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National Disability Radio

National Disability Radio

著者: National Disability Rights Network
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An insightful podcast by the National Disability Rights Network offering advocacy tools, heartfelt storytelling, and real-world policy insights—accessible whether you’re an advocate in the field or just someone who cares deeply about disability rights.© 2020 National Disability Rights Network マネジメント マネジメント・リーダーシップ 心理学 心理学・心の健康 社会科学 経済学 衛生・健康的な生活
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  • Changing Laws Can Change Lives
    2026/08/25
    This episode of National Disability Radio highlights a recent disability rights victory in Colorado, where advocates successfully worked to repeal a law that permitted the forced sterilization of people with disabilities. One of our very own P&As, Disability Justice in Colorado, was instrumental in making this happen! Hear from policy leaders and self-advocates behind the effort as they discuss coalition-building, and why disability rights progress depends on keeping people with disabilities at the center of the conversation. **NOTE** Disability Law Colorado has recently rebranded to Disability Justice! Check out their new messaging and branding on the web and across their socials: Disability Justice’s Website: https://disabilityjustice.co/ Disability Justice’s Social Media Channels Facebook: https://www.facebook.com/disabilityjusticeInstagram: https://www.instagram.com/disabilityjusticeco/YouTube: https://www.youtube.com/@disabilityjusticeCO The Arc of Colorado’s Website: https://www.thearcofco.org/ The Arc of Colorado’s Social Media Channels: Facebook: https://www.facebook.com/TheArcofColoradoInstagram: https://www.instagram.com/arcofcolorado/LinkedIn: https://www.linkedin.com/company/the-arc-of-colorado/X (Twitter): https://x.com/thearcofcoYouTube: https://www.youtube.com/@TheArcofColorado The Arc of the United States’ Website: https://thearc.org/ The Arc of the United States’ Social Media Channels Facebook: https://www.facebook.com/thearcus/Instagram: https://www.instagram.com/thearc_us/LinkedIn: https://www.linkedin.com/company/thearcus/YouTube: https://www.youtube.com/@thearc_us Transcript: Michelle Bishop: Okay. Sorry, sorry. I can get serious. We can do this. Wait, are we recording? Alden Blevins: Yes. Michelle Bishop: Oh, okay. Stephanie Flynt McEben: Well, there's our cold open. Here we go. Michelle Bishop: Hi everyone, and welcome back to National Disability Radio, the official podcast of the National Disability Rights Network, where we share with you stories and conversations that advance the rights, voices, and leadership of people with [00:00:30] disabilities. I'm Michelle Bishop, one of your co-hosts, and today we are really excited to be joined by some of our own, two folks we were able to connect with through our own network of organizations across the US. We're going to be talking with Disability Law Colorado about some of the recent amazing advocacy work that they've been doing. But before we do that, I'm going to kick it to my co-hosts. Stephanie Flynt McEben: That's right. Hey, everybody. Stephanie Flynt McEben, public policy analyst with the National Disability Rights Network and two-thirds of [00:01:00] your podcast hosting team. But yeah, wanted to kick it off to our wonderful guests. Jack Johnson: Sure. Yeah, thank you for having me. So I'm Jack Johnson. I work at Disability Law Colorado as our public policy liaison, the one and only, so I'm a team of one here in Colorado, but am joined by a lot of great advocates in our network through our community partners, as well as all of the people that work at Disability Law Colorado who bring their lived experience to our policy [00:01:30] work and their expertise in their specific areas that they work in every day. And here in Colorado, we have a very busy legislative session and a very active legislature, which means we get to do a lot of fun work. And I get to work with Molly all the time, which I'm really grateful for, and I can pass it over to her. Molly Kirkham: Perfect. Well, yeah, thank you all. I'm Molly. I work for the Arc of Colorado as a legislative policy advocate, which basically means I get to talk to senators, [00:02:00] representatives, about bills and issues that matter to individual with disabilities. And aside from that, I'm also past president of SFO and vice president of Speaking for Ourself Colorado and People First. Speaking for Ourselves is a statewide group and People First is local. And I've always been connected to disabilities. Stephanie Flynt McEben: Awesome. Thank you so much, Molly. I'm going to pass on to Alden. Alden Blevins: [00:02:30] Yeah, I was just going to say I'm so glad that you're both here today. I think this type of legislative advocacy work is so important. I used to work at a P&A myself in Virginia, and back when I was doing their communications and kind of stressing the importance of the work, I kept coming back to the key phrase that changing laws can change lives. And I think that work like you guys have done on this bill that we're going to talk about today is something that could maybe be a blueprint for other P&As across the United States as they struggle with similar things [00:03:00] in their legislatures. So thank you so much for being here with us today. Michelle Bishop: Yes, we're excited to talk about this, especially anytime we get a chance to highlight some of the incredible work that's being done in our own network. That's our favorite thing to do. So first...
