Posts Tagged ‘Black Lives Matter’

The Art of Adjustment – Light it Up with Andres Jay Molina

Wednesday, May 15th, 2024
IMAGE DESCRIPTION: Jay, a Dominican man with a goatee and glasses perched on his bald head, sits in a wheelchair outside on a sunny day in front of a river. He wears a light blue short sleeve top and looks straight to camera. (Photo credit: Elias Williams)

Photo credit: Elias Williams

Before my final guest in this second to last episode of the season became a Film Maker, Poet and Motion Graphic Artis, he had to find himself.

Andres Jay Molina, Co Director of the documentary film, “Fire Through Dry Grass” is an example of :

“It ain’t where you’re from, it’s where you’re at!” – Rakim

This episode highlights some themes to help get there:
* Finding community
* Trust
* Being prepared for opportunity

I think you’re gonna dig this one!

Listen

Resources

Open Doors NYC

Transcript

Show the transcript


TR
When it comes to adjusting to disability, do the specifics of a person’s disability really matter?
I’m talking about when it comes to living your life? Finding meaning and your purpose?
Personally, I think these are things we all desire.
Not based on our so called race, economic status or abilities but rather our humanity.

My final guest In this second to last episode of The Art of Adjustment, where we continue to highlight the role art plays in that process, is film maker, Andres Molina.

Andres “Jay” Molina:
But everybody calls me Jay .

Forty six year old Spanish man, light skin wearing a Vegas Raiders hoodie and hat. My pronouns are He/Him.

TR
Welcome to Reid My Mind Radio! I’m Thomas Reid your host and producer.
This may be your first time here, so let me explain the rules.
We don’t officially begin until the drum drops! I’m talking about…

— “Theme music. Every good hero should have some!”, Keenan Ivory Wayans, “I’m Gonna Git You Sucka”

— Reid My Mind Radio Intro
Andres “Jay” Molina:
I was living in the hood. In New York, in the lower east side of Manhattan. I used to be a truck driver. At some point there, I decided that I didn’t want to work as a driver anymore.

I started selling drugs. A few years after that, I got arrested, and I did some time in jail.

TR
After prison, Jay had to do some time in a drug program where he contracted a rare form of Pneumonia.
It put him in the hospital for a couple of years.

Andres “Jay” Molina:
Being so long in bed, I lost a lot of muscle mass. I lost my motor functions. I don’t walk today, I became disabled. All this happen in 2014.
— Sounds of busy city streets….

I used to be the type that didn’t really care much about disabled people. When I used to take the bus to go to work, usually there would be a couple of disabled guys, people around the route that I take. And as soon as the bus used to stop to pick them up, I used to be the first one in the bus, “Fuck, these fucking disabled guys. It’s gonna make me late now.”

TR
Hard to hear?
I’m in no way condoning this way of thinking.
Yet, as someone who grew up in New York and traveled to and from school and work on buses and trains, this is not an uncommon attitude.

I remember being on the train headed to class and someone got sick or passed out.
The conductor in these situations isn’t allowed to move the train.
The person even if they are conscious has to remain on the train until the EMT’s arrive.

Even the little old lady clutching her rosary beads is like, “Get them off the bleep bleep bleep train!”

— “Stand clear of the closing doors please!”, Vintage recording of NY transit Subway Announcement
— “New York, New York! (Voice pitched to an ominous deep voice)

Andres “Jay” Molina:
And then it hit me like a smack in the face because now I am one of those people.

Music begins A menacing synth loops and launches into a gritty, slow dark, Hip Hop beat.

TR
Following those years in the hospital, Jay needed physical rehab. He was sent to the Coler Nursing Home on Roosevelt Island. Just off the eastern coast of Midtown Manhattan.

Andres “Jay” Molina:
When I first got to the nursing home I didn’t know anybody of course, So I was just hanging out by myself. And then one of the nurses told me, go outside, there’s people just like you, young like you, and you can talk to them.

TR
Different groups of people congregated Outside the home. It’s a nursing home so the majority are seniors.

Andres “Jay” Molina:
But when I saw these guys actually, one of them looked Dominican, I’m Dominican. And that attracted me more. And as soon as I approached them, they just looked at me and said, “Come on man you with us”. and I started hanging out with them. And that’s when we became friends.

Andres “Jay” Molina:
I identified with them. They all looked like they came from the same background that I did. The way they talk. The way they joked around with each other.
It looked more like disabled people from the hood. That’s why I went to them right away.

TR in Conversation with Andres “Jay” Molina:
How important was that for you to have this group of other Black and Brown Brothers Who were in a similar situation?

Andres “Jay” Molina:
I felt really comfortable. They started taking care of me.

TR
they did more than congregate outside the nursing home. They broke bread together.
At the time, Jay was fresh out of the hospital. he didn’t have any money. So they all chipped in to cover Jay.

They helped each other.

Andres “Jay” Molina:
Even though I don’t walk I am what is consider independent, I can move my hands. I could move around. Most of my friends are gun violence survivors.
They are paraplegic’s and quadplegic’s, they don’t really have movement in their hands and bodies. So I started helping them.

So for example, I used to roll the blunts for them.

TR
It goes beyond rolling’ the weed, putting the blunt in their mouths and lighting it. Jay would feed his brothers as well.

Andres “Jay” Molina:
So we became close because of that. We got like a family like, I take care of you, you take care of me.

— Nino Brown A toast! (Clinking Champagne glasses)
Am I my brother’s keeper?
CMB Yes I am.

Nino Brown Am I my brother’s keeper?
CMB Yes I am.”, “New Jack City”

TR
While Jay and the other brothers continued to grow their friendship outside the nursing home, they didn’t realize they were being watched.

Andres “Jay” Molina:
A white lady called Jennilie Brewster was doing volunteer work here in the nursing home. She noticed that they didn’t have programs or projects for younger people. Usually, it was about the older crowd. She wanted to do something for us. And she started a writing workshop.

She used to come around to ask us to go to these writing workshops.
But at first we were leery, we were like white people probably police, because we were out there smoking weed.

— Whoop Whoop, Sound of the Police! KRS One

Weed wasn’t legal in New York yet.

Now we’re doing something that we’re not supposed to be doing. And then we had this white woman coming around asking questions.

She was being really persistent. She kept coming. And then one day, we decided to go to one of the workshops just to see what she was talking about.

And she started encouraging us to write about our lived experiences. To write about things that we wanted to write about.

TR
J’s first poem tapped into his memory of living on the lower east side of Manhattan in 2001.

Andres “Jay” Molina:
About how I felt about being part of 9 11

— News clip featuring Brian Gumble after the first tower was hit and before any information was known.

Andres “Jay” Molina:
Every piece of poetry that we do is about reality. It’s about what we went through.

TR
The group worked with poetry coaches during the workshops. The next thing you know, the crew was hype, excited about poetry.

Music ends!

Andres “Jay” Molina:
And that’s when we formed the Reality Poets.

TR
The Reality Poets which includes the crew of brothers Jay was invited to join and some others, are a part of what became known as Open Doors NYC.

According to OpenDoorsNYC.org, the group produces artistic collaborations, programs and mobilizing campaigns focused on community building, disability justice and gun violence prevention.

“Hit in the neck I ain’t even feel the burn.
Paralyzed instantly.
Praying to God, please don’t take me now
I got a little girl to look after and
I’m not trying to look after her from the sky”, Reality poet

OPEN DOORS is a project of the Center for Transformative Action-a 501 (c) 3 affiliated with Cornell University.

TR in Conversation with Andres “Jay” Molina:
What was your experience with poetry prior to disability?

Andres “Jay” Molina:
no experience at all. I never wrote a poem in my life ever. Didn’t even know how to write a poem.

