Posts Tagged ‘Podcast’

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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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.

On Twitter I’m at tsreid

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

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

— A hint of “This Christmas” by Donny Hathaway

The holidays are among us. If you’re looking for a way to give yourself a present while supporting what I’m hoping is your favorite podcast… one of your favorites? A podcast you’re kinda diggin’?

Anyway, go on over to ReidMyMind.com and hit that link that says Shop.

Purchase a shirt, hoodie or any item to show your rockin’ with Reid My Mind Radio! Or maybe you want to show your support for Flipping the Script on Audio Description. or of course, Young Gifted Black & Disabled.

All support is truly appreciated.

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

A Season for Honoring Ourselves

Wednesday, May 26th, 2021

To conclude this first season of the podcast which fully focused on those adjusting to blindness, I share a few thoughts from guests featured so far in 2021. Some of these comments were not included in the original episodes.

This episode also includes some of what’s in store for the next season beginning in July. Plus, I too am personally headed into a new season of my life.

Please rate & review Reid My Mind Radio on Apple Podcast. It helps more people learn what we’re doing over here!

Listen

Transcript

Show the transcript

TR:
Greetings! My name is Thomas Reid, host and producer of this here podcast called Reid My Mind Radio.

We’re just about half way through the year. And this year has been full of emotions. I’m realizing now that 2021may be the start of a new season in my life.

Later this year, I’m sort of joining that category of parents known as empty nesters.

Both of my baby girls are moving on in their education in pursuit of what I hope is their passions. my oldest is headed to grad school. Shout out to Temple University and just a few miles away, her little sister will be at Villanova. Proud Dad in full effect.

Things are really going to be different around here.

— Audio – Knock on the door

TR:

Uh, come in.

Marlett:

I need you to come wash these dishes please!

TR:

Okay, I’ll be right there.
Maybe not that different after all.

I’ll be right back y’all!
Audio: Reid My Mind Theme Music

TR:

Creating content for people adjusting to blindness and disability has some inherent obstacles to overcome.

For example, much of my targeted audience may not even be online. After all, they need to learn how to use the Access Technology assuming they were familiar and comfortable using computers prior to their loss of sight. If they were not, well that could be a very frustrating challenge that not everyone is willing to take.

Then there are those who don’t even want to see themselves as Blind and definitely not disabled so why in the world am I including that in my description. Compelling people impacted by all degrees of blindness and disability?

I’m sure some may not even think that’s possible. “What’s compelling about a person with a disability?”

In this first part of 2021 I really wanted to highlight exactly that. I wanted to really make sure this podcast is being a resource for all those new to blindness. When I say a resource, I don’t mean providing steps 1 through 10 on completing a specific task. I mean the sort of resource that stimulates that confidence and belief in the idea that it’s possible. not by me shouting at you and telling you you are a winner and coming up with a cool slogan but rather, introducing you to the cool people who are either doing it or have done it already.

One great example of what’s possible when we change our perspective is my friend Cathy Kudlick. Among many things, she discuses the important role history played in her moving from denial to where she is today.

Cathy:
I direct the Longmore Institute, it’s a cultural center that tries to put disability at the center of all culture and academics. It celebrates scholar activism, and tries to get people to think about disability as a creative, generative force for change, and to really revolutionize social views around disability.

We believe in a world where everyone thinks that disabled people, they get better, and that the world is better because of disabled people. And that’s a very radical idea, but we do it through the film festival, we do it through lot of online programming over the past year with different cultural groups and trying to look at intersections and look at convergences and all of these ways that di sability is not just pity and tragedy and trauma and terror and all of those, but to really see it as a creative force.

TR:

Where we get to in our thinking about disability is going to be based on a variety of factors.
Like how we process information and our ability to be self-aware.

Pramit Bhargava, founder of the Louie app, was so generous with his sharing. He admitted he never considered disability because he was caught up in his own climb up the corporate ladder.

He also realized how he wasn’t putting in the work that he needed to do which included learning how to use a screen reader as well as other blindness skills.

Pramit:

In fact, If I can Thomas add to that, sometimes what happens We process somebody as low vision, or no vision as saying, oh, he cannot see. But I think important thing is what is going on in that person’s mind. Right, and how do we process it? How do we deal with that condition? I think that’s the bottom line.

TR:

In this season of Reid My Mind Radio, I really wanted to bring you a different idea of what many people often consider when they think of blindness and disability.

Disability impacts across race, gender, sexuality. However, so often in the media we only see a specific white cis gender privilege experience.

Similarly, we often see a very specific version of success. Usually that is based on financial statements, awards and recognition.

