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Celebrate #ADA30 July 26, 2020

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ADVOCACY

Editor’s Note:

On July 26, 1990, the Americans with Disabilities Act (ADA) was signed into law. Every year at this time I recommend a moving PBS documentary about the Disability Rights Movement called “Lives Worth Living.” This year I’m adding Crip Camp, another film that highlights the disability revolution.

Americans With Disability Act Turns 30 Today

While I am not a sociologist I am an empathic person who respects humanity and believes in doing the right thing. Being born into a couple of marginalized groups allowed me to become uncomfortably familiar with discrimination and exclusion. Even so, because I value human life and deeply appreciate diversity, I refused to allow my circumstances to define who I am. Then later in life, I acquired a disability.

Living with a disability is a life-altering uniquely personalized situation that’s been physically and emotionally draining. Adding to this heaviness, confronting an additional layer of discrimination makes day to day life even more uncertain. Losing my independence has been frustrating and enlightening.

Because of my background, I’ve always known that the world we live in isn’t fair or equitable for everyone. As complex as we are as humans, no one can possibly understand what it’s like to live in the body of another person. Even so, our need to classify everything including people, makes it more difficult for us to see our commonalities. The further we drill down these classifications the lesser the value of those belonging to certain groups like, for instance, people with disabilities.

An Ugly History

Here in the United States, it was against the law to be in public spaces if you were “diseased, maimed, mutilated, or in any way deformed, so as to be an unsightly or disgusting object.” As unbelievable as it might seem “The Ugly Laws” as they came to be known in 1975, were enacted in the late 1860s. These ‘laws‘ encompassed the “poor, the homeless, vagrants, and those with visible disabilities.”

Eugenics, also known as a movement to improve the human race, was a process where people who met certain criteria were sterilized to prevent them from reproducing. The laws were put in place by our government and/or the people who thought they were superior to everyone else.

The Fight For Disability Rights Continues

I think the difference between those who fight for social justice and those who are against it is our view on humanity. People who respect differences and are open to accepting others as they are with empathy understand that “life,” no matter who it belongs to, matters. Even the elitists have no more or less value than those whom they deem less than.

“Around 15 percent of the world’s population, or estimated 1 billion people, live with disabilities. They are the world’s largest minority.”* The thing that sets our community apart from other minority groups is we are wholly inclusive. Anyone at any age, social status, ethnicity, religion, gender, etc. can become a member at any point in their lives. What’s sad is some of us take the stance that disability rights are ‘not our problem,’ that is until we become disabled. However, being ‘temporarily-abled’ as the majority of us are, makes it our problem.

People with disabilities share many of the same characteristics of our temporarily-abled counterparts, we simply do things a little differently. We’ve come a long way since the ADA became law however the fight for Accessibility, Inclusion, and Representation continues.

*Resource: Fact Sheet on Persons with Disabilities

Disability Rights Are Human Rights

So what can you do to become part of the movement?

  • Empathize: I think the most important thing any of us can do, is to check our assumptions at the door. It’s wrong to assume people with disabilities have no value or worse yet, no skills or aspirations.
  • Educate: Increase your understanding of the wide range of disabilities and become more culturally aware and sensitive to the needs of the community. Not every disability is hidden and each person’s story is unique.
  • Embrace: Opening your world to include people with disabilities by volunteering for organizations that support the disability community is a win-win. The organization and the people it supports will benefit from the gift of your time. You will increase your knowledge and build relationships with people who will expand your heart.
  • Respect: No one, wants to be reduced. It’s hard enough being human, so let’s eliminate this idea that disability equals deficit. Learning to appreciate differences and accepting people where they are is at the heart of humanity. If you subscribe to the idea that humanity is imperfect, respecting differences can begin with embracing our own flaws. After all, we are all human.

Let’s continue to strive for inclusivity in all areas of life. Hopefully, there will come a time when we fully embrace our differences without condescension. Until then, celebrate Celebrate #ADA30 with me. What other ways can you think of to impact the disability movement?

