Portraits of Persons with Disabilities: Katie Curnow

“How do we get people to see, to see disability in themselves, that shame and stigma, and like to be eased of that? That takes society to change, so like the chicken or the egg? Do we help people disabilities you know, embracing and taking pride in themselves and their lived experience, is it getting society to change the way they think about it? So we're not born with these ideas of ourselves?”

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Portraits of Persons with Disabilities: Gina DeShong

I hope I die warmed by the life that I tried to live.
— Nikki Giovanni, The Collected Poetry, 1968-1998
A 59 year old, African American woman stands for a portrait. She has a cane in her right hand, which is barely visible. She is wearing a red blouse with a black and white floral pattern. She has short curly hair and has a large smile across her face.

Gina DeShong, Flint, Michigan 2023

This interview was held at The Disability Network in Flint, Michigan where Gina, 59 (she/her), is the Program Director. She is a stroke survivor, avid reader and hometown girl.

For more Portraits of Persons with Disabilities interviews, click here.

Laura: Would you mind sharing a bit about your disability?

Gina: Not at all. A little over a year ago, I had a stroke. So now, I sometimes use a cane, but I’m getting better. I also have high blood pressure, diabetes, and asthma, which can be pretty debilitating at times.

Laura: Have you had asthma your whole life?

Gina: No, I developed it in my 20s from smoke inhalation.

Laura: Was it from being around smokers, or was there something else?

Gina: I was working in a restaurant, and the kitchen ventilation broke. We didn’t realize it right away, and I just started making a weird noise. I didn’t know why until my mom said, "I think you’re having an asthma attack." So we went to the hospital, and sure enough. It’s been years now, and I manage it pretty well. But I cannot be around smoke or even popcorn—popcorn is my biggest trigger. If I go to the movies, my friends have to check the air quality first.

Laura: Wow, that sounds so frustrating. When you do have an asthma attack, do you need to go to the hospital, or do you manage it at home?

Gina: I have a nebulizer and rescue inhalers. These days, I rarely need medical help because I know how to handle it.

Laura: That’s good. So, what do you like to do for fun?

Gina: My favorite things are reading and traveling. Most of my siblings live in Columbus, Ohio, so I love visiting and spending time with them.

Laura: Has using a cane affected your ability to travel?

Gina: Not really. In fact, I think people are kinder when they see the cane. I get a lot of "Do you want to sit here?" and "Are you okay?" I’m very independent, but I do think people are more considerate.

Laura: I’ve noticed that when I use a mobility aid, too. People suddenly see you more.

Gina: Exactly. They want to help, they want to make sure you’re okay.

Laura: Do you have a favorite travel destination?

Gina: Jamaica. I’d love to go back.

Laura: I hear it’s beautiful.

Gina: It is. The people, the island—it was all just wonderful.

Laura: How long were you there?

Gina: A week.

Laura: What motivates or inspires you?

Gina: I think it comes from the way I was raised. My parents and grandparents always said, "Just keep trying, keep pushing. Whatever you do, do it with excellence." And being a Black woman, plus always being a big girl, my mom used to say, "You have to do better because people will judge you differently." That stuck with me. I also wake up every day and pray, "Let me be a blessing to someone today." That’s what keeps me going—knowing that people depend on me. I have the biggest team here, and I can’t fall apart because they need me.

Laura: You have quite the leadership role here. It sounds like your upbringing prepared you for it. Are you from Michigan originally?

Gina: Yep, born and raised. I live in the house I grew up in, just outside of Flint in Mount Morris. But I’m from Flint, went to Beecher High School. Have you heard of it?

Laura: I’m from Chicago, so I know Beecher, Illinois, but not Beecher High.

Gina: It’s a close-knit community. I was at a meeting this week, and when someone heard I was from Beecher, she said, "Bucks for life!" That’s what we always say.

Laura: That’s awesome. I really liked the people I grew up with, but everyone went their separate ways after high school. Do a lot of the people you grew up with still live in the area?

Gina: Yeah, a lot of us came back.

Laura: That says a lot about the place. How did you end up working at the Disability Network?

Gina: I used to work at Michigan Rehabilitation Services as a job developer, teaching job skills classes. Luke, my boss now, used to come to meetings there. One day, he sat in on one of my classes, and afterward, he came up to me and said, "I need you to come work for me." And that’s how I got here.