Music begins, “Hooray for Hollywood”
— Explainer video about the film making process.

Andres “Jay” Molina:
I started thinking about how are movies made? What are the steps that go about making them? And that always intrigued me.
And that was always what I was after, making a film, documentary, feature film, a fiction film. Just something I think that would be fire.

TR in Conversation with Andres “Jay” Molina:
So was that an interest before disability?

Andres “Jay” Molina:
After.

I actually taught myself how to work with Premiere Pro. And I also taught myself how to work with After Effects. Taught myself Photoshop too. So I basically became a motion graphics artist.

TR
I can’t help but think about the importance of access.
To people, information, technology all based on our personal abilities.
But still, it begins with That desire to pursue our interest. Which comes down to trust in ourselves.

— Fire Through Dry Grass Trailer

Andres “Jay” Molina:
I wanted to make a documentary about the reality Poets. About everything that we went through and all our accomplishments.

And then in the middle of that, COVID hits.

a hospital called Elmhurst Hospital . in Queens, New York, was the epicenter of the pandemic. And they brought a patient from this hospital, into my room, put him in the bed right next to me. This patient had COVID. He was coughing the whole time he was there, gasping for air.

I have a lot of underlying conditions.

I felt betrayed. All these freaking people don’t care about me. They don’t care if I die or not.

TR
Feeling powerless, Jay reached out to someone he could trust.
Someone he believed cared about him.

Andres “Jay” Molina:
I call the director of open doors, Jennilie Brewster. I told her about the situation.

And she said, Jay, you are an aspiring filmmaker. why don’t we just make a film about this?

— ” A nursing home is ground zero. But it just takes one person with a virus and then it is fire through dry grass”, NY Gov. Anrew Cuomo

TR
Prior to the pandemic, Jay was working with an experienced filmmaker after receiving a grant from the New York City Mayor’s Office.

Andres “Jay” Molina:
Alexis Neophytides was my mentor. We were working together for a few years before COVID.
I call Alexis right away. And I told her about what I wanted to do. And she said, let’s make this documentary together.

TR
The film, Fire Through Dry Grass, captures the early days of the Covid 19 Pandemic from the perspective of Jay and some of the other Reality Poets. Literally, it’s from their perspective.

Andres “Jay” Molina:
We got like about four GoPro’s and I started clamping them myself to the chairs.

the GoPro shot is like a camera. They have a really big memory card like 60 gigabytes.

TR
Jay and the crew traveled throughout the nursing home documenting what was actually taking place.

Andres “Jay” Molina:
going to different offices within the facility and just recording everything.

TR
We’re talking about two Terabytes of video.

Andres “Jay” Molina:
We also have a lot of footage from outside of the facility. My collaborator, Alexis’ husband, were the ones coming and recording everything from the outside.

Every two or three days, I will just collect the GoPro, download myself into my computer And then upload into our Google Drive.

Andres “Jay” Molina:
As we started talking more and more about the film. We pitched the idea to ITVS public television, PBS channel. They liked it and they actually gave us the funding for it. So we started hiring people to work with us. The job was to watch the footage, and highlight and put aside anything that seemed important.

TR
In addition to zoom footage from the members of Open Doors in conversation as they continued to meet, there’s also arial shots taken from a drone.

Fire Through Dry Grass not only helped tell the story of the dangerous conditions being faced by both
residents and staff during the pandemic, but
it also raises the issue of disabled access to community housing.

Andres “Jay” Molina:
All of us have different agendas.
Most of the guys do want to move out. They always in the hunt for apartments.
Some of them are just here because they haven’t found one yet.

TR
Jay himself was offered multiple apartments. But they were often located in housing projects throughout the city. He didn’t feel safe and they were located far from his family in downtown Manhattan.
That was years ago, before chronic kidney disease.

Andres “Jay” Molina:
Which means I am on dialysis.
Even though I could live in the community and just go to the dialysis center, it’s much easier for me to live here.
All I got to do is get on my chair and go to the third floor and do the dialysis session.

TR
Community housing for disabled people is not just about access to shelter.
It’s about having the agency to control your own life and make your own choices.

— “Leave me alone, I want to be free from being told how to live my life
By rules, regulations, laws, bylaws, loop holes, pot holes and assholes
Let me be free to make the decisions that best serve me”, Peter Yearwood, Reality Poet

TR
Ultimately, the message that Fire Through Dry Grass makes clear is Nursing Home Lives Matter.

Andres “Jay” Molina:
During COVID Our now director of open borders, Vincent Pierce , wrote up a petition to get the CEO at that point of Coler, Robert Hughes, removed from his post.

We felt , he wasn’t advocating for us.

He was letting the Department of Health and CMS run all over us, take our freedom away. We felt that we were basically having our human rights violated.
And he wrote that petition to get the CEO removed from his posts, and other organizations saw this, and started supporting us.

That was around the time of Black Lives Matter. they formed Nursing Home Lives Matter.

TR
Robert Hughes, the CEO of Kohl at the time wasn’t fired, but I can imagine, the pressure got to him.

Andres “Jay” Molina:
The CEO retired in 2022.

TR in Conversation with Andres “Jay” Molina:
What can people do if they want to be of help? How can people support?

Music begins Bright, upbeat, ambient music that sounds like lights bubbling to the surface.

Andres “Jay” Molina:
Go to OpenDoorsNYC.org, that’s our home page. There’s a Nursing Home Lives Matter link. When you hit it you go to the Nursing Home Live Matter page. You can join in, leave your comments, leave your ideas on how you think is the best way to change nursing homes. In the country Not just here in New York.

TR
Today, despite the convenience and ease of access to dialysis treatments, Jays opened to living in the community.

Andres “Jay” Molina:
If I find myself in a situation in which I get an apartment, close to my family, my friends, my mother, my sister. I probably think about it again to move

TR in Conversation with Andres “Jay” Molina:
Do you think that would impact the reality poet’s if y’all are all, not in the nursing home together?

Andres “Jay” Molina:
No, because we also have two members that don’t live here.
Even though we do get together in person, we usually do everything virtually. Most of our meetings and events are usually through zoom calls. But every once in a while we do have in person meeting or event or project. And we just take an Uber, Access Ride to the location and get together.

TR
Since the making of this film, two of the Reality Poets have moved back into the community.

TR in Conversation with Andres “Jay” Molina:
Are there any things you learned about disability from making this film?

Andres “Jay” Molina:
Disabled people been living in what we call a system of oppression for over 100 years, in which we are treated differently, we are treated like second hand citizens
we are not being respected, we are not given the tools or help that we need to advance ourselves in life. And that’s what we are trying to break with this nursing home lives matter movement, that we matter , we are human beings too.

You still have a mind, you have a purpose, you have a say in your life, and the way you want to live your life, and that should be respected . And that should be enhanced, embellish by the people in power.

TR in Conversation with Andres “Jay” Molina:
Do you think there’s a power in film to do any of that as a filmmaker yourself?

Andres “Jay” Molina:
Of course!

We have advocated a lot for disabled people through the years of us being together.

We have done this movement Nursing Home Lives Matter. We are putting disabled people on the map.

Even though it has gotten better in Hollywood, a lot of disabled artist have been hired now, we think there’s room for more.
Not just actors and directors and screen writers, artists, poets, graphic designers all different type of arts.

I was talking to the group about making the documentary that I wanted to make originally before COVID about the Reality Poets, to show people if you try you could do it you can make it.

Music comes to an end.

TR in Conversation with Andres “Jay” Molina:
One of the things that you said is that when you became disabled, it sort of helped you discover yourself. And I’m curious to know, how do you feel about that man today?