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Seeing Beauty Through A New Spktrm

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ABBY’S CORNER | AUDIO INTERVIEW

Intro:

Hey, everybody. It’s Abby. I hope everyone’s doing great. I don’t know what the weather is like in your all’s area, but boy is it hot in my area today, but it’s even hotter because I get to hang out with Jasmine Glass, the creator and founder of innovative makeup, Spktrm Beauty. Jasmine, it is so fun hanging out with you today.

Seeing Beauty Through a New Spktrm (Abby interviews Jasmine Glass)

Jasmine:

I’m so glad to be here. Thanks for having me, Abby.

Abby:

We were chatting before this. You know my obsession with lipstick and I was talking to Steph, our creator of BBB and me, and she’s telling me all about your lipstick and, oh my gosh, can you please share with everybody?

Jasmine:

Absolutely. We’re about to launch our second product, which is an inclusive range of nude, true nude lipsticks. There’s been a lot of progress made with foundation shade ranges expanding over the past few years, but still very few brands that are offering a true nude match for people with varied skin tones. That’s one aspect of the product and we also have been working with Bold Blind Beauty as consultants because we have decided to incorporate braille into all of our packaging moving forward to be of service to the visually impaired community as well. We’re very excited about this launch for those reasons.

Abby:

I have never myself been able to find a good match for a nude lipstick. It always makes me look kind of pale or it’s not, so I love this. I want to talk about that for one second and then of course we’re going to get into the braille because, oh my gosh, I’m shaking with excitement. I want to talk with a nude lipstick, I just feel like it can really bring out my own natural beauty. Are you all about that?

Jasmine:

I love a good nude and I feel like it’s a good daytime look, a little more subtle and I just think it’s important that we make available all products that all different communities are looking for. That’s really the goal here is to draw attention to the fact that there is still a limited amount of these shades available. I’ve had conversations with our beauty consultant, Julissa, who is a black woman, and she’s talked to me about the fact that black women are still using eyebrow and eyeliner pencils on their lips at this point or having to blend colors together or just using other products that aren’t lipstick to create that look. This is a step in the right direction and we hope other brands will follow suit.

Abby:

You’re a leader, a real leader, and it’s awesome. I like a good day too. It’s awesome and I just feels delicate. I just feel like I’m featuring my own beauty that I have within. Tell us all about the braille. What inspired that?

Jasmine:

Gosh, it’s been such an inspiring journey all around. My whole team has been educating ourselves through several different resources, including working with Bold Blind Beauty along this process. I was not even aware when we started this journey how many people there are in the world that are either totally blind or visually impaired. I believe it’s around 400,000*. We started thinking about the experience of a visually impaired person going into a major beauty department store, having not a single brand that is offering braille on their products and it’s really an area of the many areas of the beauty industry is lacking still at this point, despite a lot of progress that has been made. It’s something that we wanted to address because I think it will make a lot of people think in new ways, put themselves in the shoes of somebody who has a different human experience than they do and really just to continue to expand our mission to be inclusive of people from all walks of life and to be able to provide what they need to have a positive experience with beauty.

Abby:

Can you tell us where you’re going to put the braille on the packaging and what it states?

Jasmine:

Sure. We have our brand name in braille on the lipstick tube itself, and we also have the shade distinctions. We are associating them with skin tones to make it easier for people who have never seen color to understand. Our shades go from deepest to fairest and in each category, there’s a one, two, three, so you can get an idea of the shade range within that category of deep or tan. We’re also going to add some additional information on our website in the coming weeks. We plan to create a YouTube video to explain the functionality further, so we really encourage people to go check that out too. Then on the box we’re going to have a QR code so that you can just scan that and easily get to our website to find that additional information.

Abby:

Can you tell us about your product? I read that it’s animal and cruelty free, which is such a plus for me because I am all about natural and bringing wonderful beauty to life nature. Can you talk to us about that?

