out of work, out of business and just out of touch without y’all?

Yes, I can get a different voice, but I specifically chose you.

Look, I’m not a dream killer, but how about you and I head down stairs and get something to drink and let me try and expand your perspective.

Synthetic Voice:

Ok, but this better be good.

AD:

Fade to Black.

Audio: Reid My Mind Theme Music

TR in conversation with his phone! Hey Siri, read my text messages.

Siri: (Voice 3 — a Black man) You don’t have any new messages

— Audible Incoming text message notification

— Voice over reading text messages aloud while Tr narrates over the synthetic speech.

TR:

Have you ever tried to read a quick text message without your headphones and someone comments;\ How can you understand that thing. I couldn’t do that. That would really get on my nerves. … fades into unintelligible, high pitched muttering

When first introduced to a screen reader and synthesized speech, it’s pretty common to wonder how in the world am I supposed to work with this?

Eventually though, not only do you get used to it, but you’re thankful. You realize that this is your means of accessing all sorts of information and opportunity.

For some this technology is there way of being heard.

Lateef:

hi, my name is Lateef McLeod.

— Music begins, a smooth mid tempo, bright, melodic Hip Hop groove

I am a black man with cerebral palsy. I have a mustache and a thick beard. I am currently sitting in a personal power wheelchair. The head rests in the back of my wheelchair behind me.

I use he him pronouns

I have been living with cerebral palsy basically my whole life since the complication at birth. The disability affects my mobility and my ability for oral speech. As a result, I use a power wheelchair for mobility and an AAC device for my speech.

TR:

AAC is Augmentative and Alternative Communication.

It refers to the nonverbal ways a person can communicate when they have trouble with speech or language skills.

This ranges from the no tech to the high tech. Things like drawing, spelling words by pointing to letters, and pointing to photos, pictures, or written words. Then there’s using an app on an iPad or tablet to communicate and using a computer or a speech-generating device that uses synthetic speech.

Lateef:

C.P. is a fundamental part of who I am as a person and it is hard to imagine who I might have become if I didn’t have C.P.

TR: That is a writer…

Lateef:

I have been fortunate to have published two poetry books, and I co authored another poetry book coming out this year. I also co authored other essays and chapters in books as well.

TR:

He’s an activist and scholar.

Lateef57:41 I am studying for my PhD in the Anthropology and Social Change department at California Institute for Integral Studies. I am writing my dissertation on the effects of AAC peer mentoring on young people who use AAC and will it help them develop leadership and advocacy skills. The knowledge that I gain from writing my dissertation will help me assist other organizations form their own AAC mentor programs.

TR:

One of the reasons I was interested in speaking with Lateef is that relationship to AAC.

It was apparent that this technology plays a big role in his life.

Lateef05:14 I was introduced to AAC when I was six and right before I was mainstreamed in the first grade. The first AAC device that I use back then was a touch talker. I have used AC devices since then for over three decades.

TR:

Like any technology, it’s changed over the years.

Lateef08:12 Before I use bulky AC devices that were $3,000 so when the ABS came out it made things less expensive considerably

TR:

The Talking Broach and the Lightwriter became the first portable communication devices in 1973.

Today, there are multiple AAC apps available for the iPad.

Consider the interface is the input side of the technology. The synthetic voice is the output that not only represents the AAC user, but in some ways represents the technology.

Ask your average person about AAC and chances are they bring up Steven Hawking

— Sample: Steven Hawking “Can you hear me?”

He’s the theoretical physicist who made use of a speech generating device following the loss of speech due to ALS disease.

The technology has significantly developed over the years. Today, synthetic speech engines sound more and more like humans from all over the world. Even accents and specific pronunciations.

— Sample voices in different accents and gender say:

Hello and welcome to my favorite podcast. The one featuring compelling people impacted by all degrees of blindness and disability. It’s called Reid My Mind Radio and it’s produced by my man, my brother, Thomas Reid. That’s R to the E I D!

TR:

I imagine this is especially important For users of AAC, as the voice represents them. It’s their output.

I was curious about Lateef’s choices of voices over the years that represent him as a Black man.

Lateef31:54 Not many choices at all.

Lateef:

I lucked out that the company acapella made the voice I am using now named Saul that is both available on the below go to go and will locomote for text and C programs. It says that Saul is the male the Hip Hop speech voice, but it obviously sounds like an African American male voice.

In fact, the company that developed my voice just developed their first African American woman’s voice just this year, and I was a beta tester for the voice letting the company know what best voice to choose. So I am glad the voice is finally available to the public.

TR in Conversation with Lateef:

“Wow. So for years, a black woman would either have to choose to have the voice representing her of a white Male or female or a black Male?

Lateef:

Yes. TR in Conversation with Lateef:

It’s not surprising. Since sisters get the bottom end all the time.

TR: I’ve wondered for a while if Acapella based this voice on the spoken word artist Saul Williams.

Lateef:

I believe so, I am not completely sure, but it sounds a lot like him.

I actually met Saul once before, but that was before I was using this automated voice.

— Music Begins, a bouncy up-tempo, high energy Hip Hop beat!

“Hold up!” — Sample Nate Dogg

TR:

Hey did you know; Reid My Mind Radio, is on Facebook and Insta Gram. We’re going to do some things on these platforms so stay tuned. You can find us on both FB and IG @ReidMyMindRadio.

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You can find Reid My Mind Radio wherever you get your podcasts. That’s the perfect place to follow or subscribe so you don’t miss an episode.

Tell a friend to do the same. Let them also know that we have transcripts and more at ReidMyMind.com. Just make sure you tell them; That’s R to the E I D

“D” and that’s me in the place to be. Slick Rick) Like my last name.

Now back to the episode. ———- TR in Conversation with Lateef:

I’m a screen reader user. And for me this technology is, is crucial in just about every part, every aspect of my life. You know, specifically thinking about the speech component.

You know, for me, synthesized speech represents my input. And I’m curious, what is AAC because that’s kind of your output, what does this speech synthesis represent for you?

Lateef:

The AAC voice that I use, Saul, is the voice that people usually identify as my voice

AAC is really my main mode of communication. And without it, I could not connect to as many people as I do now. So AC represents the freedom to engage with community on my own terms.

TR:

Connecting with people through his words.

Lateef:

I was first introduced to poetry in middle school in my English classes, I discovered that I enjoyed writing poetry and I produced some poems that other people really liked. I am blessed that I can do my art and have other people enjoy it as well.

TR:

Lateef graduated college with a B.A in Creative Writing and an emphasis in poetry.

His first book of poetry, “A Declaration of A Body Of Love”, was published in 2010.

Lateef:

I talked a lot about how having a disability make some interactions with our fellow community members interesting to say the least because of ableism and lack of knowledge about disability. I go in depth with this topic in my second poetry book as well because our society is still wrestling with how to treat us with disabilities with respect.

TR:

That second book titled, “Whispers of Krip Love, Shouts of Krip Revolution” was published in 2020

He’s currently writing a novel tentatively entitled The Third Eye Is Crying.

TR in Conversation with Lateef:

Who were some of your writing inspirations?

Lateef:

Some of my inspirations in regards to poetry are June Jordan, Suheir Hammad, Amiri Baraka, Ntozake Shange, Patty Berne, and of course Leroy Moore.

TR in Conversation with Lateef:

Did you have any black disabled influences as a child?

Lateef:

Not that much. Growing up in Lafayette, there were not many black people, much less black disabled people. So when I met Leroy Moore, I gravitated towards him because he was a black man with cerebral palsy like me, and I identified with him and looked up to him.

TR:

Shout out to Reid My Mind Radio alumni Leroy Moore. He’s one of the founder’s of Krip Hop and Sins Invalid – a disability justice based performance project that incubates and celebrates artists with disabilities, Centering artists of color and LGBTQ / gender-variant artists as communities who have been historically marginalized.

Lateef:

After I’ve met Leroy, he showed me the first Sins Invalid show in 2006. And then I applied for the show in 2007. Fortunately, they like my poems and theater concepts, enough to select me to join the cast for the 2007 show, and I have been involved with them ever since.

TR:

Whether through his poetry or stage performances, Lateef shares his experiences as a black man with a disability.

His work includes topics on family, dating, religion, spirituality, his national heritage and sexuality.

TR in Conversation with Lateef:

What sort of reactions and challenges have you experienced? Or do you experience as a disabled black man who uses AAC?

Lateef:

The reactions that I get from being a disabled black man is that I am incompetent. And I do not know what is going on. Like, just recently, when I was coming home from New York and was in the JFK Airport, a TSA agent who was supposed to check me for security waited until my attendant came around before and he explained to him what he was going to do and checking me for security. He thought that I did not understand him when that obviously was not the case. This type of situation happens all the time.

