Living the Dream with Curveball
Oct 4, 2026 · 42 min · 11 segments
Send us Fan Mail Send us Fan Mail In this powerful episode of Living the Dream with Curveball, we dive deep into the themes of disability…
Jennifer Chassman BrowneGuestKeisha GreavesGuestCurtisHostAbsolutely.
So Keisha, what would you say to someone who may allow their disability or chronic illness define the person who they think they are?
Um, I would say, see, it's such a tough, um, question for me because I know in the beginning I was in denial.
It's like, although, like, the doctor told me that, we, the testing is confirmed, I'm just like, "No, I think, you know, next time I go to the appointment she's gonna say, 'Oh, we got your test results mixed up.'" So I get it.
So it's like, like, sometimes I'm not like, "Oh yeah, girl, you gotta get through it and..." et cetera, because we all deal with it in a different way.
Some people may get a diagnosis and start videotaping it and, you know, expressing themselves, and that's dope.
You know, I think that's awesome, but, you know, like, everybody's the same.
Like, when I wro- wrote my first blog about my diagnosis, it's like it took me as I was writing and saying it out loud like, "Oh, wow, I got muscular dystrophy.
That's crazy." So it was just interesting that it took me to write that blog that I first kinda shared everything, like, with friends on Facebook, and they was like, "Oh, wow, I, I never knew." But you know, it can be a lot, but I would say just all you can do is take each day at a time.
What I say even to this day is what inspired me is, you know Jillian Mercado, the fashion model? And she has muscular dystrophy like me, so one day I, like, just saw her on, like, the website.
I was like, "Oh my God, she has muscular dystrophy like me." Like, it just made me feel, like, awesome.
And so that was another person I, like, always remember from the beginning early stages.
Sure, and then I got a question for you.
'Cause I think, like, I talked about not, like, hiding my disability, and then when it couldn't be hidden anymore, I was a person who didn't really have a community of other people with disabilities.
Absolutely.
So Keisha, what would you say to someone who may allow their disability or chronic illness define the person who they think they are?
Um, I would say, see, it's such a tough, um, question for me because I know in the beginning I was in denial.
It's like, although, like, the doctor told me that, we, the testing is confirmed, I'm just like, "No, I think, you know, next time I go to the appointment she's gonna say, 'Oh, we got your test results mixed up.'" So I get it.
So it's like, like, sometimes I'm not like, "Oh yeah, girl, you gotta get through it and..." et cetera, because we all deal with it in a different way.
Some people may get a diagnosis and start videotaping it and, you know, expressing themselves, and that's dope.
You know, I think that's awesome, but, you know, like, everybody's the same.
Like, when I wro- wrote my first blog about my diagnosis, it's like it took me as I was writing and saying it out loud like, "Oh, wow, I got muscular dystrophy.
That's crazy." So it was just interesting that it took me to write that blog that I first kinda shared everything, like, with friends on Facebook, and they was like, "Oh, wow, I, I never knew." But you know, it can be a lot, but I would say just all you can do is take each day at a time.
What I say even to this day is what inspired me is, you know Jillian Mercado, the fashion model? And she has muscular dystrophy like me, so one day I, like, just saw her on, like, the website.
I was like, "Oh my God, she has muscular dystrophy like me." Like, it just made me feel, like, awesome.
And so that was another person I, like, always remember from the beginning early stages.
Sure, and then I got a question for you.
'Cause I think, like, I talked about not, like, hiding my disability, and then when it couldn't be hidden anymore, I was a person who didn't really have a community of other people with disabilities.
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