Andres “Jay” Molina:
Well, I feel like I’m a better person now. Somebody that looks out for his people, people in pain, disabled people, People who need help.
Even though I’m in a wheelchair, whenever I see somebody, you know, like they can’t do it, I tie the shoes, I fix the pants, or fix the shirts, I fix the hats.
if they need me to feed them I will feed them. I’m more in touch with humanity now, which I wasn’t really before.

I didn’t really have a purpose. I found my calling.
, I became a poet. I became a filmmaker, motion graphics artist, Photoshop.

I tell people that I don’t regret me being disabled. And people are like “what you crazy” and I’m like I don’t regret it.

I found myself after I became disabled.

Music begins A very bright, inspirational piano loop that opens to a lively bright up tempo beat.

TR
Salutes to Film Maker, Poet and the newest addition to the Reid My Mind Radio Family, Andre Jay Molina. (Name extended like sports announcer)

— Airhorn

Shout out to all of the Reality Poets and everyone involved in the making of this film.

Fire Through Dry Grass goes beyond the experience of disabled people in nursing homes.
It’s about brotherhood, community, trusting in others and finding your purpose.

You can watch Fire Through Dry Grass on PBS online or the app.

I’m looking forward to more films from Jay on the big screen or other streaming platforms.

Andres “Jay” Molina:
I have ideas.
We wrote a play a few years ago called Fade about disabled men, that co own a barbershop.

— Scene from the play

So the play we had it in a theater for like a weekend, and it was received really, really good. So I’m thinking about making that into an animation stop film.

TR in Conversation with Andres “Jay” Molina:
I like it. And if you need some extra voice talent, let a brother know.

TR
Look don’t shame me. My clock is ticking, if I’m gonna put some points on the board, I have to take the shot!

— Basketball shot clock expiring and swoosh of the ball through the hoop.

TR
Listening to Jay talk about meeting the brothers outside of the nursing home, their camaraderie and their opportunity to collaborate really makes me think I’m still in search of my tribe.
I’ll talk about some of that in my final self-portrait in the next and final episode of this season. The Art of Adjustment.

As I said in the opening of the episode, the details don’t matter as much as we think when it comes to the experience of adjusting

Can you relate to Jay’s story?

Some people focus on differences. I don’t necessarily think that’s bad. Unless you’re judging or viewing through a narrow lens closed to any sort of empathy.

When I hear Jay’s story, I think about the importance of access to explore and pursue our interests.
I’m reminded that , unfortunately, these opportunities aren’t afforded to everyone equally.
Some neighborhoods and schools have programs that encourage young people to explore their creativity.
Some families have the ability and knowledge to make opportunities for their children.

Adjusting to disability can feel like time has stopped.
It’s like being in the middle of a game and the coach pulls you out.
You were just warming up and now you’re riding the bench to no where.

However, time, is access.

For Jay, disability gave him the time to learn a craft. This put him in the position to tell the story of what was taking place in the nursing home during the pandemic. He was prepared and equipped for what became an opportunity.

The older I get, the more I realize how time is limited and therefore quite valuable.

If you’re someone new to disability and feel stagnant, consider this your chance to prepare for an opportunity waiting to present itself to you in the not so distant future.
Hopefully it won’t be during a life threatening pandemic.
But whatever it is, I hope you recognize it and like Jay, light it up!

— Sound of a lighter and an increasing burning fire.

TR:
By the way, you know what else is hot?
Reid My Mind Radio baby.

— “Fire!”

Let’s continue to spread it!

Tell your friends, enemies and perfect strangers that they can get it wherever they listen to podcasts.

There’s transcripts and more at ReidMyMind.com.

The only way to get there I promise you, is by spelling it right…
that’s R to the E, I D!
— Sample “D…, and that’s me in the place to be!”, Slick Rick

Like my last name!

— Reid My Mind Radio Outro

Peace!

Hide the transcript

2020: The Year of Adjusting, Not A Just Thing

Wednesday, December 9th, 2020

I’m pretty sure most people will be glad to see 2020 come to an end.

But it didn’t start out that way. In fact, the year for so many was a symbol of a bright future, as in 2020 Vision. That idea can really be misleading!

Whether we’re talking about blindness specifically or the Covid19 pandemic,2020 was all about adjusting.

Police senseless killings, Black Lives Matter, Healthcare, we are lacking a just thing!

A look back at 2020 from this podcast’s perspective in just 20 minutes and 20 seconds!

Listen

Resources

Shout out to V! AKA Victoria Clare on her new single “By Any Means” Featuring, wait for it… me, the T. R to the E I D!

Transcript

Show the transcript

Audio: Oprah Winfrey’s 2020 Vision…
Oprah: “OMG! It’s about to happen (Crowd cheers) So of the nine visionaries joining us on the WW presents ah 2020 Vision Tour: Your Life in Focus, there’s only one man,

TR: Yeh, yeh!

Oprah: but when it’s one of the most recognizable,

TR: Mm!

Oprah: big hearted,

TR: that’s real

Oprah: delightful, fun,

TR: Ha, ha!

Oprah: strong

TR: Hey!
people on the planet, he’s all you need. Please welcome Dwayne the Rock Johnson!
Audio: Record Scratch

TR: What the… Fine, who needs them, when I got the Reid My Mind Radio Family!

Audio: Reid My Mind Theme Music

TR:

2020 is Ableist AF!

— Music begins with a bass boom into a bouncing Hip Hop beat —

I’m talking about this idea of perfect vision, used as a metaphor for a flawless; plan or strategy, objective or goal and yes even sight.

Audio Samples…

So much of this is perception, which is subjective. Assigning the label of perfect to something automatically creates a ranking system or hierarchy.

It’s not surprising that so many people in 2019 and earlier, decided that 2020, the number associated with perfect vision, was an indication of a better time to come in their lives. The time to create or invoke that plan. Maybe get into shape, return to school, start that new career. Whatever it was, 2020 began with real optimism.

In my early days of adjusting to becoming Blind, I can recall declaring random days, months and year as my time. The right time to start fresh. To look at the future with real hope seeing only opportunity.

I too kicked off 2020 with this energy for very specific reasons. That includes personal opportunities that were presenting themselves. Nothing grandiose but some that I could eventually see as the early steps in building a solid foundation.

One of the themes of 2020 has to be adjusting. Reid My Mind Radio has been focusing on this for years.
Victoria Clare, an artist in the UK, helped me kick-off the year with her story of adjusting to Blindness or as they like to say, sight loss.

Audio: Bumper
— Audio clip from: “Adjusting to Vision Loss – A Creative Approach with Victoria Clare” begins —
VC:

I went out in my Dad’s shed, I got a big old’ block of wood, stole some of his chisels, used his mallet and started creating. It was amazing. I turned my world around because it made me realize alright, I’ve been diagnosed with this sight loss but nobody’s taken away the skills that I’ve always had. They’re still there.

— Audio clip ends —

Audio: Bumper

TR:

More on her latest artistic endeavor a little later!

February came around and I was feeling pretty good. I was swimming on a regular basis – which truly means a great deal to me. That itself is an access story for another time.

I also got the chance to introduce you to my man, Ajani AJ Murray! In his episode Starting with Imagination, we see that no matter the disability, the idea that begins with our thought or imagination can sometimes be delayed by access. Notice I said delayed, not halted or deferred.

— Audio clip from: “Ajani AJ Murray – Starting with Imagination” begins —

AJ:

I always had this dream of being an actor. It was something that was always looming in the back of my mind. It was always in my spirit, but I didn’t know how to physically make the connection. I couldn’t necessarily afford acting classes at the time and I wasn’t in high school at the time to be a part of an acting club.

That idea of working within your reach continued. In the episode Climbing Accessible Heights with Matthew Shifrin, Matt talked about his work with Lego and the objective of his advocacy to give that access to others.