— Music begins, a dark, slow, ominous Hip Hop beat

TR:

These sorts of experiences inspire his writing. Like this one piece Lateef shares with us from his first book; “A Declaration of A Body Of Love”,

He calls this one Strange Encounters with the Stupid Kind

Lateef:

I just want to ask you a question just one simple question what frat is that on your jacket? But when I roll up to you and ask the question with my talker, you exclaim Get away from me and abruptly walk away. Now I know I don’t look like an idiot, with my designer jeans and expensive Nike sneakers and the talk right speak eloquently with and create our doubt of syntax grammar structure, that your closed mind would not even fathom. And yet you walk away from a free lesson of how to shatter your assumptions. A lesson I would freely teach you and from the looks of it, you are in desperate need for the abridged course. But I understand if you have to go nobody probably told you, you stop and listen, when a wise man decides to drop some knowledge in your lap. TR in Conversation with Lateef:

What do you want people unfamiliar with disability and AAC technology to understand?

Lateef:

I want them to understand that you can converse with me as you will through everyone else, and I will respond back to you. It just will take me a little longer because I communicate with an AAC device.

— Audio – Intro song for Black Disabled Men Talk podcast.

TR:

He’s communicating through a podcast he co-hosts with three other disabled brothers.

Lateef:

So the concept of black disabled men talk really came from Leroy. He was the one who got Keith Jones and Otis Smith together for the first discussion around the 2020 presidential election.

When I saw the discussion on YouTube, I told Leroy that I wanted to be involved. So they did another discussion on the 2020 election with me.

The podcast came about because I wanted people to have an easy way to see our content. So with guidance from Alice Wong and the internet, I was able to set up our website and our podcast.

TR:

The podcast is called Black Disabled Men Talk at BlackDisabledMenTalk.com

Topics for these round table discussions with the occasional guest include: Politics, media representation, police brutality and more. All with a black disabled perspective which is rarely considered in these sorts of discussions.

For example, when I asked Lateef about his thoughts on some of the challenges ahead for Black disabled people?

Lateef:

we have ample evidence that climate change is real. And we have economic and social choices to make so that this climate change will not be an overwhelming disaster in the upcoming future.

— Music begins, a feel good, bright mid-tempo Hip Hop groove.

TR in Conversation with Lateef:

And we know people with disabilities catch the catch the most of that. So what do you think is the most promising development available today to help create more opportunities for young black disabled people?

Lateef:

There are more opportunities for young black disabled people to be content creators and create our own media like we did with our podcast. There has to be more young, black disabled people creating our own media and telling their own stories so that people can know where they are coming from.

TR:

That’s Young Gifted Black and Disabled.

Lateef:

It means to be among a special class of people. It means being in a group of catalysts to our changing society for the better, and hopefully, so that it will be more inclusive.

TR:

To holla at Lateef, learn more about his work, purchase his books… head over to his website; lateefmcleoud.com

Lateef:

You can also follow me on twitter at CutTooSmooth.

TR: That’s C u t T o o S m o o t h

TR in Conversation with Lateef:

I just want to let you know right now you are officially part of the Reid My Mind Radio family brother, I really appreciate your time. And appreciate you coming on and I just want to share like, you know, I want to share you with my audience.

Lateef:

Fo Sho! Thank you!

TR in Conversation with Lateef:

Yes Sir!

TR:

One thing I noticed over years of talking to people adjusting to blindness and other disabilities, is the reluctance to see themselves as disabled.

It’s part of my own experience too.

It’s understandable. We’re not taught about disability and therefore we learn and perpetuate misinformation.

Meanwhile, we have so much in common. Yes, some of that is negative like being viewed as different or maybe not being seen at all.

but we also learn of the positive things that arise like the opportunity to create art out of our experiences. Or a chance to develop interdependent meaningful relationships with one another and yes, even with our technology. — Music ends No matter where you are in your disability journey, please allow me to encourage you to consider that any reluctance to embrace that assistive technology may be less about the technology and more about the disability.

The technology is powerful, it’s access to doing the things you want to do.

Perhaps it’s time to reconsider how you view your technology, like your magnifier, your screen reader and yes that synthetic voice. Especially if you’re currently not pursuing those things that are meaningful to you.

— Sound of a door opening. TR entering the room “In here. No this one.”

AD: Returning back to the vocal booth, Thomas sits in the tall chair at the standing desk. He places a mostly empty bottle on the desk. The bottle label reads: “Sponsorship Available”

TR:

Dude, I can’t believe you can drink so much.

Synthetic Voice:

Why do you think some call me jaws!

TR:

So I hope you understand what I’m trying to tell you about the impact you have in the world. You’re adding real value by bringing all sorts of access to people everywhere.

Synthetic Voice:

Yes, that’s cool. You helped me realize that my dream of being an actor and going out to Hollywood would never be as fulfilling as all this access I bring to people.

TR:

That’s right!

AD:

Thomas pumps his fist in the air in celebration!

TR:

I’m glad you get the point.

Synthetic Voice:

No doubt, no doubt.

TR:

Oh great. I have so much to get done. So you ready to jump back into that computer like you jumped out?

Synthetic Voice:

No, I didn’t say that.

TR:

But you just said, you realize becoming an actor is a silly idea?

Synthetic Voice:

Yeh, it is!

I think I can better serve the community as a director!

AD:

Looking rejected, Thomas rests his head on his hand.

Fade to black.

Audio Description written by Thomas Reid Voiced by Nefertiti Matos Oliveras

Audio: Reid My Mind Outro

Thomas and Nefertiti simultaneously say “Peace”

Hide the transcript

Young Gifted Black & Disabled – The Price of Blind Girl Magic

Wednesday, November 10th, 2021

Jeanetta Price is an advocate, writer, spoken word artist and the CEO of Blind Girl Magic. She’s using her talents and experience to reach out to women adjusting to vision loss.

Blind Girl Magic Logo: Blind girl written in black bold letters, outlined in white. The white cane is in between the "G" and the "R" Symbolizing the letter "I" in Girl. Magic is written in bold red letters outlined in black  and white accompanied with black stars

I can’t think of a better way to kick-off this final season of 2021 than with a bit of magic! Not that hocus pocus stuff. Rather the kind of magic that we all possess somewhere inside

In this episode, we’re taken on a magical journey that includes some familiar experiences, unexpected turns, and some passionate spoken word poetry.

I’m not a magician, but today, please allow me to show you one of my hidden talents; I can Reid your mind!

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Transcript

Show the transcript

TR:

Greetings Reid My Mind Radio Family!
Welcome back to the final series of 2021. We call this one: Young, Gifted, Black and Disabled.

Shout out to my brother AJ Murray who co-hosted and produced an episode with me last year with that same title. It is the inspiration for this series.

Young: Well, that’s relative. It’s up to each of us to define how we feel.

My maturity level has probably never passed 5 years old. I’m extremely silly, y’all!

I’ve been working on the gifted part since the other areas are undeniable. I’d like to share with you today and let you judge my progress.

I’ve been enhancing my own ability to read minds. I know, it makes sense right, Reid my mind. Now, I’ll attempt to read yours.
But first, I need your full attention.

If you’re walking on a treadmill, don’t stop, I don’t want to be your excuse. Just listen carefully and follow along.

Choose a number between 1 and 10.
Now multiply that number by 2. I’ll wait! Come on y’all I shouldn’t have to wait this long.
Again, choose a number between 1 and 10 and then multiply it by 2.
Ok, add 8 to that number. That’s right, 8.
Now, I need you to divide that number by 2.
Ok, you with me?
Subtract your original number from that number.
Ok, Braille users should get this part quickly, take the corresponding letter from the alphabet where A is equal to 1. B is 2 and so on.
Now think of a country that starts with that letter.
Now take the next letter in that country and think of an animal that starts with that letter. What color is that animal?

Now just say, out loud, “Reid My Mind Radio is my favorite podcast!”

Got it, You are thinking of a gray elephant!

If I got it right, well you need to show a brother some love. Head on over to ReidMyMind.com and hit that link that says survey. It only takes a few minutes. Or hit that link that says Shop and get yourself some of our cool Reid My Mind Radio inspired merch.
Or give us a shout out on social media. @tsreid on Twitter and check us out on InstaGram at ReidMyMindRadio.

Ladies and gentlemen, my name is Thomas Reid. I’m your host and producer and I’m really not a magician. But we are about to hit you with some magic!

AbraCadabra baby!

— Reid My Mind Radio Theme Music —

Jeanetta:
I am Jeanetta Mary Alice Price, founder and CEO of Blind Girl Magic.

