Podcasts about disability advocacy

Over 50 years ago, Robert Soto's life took a sharp turn after a devastating motorcycle racing crash. But what might have ended his momentum instead sparked a powerful legacy. In this episode of Walk and Roll Live – Disability Stories, Robert joins us to share his incredible journey—from walking with crutches to embracing life in a wheelchair, from a successful career to becoming a dedicated advocate with Triumph Foundation. His story is one of resilience, reinvention, and relentless spirit. Whether you're a fan of racing, a compelling story, or passionate about disability advocacy, Robert's voice offers insight, hope, and a touch of humor. Walk and Roll Live 

Andrea Pacheco is a beauty pageant titleholder who is breaking stereotypes and bringing disabilities to the forefront. Andrea was born with Okihiro Syndrome, and despite being underestimated her whole life, she become Miss Canada United World 2024. Brought to you By: The Sonar Network https://thesonarnetwork.com/

Episode 150 wraps up the "disabled people as NPCs" arc I've had going for the last few episodes.Support the showNew Website: badattitudespod.comBad Attitudes Shop: badattitudesshop.etsy.comBecome a Member: ko-fi.com/badattitudespod Follow @badattitudespod on Instagram, Facebook, Threads, and BlueSkyBe sure to leave a rating or review wherever you listen!FairyNerdy: https://linktr.ee/fairynerdy

About the Guest(s):Emily Ladau is an activist, writer, and speaker, known for her relentless advocacy for disability rights. With a decade of experience, Emily serves as the editor of Able News, a digital newspaper amplifying the voices and stories of New York's vibrant disability community. Her involvement in disability rights extends beyond writing, as she continually seeks to inspire and challenge societal perceptions through her speaking engagements and published works, including her book aimed at bridging understanding between disabled and non-disabled communities.Episode Summary:In this stimulating episode of Think Inclusive, host Tim Villegas engages with long-time friend and leading disability advocate Emily Ladau. As they delve into pressing issues confronting minority groups, Emily reflects on the systematic erosion of rights for the disability community, particularly those with multiple marginalized identities. She provides personal insights into navigating these challenges while expressing the uncertainties of future potentials for individuals' rights, especially under the current sociopolitical climate of 2025.The conversation moves to explore the intricacies of communicating effectively with diverse audiences, with an emphasis on thoughtfully engaging conservative politicians. Emily shares the balance of maintaining authenticity while strategically choosing words that resonate across party lines, addressing the need for cross-aisle dialogue in advancing disability rights. She also provides crucial advice for those striving to be allies, emphasizing the importance of mindful communication and adaptive advocacy efforts as tools for sustaining momentum in inclusivity goals. This episode is a rich tapestry of personal reflection and strategic insights, capturing the pulse of advocacy in challenging times.Complete show notes and transcript: https://mcie.org/think-inclusive/Key Takeaways:-The current sociopolitical environment is eroding disability rights, with advocates like Emily Ladau emphasizing the dire impacts on those with multiple marginalized identities.-Strategic vagueness in political rhetoric is creating an environment of fear and uncertainty, where advocacy requires deliberate and thoughtful communication.-Emily Ladau underscores the necessity of adjusting language to gain support from conservative audiences by aligning advocacy messages with core values.-Recognizing the limits of individual capacity, Emily advises allies to engage in advocacy through manageable actions without compromising personal well-being.-She stresses the significance of platforms like social media in advocating for disability rights, highlighting its dual role in fostering community and echo chambers.Resources:Emily's Website: https://emilyladau.com/Able News: https://ablenews.com/Thank you to our sponsor, IXL: https://ixl.com/inclusive Hosted on Acast. See acast.com/privacy for more information.

They said she'd never walk again. They were dead wrong.Holly's battle with Guillain-Barré Syndrome left her paralyzed and fighting for her life. Now she's fighting to tell her story—raw, unfiltered, and without permission. This isn't your typical medical recovery podcast. It's a brutal awakening to what happens when your body betrays you and the healthcare system fails you simultaneously.Each week, Holly exposes the harsh realities of GBS recovery that doctors don't warn you about, shares battle-tested strategies that actually work, and interviews survivors who refused to become statistics.Your body may have limitations, but your spirit shouldn't be one of them.Follow Holly's journey: Instagram: @hollyaftergbs Facebook: facebook.com/hollyaftergbs YouTube: youtube.com/hollyaftergbsWelcome to the No BS Wealth Podcast with Stoy Hall, your candid guide to financial clarity. In our third year, we're spicing things up by enhancing community ties and bringing you straight, no-fluff financial insights. Connect with us on NoBSWealthPodcast.com, and follow Stoy on social media for the latest episodes and expert discussions. Tune in, join the conversation, and transform your financial journey with us—no BS!As always we ask you to comment, DM, whatever it takes to have a conversation to help you take the next step in your journey, reach out on any platform!Twitter, FaceBook, Instagram, Tiktok, LinkedinDISCLOSURE: Awards and rankings by third parties are not indicative of future performance or client investment success. Past performance does not guarantee future results. All investment strategies carry profit/loss potential and cannot eliminate investment risks. Information discussed may not reflect current positions/recommendations. While believed accurate, Black Mammoth does not guarantee information accuracy. This broadcast is not a solicitation for securities transactions or personalized investment advice. Tax/estate planning information is general - consult professionals for specific situations. Full disclosures at www.blackmammoth.com.

When Heather Avis says she's one of “the lucky few,” she means it. In this episode, we talk about growing up with our children with Down syndrome, what it means to delight in our kids, and how all of us can participate in shifting the narrative around disability toward love and belonging. Our conversation highlights her new children's book, I Like You So Much, and focuses on:Proclaiming the worth of our childrenThe role of children's books in shifting disability narrativesUnderstanding identityExploring mutuality in relationshipsThe importance of spaces of belongingDelight and celebration in parentingMENTIONED IN THIS EPISODE:I Like You So Much by Heather AvisMore of Heather's booksThe Lucky Few podcastSmall Talk by Amy Julia BeckerHeather's SubstackReimagining the Good Life WorkshopSubscribe to Amy Julia's Substack newsletter_WATCH this conversation on YouTube by clicking here. READ the full transcript and access detailed show notes by clicking here or visiting amyjuliabecker.com/podcast._ABOUT:Heather Avis is a New York Times bestselling author, public speaker, podcaster, and a Down syndrome advocate. She is the founder of and chief visionary officer at The Lucky Few, an advocacy organization dedicated to shouting worth, shifting narratives, and reimagining what it looks like when we create spaces of belonging. She lives in Southern California with her husband Josh and three kids, Macyn, Truly, and August and two Goldendoodles, Maeby and George Michael.Website: https://www.heatheravis.com/Instagram: https://www.instagram.com/theluckyfewofficial/Facebook: https://www.facebook.com/TheLuckyFewOfficial/YouTube: https://www.youtube.com/channel/UC99_OFh29y9lVqZyHY2XztwPodcast: https://podcasts.apple.com/us/podcast/the-lucky-few/id1349646917New Book, I Like You So Much: https://www.amazon.com/Like-You-So-Much-Celebrating/dp/0310166594/Photo Credit: © Camilynne Photography___Let's stay in touch. Subscribe to my newsletter to receive weekly reflections that challenge assumptions about the good life, proclaim the inherent belovedness of every human being, and envision a world of belonging where everyone matters.We want to hear your thoughts. Send us a text!Connect with me: Instagram Facebook YouTube Website Thanks for listening!