Audio: Bumper

— Audio clip from: “Climbing Accessible Heights with Matthew Shifrin” begins —

MS:

I just wanted people to have this resource because I’d benefited so much from it. Not all Blind kids have people that could write instructions for them. Everyone deserves to be able to build and to learn from what they’ve build.

— Audio clip ends —

Audio: Bumper

TR:

Sharing our experiences with others is so important. Dr. Mona Minkara from Planes, Trains and Canes used the power of show not tell, to capture the wide range of responses to a Blind person traveling alone. And as we know, those reactions are filled with nuance.

— Audio clip from: “Taking A Ride with Planes Trains and Canes” begins —
[TR in conversation with MM:]

Wait up. You said he was nice?

MM:

I’m saying he was nice yes. (Laughing)

[TR in conversation with MM:]

Did you feel that way in the beginning? From the video, I took this guy like he was being condescending.

MM:

Oh, he was totally being condescending. I think it’s just the norm there to kind of treat people with disabilities like we are a bunch of 5 year olds.
— Audio clip ends —

TR:

Traveling is less about the destination than the journey. In the episode John Samuel: Guided By Angels, we see it’s about who you’re traveling with and what you do once you arrive!

Audio bumper
— Audio clip from “John Samuel: Guided By Angels” begins —

[TR in conversation with JS:]

And you just happen to be standing next to her. There’s such a pattern with you.

JS:

I know man; I can’t make this stuff up. I got angels all over the place.
— Audio clip ends —

TR:

While many people were progressing with their 2020 Vision plans, looming underneath it all was Covid 19. We were advised to take individual precautions; wash your hands, don’t touch your face, use hand sanitizer and somehow that translated to get as much toilet paper as you can!

I invited my wife Marlett on to compare what we experienced as a family adjusting to blindness and what the world was going through in the midst of the pandemic.

— Audio clip from: “A Peak at Finding A New Normal” begins —

Marlett:

Social distancing, that’s funny to me because no one really came around We understood about social distancing people were doing that to us for quite some time. Distancing themselves from us.

[TR in conversation with Marlett:]

Damn!

Marlett:

Well it’s true.
— Audio clip ends —

— Audio clip ends —

— Music ends —
TR:
If 2020’s perfect visual acuity has shown anything, it’s the inequity in our society.
Covid 19 zoomed in on the drastic differences in healthcare.

— Audio clip begins from “Corona – So Many Parts” —
Audio: Instrumental “Quiet Storm” Mobb Deep

Audio: Covid19 related News montage

– “The Pandemic seems to be disproportionally affecting people of color”
– “African Americans have been hardest hit by the virus. Despite accounting for 14 percent of Michigan’s population they represent 41 percent of its Covid victims.
— Audio clip ends —

TR:

In this same episode, Corona: So Many parts, I went on to compare the adaptations made in society in response to the Corona with those people with disabilities have been seeking for years.
— Audio clip from: “Corona – So Many parts” begins ”

All of a sudden!

Audio: Gazoo (from The Flintstones)

Have you noticed all of the corporations now accommodating their employees with work from home access?
The online conferences and entertainment now available.
Everything getting done online.

If inaccessibility is manmade then maybe man can fix it,
Audio: “That’s right!” from Harry Belafonte’s “Man is Smart Woman is Smarter”

TR:

Huh!

Audio: “That’s right!” from Harry Belafonte’s “Man is Smart Woman is Smarter”
— Audio clip ends —

TR:

Swindler, Scam artist, Liar, Snake oil peddler, Divider, yet in this past election, many have and continue to support him and his white house administration.
. Some of those supporters I’m sure have the absolute worst intentions. They are white nationalists. But there are some who have simply been played. And one of the rules that we need to remember is everyone gets got at some point in their lives.

I shared a story where I was duped into being a part of a dog and pony show disguised as a demonstration and discussion about Blindness.

— Audio clip from: “Live Inspiration Porn – I Got Duped” begins —
Well, in this particular case, while the dog and ponies sat up in front and this one off to the side a bit, the sighted donors were led into their temporary world of vision loss.

Reluctantly at first, one after the other each slowly began trying on the glasses.

“Oh my”…. “wow”
“where did you go Jeanie?”

And then the real fun began as they exchanged glasses with one another. Laughing as they realized how little they could actually see. Unable to find things they placed on the conference table. The host joking as she moved their cups of coffee.

Meanwhile, the dogs and ponies sat up front. While the jackasses continued with their disability experiment.

Empathy, I didn’t see that. But a check was written.

I don’t remember how the event finally ended, but I do know that was it for me. I checked out. There may have been some additional conversation but I doubt I had much to say to anyone after bearing witness to that display of ableism. I vowed to never be a part of anything even remotely like that.

I could easily imagine each of the donors around the table going home fulfilled and thinking “I should really count my blessings, because there’s always someone worse off in the world.”
— Audio clip ends —

— Audio clip from: “George W. Bush Fool Me Once” begins —

GWB: there’s an old saying in Tennessee, I know it’s in Texas probably in Tennessee but it says fool me once… (long pause) shame on…, shame on you. (long pause) Fool me can’t get fooled again!
— Audio clip ends —

TR:

You know, learn from your experiences

— Music begins – A bouncy energetic Hip Hop beat —
TR:

Hey! Do you enjoy listening to this podcast?
Do you have a topic you want to recommend?
Reach out.
email ReidMyMindRadio@gmail.com or call 570-798-7343 and leave a voice mail. Like this;

Voice Mail:

I’m calling because I listened to the Reid My Mind and I thought that episode on Charles Blackwell was just fantastic!

TR:
That was actually Mr. Blackwell himself playing a little joke on me. He said I could use it and I would either way because he doesn’t have a computer so he won’t find out!

If you do have a computer or a phone that is online and you want to stay updated to what’s happening here;
Subscribe wherever you get podcasts!
Transcripts & more are over at ReidMyMind.com.
That’s R to the E I D
(Audio: “D and that’s me in the place to be” Slick Rick)
Like my last name.

And now back to the episode
—
Audio Bumper:

“Come on chop chop, the Doctor will see you now!”

TR:

Well not really. But let me break down 20/20 as a fraction signifying normal vision.

The numerator, (the top number in the fraction), , represents – 20 feet. The denominator represents the distance in feet where a “normally” sighted person can see that same thing.

So, someone with 20/20 vision is seeing as expected.

A person with 20/200 can see from 20 feet away what a normally sighted person sees from 200 feet.

When it comes to an awareness of police brutality, Black people been having 20/20 vision. I’d add Indigenous and many people of color as well. I’d even add woke White people somewhere on the spectrum.

But too much of America has been hovering around that 20/200 acuity. They’ve been legally Blind to police brutality forever. There’s no lens to help them see the systematic racism not only in the police departments across this nation, but also throughout our society. At least not long enough to actually do something about it.

The Covid 19 pandemic created the environment enabling the magnification of the brutal killing of George Floyd, the murder of Brionna Taylor and the injustice that followed.

I wanted to be hopeful that the initial attention and outrage would be a catalyst for real change throughout society. I talked about how these events have and continue to impact me and my family. I even talked about it in the realm of Blindness advocacy!

— Audio clip from: “Let Me Hear You Say Black Lives Matter” begins —

TR:

All the organizations that are either of or for the blind want the same thing; independence, security opportunity for all Blind people. Who does this really include? For some, blindness skills training isn’t going to be enough to have an opportunity to reach that goal.

For me personally to believe these organizations and others are really about independence for all, I’m going to have to see them lead the way. That leadership needs to come from those in power right now.