Well, either I’m going to be a part of the problem or I’m going to set out to actively do something about that.

In March I was really happy to bring you an episode featuring Lachi. She’s a musician, producer and just someone who does whatever she wants to do and of course I say that with the ut most respect.

During our conversation she shared a bit on success and it’s definitely something I can rock with!

Lachi:

And when I say success, I mean, right now people would consider me successful just because, you know, I’ve been doing international songs and touring and I’m all over the place and do a lot of great things with a lot of spins. And being on the Grammy panels, but honestly, my success started when I was just able to come out of my shell and showcase to everybody that I’m really good.

TR:

Similarly when I met young brother Envizion who in his own words said he owns everything about his blindness. We saw how he made a clear decision based on what was important to him immediately after losing his sight. That continues as he pursues his passion. To me, that’s an important level of success that needs to be recognized.

Embracing every part of yourself and staying focused on your goal.

Envizion:

I have this tag where I say (singing…) I don’t see nobody.

It’s a hater blocking term. Yeah, really. I’m blind. It’s all of that. And when you’re on your way to the top two, you don’t want to be focused on everybody.

— Applause …
— “We interrupt this program for a special news bulletin!” (Classic News Announcer)
— Applause continues… “Can you feel it?” (The Jacksons, Live in Concert)

TR:

That’s the message that we’re sharing!

— Applause continues… “Can you feel it?” (The Jacksons, Live in Concert)

TR:

I’m talking about this podcast!

— Music begins, Cool up tempo Hip Hop beat

TR:

For whatever reason, rating and reviewing the podcast on Apple Podcast actually helps.

Right now, we have a 5 star rating. That means if this was food being cooked up twice a month, it’s considered delicious.

Then there’s the actual reviews. Check out what people are saying:

Pioneer 94 says: Love the AJ episode it’s so well produced. Can’t wait to listen for more.

Angel Sweetheart says: Download and start listening now!
This podcast is very well put together. A strong activist in our community. Face with heart shaped eyes, grinning face
Grinning face with starry eyes, hands with medium dark skin tone raised in celebration, thumbs up with medium dark skin tone, flex bicep with dark skin tone

Thank you so much and I love the emoji’s.

shnupperdoodlez says; Great podcast
Engaging light hearted and fun, even when talking about the tough stuf. I enjoy popping in to learn more. your voice is needed out here

Hey Shnuppledoodlez, I appreciate you, but I’m going to need a bit more commitment from you. You are family so I’d expect you to be here on a regular basis. I miss you when you’re gone too long!

Blind Widow says This man knows his topic
I highly recommend this podcast to help people learn about disability and blindness and become comfortable with it and in all aspects of it.
It affects every aspect of our lives.
Ffor me a woman who is blind, acceptance in the arena of online dating as an older adult, the more normal people see us the better it is for everyone.

Blind Widow, I see you as super intelligent, powerful and go ahead with your bad self in the online dating arena. You’re a Gladiator, but don’t hurt them out there too badly love.

I hope I’ll be able to see more 5 star ratings and even more cool reviews. And go ahead and feel free to throw those emoji’s up there. You know that fire, raised fists, hearts and all that.

— Music ends abruptly.

— Now we return back to our show (Classic News Announcer)

TR:

Success is getting to know yourself and being comfortable with that person. Acquiring a disability later in life can feel as though you have to do this all over again.

It goes beyond the emotional. Catarina Rivera aka Blindish Latina recognized a real need to consider her blindness when moving through life.

Catarina:

I just started to see disability as something that I would incorporate into my life decisions, but not let it dictate my life.

When I was in college, the first thing that was happening to me with night blindness, and I had some issues with peripheral vision, as well. And I remember that I decided not to drink alcohol, because I didn’t want to impair myself any further, I saw that people were really cutting loose and partying. I remember thinking to myself is it’s every person for themselves here, I’m not gonna, I’m not gonna get caught unaware, because, you know, I was a freshman.

My friends would help me navigate parties, I would dance, I would focus more on dancing, because I couldn’t hear people when the music was loud, and I love to dance. It didn’t stop me from having a good time. And making friendships and living life.

TR:

Whether disabled or not, chances are we experience something in life that changes our course. Most people I know had different plans for their lives. Yet, looking deeper, you may realize that your life contains the things that you were actually seeking. Love, friendships, opportunity

These episode make up the first season of 2021. All focused on that adjustment experience.

Lawyer and fellow podcaster Qudsiya Naqui beautifully wrapped up her episode and the season with some thoughts that can only come from someone who has been through their own adjustment experience.