Jasmine:

Our products are currently cruelty-free and actually we’re really excited that we are now going to be expanding into being fully clean as well by Credo Beauty and Sephora’s clean standards. I believe there is a list of 50 chemicals that you have to keep out of your product and I recently added somebody to my team, Julia, whose family’s been in beauty manufacturing for 50 years. She’s just a powerhouse of knowledge in this area, so with these additional resources on the Spktrm team now, we’re able to make strides in these areas. We really want to be mindful of every aspect of the brand and to be approaching it from an ethical perspective. This’ll be exciting progress for us as well.

Abby:

I cannot wait to give this a try. I really cannot. I just love what you’re doing and your passion behind it. This is just thrilling to me. If people wanted to find out more about your product and when it’s going to be introduced and where to purchase it and all that fun stuff, where could they go?

Jasmine:

I would encourage people to go to our Instagram first because that is the place that we’ll be announcing our launch. We’re working on some website updates right now related to compliance for visually impaired individuals, so that’s still in process, but if you follow us on Instagram at spktrm.beauty, you’ll be the first to know when our lipstick and rebrand launch happens.

Abby:

I’m already following you, but I’m just going to go spread the word even more. I cannot wait about this. I am jumping for joy. I am so excited about it. It’s going to be so much fun. Is there anything else you’d like to share with us?

Jasmine:

That’s it for now, but we’ll be making a lot of updates on our Instagram, so definitely keep your eyes peeled there.

Abby:

Oh, I totally will, and I cannot wait for this. You guys, this is Jasmine Glass of Spktrm Beauty. I’m [inaudible 00:07:25] keeping it real, keeping it natural, keeping it lovely one cane tap at a time. This is Abby with Bold Blind Beauty and thanks so much for tuning in with me and my friend. Oh, this is so fun. I have a good one guys.

Globally the number of people of all ages visually impaired is estimated to be 285 million, of whom 39 million are blind. ~Word Health Organization

Connecting With Spktrm Beauty:

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June Men In Motion | Robert Kingett

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MEN IN MOTION

Editor’s Note:

Robert Kingett, he’s Bold Blind and full of Pride. From the moment he was born, he was destined to be an overcomer and a person unafraid to be exactly who he is. In celebration of Pride Month, Bold Blind Beauty is thrilled to introduce you to Journalist and Author of Off the Grid: Living Blind Without the Internet, Robert Kingett.

Born A Miracle

I’ve always been somewhat of a miracle baby, or person, I guess you could say now. I fully embrace it, though, and yes, even the inspirational label that gets placed on me sometimes. I embrace it all because I just simply don’t have time to quibble over a slightly incorrect label.

My miracle journey started in 1989 where I was a premature baby. It’s so wild, because my birth certificate says six ounces. I was born in September. I have no idea when I was actually supposed to be born, but I came out defying all odds from the beginning.

I was born with Retinopathy of prematurity (ROP), as well as cerebral palsy. I wasn’t supposed to walk. I wasn’t supposed to talk either. My mobility was supposed to be very limited throughout my whole life. And, to a certain extent, that’s true now that I’m older, but back then, I did walk, and I did talk. I overcame so much at such a young age. I still had communication issues though. I stammered badly as a kid and still do. Which, ironically, is why I enjoy and embrace writing so feverishly.

On His Terms

I was born in New York but grew up in Saint Augustine FL. I attended the Florida School for the Deaf and the Blind and that’s how my path to adaptive technology and accessibility consulting came to be, but more on that later. I’m probably one of the very few kids that actively refused mainstream school. I rejected it firmly. I hated the thought of attending a mainstream school. I knew I was getting the adaptive technology and mobility training that would help me later on in life. I didn’t want to waste my time advocating for everything under the sun. I knew that advocacy would come later, certainly, in college, so I wanted my high school to be as painless and as inclusive to my visual impairment as humanly possible and I just didn’t see that in a mainstream school.