I’m going to need to hear them simply say it; “Black Lives Matter”

Audio Montage of individuals saying “Black Lives Matter!” Concludes with all simultaneously saying it.
— Audio clip ends —

TR:

I’ve been thinking about these intersections and specifically about the experiences of Black disabled people no matter the disability.
So I teamed up with RMM Radio alumni AJ to co-produce and host Young Gifted Black & Disabled! Along with our guests, Rasheera Dobson and D’arcee Charington, we talked about all sorts of issues including the lack of Black disabled images in the media.

— Audio clip from “Young Gifted Black and Disabled” begins —

Rasheera:

I get a little sad. I never saw anyone like me. I never saw a girl with disabilities in Essence magazine. Struggling with low self-esteem growing up I think it had a lot to do with the fact that I was reading Essence magazine, Ebony magazine Jet magazine reading the stories of Toni Morrison and hearing the Black struggle but I never read about the disability struggle.

It Matters, it really does.
— Audio clips ends —

TR:

Yet D’arcee shared how there’s so much to be proud about.

— Audio clip from “Young Gifted Black and Disabled” begins —

D’Arcee:

I was just thinking of the Morpheus quote from The Matrix Reloaded, which I recently saw. When he was in Zion, when he was talking to everyone trying to calm them down and what he said is; what I remember most is after a century of struggle I remember that which matters most.

Audio from Matrix Reloaded: “We are still here!” Crowd roars in applause!

That resonates so deeply with who I am as a person.
— Audio clip ends —

— Audio clip from “Young Gifted Black and Disabled” begins —

AJ:

The full story of the black experience hasn’t been written yet.
There are plenty more chapters yet to be explored.
— Audio clip ends —

TR:

That exploration includes the experiences of people like Artist, Poet, Writer Mr. Charles Curtis Blackwell and his words of hope and inspiration.

— Audio clip from: “Charles Curtis Blackwell – Words of Meaning Empowerment & Inspiration” begins —

CC Blackwell:

I realized ok, God gave me this talent and with this talent he’s kind of helped raise me up from that bed of poor self-esteem. Lift me up and encouraged me and inspired me. And I have to take care of this talent. I have to nourish it, be kind to it, treat it right and try to use it.

— Audio clip ends —

Audio Bumper:
Uplifting music with a beat could work to close out from here.

TR:

With over 250,000 people lost from Covid in the US alone and millions affected, it’s hard to say anything good came out of the pandemic.

I did however have to acknowledge the accessible content coming from the team that brings you the Superfest Film Festival. Director of the Paul K. Longmore Institute on Disability
center Cathy kudlick talked about the types of films featured at Superfest.
— Audio clip begins from : “Superfest Disability Film festival: Going Above & Beyond”

Cathy:

“… we highlight what we think is disability 201 – films that share the creativity and the ingenuity or the unexpectedness or the intersections of disability with other kinds of identities.
— Audio clip ends —

TR:

Associate Director of the Longmore Center and Superfest Coordinator, Emily Beitikss talked about the festival’s commitment to access including Audio Description.

— Audio clip begin from: “Superfest Disability Film festival: Going Above & Beyond”
Emily:

So much of our work is working with these film makers to teach them, think about the problem and have tough conversations as we do it so that hopefully people are thinking about it in advance of making their films.

— Audio clip end —

TR:

Including AD as an ongoing topic of discussion fully aligns with the objective of this podcast. It’s never just about entertainment. Media isn’t just about entertainment. Access isn’t just about entertainment!

This year we featured a bit of a history lesson on Audio Description. Rick Boggs of Audio Eyes took us through the involvement of Blind people in AD from its inception.
— Audio clip from: “Viewing Audio Description History Through Audio Eyes with Rick Boggs” begins —

Rick:

What I’m proud to say about Audio Description is Audio description as created by Blind people. And every innovation and advancement in Audio Description that has really contributed to what it is now was made by Blind people.
— Audio clip ends —

TR:

We continued with IDC’s Director of Audio Description Eric Wickstrom on what makes quality AD
— Audio clip from: “Audio Description with IDC: Good Enough isn’t Good Enough!” begins —

Eric:

There’s too much good enough is good enough. For us and our standards at IDC, no we’re not striving for good we’re striving for great!
— Audio clip ends —

TR:
A big part of that great is in the writing. Head Writer Liz Guttman shared her passion for AD.
Liz
— Audio clip from: “Audio Description with IDC: Good Enough isn’t Good Enough!” begins —

Liz:

I go to work every day and I get to write, think hard about the best way, the most vivid and concise way to convey something that’s on screen. So that someone who’s listening to it will get the same feeling that I have watching it. And to help bring us all in to the same level. Especially since I have become more familiar with the Disabled and Blind and Low vision community. I have friends in that community now. I care about their experience.

— Audio clip ends —

TR:

In Flipping the Script on Audio Description, we expanded the conversation to be a bit more critical and inclusive of those involved in AD from varying perspectives.

Like Media Accessibility Provider, Alejandra Ospina

— Audio clip from: “Flipping the Script on Audio Description” begins —

Alejandra:

I do Close Captioning and I do transcription and I do translation and Audio Description and so I like to imagine the things I’m doing all sort of promote access to content. I don’t consider myself as often a content creator but I like to facilitate people getting to see or hear or know what they’re watching.
— Audio clip ends —

TR:

In the second installment we heard from four Voice Over artists also narrating AD. We talked a bit about the inequities and the importance of authentic voice representation. Inger Tudor well she just broke it down to the very last compound!

— Audio clip from: “Flipping the Script on Audio Description Part Two – Voice matters” begins —

TR:

I know some people hear this and say, why should it matter? Shouldn’t anyone with a suitable clear voice just be able to voice characters or narrate films no matter their race, ethnicity, gender etc.?

Inger:

Hold on a minute. Four hundred years, we haven’t had the opportunity to do a lot of stuff, take a seat for a moment because I guarantee you your seat for a moment will not end up being four hundred years. Then when we get to the place where everybody can do everything that’s fine, but we’re not there yet and we need to catch up so give us a minute, ok?

[TR in conversation with Inger:]

There it is!

— Music ends with a base drop that pulsates and slowly fades out.
— Audio clip ends —

TR:

We went outside of the US in the third installment. No real surprise, the guidelines used in Canada and the UK tend not to include race, color or ethnicity in Audio Description.

Fortunately, there’s people such as Rebecca Singh of Superior Description Services in Toronto who are changing that.

— Audio clip from: “Flipping the Script on Audio Description Part Three – Moving Beyond Just US” begins —

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.
— Audio clip ends —

TR:

2020 doesn’t seem very fair.

The success achieved by other countries in their handling of this virus shows this pandemic, could have just been a thing! way too many lives lost that could have been prevented if we all spent a bit more time adjusting.

If only we learned from our past – you know 2020 hindsight? Oh wait!

Audio: 2020 Hindsight, Dilated peoples

Big shout out to all of the Reid My Mind Radio family. Whether you been rocking with me for just a few episodes or 100 plus!

One of our family members and alumni, Victoria Clare reached out during the pandemic to see if I’d be interested in collaborating with her on a song she was writing. She wanted to include a rap break and thought I could make it work. I said yes!
The song is available just about wherever you buy or stream music. It’s called By Any Means – it’s an upbeat dance track written to empower and inspire women who reach that point when they need to go inward and pull out that strength. I’ll link to the track on this episodes blog post.

If you like what’s been happening here on the podcast please pass it on. I know there’s a lot of people who would benefit from meeting others impacted by all degrees of blindness and disability.

Some have asked if there’s a way to financially contribute to the show.

If you are so inclined, you can donate via PayPal to ReidMyMindRadio@gmail.com.
All funds go to supporting the podcast.

Finally, I want to close this episode a bit differently in memory of someone I lost this year. A teacher of mine who said as a teacher he was there to quench our thirst but would eventually melt away. He was wrong! He ain’t going anywhere!