Qudsiya:

Everyone has their own journey and their own experience and their own way of going through those stages of grief and getting to the other side, or whatever the other side looks like, and that’s okay. And you have to be kind to yourself, but know that there’s a community waiting for you. And there’s a lot of possibility and that you are a whole person. And your blindness is a part of that. And it is a really beautiful part of that. That’s something that you should honor about yourself.

TR:

Honor about yourself. I really like that.

Do you ever consider the decisions that we make that actually dishonor ourselves? It could be decisions based on money alone, how we spend our time or how we perceive our own value.

Honoring ourselves, that’s what this podcast is all about!

If you missed any of the episodes this year, I truly encourage you to take a listen.

Going forward in 2021 , we’re touching on topics. We’ll start with Audio Description. Now, at first you may think, wait, what more can we talk about with AD?
Well, I guess you’re going to have to wait and see. You know, it’s right there, but in order to really get into it, you have to Flip the Script.

I’m taking the month of June off. The podcast will be back in July
To make sure you don’t miss anything, my suggestion is that you follow the podcast on your favorite platform. Apple, Spotify, Google, whatever man!

You can also find it at ReidMyMind.com where we have all the transcripts and other resources too.

Now all that’s left is for you to properly spell that. Let me help you… it’s R to the E I D
(“D! And that’s me in the place to be!” Slick Rick)

Like my last name.

Audio: Reid My Mind Outro

Peace!

Hide the transcript

Qudsiya Naqui – Becoming an A+ Blind Person

Wednesday, May 12th, 2021

The vision loss experience is different for everyone. Our responses to circumstances determines our outlook. Then again, our outlook on life can signal how we handle the tough situations.

Qudsiya is wearing a blue shirt and smiling besides plants outside of a building

Qudsiya Naqui, founder and host of the podcast Down to the Struts, shares several transformative moments throughout her blindness journey.

She discusses going from someone who hides their white cane to a proud Blind person who chooses to advocate on behalf of all people with disabilities.

Listen

Resources

Down to the Struts
WOC World

Transcript

Show the transcript

— Ambient music begins…

TR:

Greetings Reid My Mind Radio Family!
Welcome back to the podcast bringing you compelling people impacted by all degrees of blindness and disability.
You know, we’ve been here since 2014 so make sure you take a look in the archive if you’re new in these parts.

My name is Thomas Reid and I get to serve as host and producer.
I like to consider each of these individual episodes as a part of a larger collective story.
If you know anyone new to blindness or disability in general, please go ahead and let them know what’s happening here.
I’m confident that they would find a lot of value in the lived experiences stored in these audio file (and transcripts).
All just waiting for the right person.

Today’s episode is the latest addition to this growing archive that will not disappoint.
So let’s get down to it!

Audio: Reid My Mind Theme Music

Qudsiya:

My story of blindness is, to take a page out of Michelle Obama’s words, it’s a story of becoming.

My name is Qudsiya Naqui. And I am a lawyer and I’m based in Washington DC. I use she her hers pronouns.

I am a South Asian woman. I’m quite petite. I’m about five one. Right now I have sort of long, dark brown black hair that’s very long because of the pandemic and I haven’t been able to cut it and have kind of medium brown skin and brown eyes.

TR:

Qudsiya is the host of Down to the Struts, a podcast that explores the inner workings of
disability design and it’s various intersections.

Today, she shares some of the transformational experiences along her journey that helped shaped her view of blindness.

At 2 years old, Qudsiya was diagnosed with a congenital degenerative condition.
By the time she began reading, standard print was sufficient.

qudsiya:

But I had trouble in dark and dim places.

We were blessed and fortunate to be able to live in homes that worked for me. That had lots of sunlight, and we had lots of extra lighting. So that was the way that we kind of help make the environment accessible for me.

My mom was proactive and had me in sort of rehabilitation services with the state agency.

— Melancholy Ambient Music begins
TR:

That’s the New Jersey State Commission for the Blind, where she received mobility training and other blindness skills as a child

Qudsiya:

My usable vision was so good when I was young that I wasn’t quite understanding sometimes, like, why I had to use a mobility cane because

oftentimes, the trainer would come during the day, and I could see really well during the day.

When I reflect on it, I’m like, why didn’t they train me with the cane? At night? When I actually couldn’t see and then I would understand the benefit of it.

I had a hard time explaining to people what my situation was also because I present as sighted I don’t fit the sort of stereotypical appearance of what a blind person looks like. And so I sort of passed for lack of a better word because I didn’t have a vocabulary to talk about my disability, I didn’t even use the word disability, disability wasn’t even in my lexicon when I was a child and a teenager and even a young adult. I really struggled.

TR:

As a child, struggling with bullying and making friends.

