Podcasts about disability advocacy

The amended Employment Equity Act came into effect on 1 January 2025, introducing a 3 percent target for the employment of persons with disabilities. But what does this mean in practice, and will it create real opportunities or just raise another quota? Ari Seirlis, long-time disability rights advocate, former CEO of the QuadPara Association of South Africa, and member of the Presidential Working Group on Disability, speaks to Lester Kiewit about the promise and pitfalls of the new act, the barriers that still exist in workplaces, and the value persons with disabilities bring every day. Good Morning Cape Town with Lester Kiewit is a podcast of the CapeTalk breakfast show. This programme is your authentic Cape Town wake-up call. Good Morning Cape Town with Lester Kiewit is informative, enlightening and accessible. The team’s ability to spot & share relevant and unusual stories make the programme inclusive and thought-provoking. Don’t miss the popular World View feature at 7:45am daily. Listen out for #LesterInYourLounge which is an outside broadcast – from the home of a listener in a different part of Cape Town - on the first Wednesday of every month. This show introduces you to interesting Capetonians as well as their favourite communities, habits, local personalities and neighbourhood news. Thank you for listening to a podcast from Good Morning Cape Town with Lester Kiewit. Listen live on Primedia+ weekdays between 06:00 and 09:00 (SA Time) to Good Morning CapeTalk with Lester Kiewit broadcast on CapeTalk https://buff.ly/NnFM3Nk For more from the show go to https://buff.ly/xGkqLbT or find all the catch-up podcasts here https://buff.ly/f9Eeb7i Subscribe to the CapeTalk Daily and Weekly Newsletters https://buff.ly/sbvVZD5 Follow us on social media CapeTalk on Facebook: https://www.facebook.com/CapeTalk CapeTalk on TikTok: https://www.tiktok.com/@capetalk CapeTalk on Instagram: https://www.instagram.com/ CapeTalk on X: https://x.com/CapeTalk CapeTalk on YouTube: https://www.youtube.com/@CapeTalk567See omnystudio.com/listener for privacy information.

Steven Scott and Shaun Preece dive into everyday frustrations, from robots that can't close dishwashers to AI-powered home assistants that randomly skip podcast episodes. Along the way, they share laughs, listener rants, and reflections on accessibility, independence, and the realities of being blind in a tech-driven world.Thanks to Turtleback Low Vision for sponsoring this episode of Double Tap. As a thank you to the Double Tap community, Turtleback is offering 12% off your entire order with promo code DT12. Visit https://www.turtlebacklv.com to shop the full lineup!In this lively Double Tap episode, Steven and Shaun start with coffee mishaps—hand wash–flavoured brews included—before exploring the quirks of modern “smart” tech. They discuss a new humanoid home robot that promises to wash dishes, fold laundry, and answer the door, but can barely manage a dishwasher without remote human help. Listener Frank from Northeast England writes in with a double rant: his Alexa keeps jumping episodes, and his local council's bin habits make pavements hazardous. His story sparks a deeper conversation about the persistence of “Does he take sugar?” attitudes toward blind people. Steven and Shaun highlight the importance of self-advocacy, the limits of sighted intervention, and the ongoing challenge of poor local services. Through humour and honest commentary, the hosts consider the future of work in an AI-driven world, the value of human capability, and why accessible technology still matters. 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. Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