Yes, it's another episode about Doctor Who. No, I am NOT sorry.Support the showNew Website: badattitudespod.comBad Attitudes Shop: badattitudesshop.etsy.comBecome a Member: ko-fi.com/badattitudespod Follow @badattitudespod on Instagram, Facebook, Threads, and BlueSkyBe sure to leave a rating or review wherever you listen!FairyNerdy: https://linktr.ee/fairynerdy

In this episode of the Real Estate Pros podcast, Barry Long shares his inspiring journey from a life-altering motorcycle accident to becoming a leading advocate for accessibility in real estate. He discusses the challenges faced by individuals with disabilities in finding accessible housing and how he has worked with multiple listing services (MLS) to create a system for identifying accessible features in homes. Barry emphasizes the importance of education and training for real estate agents to better serve clients with mobility needs. He also highlights the significance of attitude, support systems, and mentorship in overcoming life's challenges. Barry's future projects, including a TV show titled 'Barry's Accessible World,' aim to further raise awareness about accessibility issues.   Professional Real Estate Investors - How we can help you: Investor Fuel Mastermind:  Learn more about the Investor Fuel Mastermind, including 100% deal financing, massive discounts from vendors and sponsors you're already using, our world class community of over 150 members, and SO much more here: http://www.investorfuel.com/apply   Investor Machine Marketing Partnership:  Are you looking for consistent, high quality lead generation? Investor Machine is America's #1 lead generation service professional investors. Investor Machine provides true ‘white glove' support to help you build the perfect marketing plan, then we'll execute it for you…talking and working together on an ongoing basis to help you hit YOUR goals! Learn more here: http://www.investormachine.com   Coaching with Mike Hambright:  Interested in 1 on 1 coaching with Mike Hambright? Mike coaches entrepreneurs looking to level up, build coaching or service based businesses (Mike runs multiple 7 and 8 figure a year businesses), building a coaching program and more. Learn more here: https://investorfuel.com/coachingwithmike   Attend a Vacation/Mastermind Retreat with Mike Hambright: Interested in joining a “mini-mastermind” with Mike and his private clients on an upcoming “Retreat”, either at locations like Cabo San Lucas, Napa, Park City ski trip, Yellowstone, or even at Mike's East Texas “Big H Ranch”? Learn more here: http://www.investorfuel.com/retreat   Property Insurance: Join the largest and most investor friendly property insurance provider in 2 minutes. Free to join, and insure all your flips and rentals within minutes! There is NO easier insurance provider on the planet (turn insurance on or off in 1 minute without talking to anyone!), and there's no 15-30% agent mark up through this platform!  Register here: https://myinvestorinsurance.com/   New Real Estate Investors - How we can work together: Investor Fuel Club (Coaching and Deal Partner Community): Looking to kickstart your real estate investing career? Join our one of a kind Coaching Community, Investor Fuel Club, where you'll get trained by some of the best real estate investors in America, and partner with them on deals! You don't need $ for deals…we'll partner with you and hold your hand along the way! Learn More here: http://www.investorfuel.com/club   —--------------------

Disabled people don't exist for the majority of non-disabled society. They don't think about us, they don't care about us, and they only accept seeing us in certain limited circumstances. We're basically NPCs.Support the showNew Website: badattitudespod.comBad Attitudes Shop: badattitudesshop.etsy.comBecome a Member: ko-fi.com/badattitudespod Follow @badattitudespod on Instagram, Facebook, Threads, and BlueSkyBe sure to leave a rating or review wherever you listen!FairyNerdy: https://linktr.ee/fairynerdy

This episode is supported by Pneuma Solutions. Creators of accessible tools like Remote Incident Manager and Scribe. Get $20 off with code dt20 at https://pneumasolutions.com/ and enter to win a free subscription at doubletaponair.com/subscribe! Get an inside look at the Inclusive Africa Conference 2025 in Nairobi, Kenya. Discover powerful conversations on assistive technology, education, accessibility, and the future of disability inclusion across the continent.In this special episode of Double Tap, Steven Scott and Shaun Preece bring you exclusive interviews from the Inclusive Africa Conference in Nairobi. Julius Mbura, known online as Julio Supercharged, shares his role in youth advocacy and assistive tech innovation in Kenya, as well as the significance of the newly passed Disability Act of 2025.Namibian artist and activist Alvarita Benedito discusses stigmatization, lack of educational inclusion, and her creative journey from music to TikTok advocacy. Also, Lesotho's Refiloehape Sesinyi offers a deeply personal perspective on educational inequality, gender-based barriers, and youth empowerment, emphasizing the need for technology and policy to drive inclusion.Chapters00:00 - Introduction00:22 - Coverage of Inclusive Africa Conference05:43 - Interview with Julius Mbura from Kenya21:48 - Interview with Alvarita Benedito, Singer/Songwriter from Namibia35:35 - Sign up for the newsletter36:34 - Sponsor: Pneuma Solutions38:21 - Interview with Refiloehape Sesinyi, disability rights advocate from Lesotho56:11 - Final thoughts and more to comeRelevant LinksJulio Supercharged YouTube: https://www.youtube.com/c/JulioSuperchargeAlvara on TikTok & Instagram: https://www.instagram.com/alvara.musicDouble Tap Newsletter: https://doubletaponair.com/subscribe Find Double Tap online: YouTube, Double Tap Website---Follow on:YouTube: https://www.doubletaponair.com/youtubeX (formerly Twitter): https://www.doubletaponair.com/xInstagram: https://www.doubletaponair.com/instagramTikTok: https://www.doubletaponair.com/tiktokThreads: https://www.doubletaponair.com/threadsFacebook: https://www.doubletaponair.com/facebookLinkedIn: https://www.doubletaponair.com/linkedin Subscribe to the Podcast:Apple: https://www.doubletaponair.com/appleSpotify: https://www.doubletaponair.com/spotifyRSS: https://www.doubletaponair.com/podcastiHeadRadio: https://www.doubletaponair.com/iheart About Double TapHosted by the insightful duo, Steven Scott and Shaun Preece, Double Tap is a treasure trove of information for anyone who's blind or partially sighted and has a passion for tech. Steven and Shaun not only demystify tech, but they also regularly feature interviews and welcome guests from the community, fostering an interactive and engaging environment. Tune in every day of the week, and you'll discover how technology can seamlessly integrate into your life, enhancing daily tasks and experiences, even if your sight is limited. "Double Tap" is a registered trademark of Double Tap Productions Inc.