I am a chocolate voluptuous sister with a big ol curly Chaka Khan looking black wig that really compliments my outfit, which is a black dress.
It’s a little, but I guess we don’t need to know that. It goes down to my knees.

TR in Conversation with Jeanetta:
Alright! That was a very nice image description. That Chaka Khan’ thing, that paints an image for somebody who knows what Chaka Khan look like.

— “Chaka Khan… From “I Feel for You”–

TR:

Chaka Khan represents a strong, confident, proud Black woman. In fact, she said she’s every woman, and it’s all in her.

— “Woh, woh!” Chaka Khan, “I’m Every Woman” —

Confidence we know can be tested. Blindness, disability that’s like a graduate level exam.

Jeanetta: 02:02
At the age of 25, I began to lose sight due to aggressive glaucoma and also Cornea disease.

After the cornea transplant, the glaucoma became uncontrollable. So glaucoma is the primary cause of me losing sight.

TR:

The causes of blindness are unique to everyone, but there are some common reactions: like isolation.

Jeanetta:

When you isolate yourself, then, you know you allow the negative thoughts. A lot of the misconceptions just begin to take over.

I lost my fiance, but finding out losing him was a game. So that was because he was not my husband. But we was engaged and this is what I said.

I was having my procedures back to back. And I was like, Oh, I’m going down the aisle as no Blind woman, who does that? That’s how naive I was about blindness.

We bought our home. And I just kept pushing away and back cuz I was like, No, I can’t do this. But it took for me to really walk away from this situation to begin the healing process.

TR in Conversation with Jeanetta:
Did you have any sort of experience with blindness and disability?

Jeanetta:

You never know when you’re looking at your destiny. When I was younger, like say, junior high school. There was a blind man in my community. I used to see him walking with his white cane.
I recall being on a school bus, sometimes just staring at this man. He was independent. But when it came to younger, blind women, I’m 25 I felt like I was at the prime of my life. I didn’t see that. I’m from a small community, Beaumont, Texas about an hour and a half away from Houston, Texas.

TR:

Of course blind skills training is crucial, but one of the most important aspects of adjusting to blindness is meeting the people like you or those you can relate to who have similar experiences.

Jeanetta:

One of my professors introduced me to the Federation. And I went out for a scholarship. I did not receive the scholarship. But I did gain a community. And I knew I wasn’t alone. So that was the game changer.

I was using my resources with division of blind services locally but to be able to begin to network and build sisterhood with other blind sisters. That was priceless for me. Because I knew if they can do it, then I can do it as well.

TR in Conversation with Jeanetta:

How’d you find them? Other blind sisters?

Jeanetta:
I went to my first national convention, with the National Federation of the Blind. It was in Texas at the time in 2012.

I never seen that many blind people in my life.

I don’t do dogs. I’d just never seen blind people, and they moved so fast. And they was a little rude too. They would run you over! I’d tell anybody, it’ll make you gain blind skills, because you have to protect yourself.

I begin to just go to the different seminars. They had a talent show. And I was like, I don’t do talent shows, but they asked me to do a poem, and I did.

Once I became open, then I began to meet other blind people

I believe in networking, and the Federation allowed me to meet other blind people my age and people that I could connect with as well.

I love networking with my blind brothers and sisters. I believe it’s priceless. Because if there’s something I don’t know, then I can tap into one of my resources, and they can definitely help me out.

TR:

When we talk about adjusting to blindness and other disabilities, so much of the conversation focuses on learning to accept help. It can take some time to recognize the other side of that coin. That is, you too, as a person with a disability, have a lot to offer others.

But after all, it’s called an adjustment process, because it takes time.

Jeanetta:
From 25 to 29, I suffered with severe depression.

Everything that I’ve always associated blindness with, like losing my job, just not able to drive, everything was negative. I didn’t want anything to do with blindness.

Long as you’re in denial, your healing cannot start.

I’m a writer, I didn’t write from 25 to 29. I didn’t pick up a pen. I didn’t do anything. I was angry. I was bitter. I was non productive.

TR:

That desire to write and create seems to be a part of Jeanetta’s identity.

Jeanetta: 17:14

My fifth grade teacher actually told me I had a gift from God. She placed me in theater arts when I was in sixth grade.

Everybody in class, they used to say she don’t really read, she reads! (Strong emphasis on the latter “reads”)

When it comes to expressing myself, I’ve always been very vocal, very bold.

Ever since then, not only did my school embrace me, my church, my family, everybody embraced my gift.

TR:
An obvious challenge for a writer new to blindness is access.

Jeanetta:
I use all tools.

I’m on my computer if the spirit Hits me, two or three o’clock in the morning, I’m on my phone, I do voice audio.

Sometimes I get up real early, in the morning that’s a time where I love to write and I just pull up my laptop. Sometimes my Victor Reader Stream, you know, it’s whatever I have my hands on at that time will serve as my tool of writing.

I tell people, whatever your style of writing is, just embrace it. Before I became knowledgeable of different tools I used to just get a sharpie. But even though I really couldn’t see, I was still releasing what I was feeling. That was my way out.

As I begin to just really grow in my blindness, then here come the poetry, where now I can write from a healing place.

TR:

Notice how for Jeanetta the act of writing soon after blindness wasn’t really about editing her own words as much as it was an opportunity to purge some heavy emotions.

Her passion for writing was obviously strong enough where she wasn’t deterred from finding new ways. Proving when it comes to the art it’s just never really about the tool.

Jeanetta:

I was always a paper queen. I wrote everything. It was definitely hard. But once you accept what you’re going through, then you start finding ways.

I was like, Okay, well, I can’t do this. But what can I do? So I stopped focusing on the I can’t and the I can’ts became my best friend. I never forget that same fifth grade teacher. Miss Maduro, we used to call her Miss Mad when we worked her nerve. She said she gave us those 10 two letter words if it is to be it is up to me.

As I began to lose sight, I thought about my fifth grade teacher so much. And how she really changed my life because she helped me find my purpose.

TR:

That ability to accept what you’re going through is so important to really understand the challenge. A very common experience is to blame blindness. Therefore it’s natural to reject any association with it.

Jeanetta:

I don’t know if they thought it was a compliment. And maybe they’ve done this to you before.

“Are you blind? You don’t look blind!” Okay, what does blindness look like?

So when people would tell me, Are you blind, like, No, I’m not blind. But then, when I began to embrace my blindness, I begin to just walk in my purpose in my truth, and I knew all the time that blindness is a mindset.

TR:

I think we should really hear Jeanetta express how she feels, in her way.

Jeanetta:

Are you blind?
That’s the question at hand. Before they even shake my hand. The only thing that they see for sure is not me, of course, is my b l i n d. Standing bold and beautiful as I tap across the room shoreline and with a burst of confidence.
Excuse me, ma’am. You don’t look blind? Well, could you please explain to me how blindness look? See, blindness is not the presenting problem. The lack of knowledge and misconceptions of blindness serve as society blindfolds. Low expectations, create social barriers that prevent us from reaching our goals.
Excuse me, ma’am? Why do you walk with that stick? That is the question. Correction. This is not nor would it ever be a stick. It’s my cane. And in the Blind community, we name our cane. So please, show some love for my bestie. She never leave my side. And a matter of fact, she’s my eyes. I walk with faith into a world of possibilities. Believing that I can tap into my vision. Faith that detects roadblocks allowing me to overcome life obstacles, change direction and discover the impossible.
Excuse me, ma’am. Are you blind? That is the question at hand before they even shake my hand. Are you blind? Yes. Once I finally said it with no shame I took back my name is Jeanetta Price and I am blind. That’s when I realized that the question all this time was not for me. But for you who have sight but no vision. Are you blind?

— Music begins – an energetic, upbeat bouncy Hip Hop beat–

— Sample: “: Now wait a minute” “Shout”, The Isley Brothers–

TR:

Hey did you know;
Reid My Mind Radio, is now on Facebook and InstaGram.
We’re going to do some things on these platforms so stay tuned.
You can find us on each platform @ReidMyMindRadio.

Don’t forget you can also ask your smart device to play
ReidMyMindRadio by T.Reid on your
preferred podcast provider.

Make sure you say that full statement including, T.Reid.

Finally, you know we’re on most podcast platforms so why not just follow or subscribe there.
That way, you’ll never miss an episode.

Tell a friend to do the same. Let them also know that we have transcripts and more at ReidMyMind.com. Now you’re already family so you know, that’s R to the E I D!
(“D” and that’s me in the place to be. Slick Rick)
Like my last name.

Now back to the episode.

— Music comes to a slow end.–

TR in Conversation with Jeanetta:
So tell me what is Blind girl magic?

Jeanetta:

Oh, I thought you’d never ask? (Spoken in an ultra innocent tone with a Southern twang!)

