Archive for the ‘African American’ Category

Reid My Mind Radio: At the Intersection of Black and Blind

Wednesday, January 18th, 2017

Many would assume growing up blind in the 1950’s & 60’s had its challenges. What about growing up Black and Blind attending a segregated school for the blind?

Robert Lewis at work at the Radio Reading Network of Maryland

In this latest Reid My Mind Radio you hear from the Executive Director of the Radio Reading Network of Maryland, Robert Lewis.

We talk about;

  • Attending a segregated school for the blind
  • How being blind saved his life
  • Playing music with Stevie Wonder and much more.

Plus in the special podcast edition, we include some of his personal music suggestions for those times when you just need a lift!

 

Subscribe bit.ly/RMMRadioSubscribe

 

Press Play below to Listen now!

 

Transcript

Show the transcript

TR:Happy New Year!

I know some of us are not feeling that happy in 2017 and possibly longer. I don’t know like 4 years!
Well, as long as we’re not six feet under or my personal favorite stuffed into an ern sitting on a mantle… we’re good and we can make things happen.
We can fight…fight the power!
But first a new Gatewave piece I know you’re going to like and some extra immediately following!
Hit me!

[Audio: RMMRadio Theme Music]

 

TR:
Meet Robert Lewis, the Executive Director of the Radio Reading Network of Maryland. With over 35 years in the business, he is more than qualified to run the network. We’ll hear more on that, but it’s his life experiences that are truly compelling and offer a glimpse to what it was like growing up as an African American attending a segregated school for the blind.

 

RL:
I went to the Maryland School for the Blind, here in Baltimore Maryland. It was a wonderful place to go to school. I started there in 1954. It was a nice school but in the very beginning there was one side for the blacks and one side for the whites. And you were not allowed to sleep on the white campus . The two races went together for school but after that we would go our separate ways the first couple of years that I was there. That’s the way they had the whole setup.

Things were done to you or things were done that would not be tolerated today.

In the beginning they wouldn’t  buy Black kids Braille writers and things of that nature until like 50’s or more like in the 60’s. They started doing some things for Black kids that they didn’t do before and they would do them for the white kids.

You would be surprised what we had to deal with  in the 50’s and 60’s in a blind school.

 

TR:
The discrimination, limited social interactions, like at parties.

RL
As soon as we started to dance with one of the  white girls, the party was over. That party was ended!
They weren’t going to have that.

Society makes people prejudice. If they had left us alone it would never had happen, but because the teachers and because of the house parents and so forth  letting you know that you were black, who cared?
The students didn’t care!

The Lion’s Club used to come out and deal with us.
And at one time the Lion’s Club did not deal with Black kids.

 

TR:
the discrimination lead to varying degrees of abuse.

During a school Halloween party, a member of the Lions Club was responsible for guiding Robert to his chair.

 

RL:

He grabbed both my arms and walked me backwards to the chair.
I’m a 6 year old kid and this is a full grown man and he was squeezing my arms as hard as he could to try and make me cry and I said to myself he’s trying to hurt me but I’m not going to let him know that it hurt. So I didn’t and after he got me to the chair he pushed me down with a little bit of force. That was his way of saying well I don’t really like doing this or I don’t like Black people and I don’t like Black kids.

 

TR:
There was the even more abusive punishments dealt out by those charged with protecting and educating blind children.

 

RL:
Some of the Black kids were punished to the point that we had to stand out in the hall at night with no clothes on.
First we didn’t understand it but then we realized that the person that was doing that may have had a little problem on the side.

 

TR:
The discrimination continued as Robert traveled outside of the state competing with the school Wrestling team. He recalls, they couldn’t eat in restaurants.

 

RL:
We went to one restaurant and the lady said you got to eat as fast as you can so we can get you out of here before the owner comes  back because if he saw we had Black people here he would fire me!

 

TR:
In North Carolina, it was more than getting a meal.

 

RL:
Guys jumped out of the car and came over and they were going to beat us
all up.
We had no idea … What is this all about? Is it because we are blind; no, it’s  because you’re black and you’re blind!

 

TR:
Eventually, the segregation came to an end. The children lived together.

At first the parents were very upset about it and they didn’t really want it but  in order for the school to get money from the state, they had to integrate the school.

 

TR:
Remember, Robert described the time he spent at the Maryland School for the Blind as wonderful. Discrimination and racism were just a part of his school life.

We had a lot of terrible things that we dealt with but  we also had good things because we had a lot of white friends that we went to school with that would do anything in the world for us.