Today I'm joined by Ilaria Naef, Italy's first wheelchair motocross rider! She shares her experiences with WCMX as well as her opinion on accessibility around the world.Ilaria's Instagram: ilawheelieIlaria's Facebook: https://www.facebook.com/ilawheelieSupport the showNew Website: badattitudespod.comBad Attitudes Shop: badattitudesshop.etsy.comBecome a Member: ko-fi.com/badattitudespod Follow @badattitudespod on Instagram, Facebook, Threads, and BlueSkyBe sure to leave a rating or review wherever you listen!FairyNerdy: https://linktr.ee/fairynerdy

 Episode 7 is here! We're joined by Jackson Botsford, DAKC's accessibility specialist, to talk about the ADA, inclusive design, and what it really takes to make spaces accessible for everyone.

The entertainment industry needs to stop pretending that there are disabled actors available to fill disabled roles and start admitting that it just doesn't want to put in the effort to find them.Support the showNew Website: badattitudespod.comBad Attitudes Shop: badattitudesshop.etsy.comBecome a Member: ko-fi.com/badattitudespod Follow @badattitudespod on Instagram, Facebook, Threads, and BlueSkyBe sure to leave a rating or review wherever you listen!FairyNerdy: https://linktr.ee/fairynerdy

Imagine having your world turned completely upside down in your early twenties – from travelling and building a thriving career to suddenly facing life-threatening medical complications. In this robust conversation, I speak with the extraordinary Lisa Cox, whose journey from stroke survivor to internationally awarded disability advocate will challenge how you think about disability, resilience, and representation.Lisa shares the raw truth about navigating life after acquiring multiple disabilities at age 24, including partial blindness, amputations, and a permanent brain injury. Yet her story isn't one of defeat – it's a testament to redefining purpose and challenging societal perceptions. With humour, wisdom and unflinching honesty, Lisa reveals how her disability became her unexpected superpower and why representation matters for the 20% of our population living with disabilities.Key TakeawaysDisability is everybody's issueWith approximately 20% of the population having disabilities and the UN stating we'll all experience disability at some point in our lives, making things more inclusive benefits everyone, not just those currently living with disabilities.Identity beyond disabilityLisa powerfully shares how her most significant challenges weren't about appearance, but about the loss of ability. She emphasises that people with disabilities have diverse interests and shouldn't be reduced to their medical conditions – "We're not a monolith."Representation drives social changeFrom marketing campaigns to political leadership, disability visibility in media and public life directly impacts education, healthcare, and employment opportunities. Small wins like wheelchair Barbie might seem insignificant, but they create ripple effects for systemic change.Allyship starts with small actionsYou don't need to rewrite government policy to make a difference. Sharing social posts, helping someone get workplace accommodations, or simply treating disability as normal can create meaningful change. The disability community needs allies outside their "bubble."Moving ForwardLisa's journey reminds us that while challenging societal perceptions takes time, each small step matters. Whether you're navigating your own health transitions, supporting someone with a disability, or simply wanting to be a better ally, remember that authentic representation and inclusion create a world that benefits everyone.As Lisa wisely notes about preparation for aging: "I go to the gym a few times a week because I know that my 80-year-old version of me is going to have extra mobility challenges. So I'm planning for that now." What a powerful reminder that midlife is the perfect time to lay the groundwork for our future selves.Visit www.lisacox.co for her social links and to read more.Lisa is a proud advocate for the charity Youngcare: www.youngcare.com.au Instagram: https://www.instagram.com/lisacox.co/LinkedIn - https://www.linkedin.com/in/lisacox-authorspeakerconsultant/Remember to subscribe to the Redefining Midlife podcast and leave a review if you enjoyed this episode! Your support helps more midlife women find these empowering conversations.Connect with meJoin Better Than Before: joclarkcoaching.com/better Share your journey with me by sending me a message on Instagram at https://www.instagram.com/joclarkcoaching/ LinkedIn https://www.linkedin.com/in/joclarkcoaching/⁠Email me your success story at jo@joclarkcoaching.com. What you do today shapes your tomorrow. Your health matters because YOU matter.Here's to redefining midlife and making our next half of life even better than the first.

✈️ This week's episode features Gerald R. Ford International Airport and their new sensory room — a calming, thoughtfully designed space for travelers with sensory sensitivities. We talk about why spaces like this matter, how they came to be, and what true accessibility looks like in busy public environments. Because inclusion should be built into every journey.

Creating Inclusive Spaces: Disability Advocacy, Outdoor Access, and Inclusion in Your Community.Welcome back to the Outdoor Adventure Series. In today's episode, we sit down with Jenna Udenberg, an inspiring disability advocate, accessibility educator, and author of the book Within My Spokes. Growing up in the rugged beauty of northern Minnesota, Jenna's journey has been shaped by her early diagnosis of juvenile rheumatoid arthritis and a lifetime of navigating—and working to improve—accessibility in her community.Jenna shares how her love of the outdoors, music, and resilient spirit led her from being a band director to founding her nonprofit, Above and Beyond with You. She opens up about the challenges and triumphs she faced as a wheelchair user in a rural setting, the evolution of accessibility in her hometown of Two Harbors, and her drive to ensure everyone can enjoy nature's wonders.DISCUSSION00:00 "Introductions"03:22 Overcoming Trauma Through Music09:25 "Supportive Band Teachers' Impact"10:02 Adaptation Challenges in Education14:12 Improving Accessibility Conversations17:28 Adaptive Outdoor Exploration22:15 Community Connection Through Stories24:13 "True Accessibility Needs Better Communication"27:55 Embracing the Book Writing Journey33:04 Enhancing Accessibility in Storytelling37:21 "Embrace Curiosity and Overcome Labels"LEARN MORETo learn more about Jenna and her work, visit her website at https://www.aboveandbeyondwithu.org/ and follow her on these social sites: Facebook: https://www.facebook.com/profile.php?id=100091881005060Instagram: https://www.instagram.com/aboveandbeyondwithu/LinkedIn: https://www.linkedin.com/company/above-beyond-with-u/Click here to pick up a copy of Jenna's book, " Within My Spokes: A Tapestry of Pain, Growth & Freedom.NEXT STEPSIf you enjoy podcasts devoted to outdoor adventure, find us online at https://outdooradventureseries.com. We welcome likes, comments, and shares.KEYWORDSJenna Udenberg, Accessibility, Disability, Diversity & Inclusion, Author, Two Harbors, Howard Fox, Outdoor Adventure Series, Podcast, PodMatch#JennaUdenberg #OutdoorAccessibility #Disability #DiversityAndInclusion #Author #TwoHarborsMN #OutdoorAdventureSeries #Podcast #PodMatchMy Favorite Podcast Tools: Production by Descript Hosting Buzzsprout Show Notes by Castmagic Website powered by Podpage Be a Podcast Guest by PodMatch