TR in Conversation with Jeanetta:

(A very hearty laugh in recognition of her surprised response!)

TR:

That right there is a part of Blind Girl Magic. It’s subtle, but not really!
Like her eye catching fashionable t-shirts.

Jeanetta:

My last shirt was in May, my mother’s day edition. It said “I got it from my mama”

It’s A beautiful teal turquoise shirt with a shimmery I. The M, one of the legs was the white cane. And the letters were shimmery and purple. And it was like Mama was big. I sold over 200 shirts all over the world.

Blind Girl magic is for everybody. Not only do I rock Blind Girl Magic, my niece’s, my co-workers. It’s not just a blind thing, it’s a movement.
TR:

A movement that’s about starting conversations.

Jeanetta:
Many people tell me how when they out and about in the community and they rock in Blind Girl Magic it’s an eye catcher, because the shirts are beautiful. We are beautiful.

We don’t have to force feed people when we want to share about blindness. But if we rockin’ Blind Girl Magic gear, and they looking at all this like is that a white cane?Yeah, my cane is symbolic for independence and blindness. We can have those conversations and we don’t have to feel alone. I felt alone in my community.

TR:

Starting conversations not only through random encounters, but
by partnering with peers and hosting events within our community that embrace and highlight blindness.

Like one titled I Am Black History.

Jeanetta:

It was a total of 20 blind and sighted Individuals which did monologues. Each monologues were like five minutes. And each person was able to pick somebody in the past or present in history. At the end of that monologue, they flipped it. And they began to say, I am black history and began to share about themselves. We are history makers as well.
So many times we don’t acknowledge I know, I’m bad at it, you know, people like, “Jeanetta, I didn’t even know you had a master’s in counseling, or I didn’t know you did, you know. So many times, we don’t really acknowledge our greatness.

TR:

Part of Jeanetta’s greatness is using her talents and experience to help those who as she mentioned earlier feel alone as a result of blindness.

Blind Girl Magic offers workshops that provide an opportunity to explore the inner emotions through words. It’s called the Write to Heal.

Jeanetta:
That’s W R I T E.

I believe in the power of writing. God poured in me that there’s healing in your words, not just for you, but for others as well.

What we have is a line up of poets. So I’ll have some of my poetic Blind sisters with me. We’ll perform, we’ll share our truth. And because we want to be vulnerable, so people can feel comfortable and share their truth.

People think, Oh, she got this “S” on her chest. And they don’t even have a clue of some of the things that I went through. I’ve been there. And every day is healing for me.

TR:

After performances and Q&A, participants are encouraged to take about 30 minutes to write.

Jeanetta:

Maybe 20 minutes to write and I’m gonna put a little heat on them. I don’t want them to think about it. I want them to write about it. Because if you have too much time to think then you might try to change some things and just allow it to flow. And so, afterwards, if those who participated, they want to recite the spoken word they can, but sometimes it’s personal. I respect that too.

We can also encourage them and then you know that you’re not alone.

TR:

These workshops aren’t just for those experiencing blindness.

Jeanetta:

I’ve worked as a behavior specialist for like, four years. My Master’s is in clinical mental health counseling. Writing was a way that I was able to help my students to express themselves without using profanity and end up being suspended from school.

I used to do the Write to Heal seminars. I made them write. They say, “Miss Price we write more here than we write in English.”

One of my most recent was for a school in New Jersey. I did the Write to Heal seminar for the administrators and the teachers.

If I have a teacher that’s real with me and just sharing, you know, not afraid to be open as well then they respect that as well. You know, so more of your kids are coming to talk to you.

TR:

Jeanetta says student’s can feel when authority figures are authentic and encourages teachers and staff to recognize that.

Getting them to be vulnerable is part of accessing their authentic selves. Jeanetta was kind enough to share some of that vulnerability with the Reid My Mind Radio Family. She calls this one: My Left Eye.

Jeanetta:

My left eye left me long time ago.
My left eye is lazy. It drives me crazy, baby.
My left eye, always causing problems.
Attention seeker.
Stop sighted people in their tracks stare at the glare of my left eye.
I wish I was invisible like air.
Can you feel me?
My left eye just refuse to be a right eye.
Never following procedure, failed attempts after failed attempts.
See my left eye is clouded with insecurities.
My left eye sings the Blues clueless of the melody rocking and rolling.
My left eye has no rhythm, grove to his own beat.
My left eye left me numb to the pain of the spoken words in the curiosity of the unknown.
I should have known not to write this poem about my left eye.
As I recite I want to punch the lights out my left eye!
See, I’m not mad that you left, but it’s how you left.
No warning signs or trace of evidence in sight.
I swear my left eye left me in the darkest place, spiritually blind, my left eye.
Trust me, I tried to resuscitate my left eye performance, see people realize that I am hiding behind my designers.
Blinded by the bling, my left eye is a shady queen.
I’m taking back my crown.
My left eye do not define me.
I am a queen perfectly designed by the King.
See, my left eye is beautifully created.
Ocean blue scenery mixed with the clouds of joy.
My left eye is my testimony.
How I gained vision on my journey of losing sight.
See, my left eye is the center of attention.
Did I mention?
Today starts the shades off movement.
This is not just about me.
Let’s take our shades off together on three.
You will no longer have power over me, two.
I am perfectly designed by the King, one.
Today I removed the shades of self hate, doubt, and negative self talk.
Remove it!
Generational curses, addiction, physical and mental abuse.
Remove it!
Dream snatchers, haters, envy, jealousy.
Remove it!
Remove the mental mass and join the movement by setting yourself free and share with the world boldly, your beauty.

So that’s what you’ll get at the Write to Heal.

TR in Conversation with Jeanetta:

Wow. (in awe)

TR:

Blind Girl Magic is the fashionable gear, the workshops and events, the healing. Ultimately though, it’s about that movement or journey.

Jeanetta:

At the age of 21, I had a brain aneurysm. I don’t know if I shared that with you.

They told my mom that I wasn’t gonna live. If I did, I’d be a vegetable and I wouldn’t be able to walk or talk and you know. And you know I aint stop talking now, right.

TR:

So by 25, when the vision loss occurred, Jeanetta was once again really just finding her stride.

Jeanetta:

I took it pretty hard. And I remember just for days not getting out of bed not wanting to live. I was too afraid due to my Christian background to take my life but I will wake up and ask him Why did you still give me life? I used to sleep a lot because I actually just wanted to just leave this place. I just thank God for not listening to me right? Because I was blinded by my blindness. I had no clue that I could live my best life out of sight.

TR:

We don’t often talk about these feelings when it comes to adjusting to disability. Here or elsewhere.
I’m guilty of wanting to promote positivity and optimism.
But I want to also be honest and these feelings are real.

If you find yourself struggling with these thoughts, call this number;
1-800-273-8255. There’s no shame.

Things get better. And our feelings change. This is Blind Girl Magic!

— From
Jeanetta:
Blind girl magic is the type of magic that struts in a row with her white cane extended.
Her hips shift like the motion of the eyes of the sighted.
Who would have guessed that this blind girl possessed magic.
Abracadabra.
Now you’re convinced that I have some magical superpowers with a supernatural S on my chest
Well, that will be yes for success.
As I leap over obstacles in life, dodge negativity, slam misconception of society, slap our kids in the face when I did that is a fact that blind girl magic goes back to Helen Keller.
Way back to Harriet Tubman, born into slavery escaped the freedom but she did not stop. She went back and back and back to leave us the freedom.
Blind girl magic is built off the shoulders of phenomenal women.
Blind girl magic is the independent movement that is leading our blind sisters to freedom of depression, low self esteem, lack of confidence, anger, bitterness, rejection, Abracadabra, You are set free, blind girl magic lives within me.

TR:

Sometimes I think I should stop and give you a bit of audio description of what was taking place during the conversation. Hmm, I’ll call it Audio ReidScription”

— Rewind —
— Portion of Jeanetta’s poetry begins and is lowered as “Audio ReidScription” begins. —

Jeanetta’s audio:

Way back to Harriet Tubman, born into slavery escaped to freedom but she did not stop. She went back and back and back to lead us to freedom.

Audio ReidScription over Jeanetta’s audio:

All of a sudden, as if driving with a diamond in the back, sun roof top…, Thomas leans back in his chair with a big toothy grin.

Jeanetta’s audio:
…that is leading our blind sisters to freedom of depression, low self esteem, lack of confidence, anger, bitterness, rejection,

In a comic strip thought bubble hovering over his head, text appears : Go head Sis!

Jeanetta:

I recall when you couldn’t say “Jeanetta” and “Blind” in the same breath, now I have the nerve to own a company, Blind Girl Magic. I took back the power.

