Archive for the ‘Fatherhood’ Category

Reid My Mind Radio: For the Love of Honey

Wednesday, October 11th, 2017

Picture of Ojok Simon in front of a blue covered background.

This third segment features Ojok Simon. Attacked as a boy in Uganda by the infamous army of Joseph Kony, hear his journey to becoming one of the first three Holman Prize winners as an Entrepreneur who is about more than just bizzzzness!

Resources

Transcript

Show the transcript

TR:
What’s up RMM Radio Family…I’m excited for another Holman Prize winner story, but I’m also a little down. It’s the third in the series of 3!
Well when I get down, I sing the blues.

[Audio: Muddy Waters, Honey Bee]

TR:
Nah, I’m not blue! Let’s Go!

[Audio: Reid My Mind Radio Theme Music]

TR:

Today we conclude our three part series featuring
all of the Holman Prize recipients.

The prize is named in honor of James Holman. Known as the Blind Traveler, Holman completed a series of solo journeys taking him to all inhabited continents.

Sponsored by the San Francisco Lighthouse $25,000 is given to each of the winners who are all legally blind and in their own way exhibit the adventurous spirit and attitude of James Holman

In order to meet our third winner, I had to travel to Uganda in East Africa. Well, via Skype!

Ojok:

I am Ojok Simon from Uganda. I am from the northern district of Gulu.

I was a child growing up in a rural community. I used to play a lot with all my fellow peers. We enjoyed hunting for wild honey . We liked playing hide and seek games. I used to have a lot friends. many people would come and play around with me . they would come to listen to my stories . I liked creating jokes . I liked giving tough predictions in the future. So I’m that kind of crazy person.

My ambition was to be a military doctor.

TR:
Sounds like what we would think about as life for a young boy.

However, during the late 1980’s
Joseph Kony came into power and his Lord’s Resistance Army
terrorized Northern Uganda.

The LRA is Known for forcing children to serve in their army and
all sorts of brutal atrocities.
At 9 years old, Ojok’s home in Gulu was the site one such incident.

Ojok:

They found me and my mother were still in the house. And they thought that being a child I was going to run away. So they started to beat me at the temple of my head using the butt of the gun. I fell down with a lot of pain. I didn’t know and my parents didn’t know that there was that kind of internal injuries of my sight. After three years they started to realize that my vision started deteriorating and there was no medical attention that I could seek because everybody, every area was in war. The doctors live in fear so you can’t get medical attention. After five years I had to go and join the blind school. Even when I was trying to seek the medical attention through the blind school there was no equipment so that they could help me so I had to remain with the condition like that.

TR:
That condition Ojok described is low vision. It’s important to note that the School for the Blind in Uganda doesn’t take acuity into consideration when creating the curriculum. Everyone is taught Braille for example, large print is not an option.

Another part of his studies included what Ojok refers to as psycho social support or therapy, which is what helped him eventually come to terms with the
permanence of his condition.

Yet, at 9 years old with lots of friends looking up to Ojok that adjustment had to be difficult.

Ojok:
When I was growing up as a boy among my friends I used to like Football. I used to play like a goal keeper so when my vision started losing I started losing friends because I could not handle the ball the way they feel like their leader should be. They said you are blind so cannot associate yourself with us. Life became horrible. To make the matters worse we used to love hunting for wild honey.

[TR in conversation with Ojok]
I don’t know anything about hunting for honey, like what is that process like?

Ojok:
Hunting for wild honey, it’s wild honey ok… of course we live in a community where a lot of bees swarm ok. They keep moving around looking for their house so that they could get accommodated like the hive, but people doesn’t take care of providing a house for the. Now the bees will end up handing on the big thick trees .

[TR in conversation with Ojok]

When they find that honey, there’s no bees there? The bees are somewhere else?

Ojok:
No the bees will also be there because they live together and protect the honey because you know honey is a food for bees as well.

[TR in conversation with Ojok]

… right, but how do you deal with the bees when you’re trying to take the honey?

Ojok:
They do it in a local way. They will get fire and they will burn the bees. Now when the bees run away, that’s when they will harvest the honey. They will not take care of the bees. Now for me it became a challenge because imagine with your poor vision climbing up the trees and trying to move and walk on the branches, balancing so that you can go and remove the honey. So since for me I like also moving in the bush during the daytime because I have some little sight I would get where the honey nests are but at night I could not locate the situation so my peers use that opportunity so that they can get the wild honey . They would take it to their grandparents, they will receive a lot of praises, they would sing them that they are great men and served them with the good food. So now I’m missing those love from my grandparents.

TR:
Chances are, you’re like me. You probably don’t know much about wild honey and didn’t realize it had such value. As we will see, this is just the bee ginning of all this sweet nectar has to offer.

Ojok:

While I was pursuing my studies one day during holiday… Remember I told you that we are also in the war torn area, people then were taken to concentration camps. I was now walking around our broken home where we used to stay. Now while I was walking around there, bees were stinging me from all directions. Then with my poor vision I was trying to run. The direction where I was running that was where the bees were coming from . Then I came across an abandoned clay pot. it was just on the ground. There were bees in that clay pot and I said wow now what can I do. Then I went back home and I came back now because this is on the ground and is in the area where I know , then I harvested the honey. I took it to my mother. She became happy eating the honey.

TR:

Realizing he could easily harvest the honey from this more accessible method, Ojok devised a plan. While his mother was out of the house, Ojok
helped himself to one of her clay pots.

Ojok:

Who has taken this pot of mine… who has taken this pot of mine?

I don’t know… I even denied so, I got the pot and took it next to the one I found in the abandoned home and left those there. Now two pots. I went back to school. Now during another holiday I came back and found both pots are colonized with the honey. And that became the turning point for me.

TR:

Harvesting the honey, Ojok was once again able to surprise his mother.

Ojok:

I took it to my mother and she said hey where are you always getting this honey. I said yes, I have my techniques.

TR:
Ojok admitted to his mother that part of his technique included taking her pot…
His make shift hives produced more honey than his family could consume.

Ojok:

Some of my friends, they started being friendly to me because they want to eat the honey. If you want to eat the honey be my friend so that I can sell you.

TR:

Hiving Bees and harvesting the honey using
clay pots isn’t very sustainable. Drawing the bees away with fire in order to gather the honey, kills some of the bees. Reading more about the process of Bee Keeping in Africa Ojok invested in a new type of hive, while still pursuing his Bachelor’s degree.

Ojok:

I found now they were selling a hollow tree. They would cut the log of a tree then they would produce a hole inside. There are doors so that the bees would stay inside. Bee keeping was not for commercial or social change but just because I love eating honey I want to get praises. So I just continue with the bee keeping. After my formal studies I returned back to my village. I started doing human rights activism for people with disability through the convention on the rights of people with disabilities.

TR:
As an advocate, Ojok was informing others with disabilities about their human rights and how they could live independently.

Remember, Bee keeping to Ojok was a hobby, but his advocacy work led to his discovery of more possibilities.

Ojok:

Then I started meeting some of my fellow blind people that we used to live with them during the school time, but they did not finish their studies. And now they were saying their poor. they don’t have any source of income. I would spend all of my salary on them. When they asked me for soap, I’d give them. When they asked me for something little I’d give them. Then I asked myself self, how long would I keep on helping people like this? Is this really sustainable?

TR:

Ojok’s two original clay pots turned into 12 income producing hives. He wondered why such an idea couldn’t do the same for others.

Ojok:

They don’t have any source of income but for me I’m getting my normal salary. But on another side, my hives are also there. After 7 years I resigned. I decided to go for Entrepreneurship training in India with the organization called Kanthari, which is Braille without Borders.

[Audio: Oprah Winfrey Show featuring sabriye tenberken]

TR
sabriye tenberken started the first school for the blind in Tibet – where blindness is viewed as a curse for something done in a prior life. This school formed the foundation of Braille Without Borders, an organization empowering blind people to take their lives in their own hands.

In 2005 she co-founded kanthari in Kerala, South India. Kanthari fosters participants from all over the world, who, like Sabriye, have a passion to make the world a better place and the strength to be forces of good rather than victims of circumstance.

A kanthari is a plant that grows wild in every backyard of Kerala, a small but very spicy chili with a number of medicinal values. It’s also a symbol for those who have the guts to challenge harmful traditions and the status quo, who have fire in their belly and
a lot of innovative ideas to make a positive difference.

Ojok:
Then I came back. I started now launching my idea venture of providing employment to blind people. Then I started training 22 blind and low vision both men and females from the age of 20 and above. My target is to target those who are already out of school so that they can get employment.

I give them start up kits, like the bee hive. I give them 5 of them each. Then later I started giving them an improved type of bee hive which I too have it’s called Top Bar.

[TR in conversation with Ojok]

Top Bar!

Ojok:
Then I follow them up and I build their capacity and I add them two top bar each.

[TR in conversation with Ojok]

So what’s the difference between that and the other one, the traditional one?

Ojok:
The top bar will produce more honey and then would last longer than the traditional hive.

TR:

The initial 22 students, turned into 38. The lessons, go beyond harvesting honey and
include orientation and mobility, leadership skills

Ojok:

Now something I could not provide they can advocate for their own needs, because bee keeping might not answer all their problems. But it’s just like a spring board.