Qudsiya:

I do think it shaped a lot of my identity. I was quite introverted, I love to read. It definitely did shape who I was when I was younger in slightly more negative ways, I felt like it was something I had to hide and that I had some degree of shame about. That really affected my willingness and desire to engage socially and to make friends and to put myself out there.

TR:

There are two main perspectives in viewing disability.
Whether you’re familiar with them or not, you may recognize your own way of thinking.

The medical model. This approach sees the problem as the illness, disease or injury. The focus is on fixing the person.

Qudsiya:

I started losing vision really quite rapidly kind of at the end of college when I was 22. At that same time, there was a experimental gene therapy. That became available and my parents really were encouraging me. They had very good intentions, and they love me very much. They wanted me to feel good about myself and be successful. And their pathway towards that was, you know, to have this therapy that would help me either gain vision back or halt the degeneration.

I did enroll in the clinical trial. I really believe that people should have choices about how they want to live, I have a little bit more healthy skepticism about that, because so much of it is rooted in ableism, which is a term that I use a lot now, but was really unaware of at that time.

— Ambient music ends

TR:

That’s the discrimination of and social prejudice against people with disabilities based on the belief that typical abilities are superior.
It assumes that disabled people require ‘fixing’ and
defines people by their disability.

Qudsiya says she’s unsure if the therapy has helped reduce the degeneration but notes she didn’t regain any vision.
She did however slowly begin inching toward that alternative way of viewing disability, but first, she had to go through some things.

Qudsiya:

I went through a really dark time in my 20s, just trying to like sort of, quote, fix myself,

When I was young they told me that my vision would be stable, you know that I had nothing to like, quote, worry about, and it would just be the same as it was. And that was pretty doable.

TR:

While preparing to enter Law School at Temple University, Qudsiya began seeing a new doctor who explained that her vision loss was degenerative.

Qudsiya:

That really explained what I was experiencing in the two or three years prior, reading was starting to become really difficult.

Law school, is very difficult for a whole host of reasons. And it’s a difficult environment, it’s just a lot of work. It’s very hard. And there’s a lot of reading, like hundreds and hundreds and hundreds of pages of reading a week.

TR:

Since grade school, Qudsiya prided herself on her ability to study hard and have the grades to reflect that effort.

Her vision and grades both deteriorating she considered dropping out.

Qudsiya:

And somehow, I didn’t, I had a couple of really amazing professors. And then I got a really cool internship at the ACLU of Pennsylvania, the summer after my first year, because I happened to meet the Legal Director at a career fair. And we just totally hit it off. And she was an incredibly supportive person. And between her and a couple of my professors, I just, I stayed and I didn’t quit, and I didn’t give up. I started to explore text to voice software and the different kinds of technologies that were emerging. Blind people have been using it for years.

I kind of taught myself to learn by listening because I’d always been a visual learner. And I had to completely transform the way my brain worked. And I was able, it took me a long time. And it was hard, but I did it.

TR:

The grades improved, her self confidence returned and she was making strides in her blindness journey.

Qudsiya:

Oftentimes, a lot of sighted techniques are foisted on you. Like there’s always the imperative for you to use your eyes. But that was the first time I started to realize you know what, like, it’s not about like forcing me to use my eyes if my eyes aren’t the most efficient way to get something done. And so I started to like embrace like new Non sighted ways of doing things which made me a lot more efficient and made things easier for me.

The day that I said, I need to use jaws 100% of the time, like changed my life.

TR:

But what about accepting that white cane?

Qudsiya:

There was so much stigma for me associated with it. Shame.

I got myself into real difficulty. There was one time I was in Penn Station, and I fell on the train tracks.

TR:

Thankfully, the train wasn’t moving and someone quickly pulled her up.

Although already familiar with proper cane technique, Qudsiya wasn’t a practicing user. Living in New York City at the time, she
reached out to the New York Commission for the Blind and got herself an Orientation and Mobility instructor.

Qudsiya:

I said, I need you to force me to use it in front of you until I get to a point where I’m okay with it in myself.

We worked every day a couple times a week for like an hour and little by little after a while, I started to just feel comfortable with the cane.

I went from someone who would carry the cane folded up in their purse, never even think about it, to a person who now uses a cane pretty much all day all the time and never is without it and has a very healthy relationship with it. That took a long time. And it took a lot of struggle and a lot of moving past my own stereotypes and my own ableism

TR:

Qudsiya offers some additional thoughts on what could be helpful in decreasing the stigma associated with blindness and disability.

Qudsiya:

There’s such a lack of education in a young age to a culture eight children to the concept of disability and like these disability positive messages.