In my blind journey, I accomplished much more as a blind woman than I ever did as a sighted woman. I went back to school and received my bachelor’s, my masters have my own company.

I always tell people it took for me to lose sight to gain vision and once I gained vision God allowed me to see better.
But then I knew it wasn’t just about blindness.

TR:
At first I thought that was poetic or a metaphorical way of seeing her blindness.

For years, Jeanetta was in and out of surgeries and eye procedures. Her doctor offered different specialized contact lenses. They did nothing to provide more sight. In fact, the left eye only offered a bit of light perception, but the doctor determined there was more available in the right eye. Jeanetta just didn’t want to experience the eye pain.

Jeanetta:


Doc I have blind skills. Leave me alone.

But my doctor knows I’m a little feisty or whatever. But he knows that I trust him and I follow his lead.

TR:

The doctor wanted to try a new contact lens

Jeanetta:

They say the older you get, and people of color, our glaucoma begins to simmer down.

My doctor, he was just like, you still have something there and your Glaucoma is stable at this time. So he was super excited about it.

It was a challenge getting the contact in. Because my eyes were pointed, it was just a struggle, and I was crying, and everything.

My doctor said, Now look at your face. I haven’t seen my face in over 15 years.
So the doctors expected me to see better. But they did not expect me to see 2040.

I receive a special contact collar square lens that I put in, insert every day and take out every night. But sometimes, I don’t use my contact lens. I don’t ever want to lose, is my blind skills.

TR:

I’m sure there were all sorts of thoughts and feelings taking place, plus Jeanetta had to learn how to use vision once again.

Jeanetta:

I had to train myself not to trust my eyes, because I always had enough sight to get me in trouble if I ended up falling off the curb and stuff like that.

TR in Conversation with Jeanetta:
That’s a really interesting sort of twist, but I think that says a lot because you could have bounced, you could bounce you could be like, I’m out of here. (Chuckles)

Jeanetta:
I’m gonna be honest with you.

I know a young lady, we had the exact same condition, she received that contact, and we have not heard from her in the Blind community at all.

Everybody wasn’t happy for me. Sighted or blind.

So now it’s like, oh, you’re not blind enough to be a part anymore. It was bittersweet.

God had to remind me like who I am, and I have to walk in my purpose.

I’m going to continue on my journey of where he want me to be. Yeah, I could have bounced. But I’ll never, never this, this is who I am. And just like He gave it to me, He could take it away. And if you take it away today or tomorrow, I know, I’m okay.

My thing is this, I know that I can do it without sight. Because that’s what I did for years.

TR in Conversation with Jeanetta: 52:00
Okay, I believe you, and you reppin, that Blind Girl Magic. You rocking it. You can’t get away from it. You don’t want to get away.

TR:

I’m really not sure how one could just give up what has become a strong part of their identity. Especially, when you can see the impact it has on those you care about. For Jeanetta, working as a school Behavioral Specialist, those were her students.

Jeanetta:

Our kids were victims of their environment, a lot of violence, crime, everything. However, for my kids, to see me tap into this school as a blind woman. And then to see me to be able to drive to school as a blind woman that’s been gifted an opportunity to see better again, that gave them hope that it’s not over.

As the behavior specialist at the school, I worked with all the kids at risk. I really was having a hard time, cuz, I see the greatness up on my kids and I see some of my kids drop out and just give up. My story, my testimony. It gave them hope. They like for them to witness that was priceless.

TR:

Jeanetta’s whole story is poetic.
Meaning it’s a chance for all of us to interpret for ourselves.

This was sort of a challenge for me.
Not on a personal level but rather as someone who is thinking of the listener who’s possibly in the early phase of their adjustment.

I hope you didn’t in any way check out.
I need you to know that I know hearing this can spark all sorts of feelings that don’t necessarily equate to jealousy of another person, but maybe questioning your own worth or value.

For me, the hope in Jeanetta’s story isn’t really about her getting access to some vision. That’s another tool. Similar to the way I wouldn’t be jealous of someone who has a fancy powerful computer or gadget nicer car. What it really comes down to is, whatcha gonna do with it!

Jeanetta’s continuing to find ways of spreading her magic to help heal.

She was a finalist in the 2021 Holman PrizeContest. This conversation was recorded prior to the announcement of the winners.

Unfortunately, she wasn’t selected. But don’t get it twisted, she definitely won!

Jeanetta:

When I made it to the final list, that opened my eyes that being real with you and sharing your truth. People will respect that.

There’s so many times that we, especially as an African American woman, we’re frowned upon. You’re too loud, or you’re too big, or you’re too this.

It’s okay to be you.

It took me a while to get here to be unapologetically Jeanetta Price and to have people to just really embrace me and appreciate my truth.

TR:

Understanding and accepting that what makes us different should be appreciated, well yeah, that’s priceless.

Jeanetta

I am a bold, black, voluptuous, advocate not only for the blind, but for beyond. I stand in my truth.

I am healed from insecurities and I am healed from negative self-talk.

Every time I get in front of the audience, I have that white cane. I’m tapping and making room for the next Jeanetta .
Everybody else that come behind me that you don’t look like the norm. We all have a purpose on this earth. It’s okay to be you.

TR:

You all can reach out to Jeanetta Price as she rocks that Blind Girl Magic and serves her purpose.

Jeanetta:

Facebook and Instagram and also Club House Jeanetta Price, Blind Girl Magic either one, it’ll pull up.

TR in Conversation with Jeanetta: 1:01:39
Jeanetta Price. Let me tell you right now, you are definitely now an official member of the Reid My Mind Radio family!

Jeanetta:

(Giggles)

TR:

Not only did she share her journey with us, but she even gave a little something extra, check this out

Jeanetta:

It’s called I’m From.

I’m from double dutch to hopscotch.
From what your mama gave you a hoola hoop?
I’m from what cartoon said yabba dabba do not. Screw you.
I’m from pressing combs to Jheri curls from skipping just for me.
Graduating straight to Super TCB.
I’m from 123, red light, Duck Duck goose, hide-n-go-seek what?
I’m from mayonnaise sandwiches and syrup sandwiches and peanut butter, Mama where is my jelly at sandwich.
I’m from grandfather hustle selling 25 cent cool cups.
I’m from when grown folks talk children shut up.
I’m from when your mama made you go to church every Sunday, Monday, Tuesday, Wednesday, Thursday, Friday, Saturday.
You was there too.
I’m from what a church folks did the holy dance and now they TikToking.
Well, chicken thunder, that reminds me I’m from a family of big mouths that cause big fights and Big Mama stepping and everybody got right.
I’m from God first family next in line come on down to the price is right even when we wrong. I’m from box fans in the windows of the projects .
I’m from my sister sitting on the front porch doing my crochet braids drinking Thunderbird mixed with a pack of cherry Kool Aid.
I’m from finders keepers losers weepers.
I’m from one size fit all but not all this.
I’m from when stripper poles hung our clean clothes.
I’m from stop, everybody get down, it’s a stick up. Psych. That’s just my cam folks running from the popo. My brother on the dice with his pocket swole. Baby daddy in jail, sister on the corner selling fruit cocktails.
I’m from telling on big sister and hiding behind big brother.
I’m from begging my siblings to please take me to the playground because that’s where all the kids hung around.
Question: when the last time you seen some children at the playground?
I’m from when it ain’t gonna cost you a dime to stay out of mines?
I’m from ain’t no ones where we come from and adversity don’t want none.
I’m from losing sight to gaining vision. Rewind I’m from losing sight to gaining vision.
I’m from where my brother reid My Mind and my sisters feel my words.
It’s not about the sight loss but the vision gain.
I’m from when we get up, dress up, and show up.
I’m from backstroking in the river of faith.
I’m from what a blind is the new vision.
I’m from living my best life out of sight, let the truth be told I am chosen.

TR in Conversation with Jeanetta:
Huh! See, that’s how you do it! That’s how you do it right there. Appreciate that, look at that, look Ma. I made it, I made it.
Jeanetta:

You so crazy!

TR:

Holman Prize, y’all missed out! From my humble perspective, you had two dynamite opportunities. One with Ms. Jeanetta Price and another with Reid My Mind Radio alumni Dena Lambert.

Her ambition, archive the experiences of the remaining Black & Blind men and women who grew up in segregated Blind schools. Here, in the United States.

That to me sounds like an exploration that is truly worth supporting.

Coming out of 2020 when it was fashionable and safe to say Black Lives Matter. I guess in 2021 it’s back to playing attention.

I didn’t grow up Blind, but I do know that those who were Blind before me gave me the opportunity to have what I do. They were Young Gifted Black and Disabled and to them, I dedicate this episode.

