Episodes

  • Indigenous artist born with one arm, one leg creates colorful world (Enable: The Disability Podcast)

    Indigenous artist born with one arm, one leg creates colorful world (Enable: The Disability Podcast)
    Jan 7 2026
    Frank Buffalo Hyde, an Indigenous artist who's been featured at the Smithsonian National Museum of the American Indian and other museums across the United States, was born with one arm and one leg due to a birth defect after his father was exposed to Agent Orange. In this episode of "Enable: The Disability Podcast," he speaks about the use of prosthetics and other resources, the ways he tried to avoid feeling different as a child, the healing power of humor and pop culture in his colorful artwork, and even Bigfoot, Sasquatch, UFOs and cryptozoology. "For me, I came into the art scene and became a professional artist at a time where I had to fit into a world that wasn't necessarily made for me so I didn't necessarily let my disability define me," Hyde says. "People would find out later when I sign my work and... [be] pretty shocked. And a lot of people would ask me, you know: 'Are you left-handed?' (laughs) I'm like, 'Yes.'" Frank Buffalo Hyde's website: https://frankbuffalohyde.com/ “Enable: The Disability Podcast,” which highlights amazing people with disabilities and different abilities, releases new episodes weekly on YouTube and all major podcast platforms. Follow facebook.com/enablepodcast or @enablepodcast on Instagram and TikTok for more. Note: Views expressed in this podcast do not necessarily reflect the views of Advance Local. Learn more about your ad choices. Visit megaphone.fm/adchoices
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    18 mins
  • Spina Bifida Warrior: Facing challenges head on (Enable: The Disability Podcast)

    Spina Bifida Warrior: Facing challenges head on (Enable: The Disability Podcast)
    Dec 18 2025
    Derrek Cooke, who was born with Spina Bifida, speaks with “Enable: The Disability Podcast” about what it means to be a "Spina Bifida Warrior" and facing challenges head on. He also spoke about who his heroes are, the resources and support he receives, and the near-death experience that taught him to enjoy life to the fullest. He created Derrek's Bags for other people with disabilities to carry catheters and similar medical equipment, featuring positive phrases like "Disability is not a bad word," and donates 34% of the proceeds to the Spina Bifida Association of New York State. Derrek's Bags: https://www.etsy.com/shop/DerreksBags Spina Bifida Association of New York State: https://sbanys.org/ National Spinia Bifida Association: https://www.spinabifidaassociation.org/ “Enable: The Disability Podcast,” which highlights amazing people with disabilities and different abilities, releases new episodes weekly on YouTube and all major podcast platforms. Follow facebook.com/enablepodcast or @enablepodcast on Instagram and TikTok for more. Note: Views expressed in this podcast do not necessarily reflect the views of Advance Local. Learn more about your ad choices. Visit megaphone.fm/adchoices
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    24 mins
  • The R-word and why you should never underestimate people's special abilities (Enable Podcast)

    The R-word and why you should never underestimate people's special abilities (Enable Podcast)
    Dec 10 2025
    Skip Clark, whose son Zach has Down syndrome, speaks with “Enable: The Disability Podcast” about the pain of hearing the R-word and why you should never underestimate a person's special abilities. He also speaks about Zach's love of baseball and music; resources and support; and the fun their family has together. "Don't underestimate them, don't call them names," said Clark, a radio DJ and host of the "Skip Happens" podcast. "They're doing the best they can and they're doing damn well at it... My son's one of the smartest people around." “Enable: The Disability Podcast,” which highlights amazing people with disabilities and different abilities, releases new episodes weekly on YouTube and all major podcast platforms. Follow facebook.com/enablepodcast or @enablepodcast on Instagram and TikTok for more. Note: Views expressed in this podcast do not necessarily reflect the views of Advance Local. Learn more about your ad choices. Visit megaphone.fm/adchoices
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    24 mins
  • "Scariest day of my life": An amputee's physical & mental journey (Enable: The Disability Podcast)

    "Scariest day of my life": An amputee's physical & mental journey (Enable: The Disability Podcast)
    Dec 3 2025
    Lindsay Hicks talks with “Enable: The Disability Podcast” about her experiences as an amputee, the high cost of prosthetics, and the mental and physical challenges that come with an amputated leg. She's also an athlete, a mom to a neurodivergent child, and a disability advocate helping raise money for other amputees to get prosthetic devices and support. "When I was 22, walking into that hospital, knowing I'm about to get my leg amputated, was the scariest day of my life," Lindsay says. "And so when I woke up, the first thing I did was flip that cover back and look to see if that leg was gone. And sure enough, it was gone... I felt like I was Lindsay one way before the amputation. And then I was a different Lindsay after the amputation. And it's like I was two different people." Lindsay is raising money for Liberty Health to help provide access to prosthetic and orthotic services for underserved populations https://gofund.me/f834ad908 You can also follow Lindsay for updates on her journey at / lindsay.hicks.7106 “Enable: The Disability Podcast,” which highlights amazing people with disabilities and different abilities, releases new episodes weekly on YouTube and all major podcast platforms. Follow facebook.com/enablepodcast or @enablepodcast on Instagram and TikTok for more. Note: Views expressed in this podcast do not necessarily reflect the views of Advance Local. Learn more about your ad choices. Visit megaphone.fm/adchoices
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    34 mins
  • Scott Kelly: Jonas Brothers, military disability benefits, more (Enable: The Disability Podcast)