Send us a textIn this episode of ADC's Parenting Adult Children podcast, host James Moffitt is joined by John Fela and Katy Moffitt to discuss the challenges and experiences of parenting children with disabilities. John shares his journey as a parent of a nonverbal autistic son, highlighting the fears and realities of finding suitable care and community for his child. Katy, with her extensive experience in special education, adds insights into the educational needs and social dynamics of children with disabilities. The conversation delves into the importance of community support, the role of churches in disability ministry, and the need for awareness and acceptance in society.Keywordsparenting, disability advocacy, autism, special education, community support, church ministry, awareness, acceptance, nonverbal communication, special needsTakeawaysJohn Fela describes himself as the 'Swiss Army knife of disability advocacy.'John's son, Chris, is nonverbal and autistic, requiring specialized care.Katy has over 25 years of experience in special education.The importance of finding a supportive community for families with disabilities.Challenges in finding suitable educational and living environments for children with disabilities.The role of churches in providing support and inclusion for families with disabilities.John emphasizes the need for awareness and acceptance in society.The fear of the future and loneliness as a parent of a child with disabilities.The significance of communication tools like TouchChat for nonverbal individuals.John's advocacy work includes writing, speaking, and creating support groups for fathers.Title OptionsNavigating Disability Advocacy with John FelaParenting Challenges: A Journey with John and KatyBuilding Community Support for Special Needs FamiliesThe Role of Churches in Disability MinistryJohn Fela: A Voice for Disability AdvocacyUnderstanding Autism: Insights from John FelaSpecial Education and Parenting: Katy's PerspectiveCreating Inclusive Communities for DisabilitiesJohn Fela's Advocacy JourneySupporting Nonverbal Communication in AutismSound bitesSwiss Army knife of disability advocacyFear of the future and lonelinessImportance of community supportRole of churches in inclusionAwareness and acceptance in societyNonverbal communication toolsChallenges in special educationBuilding support groups for fathersNavigating disability advocacyCreating inclusive communitiesChapters00:00:00 Introduction and Guest Introductions00:00:00 John Fela's Advocacy Journey00:00:00 Parenting a Nonverbal Autistic Child00:00:01 Educational and Living Challenges Listen here for our sponsors list. Many thanks to them for helping to underwrite the costs of producing this podcast. Support the showSocial Media Links https://www.youtube.com/@JamesMoffitt https://www.instagram.com/parentingadultchildren125/ https://www.tiktok.com/@chiefpropellerhead ABC's of Parenting Adult Children Facebook Page https://www.facebook.com/profile.php?id=61581576308055 r/parentingadultchildren Feel free to subscribe to these channels and share the links with your social media portals.

In this episode, Kyle and Sean discuss the importance of disability employment and accessible travel with guest Daniel Van Sant, Director of Disability Policy at the Harkin Institute. They explore the challenges faced by disabled individuals in the workforce, the significance of National Disability Employment Awareness Month, and the barriers to travel for those with disabilities. Daniel shares insights on advocacy, the need for positive representation of disabled individuals, and the current trends in airline accessibility. The conversation emphasizes the importance of visibility and self-advocacy in creating a more inclusive society.

It's surprisingly easy for people to think labels don't mean anything, but they can actually be quite powerful.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 neurodivergent and considering starting your own business, boy, have I got the episode for you!Follow my guest, Kaylie Chandler, on social media:Instagram: @kaybowzieThreads: @kaybowzieTikTok: @kaybowzieYouTube: @kaybowzieSupport 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

Grey's Anatomy isn't a stranger to disability-related storylines. So why was this time different?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

On the weeks episode of BVC Pastor Speak we discuss the successes and needs of the disability community with Jawanda Mast from the National Down Syndrome Congress. You'll hear impactful stories and learn how to be an advocate in everyday life. The NDSC can be found at NDSCcenter.org and the Action Alerts can be found on the Policy & Advocacy page.

Disagree with me or not, it's a hill I will die on: Pregnancy is not a disability.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

I hope my SSA examiner doesn't listen to this episode.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 Clare senator is calling on the Public Expenditure Minister to clarity the measures in Budget 2026 that will assist those with disabilities. The Disability Federation of Ireland has described this year's package as a "devastating setback for disabled people unable to work", claiming they'll "see their incomes fall with the removal of vital social protection supports". A €619 million increase in funding for disability services has been announced this week, with disability allowance rising by €10 to €254. Speaking in the Seanad, Ennistymon Senator Martin Conway advocacy groups haven't minced words when expressing their dissatisfaction with the measures unveiled.

Sometimes what hurts most isn't the migraine itself—it's living in a world that doesn't understand it and isn't built to support it. While visible disabilities often receive accommodations, migraine remains largely invisible—leaving millions to navigate environments that dismiss, overlook, or even worsen their pain.This episode of The Migraine Heroes Podcast explores the urgent need for advocacy in migraine care, blending personal storytelling with practical solutions. Hosted by Diane Ducarme, who has guided hundreds of women in reshaping their healing journeys, we look at how resilience and community can rewrite the narrative of living with this invisible disability.You'll discover:

You might be surprised to learn I'm not automatically on the side of the disabled person in a given situation.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