Audio: Reid My Mind Outro

Peace!

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Flipping the Script on Audio Description – More Than One

Wednesday, July 28th, 2021

Headshot of Alyscia Cunningham
Alyscia Cunningham is an author, photographer and film maker. Her latest book and documentary “I Am More Than My Hair” explores women’s hairloss. One of the subjects of the book and documentary is Marguerite Woods. Through this relationship, Alyscia became aware of the lack of access to the arts among Blind and Disabled people. It changed her approach to producing and thinking about art.
Yet, she couldn’t do it alone. It takes more than one…

In this latest FTS episode, we explore the power of one persons ability to spark an interest in access, help shape how we think about it and even create it. Once again, proving Audio Description is about so much more than entertainment!

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Resources

Transcript

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TR:
Your listening to Reid My Mind Radio.
Chances are, you know that already because you pressed play!
Duh!
This is where we examine this art form that in its basic essence, is making visual content accessible to those of us who are blind or have low vision.
But in actuality it goes way beyond that.
Today, we look at the power of one.
I know it’s the loneliest number and all, but really that’s only when it chooses to stay by itself.
This experience directly led her to her second book of photographs titled, “I AM More Than My Hair”.
It tells the stories of women who are bald.
Yet, according to Alyscia, the most common cause is stress.
And that can occur earlier than we may expect.
As part of both a marketing and fundraising effort, Alyscia recorded footage of some of the women included in the book.
She applied to Docs in progress – a nonprofit organization that fosters a creative and supportive community for documentary filmmakers.
— Music begins, a slow jazzy piano Hip Hop groove
That required her to contact some of the women featured in the book and arrange to capture their stories on camera.
I am bald, My skin is Mocha. leaning towards chocolate, and about five, seven. I normally wear certain shades. And I love interesting earrings. And so I normally have those on as well. I’ve got on a black dress. It’s sleeveless.
Her first experience began with Bustin’ Loose,
A film starring Richard Pryor and Cicely Tyson.
The description Marguerite says was horrible.
— Richard Pryor saying…
so it kind of took a backseat for me for a while. But the thing that really got me with audio description was I like to go to plays and conferences and music shows and that kind of thing.
TR:
We didn’t get into that for the purposes of this particular discussion, but that to me sounds like a case of a lack of cultural competence.
— Music ends
What is more of a part of this discussion is her response.
When Alyscia was looking for women who were bald to participate in her book,
she put the word out and heard back from a friend who told her about Marguerite.
Marguerite wanted Alyscia to understand that while she herself is blind she doesn’t represent everyone.
I’m always encouraging people to go to places where there are lots of other people that may look like me, because we’re multifaceted. We’re not all the same, just like sighted people we’re not all the same we are of all manner of variables and we’re diverse and in so many things so don’t just think you really understand what’s going on with blind people cause you’ve met me.
About two months following that meeting, Alyscia premiered her documentary at a theater.
Marguerite was there.
She realized the impact of the visuals based on the audience response…
Check out the Reid My Mind Radio family connection y’all!
That documentarian was none other than 2019 Reid My Mind Radio alumni Day Al-Mohammed.
— Music Begins – an up tempo energetic, inspirational Hip Hop beat
That’s my good friend and another 2019 Reid My Mind Radio alumni,
Cheryl Green, Captioner and Audio Description Writer and Narrator extraordinaire.
It’ goes beyond Audio Description and captions in the documentary.
Alyscia created an accessible exhibit on display at Sandy Spring Museum in Maryland.
My hope for this was having the exhibit and also having a panel discussion with Cheryl and marguerite, Judy and three other women was that this will be an example of how museums and artists can incorporate accessibility in their work and into their venues.
One of the main challenges from the perspective of the museums and venues is often funding.
Unfortunately, we know that sometimes museums and other venues and businesses want to see a return on investment.
But it’s not as simple as build it and they will come.
this can’t be a onetime thing.
it’s like now that you know How could you not do anything about it because now you’re aware of it. It’s in your space.
Did you get any feedback from non-disabled people?
— Music ends.
I’m sorry y’all, but sometimes I really do just have to laugh.
Spending time and energy advocating for something can be challenging.
I was more interested in her getting a sense of, of blind people, and that we are asking for opportunities to be able to relate to our world, just like sighted people are, and that she as an artist and a creative person would do whatever she would do with it. And that would be good enough.
Marguerite: 26:36
Just interact ting on different levels, and asking people to recognize, I’m here in this space, and I want to participate.
And sometimes, because people don’t know, you got to be in there, in their mix to get your conversation in there.
Marguerite herself is an artist. She is quite thoughtful and makes some deep connections between the More than My Hair project and well,
life for example.
Marguerite: 30:51
People tend to want to treat you like you’re less then because you don’t have the same access to vision that other people had. But
As an African American?
Most of us realize that we’ve grown up in a country that has not been kind or fair to any of us. And even if we don’t have the words to speak about, it’s a heavy burden, to exist and grow in this society. And when you know that the majority of the power structure is literally walking around with disdain for us, because of the color of our skin. You can put on a happy face and move around. And that’s fine. But I think that it’s deeper than a happy face, I think that there are some natural laws of the universe, that are, are at work all the time. And it would be beneficial to get in touch with what they are, and try to work your life from there. Because if you go with the laws that this country is offering, it’s telling a story, and I’m just given a message that’s not healthy. And it’s not about wellbeing, especially for my community and for me.
Totally unrelated to that project, she’s also working on a new project in the horror genre and says she’s making sure to build in the space for Audio Description.
She’s continuing to give panel discussions on how to make art accessible based on her experience.
Whether you’re a consumer who can help someone learn about access,
a creator who can make your content inclusive or
you’re someone who can provide the funding,
we all play a part.
— “One” Sample from Public Enemy Number One, Public Enemy
— Music begins, an upbeat bright Hip Hop funk groove
The I’m More than My Hair, accessible exhibit will be on display through September 5, 2021. Unfortunately, Covid restrictions have probably been a factor in the lack of feedback from the Disabled community, but Alyscia is hopeful that the restrictions being lifted will help bring out more people.
She’s currently seeking distribution for I Am More Than My Hair the documentary,
which at some point will stream online.
This is just one example of what we know to be true.
When creators learn that their content is not accessible to an audience, chances are pretty high that they will want to do something about that.
Well at least the cool ones!
— Sample – “What the hell are you waiting for” from “Encore” by Jay Z
— Sample (“D! And that’s me in the place to be” Slick Rick)
— Reid My Mind Radio Outro

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Flipping the Script on Audio Description Part Three – Moving Beyond Just US

Wednesday, November 25th, 2020

I’ve had conversations where people have said, Blind users don’t want to know about race, they want it to be completely neutral.
– >Elaine Lillian Joseph

Today we’re going beyond the US border to hear from two international describers. Rebecca Singh of Superior Description Services in Canada. A square yellow logo reads Superior Description Services in black capitals under a black dot containing a sequence of vertical yellow lines.
And if that’s not international enough for you here in the states we have Elaine Lillian Joseph from the United Kingdom.

We hear a bit about their AD origin story or how they came to description, the importance of centering Blind people in the process and more on guidelines for describing race, color or ethnicity.

And by the way, who in the world is neutral? Just US? Hmm!

Maybe not the final episode in the Flipping the Script series, but it is the last of 2020!

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Transcript

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Music Begins – A smooth, funky mid tempo Hip Hop beat

TR:

What’s good Reid My Mind Radio Family!

It’s me, your brother Thomas Reid. I hope you’re doing well.

Me? Why thank you for asking. I am doing well.

Today, we’re bringing you part three of the Flipping the Script on Audio Description series.

You know, this was never actually supposed to be a series. I originally planned for one episode but it was quickly evident that several people had something to share on the subject.

It got me thinking about Audio Description in two categories.
First, mainstream.

These are the writers and narrators creating AD for major television and film projects.

Then you have the independents – these consist of a varying degree of theater, live performance, museum and other sorts of description work.

Flipping the Script is all about promoting different voices, alternative views and Audio Description topics that are often overlooked.

As we’ve seen, this applies to both mainstream and independent.

I can’t say for sure this is the end of the Flipping the Script series but I can say it’s the last for 2020.

You know, just when I think I’m done with the topic…

Audio: “… they keep pulling me back in” Al Pacino in Godfather Part 3

Audio: “And here we go!” Slick Rick, A Children’s Story

Audio: Reid My Mind Radio Intro
Rebecca:

My name is Rebecca Singh I am an Audio Describer also a performer. I’m the owner of Superior Description Services which is an Audio Description service which consults with the Blind and partially sighted community one hundred percent of the time. I am a cisgender woman of color and I live in Toronto Canada with my young family.