Disability cannot truly be (nor does it need to be) overcome. What disabled people really overcome is EVERYTHING ELSE.Support the showNew Website: badattitudespod.comBad Attitudes Shop: badattitudesshop.etsy.comBecome a Member: ko-fi.com/badattitudespod Follow @badattitudespod on Instagram, Facebook, Threads, and BlueSkyBe sure to leave a rating or review wherever you listen!FairyNerdy: https://linktr.ee/fairynerdy

In this episode of 'This is Beacon's #jointheconversationseries, hosts Reuben, Brandon delve into an insightful discussion with actress, writer, and director Rachel Handler. As a disability advocate and a recent participant in the Easterseals Disability Film Challenge, Rachel shares her inspiring journey in the film industry, her relocation from Jersey City to the Hudson Valley, and the profound impact of authentic disability representation in media. The conversation covers the challenges and triumphs of her career, the significance of the Disability Film Challenge, and the crucial need for inclusiveness in Hollywood. Rachel also highlights her personal experiences and creative endeavors, providing a compelling narrative of resilience, adaptability, and artistic passion. 00:00 Introduction and Welcome00:33 Meet Rachel: Actress, Writer, and Advocate01:03 Life in Beacon and Personal Background09:19 Challenges and Triumphs in the Film Industry13:01 The Disability Film Challenge Experience18:53 Community Support and Filmmaking in Hudson Valley28:51 Backlash and Representation in Media29:48 Authentic Casting and Inclusivity31:25 Challenges and Stereotypes in Hollywood33:04 Intersectionality and Disability34:08 The Disability Film Challenge37:10 Promoting the Film Challenge39:21 Impact and Opportunities from the Challenge43:24 Personal Experiences and Microaggressions45:33 Behind the Scenes of Filmmaking49:05 Final Thoughts and Future Plans

More great disability representation from Doctor Who. I've never lied about being a nerd.Support the showNew Website: badattitudespod.comBad Attitudes Shop: badattitudesshop.etsy.comBecome a Member: ko-fi.com/badattitudespod Follow @badattitudespod on Instagram, Facebook, Threads, and BlueSkyBe sure to leave a rating or review wherever you listen!FairyNerdy: https://linktr.ee/fairynerdy

RFK proposes a "disease registry" to track citizens with autism. What could possibly go wrong?Support the showNew Website: badattitudespod.comBad Attitudes Shop: badattitudesshop.etsy.comBecome a Member: ko-fi.com/badattitudespod Follow @badattitudespod on Instagram, Facebook, Threads, and BlueSkyBe sure to leave a rating or review wherever you listen!FairyNerdy: https://linktr.ee/fairynerdy

Yayne Abeba fills in for Brian as host of 'Headliners on the Headlines,' featuring this week's comedians Tony Dijamco and Dave Burleigh. The episode covers a wide range of current events and topics, beginning with humorous discussions about Pete's drunken texts revealing war plans, segueing into a critique of the media and political ineptitude. They discuss the GOP's internal conflicts, media compliance to political pressures, and the hypocrisy in political actions. The conversation touches on Elon Musk's impact on Tesla and his handling of government roles, the importance of journalism and reliable news sources, and the legacy media's failings. They also delve into disability advocacy, discussing RFK's controversial autism database project. --Connect with our Guests...Yayne Abeba - @YayneAbebaComedy on TikTokTony Dijamco - @TonyDijamco on InstagramDave Burleigh - @Dave_Burleigh on Instagram  --For more from Brian...Visit his website: www.BrianCopeland.comFollow on Social Media: Instagram - @CopelandsCorner & @BrianCopieEmail: BrianCopelandShow@Gmail.com --Copeland's Corner is Created, Hosted, & Executive Produced by Brian Copeland. This Show is Recorded & Mixed by Charlene Goto with Go-To Productions. Visit Go-To Productions for all your Podcast & Media needs.Our Booking Producer is Tom Sawyer. For any show inquiries, please email CopelandsCornerPodcast@gmail.com

CW: AbortionIceland has all but eradicated Down syndrome from its population, but at what cost?Support the showNew Website: badattitudespod.comBad Attitudes Shop: badattitudesshop.etsy.comBecome a Member: ko-fi.com/badattitudespod Follow @badattitudespod on Instagram, Facebook, Threads, and BlueSkyBe sure to leave a rating or review wherever you listen!FairyNerdy: https://linktr.ee/fairynerdy

Physician and psychologist Heidi Feldman is a pioneer in the field of developmental behavioral pediatrics who says that the world's understanding of childhood disability is changing and so too are the ways we approach it. Where once institutionalization was common, today we find integrative, family-centered approaches, charting a more humane, hopeful path forward. For example, for children born prematurely with increased likelihood of disability, increasing skin-to-skin contact – what is called  “kangaroo care” – can literally reshape that child's brain development, she tells host Russ Altman on this episode of Stanford Engineering's The Future of Everything podcast.Have a question for Russ? Send it our way in writing or via voice memo, and it might be featured on an upcoming episode. Please introduce yourself, let us know where you're listening from, and share your question. You can send questions to thefutureofeverything@stanford.edu.Episode Reference Links:Stanford Profile: Heidi M. FeldmanConnect With Us:Episode Transcripts >>> The Future of Everything WebsiteConnect with Russ >>> Threads / Bluesky / MastodonConnect with School of Engineering >>> Twitter/X / Instagram / LinkedIn / FacebookChapters:(00:00:00) IntroductionRuss Altman introduces guest  Heidi Feldman, professor of pediatrics at Stanford University.(00:03:26) Path to Developmental PediatricsHeidi's journey from education to developmental-behavioral pediatrics.(00:05:10) The Emergence of Developmental PediatricsHow developmental disabilities entered the medical mainstream.(00:07:30) Common Disorders in ChildrenThe most prevalent disabilities seen in practice and diagnostic trends.(00:09:46) Preterm Birth and Disability RiskWhy premature birth is a major risk factor for developmental challenges.(00:13:53) Brain Connections and OutcomesHow white matter and brain circuitry impact development.(00:17:09) Kangaroo Care's PotentialHow skin-to-skin contact positively influences brain development.(00:21:30) Inclusive Family and Community SupportWhy integrated care and inclusive classrooms benefit all children.(00:23:37) Social and Economic UpsidesCost savings and increased independence from inclusive care.(00:24:33) Transitioning to Adult CareGaps and opportunities in supporting disabled youth into adulthood.(00:27:12) Using AI to Improve Care QualityAI models help track whether care guidelines are being followed.(00:31:00) Conclusion Connect With Us:Episode Transcripts >>> The Future of Everything WebsiteConnect with Russ >>> Threads / Bluesky / MastodonConnect with School of Engineering >>>Twitter/X / Instagram / LinkedIn / Facebook