Laura: Do you miss teaching classes?

Gina: No.

Laura: Haha, fair. Do you feel like leadership is where you thrive?

Gina: Yeah. I’m a take-charge kind of person. I don’t know if that’s good or bad, but it’s who I am.

Laura: I think people need that. So, you mentioned you love reading. What do you like to read?

Gina: Urban fantasy is my favorite genre. I also love mysteries.

Laura: Me too—I love a good page-turner.

Gina: And I love book series. I like getting to know the characters and staying involved in their world.

Laura: Any recommendations?

Gina: The October Daye series by Seanan McGuire. It’s urban fantasy and one of my favorites.

Laura: I’ll have to check it out. I’m in a book club, and we’re always looking for new reads. Do you take turns picking books in yours?

Gina: Yeah. There are about 10 of us.

Laura: Mine is four people, and usually only two of us have read the book. It’s more of a social thing for some. 

Gina: We do ours on Zoom most of the time since some members live in Detroit and out of state. But I love when we meet at the library.

Laura: Have you ever organized your books by color?

Gina: No, but I love how that looks. I don’t like giving books away! My uncle always says, "Why don’t you stack them up and put a mattress on top?"

Laura: Haha, they’re treasures!

Gina: Exactly. I used to manage a bookstore, and it was the best job.

Laura: Would you ever go back to that?

Gina: If it paid enough, yeah. But, you know, retail. I worked in women’s fashion for over 20 years too. I just stopped four years ago. I always had two jobs.

Laura: Wow. So, you like to stay busy?

Gina: Yeah. I’m single, no kids, so work gives me focus. But I am a dog mom.

Laura: What kind of dog?

Gina: A dachshund-shih tzu mix. My other dachshund passed away about a month and a half ago—she was 15. I have a picture of her in my office.

Laura: I’m sorry.

Gina: She was beautiful and so sweet. Her name was TeeTee. My new dog, Rocky, is the opposite—he barks all the time.

Laura: Final question—what change would you like to see for disabled people in the future?

Gina: I want people to see our abilities, not just our disabilities. Don’t see my cane—see me.

Laura: Seeing the whole person.

Gina: Exactly. And I want disabled people to see themselves that way too.

Laura: That’s a powerful message.

Gina: Nikki Giovanni said, "I hope that when I die, I am warmed by the life I tried to live." That’s my favorite quote.

Laura: That’s beautiful.

Portraits of Persons with Disabilities: Mia Diaz Garcia Wells

An interview with Mia Diaz Garcia Wells. They share their story about living with Generalized Anxiety Disorder, Social Anxiety and Major Depressive Disorder. Mia shares their experiences with identity and self-expression, and desires more intersectional inclusivity in disability movements. They talk about coming out as disabled and LGBTQIA.

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Portraits of Persons with Disabilities: Jessica Mae Dixon

When you have a visible disability, your disability introduces you before you ever get to introduce yourself. And that’s a shame, because I’m so much more than that.
— Jessica Mae Dixon
Portrait of a white skinned woman, with a short gray bob, smiling at the camera. She has brown eyes and is wearing a long sleeved, v-neck black shirt. She is holding two forearm crutches.

Jessica Mae Dixon, Flint, MI

Would you mind sharing about your disability?

Jessica: I always say I double, triple dip in the disability pool. I was born with cerebral palsy, and I also identify with a mood disorder. I have depression, anxiety, asthma, and high blood pressure, which I manage with medication. I think that’s it—not that I’m trying to acquire more! But I always remind people: at some point in your life, you’ll be part of the disability community, whether temporarily or permanently. Aging, in itself, is a disability.

Laura: Cerebral palsy (CP)— that’s something you’re born with?

Jessica: Yeah, it’s considered a developmental disability. It affects my motor skills and balance, specifically on my right side, both upper and lower extremities. Some people with CP have cognitive impairments, while others never walk or talk. Then there are cases where you’d barely notice it.

I met someone once who told me she had CP, and I thought, bullshit. It took me a while to notice, but it was there—very subtle. That’s what I love about disability. It’s such a broad spectrum. And I have to remind people, just because I have CP doesn’t mean I know everyone with CP.

Laura: And you don’t represent everyone with CP either.

Jessica: Exactly. I even went on a date with a guy who had CP once—it was horrible. He wasn’t comfortable with his disability, and then he fell during our date and got so mad. I get it—I get frustrated too—but I was like, Dude, you’re with me.