When we finished our conversations he’d say “May we remain” I think of that now like a little prayer.

Reid My Mind Radio Family, I wish you all a very joyous holiday season and great things in 2021!

May We Remain!!

Audio: Reid My Mind Outro

Peace!

Hide the transcript

Let Me Hear You Say Black Lives Matter

Wednesday, June 17th, 2020

In gold lettering on top of a red, black & green background appears "Reid My Mind Radio."

the title says it all! It’s the place we have to start if we are really going to make change in this country & world. I’m talking about individuals as well as society. And included among that group are the blindness consumer advocacy organizations; ACB and NFB. While there are differences in the founding philosophies of each, at the core both of these groups strive for Blind people to have the same rights as our sighted peers. Do they really mean all Blind people? I want to believe they do, but I guess I’m going to need to hear them say it; Black Lives Matter!

I’m trying to remain optimistic but right now, it really takes a lot of effort to be hopeful. I was reminded of a story from the Reid My Mind Radio archive that in a way illustrates some of what needs to happen in order to really move forward.

Listen

Transcript

Show the transcript


Audio: Music… “Mission Start”

TR:

Welcome to or back to the podcast! My name is Thomas Reid and I’m the host and producer of Reid My Mind Radio – the podcast bringing you compelling people impacted by all degrees of blindness and disability. Sometimes I share experiences of my own as a man adjusting to becoming Blind as an adult.

today, well, it’s right there in the title. That is, the place we have to start if we are really going to make change. I’m talking about individuals, society and yes blindness & disability advocacy organizations.

If you’re part of the Reid My Mind Radio family, you know I’m pretty optimistic. It takes a lot of effort right now, but I’m trying y’all, trying to remain hopeful.
Audio: News commentator announcing global protests in London, Australia, Japan, Korea & Germany. All mixed with the chants of Black Lives matter!

TR:
That solidarity & declaration that I’m hearing from around the world, feels good, but I
need to hear it from voices much closer to home.

Audio: Montage of voices saying Black Lives matter. Each panned along the stereo spectrum.

TR:
Let’s go!

Audio: The final voice says;
“Yo, Black Lives matter!” The voice of Siri from the IPhone says” Send”

Audio: Reid My Mind Radio Theme Music

Audio: Sounds of dinner table/kitchen conversation from the Reid family household.

TR:

Like a lot of families meals are a time to come together. Not only to prepare and enjoy the food but also to check in with one another.
In the Reid household, we established some rules years ago around what was acceptable during meals. Like we don’t answer phone calls, we don’t look at our devices but rather we stay in the moment while we are eating together.

Audio: News commentator on the killing of George Floyd and protests.

TR:

Unfortunately, no matter how much I would like the rule to be in effect, just while we’re eating, there are times we can’t really afford to keep them. The most recent murders of Ahmaud Aubrey and George Floyd, the protests and of course, the self-described nationalist in the White House have caused us to rescind the rules. Both of my kids need to discuss all of this.

Riana who will be 23 soon is extremely passionate when it comes to issues around social justice. She needs to be active and she’s figuring out the best ways for her to do that. For example, donating to protester bail funds, continuing to educate herself through reading and research and sharing resources with her network.

Raven is younger, more internal and is really figuring out how to articulate her thoughts. Her friend groups are very diverse and she recognizes the differences and really appreciates them. Recently, she had to deal with the outing of a classmate, one in particular which has garnered a lot of national attention. This young 17 year old made very public awful racist comments. Listen to the statement from a young girl from Generation Z. Some thought this would be the post racial generation free from racism. Notice how deliberately she shares her revelation.

If you are triggered by little racists using the N word, skip ahead about 34 seconds.

17 Year Old Racist:

So, I’ve been seeing this video going around about why Brown people should be able to say the N word. So I’m here to tell you why white people should be able to say the N word. Because we made it up and none of you guys would be able to say that word if my ancestors didn’t decide to call you Black people Niggers all the way back in those old days. And so what do you guys do to try and show your appreciation, for coming up with your best word to call your best friend Nigga as you pass each other in the hall? You do what all good Black people do, you stole it. So all I’m doing here is trying to take back what’s already ours.

Audio: Ambient music

TR:

If it was shocking to you because you never heard this sort of language, it’s time to acknowledge your privilege. It’s not a time to pat yourself on the back because you raised your children to be color blind. It’s not a time to feel the need to share how you cried when Dr. King was assassinated or even you know someone who is Black. That doesn’t work towards a solution which makes you part of the problem.

Not even the four walls of our comfortable home can keep my family protected from the reality of violence against Black men, women and children. Like trying to explain to my kids how Travon Martin’s murderer was not going to face prison. Michael Brown’s killer would just walk free.

Riana has goals of moving out on her own. Meanwhile Breonna Taylor a 26 year old Emergency Medical Technician gets shot 8 times in her own home by police after wrongfully busting in her house in search of a suspect already in custody.

Audio: Two young children saying “Black Lives Matter”

Raven right now is learning to drive and I have to think of Sandra Bland and the others who have ultimately have fatal encounters with police because their driving while Black.

A word of caution:
What you’re about to hear is an example of the trauma and fear associated with police brutality. If the threat of violence is triggering, please skip ahead about 2 minutes.

Audio: Woman passionately trying to help a young Black man while he is being surrounded by police. We find out her boyfriend was also killed by police. The audio ends with her sobbing for them to simply put their guns away while begging the young man not to move.

TR:

Y’all know this isn’t about my privileged dinner time, right?

for Black people, it’s not only the threat of violence and interactions with police, but not dealing with the feelings around these murders is like allowing a virus to infect our bodies. We can wash our hands regularly, sanitize every package that comes into our homes, eat organic food but how do we protect ourselves from feeling as though we don’t matter.

Audio: A woman saying Black Lives Matter.

TR:

Being totally Blind doesn’t stop the images of these horrible killings from being engrained in my mind. I don’t need to see video of Michael Brown’s body left on the street after being murdered, I don’t need to see Ahmaud Aubrey being shot down or this deranged so called officer kneeling on George Floyd’s neck to understand what that looks like. In fact, these images involuntarily flash in my mind without ever having seen them.

Recently I tweeted that I was waiting to hear a show of solidarity from the blindness organizations. I soon read one from NFB and then specifically questioned if ACB was going to show their support. They did. They also directed a tweet to me that they were waiting on a review before posting.

My response was that I was happy to see them done but the real statement will be seen in their actions like representation on their boards and leadership position and outreach.

Both statements were weak. In general, any solidarity statement at this point in time that does not include the simple phrase acknowledging that Black Lives Matter, it doesn’t have much weight in my opinion.

Audio: fire engine racing towards a burning building.

If a house was burning on a block of 10, should the fire department show equal attention to each house. Wouldn’t it be fair to first put the one fire out? Save the family in the house. Apparently some would prefer the fire department drive right past the burning house in order to make it clear that all the houses on the block are important. Meanwhile, do you all smell that smoke, the other homes on the block are beginning to burn.

Audio: Young man says Black Lives Matter

TR:

If a solidarity statement had to be generated by the Black or multi-cultural segment of the organization, it’s starting from the wrong place. Is that because some blind people like to think their blindness makes them immune to racism? Funny thing is most Blind people have had sight at some point. In fact, most Blind people aren’t even totally Blind. You’re not being honest with yourselves if you think racism doesn’t affect you. As if you don’t benefit from white supremacy.

Audio: Do Blind People See Race…

From Tommy Edison YouTube Channel:
“Martin Luther King always talked about don’t judge a man by he color of his skin but by the content of his character. And I have to be honest with you I think people like myself and other Blind people are the best at that because we don’t see the color of their skin.”