Caring for a loved one with disabilities can feel like an endless marathon of emotional and logistical challenges that drain your energy and test your resilience. Most people struggle silently, unsure how to balance their own needs with the intense support requirements of their family member. Diana Carson's journey offers a powerful roadmap for anyone feeling overwhelmed by caregiving, showing how strategic advocacy and personal growth can transform what seems like an insurmountable obstacle into a path of profound connection and purpose. Her story isn't just about overcoming systemic barriers, but about discovering inner strength and creating meaningful support networks that honor both the caregiver and the person being cared for. Through her experiences with her brother Joaquin, Diana reveals practical strategies for maintaining hope, building community, and nurturing yourself while championing the rights and dignity of those with disabilities.What You'll Learn:Reframing disability: how shifting perspective unlocks new possibilities.The sister's love that completely reshaped her brother's future.Diana's bold approach to fighting for her brother's freedom.Turning personal struggles into a mission of compassion and impact.Therapy as the breakthrough tool for healing complex family dynamics.Why you need to start making gratitude a daily practice.The difference between disability awareness and true access for all people.

In another move to demonize the autistic community, the Trump administration has announced that Tylenol is linked to autism, despite very little evidence to suggest it.Sources used in this episode:https://www.cbsnews.com/news/trump-rfk-jr-distort-facts-autism-tylenol-vaccines/https://people.com/what-is-leucovorin-the-supplement-rfk-jr-claims-treats-autism-11814634Support 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

Latima Anderson Mason is an inspiring advocate and a dedicated mother to her daughter who has a disability. As her daughter transitions into adulthood, Latima has taken an active role in navigating the complexities of aging out of support services and exploring guardianship options. Her personal experiences have fueled her passion for advocacy, guiding other families through similar challenges with empathy and insight. Latima is currently engaging in workshops and legal processes to ensure her daughter's rights and independence are upheld as she enters this new life stage.Episode Summary:In this episode of DSP Talk, host Asheley Blaise engages in a poignant conversation with Latima Anderson Mason, a devoted mother and advocate for her daughter with disabilities. As Anika approaches adulthood, Latima shares the intricacies of the aging-out process, especially focusing on the transition from high school to adult services at the age of 21. By sharing her story, Latima helps to shed light on the critical path of securing guardianship while balancing her daughter's rights and independence—offering listeners a glimpse into the challenges and victories experienced by families navigating a similar journey.Latima Anderson Mason provides insight into the emotional and practical challenges of securing guardianship for her daughter, Anika, who is aging out of services. The discussion highlights essential topics such as the significance of understanding legal processes and maintaining the child's voice in critical decisions. Key resources such as AHRC New York workshops are mentioned, offering needed support to families. The episode concludes with Latima's personal hopes for a future where individuals with disabilities are seen and heard beyond their limitations. This episode is a must-listen for families and advocates in the disability community, providing relatable and beneficial guidance.Key Takeaways:Aging Out Process: Children with disabilities are entitled to services through the Individuals with Disabilities Education Act (IDEA) until they turn 21 (in NY, other States it can be up to 22).Guardianship: is a court process that allows a parent or caregiver to make legal, medical, or financial decisions for an adult child who is unable to make such decisions independently. (Source Planning for Children with Disabilities Aging Out of the School System - , May 01, 2025)Effective Communication: Continuously explaining processes and decisions to a child with disabilities helps in understanding and decision-making.Alternatives to Guardianship: Supported decision-making (SDM) is a practice by which people with intellectual and developmental disabilities (I/DD) are able to make their own decisions with the support of trusted persons in their lives and retain all their legal and civil rights. (Source: What is Supported Decision-Making? – SDMNY)Resources:AHRC New York: Guardianship ServicesOPWDD Transition Services Recorded Webinar May 9, 2024 Hosted on Acast. See acast.com/privacy for more information.

Medicare is going to introduce a pilot program using AI to determine claims and denials for patients. 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

In this episode, disability advocate and Steptember ambassador Sophie Geeves shares her journey from early intervention with the Cerebral Palsy Alliance to presenting evidence in Parliament. She opens up about the role of CPA in her life, what Steptember means to her, why inclusion in education is still a fight, and how she navigates belonging in both disability culture and mainstream society. Key Moments: [7:26] Why Steptember is about “movement in all forms” and how funds support babies and families. [10:12] Transitioning from child to adult services with CPA. [12:30] Sophie’s experience giving evidence to the NSW Upper House inquiry on education. [23:31] Her advice for young disabled people finding their voice. Connect with Peta: Instagram: @petahooke Website: www.icantstandpodcast.com Email: icantstandpodcast@gmail.com Episode Transcript: https://www.icantstandpodcast.comSee omnystudio.com/listener for privacy information.