The Swiss Army Knife of Disability Advocacy: A Conversation with John Fela In this episode of the Wheel With It Podcast, host Devon Wieters talks with John Fela, who describes himself as the Swiss Army Knife of disability advocacy. John shares his journey as a parent of a son with autism and his roles as an advocate, teacher, and member of Johnny and Friends, a global Christian disability organization. John discusses the importance of community, the challenges faced by families and individuals with disabilities, and his Three C's strategy for managing blended families. Tune in to hear real conversations about disability advocacy, community building, and more. Follow John Fela on Instagram (https://www.instagram.com/john_fela_1/), X (formerly Twitter) (https://x.com/jfelageller74), Facebook (https://www.facebook.com/johnsspecialneedsblog/), and visit his website at https://johnfela.com/. Check out all the links in the show notes and subscribe to stay updated with our episodes. For all things Wheel With It Podcast, visit https://linktr.ee/wheelwithitpod.00:00 Introduction to Disability Advocacy00:59 Meet Our Guest: John Fela01:18 John's Journey in Disability Advocacy03:36 Challenges and Triumphs of Parenting a Child with Disabilities09:58 The Three Cs for Blended Families14:55 Joni and Friends: A Global Outreach21:11 Navigating Education and Independence28:23 The Importance of Community35:42 Closing Remarks and Resources

Boycotting is a privilege. Not everyone is able (physically, financially, or otherwise) to participate. Shame should not be part of the package.Support the showNew Website: badattitudespod.comBad Attitudes Shop: badattitudesshop.etsy.comBecome a Member: ko-fi.com/badattitudespod Follow @badattitudespod on Instagram, Facebook, Threads, and BlueSkyBe sure to leave a rating or review wherever you listen!FairyNerdy: https://linktr.ee/fairynerdy

Have a comment or question? Click this sentence to send us a message, and we might answer it in a future episode.Welcome to Season 5, Episode 12 of Winning Isn't Easy. In this episode, we'll dive into the complicated topic of "Disability in the Modern World, Advocacy, and More with Guest Hollis Peirce."Join attorney Nancy L. Cavey, a leading expert in disability claims, and special guest Hollis Peirce for an insightful discussion on disability advocacy, the realities of living with a disability in today's world, and more. Hollis, born with muscular dystrophy, shares his personal journey, offering a firsthand perspective on how disability impacts his daily life - highlighting that living with a disability can often feel like a full-time job. He also discusses the challenges faced by those with disabilities in the modern world and explores ways people can get involved in disability advocacy.In this episode, we'll cover the following topics:One - Hollis' Personal Journey and ExperienceTwo - Disability in the Modern WorldThree - Advocacy and PerspectiveWhether you're a claimant, or simply seeking valuable insights into the disability claims landscape, this episode provides essential guidance to help you succeed in your journey. Don't miss it.Hollis, who hosts the podcast 21st Century Disability, can be found at the following:Website: https://www.21stcenturydisability.com/Instagram: https://www.instagram.com/21stcenturydisability/Facebook: https://www.facebook.com/21stcenturydisabilityBluesky: https://bsky.app/profile/21stcentdisability.bsky.socialLinkedIn: https://www.linkedin.com/in/hollis-peirce-347122239/Listen to Our Sister Podcast:We have a sister podcast - Winning Isn't Easy: Navigating Your Social Security Disability Claim. Give it a listen: https://wiessdpodcast.buzzsprout.com/Resources Mentioned in This Episode:LINK TO ROBBED OF YOUR PEACE OF MIND: https://mailchi.mp/caveylaw/ltd-robbed-of-your-piece-of-mindLINK TO THE DISABILITY INSURANCE CLAIM SURVIVAL GUIDE FOR PROFESSIONALS: https://mailchi.mp/caveylaw/professionals-guide-to-ltd-benefitsFREE CONSULT LINK: https://caveylaw.com/contact-us/Need Help Today?:Need help with your Long-Term Disability or ERISA claim? Have questions? Please feel welcome to reach out to use for a FREE consultation. Just mention you listened to our podcast.Review, like, and give us a thumbs up wherever you are listening to Winning Isn't Easy. We love to see your feedback about our podcast, and it helps us grow and improve.Please remember that the content shared is for informational purposes only, and should not replace personalized legal advice or guidance from qualified professionals.

In this powerful episode of IDD Health Matters, Dr. Craig Escudé sits down with renowned disability advocate Liz Weintraub to explore what true health equity looks like for people with intellectual and developmental disabilities (IDD). Liz, a senior policy specialist at the Association of University Centers on Disabilities (AUCD), brings her lived experience and professional expertise to the conversation—sharing insights on advocacy, accessible healthcare, and the importance of plain language in medical settings. Liz discusses AUCD's national impact through 62 university-based centers across the U.S. and territories, her work on Capitol Hill, and key legislative priorities like ending subminimum wage (14c) and expanding home and community-based services. She also opens up about her own healthcare journey after a diabetes diagnosis, emphasizing the need for clear communication and respect for patient autonomy. Listeners will also learn about Tuesdays with Liz: Disability Policy for All, Liz's YouTube show that makes complex policy issues accessible to everyone. She shares how self-advocacy helped her transition out of institutional care and inspired her to empower others to do the same. Tune in to hear Liz's three essential tips for improving healthcare for people with IDD and why her message of "healthcare for all" is more important than ever.

I had such a fun time talking with this week's guest, Diana Hurtado. We touched on so many important topics, and I can't wait to see her big career break!Diana's talent agency: ZebedeeFollow Diana on Instagram: @wheelie.funnySupport the showNew Website: badattitudespod.comBad Attitudes Shop: badattitudesshop.etsy.comBecome a Member: ko-fi.com/badattitudespod Follow @badattitudespod on Instagram, Facebook, Threads, and BlueSkyBe sure to leave a rating or review wherever you listen!FairyNerdy: https://linktr.ee/fairynerdy

In this powerful episode of IDD Health Matters, Dr. Craig Escudé sits down with renowned disability advocate Liz Weintraub to explore what true health equity looks like for people with intellectual and developmental disabilities (IDD). Liz, a senior policy specialist at the Association of University Centers on Disabilities (AUCD), brings her lived experience and professional expertise to the conversation—sharing insights on advocacy, accessible healthcare, and the importance of plain language in medical settings. Liz discusses AUCD's national impact through 62 university-based centers across the U.S. and territories, her work on Capitol Hill, and key legislative priorities like ending subminimum wage (14c) and expanding home and community-based services. She also opens up about her own healthcare journey after a diabetes diagnosis, emphasizing the need for clear communication and respect for patient autonomy. Listeners will also learn about Tuesdays with Liz: Disability Policy for All, Liz's YouTube show that makes complex policy issues accessible to everyone. She shares how self-advocacy helped her transition out of institutional care and inspired her to empower others to do the same. Tune in to hear Liz's three essential tips for improving healthcare for people with IDD and why her message of "healthcare for all" is more important than ever.