From YouTube, “Can Blind People See Race” Freedom is mine official.
“Can Blind people see race? Given that we identify a person’s race primarily by their appearance, what elements do the visually impaired use to perceive race. Several studies have been done into this area and the conclusion is definitely yes, visually impaired people can perceive race.”

TR:

History has shown when it comes to so called racial issues, America is all about weak statements.

America doesn’t want to examine their role. You know what, let me say that again to not sugar coat it …

Audio: Music…

TR:
White America doesn’t want to do the work to fix racial injustice.

I see the same right now from blindness organizations. Asking Black people to lead this effort isn’t the fix. Rather, once again for Black people, our dinner time with our families are being interrupted.

Why not start with a real self-evaluation. Have a conversation among the organization’s leadership and board about race. Whether personal but more specifically as it relates to the organization. Look back, how many members are even in the organization? How often does the leadership interact with them and what have those interactions been about? How often do we hear from Black people at our meetings and conferences. have we ever truly done any outreach or did we wait for those Black people in the organization to recruit others?

This is a problem that existed in this country for 400 years and won’t be fixed with one statement. it won’t be fixed in our lifetimes. It requires a lot of work that starts with honest self-examination.

To be clear, I think it’s time for these organizations to truly look at the intersections between disability and other identities. The majority of police brutality cases impact Black people with disabilities. Women with disabilities experience an overwhelming number of sexual attacks, LGBTQ and Trans communities have a significant population of people with disabilities. And Black Trans gender men & women need our support. Honestly, if you have a problem with that then you need to ask yourself if you’re really about justice.

All the organizations that are either of or for the blind want the same thing; independence, security opportunity for all Blind people. Who does this really include? For some, blindness skills training isn’t going to be enough to have an opportunity to reach that goal.

For me personally to believe these organizations and others are really about independence for all, I’m going to have to see them lead the way. That leadership needs to come from those in power right now.

I’m going to need to hear them simply say it; “Black Lives Matter”

Audio Montage of individuals saying “Black Lives Matter!” Concludes with all simultaneously saying it.

TR:

In producing this podcast, I’m always searching for the right mix of education, resource sharing and entertainment. As I usually believe our stories have more to offer outside of those adjusting to blindness, I recalled this travel story from the Reid My Mind Radio archive.

Audio from “Traveling Zen”

Audio: Biggie Story to tell

TR:
Just this past Thursday I was traveling to Mobile Alabama –
Yes, Mobile Alabama…
Why?
Well that’s not really for this discussion.

In fact, let’s go revisit the day…

Audio: Car pulling to curb

TR:

Exiting the chauffeur driven Suburban I’m met by one of the Allentown Airport staff responsible for
Assisting travelers through the airport. I refer to them as the Meet and greet staff.
Normally, I have to get to the check in counter in order to request this, but luck
Just had it a very nice gentlemen by the name of Tom was waiting on the curb for someone who needed assistance.

Audio: SoundOfAirport – Check-in/Security

Smoothly clearing the check in process and
Security, Tom informs me that my flight is delayed just as we reach the gate.
It was close to 12 PM. And my flight was originally scheduled to leave at 1 O’clock and
Arrive in Atlanta at 3 PM for a connecting flight To Mobile at 5:15 PM.

Ok, no worries a departure at 2 is fine, I’ll get to Atlanta by 4. No problem, even though Atlanta’s airport
Is huge, I’d still have time to make my flight. And I’d rather wait in Allentown airport which is way smaller and comfortable.

At 2 O’clock I’m told we’re now Departing at 2:30.
Now this is a potential problem! With a connecting flight at 5:15…
There’s a good chance I’ll miss my flight.

I go over to the ticket agent to see what I can do about this potential dilemma.
Rosita, the ticket agent schedules me for the later flight Which leaves Atlanta at 9:15,
In the event I missed the 5:15 flight.

Requiring the assistance of a meet and greet means I’m one of the last people off the flight. This Adds to the probability that I
May miss my connection. On the flip side, I’m one of the first on the plane!

I’m pretty relaxed already, but now I decide it’s time for me to go into a Zen state of mind. One thing about adjusting to blindness, it means
Becoming accustomed to waiting.

The ticket agent announces over the PA that it’s time to board.

I grab my coat, bag and cane and proceed to the counter. I board with one of the ticket agents.
I ask her if she could somehow call ahead and make sure a meet and greet is there
When we arrive so I can exit the plane quickly and make my connection. She takes my boarding pass and says she would do that.

Sitting in the window seat, I strike up a conversation with my seatmate when he arrives on board Delta Flight 5387. I tell him about
My connection issue. He seems to think I have a strong chance of making the flight.
We chat a little more, I put my headphones on, and open my Audible app to read my book. I’m good, I’m pretty relaxed and calm… I accept what I can’t control!

At around a little after 4, the pilot announces that we’re about to descend and
We’re scheduled to arrive on time 4:40. My seatmate, nudges me,
I think you’re gonna make it, he says. Knowing what I know about the wait for a meet and greet
I tell him, “Meh, we’ll see! I’ll still have to wait for assistance…”

At 4:45 we’re on the ground taxiing to the gateway
I take out my phone and check the Delta app to determine the status of my next flight. There’s significant bad weather so I’m hoping
My next flight would be slightly delayed. Nothing…
The pilot announces we’re going to terminal C gate 33. By 5 PM we’re still on the tar waiting to be directed into our new gate, D 33.
My seatmate is excitedly telling me I can make that flight.
“Just run out of here you can make it he says. I’m thinking did he not hear me when I said I need to wait for assistance.

I check the app again, it now says my next flight is boarding and scheduled to leave on time.
At gate D29. I tell my seatmate… Aww you can do it! He says as
he stands up to retrieve his bags from the overhead. I ask him to pass me my back pack and folded up cane.
Is this yours too, he asks
A folded up white cane, I ask… Yes! Now, He sounds confused… I think it sinks in…

My man, I say… do you think you can help me Get to d29… it has to be right near this gate.
I didn’t think it would be a bother, he wasn’t connecting to another flight. Yeah! He exclaims
I say to him… “get in front of me and let
Me hold onto your right elbow.” He complies…
I grab my bag and we take off.

Audio: Victory music

My seatmate now ripping through the narrow aisle. And my shoulders knocking into chairs and walls
He apologizes… Bro, I can take a hit let’s do this… turn it up. Yeah, he exclaims again now even more determined to accomplish his goal…
We zoom past the flight attendants who say something about An assistant… I don’t bother responding, no time for that
My seatmate and I are now a team and we’re on a mission.
“He’s my blocker “I think to myself and we’re gonna score this touch down…

We can do this, I hear him say as we rip past the ticket agent at gate 33… As we’re quickly and purposefully walking, in search of gate D29-
I hear my name. … Paging Mr. Reid, Thomas Reid… That’s me I tell him.
“He’s here, he’s here” yells my Blocker… He’s here, he’s here…says the ticket agent at D29 into a telephone…

We get to the podium at gate 29… Touchdown!!!

As if rehearsed, We do a two hand high five, chest bump, all While the ticket agent and bystanders applaud….

Ok, that would have been the movie version celebration.

Instead, the ticket agent asked for my boarding pass… I retrieve my boarding pass
Thank my team mate and I’m hurried onto my next flight.

I didn’t get his name or even had the chance to Shake his hand, but man I appreciated him.

Sitting on my final flight to Alabama considering how through that entire process
I felt quite comfortable and calm with just going with the flow. I thought about the first part of that very well known
Serenity prayer: God grant me the serenity to accept the things I cannot change; courage to change the things I can; and wisdom to know the difference.

This experience reinforces what I believe is the power of team work. I thought about how this pertains to lessons
for those adjusting to blindness or for that matter adjusting to any sort of change.

I’ve always been one to think of that very broad definition of independent as doing something by myself.