I knew that society saw me as another worldly being that wasn’t worth nurturing as a disabled person, so I perceived mainstream school to just be an academic hassle. It probably would have done wonders for my social life, but I didn’t care about having an active social life when I was younger. I also didn’t want to be around sighted people unless it was on my own terms because, I believed, that my academics would suffer because I’d be trying to develop social justifications. I thought my energy would be wiped because I’d have to constantly demonstrate to sighted people that I’m worthy of existing and taken seriously. At a blind school, disabilities didn’t factor into my acceptance. 

Another reason why a big part of that unwillingness to fight for a mainstream education was so strong is because I was getting a very accessible education. I also was just trying to get through the day, and to my eventual long-term goal of becoming influential. Even if it was silent influence, I wanted to actively chip away at the social barriers disabled people face on a daily basis.

From Scrapper To Success

My home life wasn’t that great. I was abused, both physically, mentally, emotionally, and otherwise. My mother, who was a single parent, didn’t know how to deal with her own daemons so she took them out on me. She was a heavy drinker and, yes, there would be beatings. I often went hungry, so I absolutely empathize with someone when they tell people they don’t know what real hunger feels like. People will never fully grasp it, I realized, so I just had to survive. Get out. Become as successful as I could possibly be and hope I make a small difference in the world, even if it’s educating someone about blindness or starts a chain reaction that makes things more accessible for many in my generation and beyond.

I developed a strong sense of advocacy in my teen years. I’ve never been good at giving a punchy media bite that goes viral or gets people talking. I knew I’d never be in the spotlight however, I knew my strength was in planning and strategic implementations. Oh, and trickle-down advocacy—chain reaction advocacy, as I call it.

I’m very career-driven, and very focused, which is probably why I’m still single. I’m very proudly gay and or queer. I use those words interchangeably to describe my sexuality. I’m definitely not bisexual though, I’m very much gay. But, often, the men I’m attracted to are sighted and have no idea how to keep up with my career drive. That’s something that will, eventually, slow down I’m sure as I get even older, but for now, I’m very focused. I find the idea of romance and love is just something that I will find when it finds me, and grabs hold of me. That’s ironic because I’m an extremely romantic person. I’m very empathetic but extremely strong, personality-wise. I guess you could say I’m a mashup of imperfections that changes people’s lives in small ways.

The Path To Journalism

My advocacy started when I created the first-ever newspaper for the blind at FSDB. That proved to me that I could give people chances and opportunities if I just kept being persistent. As a result, well, I’m very politically active now. Very progressive. Very forward-thinking. And yes, I’m a proud feminist and trans ally. I knew I had the power to change lives through journalism and fiction, so I began writing. Fiction, advocacy journeys, telling people’s stories. I find that very few people have media literacy skills today. I mean, even in my generation and younger. I read, constantly. I even read mainstream news everybody likes to rag on so much, but again, very few people just simply don’t know how the media works in general, which is why I don’t get into small fights online about mainstream media and agendas and biases and otherwise. It’s all trite ignorance and a complete waste of my time. Besides, I have a socialist revolution to start. Just kidding. Or am I?

My writing eventually created the Accessible Netflix Project, which actually got Netflix to provide audio description platform-wide wherever possible. This was a huge accomplishment, but my work isn’t over with. My real love is books. Especially diverse books, and audiobooks, and the publishing industry. I’m working to eventually make it so that seeing blindness in fiction is common while continuing to be a very strong ally to my fellow minorities.

Unicorns, Cookies & Education

I always find it really weird when someone asks me what my hobbies are. My hobbies are extremely plain and ordinary. Like, who doesn’t like listening to music and watching TV shows with audio description? I know a few people who don’t like reading, but I just imagine them as very confused unicorns and continue loving books and literature. I read, certainly. I watch very dark comedy. I listen to boy bands. I steal rainbow tinged cookies from unsuspecting glittering cats in my spare time. I’m so done with being normal. It’s overrated. 