They started realizing that yes they are human beings. For instance, among the 38 people that I already trained which are practicing bee keeping, three of them actually they have grown more than my capacity. They became recognized in the society even they are now elected leaders to go and defend people who are visually impaired with the local government in the community – which is above me. Even I call them my boss… (laughs)

[TR in conversation with Ojok]

Laughs… How does that feel?

Ojok:
Actually, I feel relief. Inside me I said yes, this is what I want to do. Like a bearing in a bicycle, the bearing is very tiny but it play an important role of making the bicycle to go faster. So I just said yes I’m not being seen but I can see the impact. This has given me the answer I have been looking for.

TR:

Ojok was already seeing some success with his venture. Learning of the Holman Prize competition through his kanthari mentor he submitted his video.

[Audio from Ojok Holman Prize Ambition Video

Ojok:
I would use the prize to empower blind and partially sighted person to be bee keepers in their home. Beneficiaries will be trained in different types of bee hives, introduction to be keeping, honey harvesting, mobility and orientation and they will be sent back to their home to work in their own bee farm. And five years from now I can see blind and partially sighted person being great entrepreneurs…]

Ojok:
When I found out I was a winner I said I can’t believe it…

I think my answer is being well known globally. It’s not only in Uganda because my biggest dream is to create an incubation center that will provide more employment for people with visually impairment through bee keeping by creating a honey factory where they would also now process their honey and they would market and they would do all those things. Those who might not practice bee keeping those who are skillful in other demonstration work and they would also be brought in the system. So after saying that hey I’m I winner I said yes my answer is coming slowly by slowly and I think one day the whole world will know that there are a certain group of visually impaired persons in east Africa in Uganda who are providing the world with tropical honey that is very healthy.

TR:

Creating big goals and achieving them isn’t new to this Holman Prize winner.

Ojok:

I’m the first visually impaired person in my district to go up to the university so I had to show that I can bear fruits. If everything dwells on me then I would carry a lot of burdens. I need them to start carrying their own burdens, but at the moment they’re still dealing with low self-esteem a lot of stigmatization, negative attitude… they still believe in the status quo that if you are disabled or you are visually impaired you cannot do any developmental thing which makes them not so productive.

[TR in conversation with Ojok]

Yeh, and so they start to feed into that mind set and start to believe it and then that’s it, once they believe it they stay there.

Ojok:
Exactly!

TR:

Like James Holman, Ojok Simon has ventured out beyond his immediate surroundings. Forming the right relationships with others who
can support his journey like;
His instructors at Kanthari in India providing Entrepreneurship training.
Working with mentors like Italian Bee Keepers to learn state of the art methods in bee keeping.
Capturing the attention of the San Francisco Lighthouse to
help expand not only his financing but
chances are increasing his exposure and helping him make more relationships to help reach that goal

In the book A Sense of the World, Howa Blind Man Became History’s Greatest Traveler; author Jason Roberts writes about Holman’s encounter’s with François Huber – who Robert’s writes was the most famous blind man in the world at that time.

Losing his sight at 15, Huber’s research is said to have laid the foundations of the scientific knowledge of the life history of the
honey bee.

[TR in conversation with Ojok]

What have you learned from your experience. I mean from that moment where you were 9 and you were getting brutality attacked. It sounds like you had several years of therapy. The dealing with the loss and all of that it sounds like that probably helped you a great deal but in general how do you look back on your life?

Ojok:
When I look back, look back on myself right now I would just say good enough it happened when I was still a child and I managed to cope with the situation, that’s one.

And then two, the best important thing is to have accept yourself the way you are and then learn how to live with it. I’ve learned my weakness and how I can turn my weaknesses into opportunities.
And also I say yes, having the heart of forgiveness. you need to forgive one another. If these people who had beaten me I could get them you’ll just derail yourself from mercy. You just waste a lot of your energy for nothing. You need to forgive them because maybe they did it not knowing . Maybe also they were under certain influences. If they were to come across me I think they would also realize that I’m not saying I’m in a better situation but I might have the material to also help them. If you have the heart of forgiveness even to those of my friends who used to insult me … I’ve forgiven them and now we are still good friends.

[TR in conversation with Ojok]

Wow, how long did that take you to get to that point because, that’s not just about blindness that’s life. And just about everybody can use that. What got you there?

Ojok:
When I look back…

It was a gradual process. One the formal education that I went through. I was feeding my brain with knowledge and though I not yet done it that much, I need to go for my Master’s in the future. It makes me to start analyzing each and every persons act and I say yes maybe they are doing that out of ignorance. Maybe they are doing that because they have not reached the level I have reached. So it took me more than 10 to 15 years when I started learning yes, I need to do this, I need to forgive, I need to accept my situation. I need to learn and do things.

slowly by slowly I was meeting different
characters.

I remember one of my good mentors from Uganda. Sorry she lost her life. She was my good teacher, I think she was also in the World Blind Union that is the late Sandira Frances. She was a totally blind person and she managed to struggle with her life and I was able to learn (from her).

Wherever she is she also feels happy that yes I’ve left somebody who is helping to carry on the work that I’ve been doing.

TR:

Carrying on the work, that sounds like what the Holman Prize is all about.

This brings to mind the African American proverb that dates back to a time it was illegal for enslaved Africans in America to know how to read.

Understanding the power of knowledge those who did learn would teach another. Encouraging them to do the same with the phrase; Each one teach one.!

Blinded as a young boy, Ojok Simon’s life could have easily went down a different path. His ability to find the sweet honey among the destruction left behind in a torn community, wasn’t a onetime thing.

That’s how he appears to live his life.

Ojok is currently engaged and has four children. That includes two young girls who were orphaned and he decided to adopt in order to help spare them what in those circumstances is often a dark future.

If you want to learn more about Ojok’s plans or maybe even see how you can support his goal , you can reach him through his organization’s website. HiveUganda.org.

The official place to learn more about the Holman Prize and even follow the progress of the winners is HolmanPrize.org.

I’m hoping each of these winners will be interested in speaking with me in the future about their progress experiences and of course lessons learned.

I’m Thomas Reid, for Gatewave Radio,

[Ojok from interview: “I love eating honey, I want to get praises!”]

audio for independent living!

[Barbara Streisand’s “Queen Bee” from A Star is Born
The beat loops with background singing what sounds like a bee buzzing….
acapella we hear her sing… “The Queen Bee’s never gonna be alone”
]

## TR:

How freaking cool was that!

I didn’t think this interview was going to happen. I mean connecting via Skype and speaking with someone in my own state can be a challenge. Here’s how it went down.

[Audio collage of TR attempting to get in touch with Ojok via Skype… includes sounds of me drumming on my desk to the Skype music… After multiple attempts which included failure due to storms in Uganda we connected.]

TR:
But Ojok was able to increase his bandwidth on the fly.

I heard about the sophistication of the cell phone market in Africa. So much of the continent’s commerce is done via telephone transactions. The wireless market made that possible without the infrastructure required for wired services.

The cool thing about technology, remember is not the technology but rather what we do with it.

Sort of like the honey… Ojok is harnessing that natural resource to empower others.

This in itself is a powerful statement. If you know anything about how Africa has been repeatedly been robbed of its natural resources, maybe this story takes on another meaning for you.

Big shout out to Ojok Simon, Ahmet Ustunel and Penny Melville-Brown, the first class of Holman Prize Winners.

Join me in wishing them the most success… do what winners do yawl… keep winning!

You too can keep winning… you know what you have to do right?

Subscribe to this podcast on Apple Podcast, Google Play, Stitcher, Tune In Radio or Sound Cloud. Then tell 3 friends…. why three… I told you when we started this series…
[Audio. De La Soul… 3 is the Magic Number!]

[RMMOutro]
Peace

Hide the transcript

Reid My Mind Radio – 14 Year Old Makes Talking Laundry Machine

Wednesday, August 30th, 2017

TReid in front of washing machine which appears to be talking... machine says "47 minutes remaining on the wash cycle!
Touch screens and digital displays look sexy and futuristic, but for those who are blind or low vision these can present a real access issue.

Jack DuPlessis, a 14 year old programmer stepped up to the challenge of making a washer and dryer talk! Hear how he did it and the possible impact this can have on the future of appliances.

Resources

More of Jack’s work on Git Hub
* Purchase from First Build

Transcript

Show the transcript

TR :
What’s up RMMRadio family.
We’re getting right into this today.

And I can tell you from the jump, there’s know original musical creations in this episode.
[Applause]
Oh seriously who did that… that’s not cool!

[Reid My Mind Theme]

TR:
Accessibility issues are everywhere. Transportation, information like the printed word or that which appears in movies but isn’t spoken and too often employment.
When you think about the problem solvers who find solutions to these types of access issues, you may not think he’d sound like:
[TR in conversation with JD]
How are you?
JD:
I’m good!

TR:
… Well, like a 14 year old young man.
That’s Jack DuPlessis,.

Jack developed a way to make an otherwise inaccessible washer & Dryer talk.

Many of the newer appliances on the market today whether stove tops, microwaves and laundry machines are using digital displays and no real tactile options.

I spoke with Sam DuPlessis now known as Jack’s Dad.
I wanted to learn more about First Build, where this project all began.