This is the very first episode of my new podcast, Take the Next Step, and I'm sharing it here so you won't miss the launch. Be sure to follow Take the Next Step with Amy Julia Becker wherever you listen so you don't miss future episodes. (New episodes of Reimagining the Good Life are coming in October!)Follow the new podcast at: amyjuliabecker.com/step/__Feeling overwhelmed by the challenges of disability? Katherine Wolf, author, advocate, and co-founder of Hope Heals, joins Amy Julia Becker to explore how families can reimagine disability, build connection, and celebrate life. From the dinner table to the slow work of recovery, learn how to find delight in the story you have. Discover:How to experience joy in the process, not just the outcomeDaily habits to cultivate gratitude and delightHow to build a supportive, connected communityWhy purpose and contribution matter for every family_MENTIONED IN THIS EPISODE:Katherine's books, resources, gatherings, and inter-ability communities: hopeheals.com. Luke 14_WATCH this conversation on YouTube: Amy Julia Becker on YouTubeSUBSCRIBE to Amy Julia's Substack: amyjuliabecker.substack.comJOIN the conversation on Instagram: @amyjuliabeckerLISTEN to more episodes: amyjuliabecker.com/shows/_ABOUT OUR GUEST:Katherine Wolf is an author, advocate, and co-founder of Hope Heals. After she survived a near-fatal brainstem stroke at age 26, her family's journey through disability has become a public witness that good and hard can co-exist in the same story. Through caregiving, storytelling, and lived theology, Katherine is inviting others into a vision of hope, interdependence, and embodied resilience. She and her husband Jay live in Atlanta with their two sons.Website: www.hopeheals.com Instagram: @hopeheals_Take the Next Step is produced in collaboration with Hope Heals. Hope Heals creates sacred spaces of belonging and belovedness for families affected by disabilities to experience sustaining hope in the context of inclusive, intentional, inter-ability communities. Find out more about our resources, gatherings, and inter-ability communities at hopeheals.com. Follow us on Instagram @hopeheals.We want to hear your thoughts. Send us a text!Connect with me: Instagram Facebook YouTube Website Thanks for listening!

Florida's intention to do away with vaccine mandates has terrible implications for all of us, but especially for vulnerable populations.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

I'm so excited to share something new with you! My new show, Take the Next Step, is a podcast for families experiencing disability—filled with real talk, real tools, and real hope. Tune in over at Take the Next Step each week for conversations with parents, therapists, and advocates about how we can cultivate belonging and build a flourishing future for the entire family.You can find the new show by searching "Take the Next Step with Amy Julia Becker" on your podcast app, or find it online at amyjuliabecker.com/stepAnd stay tuned - new episodes of Reimagining the Good Life coming in October.__WATCH this conversation on YouTube: Amy Julia Becker on YouTubeSUBSCRIBE to Amy Julia's Substack: amyjuliabecker.substack.comJOIN the conversation on Instagram: @amyjuliabeckerLISTEN to more episodes: amyjuliabecker.com/shows/_Take the Next Step is produced in collaboration with Hope Heals. Hope Heals creates sacred spaces of belonging and belovedness for families affected by disabilities to experience sustaining hope in the context of inclusive, intentional, inter-ability communities. Find out more about our resources, gatherings, and inter-ability communities at hopeheals.com. Follow us on Instagram @hopeheals.We want to hear your thoughts. Send us a text!Connect with me: Instagram Facebook YouTube Website Thanks for listening!

Joslynn's journey began with a profound lesson from her mother's courage, a choice to speak up that broke a legacy of silence and shaped a lifetime of advocacy. Starting as an 11-year-old volunteer in an adaptive soccer program, Joslynn's found community and purpose that ignited her career dedicated to disability services, challenging systems, and helping others find their voice.From navigating pushback in professional and personal spaces to transforming doubt into "speed bumps" rather than barriers, Joslynn's story is one of resilience, persistence, and purpose-driven work. She shares the powerful mindset of "Don't say no, say how," turning obstacles into opportunities to create real change.If you've ever felt held back by "no" or wondered how to keep pushing for what matters despite the odds, this episode offers a raw and inspiring perspective on advocacy, breaking cycles, and finding strength in vulnerability.Earth Monster is the storytelling podcast that uncovers the real stories and biggest ideas that shape our lives. Subscribe for more episodes that celebrate the messy, beautiful journey of being human.