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    37 分
  • Public Policy Pod: Putting the FUN in funding
    2026/07/28
    Video Version: What does it actually mean when disability advocacy is “level funded”? What are federal appropriations, and why are they such a big deal for disability rights? On this episode of National Disability Radio, Alden Blevins (Communications Manager), Stephanie Flynt McEben (Public Policy Analyst), and Eric Buehlmann (Deputy Director for Public Policy) pull back the curtain on the federal funding process and what it means for the Protection and Advocacy (P&A) network. They discuss the successful FY26 funding fight, why advocacy on Capitol Hill matters, and how everyday people can help. You also get the added bonus of hill-day survival tips, advocacy myths and truths, and a very important debate about coffee and tea. Transcript: Alden Blevins: Hello, and welcome to National Disability Radio. I am here today with two wonderful people who are about to introduce themselves. I am Alden Blevins, Communications Manager here at NDRN. I have my own lived experience with disability and I’m really glad to be here today. What about you guys? Who are you, What do you do? Stephanie Flynt…: Yeah, I’m Stephanie Flynt McEben. I am also one of your hosts of the podcast and NDRN’s Public Policy Analyst. And I have beef with a music streaming app, and I’m not going to talk about which one, but let’s just say that this [00:00:30] music streaming app told me that I was 67 for Christmas this year. And then it had the audacity to… Oh gosh, what was the playlist the other morning that was recommended? It was Old Camping Man Sunday Morning, and it was really weird. Why? I don’t listen to old camping man music unless James Taylor and Chappell Roan and Taylor Swift count as that. But anyway, hope everybody else is having a good day. And hey, if Spotify thinks [00:01:00] you’re old, you’re just… I don’t know. You’re young at heart, anyway. Alden Blevins: I think it clocked my age exactly. And I must say that I listened to a lot of Lady Gaga and Kesha in the last year. Stephanie Flynt…: Yes. Alden Blevins: And to be fair- Stephanie Flynt…: You were in the 2010’s era. Alden Blevins: They were still the two most popular artists when I was graduating from high school, so they clocked me. They clocked me for sure. Stephanie Flynt…: Oh my gosh. Time to introduce Eric, who is our Deputy Executive [00:01:30] Director for Public Policy. How are you doing? It’s great for you to be here. Eric Buehlmann: Great, it’s wonderful to be here. Evidently, your phone must be listening to my music then in that way [inaudible 00:01:44] Stephanie Flynt…: Maybe so. I don’t know what’s going on, but I don’t know how I feel about it. And also, I guess… I don’t know. I guess the Spotify age thing is eclectic because my top artist was Taylor Swift, so I don’t know. Anywho. Eric Buehlmann: So I’m Eric Buehlmann. I’m the Deputy Executive [00:02:00] Director for Public Policy. As Stephanie said, my first choice is not Taylor Swift, but my wife listens to it a lot. So when I’m in the car with her, that’s what I’m listening to. Alden Blevins: This is National Disability Radio. We are the official podcast of the National Disability Rights Network. The National Disability Rights Network works in Washington DC and around the country on behalf of the protection [00:02:30] and advocacy systems, the P&As and the client assistance programs or CAP. We are the nation’s largest provider of legal advocacy services for people with disabilities. The first thing we want to talk about is some big and good news. The P&A network was funded for the rest of FY26. Can we get a hallelujah? Stephanie Flynt…: Yay, woo-hoo! Alden Blevins: The first thing I was just going to ask is, Eric, can you explain to us why it’s a big deal that we were funded and level funded, [00:03:00] and kind of what it took for us to get to this point? Eric Buehlmann: In terms of being able to, why we were able to do this, it’s really our members reaching out to all the representatives, all the senators, making the case, all the good work that the P&As and the CAPs do, and showing all the examples and saying, “Look, if you don’t fund us, this is what’s going to happen, is that person with a disability is not going to be able to get accessible housing or accessible transportation, or the student’s going to be able to go to school or someone’s going to have an assistive [00:03:30] technology device or rampant abuse and neglect are going to be occurring in either the community or institution.” So they made those cases. Congress said, “We agree with you.” And the best we could hope for at this time was at least maintaining our funding and not losing it. Alden Blevins: I think it’s really important to remember that this is not just numbers on a spreadsheet, this has real world impacts on peoples’ lives, the lives of people with disabilities, whether or not they can access enforcement of their civil rights, so [00...