Ironically speaking, my career path has never been regular, either. I dropped out of college, published a book, wrote for free, did accessibility consulting, became more progressive, posted accessibility rants onto the web, and, finally, became an expert witness for a law firm here in Chicago. I’d like to take this opportunity to tell all the responsible readers to stay in school, even if I loath private colleges with every fiber of my peculiar soul. Seriously. I think education is the most important facet in someone’s life. Encourage reading. Encourage creativity, because that’s what truly makes the world go round.

Image Description:

Featured image is the Beyond Sight Magazine cover. Robert’s photo is on the cover, he is wearing a black tee-shirt with the word “PR💛UD” in rainbow colors. The masthead is teal with “Beyond Sight Magazine” in black text. The dot on the ‘i’ in ‘sight’ is the eye used for our 2020 Year of Vision Campaign (described HERE). There are 2 lines of black text that say “Bold blind and full of” the third line ‘PRIDE’ is in rainbow colors. In the bottom left corner is a teal circle with an illustration of a blind man in motion with his white cane and “Men In Motion” is in yellow text under the circle.

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Lights! Camera! Audio Description Action!

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ABBY’S CORNER | AUDIO INTERVIEW

Featuring Roy Samuelson

Hey, guys. It’s me, Abby, I hope everyone is continuing to do well as we begin to ease restrictions related to the COVID-19 pandemic.

Today I have a real treat for you. I recently had the honor of interviewing an extraordinary person who is extremely passionate about the work he does. As a top Hollywood voiceover artist, today’s guest is also a tireless advocate for the blind and low vision community and an overall nice guy. I can barely wait to get started. You can listen to our interview, read the transcript, or do both. Enjoy!

I’m a narrator but I’m playing the role of your friend that’s sitting next to you and making sure that I’m not getting in the way of the story. And what I try to do is make sure that I bring that emotional nuance to the scene so that I don’t get in the way but you can stay fully immersed in it. 

~Roy Samuelson

Abby:

Hey everybody this is Abby and I’m hanging out with one of the coolest guys that I know. And you’re thinking who is that? I’m going to tell you who it is: I’m hanging out with Roy Samuelson. And who is that you say? He is an Audio Descriptor Narrator who I’m crazy about. He is just awesome and he’s done so much work and he’s totally, totally fun to watch movies with and talk about things and boy I just had the best time this morning hanging out and chatting. How are you today?

Roy:

Doing great Abby, thanks so much for having me, this is cool! 

Abby:

You’ve taught me so much about audio description and like what it means to you and what it is so can you please share it with others because I want everybody to know what we’ve talked about.

Roy:

Yes, audio description is a way for a narration track that you listen to talking about what’s happening on screen so the visual elements of a movie or tv show and it’s a way to bring access to those, to someone who might be blind or low vision or other people who might not be looking at the screen right now.

Abby:

And let me tell you guys, it’s super exciting for me because you know I’m into everything and I mean everything. So when I got to actually watch this movie and know what’s happening without having to interrupt my friends I’m like oh my gosh what’s happening now because there’s a visual scene gosh what you do is really brings it to life can you talk about how you make that happen?

Roy:

Sure, so it’s a big process it’s not just me there’s audio description has been around for decades believe it or not and now it’s at the point where companies bring in a special writer who writes a special audio description script based on what’s happening on screen. And I don’t get involved in the writing, it’s a really specialized skill and those people bring the script to life by watching the movie or tv show and they sometimes get a shooting script. So there’s a lot of research that’s done even before it’s in my hands. People look it over and make sure it’s edited right, make sure the timing is right so that when I get the script that I know when to come in between lines of dialogue. There’s all sorts of really specific decisions that are made before it even gets to me. And then when I get it I read a script into a mic and sometimes I’m directed and told what to do as far as making sure I’m matching the emotional tone of the scene and then it’s edited and mixed and sent out to along with a movie or tv show. 

Abby:

That for you is like art to me and you know why? Because I have all these friends that can see and a friend of mine that used to be able to see and she can’t see now and she’s comparing what it was like to watch a movie before like when she could see because there’s so many takes to it. You had mentioned when we talked about this too like a picture is worth a thousand words which has so stuck with me and getting the right narration into that to bring a piece to life when there’s so much going on in those clips, has to be really, is it crazy hard to do?