An episode about a deceptively simple topic: restaurant seating.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

What does it take to turn one of the nation's largest disability communities into a Ramiro Alvarez political force? In Detroit, where more than 30% of residents live with a disability, grassroots organizing has led to a groundbreaking victory: $8.4 million in the city's 2025 budget is now dedicated to disability services. Join Pushing Limits this Friday as we continue our 2-part series on role model disability organizations. We talk with grassroots disability movement leader, Ramiro Alvarez, Communications Director at Detroit Disability Power. Listen in as we discuss how the organization built collective strength over eight years and won real change for the community. This episode is hosted by Adrienne Lauby and produced by Jacob Lesner-Buxton with editing assistance by Dominick Trevethan and Denny Daughters.   The post Disability Advocacy in the Motor City – Pushing Limits – August 29, 2025 appeared first on KPFA.

We all buy into at least one conspiracy theory. This one's mine.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

Send us a textIn this episode of The Different Ability® Podcast, I sit down with the incredible Kat Paz, a disability advocate with a heart for cheering others on. Kat shares her story of immigrating from the Philippines to San Francisco at just 16 years old, experiencing culture shock, and how her brother with special needs shaped her purpose in life. Together, Katey and Kat talk about community, advocacy, and celebrating the power of supporting others. Get ready for an uplifting and joy-filled conversation with someone who truly embodies what it means to advocate with love.Kat's BioKatrina "Kat" Paz is a leadership enthusiast, business owner, and now a bestselling author. Born in Manila, Philippines, to a professor and an entrepreneur, Kat values education and entrepreneurship. After earning a master's from Johns Hopkins School of Public Health, she entered the biotech and pharmaceutical industry, eventually managing over 30 individuals. Recently, Kat launched LeapGround, a venture focused on providing accessible digital marketing services to founders with disabilities.Connect with KatWebsiteFacebookLinkedInInstagramThe BookGet your copy of Trailblazing and Transforming: Success Stories of Entrepreneurs with Disabilities HERE! Stay in the loop with the new Different Ability® product I'll be launching!Sign Up Here!Shop new products here!Places you can reach me at:Website:https://kateyfortun.com/https://kateyfortun.com/podcastInstagram:https://www.instagram.com/kateyfortun/https://www.instagram.com/differentabilitypodcast/

I miss the days when my brain functioned like a well-oiled machine. These days it functions more like someone slipping in oil.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 ListenABLE podcast, hosts Angus and Dylan sit down with Sara Shams — a pharmacist, model, and disability advocate — to share her inspiring journey as a bilateral above-knee amputee living with the rare genetic condition tibial hemimelia. Sara opens up about her early life and multiple surgeries, how advances in prosthetics technology have shaped her independence, and the confidence she’s built through advocacy and representation in media. The conversation dives into cultural perspectives on disability, the impact of the Shift 20 initiative on increasing authentic representation, and how brands can move beyond tokenism to embrace true inclusion. From breaking into the modelling industry to launching consultancy work for accessible runways, Sara shares the importance of personal choice in mobility aids, resilience in the face of stigma, and the power of visibility in changing perceptions. What You’ll Learn: How prosthetic advancements are transforming independence and mobility. Why authentic representation matters for the disability community. The business and social impact of the Shift 20 initiative. How to address tokenism through education and cultural change. The role of confidence, resilience, and personal choice in disability advocacy. Get in contact with Sara: https://sarashams.au/ Connect on LinkedIn: https://www.linkedin.com/in/sarashams Watch the Full Episode with Captions Here: https://youtu.be/ux5keqFJjTM Recorded, edited and produced by Angus' Podcast Company: www.sessioninprogress.com.au Chapters:00:00 Introduction to the Podcast and Guests03:00 Sara Shams: A Journey Through Disability05:53 Understanding Tibial Hemimelia and Its Impact08:56 Surgical Journey and Early Life Experiences12:04 Evolution of Prosthetics and Technology15:01 Building Confidence and Embracing Disability17:54 Cultural Perspectives on Disability18:25 The Journey into Modeling21:37 Advocacy through Shift 20 Initiative22:42 Navigating Tokenism and Authentic Representation26:51 Launching her Consultancy30:16 The Balance of Representation and TokenismSee omnystudio.com/listener for privacy information.