Maryland School for the Blind had one of the best wrestling and track teams in the country so we went all over the place.
We learned so much and we had so much fun as far as the students together.
We had a really good soul band good jazz band.
I grew up with the Beatles . I grew up with the platters. I grew up with Elvis Presley.
Some of the kids that were white, we learned their music and they learned ours.
I would come home and my sister would say here comes the little white boy!

 

TR:
In some sense, Robert really does straddle two identities. Not black and white, but rather black and blind.
The intersection of the two present a fully unique experience.

As a young African American growing up in Baltimore Maryland in the 1950’s and 60’s , Robert observed the events taking place in his neighborhood from a different perspective.

 

RL:
I heard one day when the police came out and they sicked the Shepard on the neighborhood and one guy named frank grabbed the dog around his neck and killed him.
You could hear in the wagon, you could hear the beating he was getting.

 

TR:
The wagon he refers to is the police patty wagon used to round up and transport suspects charged with criminal acts.
Robert says that the recent episodes of police brutality in cities like Baltimore aren’t new.

RL:

When they would beat the kids in the wagon, you could hear the wagon going up and down. if they wanted to find out  if you were telling the truth they would take a phone book and put it on top of your head and then hit it with a police stick. And there were no scars. What they would do is open the window.  they’d say you can tell us what we need to know or you can jump out the window. or take the beating.

 

TR:
Once , the additional identity of being blind could have possibly saved his life. As a young boy traveling in the car with his family, he recalls when an officer stopped his father for speeding.

 

RL:
the police was giving my father a ticket and I reached out to touch his gun and the policeman stepped back and drew his gun to shoot me. My father said oh please don’t shoot my son, he’s blind. And the policeman said oh he’s blind? So he took the bullets out of the gun and put it in my hand and let me play with it . He said, I’m not going to give you a ticket I’ll let you go this time. He said, but every day  for the next week I want you to buy your son an ice cream cone and every night for the rest of the week he’d come by the neighborhood and say did your father  buy you an ice cream?

 

TR:
By no means was Robert’s childhood full of violence.
residing on the school campus during the week, he returned home on weekends.

RL:
Man it was fun because I could come home and tell  them what I learned as far as in school, but then I could get on the roller skates and skate up and down the sidewalk and ride my two wheel bike. My grandfather was a mechanic, I had my hands inside automobiles. My mother would take me to the five and dime store and let me buy a toy. She treated me just like she did all of her other kids. My cousin Mack Lewis had a boxing gym in Baltimore. He was a very well-known manager of boxing. He would train Larry Middleton Vincent Pettway… some of the big time boxers. I would go over to the gym and listen to the guys box. I’d go around listening to musicians. I went over to the stable and rode the horses. I could honestly say I felt just like any kid that could see because I really think I had some angels looking out for me. I really enjoyed hearing things and dealing with things that I dealt with  you know in the neighborhood. Friday nights and Saturday nights was a great time because everybody had a good time. They had crab feasts. They’d walk up and down the street.

 

TR:{In conversation with Robert.}
So you were not at all isolated. You were definitely part of the community  it sounds like.

 

RL:
I was part of the community, yes!

 

TR:
Community, in his neighborhood, school and even activities that lead to lifelong passions like music.

 

RL:
I got my start playing marching band music. I played Sousaphone in the band. I played the Base Drum and from there I went to a complete drum kit. Being totally blind and a drummer, drummer’s completely different than other musicians. When you go and tell people you are blind and you play drums … I told one guy and he said I mean, I could see you playing the horn, but ain’t no way in the world I can see you playing the drum set cause you blind. How you gonna find the drums and the cymbals. I play an 18 piece drum kit! I’m a very good drummer.

I played with 15 and 18 piece bands.

I played with Stevie before.

 

TR:
So we’re clear, he’s talking about Stevie Wonder.

 

RL:
He came to the Maryland School for the Blind and we played  together.

 

TR:
Today, Robert is back on the campus of the Maryland School for the blind.
Not with the school, but rather in his job with the Maryland Radio Reading  Network, a radio reading service for the blind and others with print disabilities.

 

RL:
I started as a board operator and I’d go to work and people would whisper and say is he blind? This is a radio reading service but they had no blind people working there. I started as a board operator and moved up the ladder and I became the Executive Director.

 

TR :
Some of his responsibilities?

 

RL:
Fundraising, directing,   , setting up all the program, fire those that need to be fired or hire the people that need to be hired.

 

TR: {In conversation with Robert}
What would you say are the aspects of your specific experience  that have either helped or make your job more challenging?