Roy:

Well, I bring a lot of my voiceover experience to audio description. So it is called audio description narration, but what I like to do, there’s a bunch of training that I’ve had for voiceover work. Whether it’s commercial work or doing video games or animation or even taking an improv class or an acting class that helps inform what I bring to audio description. So yeah, I’m a narrator but I’m playing the role of your friend that’s sitting next to you and making sure that I’m not getting in the way of the story. And what I try to do is make sure that I bring that emotional nuance to the scene so that I don’t get in the way but you can stay fully immersed in it. So, in that sense yeah, it is an art and a craft, [laughs] arts and crafts that you can go shopping at Michael’s for…

Abby:

[laughs]

Roy:

but it’s something that you can bring, that I love to bring to the script. For me it’s a little more than just reading the words.

Abby:

What I wanted to know is when you are working with doing all of this like, you’ve talked about all of your background you’ve brought to this. When did you get so excited about audio description? What made you think ‘hey this is what I want to do?’

Roy:

Oh, there’s like three levels to it. There were three phases, like when I first found out about it, I had an audition and I went in and I recorded a scene from a movie with an audio description script. And at the end of it, you know normally when I do an audition I’m like ‘oh I hope I book it.’ In this case, that feeling of ‘oh, I hope I book it’ was there but there was this extra element and it was this excitement of [dramatic voice] ‘I’ve never heard of this before, this is amazing!’ And it combines so many different elements of what I was doing in voiceover in such a beautiful way that, that passion; so like on the technical side was really high. And then maybe a few years ago I started connecting with our audiences on social media and learning what they want and how they would love to have audio description and it became this extra phase where it’s like ‘oh okay I can do this, and finding out how to bring the story to life in a way that the audiences want. And that’s been the most rewarding part. And now it sounds like being part of the overall conversation, there were over 4,100 audio description tracks available as of early May 2020, that’s… 

Abby:

[gasp}

Roy:

so exciting! And it keeps on growing that these streaming services are opting into it outside of the FCC mandates, so they recognize the value.

Abby:

You’re talking about people that are blind or vision impaired, are they involved in any of the work you do?

Roy:

Yeah, especially now that, oh gosh, there’s so many different directions to go here. Our blind and low vision audiences have definitely been speaking up about what they want that the conversation has changed from ‘does it have it or not?’ which is such an important conversation, being able to make sure that audio description is as ubiquitous and everywhere as closed captioning, that is a huge element. The other thing that’s happening is the quality, the excellence of audio description that a lot of companies that provide audio description are going above and beyond to provide the best they can. And with that, it’s making sure that blind and low vision audiences and advisors and guides are involved in at least some part of the creation. There’s a company that is owned by a blind owner and he’s been very clear about making sure that he hires disabled actors to do the narration; blind, low vision or otherwise, and that kind of inclusion is starting to happen. The other companies are also making sure that their scripts have advisors so that, it’s a different experience it’s not a sighted person putting on a blindfold for an hour and a half and saying ‘oh that’s good.’ There’s something else that comes into it and this is something I think is really important is that for our audiences. You know, “nothing about us without us” is more than just checking a box or a token “gift” it’s an actual necessity to bring the quality of this work to the standard that our audiences deserve.

Abby:

What do you learn from the blind community?

Roy:

Great question and I’m going to do a little segue but to answer your question about teaching narration for audio description

Abby:

Oh yes

Roy:

So when I taught classes it’s mostly voiceover talents who are really excited to learn about it and learn the nuance and what sort of things to technically bring their performance to life for an audience. And that’s the perfect time to bring in a blind or low vision advisor. So they join us usually on like some sort of audio call where they’re listening in to the samples that the talents are giving and it’s such a beautiful two-way street. Beautiful in the sense that the voice talents are getting instant feedback about ‘oh you know that was a little too much, you were too into it’ or ‘that was a little too flat’ or ‘that really didn’t match the scene’ or ‘I was taken out of the…’ so that kind of feedback; the advisor is the director in that sense. So my role outside of giving some very general basics in the technical side is to facilitate the teaching of the talent, the voiceover talent being taught by our guide by our advisor. And it’s, the feedback that I’m getting from all sides has been this is what we want and it checks so many boxes for everyone.  