I just remember in high school I never learned about the ADA, I never learned about the Rehab Act, I never learned about disability rights history.

I feel like if I had existed in an environment that was giving me all these positive messages and welcoming messages and accessible messages about who I was, and the fact that my disability was okay. I think my outlook would have been quite different. But I was in an environment where my disability was sort of invisiblized. I see that changing now for young people. But I think we have a long way to go.

TR:

Another transitional moment for Qudsiya along her blindness journey came when she experienced job discrimination.

Qudsiya:

That was the first time in my life, I had been exposed to disability rights and Disability Law and the civil protections that are available to people to prevent against discrimination. And I didn’t really understand that I had been repeatedly discriminated against in various work settings until I had this experience that became so extreme that I had to get an advocate to help me.

TR:

She credits that person with changing her life.
Helping her become clear about the problem and to see things from a different perspective.

Qudsiya:

Okay, it’s not me, that’s the problem here. It’s the system. That’s the problem. And it’s a system that is not designed to give me access, and I need to fight for that access.

— Music begins – a bright melody that moves to a driving beat…

TR:

The social model of disability.

This views disability as a part of life and not the problem.
Rather recognizing that society erects barriers in various ways that can limit opportunities.

Qudsiya not only learned how to advocate for herself, , she found a community of people who also had a positive outlook on their own blindness and disability.

Moving to Washington DC from New York City, she was introduced to another Blind Lawyer.

Qudsiya:

She and I actually connected over something completely unrelated to blindness. We connected over the fact that we were both athletes. She was a cyclist and runner, and I was a runner also.

She was starting up this sports group in DC called the Metro Washington Association of Blind Athletes. And she kept encouraging me to come and try out tandem cycling.

I hadn’t been on a bike since I was a little kid.

I didn’t know anything about tandem. I was like, this is gonna be a disaster.

Finally she pushed me and I went and I got really into it, I just fell in love with it.

TR:

That led to other sports and activities like adaptive rock climbing,
guided running and most importantly friendships with other Blind people.

Qudsiya:

That was really transformative, mostly because I never had Blind friends in my life. And so I suddenly had this massive, wonderful, supportive, fantastic community of other Blind people that were doing all sorts of things had all sorts of professions came from all different types of backgrounds. And we just had fun together. And we support each other.

TR:

That support is invaluable. From the practical to the emotional, helping you become your best self.

Qudsiya:

I’m like a b minus blind person, and I’m trying to get to an A plus.

TR:

I think she’s being tough on herself.

Even if we’re not being graded, a community of people to learn and share with along any journey is important.

Qudsiya:

I started on that journey kind of later in life, as opposed to some of my peers who were born blind or lost their vision when they’re really young. They really became resources to me, and I just started to see the world really differently.

I’m also part of another new group that just started last summer. It’s called WOC World. W O C. It’s a group for blind women of color – a virtual community of blind women to support blind women of color.

TR in Conversation with Qudsiya: 39:15
I always like to highlight the importance of meeting people. Because I think it plays a big role. I always bring it back to the podcast, because that’s what this podcast is all about. Not everyone is in an area where they can actually have access to all of these people. And so that that transition process that I think really is impacted by meeting people may take even longer because you have no sort of model of what blindness can actually be.

— Music ends with an ambient fade out

TR:

Qudsiya is a fellow podcaster. She’s the founder and host of Down to the Struts.

Qudsiya:

A strut is like an engineering device that you’d use to hold stuff together.

It’s sort of evokes this idea of like, what are the building blocks? What holds the world together? And how do we change structures and systems.

I wanted to make non disabled people see why they need to think about things from a disability lens and why that’s important and why we should care about it.

TR:

While she was being pushed to write and publish law review articles she found her heart just wasn’t in it.

Already a consumer of audio content including books and podcasts,
she recognized the opportunity to explore some of her interests and expertise.

Qudsiya:

The article I was working on was about disability, specifically disability in the US. And its intersection with immigration, which is one of my areas of expertise as a lawyer.

I really care about disability and its intersections with other types of things like race or other types of policy issues like disability, unemployment, disability and health care.

And I am a person who has experience with like policy and research and these sorts of things.

I really care about this area of work. And I love audio content. And it’s a pandemic, and I’m sitting at home and I got nowhere to go and nothing to do. And I was like, You know what, I’m gonna do it. That’s how Down to the Struts was born.

— Music begins a Hip Hop beat opening with hi hats…

TR:

Occasionally, I’m asked about starting a podcast. My advice closely aligns with the steps Qudsiya lays out.

Qudsiya:

I decided I wanted to do an interview style show and bring a mix of sort of people with lived experience, people who are experts in their fields to talk about sort of very broadly speaking, disability design and intersectionality.