SD: First Build was started about three years ago by G.E. appliances. We’re a wholly owned subsidiary of G.E. appliances. We want to incubate new products and
we want to do it in an open and collaborative way. We have all the tools to design build and sell new products and new innovations. And we invite anybody to come in and collaborate with us. Truly we mean anybody. We’ve got an on-line presence. You can come in and sign on and use our tools and create with us or you could go online and submit ideas to our website – we call it Co creation.

TR:
Others in the community and those who visit the site vote for their favorite ideas. The more votes and idea gets;

SD:
We put them in queue to make them and see if we can make products out of them. So really let the creativity of this place and ideas of a large group, come in and help us accelerate product development where from a G.E. appliances point of view things used to take years, we want to just take weeks and months to get these ideas out there tested.

TR:
First Build isn’t just sitting around waiting for ideas to come to them.

SD:
Once a year we do something called a mega hack a thon.

TR:
Hackers usually refers to computer programmers .
A hackathon is a fast paced event that
can last for a few hours or over a weekend.
The intention is to design a new piece of software often with a specific goal in mind.

In the case of the First build hackathon, hackers includes
programmers, engineers, machinists and others.

SD:
We just take things apart and put them back together and try to create new concept products in a weekend.

This year’s Hackathon is September 9 & 10.

TR:
Last year’s hackathon inspired what would become a talking laundry machine. But it started with a Stove or cook top.

SD:
An induction cooktops that was really designed specifically to address some of the cooking issues for the visually impaired. It was a great idea it had a pan locator on a smooth cook top where the visually impaired person wouldn’t have to feel with their hands where the burner was starting to warm up. They could just feel with the pot and it kind of self-locates over the cooking surface. we’ve never seen that before. We happen to have here in Louisville. the American Printing House for the Blind. It’s been here for one hundred fifty years and it’s where they print almost all the materials and teaching aids for blind and visually impaired education in the United States. When their leadership came in and reviewed the cooktop, it had like a cap touch control. It’s not very accessible.

TR:
It was through this outreach and communication with those who are impacted by the inaccessibility, where Sam received a request.

SD:
As things get more electronic like laundry, the knobs just spin three hundred sixty degrees they don’t have a home position. They don’t even have a home beep. You’ve grown this capability but you haven’t really addressed a good universal control. If you can give me a home beep . On Something that would be great.

So I took that as an idea for laundry. Something that here at first build we could just program a test for that and have something maybe that we could
update have in the field and just have a home beep on laundry. Really easy to do. I came home and I asked Jack would he be willing to work
on something like that.

[TR in Conversation with JD]
So your father comes to you with the idea, what did you think about it when he first asked you?

JD:
Yeah, I never thought about visually impaired people using a washer and how hard it would be without something as simple as a home position. So that was just a new take on controlling a washer, but I thought it would be a fun project.

[TR in Conversation with JD& SD]
Jack did you get into programming because of your Dad? Dad, how did it happen
SD:
The cool thing that I did was I brought home a Raspberry Pi and connected to a T.V.

TR:
Sam’s not referring to an actual pie here.
He’s talking about the tiny and affordable computer that you can use to learn programming through fun, practical projects

Getting his hands on this in 4th grade along with a visual coding interface, Jack began working on small projects that included making his own games.
Eventually that led to him learning other languages and other projects like a website that lets users test their typing speed and proficiency

And of course, talking laundry machines!

JD:
So yeah, I went with it and got a working like prototype version in about a weekend or so.

[TR in conversation with JD:]
For some kids, that would deter them to even continue. “Ah this is gonna take too long”, but that’s not you, it doesn’t sound like that.

JD:
[long pause]
No!
[TR & SD: laughs]
## TR:
Jack is humble which is an endearing trait for a very bright talented young guy.
Plus, he has Dad. And Dad’s love to talk about their children.

SD:
What took a few hours that weekend, was a very limited functionality and as this thing developed and we got the feedback, Jack rewrote this to not only address just the knobs but to address many of the buttons that are on the laundry and went through four total structure rewrites. and it has turned him from a very simple piece of code into a very very elaborate piece of code and it’s all self-taught.

I’m an engineer and I lead the technical development here at First Build. The passion that we look for in successful engineers is you got to see the problem and want to solve it and Jack has that and spades. He really
sees problems and really likes to dive in to figure out what it takes to solve it.

When Jack makes a significant improvement in anything the corners of his mouth turn up ever so slightly.

TR & Dad laugh!

TR:
That code Jack wrote is now on a small device that attaches to both washer and dryer via a cable that plugs into the diagnostic ports in the back of each machine.

Turning the knob on the machine gives you immediate feedback:
[Sample Sounds]

It even allows you to press a button on the device while the machine is running and hear how much time is remaining.

[TR in conversation with JD & SD]
Have you gotten any feedback from anyone who is visually impaired who may have used the device?

JD:
Yeah…So we put a device in the Kentucky School for the Blind. So we’ve gotten good feedback from them.
And that same person who gave us the feedback about the cook top from the American printing House for the Blind, he has given us great feedback on it as well.
SD:
Not only has he been able to take their feedback you know one on one, but he’s since been able to release software that provides the features that they asked for.
[TR in conversation with JD & SD]
Congratulations to you young man! It’s a really cool thing you’re doing. Dad you too. Obviously you introduced him to it. What are you learning about accessibility?

SD:
I’ve made appliances for twenty five years and we’ve got we call it a heuristics evaluation. Where we look at the usability of controls. And from a I mean just a basic use of what could be in a control to make it more accessible I’ve learned that there are they they can actually be free and we can start putting them in appliances that we make today. If something has a tone capability instead of having it beep the the same beep as it slews through maybe a couple different selections. If it has a high and low tome Automatically it’s much more usable. With these types of insights you know we can put a home beep, it the minimum and that’s free.

We started to update our heuristics evaluation. I’m taking what we’ve learned in this point of view and seeing how we can update our control algorithm so that everything comes
out a little bit more accessible.

TR:
Of course, I had to ask about an iPhone app

SD:
That’s probably where in a few years I think many of our appliances will end up.

Wi-Fi has started to be added to our top end appliances including laundry and there is
a laundry app. One of the things Jacks work has done is uncovered these communications that Go back and forth in the app don’t exist. He’s actually telling
them the things that they need to do to create a more accessible app experience..

[Tr in conversation with JD:]
What’s your favorite piece of technology right now Jack?

JD:
My favorite piece of technology right now that I want is probably a Mac Book.

SD:
Santa Clause is getting some hints!

[Tr in conversation with SD:]
And it sounds like he’s been a real good boy!

[Tr in conversation with JD:]
Do you see yourself going more into what area? Do you want to stay with manufacturing coding, I heard games what do you want to do?

JD:
I’m not sure exactly what I want to do. As long as it involves computers, programming it will probably be good with me.

[Tr in conversation with JD:]

And accessibility too, right?

JD:
Yeah!

[Tr in conversation with JD:]
Laughs!

TR:
It’s refreshing to know that this talented young man and possible future leader in technology is already showing signs of committing to accessibility.

Right now, the First Build Talking Laundry Module is available for one GE washer and 2 dryers 1 electric and one gas.

The modules right now are being produced on demand and available for purchase
via the First Build website; firstbuild.com

It costs $99 and works for both washer and dryer. and comes with the cables and AC adapter.

The device is 5 x 5 x 2.5 inch and has built in speaker and volume control knob and includes magnets on the base to hold the unit to the side of dryer

I’m Thomas Reid for Gatewave Radio

[JD: from the piece… long pause and he then says… No!]

Audio for independent living!

TR: RMMRadio Outro

The purpose of technology is to help us accomplish a specific task. The first tools used by our ancestors in Africa could be considered assistive technology.

Accessibility, just extends the us. For too long us only included those with fully functioning… fill in the blank.
More people are understanding and being informed that just because your eyes don’t function at a certain level, you don’t hear the way others may or any other disability, that doesn’t mean you don’t have to get the same things accomplished.

I can really appreciate this story for several reasons.

I can relate to the Dad, Sam, recognizing that his son’s interest. Then challenging him to get involved with a project that has a real world purpose. Encouraging him to not only get better at coding but gaining an early lesson about technology – it should improve our lives.

There’s another lesson that can be gained… it’s about disability but even more so it’s about humanity. Everyone has unlimited potential. Disability doesn’t reduce that in anyway. People do.

People who see limitations and then whether directly or otherwise restrict someone from reaching their potential.

People who internalize that idea and restrict themselves.

People who refuse to make their products accessible even after learning that by doing so they are restricting 20 percent of the population who has some form of disability.

Whether from a business or creative perspective, not working towards a fully accessible product is a very limiting move. Convincing me once again that the limitations are in the eye of the beholder.

Accessibility advocates will tell you the goal, is accessibility included in the design phase. The time when all those involved with the creation of the product are beginning to figure out what the product will look like and how it will work. It sounds like Sam is taking steps toward that. Especially realizing that it doesn’t have to be that complicated.

We can say that Jack getting involved at 14 is right in line with that. Part of the problem is that accessibility isn’t often included in computer science curriculum.

Getting introduced to the concept of accessibility at 14 years old, makes me optimistic about the future.

You might say this is one person, one story, but that’s never really the case unless the story goes untold.

Well Jack’s story has definitely made its way around the web and I’d like to think that the accessibility conversation has been advanced a little further.