There has rightfully been pushback on referring to Governor Greg Abbott as Governor "Hot Wheels." If we're going to mock political figures, we've got to have the integrity to do so without mocking a part of them beyond their control.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 candid and insightful conversation, host Kristin Walker sits down with Reverend Dr. Stephanie Holmes to explore her personal and professional journey in autism advocacy. From her daughter's early diagnosis to her family's multi-perspective book, Dr. Holmes shares how lived experience shaped her mission to support neurodivergent individuals, couples, and families—especially in faith-based communities. Together, they discuss the historic underdiagnosis of women on the spectrum, the nuances of masking, the need for inclusive education, and the often-overlooked intersections of autism, gender, and culture. This episode is a deep dive into breaking stereotypes, amplifying autistic voices, and creating genuine inclusion in schools, marriages, and communities.​Stephanie C. Holmes graduated from Campbell University summa cum laude with a Bachelor's degree in Psychology in 1994. She then completed her Master's in Counseling  summa cum laude through Liberty University  and further pursued licensing in  the state of NC which was obtained and held from 2001 through 2009. She was an LPC in good standing. Upon moving to Georgia, with a desire to reach more people through tele- counseling, she obtained other certifications to pursue her calling of working with marriage and families with special needs nationally and internationally.  Her highest held degree is an Ed.D from Abilene Christian University, where she graduated with distinction upon completing her dissertation, “Creating an Inclusive Climate for Students on the Autism Spectrum.”​Certifications and Training​Certified Master Life Coach through International Board of Christian Counselors (IBCC)Certified Mental Health Coach through American Association of Christian Counselors.Board Certified Christian Counselor through International Board of Certified Counselors (AACC)Board Certified through Georgia Board of Examiners for Georgia Christian Counselors and TherapistsCertified Autism Specialist through IBCCESNeurodiverse Couples Certification through AANENeurodiversity Trained and Certified through Neurodiversity Training InternationalOrdained through IAOGholmesasr.com

Disabled people may feel like we have to sacrifice quality services in order to have our accessibility requirements met and we simply shouldn't have to.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 Brain & Life Podcast, co-host Dr. Daniel Correa is joined by author, adaptive fashion model, and disability advocate Sarah Todd Hammer. Sarah Todd shares her experiences with Acute Flaccid Myelitis (AFM) from diagnosis to today, highlighting the diagnosis and treatment processes and how she has continued to follow her dreams throughout the years. Dr. Correa is then joined by Dr. Kiran Thakur, a neurologist and expert in infections that affect the brain and nervous system. Dr. Thakur is an associate professor of Neurology at Columbia University and has worked around the world studying how diseases like viruses can lead to serious neurologic conditions. Dr. Thakur explains what AFM is, the effects it can have, and what can be learned about how to care for patients with rare and life-changing neurologic conditions.   Additional Resources Sarah Todd Hammer Rising Measles Cases Raise Concerns About Serious Brain Complications Acute Flaccid Myelitis (AFM)   Other Brain & Life Podcast Episodes on Similar Topics How Disability Advocate Wesley Hamilton Became Empowered by Adversity Parenting and Writing While Disabled with Jessica Slice How Paula Carozzo is Redefining Disability and Advocating for Her Community We want to hear from you! Have a question or want to hear a topic featured on the Brain & Life Podcast? Record a voicemail at 612-928-6206 Email us at BLpodcast@brainandlife.org   Social Media: Sarah Todd Hammer @sarahtoddhammer; Dr. Kiran Thakur @columbiamed Guests: Hosts: Dr. Daniel Correa @neurodrcorrea; Dr. Katy Peters @KatyPetersMDPhD

If you can't be bothered to put your shopping cart away after your shopping trip, that tells me basically everything I need to know about you.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

Disabled artists don't need AI to create. Claiming AI is an "assistive tool" for disabled artists is just an attempt to obfuscate the fact that generative AI is theft.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