 

RL:
The hardest thing is proving things to people. Proving what you can do.
If I ask someone for money and they’ll say to me well what do you do at the station? How do you know if you’re on the air or not? Or how do you know what time it is? And after a while, all of these stupid questions just get to you but, you can’t let people know they’re getting to you because they really don’t know. So you have to answer those questions as polite and as nice as you can do it. You have to be nice to people and after a while I wouldn’t say you get tired of being nice, sometimes you get tired of the way people talk down to you

I love my job and I like what I’m doing. If I sit home retired I’ll probably weigh a thousand pounds.  so I’m trying to avoid that  or find something else to do probably go into some music, but right now my whole job is what I do now with the radio station and part-time  stereo sales.

 

TR:
This is Thomas Reid
{James Brown’s “Say it Loud”
“Say it loud, I’m black”
Simultaneously…
RL:
Your Black and Blind…
James Brown’s “… And Proud!
{}

for Gatewave Radio…

Audio for Independent Living!

[Audio from : KRS1 “We’re not done” “We’re not Done”… “Check this out” from “You Must Learn”]

 

TR:The intersection between disability and race, gender and other identities is something I’d like to explore more.

It’s now part of my own life experience and with people with disabilities being the largest minority group, it’s probably an effective way to promote disability related issues.

If any of these apply to you and you have a story to share or know of someone who does, please send me an email…
ReidMyMindRadio@gmail.com.

It was a real pleasure speaking with Mr. Lewis and I hope to do so again. I can just imagine all of the other stories he could share.

In fact, there are more stories that were not included in the Gatewave piece.

Sometimes it’s hard to explain the level of ignorance people display in response to blindness or disability.

Some of the stories can be entertaining, but often they’re confusing. And as I like to say, you can’t make sense from nonsense.

As you heard in the end of the Gatewave  piece, Robert sells stereo equipment part time. After selling some equipment, he called the customer to check in with him two weeks after the sale.

 

RL:
He said, as long as you live please don’t ever call me. I said, don’t ever call you again? He said no, because I have to have eye surgery next week.

TR:
Ohhhhhh!

RL:
… and I know it’s only because I bought that equipment from you.

I said to him, did it rub off?
{laughing!!!}

He said please never, NEVER, never call me again!

I said, OK!

 

TR:

Recently I was reminded about someone who I knew for years, who didn’t say this to me but definitely treated me as if I were contagious!

And like Robert said…

 

RL:
Ok!

 

TR:

I wanted to end the conversation  on a positive note because we all know those haters are going to hate and ignorance is out here!

Plus it would only be right especially profiling someone who has been through all that he has and refers to his experience as wonderful. That’s an optimist folks!

I asked Mr. Lewis to give me some music recommendations. I thought I’d pass them on to the podcast listeners who enjoy a variety of music.

 

RL:
I don’t really listen to a lot of the new stuff.
If you’re a gospel person I consider the older gospel like Aretha Franklin or James Cleveland to be outstanding. If you really want to get into the going back into the world and listening to oldies but goodies and things of that nature think songs like “What’s to become of the broken hearted”. robins had some really good stuff out. “The Masters Call” It talks about a situation that a guy got involved with and was able to find god. When I’m really down if I want to hear something nice I listen to “Palisades Park” by Freddie Boom Boom  Canon which really is a very nice song to give you a little bit of upbeat or some things by gene Pitney  or things like that really will help you, inspire you music wise. Just getting a boost. Even down to Leslie Gore. I don’t mean songs like “It’s my party” but I mean really good songs that she did that were just outstanding; “Love and spoonful”. The Temptations had an unbelievable bunch of songs that really move me. I mean I love music. There’s so much music that that I really really enjoy. When you look at big bands sounds. I think one of the best instrumentals that I ever heard  in my life was Jimmy Smith’s “Mojo”. And only because no one plays an organ like Jimmy Smith. No one can move their hands and feet like he does; God bless the musician! He was unbelievable!
If you listen to that song and you listen to his right hand what he’s doing with his right hand is beyond what a musician can do. I enjoy so much of the old stuff. I mean Mandrill. I like a horn section. I love tower of Power. Ray Charles’ band moved media also have to put Jimi Hendrix in that line up. There’s so much harmony in some of the groups that came out of England. Crosby, Still, Nash &young. To me Cold Blood has an unbelievable band. They have Lydia Pense who sings for them. Oh my God that girl can sing!
James Brown’s band was fantastic. More so than his singing. His band was as tight as they come. But Ten Wheel Drive is also another tight band to listen to. And also Gail McCormick and Smith. They took the version of the Shirelle’s Baby it’s you. They have a horn section there that is fantastic. There’s nothing like 8 or 9 horns playing together like that . Like Tower Power does… My dream someday would be to play a song with Tower of Power or Ten Wheel Drive. These guys are tight!