I got a team of people together.

I don’t know how to design a website, I don’t know how to audio edit, I got a lot of brains together. And at first it was just for advice. But then a couple of friends of mine, really like wanted to be involved and wanted to work on it. And I was so touched by their desire to be supportive, they just loved the idea of the project.

I had a focus group of a whole bunch of friends that helped me vote on the title.

We launched our first season in October of 2020. And there’s six episodes, and we’ve just launched season two.

TR:

She narrowed her subject, figured out what aspects best fit her skills and interests.
Assembled others for advice and ended up with a team.
She’s also using a seasonal approach which I highly recommend.
It takes away some of the stress in producing regular content.
And of course, she got feedback on her podcast name. Did I mention she has herself a team?

Qudsiya:

I went to Barnard College, which is part of the women’s college that’s part of Columbia University. So I went looking for a student who was interested in audio editing. That’s how I came across Anna Wu, who is a junior at Barnard.

She brought along her friend Adrian Kahn, who does our transcripts.

I have two other friends. Ilana Nevins is our audio editor and my friend Adriana pole who is fabulous social media coordinator and manages all my Twitter and Facebook and Instagram so I don’t have to. (Laughs )

I’m scared of social media!

TR:

Yes, I’ll admit it, I am a bit envious of her team.

A lot of thought and planning went into the creation of Down to the Struts. Ultimately, it’s figuring out what you want. I get the sense that this is how Qudsiya operates.

Qudsiya:
I realized very, very quickly, that I did not want to be a practicing attorney, I think I probably even knew that before law school, but I knew I was interested in immigration, and I knew I was interested in kind of policy.

A lot of the policy people were like, Well, you can’t really fix the system if you don’t understand the experience of people who are going through it.

So I did practice immigration law, representing asylum seekers and survivors of domestic violence.

And then I went to a different organization where I was managing the program that was delivering services to unaccompanied children who were in federal custody, on the border and in other parts of the country.

TR:

She continued doing that work for a different organization while expanding into disaster recovery and other areas.

— Music ends…

Qudsiya:

now most recently, I’m at a big research like policy institution working on civil court reform work. Making this civil court system for like people who experience evictions and debt collection lawsuits and have to deal with child support cases and things like that to making the system more accessible especially for people who don’t have lawyers, and I bring a lot of my disability kind of focus in there too, because, especially with all the technology and courts, like a big concern is like making sure everything’s accessible.

I feel like, it all kind of bleeds together.

TR in Conversation with Qudsiya:

What do you want people to sort of take away from your podcast?

Qudsiya:

For disabled people, I want them to leave the podcast feeling like their issues are being addressed, that I’m exposing and uncovering the barriers they face and providing positive solutions and proactive solutions to how we can break down those barriers and fix those problems. And for

For the non disabled people I want their eyes to be opened to how the systems and structures that we live inside, whether that’s the immigration system, whether that’s the education system, whether that’s health care, how, they affect disabled people, and how ableism plays a role in that. So that they can walk away and know, there’s solutions to solve them. And I want that information to get out to the people who are the decision makers and the stakeholders in the system so that they can start to make change.

TR:
Think about the importance of all the transitional moments Qudsiya experienced.
From her battle with the white cane to experiencing discrimination on the job
which led to her meeting people who would come to positively influence her life.
Combine these experiences with her own positive attitude and drive and consider her advice for those new to vision loss.

Qudsiya:

Everyone has their own journey and their own experience and their own way of going through those stages of grief and getting to the other side, or whatever the other side looks like, and that’s okay. And you have to be kind to yourself, but know that there’s a community waiting for you. And there’s a lot of possibility and that you are a whole person. And your blindness is a part of that. And it is a really beautiful part of that. That’s something that you should honor about yourself.

— Music begins, a bright inspiring Hip Hop beat

TR in Conversation with Qudsiya:

Qudsiya, you know that you are now an official, and I want to say it twice, an official member of the Reid, My MindRadio family now that you’ve been on the podcast, you know that right?

Qudsiya:

Oh, that’s awesome. Thank you. Thank you for welcoming me into the family.

(TR & Qudsiya laugh…)

TR:

To get in contact with Qudsiya and or where to find the podcast;

Qudsiya:

You can email us at down to the struts@gmail.com. You can find our website which is www got down to the struts.com. We’re also on Facebook, Twitter and Instagram at down to the struts. And you can subscribe rate review the podcast on Apple podcast, Spotify, Stitcher, or wherever you love to listen, so definitely check it out.

TR in Conversation with Qudsiya: 1:00:19
Spoken like a true podcaster.