Shout out to Sam and Jack DuPlessis First Build and GE for advancing access for those who are blind or visually impaired.

And here’s hoping Santa is listening to this episode of the podcast and Jack finds some cool stuff under that tree this year!

You know what else is cool? Yes, you do!
Subscribing to this here podcast. You can subscribe on Apple, Google Play, Stitcher, Tune In Radio and follow on Sound Cloud.

Give the podcast a rating, a review and or tell a friend or two to take a listen.

Peace!

Hide the transcript

Reid My MindRadio – Fears of a Blind Nomad

Wednesday, June 7th, 2017

Jim Paradiso at the Inca Ruins
When I heard about Jim Paradiso, I had to find out more. He’s a Blind Nomad… I had to hear his story. Turns out it’s so much more than that… he’s forcing you to challenge what you think is possible. That is, if you believe!

Take a listen and let me know; do you believe?

Resources

Transcript

Show the transcript

TR:
What’s good fine people.

I have a lot to say about this episode so I’m just going to get right into it.

Well of course after the intro…

The best way to kick this one off…
[Audio: Been Around the World, Notorious BIG]
[Audio: RMMRadio Theme]

JP:
By the way what I’m about to tell you is true and I don’t give a damn if you believe it or not!

TR:
Any story that begins like that, well, you know it has to be good. whether it’s true or not, that’s for you to decide.

That voice you just heard is Jim Paradiso.
you can call Jim, a nomad!

A modern day nomad refers to people; often those with an online virtual business, where one’s income isn’t tied to a brick and mortar location.
Earning 60K for example and living outside of the US on various continents can really stretch that dollar.

That’s not exactly Jim’s situation. He’s been living a version of this lifestyle for over a year now and is currently in Loja, Ecuador.

According to Jim;

JP:
The adventure is the journey

TR:
With that said, let’s begin with the journey that lead Jim to Loha Ecuador.

JP:

I was talking to a friend, he was moving to Vilcabamba and I’d never heard of Vilcabamba and I said it sounds like a good name so I left to go to Vilcabamba. Which is a fifteen hour ride on a bus from. Manta to Vilcabamba. So it took me four weeks to get there.

I get into Cuenca and of course with me now I’m traveling alone for the first time. And I’m up in this Hostel, I said well OK, so I posted on FB { I’m in Cuenca, what’s there to do for a blind man traveling on his own?

TR:
Ok, , the fact that Jim is blind for most people probably makes the idea of him living a life as a nomad and traveling in unknown places, is maybe;
Very frightening?
Unbelievable?

Well, then let’s pause on the journey through Ecuador for a moment and hear what some may think is an unbelievable adventure of Jim’s vision loss
and the series of preceding events .

JP:
I had an aneurism Thirteen years ago on my left eye. And they tried to fix it and they screwed up the eye entirely. Then three years ago I woke up one morning and I had an aneurism in the other I. And I went through ocular injections and everything else that went with it and I had a bad reaction to the ocular injections which caused me to have a stroke.

so I was living with a girlfriend who decided she didn’t want to be with a blind man.

I ended up homeless. I was a month from being blind enough to qualify for Social Security. I was unemployed and Basically I was living on the couch of a motor home
that belong to a friend of mine who was in a retirement community.

So I get a phone call from my brother who was living in Ecuador and he said Well Linda is looking for a manager for a B&B would you like the job? I said, well what’s the pay. Room and board and fifty dollars a week.

Ok, I could be homeless in a motorhome in Florida or I could be homeless on a beach in Ecuador?
kind of a no brainer to me.

TR in conversation with JP:
and I’m sure fifty dollars is different in Ecuador than in Florida.

JP:
It doesn’t make any difference as long as you got food and shelter who cares about the rest of it. I live very inexpensively because that money doesn’t mean anything to me anymore.

I went for a pedicure because I couldn’t see my toe nails and I was catching them on my socks and when she cut the calluses off the bottom my feet so when I went for a walk on the beach I ended up getting third degree burns on the bottom of my feet.

I picked up a flesh eating bacteria and I had to be medivac the act from Ecuador to the United States after two operations down here and five days in the hospital.
The flesh eating bacteria that I picked up is usually fatal within seventy two hours and the only cure for it is amputation; actually they call it debridement which really is amputation. They have to remove all of the bacterial growth because it doubles in size every nine minutes.
Once I got back into the United States they put me in the teaching hospital in Shands of which this was the second case they had in fifty years of this particular virus. They amputated two toes and debride most of my foot and then they had to regrow it in an oxygen rich environment.

This took ten weeks and then they put me in a nursing home for a month. Rehab they call it but it actually was a nursing home.

While I was there I had an abscess on the back of my head so I went to the doctors when I had my foot looked at and they slants the abscess and said this isn’t right so they sent me to a Dermatologist.
Well when they slants it they gave me MRSA – which is another flesh eating bacteria. While I was at the doctor’s they said oh I don’t like these moles on your back let me have them biopsied. Well as it turned out I had skin cancer. They had to operate on my back and removed the skin cancer. Which I thought we were just going to remove a mole but they ended up doing 19 stitches on each side and trenched both sides of my back. Then they had to put me on different antibiotics in order to kill the MRSA they gave me and then when they removed that they discovered it was a tumor. Then they had to remove that. And that was in six months.

At that point I was afraid of dying.

When I finally got settled with Social Security Disability, I Flew back to Ecuador.

TR in conversation with JP:
Why?

JP:
Because my kids wanted to put me in a retirement villa.

TR in conversation with JP:
How many kids do you have?

JP:

Again that’s an odd story…

I have four kids but they’re not mine.
TR in conversation with JP:
Oh Ok!

JP:
My ex-wife’s two kids from her previous marriage.
And I have her ex-husband’s two kids from his previous marriage.

TR in conversation with JP:
OK that’s a new situation!

You have her ex-husband’s kids? (laughing!)

JP:
They all consider me dad and I was always there for them.

By the way, have you ever heard a story this ridiculous?

TR in conversation with JP:
so many people stories that I have heard of do have like one thing on top of the other you know but this flesh eating viruses and tumors, yeah… you’re winning!
– laughs!

TR:
Now, returning to Ecuador Jim met up with a friend.

JP:
He didn’t have any money and I said OK I need someone to travel with because blind people can’t travel alone!

Well I spent three weeks in the Andes and then two weeks in the Galapagos. Then we came back and we went up to Colombia – we spent three months in Colombia. Then we took a cruise and went from Cartagena through Panama, Costa Rica, Jamaica and Grand Cayman. And then circled around back and then went hiking in the mountains and Colombia

TR:
That friend Jim was traveling with was 42 and at the time Jim was 60.
Plus he was still recovering from flesh eating diseases,
multiple cancer surgeries and newly adjusting to blindness.

He learned a valuable lesson.

JP:

There are some things that are worse than traveling alone and that’s traveling with somebody else!

So at Christmas I flew back to Manta.
TR in conversation with JP:
So Jim can I ask you… you just
shared all of that … I mean you talked about a cruise and
flying to the Galapagos and stuff so you’re financing that on the Social Security?

JP:
Yeah!

TR in conversation with JP:
OK! And at this point you’re not paying rent or anything like that just traveling so you’re a Nomad.

JP:
Right, I’m a Nomad, I’m homeless.
I’m doing this on $1,127 a month.

So anyways when I got back to Manta I had infected my foot again and I had to stay off it for six weeks which drove me nuts.

So I was talking to a friend he was moving to Vilcabamba and I’d never heard of….

TR:
That brings us back to Jim’s journey.

When we left off, he was on his way to Vilcabamba
and stopped in a Hostel in Cuenca
where he posted the question

JP:
In Cuenca, what’s there to do for a blind man traveling on his own?

One guy suggested why don’t you head up to Ingaperka which is a Aztec ruin in the Andes which would be Eastern Ecuador.

TR:
So off he went to Ingaperka to find the ancient Inca Ruins.

Now if you’re thinking Jim is probably fluent in Spanish
or of course everyone speaks English,
well you’re wrong.
In fact, most people in the town of Ingaperka speak a dialect of the Incas.

JP:
The bus let me off in the middle of this town. I have no clue where I am I finally find somebody that speaks about four words of English.
And she asked me what I was doing and I say I was looking for the ruins. And she says ruins Cinco. I said Cinco kilometers. She says no Cinco minutos. I said where and she say aqui and pointed me to a road and so I walk up the road. I walk into this beautiful state park.

TR:
After receiving a tour of the ruins
well, it’s time for Jim to begin making his way to Vilcabamba.
He catches one bus to Cuenca and another to Loja.
Which is where he of course posts to Facebook:

JP:
What’s there to do for a blind man travelling alone through Loja?

Well this woman posts back well I have these two. English students who
are blind and would like to meet you. They’re sisters. So I meet them for coffee they come in on the arm of somebody crab walking because they don’t travel alone they’re in their thirty’s and they’ve been blind all their life.

They sit down and we’re talking and one of them looks at me and says who are you traveling with? I said nobody.

She Says Do you speak Spanish? I said no she said you can’t do that! I said yeah, I can!

TR:
By now you probably get the impression that the response, yes I can,
that’s something Jim is quite used to saying!