Tune in to hear from Scott Ford, camp director of Michigan Blind Athletic Association's Sports camp! Give it a listen and be sure to visit https://buff.ly/sgpc3k2 for more information and camp registration!

Have you ever felt disconnected from your body—or grieved the version of it you used to know? I have. And in this episode of Unleash Your Inner Creative, I'm talking with disability advocate and author Jayne Mattingly about something we don't hear enough about: body grief, and how it can quietly block our creativity and self-love.Here's what I've come to realize: when we lose trust in our bodies, we often lose connection to ourselves and therefore our creative voice. But when we start rebuilding that trust—even slowly—we open the door to healing, peace, and creative freedom.Jayne created a powerful framework to help us understand and move through body grief, and in this episode, she shares her story, how it applies to you, and how getting into a relationship with your body can shift everything—from how you heal to how you create.From this episode, you'll learn:-What body grief is and how to recognize it in your own life-The 7 stages of body grief and how to move through them-How to begin rebuilding trust with your body—at any stage-Why healing your relationship with your body can unlock your creativityTW: Eating Disorders and Mental Health More on JayneUnleash is Nominated for a Webby Award and we need your help to win! Vote here: https://vote.webbyawards.com/PublicVoting#/2025/podcasts/shows/creativity-marketing ✨ Want personalized support to reconnect with your creativity yourself and share your work with the world? I'm a creative coach who helps artists, entrepreneurs, and multi-passionate creatives move through self-doubt and unleash their authentic voice.

Subtitles have seen an increase in use in recent years. Is it due to the dumbing down of the viewing public, or are the reasons more mundane?Support the showNew Website: badattitudespod.comBad Attitudes Shop: badattitudesshop.etsy.comBecome a Member: ko-fi.com/badattitudespod Follow @badattitudespod on Instagram, Facebook, Threads, and BlueSkyBe sure to leave a rating or review wherever you listen!FairyNerdy: https://linktr.ee/fairynerdy

Sophie Etheridge is redefining open water swimming. A marathon swimmer, coach, and disability advocate, she made history in 2023 by becoming the first person with Complex Regional Pain Syndrome to swim the English Channel solo—setting a World Record for the longest English Channel Swim at an astonishing 29 hours and 4 minutes. In this episode of the Tough Girl Podcast, Sophie takes us behind the scenes of her record-breaking swim, sharing the physical and mental challenges she faced during nearly 30 hours in the water. From training and preparation to the unexpected obstacles that tested her resilience, Sophie's story is a testament to determination, adaptability, and the power of a strong support team. She also speaks about her work in making swimming more accessible, advocating for better opportunities for disabled swimmers, and why she believes everyone should have the chance to experience the freedom of open water. Tune in for an inspiring conversation about overcoming adversity, pushing boundaries, and the true meaning of endurance. *** Catch the latest episodes of the Tough Girl Podcast, dropping every Tuesday at 7 am UK time! Don't forget to subscribe so you won't miss the inspiring journeys and incredible stories of tough women.  Want to play a part in uplifting female representation in the media? Support the Tough Girl Podcast on Patreon! Your generosity helps shine a spotlight on female role models in the world of adventure and physical challenges. Join us in making a positive impact by visiting www.patreon.com/toughgirlpodcast. Thank you for your amazing support! *** Show notes Who is Sophie  Ultra marathon swimmer and adaptive athlete. Previously peaking to Sophie on the Tough Girl Podcast (TGP) in August 23rd 2022  Being the founder of ADOWS - Adaptive and Disabled Open Water Swimmers  What we talked about the first time we spoke on the TGP What was happening in 2022 The English Channel Relay Swim  Marathon Swimming Federation  Thinking about doing a solo English Channel swim  Swimming Teachers Association (STA) Conference  Wanting to complete the original swimming triple crown as a disabled person Getting sponsored to swim the English Channel  What changed going forward  Needing to have a medical and do a qualification swim  Wanting to learn as much as she could about swimming the English Channel solo Going on a swim camp in Wales by herself and travelling solo  Why 2023 was a very quick year, but took a long time Sharing her goal of a solo swim  Having 8 months to train  Starlight - shining a light on disability swimming  Up-skilling swimming teachers and training them how to teach disabled people how to swim  Having no doubts and the power of words and language  Not being able to tread water and how that changed the feeding process The multiple challenges that Sophie would have to face during the swim  Having a great crew and team around her  Going on a spring tide and getting the last slot available to swim the channel  The fear of getting out of the water at the end of the swim and not being able to use her legs… Expecting to do the swim in 18/19 hours The strategy and the plan for the swim Night swimming  Swimming sideways for 7 hours and not being able to make any progress forward 29hrs 4 mins…. Swimming!  Why it became more of a mental challenge  Aiming to swim for 24hrs! Setting 3 world records and not knowing until back on the boat Reaching France  Getting back on the boat and heading back to England Not celebrating straight away  Getting a huge amount of press Raising over £6,000 for STA  Fundraising for Level Water  How to connect with Sophie and follow along with her challenges Final words of advice Find out the starting point  Give yourself permission to let go and to try new things Why you never know where the journey is going to take you    Social Media Website/Blog: sophie-adaptive-athlete.com  Instagram: @sophie_adaptive_athlete Facebook: @sophie_adaptive_athlete  

Meet Stephanie Evans, a dedicated advocate for mental health and disability rights from St. John's, Newfoundland and Labrador. With a social work degree, she's committed to supporting individuals through advocacy and plans to open a private practice. Stephanie serves as chairperson for NEADS, driving impactful change for students with disabilities. She also contributes to the Wavemakers Advisory Board and the Dawn Canada Hummingbird Network. An avid outdoor enthusiast, she finds healing in nature through hiking and sports. Passionate about creating equitable spaces, Stephanie's volunteer work reflects her unwavering dedication to uplifting and empowering others.

They're coming for Social Security? I'm SHOCKED. Who could have predicted this? WHO?Support the showNew Website: badattitudespod.comBad Attitudes Shop: badattitudesshop.etsy.comBecome a Member: ko-fi.com/badattitudespod Follow @badattitudespod on Instagram, Facebook, Threads, and BlueSkyBe sure to leave a rating or review wherever you listen!FairyNerdy: https://linktr.ee/fairynerdy

The More Sibyl Podcast Presents: 장애인의 희망|The One with Ms. Crystal Chigbu - Beyond the Limb: A Mother's Fight for Disability Advocacy & Inclusion| Episode 7 (2025)Imagine being a new mom, filled with joy and anticipation—only to be told that your child will need an amputation. The shock, the fear, the overwhelming uncertainty. Now, imagine channeling that pain into a movement that transforms not just your child's life but the lives of thousands. That's exactly what Crystal Chigbu, founder of The Irede Foundation, has done. In this episode, Crystal shares her incredible journey from corporate leadership at Procter & Gamble to becoming a pioneer in disability advocacy in Nigeria. Her personal experience raising a child with limb loss led to the creation of a foundation that has provided over 600 prosthetic limbs to children across Africa, restoring their mobility, confidence, and hope.Crystal takes us through the challenges and triumphs of navigating career transitions with purpose and resilience, the realities of building and sustaining a successful social enterprise, and the role of mentorship, coaching, and gender dynamics in professional growth. She opens up about overcoming grief and emotional hurdles, the importance of storytelling with dignity in disability advocacy, and the groundbreaking innovations in prosthetics and the future of local production in Nigeria. We also explore fundraising and scaling a non-profit with credibility and transparency, ensuring long-term impact.Crystal's journey is a testament to the power of community, purpose, and persistence. You can help amplify this impact! Support The Irede Foundation by:

What does it take to become a "Swiss Army Knife of Disability Advocacy"? For John Feller, it began with the birth of his son with autism who is now 16 and nonverbal. His journey from confused parent to national advocate reveals the profound challenges and unexpected gifts that come with raising a child with disabilities.The path wasn't always clear. John candidly shares his initial struggle to accept his son's diagnosis and find his footing as a father when traditional parenting roles were upended. "What I struggled with in the beginning was finding my role," he explains. "I couldn't be the breadwinner, I couldn't manage all the therapies—so who was I as a parent, as a husband, as a father?" This identity crisis eventually led him to discover his true gifts in advocacy, networking, and relationship-building.Education presents particular challenges for families navigating disability. John offers valuable insights about the realities of public versus private schooling, cautioning parents not to be deceived by appearances: "Anything looks good on a website." His family ultimately made the difficult decision to place their son in a residential facility a thousand miles from home—a choice requiring tremendous surrender but proving beneficial for their son's development.Communication with a nonverbal child requires creativity and patience. Through a combination of body language interpretation, basic signing, and assistive technology, John has found ways to connect with his son. He emphasizes the importance of addressing individuals with disabilities directly rather than speaking about them as if they aren't present: "He doesn't speak, but he does hear."The conversation takes a powerful turn when John discusses the vital importance of community support. Having transitioned from feeling completely alone to building a national network, he now helps other families find their lifelines. His work with Joni and Friends, a global Christian disability ministry, allows him to help churches create welcoming environments for people with all types of disabilities—visible and invisible.Looking toward the future, John confronts the reality many special needs parents face: what happens when they're no longer there? With his son being an only child, creating intentional community becomes even more critical. Who will check on him, celebrate birthdays, or simply offer a hug?Whether you're navigating disability personally or seeking to better support those who are, John's story offers profound wisdom about finding purpose through unexpected challenges and building communities that sustain us through life's most difficult journeys.Let me know what you think of this episode? Support the showSupport the Podcast. https://buymeacoffee.com/dorseyrossSocial Media Links, Instagram https://www.instagram.com/dorsey.ross/ Facebook https://www.facebook.com/DROCKROSS/ My Book Amazon Book Overcomer https://bit.ly/4h7NGIP

We're back with the rest of my conversation with Michael Murphy, discussing his experience with NLD (NVLD) and his book-writing and Sudoku endeavors!Support the showNew Website: badattitudespod.comBad Attitudes Shop: badattitudesshop.etsy.comBecome a Member: ko-fi.com/badattitudespod Follow @badattitudespod on Instagram, Facebook, Threads, and BlueSkyBe sure to leave a rating or review wherever you listen!FairyNerdy: https://linktr.ee/fairynerdy

Guest and HostGuest: Precious Perez, President at RAMPD | On LinkedIn: https://www.linkedin.com/in/precious-perez-a0548915b/ | Website: https://preciousperezmusica.com/Host: Sean Martin, Co-Founder at ITSPmagazine and Host of Redefining CyberSecurity Podcast & Music Evolves Podcast | Website: https://www.seanmartin.com/Show NotesThe intersection of music, technology, and accessibility is shaping how artists create, perform, and share their work. In this episode of Music Evolves, host Sean Martin speaks with singer, songwriter, and educator Precious Perez, a Berklee College of Music graduate with degrees in music education and vocal performance. As a blind Latina artist and disability advocate, Perez shares her journey in music, the role of technology in her creative process, and how she works to increase opportunities for musicians with disabilities.A Life Shaped by MusicPerez's passion for music started early, surrounded by the diverse sounds of her Puerto Rican household. From salsa and reggaeton to R&B and pop, her exposure to various genres helped shape her identity as an artist. She recalls her first songwriting experience in fourth grade, when she transformed a poem into a song with the help of a music teacher. That moment solidified her desire to pursue music professionally, leading her to Berklee, where she refined her skills in both performance and education.As a blind musician, Perez explains how she interacts with music differently from sighted artists. She describes her early experiences learning Braille music and how tactile memory plays a role in understanding composition. While she primarily relies on her ear, her knowledge of Braille notation helps her analyze rhythm and structure in a unique way.Technology as a Tool for InclusionFor Perez, technology has been both a gateway and a challenge. She demonstrates how she uses a BrailleSense note taker, a device that allows her to type lyrics and read them in Braille while composing. She also shares how screen reading software enables her to navigate recording software like Logic Pro and Pro Tools, ensuring she can produce and edit her music independently.Beyond the studio, accessibility in live performance is another key consideration. Whether using in-ear monitors or giving cues to her bandmates through verbal or physical signals, Perez emphasizes that clear communication and collaboration make performances seamless.Advocating for Disability Representation in MusicPerez is also the president of RAMPD (Recording Artists and Music Professionals with Disabilities), an organization founded by recording artist Lachi and NPR Tiny Desk Contest winner Gaelynn Lea. RAMPD is dedicated to amplifying disability culture, promoting accessibility, and ensuring that disabled artists have equitable opportunities in the music industry. The organization consults with major industry events like the Grammys, NAMM, and Folk Alliance to improve accessibility and representation.She stresses that disability is an often-overlooked part of diversity and that anyone, at any time, could join this community due to illness, injury, or aging. Through RAMPD, Perez and her colleagues are breaking down barriers and proving that disabled musicians are just as competitive and professional as their peers.A New Era of MusicPerez is embracing a new era in her music, blending her Latin roots with her pop and R&B influences. She performs her latest song, Rosé, a Spanish-language track about embracing the present moment with a loved one despite life's difficulties. With plans to record a new project with We Could Be Music in Costa Rica, she is leaning into the Latin music space in a way she has always envisioned.Her story is one of resilience, innovation, and passion. From navigating music education as a blind student to advocating for industry-wide accessibility, Perez is proving that talent and determination—not sight—define an artist's success.Listen to the full episode to hear Precious Perez's insights on technology, performance, and advocacy in music.SponsorsAre you interested in sponsoring this show or placing an ad in the podcast?Sponsorship