(TR & Qudsiya Laugh)

TR:

I really liked the way Qudsiya identifies and appreciates the different moments throughout her journey for the value they helped bring to her life.

Once again shout out to Qudsiya, I really enjoyed our conversation.

If you too enjoyed it well you can always feel free to let me know that or any other comments you may have by emailing me at ReidMyMindRadio@gmail.com.
Tell others about the podcast so they can listen for themselves. All I want to do here is to reach as many people experiencing vision loss as early as possible.

You know we have transcripts and more over at ReidMyMind.com right?

And I know you know, that I know you know, it’s R to the E I D
(“D, and that’s me in the place to be! Slick Rick)
)
Like my last name.

Audio: Reid My Mind Outro

Peace!

Hide the transcript

The 2019 Rap Up… Yes, Rap Up!

Wednesday, December 18th, 2019

A brief update about what’s been going on with the podcast as well as some thoughts on the future. I’d really appreciate feedback!

I was inspired to take a look back at this year’s episodes and create an “original” production I’m calling the RMM Radio 2019 Rap Up. It features my daughter Raven Reid along with yours truly spittin’ that fire!

Shout out to DJ Pain 1 for this free beat on YouTube that just inspired the hook!

“It’s 2019|And it’s the end of the year| Here’s some episodes, that you should really hear| 2020’s on the way| We don’t have long to go| Do the right thing, subscribe| Reid My Mind Radio”

Happy Holidays!

Listen

The 2019 Rap Up Video

Ok, maybe I was just having way too much fun… I decided to make a video of the Rap Up song.

The video simply contains mainly still images of those episodes featured in the song. Since it features my baby girl Raven, I decided to take some footage from a video of her when she was much younger, maybe 3 or 4 years old!

Transcript

Show the transcript

TR:
Happy Holidays Family!

Ok, so this is the actual last episode of the year. Although I consider these sort of extra. To me the real nourishment, the value are the people you meet every two weeks. Those are the people you should know. Me, I’m just the guy who enjoys bringing them to you.

Oh, if you’re new here, please be sure to check out the meat and potatoes, those other episodes I referred to. And allow me to introduce myself to you I’m Thomas Reid host producer and the extra garnishment on the plate and I guess I’m the Chef who serves it all up! I’m also the pro at running the heck out of a metaphor.

Audio: Reid My Mind Theme Music

TR:

In 2018, I started thinking about taking this podcast to what I considered a next step. That’s moving from a passion project, aka a total personal expense to a sustainable venture; at the very least having the expenses covered.

At the most, I’d expand the podcast in scope and frequency. That would include multiple producers and other talent. Specifically, blind or low vision producers and those with disabilities.

That shot was with the Google PRX Podcast Creators Program.

When Google announced they were getting into the podcast business, they also decided to team up with PRX, the Public Radio Exchange to help find and train podcasters that were creating for diverse or marginalized communities.

I figured, I meet these qualifications! I applied.

I made it to the semifinals but ended up not making it all the way. I was encouraged to try again during the second round of the program this year. I did.

Out of something like 10,000 entries, I’m happy to report that Reid My Mind Radio made it to the finals. We didn’t win, but we sure enough didn’t lose!

The PRX team invited two other runner up teams and myself to join the 6 winning teams in Boston for a podcast training boot camp. It was very cool. I met some great podcasters from around the world including Brazil, Columbia, India, Lebanon and Spain. And then some much closer including the only winning team from the US in New York/New Jersey and the other two runner ups from Boston and Oakland.

A big shout out to all of the teams including the PRX training team. It was cool to be among other podcast creators.

Audio: “What’s Your Name?”

One of the things that I’ve been thinking about is the name of this podcast. I know it doesn’t exactly communicate the goal of the show. Obviously, there are better names that I could come up with that would make for better Search Engine Optimization especially for those searching Apple Podcast based on a topic like; adjusting to Blindness or disability.

On the last day of the Google PRX Podcast Creators Program Training Boot Camp, each team had to present their show to a panel of podcast industry experts.

Audio: Mark Intro…RMMRadio

That was my intro, you know I got hype right?

Anyway, some of the feedback I expected was around the name. A lot of people actually were interested in hearing more about the personal experiences. That’s something I’ve been told on several occasions, but have resisted for various reasons.

If I do eventually decide to re-brand what we do here, I will definitely keep Reid My Mind Radio and maybe start to share more of my personal experiences and maybe comment more about blindness and disability related events and issues.

What do you think about me changing the name of the show going forward? Maybe re-branding and repurposing Reid My Mind Radio?

let me know if you would be interested in listening to this type of thing. ReidMyMindRadio@gmail.com or 570.798.7343.