JP:
I’m here!
She takes me over to the elementary school which I’ll tell you is like a prison. Two meter high concrete walls surrounding it with broken bottles over the top of it and they’re all concrete bunkers and it’s just… it’s got mold it’s just… it’s a horrible place.

TR in conversation with JP:
Is that specifically just for blind children or is that…

JP:
Yes, it’s specifically for blind children. And there are residents there and there are day people that come from the city and this is the only blind school for elementary school children in the area. And she tells me that they don’t teach mobility there because they had to cut they cut their budget and the person they cut from the budget was the mobility trainer.

Now my experience with mobility training is I am blind
and I am mobile. There are my qualifications for the position… so now I’m the mobility trainer.

TR:
See what I mean by saying yes…
Jim not only said yes to teaching others who are blind to use the
white cane and more, but he has a pretty packed schedule.

JP:
I’m working four days a week from eleven to one at the elementary school. I work five days a week teaching conversational English at a college and I work two nights a week teaching mobility and technology at the high school.
I’m starting a nonprofit… We’ve got a doctor. Who is volunteering his time services to do prosthetic eyes on the kids that have missing eyes plus I have the Go Fund Me going…other than that I’m not really that busy!

TR:
That Go Fund me is a campaign to raise money to purchase white canes,
iPhones or iPads to provide children with GPS capabilities
in order to improve their mobility.

You can find more at:
http://GoFundMe.com/3noxfco

If you’re wondering what are the living conditions for a blind nomad
in Ecuador
Jim says his apartment in Ecuador
would probably rent for several thousand in New York City.

JP:
It’s the studio penthouse with a balcony view of the mountains. Glass all the way around its fully furnished. It has a hot tub, a walk in shower. The bathroom is ten by twenty and I pay $350 a month for it including utilities.

TR:
Jim’s a volunteer! He’s not paid for any of his work.
Well not in the traditional sense!

JP:
What I get from a kid who comes up and hugged me. You know – I’ve got children that actually… they don’t speak the language that I speak and they cannot express themselves on how much they really appreciate me.

I get people hugging me all the time. That’s what I get paid in!

While I still have work to do here I’m not leaving. It’s just different it’s a different lifestyle I found a place where they need me so I’m staying. When they don’t need me any more I’ll go somewhere else.
TR in conversation with JP:
How do you feel today about everything that happened? That whole crazy story you told me.

JP:
I will tell you something that you will very seldom hear from a blind person.

Going blind was the greatest opportunity of my life! Without that none of this would have happened. And that’s how I look at it.

TR:
And isn’t that what it boils down too!
How we choose to look at it!

Jim is actually looking for an assistant volunteer
to join him in Ecuador.
He needs help with some of those things he’s doing like
teaching mobility and technology.

He can provide room and board, but
the candidate needs to pay for their own travel.
Oh, yes, and the candidate must be blind.

Jim can be contacted directly through his Facebook page titled:
Blind Jim Can’t do That!
(Yeh, I can!)

I’m Thomas Reid
for Gatewave Radio,
[JP: I don’t give a damn if you Believe it or not ]
Audio for Independent Living.

TR:
I have never described myself as a journalist.
In fact, I make sure to say, I’m not.
I am a self-described Advocate who uses audio to make a point.
I don’t hide my opinion,
I choose the stories I want to tell and have a real solid perspective.
The idea of a journalist is that they supposedly don’t have that bias.
I don’t believe that at all!
However, A journalist would have done some real fact checking of Jim’s story.

They would have contacted various sources to try and confirm
his account of the events.

I am a New Yorker,
I instinctively don’t believe you!
It’s something I am really trying to rid myself of but it’s so ingrained in my being it’s really hard to separate.

I know there are some who will listen to this and not believe him.

Some will assume he has some residual vision – and say
that’s the reason he can do it.

Jim does have a bit of light perception which allows him
to see shadows out of a part of one eye.

Some will think it’s his nature.
Well, it’s probably fair to say Jim is something of an adventurer.
Before losing his sight he was a professional scuba diver diving throughout
the US and Caribbean.

That included salvage work for insurance companies, body recovery,
owning his own diving school and treasure diving in the Caribbean.

So here’s the thing…

I do believe Jim.

Jim is 100 percent telling the truth about the fears of a blind traveler.

Those fears are not just contained within the person who is blind.

You know that because as you were listening you felt uncomfortable.

You know you did.

I don’t care if you are sighted or
any degree of blind, you felt it!

I felt it! And feeling that way upset me.

I travel alone to different states but I had a fully planned itinerary.

Jim’s story made me challenge how I look at the world
and what I really believe is possible.

During our conversation a woman interrupted Jim and I asked him to explain what happened.

JP:
some woman just walked up to me and said You’re an inspiration to the people down here. I overheard your conversation.

I have people walking up to me on the street constantly doing that.

TR in conversation with JP:
How does that feel?

JP:
I don’t think I’m anything special.

I think everybody has it within themselves just that I choose to do that my question to people is Why don’t you choose to do it.

There are so many people out there that don’t want to leave their house and it bothers me.

TR in conversation with JP:
Why?

JP:
I’ve met so many blind people in my. Limited time being blind. And most of them tell me that they have limitations on everything they do.

You know they tell me it’s OK that you can do this but I can’t and then they give me a list of reasons why they can’t.

TR in conversation with JP:
What are some of those reasons?

JP:
Oh I could get hurt I could fall down. I could get lost.

So what’s the big deal you don’t think I get lost you don’t think I fall down you don’t think I get hurt?

TR:
I think it’s fair to acknowledge that the emotions behind these thoughts are real. But Fear you may have heard
is an acronym for False evidence appearing real.

You know what else is real!

Our perspective!
And we can actually control that!

JP:
I survived cancer. I’m blind. I survived the flesh eating bacteria What are you going to do to me that God hasn’t done already? It’s true! What fear do I have now. They told me I was going to die on three different occasions.

TR in conversation with JP:
you know you’re going to go at some point.

JP:
Right, we’re all gonna go some time!
I’d rather go out swinging then go out crying.

There is nothing holding you back but yourself.
I was at a Blind I Can meeting I can do is what they call it…

And they were talking about having an outing and they were talking about going out to lunch.

I mean, what is going to lunch proof for a blind person. Everybody eats!

They asked me what my idea of a good outing was…

There’s a place in Florida in Orlando called Machine Gun America. It’s automatic weapons… what the hell could possibly go wrong!

TR in conversation with JP:
Laughing!… I love it!

JP:

Make yourself feel alive.

You’re dead, nobody’s told you!

TR:
Jim, like many who lose their vision later in life, especially over the age of 55, never even had real mobility training.

JP:
My mobility training consisted of twenty minutes.

I learned everything on the internet and by myself reading books so when
they finally picked up my paperwork they put me through … they put me in front of a mobility trainer who told me that in familiar surroundings I was Ok, but I needed work in unfamiliar surroundings.

So I was hiking staying at an Echo lodge called Ukuku in Columbia it’s outside of Ibagué.

It’s a two kilometer hike up a mountain across three rivers. To get to this and the last river you crossed There’s a log and you got to balance on a log to cross the river.

Now do you know the proper caning technique for crossing a log bridge?

TR in conversation with JP:
Laughing… No I do not!

I think mine would be to straddle the log and then slowly go across. That would be my technique.
But that’s just me!

JP:

So I had to call back to the person who was in charge of the mobility training and I said, hey Tom what’s the proper caning techniques for crossing a log bridge?

TR in conversation with JP: To the avenue.
Oh my gosh! Did they have any advice for you?

JP:
Oh hell no.

TR:
But don’t get it twisted,
Jim isn’t some sort of blind Evel Knievel.
(If you’re younger than 40 Google him!

Jim is practical about his travel.

JP:
I have a theory. It’s really simple when I get to a town if I check into a Hostel I get the business card of the Hostel, put it in my wallet.

If I get really lost I take the business card and I give it to a cab driver and I ask the cab driver donde esta aqui… where is this? And he takes me there.

TR:
That practical advice goes beyond travel…

JP:
I’m trying to convince people that just because you have a problem doesn’t mean you can’t get your ass out and do something.

I listen to people tell me they can’t get a job. Well, go volunteer and get some experience!

TR:
I’m hoping to speak with Jim again.

And who knows maybe that will be in person, in Ecuador.

There are links on Reid My Mind.com to both the Go Fund Me and his Facebook page if you want to communicate directly with Jim.

I usually close with my reminder for you to subscribe to the podcast…

well today, I’m closing out with part of a favorite quote taken from Jim’s Facebook page.

Maybe someone will find it helpful… I think Jim may have.

Falling down is a part of life, getting back up is living.”

Peace

Hide the transcript

Reid My Mind Radio – The Reidwind Episode

Wednesday, April 26th, 2017

Sometimes it’s worth pausing to take a look at your work. Maybe a time to reflect, re-evaluate or maybe just slow down to pick some others up as you continue along the way.

Today we rewind, or rather Reidwind, and take a look back at some of the prior episodes in the past six months.

There’s lots of ways to consume this content… Sound Cloud, Apple Podcast and others, even transcript.

Transcript

Show the transcript

TR:
For more than 2 years I have been producing this podcast.

The last 6 months or so include episodes that exemplify some of the reasons I enjoy doing this.

Today, let’s take a quick look back.

If you’re new here it’s a great way to introduce you to some of what Reid My Mind Radio is all about.