In this episode, I chat with Jude Bronstein, a disability advocate and fellow olah. We discuss what their life is like dealing with having cerebral palsy, how to be a disabilities advocate and owning your struggles without pushing yourself too hard. Jude shares how to learn to accept your different states of mind rather than resist them.I hope you appreciate this real, down-to-earth and honest episode. Follow Jude's work at disabledreamer.com or on Instagram @disabledreamer.(0:00-4:00) - Jude is a long time podcast listener!(4:00-15:00) - Cerebral Palsy and writing as a coping mechanism(15:00-26:51) - Being a disability advocate(26:51-35:00) - How to build a positive mindset during difficult times(35:00-38:00) - IFS theories (38:00-end) - Advice for getting through hard times 

I'm happy to welcome my first listener-turned-guest, Michael Murphy. Michael lives with photosensitive epilepsy and non-verbal learning disorder, and is undertaking the task of reworking the Americans with Disabilities Act. In this episode, we discuss the ADA in depth, as well as Michael's experiences with epilepsy. Be sure to tune in next week for the conclusion of our conversation.Support the showNew Website: badattitudespod.comBad Attitudes Shop: badattitudesshop.etsy.comBecome a Member: ko-fi.com/badattitudespod Follow @badattitudespod on Instagram, Facebook, Threads, and BlueSkyBe sure to leave a rating or review wherever you listen!FairyNerdy: https://linktr.ee/fairynerdy

A reflection on the documentary, "Super/Man: The Christopher Reeve Story" and Christopher Reeve's legacy as an actor, director, and disabled person.Support the showNew Website: badattitudespod.comBad Attitudes Shop: badattitudesshop.etsy.comBecome a Member: ko-fi.com/badattitudespod Follow @badattitudespod on Instagram, Facebook, Threads, and BlueSkyBe sure to leave a rating or review wherever you listen!FairyNerdy: https://linktr.ee/fairynerdy

In this episode of the Running Wine Mom podcast, host Samantha Cieslinski speaks with Marcela Maranon, the first disabled Latina to climb Mount Kilimanjaro. Marcela shares her inspiring journey of overcoming adversity, her adventures traveling to the seven wonders of the world, and her commitment to advocating for accessibility and inclusion for individuals with disabilities. She discusses her House of Hope project, which aims to support disabled children in Tanzania, and emphasizes the importance of community and allyship in creating a more inclusive world.@thejourneyofabravewoman@therunningwinemom_

Charlene Wheeless, author of You Are Enough! and I recap the latest 5 Things (good vibes in DEI) in just 15 minutes. This week our conversation is about Beyoncé breaking ceilings, Goodell holding the line, disability advocates making moves, and more!Here are this week's good vibes:Equality Wins for Families and WorkersBeyoncé Breaks Country Music CeilingGoodell Holds the Line on DiversityDisability Advocates Drive Uber ChangeFirst-of-Its-Kind Hospital Redefines Disability CareGood Vibes to Go: Bernadette's GVTG: It's Black History Month! Buy Black by shopping for a beautiful variety of products from tons of merchants. Buy Black's mission is “To drive traffic and revenue to Black-owned businesses in order to close the revenue disparity gap between Black-owned businesses and their non-Black counterparts.Charlene's GVTG: Buy Black all year round – and choose love.Read the StoriesConnect with Charlene WheelessWatch the show on YouTube. Join thousands of readers by subscribing to the 5 Things newsletter. Enjoy some good vibes in DEI every Saturday morning. https://5thingsdei.com/

I must be prescient because a whole lot of what I said in this episode has come to pass.Let's take a look at the story that gripped the nation in the days and weeks leading up to Christmas: the death of United Healthcare CEO Bryan Thompson, and the eventual arrest of Luigi Mangione.Support the showNew Website: badattitudespod.comBad Attitudes Shop: badattitudesshop.etsy.comBecome a Member: ko-fi.com/badattitudespod Follow @badattitudespod on Instagram, Facebook, Threads, and BlueSkyBe sure to leave a rating or review wherever you listen!FairyNerdy: https://linktr.ee/fairynerdy

We're doing something a little lighter this week. Tattoos! I'm getting a new one soon, and I wanted to reiterate why tattoos are so meaningful to me as a disabled person.Support the showNew Website: badattitudespod.comBad Attitudes Shop: badattitudesshop.etsy.comBecome a Member: ko-fi.com/badattitudespod Follow @badattitudespod on Instagram, Facebook, Threads, and BlueSkyBe sure to leave a rating or review wherever you listen!FairyNerdy: https://linktr.ee/fairynerdy

CW: N@zis, brief mention of sexual assaultIt's been a while since I've dropped this many f-bombs in an episode. You've been warned.Note: I cannot confirm or deny that Elon Musk has autism, but whether he does or doesn't isn't really the point.Support the showNew Website: badattitudespod.comBad Attitudes Shop: badattitudesshop.etsy.comBecome a Member: ko-fi.com/badattitudespod Follow @badattitudespod on Instagram, Facebook, Threads, and BlueSkyBe sure to leave a rating or review wherever you listen!FairyNerdy: https://linktr.ee/fairynerdy

If you're struggling to keep people engaged and loyal in your product or business, check out my FREE gamification course to learn how to do just that: bit.ly/freegamificationcourse-web "Questify Your Life" system that also works alongside disabilities. We sit with Sierra Grandy to discuss how she gamifies life using her unique "Questify Your Life" system. They explore Sierra's approach to living life as a series of quests and how gamification can drive engagement and personal growth. Sierra Grandy is a recent lawyer, disability advocate, and business owner. She plays her life as if it were a quest and teaches others to do the same by using her "Questify Your Life" system. Rob is a host and consultant at Professor Game as well as an expert, international speaker and advocate for the use of gamification and games-based solutions, especially in education and learning. He's also a professor and workshop facilitator for the topics of the podcast and LEGO SERIOUS PLAY (LSP) for top higher education institutions that include EFMD, IE Business School and EBS among others in Europe, America and Asia.   Guest Links and Info Websites: SierraGrandy.com QuestifyYourLife.com (website in progress-soon to launch) LinkedIn: Sierra Grandy Instagram: @sierramgrandy TikTok: @questifyyourlifesierra Substack: questifyyourlife.substack.com   Links to episode mentions: Proposed guest: Brennan Lee Mulligan Recommended book: The Gifts of Imperfection by Brené Brown Mindset by Carol Dweck Favorite game: Tabletop: Dungeons & Dragons Party Game: Business Walrus Video Game: Dark Cloud 2   Lets's do stuff together! Get started in Gamification for FREE! LinkedIn Twitter Facebook Instagram TikTok YouTube Ask a question

There's an important element to Wicked outside of the friendship between Elphaba and Galinda: Elphaba's sister, Nessarose. I found the disability representation to be strong, and in this episode, I discuss a few different points of Nessa's story.Support the showNew Website: badattitudespod.comBad Attitudes Shop: badattitudesshop.etsy.comBecome a Member: ko-fi.com/badattitudespod Follow @badattitudespod on Instagram, Facebook, and ThreadsBe sure to leave a rating or review wherever you listen!FairyNerdy: https://linktr.ee/fairynerdy