All in all, it was a good year for the podcast.

This is where I should insert flashbacks from this year’s episodes. You know a wrap up.

Then, as I was sleeping I had a thought or maybe it was a dream. Maybe

Audio: Dream harp

Audio: Reid My Mind Radio 2019 Rap Up

Music begins…

TR Talking:

So I figured this year 2019 we should do like a wrap up. It’s Christmas time right? Well not a wrap. Really it’s an rap.

“Coo Caw” Bird wings flapping…

I did bring somebody to help me out. Close out the year, you know, in a special way

Music Crescendo….

My baby girl, Raven Reid, get ’em, hah!

Chorus Raven Reid sings…
It’s Twenty Nineteen
And it’s the end of the year
Here’s some episodes
that you should really hear
2020’s on the way
We don’t have long to go
Do the right thing, Subscribe
Reid My Mind Radio

Verse – TR:
First ep in 2019, I was talking opportunity
Just feeling positive for you and me
Next was the first of more to come
The topic, Audio Description ,
“Read by Roy Samuelson” (Audio from Audio Description)

Episode 3 was right on time
Yes, celebrating 15 years of being blind

Black Disabled History was episode 4
Straight from Krip Hop called my man Leroy Moore
(Audio: Leroy Moore says “Krip Hop!)

Now William Greer, he was referred to me
He’s from the film fest, cinema touching disability

Access is Art, you should know what I mean
If not check Episode 6 with my friend Cheryl Green
(Audio: Cheryl says, “It’s about equity!”)

Shout out Alice Wong amplifying
(Audio: Alice says “Disabled voices of color”)
That’s why Disability Visibility.com is like no other

We say Representation matters, they say what’s the fuss
I’ll remember in the dark, hashtag LetUsPlayUs?

Chorus Raven Reid sings…
It’s Twenty Nineteen
And it’s the end of the year
Here’s some episodes
that you should really hear
2020’s on the way
We don’t have long to go
Do the right thing, Subscribe
Reid My Mind Radio

Verse 2 – TR:
Day Al Mohammed produced and directed the Invalid Corps
She does policy, writes books and a whole lot more
(Audio: Day says: “Invalid Corps”)
Elizabeth Sammons is an author touring the country in an RV
At least that’s where she was when she spoke with me!

I Always rep the BX, New York City
Shout out to Prince Bri, Power Not Pity
(Audio: Power not Pity opening music…)
Is there room for the blind on the AD scene
Ask blind consultant, her name’s Colleen

Audio Description there’s more to the game
like describing Sports, Conferences, right Kat Germaine
(Audio: Kat Germain says “Yes”)
Next 3 eps feature the spark event
Sue talked about it and she’ll be back again!
(Audio: Sue says” We’ll sit down for another one”)
Mom and author Kristin Smedley was there live
She says It’s not just her kids but we can all thrive.

She started Captivating, Bold Blind Beauty Oh Boy!
Third time on the podcast, what’s up Steph McCoy
(Audio: Steph laughs…)
Chorus:

TR: “Take it to the bridge”

Bridge Raven Reid Spoken Word…

Since 2014 when this podcast was kicked off
It was geared to anyone feeling vision loss

See, those newly adjusting, it’s their own abilities they question
Reid My Mind Radio is changing perceptions

If you haven’t done so yet, hurry, act fast
Subscribe at ReidMyMind.com or wherever you get podcasts!

Make sure you spell Reid, R E I D
The podcast making blindness funky!

Verse 3:

Question, are Leaders made or are they born
The answer comes from AFB’s Megan Aragon

Landing your dream job is more strategy than luck
Coach Nancy gives some game plus she gives a duck
(Audio: “Quack, Quack”)

Audio description & physically integrated dance
Alice Sheppard, Laurel Lawson, Audimance

Man, this year flew by, like 1 2 3
Closing it out, my Bro Joe Strechay,
(Audio: Apple TV Plus)
See!

TR: “Daddy Daughter let’s go!”

Chorus – Raven Reid & T.Reid: (Repeats)
It’s Twenty Nineteen
And it’s the end of the year
Here’s some episodes
that you should really hear
2020’s on the way
We don’t have long to go
Do the right thing, Subscribe
Reid My Mind Radio

TR:
That was fun!

Merry Christmas, Happy Chanukah, Happy Kwanza Happy Three Kings Day whatever you celebrate or don’t.

All the best to you, Reid My Mind Radio Family from the entire Reid family.

And of course, so there’s no confusion, that’s R to the E I D, like my last name!

Audio: Reid My Mind Radio outro

Peace

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The 2019 Rap Up… Yes, Rap Up!