I say some because part of the stress and the joy of doing this is it’s mine… I can do whatever the Bleep I wanna do…

Like right now… I wanna drop my intro music!

[Audio Reid My Mind Theme Music…]

TR:
This podcast is a place for me to share opinions. Like…

After attending the Pennsylvania Council of the Blind conference; where people with vision loss are the main attendees, the environment is made very accessible. Unfortunately, outside of these types of experiences, this rarely occurs.

TR: From [” Are Blind Conferences Fantasy” Posted November 2, 2016](http://reidmymind.com/reid-my-mind-radio-are-blind-conferences-fantasy/)
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.

TR:
Whenever possible, I like to include my daughters in my podcast.
I just enjoy their company,
when we hang out it’s always fun …
we laugh and act silly.
We share our sense of humor so it’s going to be fun.

In early December I tried to convince them
to do their own episode of the podcast as they did a few years ago, but
this time with a special twist.
From [“Join the Coalition” Posted December 31, 2017](http://reidmymind.com/reid-my-mind-radio-join-the-coalition/)

[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…]

TR:
They came around and we
closed the year with the [Rizzle Razzle episode](http://reidmymind.com/reid-my-mind-radio-rizzle-razzle-year-end-special/)
Even though they sabotage my microphone!

*This episode did not include transcripts as it was very much dependent on the music being discussed.

TR:
Reid My Mind is more than personal …
it’s about telling people’s stories…

People adjusting to blindness like
Robert Ott who drew from his martial arts background to move forward after losing his sight to a gun shot womb.

RO:
I couldn’t believe this was happening to me. Everything was racing through my mind. I’ve got pictures of me doing dive rolls over large groups of people and doing splits in the air. I used to go running a lot on the beach and hand springs and just all kinds of beautiful great stuff. I was so weak I couldn’t even do a push-up and now I’m blind. I can’t get around, my independence, my confidence, my self-esteem, my balance.

TR:
While these stories are specific to adjusting to blindness,
it’s easy to see how everyone has their own way of responding.

Maria Johnson, AKA Girl Gone Blind , decided to share her experiences and challenges on her own blog. …
She spoke very candidly of her adjustment process.
One memorable moment was some of her personal words of encouragement that led to a little creativity …

In [“Who is Girl gone Blind”](http://reidmymind.com/reid-my-mind-radio-who-is-girl-gone-blind/) I included a “song” created using Maria’s words specifically “I got this”.

TR:
I don’t like to use the often referred to idea of
overcoming blindness or disability and accomplishing goals.
I like to think of working with what you have …
making the most out of your situation and counting your blessings…
Like young Ant, the first female blind rapper
From [“Meet Young Ant, First Female Blind Rapper”](http://reidmymind.com/reid-my-mind-radio-meet-young-ant-first-female-rapper-whos-blind/)

TReid:
Young Ant in the building!

YA:
Young Ant in the building!

Treid:
Uh Oh!

So the way I look at this; Antynette is the person, Young Ant is the rapper!

YA:
[Laugh!] Yeah, that’s right!

TReid:
Alright, so first who is Antynette?

YA:
Antynette is a young lady who has been through a lot in a little bit over a year and half and is trying to find her through it with adjusting and coping
and in different techniques that I’m learning and trying to find different avenues of expressing how I’m feeling.

[Intro to “Count your Blessings” by Young Ant]

TReid:
Beautiful!
I lost my sight about 13 years ago. And so…

YA:
Really!

TReid:
Yeh so one of the things that I like to hear from people adjusting to blindness is that they don’t first start with who they are with the fact that they
are blind. You said you are a young lady!
Now, tell me who’s Young Ant?

YA:
Well Young Ant is a motivational rapper!

TR:
And then some like Doctor Dre best known for Yo MTV Raps and more, who’s adjustment process is about Fighting Back…

From[“Doctor Dre’s The Fight Back”](https://t.co/CzpxqDcUXg)

Dre:
I embrace it. And in embracing it he has put me on a path  to help other people and to reach out and express myself not  just about the type 2 Diabetes
not only about the blindness but  about when something goes on and there’s a struggle sometimes embrace your struggle to find your solutions.
It doesn’t mean it’s a guarantee for a cure or a guarantee to a perfect answer  but what it does is says you know what  I’m more than what’s going on with
me.
I can also work with this.

If you have a good relationship with your family, friends and  other people and reaching out. I learn every day from so many different people  and I pay
attention and I  try to pass on some of the knowledge of what I get  so that people can help themselves

TR:
It’s more than the adjustment experience.

We heard from
Robert Lewis sharing his story of
growing up in a segregated school for blind students.

From [“At The Intersection of Black & Blind”](http://reidmymind.com/reid-my-mind-radio-at-the-intersection-of-black-and-blind/)

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:
Naru Kwinah and Leroy Moore, the two gentlemen producing the
documentary of the life of Joe Capers. Played a big role in artists like EnVogue, Tony Tony Tony and MC Hammer

From [“Who is Joe Capers”](http://reidmymind.com/reid-my-mind-radio-who-is-joe-capers/)

Naru:
Listen brother! His studio was called “J-Jams Studio: Joe did everything.  He had his mix board in Braille. He recorded, he engineered he mixed, he produced.
He did everything that you could every possibly do in the studio. And he had the greatest ear I have ever been around and I’ve  been doing music over 40
years of my life. If you had one note or one little thing off he knew and he would call you on it. You know because he was blind you thought you’d  get
away with stuff.

TR:
In that same episode we learn about Krip Hop from founder Leroy moore.

LM:

This year is our 10th Anniversary and we have loose chapters…

TR:
These include countries within Africa, the UK, Germany and Spain.

[Audio: “Tales of the Krip-Hop”, Rob da Noize Temple]

With the network formed by Leroy and co-founder Keith Jones, the two being disabled activists, the focus continues to be on education and advocacy.

LM:
So we saw Krip-Hop as a way to bring awareness around the history of disabled musicians from the Blues to Hip-Hop and really educate and to push the Hip-Hop
arena  around Ableism thinking around disability and to really say that disabled musicians have been here since the Blues.

TR:
That’s just a taste of some of what has appeared here on
Reid My Mind Radio over the past few months.

Subscribe now to make sure you are riding along during
the months to come.

You can subscribe via Apple Podcast or where ever you like to get your podcast content. That includes Stitcher and Tune In Radio.

Go check that out now, there’s lots of good stuff.

If you’re listening on Sound Cloud, hit that follow button.

I’m Thomas Reid
[Audio: Young Ant “Don’t get it wrong, I’m in my zone”]

[Audio: Reid My Mind theme music outro]
Peace

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Reid My Mind Radio: Doctor Dre’s The Fight Back

Wednesday, March 15th, 2017

Picture of Doctor Dre, seated with a tan fur jacket with the caption, Doctor Dre The Fight Back!

Doctor Dre of Yo MTV Raps, NYC’s Hot 97 Morning Show, the movie Who’s the Man? And so much more … is launching The Fight Back!

Diagnosed with Type 2 Diabetes and now blind, this fight back is about more than you probably think.

This episode features the piece produced for Gatewave radio followed by more personal conversation with Dre. Plus, you know there’s only one way to intro this podcast… if you were a morning show listener you know I had to do it…it’s the roll call!

So c’mon yawl, listen to Dre…
>scroll down a bit, , to hear the show press play!

 

Resources:

 

Transcript

Show the transcript


TR:
What’s good everybody?
This is a special episode so I’m going to jump right in…
it’s no mystery , the title of the episode says it all.

If you’re in my age group You remember when older folks said rap was a fad and
black radio didn’t play the music!

You remember when MTV played videos and they weren’t black artists let alone rap music.

Yes, this episode is featuring that Doctor Dre from YoMTV Raps and many other things like the Hot 97 morning show.
With that in mind! There’s only one way for me to kick-off the podcast…

Yeah, I’m gonna do it!

[Audio: From The Hot 97 Morning Show with Ed, Lisa & Dre
Music…
“What’s up yawl, whatcha got to say, who’s on the phone with Ed, Lisa & Dre?”]

TR:
Yo, TReid’s the name, and right now’s the time
Welcome to the podcast called Reid My Mind!

Cheah!

[Reid My Mind Intro]

TR:
Significant vision loss can force a person to face real doubts and questions.
Such as;
Why did this happen to me?
What do I do now?

Andre Brown has chosen to answer the last question by launching a fight;
well really a fight back.

It’s more than vision loss.

In  2008 Andre was diagnosed with type 2 Diabetes.

He experienced multiple complications of the disease including Charco – foot Syndrome which he says can cause a collapse of the ankle.

DD:
My vision loss came as a progression of that and not taking care of myself properly.

my vision loss was a gradual thing where I  started seeing little things across my vision. Little lines and you know things jumping.

TR:
After These lines often called floaters,  multiple surgeries to repair detached retinas,
Andre was left with some light perception.

DD:
Diagnosed as Diabetic Retinopathy but  as the Doctor said  to me , he said that’s what’s   blocking your vision, you have scar tissue in the back. He said we can’t do anything about  it until we stop the Diabetes. So once that happens then  we can do a different procedure or two to see if we can make the sight  come back.
I’ve spoken with a lot of different people and everyone has told me that my sight  returning is a very strong possibility, especially with what I am doing now.