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    42 分
  • “I Identify as Blind” disability pride, music and unmasking with Lachi
    2026/03/05
    On this episode of National Disability Radio, we sit down with award-winning recording artist, advocate, and author Lachi for a powerful conversation about disability pride, music, and unmasking. Lachi shares her journey, from navigating the music industry as a blind artist, to founding RAMPD, a coalition amplifying disability culture across the industry. We talk about what it means to say “I identify as blind,” move beyond the medical and social models of disability into a cultural model rooted in identity and joy, and remind listeners that no one can defeat someone who hasn’t given up. From glam canes to Grammy stages, this episode is about claiming space, rejecting internalized ableism, and turning perceived flaws into flexes. Transcript: Alden Blevins: It’s Lachi? I feel very- Lachi: Lachi like Versace. Alden Blevins: Lachi like… Oh, I love that. Michelle Bishop: That is the best way to explain it. Lachi: I mean, but you know what I’m saying? Come on. Alden Blevins: Well, we’re really excited about having you today because we’re all music lovers in this group here. Michelle Bishop: Yes. Alden Blevins: We talk about music all the time. Michelle Bishop: So much. Lachi: Good, good, good, good, good, good, good. I’m in the right place. Michelle Bishop: Hi everyone. Welcome back to National Disability Radio, the official podcast of the National Disability Rights Network. I am Michelle Bishop, 1/3 of your podcast hosting team. Stephanie Flynt McEben: And I’m Stephanie Flynt McEben, public policy analyst here at NDRN. Alden Blevins: I am Alden. I am a communication specialist at NDRN and I am so excited today, like I mentioned, we’re all lovers of music, so we got a guest that I’m really excited about. Lachi is an award-winning recording artist and a recording Academy Grammy’s national trustee. She’s also a disability advocate who’s been breaking barriers in the music industry and beyond. She’s the founder of RAMPD, which by the way, is such a fun play name. I really love that. And the author of the upcoming book, I Identify as Blind. So without further ado, Michelle, you’ve got some questions to kick us off, I think. Michelle Bishop: Yes. We’re so excited to have you with us. As Alden said, we are. We’re huge music lovers. I’m pretty sure we spend most of our meetings where we allegedly plan this podcast just talking about music. So you’re absolutely in the right place today, but to get us started, I mean, you’ve been open about the fact, and I’m just really interested in this as a disability rights podcast. You’ve been really open about the fact that it took you some time to really embrace your identity as a blind and disabled woman, especially in the industry that you’re in that often really rewards conformity. Can you tell us a little bit more about that journey for you, both as an artist and as someone navigating just the world with a disability? Lachi: Okay. Yeah, for sure. Hey, everybody. Lachi here, Lachi like Versace. I am a Black woman with cornrows, chilling here in New York in my studio. I also identify as blind, I identify as neurodivergent, and I identify as an Aries. So do with that what you will. Michelle Bishop: All the important points right there. Lachi: All the important points like name, age, sign. Thank you. Okay. Yeah, but I’m really glad to be here. And thank you for that question, and thank you for having me. So music has always been a very integral part of my life of growing up. Where other babies would kick in the womb, when she was pregnant with me, I was playing the piano in the womb. I don’t know how she got a piano in there, but she’s not a liar, so I’m going to take her word for it. When I was super-duper young, I didn’t really have a lot of friends, especially because of the fact that I had differences and this and that. And so I would take to music to, I guess, understand the world better and have the world understand me better. I just knew how to express myself through song and it just said the things I needed to say. It was the prayer I needed. And because of music, I started to find confidence in how to speak and how to behave and how to act. And as I got older, when I was growing up, disability was not necessarily a thing people talked about a lot in schools and teachers didn’t know what to do. My parents didn’t really know what to do. And so I would always just turn to music. It’s actually right now I’m working on a children’s album because I think that kids need to hear music that has to do with disability and neurodivergence, as well as their parents as they grow up. When I got into college, I started wanting to do music, but I studied business and finance because when I told my parents I wanted to do music, they were like, “That’s not how you spell doctor.” because they are Nigerian immigrants and everybody else in my family went to either med school and blah, blah, blah. And I was like, ...
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    42 分
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