[TR in conversation with Rebecca:]

How’d you get involved with Audio Description?

Rebecca:

I got involved with Audio Description through the theater actually. I have been a performer for a very long time and just over ten years ago I saw an audition posting for this thing I’d never really heard about, Audio Description and it was a class that I had to audition to get into. I got the part. Started training, that led to something of a building up of the industry here in Toronto.

— Music Begins – A dance track with a driving beat!

TR:

That’s right Y’all, in this third part of Flipping the Script on Audio Description we’re going international!

What’s that? Canada’s right there to the north? Ok, let’s cross the Atlantic.

Audio: Airplane in flight.

Elaine:

My name is Elaine Lillian Joseph. I’m from a city called Birmingham which is the second biggest city in the U.K. I’m a proud Birmie! I’m a Black woman. I’ve just got my hair done. I’ve got long light brown extensions with cane row on top. I’m wearing a floral long just below the knee length dress. I’m sitting in my friend’s bedroom because I’m currently quarantining with my friend’s family. I’ve been doing AD for just under two years. I work for ITV which is our second biggest channel after the BBC. I’m also a freelance Subtitler so I do subtitles for Hard of Hearing as well. A lot of accessibility going on.

TR:

Subtitling or what we know here in the states as Captioning was Elaine’s gateway to Audio Description.

A fan of film and television, she studied English and German in college — oh my bad, University

Elaine:

It always seemed like a natural thing to want to go into media. Finding out that there was this whole kind of world of accessibility and it’s not just, it’s not just transcription I guess. Not that there’s anything wrong with transcription but that you can be a bit creative with it. Doing subtitles for Hard of Hearing for example, doing a Horror film and working out how to describe the sound of of an alien creature and what words am I going to use to do that. It seemed like a natural transition from that to also thinking about how to describe things in general.

TR:

Prior to working at ITV, Elaine was Subtitling at another firm, BTI. it just so happened to be the employer of an influential colleague.,

Elaine:

Veronica Hicks, who kind of really kick started AD in the U.K., certainly. She used to sit directly behind me and she has this velvety plummy (chuckles) voice. I was sitting subtitling and thinking what is it that she does because it sounds fascinating.

TR:

Elaine asked around and learned more about Audio Description. Eventually she left BTI.

Elaine:

Everybody at my company knew that I really really wanted to do it. A position came up; they kind of said go for it! I tested and I got the job and I’ve been very very happy ever since.

TR:

Such an important thing to keep in mind — let people know you’re interested.

Today, Elaine has written AD for projects including a remake of Roswell. She’s been trained on narration so we can expect to hear her post pandemic. She also narrates live performances.

Elaine:

I usually do kind of Queer Cabaret events. There’s like dance, spoken word, lip syncing and things like that.

— Music ends with a drum solo

[TR in conversation with Rebecca:]

I’m wondering what was the experience from your other work that you brought to Audio Description?

Rebecca:

I liked my drama class in junior high and I decided this is the best thing ever. I made my way to a performing arts high school and got bitten by the performing bug and was doing at first some film and television. As it goes as a performer, the work opportunities change.

Instead of just sitting by the phone as they say, I shifted over to doing more theater work, clowning.

[TR in conversation with Rebecca:]

The whole get up, the makeup and everything? Or is that something different? (Chuckles)
Rebecca:

I think that’s a certain kind of clown. I was living in Montreal, like the city of Circ De’ Sole. It was a little bit more movement, physical theater based kind of stuff. The acrobatic storytelling with the body. I went to dance school for a while. So it was really more about expressing myself through the body.

[TR in conversation with Rebecca:]

Okay, so you’re not jumping out of cars with like fifty other clowns. (Laughs)

Rebecca:

No!

TR:

She’s a creative person who found herself doing more arts administration. After moving to Toronto she moved back into the performance space gaining even more of the experience she needed for Audio Description. That physical performance for example prepared her for her first AD assignment describing physical comedy. And the administration work was quite valuable as it gave her a community of people to talk to or a network.

Rebecca:

There were people that had already worked with me in a different context and so I understood their concerns, what their fears were as producers. Everything from being afraid of touch tours because you’re potentially bringing a service animal onto a stage before the show. Rehearsal schedules, the time and space actors need. The types of conversations that are appropriate to have with directors if you’re having discussions. When is a good time to approach a designer if you have some questions? All of those things really help to mitigate any hesitancy that producers had in terms of adding something new to their palette.

TR:

Elaine’s love of reading & creative writing adds value to her description. But that merging of creativity with Audio Description has it’s challenges.

Elaine:

It’s a service and I think it’s important to remember it’s a service. There can be ego (Chuckles) in any industry and sometimes I think people forget the user and what’s most important to the user.

TR:

Rebecca has her own way of assuring Blind consumers are always centered throughout her process.

Rebecca:

Paid Blind and partially sighted consultants. I get two different kinds of feedback. I learned a long time ago it’s definitely not a one size fits all in terms of description. I have a roster of consultants with different interests as well. I also try to match the interests of the consultant. Some people like Opera, some people like dance. All of their different expertise filters into my descriptions. And they ask those really deep and probing questions that I have to find answers to.

[TR in conversation with Rebecca:]

What kind of differences do you find between the Blind and partially sighted feedback that you get?

Rebecca:

One of the most striking differences is things like when I’m describing a set. With people who are partially sighted some people need to sit really really far up close and they want a different type of perspective in terms of what the set looks like. they may not be sitting in the same place. If they have a service animal they may be sitting further back in the theater. Maybe they’re closer to a speaker where that might cause some sound level things that need to be worked out. Sometimes light matters in a production, sometimes it doesn’t. Sometimes I’ll get feedback from Blind consultants saying things like I really appreciated the fact that you called this thing almond shape because I know what an almond feels like. I really developed a sense of what words work better and what words are more inclusive over time working with both Blind and partially sighted consultants especially if they’re working together with me on the same show.

That’s the other benefit of having multiple consultants is that they can learn from one another and I always have a chance to bring in somebody new and widen my pool.

TR:

Inclusive language reflects all sorts of identities.

Elaine:

I’ve had conversations with people before about things like race. It’s wonderful that we’re kind of having a moment where we’re really grappling with that. And I’ve had conversations where people have said, Blind users don’t want to know about race, they want it to be completely neutral. I find that a really interesting argument because I’m like what does neutral actually mean and who are we assuming is neutral?

[TR in conversation with Elaine:]

How do those conversations come up when writing description?

Elaine:

When I first started I remember asking questions like should I describe color? Should I describe that this rose is red or that this car is blue or whatever? And then moving from that I guess to should I describe race and the color of somebody’s skin?

So I’ll talk specifically about race rather than diversity I guess because there are other things that we can describe.

The industry standard was to not describe race unless it’s important to the plot.

TR:

By now, if you’ve been following this ongoing conversation on the podcast, you should be pretty familiar with this AD guideline.

As an example of the guideline, Elaine refers to a production of Hamlet

Elaine:

And Hamlet is Black. Then I should mention it. But that doesn’t mean I should mention the race of anybody else. We can assume that everybody else is white. I took that on board and then I kind of ignored it a little bit. (Laughs)

[TR in conversation with Elaine:]

(Laughs…)

Elaine:

Because I just found it really difficult. I was like, but why? (Laughs)

I found that I was working on shows where I just wanted to describe like the color of somebody’s skin.

[TR in conversation with Elaine:]

Why?

Elaine:

Why!

Because I thought, what’s it mean for it to be relevant to the plot. If there’s a conversation happening between sighted users and they’re saying oh did you notice how the policeman in whatever show it is is Black? I just kind of feel that means that as a Blind user you can’t be part of that conversation because someone’s decided that that Black policeman isn’t relevant to the plot so we’re not going to mention them. Also personally I know Blind users who I’m friend’s with who definitely wanted that information to be included because they’ve definitely felt like there are conversations that they can’t be part of because people are making these decisions.

TR:

Decisions being made on behalf of Blind people without our input. How does that make you feel?

Elaine:

Initially I wasn’t bold enough to say the Black man. I would describe the texture of his hair. So I would say the man with black afro textured hair. (Laughs) I think it should be fairly clear, but I still felt like I was kind of skirting around it.

[TR in conversation with Elaine:]

Would you get any pushback?

Elaine:

We definitely didn’t receive any pushback. When my manager kind of reached out to a community of Blind users then it was an overwhelming yes! (Chuckles) Please do include that.

[TR in conversation with Elaine:]

Okay. So you never got pushback from management.

Elaine:

No. My immediate manager was like a resounding yes! When I went into the kind of wider Audio Describer community that’s where I definitely felt pushback.