Using mobility aids

Jessica: I’ve always used assistive devices. These are Sheila [gestures to crutches]—Outdoor Sheila has an ice pick, and Indoor Sheila is for home. At home, I just use one because I think I’m a badass. It’s a small space, and everything is where I like it.

I’ve only used them for six years, and I hated them at first. Some days, I still do. But I have so much more energy when I use them. If I want to go to the park after work, I actually can. They prevent falls, but I’ve still fallen with them—they’re not a guarantee. I call them my accessories. I’m basically an action figure that comes with extras.

Laura: I love that! I found the hashtag Babes with Mobility Aids, and it made me so happy.

Jessica: Yes! I’ve used that tag before. But honestly, I don’t have many pictures of my whole body with my mobility aids. It’s not that I don’t like looking at myself, but I don’t see myself that way. Does that make sense?

Laura: It does. I have an altered gait and have used mobility aids, too. You see everyone else moving and assume you move like them.

Jessica: Exactly! I remember once, I caught my reflection in sliding doors and freaked out. I thought, No wonder people stare at me! 

And then people assume I’m in pain all the time. Sure, gaining weight or injuries can cause pain, but people think I’m suffering. No, dude—I’m just trying to get where I’m going, pay my bills, and grab a cheeseburger.

Laura: Have you always used mobility aids?

Jessica: Not always. I had a walker and a wheelchair when I was little, but by second grade, I was golden. I grew up on a farm, did everything my siblings did. Then, as I gained weight and got older, mobility got harder.

If you’d asked me three years ago, I would’ve said, I’m working on getting rid of them. Now, I think, If I don’t need them one day, great. If I do, oh well.


Growing up & aging with a disability

Jessica: It’s funny because I’m a licensed counselor. I work mostly with people who acquire disabilities. When they’re struggling with how their body has changed, I have way more grace now. I know what it’s like to have your disability evolve over time.

Laura: I was born with my disability too—Larsen’s Syndrome, a connective tissue disorder. I get what you mean. You grow up fine, but then as you age, things start to change, and suddenly it’s affecting you in a different way.

Jessica: It starts to create more barriers. And it might not even be like big barriers to people who don't know what it is to live inside your body, but to us, it's another obstacle.

It was definitely a rough road growing up and not having people similar to me, that looked like me, or thought like I did. I mean, I had a few friends in school, but they had significant disabilities, blindness, wheelchair user. And at that time, because I didn't use a lot of devices, I'm like, well, I don't really fit in that group either.

Laura: Do you know a lot of people with Cerebral Palsy (CP) now?

Jessica: I do, but here’s the thing: all the funding and research is for kids with CP. No one talks about aging with it. I just finished physical therapy for incontinence, and I learned so much. It’s not just my CP—it’s a combination of aging, being a woman, and CP. But no one talks about this stuff. Adults with disabilities kind of get lost in the fold.

Laura: Yeah, when you’re a kid, there’s a whole plan for you. Then you turn 18, and it’s like, Alright, good luck!

Jessica: Right? And they lie to you. College will be paid for, you’ll get all these resources! Nope. But that’s okay—I don’t want handouts. I want a hand up.

I remember when I was 10, I got an award from the town that I lived in for like, something I didn't even do. Just like existing. And at that time, I was so excited. I got ice cream, my picture taken with the mayor and like, it was so cool. And that was so fucking ableist. I did nothing. It's because I had a disability that people were like, let's give this little girl something.

Laura: And then as an adult, you realize—no one cares.

Jessica: And I don’t want them to. When someone at the grocery store tells me, "You’re doing such a great job," I just want to say, "Lady, move. I’m just here for tacos."

Laura: [Laughing] Constantly inspiring people, despite your best efforts.

Jessica: Someone told me yesterday, “You look like you're suffering.” And I was like, “You know what I'm suffering from? Inflation. [laughter] I could really use a raise.”


Outsider perceptions

Laura: Do you feel like more people tell you you're an inspiration now that you're using mobility aids?

Jessica: Honestly, I get more pity now than I did before. Before, I was just walking around like, I don't have time for this—I’m doing my thing. But now, with the mobility aids and just the way my body moves over time, I take a little longer. And people feel the need to step in, like, Let me help you. But I tell them, If I need help, I’ll ask.