 

TR:
Now before you go to your choice of music apps and begin listening to some of these suggestions, do yourself a favor and head over to your podcast app and subscribe to Reid My Mind Radio. It’s good for your mind, your body and your soul!

Peace!

Hide the transcript

Reid My Mind Radio – Rizzle Razzle Year End Special

Wednesday, January 4th, 2017

Taking over the Reid My Mind Radio Studio once again for a year end special…Rizzle Razzle.
I asked for your help in convincing my daughters to let me be a part of their end of year wrap up. This year, they cover music, iPhone apps and phrases. Find out who made their lists. Find out if I made the show!

Reid My Mind Radio – Join the Coalition

Wednesday, December 14th, 2016

Leading into 2017, it’s apparent that finding common ground will be even more important than ever.

If you’re looking for a New Year’s resolution , consider building coalitions. That building for me starts at home! Find out what I mean and then help me take action!

Now… what are you waiting for…
Subscribe to RMM Radio bit.ly/RMMRadioSubscribe

To listen now, hit the Play button below!

 

 

Resources

 

*No Totally Podcast, Ramp Your Voice Episode
*Ramp Your Voice
*Support the movement… Email ReidMyMindRadio

 

Transcript:

 

TReid:
I’ve been trying to figure out, what would be an appropriate topic for a year end episode of Reid My Mind Radio ?

A Bloopers reel?
A recap of my favorite episode?

Then I was inspired!

[RMMRadio Intro Music]

TReid:
A few years ago my daughters produced their own end of year show.
They chose to countdown their favorite songs of the year and talked about some of the more memorable news events according to what was then a 16 and 11 year old.
It was the first Rizzle Razzle Show!
It got about 3 to 4 times more listens than anything I put out at the time…

{Obviously slightly annoyed…} Whatever!

I loved listening to it myself. It was something they decided to do together – who could be upset with that.

So, I thought I would suggest Rizzle and Razzle once again return to the microphones for a year end wrap up show. However, this time, I thought they would invite a special guest… me, Daddy!

Sounds great right?

Since Riana or Rizzle was away in college I thought I would first approach Razzle., that’s my youngest daughter Raven

I thought Raven would definitely be up for including Daddy. She’s still here with me and we still get to spend a lot of great quality time together. She’ll love the idea.

Here’s how it all went down…

[Sound of Harp signaling going back in time…]

TReid:
Excited by the idea, I couldn’t wait for Razzle to get home from school. Our routine is when she arrives home, she comes into my office takes a seat on the couch and we talk. She shares the highlights of her day and I usually try to entertain her with silly jokes of some sort.

On this particular day, I decided I would go right into the idea…
After letting her in the front door of the house and getting my hello kiss Raven took her place on the couch in my office and I sat in my chair. With excitement I explained that I had this fabulous idea…

[TReid in conversation with Raven]
Alright, I think we need to bring back Rizzle Razzle this year…

Raven:
I agree!

TReid:
…but

Raven:
Oh no…

TReid:
… you should have a guest…

Raven:
Ooooh, who is this guest?

TReid:
… me, Daddy!

{After several seconds…}

Raven
No!

[Silence]
TReid:
Yeh, I know, you’re probably just as shocked as I am!

After about 30 minutes or so I let it go…

Maybe I went about this the wrong way.
Rizzle is the oldest, she’d be able to influence Razzle.
Even though she’s away at school, we speak everyday…
I’m ready for her call usually in the morning as she’s walking to class.
That’s when I decided, I’ll get her on my side and the show will be a go…

Here’s how that went down…
[Sound of Harp indicating going back in time.]
[Sound of iPhone ringing]
TReid:
You know, why drag it out?

Riana: “No!”

[Jay Z, What more can I say…]

[Audio sequence of both Raven and Riana saying No in various ways.]

TReid:
After several weeks, I’m finally able to speak about it without breaking down in tears.

I’m not mad at my wife’s daughters…
No seriously, those are my babies!
If it’s just supposed to be a Rizzle Razzle thing, that’s cool.
They just better not invite their mother on a show.

[Ooooh!]

Treid:
Right now with the climate in this world feeling even more divided, building coalitions, making relationships with others based on similarity seems like a real opportunity and a good idea.