Could I have done this by myself… Some may quickly say no, others may argue yes with the right circumstance as in accessible information…
like a good indoor navigation app. But honestly,…,…., it was way more fun with a team!!

Audio Bumper bringing us back to the present.
Audio: Music starts…

TR:

My seat mate and ultimately my team mate for a few minutes at least, was as far as I can tell a white guy. We worked together. I was in a position where I needed him to be out in front if I wanted to make my flight. It wasn’t my only option, but missing that flight would have meant a really long and possibly very uncomfortable delay. Not for him, but rather, just me.

Reid My Mind Radio will be back on August 4th. I have some really good episodes planned for the second half of the year but right now, I need to do a little recharging. If you’re new to the podcast, feel free to check out the archive. We have over 100 episodes and they don’t expire.

You can get that just by subscribing to Reid My Mind Radio wherever you get your podcasts. None of my stuff is behind a pay wall because I really do want it to be an accessible resource for those adjusting to blindness.
Transcripts, resources and more are over at ReidMyMind.com. And yes, that’s R to the E I D (Audio: “D, and that’s me in the place to be!” Slick Rick)

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Are Blind Conferences Fantasy

Wednesday, November 2nd, 2016

Back from another Pennsylvania Council of the Blind Conference. This is not a recap.

After all of these years, this was the first time I recall hearing that such conferences  have been described as fantasy. Fantastic! Yes, but I never heard them described as being a fantasy.

Unicorn with Sunglasses

You could say this is my opinion on  the idea or you could just say it’s what was on my mind!

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Transcript:

Just about two weeks ago now, I attended my 11th conference of the Pennsylvania Council of the Blind.

My first conference was in 2006. I attended with a group representing the newly formed Monroe County  Council of the Blind or as we called it MCCB. We were considered a young, energetic  and extremely enthusiastic bunch of new comers to the organization.

Most of the group were newly adjusting to blindness. The MCCB itself was formed after we met at a local support group and decided we wanted to do more with our energy than talk about the issues.
Don’t get me wrong, I am all for talking and sharing our stories to help one another better manage the experience, but for many of us we were used to doing more and had a need to put our energy to good use.

I’m sure each of us who attended that first conference had our own expectations. I don’t fully remember what I expected, but I know I was open to learning. I can definitely recall trying to process so many different emotions throughout the weekend and during the first few weeks to follow.

Even today some things really stand out from the experience.

Like when one of our members Mary Ann,  was given a Braille menu at an Olive Garden during dinner on our first night at the conference.

Her excitement was infectious! It was just a menu! In fact, it was just Olive Garden – no shots, I enjoy the breadsticks and salad!

As the only proficient Braille reader in the group, Mary Ann immediately designated herself as the official menu reader for the rest of the group who did not read Braille, but even for those who could read print.
And the group honored that request, not as though they had a choice!

As a new advocate at the time, I was both excited for her but yet upset that she was still so surprised by the availability of the menu. Obviously something she did not experience often.

The next morning, I got my first glimpse of an accessible tour of what I recall was a train museum.

The tour guides used descriptive language as opposed to assuming everyone could see and recognize various features about the characteristics of these historic trains.

Some of the materials were available in alternative formats to standard print including Braille and large print for those with low vision

This may not seem like a big deal for those in the know, but when you’re new to blindness and beginning to believe you have to get used to just missing out on certain things;
observing that it doesn’t really take that much effort to be included, well it’s a real awakening.

I recently heard these types of tours and activities or even the conferences themselves  described  as fantasy.
The idea is that this is not and will never be the real world. The real world I guess in the minds of those who believe this is fantasy will always  exclusively cater only to those with sight and forever exclude people with vision loss.

At various times  throughout my journey with vision loss I came close to believing things can’t change. My struggle with cynicism was only made worse  with the random encounters with those who remind me that they see me first as a blind man and their definition of that goes beyond my inability to see.
For them it’s the subconscious stereotypes and misperceptions that create their image of who I am. the things I do or don’t do are viewed through a lens painted with layers of misinformation that so much of society has been lead to believe about blindness and disability.

Being conscious of that  comes with a price.
I can sometimes put more pressure on myself to   do something “right” believing that if I veer off course or make a simple mistake I may confirmed a false truth about blindness.

The fantasy world of blind conferences or conventions actually provided me a place to practice all of my blindness skills in a friendly atmosphere.
These conferences also  offered me a chance to relieve myself of the burden of believing I had to represent every blind person in the world.

There are times when I can get up from my chair during a conference  and almost perfectly walk out of the room using my white cane and easily navigate my way to my destination.

Then there are the other times when I get a little side tracked for various reasons.

These conferences have over the years taught me that both results are okay.
There’s no perfection.
People with all levels of  Orientation and mobility skills have and do both.  People with 20/20 vision do both.

it’s not my responsibility to explain how my cane tapping against  a planter or some obstacle in the middle of the room is not a sign that I am lost, but rather me gaining access to that information to determine which is the best course to avoid that obstacle.

I can’t change what someone else sees. This is determined by their experience and knowledge , not me. I know there are those who will lump all people who are blind together.
We share the experience of blindness, but for many that’s it! We’re different in so many ways.

Maybe these conferences are considered fantasy based on the cooperation and the way people tend to work together.

Since that first conference, I watched how people with all different levels of vision loss could help one another.

The person in the elevator who has low vision searching for the right button extends their gratitude to the person with no sight whatsoever who quickly identifies the button using Braille.

the teamwork of one gentleman using his white cane while  supporting a man with both vision loss and mobility challenges , slowly losing his strength, make his way to his hotel room.

Throughout the weekend, I witnessed people  all in support of one another. I saw more to blindness than I did prior to the conference. It confirmed that  not only was I right in thinking my vision loss didn’t have to mean more than I can’t see. It didn’t reduce who I am as a person. it didn’t put me in another class of people. It didn’t in any way impact my competence, my manhood my spirit. It simply means my eyes no longer work and I need to figure out other ways to get the information that I need to do certain things.

Since 2007 I’ve been a part of the conference planning team and I have been the coordinator  since about 2010 . My hope each year is that those newly adjusting to blindness will walk away from the conference  believing  that what some see as a fantasy is really inevitable.

There are changing demographics that make accessibility  a much more mainstream term today than even in 2004 when I was first introduced to that word.

Companies like Apple have committed to accessibility  making so many things usable for people with disabilities.
Smart phones and their apps
Television and movies along with audio description
indoor navigation which basically brings  GPS inside.

All of this progress is real!
We can touch it,  put it to use today and measure its effectiveness.

However, we’re not able to count the degree in which the attitudes are changing.

For many people the last few years have been an awakening to things that have existed since this country’s beginning.

The police brutality against people of color
Law enforcement’s corruption and cover ups of these incidents
Racist ideologies and behavior throughout society.

Camera’s and demagogues like Trump bring all of this to the forefront for all to see and confront.

Meanwhile those in the communities effected have been raising their voices in protest forever. The larger society not wanting to believe it or refusing to believe this could be true simply lowered the volume control and went on with their lives.

Blindness according to multiple surveys is ranked as America’s greatest fear… even more than death.

Some of these surveys are as recent as August 2016.

We know that people fear what they don’t know or understand.

This level of ignorance in 2016 is not surprising  but also not excusable.

The other side of this ignorance are those who are overly amazed by blind people living their lives every day.

Successfully living lives shouldn’t be considered amazing.

Maybe then we raise the bar for what we expect from people with vision loss and others with disabilities. And there’s no doubt that these expectations would be met.

In no way will I frame my perspective as a fantasy. It’s in progress. The more access gained the more people will have a chance to hear our voices, learn of our stories and rid themselves of their fears. It’s happening, just watch!