There was someone at work who came up to me and said, “I’m just really worried for you.” I told them, “That’s a you thing. That’s not my problem.”

Because here’s the thing—when you have a visible disability, your disability introduces you before you ever get to introduce yourself. And that’s a shame, because I’m so much more than that. But I also recognize that people aren’t necessarily uncomfortable with disability itself—they’re uncomfortable with vulnerability. And I am literally walking around as the embodiment of vulnerability, which I think freaks them out.

Laura: Yeah, it’s like you’re out on display in a way.

Jessica: Exactly. But to me, I’m just living my life. I pay my bills. I do the things I enjoy. I wouldn’t know any different. 

People sometimes ask, “If there were a pill to ‘fix’ it, would you take it?” When I was 15, I probably would’ve said yes. Now? Pass it to the next person.

Laura: I hear you. I’ve had those conversations too, and I’m like, “No, I’m good. I don’t need to change anything.”

Jessica: It’s not that we’re fine—I mean, everyone’s kind of losing their shit. Some people are just better at hiding it than others.

Laura: That’s so true. And I feel like disability gives you a little more... I don’t know, stamina? Or at least a darker sense of humor?

Jessica: Oh, for sure. You have to, or society will eat you alive.

Laura: Otherwise you’d just cry every day.

Jessica: Which—I do that too. [laughs]


What do you do for fun?

Jessica: I spend a lot of time with my dog—he’s a pug. I like to read. And honestly? I just like spending time with people. I like eating. If someone asked me, What do you do for fun? my first answer would probably be, I eat. [Laughs]

But really, I love meeting people, connecting with them, and understanding them. I don’t even have to know them that well. I just enjoy watching how people navigate life.

But yeah, I don’t do anything too wild.I do some crafts here and there. I write poetry, but I don’t share it with anyone—it’s just something private that I do.

I love foreign films. And I love thrifting. COVID gave me a really bad thrifting habit. But I try to play by the rules—if I bring something in, I have to take something out. I can’t just keep collecting. Except when it comes to books. I have about 200 books in my apartment, and books don’t have a rule.


What motivates or inspires you?

Jessica: My curiosity.

Laura: Oh, that’s a good one. That probably explains why you love being around people, too.

Jessica: Yep. My thirst for knowledge and my curiosity—those are what drive me.

Laura: That’s such a gift to be born with.

Jessica: And I’m a Gemini, so it’s all wrapped up in there. [Laughs]


What change would you like to see for disabled people in the future? 

Jessica: That’s a really good question. I think I’d like people to recognize that we all have something. That there’s no real divide between "us" and "them."

People act like disability is this separate thing—like, Oh, you’re part of that community now. But why can’t we just recognize disability as part of the human condition? That’s what I’d like to see. More people realizing that the distance between me and them is way shorter than they think.

Laura: Yeah. Disability is a construct—that’s really all it is.

Jessica: Exactly. And it comes in many flavors. I’m just a really spicy flavor. [Laughs] And then you’ve got people who are just plain vanilla.

But seriously, people have this idea that disability has to be seen, or that it has to be tragic. Or that it has to be this big charity-driven thing. But in reality? Disability is the human experience.

Laura: So well said. Drop the mic right there. Because it is the human experience.

Picture Day with Detroit Disability Power

As a member of Detroit Disability Power, I am always looking for ways to use my photography skills to empower the disabled community. This month, we partnered to put up a community engagement event we called ‘Picture Day.‘ The goal was to engage with the Detroit community and provide people with headshots they could use for professional and networking purposes. We had a great turnout and created some beautiful portraits. Check them out below! And if you would like to get your headshot taken, contact me here.

More Headshots

In the last few weeks, I’ve taken headshots for two of my friends, Rebecca and Kit. Rebecca is an actress looking for a headshot more true to life than her current headshot. Kit is a massage therapist starting her own business who needed a headshot for her website. Both ladies are very talented and made great models. Take a look!

Corporate Headshots

In today's professional world, everyone needs a head shot. Whether it be for your LinkedIn profile or company website, a professional headshot conveys a commitment to quality. It shows potential clients and employers you value your work and take it seriously. We offer corporate headshot services for individuals and teams. Portraits start at $75. Contact me today for more info.

While you're here, check out this series we did for 2 Point Perspective below!