TR:
What he’s doing now?
Simply put, he’s fighting back!

This fight is just as much for others as it is for himself.

Andre’s in a unique position to take on this job.
You see he’s been working in support of the careers of others for years.

Andre Brown, is better known as Doctor Dre, a pioneer  in Hip Hop culture and entertainment.

Starting out in WBAU, the Adelphi University radio station in Long Island,
Doctor Dre would eventually go on to record music with his group Original Concept.

He D Jayed for the Beastie Boys.

He was involved in getting one of Hip Hop’s most prolific and influential groups, Public Enemy on to Def Jam records.

Most people know him as part of the Ed Lover and Doctor Dre Duo who
hosted “Yo MTV Raps” every weekday
between 1989 and 1995; As well as
extremely successful radio morning shows in New York City between 1993 and 1998.

DJ, musician, actor, author… and now
Doctor Dre is  in a position to bring real attention to two of today’s
very significant health crisis ;
Diabetes & Vision loss.

DD:
Well we have the program that’s called Doctor Dre’s The Fight Back.

Taking the situation and being able to talk to other people and say, I can show you through  what I’m going through  that we all can change. We all can grow.

I’m finding other people that have different or similar experiences and being able to share that. So the fight back is
how do we reach out and get so many resources to work with you to try to actually change your situation.

TR:
Changing the situation by providing access to information  including;
medical, lifestyle and technology.

DD:
I’m doing a lot of Holistic medicine along  with traditional medicine to work with my Diabetes  and just to change my diet. Just putting that under better control

I’m playing the Guinea pig so everyone can  see it.

TR   [In conversation with Dre]
When you say   you’re playing the Guinea pig what does that mean?

DD:
Sometimes you have to go out and someone has  to go oh hey does that work, well I’ll try it  let’s see

I’m not bringing guarantees, I’m trying to bring choices.

What we’re doing is trying to bring those choices to the fore front. so there no longer just whispered in a corner or you have to pull this up on the Google thing… know we’re gonna say no, here’s a bunch of things here, find a way to find something that works best for you. Here are some things that are very easily at your beck and call.

And when you have options, there’s so much more you can do.

TR:
Real life style changes that affect the way we think about nutrition.

DD:
And that’s one of my goals in The Fight Back, is to change bad thinking.  The mother of 4 who works three  jobs with four kids and they have to run to McDonald’s because they  want those Happy Meals; I want to change the Happy Meal to a life meal.

TR:
Lifestyle choices are like adjusting to vision loss; it’s personal.

DD:
you do what you feel the most comfortable doing  and you work from that position. Everybody’s an individual about it. There’s no one magic thing for one person. There’s a lot of great things out there and I  am discovering those things to help  me accomplish doing other things. I’m very open to learning.

TR [In Conversation]:
What types of things are you discovering?

DD:
I have a phone I could talk to and it  speaks and dials  and talks to me.

The technology now is catching up. I believe like Netflix has where they actually have  a program that is designed so when you’re watching a program it describes everything so you get the full affect.
I’m discovering it one at a time but I don’t know the name of everything I just go wow that exists , that’s a good idea, that’s a really good idea.

TR [In Conversation with Dre]:
that’s Audio Description.

DD:
Yes.

TR [In Conversation with Dre]:
Just for full disclosure, I’m blind myself.

DD:
Oh, ok!

TR [In Conversation with Dre]:
The experience is unique and different for everyone. So I’m trying to gauge what is your experience and how other people can relate and learn… whatever that is because that’s what experience is all about. There for everyone.
DD:
Exactly.

Well with me I understood simply when it was starting to happen  I said don’t panic.
I’ve become a person that reaches for solutions. And rather than falling into , oh my god I can’t believe this is happening  and go into depressed mode I said no  this may happen, this is what you may need to prepare to start doing. And I started preparing myself for it. I said you know what I said you know what  this may be, but darkness  won’t last forever. I said  you have God behind you  and God has already told you  this isn’t forever, this is to slow you down  this is just to make sure  that you can listen and hear what I have to say. And I started listening and hearing what he had to say  more than I started talking.

I embrace it. And in embracing it he has put me on a path  to help other people and to reach out and express myself not  just about the type 2 Diabetes not only about the blindness but  about when something goes on and there’s a struggle sometimes embrace your struggle to find your solutions.
It doesn’t mean it’s a guarantee for a cure or a guarantee to a perfect answer  but what it does is says you know what  I’m more than what’s going on with me.
I can also work with this.

If you have a good relationship with your family, friends and  other people and reaching out. I learn every day from so many different people  and I pay attention and I  try to pass on some of the knowledge of what I get  so that people can help themselves

TR:
The Fight Back is a give and take; a collaboration.

TR [In conversation with Dre]:
So what is The Fight Back, what does that look like? in the world. Is that like a  web portal

DD:
It’s going to be a website… we’re building as we speak because I didn’t want to just put something out there … like it’s easy to say we’re going to do that  and throw it out there and  people just think that’s it, that’s it… no so I said , first thing we’ll do  is I’ll go out and start talking , build different interviews up and now it’s starting to take different testimonials  from different people  and it’s attached to other situations  also , you know I’m working with  a friend of mind from a company called Rally Wing and they had family who had diabetes and their discussing stuff with me.

Another gentlemen by the name of Marvin Mizell who is Jam Master Jay’s brother  has a company called JMJ Foundation  for the youth. He has Sickle Cell and Diabetes so connecting with his thing. there’s a bunch of people that I have connected with  and I said you know what maybe I should be that focal point to bring people together. and see if we can actually work, not just to a cure and better treatments ,but to better understanding  and better conversations

So going out now and talking to different people and listening to what their saying  how they fought back
that’s what this fight back is all about.

Bring those stories to light.
Bring this action to light!
And be a little educational, be a little entertaining, be informative, and be supportive
That’s where the strength is!

TR [In conversation with Dre]:
Is the reality show still a thing?

DD:
We went out there we talked to different places, everyone was excited, yeh we want to do this, yes Dre we love it. And as more we kept talking, my idea disappeared and it became this other thing. It was like that’s not what we’re talking about .

I have a little experience in creating television programs.
We’re creating our own show. Creating our own messaging, making our own venue because the technology allows us to do this.

How do we take all these different instances and work together. Instead of just having a website, a page, you know do this  and get this. No, I want you to come on, I want you to see these different testimonials to be able to reach out to like you and to say hey I want you to talk to him because your experience can help some other people. Your conversation can help someone else who may be feeling down and go hey wow it isn’t as bad as I thought or it could be really bad so we’re going to try and reach out. Go see people shake hands, kiss babies, do whatever needs to be done. We’re going to run the ultimate campaign! The campaign of life of wellness and happiness. That’s a campaign where you just can’t be elected. there is no electoral college for that!

TR [In conversation with Dre]:
[Laughing!!]

DD:
I’m sorry! I’m so sorry!

TR [In conversation with Dre]:
Don’t apologize for that. That’s real!
[Laughing!]

DD:
My things are based on love
People want to sit back and talk about this guys this and this one’s that. Hate, hate!
I said, you know what man, hate carries weight! With love you can soar!
And I got nothing but love man!

TR:
When the site is completed, you will be able to learn more at Doctor Dre TFB.com.

There’s a quote I like to refer to that’s attributed to a Greek philosopher or motivational speaker depending on who you believe…
It’s not what happens to you, but how you react to it that matters.

Doctor Dre,  reacting with love
to make information more easily available , bring
health choices to the forefront,  create a place where
others can share their experiences, all while
remaining faithful and encouraging;

In this fight, there can be only one winner; nothing but love!

This is Thomas Reid, for Gatewave Radio;

Inserted from DD:
“Bring those stories to light. Bring this action to light! And be a little educational, be a little entertaining.”

Audio for independent living!

[Audio: Dre drop a load on em’, from “You down with MTV”]

TR:

Podcasts allow for longer exploration and intimate conversation.
In a way, I hinted to this in the Gatewave story edit.

There’s power in conversation between two people
exchanging knowledge about their shared experience.

Some things you really only feel comfortable talking about with someone who you know gets what you’re saying.
You don’t want to have to explain yourself.

The conversation could just be two people kicking around philosophical ideas.

often it’s , just talking about real practical sharing of information.
Like when Dre mentioned posting to Facebook:

DD:
One of my friends growing up he said I saw you on Facebook and I’m going how is he doing this? Isn’t he blind? And he’s like, he’s actually posting and doing this and that… I said, I have somebody doing that. The way I post is my son posts for me. He’ll put stuff up  that I need written or said or whatever we want to put on my Facebook page. So that’s fine. That’s how that works.

TR [In conversation with Dre]
You could do it yourself too you know right?

DD:
Please, I’m listening

TR [In conversation with Dre]
Ok so you have the iPhone and the app on the iPhone is , I mean it’s all accessible. It sounds like you mainly probably use Siri, the dictation?

DD:
Yes, I use Siri right now.

TR [In conversation with Dre]
So  you don’t use the keyboard at all, you never tried to use the keyboard?

DD:
No!  (Surprised!)

TR [In conversation with Dre]
Oh, you can absolutely. Do you have Voice Over turned on?

DD:
You know what,  I’ve been trying to go to the Apple store to sit there and have them explain everything that can be done , I do not probably have it turned on, no.