Abby:

I’ll tell you, my creator, Steph, you know like she’s so awesome right. What I love about her is like not only has she totally brought me to life which is super fun and we get to be this you know, expressive showing so much but she’s vision impaired which everyone knows and she’s so many things and she’s so open. She’s an African American woman, she’s over 55 and she encompasses all this creativity and she built Bold Blind Beauty and she’s bringing women of every type and men cause you know this year we’re doing Men In Motion. And the reason I bring this up is how do you see diversity in more than one way than just blindness in this field?

Roy:

Sure, so I’m a sighted white narrator; that’s what I bring to the table and with that I’m learning alot more about diversity. There is a great event that happened I think in 2019 at the television academy where it was a panel on performers with disabilities and it was also the casting people making decisions to bring in people with disabilities, not exclusively for storylines about disability but about this is a person with a disability who’s playing a character who happens to have a disability. The story wasn’t about the disability it was framed in this panel one of the best panels on disability that I’ve seen so that is one aspect of diversity. I think another aspect of disability that we can even talk about in the world of audio description is that there are other narrators who are people of color, women of color, and all sorts of things. I think that in that world of representation if you’re a blind or low vision audience member you’re going to be listening to this voice for all the things that are happening and that makes a difference. Being able to hear representation of yourself in that voice of the narrator is super important. I can’t speak to much detail about that but I’m a big proponent of more diversity in this world because it is representation and it’s a representation that is happening. I don’t know specifically the percentage, it’d be fascinating to find that out but what I do know is that the more diversity the better and that nobody loses out on that. One of the things that I’m learning is it’s these little steps that do make a difference it’s not like this big 180-degree turn. It’s like even this conversation right now I’ve changed a little bit it’s like ‘oh yeah, okay that’s another way we can approach this’ or little tiny steps and as more people choose to make those steps it becomes like a really big wave in a way that helps everybody out. It not just helps, it makes it more diverse in such a beautiful way.

Abby:

If people want to get in touch with you to learn more about what you’re doing, how can they do that? 

Roy:

There’s a few ways; I’m on social media so Twitter is @RoySamuelson. I’m also on Instagram @RoySamuelson and I do Alt text on both of those. On Facebook, I’m pretty active in the Audio Description Discussion Group which is a really lively and engaging kind of positive group of pretty close to 500 people that are both narrators, writers, and consumers, audience members. It’s a really great place to learn more about audio description and see the discussion and how it’s growing. There’s a lot of great things happening there and of course, there’s other places that I like to refer people to The Audio Description Narrators of America which is theadna.org, it’s like an IMBD list of audio description narrators based on contributions from our audiences when they hear someone. Those are the main places I like to refer people to.

Abby:

I’m Abby with Bold Blind Beauty, it’s been awesome hanging out with you guys and Roy. And keep in touch and we’re going to keep you guys rocking with some more fun stuff and we’ll post the links that Roy also references so you can keep in touch if you have questions. Have a great one. Hey, make sure you have your stilettos on and your canes tapping.     

Roy Samuelson Bio:

Roy Samuelson can be heard on the current season of Westworld as Dolores’ virtual assistant. In the world of Audio Description, he narrates Hulu’s The Great, CBS All-Access’ Star Trek: Picard, Sony’s Bloodshot, Universal’s 1917, and Spider-Man: Far From Home, among 600+ other blockbusters and series titles. He loves connecting TV, film, and streaming decision-makers with audiences who are blind or low vision.    

Image Description:

Roy looks into the camera wearing a blue shirt.