Recently, I listened to a podcast featuring a conversation between an able bodied Asian American man and an African American woman with a disability. I thought it was a good conversation especially for those not familiar with disability and interested in learning more with the intention of becoming more aware.
These two apparently met online and have learned from one another and seem to be in the process of building an alliance in order to help reduce the levels of misinformation that are all too common when it comes to the so called minority groups.
They discussed some of the ways the misinformation impacts their lives and it was easy to see the similarities. Those were only understood after the information exchange. The differences are easy!

That podcast, by the way is called “No Totally” and you can find a link to it on the post for this episode on Reid My Mind.com.

Focusing on the things that make us different from others could be isolating.
Especially if you have enough differences…

Growing up as a African American man I have been through my share of racial experiences.
I’ve had many instances where white people have tried to intimidate, dominate and even inflict bodily harm.

As an African American with Puerto Rican heritage I have even experienced some very unkind remarks from African Americans and
unfortunately I’ve been witness to Latinos insulting African Americans.

And then, just when I thought I had it all worked out, my identity in check; comfortable and confident
in my caramel colored skin with a Tahino tint
I get a whole new category … PWD or person with a disability.
And boy, this one comes with a whole new set of do’s and don’ts and can’s and cannots. Or at least perceived cans and cannots!

So I begin to read about blindness, read about disability and become involved in blindness advocacy.

The majority of my peers involved in advocacy are white.
Furthermore, the majority of those in leadership are congenitally blind or blind since a very young age.

So my group can shrink even further…

If there’s one thing I adapted to naturally throughout my life, that’s being the only one!

The only or one of very few black kids in the class beginning in grammar school.
The only one who was Puerto Rican.
The only Puerto Rican who didn’t speak Spanish….

I spent years being the only black guy in the meeting, on the project team, in the car
returning from a meeting with colleagues as the car travels through the Bronx, past the neighborhood I grew up in only to have several of my white colleagues question their safety.

[Sound as though an inner thought…
“Let the car break down now and I’m leaving all your asses! I’m good”]

If I were driving I would have went off the main road and made them all nervous, just for the LOL’s!

The differences can go even further… I didn’t even touch on the cancer thing.

[Cheers Music and re-mix!]

TReid:
It’s natural for anyone to want to go to that place where everybody knows your name…

To some extent there’s a real level of comfort being around other people who are blind.

Hanging out with friends who are black gives me an opportunity to be me too.

put me in a room with the smells of Arroz con Gandules, pernil
(even though I don’t eat pork!)
Sounds of Salsa music and people talking Spanglish! for those not in the know that’s the combo of English and Spanish… and I feel at home!

But in any situation there’s always that chance to
feel separated. It could be anything…

Hanging out with friends or a work related setting and inevitably the conversation moves to the current sport season…
As a man, I’m expected to participate…
Get ready for a real disappointment yawl, I don’t follow sports like that!

[Sound of Shocked audience response]

I think our differences make us interesting.

the problem though are those who believe that something that separates us makes one superior to another.

As we end this year and enter 2017 with a thick feeling of division in the air
I’m going to continue to respect differences based on what I said earlier and focus on supporting and building with others in those areas in which we have shared interest.

There’s too many things we can accomplish for the good of all. With that said, those who feel the same, I’m asking you to send an email to reidmymindradio at gmail.com asking Rizzle Razzle to do a show with their Dad!

I’m just saying’ why don’t they want their father in the show…
I can do a good job…
I do this… (Fading out)
They use my equipment… (fading out)
Come on, I edit it and put it on my website… {fades out}

[close music]

Reid My Mind Radio – 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!

If you haven’t yet, make sure you Subscribe to RMM Radio
– In the meantime, hit the Play button below!

 

 

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!

Reid My Mind Radio: Talking Misperceptions of Blindness

Wednesday, May 18th, 2016
Reid My Mind Radio Logo

Courtesy of RMM Graphic Designer, Raven Reid

While we’re over 30 episodes deep into RMM Radio, this is the first episode as an official podcast. That’s right, you can now subscribe to Reid My Mind Radio via the Apple Podcast app or any other podcast application.

 

In many ways it’s fitting that today’s episode feature’s Andre Watson, PhD. We’ll learn about his road to becoming a Psychologist an Olympian, a husband and Dad. Plus we’ll talk about the misperceptions of blindness and why yours truly when dealing with people, who make stupid assumptions about blindness, shouldn’t lose the desire to “take them down!”

* Reid My Mind Radio or any of its affiliates, do not hereby endorse random violence — at least not against innocent parties!* LOL!

I digress…but you should subscribe!

Or Listen now!