TR [In conversation with Dre]
Ok!

TR:
Sometimes we assume that people are supposed to just know things…
Those who do, need to be more open and welcoming in order to make that information available.
At the same time remain open to receiving new ideas.

Three words that tell me Dre is going to be fine
no matter what the end result of his vision loss turns out to be;

DD:
“Please, I’m listening!”

TR:
Please, I’m listening!

Dre doesn’t know me.
He’s been around the world and has access to people and privilege.

DD:
Having reached out to people like Stevie Wonder.

TR:
Now, who am I to challenge something that Stevie says. I only say that because what Stevie means to me.

Adjusting to blindness though, is different from living with blindness all your life.

For example, I grew up only seeing out of one eye.
The challenge to me was different compared to someone who loses an eye
later in life and never had monocular vision.
I could share some information about things they should know,
but prior to blindness I wouldn’t have been able to relate to that loss.
That adjustment is the challenge. Growing up only knowing one thing is a different experience.

Meanwhile, I too could probably benefit from some of their discoveries.

Dre knows there’s so much more to learn and is open to that information for himself and others.

Our conversation though, went deeper.

Like when I wanted  Dre to know about an aspect of blindness
that is experienced and the ramifications that are felt by too many.

TR [In conversation with Dre]

We started the conversation with a little bit about  blindness and with the things people do and do not know, right. There’s all this technology, there’s so much you know going on and one of the big big issues  when it comes down to the blind community . The image of people who are blind in terms of how that’s perceived in society,  there’s a lot of negative connotation when it comes to blindness that I realized that I had and as I met other people  you know, blind at birth or blind afterward, there’s an incredible resource out here that is not being taken advantage of. So within the blindness community and within the disability community, unemployment is 70 percent.

DD:
Yes, it is!

TR:
So many people don’t even understand that. Even in just in terms of how people can do things and the abilities that are there it’s just not known. In part of what you’re doing you may not have or may have thought about it, you are going to be a representative  of that to some degree. Whether or not you like it or not, right, people are going to look at you and they now look you as he’s blind and therefore when they think of other people who are blind they will think of you. And so the things that you’re doing are going to send a positive message  not only to people who are sighted but also to other people who are blind who may have  bought into that.

I just ask you to ponder that, you know!

DD:
I hear what you’re saying. It’s very funny that you say those things. Funny not laughing wise, funny as it’s very interesting how we do that … I now the same way  I was put upon  and told do you believe you can get your sight back, I’m going to ask you those questions to… do you believe you can get your sight back?

TR:
Now, I had lots of people say they were hoping and praying I get my sight back, but
No one outside my immediate family has ever directly asked me that question.

I know a lot of people might think that question shouldn’t have been asked.
But it was part of our conversation so in no way was I offended or upset by that. This was a conversation between two people experiencing vision loss.

This isn’t some random person asking me on the street.

My answer and Dre’s response forced me to think about how I look at that question.

My answer… next time on Reid My Mind Radio!

[Laughing….]

Just playing!

TR [In conversation with Dre]
Nah! My situation is totally different.

DD:
Mmm hmmm!

TR [In conversation with Dre]
Number 1 my cancer is a genetic cancer. I was born  with a cancer called Retinoblastoma. I lost my left eye  as a child. The tumor overtook that eye.  I had at that time, this was in 68, well 69, radiat5ion. Thirty five years later that radiation caused another huge tumor  to grow in the back of my right eye and so I had no real choice because it was right on the optic nerve and so when it’s on that optic nerve, the next step is the brain So my choice was do I take that out  and live? Now mind you my wife was pregnant with our second child, we just moved from the Bronx to the Poconos in a house… so my right eye was removed.  There’s no coming back from that.

DD:
Ahh, yes.  You can’t get an eye transplant?

TR:
No, there’s no such thing as an eye transplant. The amount of nerves  that are in the eye  is unlike any place else. But that’s ok!  I didn’t have a choice and that’s ok, you know because I  my family, I have my little girls you know and so  my thing was like you  stepping back from the industry, my thing was I’m raising my girls you know. I’m a keep working and do whatever I can and be a  you know a help to other people  be a you know, productive member of society  and all of that and I can do that when I’m blind. I like to say the only thing I can’t do is drive.

DD:
Well that tells me a funny story that  I thrown out to Stevie Wonder about doing a movie I used to tell when I was doing interviews and I still do but know people go like you’re really going to do that and I said yeah I’m going to do that. I was being interviewed and they said Dre you gonna do any more movies and I said yeah I’m going to do movies. I said right now I’m in conversation with Stevie Wonder , we’re doing this movie called Just Drive the Damn Bus! And everyone fell out. They said for real. I said yeah and in that movie you’re going to see  Stevie and I drive the bus.

TR:
Uh huh!

DD:
They were like, how are you going to do that?  I said that’s the point, you gotta see the movie. And I was joking about it right?And then I started working with  one of my partners and we started  coming up with a concept of the movie and  it was like, this could work. I said, it’s a movie! I said, but do you understand what would happen and he said  but how are you guys going to act in the movie? I said  the same way other people act  in a movie, you hit your mark, you say your lines you keep moving, that’s not an issue.

TR:
Right.

DD:
Stop making an issue of a non-issue.  And then I told, a matter of fact I told  I was talking to LL Cool j and I told him about it and he  fell out laughing. He said you’re serious. I said I’m dead serious, your gonna do that.
I don’t walk around with dark glasses on. My son says Dad put the glasses on  stop walking around… I said no people need to see my eyes the way they are. So what, it doesn’t matter.
I say this to say this to you. We may not know the technology that will exist to help you gain sight when you need it, but I believe in my heart with what you just told me and what just trinkled through me is you and I our meeting is not coincidental  and I can’t promise this, but I just have this feeling  in my gut you’re gonna get your sight, because you need to see your kids.

TR [In conversation with Dre]
[Exhales!]

DD:
I know you’re saying, how can that be done? I don’t know. I don’t have that answer yet. That answer may come next year, that may come in five years, we don’t know. When I put those goals in front of me  it gives me something to shoot for. Reality or not, that’s why I say  that thing about the movie,  just drive the damn bus… Bill said, you are nuts, you’re outta you… I said no I’m not. I said because we can do anything if you put your mind to it.  Remember seeing Star Trek the Next generation

TR [In conversation with Dre]

yeah, yeah, with Jody…

DD:
LaVar Burton! He put on a visor and  he could see. But when he went to do the movies  LaVar didn’t want that visor on his face they pulled it off and put something on his eyes…we don’t know what’s coming!

TR [In conversation with Dre]
Right!

DD
Now if I could get in a DeLorean and go sixty years forward and grab it and pull it back  and say here put this on it works

TR [In conversation with Dre]
[Laughing….]

DD:
I don’t know!

TR [In conversation with Dre]

Right, right!

DD:
But we’re back to what the Fight Back is all about, choices!

TR [In conversation with Dre]

What you just said  helped me because the obstacles in front of me are not  necessarily just based on sight. And that goes into a really deeper conversation, but when you said  you get something from  that, there’s no way  I would want to take that away from you!

TR:
I’m not a dream killer and never want to be that!

Believing in the ability to regain sight doesn’t mean  not believing in the abilities of people who are blind.

Often though, that seems to be the message we hear from different organization in their fight against blindness.

The NY Times a few weeks ago ran an article with the headline;
The Worst that Could Happen? Going Blind, People Say
The article itself discussed some of the fears, and ways to prevent or slow
certain types of eye diseases, but
it did nothing to help ease that fear for
those who are facing  that in their present or future.

That’s not cool!

They only looked at vision loss from the medical perspective  ,
prevent the disease and there’s no longer an issue!

But there’s the society side!

That fear is what leads to people not wanting to in anyway associate themselves with blindness.
That fear and miseducation leads to that 70 percent unemployment.

But Dre’s not saying that.
His approach appears to be inclusive, holistic as in a full picture.

He’s straight up keeping his options open
I can support that!

Let’s do some shout outs!

First of all Doctor Dre,
thank you brother for the conversation,
for the courage and willingness to bring options to the people!
I hope to hear more about the Fight Back in the near future.

These next two shout outs come with a recommendation…
Audio: The Cipher Show theme[]

If you are a hip hop fan and like to hear background stories
from artists, journalists and those on the business side…
you need to check the cipher show.
Host Shawn Satero was kind enough to help make this interview happen.

It’s one of my favorite podcasts.

At least once every episode you will hear a person being interviewed say, Wow, you really did your research!”

you’ll hear it at least once an episode which lets you know it’s a quality show.

Shout out to Shawn and the Cipher show!

Shout out to Bill Adler who helped coordinate this with Dre.
BTW, Sir, please continue producing that Christmas  Mix Tape,
my daughter and I look forward to that Cipher episode each year.
No comments folks, I like the different cultural Christmas music and I ain’t ashamed to say it!

If your listening right now on Sound Cloud hit that follow button.
You can subscribe  via any podcatcher on your phone or tablet,
Apple, Android it doesn’t matter we’re outchere!

We’re on Stitcher and Tune In.

Got feedback?
Hit me at reidmymindradio@gmail.com … Remember Reid, is R E I D.

Thanks for listening!

Peace!

Hide the transcript