    Scott Kelly: Jonas Brothers, military disability benefits, more (Enable: The Disability Podcast)
    Nov 26 2025
    Military veteran Scott Kelly, whose resume went viral on TikTok when it was seen at a Jonas Brothers concert, talks with “Enable: The Disability Podcast” about his experience in the U.S. Army and Special Forces, his medical retirement, and military disability benefits. He also talks about his podcast, "At the Water's Edge"; the challenges for veterans transitioning to civilian life; and the fun facts he revealed on Jimmy Fallon: He didn't know who the Jonas Brothers were and he wasn't even applying for a job at the time. Kelly also explained the difference between medical separation and medical retirement, sharing the help he received from the Care Coalition (https://www.socom.mil/care-coalition/). “Enable: The Disability Podcast,” which highlights amazing people with disabilities and different abilities, releases new episodes weekly on YouTube and all major podcast platforms. Follow facebook.com/enablepodcast or @enablepodcast on Instagram and TikTok for more. Note: Views expressed in this podcast do not necessarily reflect the views of Advance Local. Learn more about your ad choices. Visit megaphone.fm/adchoices
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    19 mins
  • Disability benefits: Who's eligible for SSDI, SSI? - Michael Liner (Enable: The Disability Podcast)

    Disability benefits: Who's eligible for SSDI, SSI? - Michael Liner (Enable: The Disability Podcast)
    Nov 20 2025
    Disability lawyer Michael Liner, head attorney and founder of Liner Legal, talks with "Enable: The Disability Podcast" about disability benefits, including SSDI (Social Security Disability Insurance) and SSI (Supplemental Security Income); who's eligible; how to apply; and important details about restrictions (such as SGA, Substantial Gainful Activity) and timelines. Liner also shares his experiences with epilepsy and motor tic syndrome, and why he's not a fan of the word "disability." "I hate the word disability because I think it's such a misnomer. Disability means you lack ability. I don't lack ability. I'm better than most people at a lot of things," he explained. "I think that what we should be talking about are diff abilities, having different abilities. With my background, if you ask me to sit and concentrate and focus on something for two hours, no chance, not gonna happen... [but] I don't have disabilities. I have different abilities." "You just need to find what you're great at and lean into it. And that's my story." For more info, visit ssa.gov/disability or connect with Liner at linerlegal.com and on TikTok @backwardshatbarrister. “Enable: The Disability Podcast,” which highlights amazing people with disabilities and different abilities, releases new episodes weekly on YouTube and all major podcast platforms. Follow facebook.com/enablepodcast or @enablepodcast on Instagram and TikTok for more. Note: Views expressed in this podcast do not necessarily reflect the views of Advance Local. Learn more about your ad choices. Visit megaphone.fm/adchoices
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    26 mins
  • 'It's not easy': Mrs. New York is Army officer and Spina Bifida mom (Enable: The Disability Podcast)

    'It's not easy': Mrs. New York is Army officer and Spina Bifida mom (Enable: The Disability Podcast)
    Nov 12 2025
    Mrs. New York 2025 winner Colonel Christina Fanitzi talks with "Enable: The Disability Podcast" about her experience in the U.S. Army, her Top 6 finish in the Mrs. America Pageant, and her platform of Spina Bifida awareness, research and resources. She was inspired by her son, Christian, who was born with Spina Bifida Myelomeningocele and Hydrocephalus – conditions that affect mobility, continence, and development. She was also named New York State's Mother of the Year in 2025, but doesn't take any of it lightly. "I think people would look at me and be like, 'Oh she's an Army officer, New York State Mother of the Year,' all this stuff. But I struggle. It's not easy. It's not effortless," she said. "It takes a lot of work." "Nothing worth it is easy," she added. "I got to give myself a lot of grace, and you got to give yourself grace... You're doing the best you could possibly do and your kid knows it." “Enable: The Disability Podcast,” which highlights amazing people with disabilities and different abilities, releases new episodes weekly on YouTube and all major podcast platforms. Follow facebook.com/enablepodcast or @enablepodcast on Instagram and TikTok for more. Note: Views expressed in this podcast do not necessarily reflect the views of Advance Local. Learn more about your ad choices. Visit megaphone.fm/adchoices
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    27 mins
  • 'How I Met Your Mother,' a rare genetic disorder, and "the cliff" (Enable: The Disability Podcast)

    'How I Met Your Mother,' a rare genetic disorder, and "the cliff" (Enable: The Disability Podcast)
    Nov 6 2025
    "How I Met Your Mother" co-creator Craig Thomas talks with "Enable: The Disability Podcast" about his son, who was born with a rare genetic disorder known as Jacobsen Syndrome. Thomas, who was working on the Emmy-winning TV show at the time, said it felt like writing for a comedy while living a drama. Those experiences helped inspire an unmade movie musical and a new book, "That's Not How It Happened," about Down syndrome and "the cliff" that families face as special needs children enter adulthood. Thomas also sheds light on the "Band vs. DJ" debate from "HIMYM," the music he had at his own wedding, and his advice for anyone who's ever felt alone and afraid to share the challenges they're facing. "That's Not How It Happened" is available now on Amazon and other major booksellers: https://www.amazon.com/Thats-Not-How-Happened-Novel/dp/0778360296/ref=sr_1_1?tag=advancesyracu-social-20 “Enable: The Disability Podcast,” which highlights amazing people with disabilities and different abilities, releases new episodes weekly on YouTube and all major podcast platforms. Follow facebook.com/enablepodcast or @enablepodcast on Instagram and TikTok for more. Note: Views expressed in this podcast due not necessarily reflect the views of Advance Local. Learn more about your ad choices. Visit megaphone.fm/adchoices
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    40 mins