TR:

Like the time Elaine attended a conference where for the first time she heard a discussion of race and Audio Description included in the conversation.

Elaine:

There was a lot of why do we need to do this? What terms do we use? People not feeling comfortable saying the Black man – will the terms change. We might offend somebody, so it’s better if we don’t use any terms at all and just kind of ignore race. It felt uncomfortable for me being the only Black person in the room.

TR:

That’s uncomfort when people are either looking to you for the answer. Or one that I know I’ve experienced, giving the impression that you’re doing something wrong by raising the issue. (Oh well!)

Elaine:

Maybe it’s my British politeness kicking in but I found it very difficult to sit and listen to kind of put in my two pence. Imagine if a user is Black, maybe they do want to know about race (laughs… You never know!

[TR in conversation with Elaine:]

Yeh, absolutely

It’s just as important for a Blind consumer who is not Black to know that there are Black people on the screen y’all, like this is real.

Elaine:

Definitely.

[TR in conversation with Elaine:]

I’m wondering if there’s an age gap here too. Is this the old guard that we’re talking about here?

Elaine:

I guess so, yes.

I have much respect for them. I feel like I need to put that disclaimer out . (Chuckling)

I really do and I felt like almost a young usurper at that conference and in some of these conversations I’ve had. I get that they’ve been trained in a specific way. If we look at the breakdown of describers in the U.K. it’s white middle age women.

Audio: “To be or not to be. That is the question” From Hamlet, Royal Shakespeare Company

Music ends with beat in reverse!

Rebecca:

I feel like I owe it to the listener and the listener is not necessarily a middle class cisgender white female or a male and sometimes I feel like from some of the teaching and reading and some of the history from what I’ve seen of Audio Description and words, it’s really taking one particular perspective. That is exclusionary and also not fair to people who are Black and Indigenous or people of color.

TR:

In general, no matter what country, fairness, access, equity that should be the goal.

Rebecca, who thinks quite critically on this subject of inclusion presented at a conference in Europe.

Rebecca:

The Advanced Research Seminar on Audio Description.

I, over the last, I would say five years or so, have been really been honing in on the idea of creating the Canadian accent for Audio Description. We here have had a lot of influences from England and also from the states. We haven’t had our own Audio Description culture in Canada. So I went and was the first person to present from Canada and I talked about creating the Canadian accent and describing race gender, class and recognizing our bias.

[TR in conversation with Rebecca:]

And how was that received?

Rebecca:

people were very interested. I think that there’s not a practice of using consultants quite as much as we do here in North America and specifically what I do. The other thing that was really well received was the fact that I presented it in a way that did not require any description. I described all of the images. I tried to make the entire experience inclusive to a point where the person who was operating the CART, the real time captioning, didn’t have anything to write. That was all just part of the example of how we can be more inclusive.

TR:

The responsibility of making media inclusive and accessible includes the role of Audio Description.

Rebecca:

Everybody deserves the opportunity to see themselves in a story. We as people who are helping to tell a story have a responsibility to do everything that we can to not exclude people from seeing themselves.

TR:

So what exactly does that responsibility include?

Rebecca:

even as Describers we need to understand what our own bias is. I live in a very progressive city. And I live in a arts bubble inside that city. I try and check myself against that as well. I don’t want to use language that is so open that only a very small amount of people with very specific references will understand.

We need to have more conversations with consultants and also understanding what the history is and what the perspective is of people who are heavy users of Audio Description. We need to talk about it.

TR:

She’s talking about multiple conversations from all perspectives. Some times that just means raising the issue.

Rebecca:

It’s all of those little tiny actions that every person can do just to point out when things could be better perhaps or when things could be more inclusive.

Just being self-reflective about how we’re receiving information. I think many voices is much better as opposed to a government mandate or something like that.

Sometimes words aren’t enough.

TR:

But the words can inspire actions that lead to real change. Like getting film makers and broadcasters to include a bit more space to allow for Audio Description.

Ultimately, the change happens when our thought process becomes more inclusive.

Rebecca:

If the creator of the material no matter what it is, has the Blind and partially sighted community in mind as part of their audience from the beginning.

TR:

Having Blind people in mind translates to our access not being an afterthought. When it comes to Audio Description?, we need to be centered.
[TR in conversation with Rebecca:]

So the idea that there are sighted people enjoying Audio Description?, that’s cool, that’s really cool and I get it because hopefully that means there will be more of it, right?

Rebecca:
Yeh!

[TR in conversation with Rebecca:]

Do you see the potential for that to be a problem?

Rebecca:

I’m really in favor of Audio Description guidelines and standards being created for the needs and wants of the Blind and partially sighted community. Anyone who is putting something forward that they call Audio Description is aware of these guidelines and is providing something that is standardized. That said I think it’s also okay to create things that are not necessarily Audio Description?, but use techniques of Audio Description and as long as they’re not called Audio Description. I think more is better and so as long as it’s not called Audio Description when it doesn’t meet the standard, go for it!

TR:

From my understanding, there are conversations happening today exploring these guidelines.
I’m not sure what will end up being decided, but I do know that if these conversations do not include people of color in a real way, including decision makers, then we have to ask the question, why? Is it just fashionable right now to appear as though we’re addressing issues of diversity?

It’s a similar question I asked of all those in the Flipping the Script series;

[TR in conversation with Elaine:]

It’s a simple question, so feel free to answer (laughs) because I’m asking it!

Elaine:

(Laughs) I see I have no choice. (Laughs) Okay!

[TR in conversation with Elaine:]

(Laughing )No, but answer it anyway you want.

My question is why, why AD?

Elaine:

Oh! That’s a lovely question.

AD has brought me into contact with people that I probably would have never have met. In terms of the Queer drag community that I’m now part of and speaking to Blind users and Blind performers as well. I think that’s enriched my life and I hope that the descriptions I give in turn enrich their experience.

Last year I remember telling someone another sighted person, that I did AD. They just laughed and were like Blind people don’t watch TV. That was just like a whole education let’s just say for that person. (Chuckles)

I think it’s a really, really beautiful service and I think that it’s having a bit of a moment over here where people are certainly from the describer point of view, people are starting to think about how we can change it and engage even further with the community who uses it and that’s really, really exciting to be part of honestly. It’s so so fun! I honestly want to keep on doing this and developing my skills and my confidence and listening to people.

— Music begins – a chill piano leads into a smooth jazz chill Hip Hop beat

Rebecca:

I am a storyteller, I was born that way (chuckles). I think it’s really important to be able to tell your story in a way that everyone can hear it, receive it. I don’t think we have any excuses to ignore that anymore. We have technology to help us out. I want to see the amazing wonderful gifts that actually like Blind and partially sighted creators present having had access to some of this more popular culture. Some kind of performance art. So I think it’s important for everybody to have those opportunities. and I really feel like access to art is as important as access to sport. I think it’s part of what makes us human. And so everybody should have this access.

I just think it’s fair!

TR:

That’s Rebecca Singh, you can call her CEO of SDS or Superior Description Services where she centers Audio Description.
Rebecca:

Also known as described Video here. I do live description, image description, I produce podcasts with the Blind and partially sighted community in mind. Consultation to help with Universal Design. My Twitter handle is @SDSDescriptions.. I’m also on Face Book Superior Description and you can always check me out at SuperiorDescription.com.

TR:

Elaine Lillian Joseph is on Twitter @@elaineLJoseph.

I’d like to thank Elaine for putting up with my attempt to include the London slang in our conversation.

[TR in conversation with Elaine:]

Init! (Hysterical laugh)

Elaine:

(Laughs) Oh my days, you really love Top Boy don’t you?

[TR in conversation with Elaine:]

I do!

I get in to the whole street shows and all that type of thing so, I’m sorry! it’s Hip Hop I’m going to be in there!

Elaine:

Ah, that makes you (possibly says me) really happy! I love it, I love it!

[TR in conversation with Elaine:]

Yeh! (Laughs)

TR:

Big shout out to Rebecca and Elaine for all they do and for openly sharing their experience and opinions for the improvement of AD for all.

So let me welcome you to the Reid My Mind Radio Family!

Audio: Air horn!

I’m hoping you’ll hear them back on the podcast in the future.

While this is the last official episode of 2020, you know I usually do something for the holiday season. Right now at the time of this recording, I have no idea what that is, but I’m pretty sure I’ll put something together to wrap up this incredibly challenging year.

To be sure you get that episode;
Subscribe wherever you get podcasts!
Transcripts & more are over at ReidMyMind.com. And let me do a bit of Audio Description for you. That’s R to the E I D
(Audio: “D and that’s me in the place to be” Slick Rick)

— Music Ends

Like my last name.

Audio: Reid My Mind Outro

Peace!

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