Lauren welcomes her guest Megan Mindy, a recent public health graduate from the University of Iowa. Megan shares her journey blending her passions for disability advocacy, inclusive recreation, and entrepreneurship. Her experiences include an internship at the University Center for Excellence in Developmental Disabilities, participation in the LEND program, and a study abroad trip to Cape Town exploring disability culture. Megan has also launched her own adaptive sports startup, Common Ground, to increase access and opportunities for athletes with disabilities. Her story highlights the power of combining personal passion, community engagement, and public health education to create real-world impact. A transcript of this episode is available at https://www.public-health.uiowa.edu/news-items/plugged-in-to-public-health-talking-disability-advocacy-inclusive-recreation-and-entrepreneurship-with-megan-mindy/ Have a question for our podcast crew or an idea for an episode? You can email them at CPH-GradAmbassador@uiowa.edu You can also support Plugged in to Public Health by sharing this episode and others with your friends, colleagues, and social networks. #publichealth #disabiltyadvocacy #inclusiverecreation

The global disability market represents a staggering $18 trillion dollars in spending power. And in this powerful episode, Tiffany Yu, founder of Diversability, TEDx speaker, and author of The Anti-Ableist Manifesto is sharing how she turned her own disability into a global movement for inclusion. After a car accident made her disabled and took her father's life, Tiffany eventually found the courage more than a decade later to share her story, helping others unlearn shame and embrace their own identities.You'll hear how Tiffany built Diversability from a college club into a thriving international community, why employers must rethink job descriptions and office norms to foster true accessibility, and how storytelling paired with data can radically shift public perception.If you want to build more inclusive communities, Tiffany's magnetic energy and practical wisdom will inspire you to see lived experience as a superpower rather than a limitation.Resources & LinksConnect with Tiffany on her website, order her book, The Anti-Ablelist Manifesto, and watch her TED talk, The Power of Exclusion.  This show is brought to you by iDonate. Your donation page is leaking donors, and iDonate's new pop-up donation form is here to fix that. See it in action. Launch the interactive demo here and experience how a well-timed form captures donors in the moment they care most. Let's Connect! Send a DM on Instagram or LinkedIn and let us know what you think of the show! My book, The Monthly Giving Mastermind, is here! Grab a copy here and learn my framework to build, grow, and sustain subscriptions for good. Want to book Dana as a speaker for your event? Click here!

What would you do if your greatest challenge became your greatest calling? For brothers Kyle and Brent Pease, the answer is racing—together. But what they've built goes far beyond the finish line. In this powerful episode, I sit down with Kyle and Brent Pease, co-founders of the Kyle Pease Foundation and Ironman finishers many times over, to talk about what it means to redefine possibility. What began as one race turned into a mission: to make endurance sports more inclusive, and to empower people with disabilities to find their own version of greatness. We dive into the early moments that sparked their journey, how they've now completed 150+ races together, and how their work through the foundation is transforming lives—not just through sport, but through employment, leadership, and connection. Kyle opens up about the physical toll of racing 16-hour days from a wheelchair, while Brent shares the emotional impact of being pushed—literally and figuratively—by his brother's unwavering drive. We talk about their unforgettable races at Kona and Boston, the birth of their inclusive employment program, and the moving story of how “five more feet” kept them going when everything inside told them to stop. At the heart of their message is a simple but transformative belief: endurance creates resilience, and everyone deserves to feel the power of crossing their own finish line.   Meet Our Guests: Kyle & Brent Pease  Brent and Kyle Pease are brothers, elite endurance athletes, and co-founders of The Kyle Pease Foundation, a nonprofit organization dedicated to promoting inclusion for individuals with disabilities in both sports and the workforce. Their story gained global recognition when they became the first push-assist brother team to complete the IRONMAN World Championship in Kona, Hawaii. Since then, they've competed in over 150 races together, becoming a symbol of what's possible when determination and brotherhood collide. Kyle, born with cerebral palsy, has shattered limitations and expectations. With a degree in Sports Management from Kennesaw State University, he not only races with Brent but also works part-time at Publix and Atlanta Braves games, spreading his message of resilience and inclusion. Through the Foundation, Kyle plays a key role in initiatives like adaptive sports equipment, inclusive employment, and scholarships, empowering others with disabilities to chase their goals. Brent, a Florida State University graduate and seasoned endurance coach, serves as the Foundation's Executive Director. His leadership has fueled programs like the Inclusive Employment Program, which helps individuals with disabilities secure meaningful work. Brent's athletic achievements, combined with his passion for advocacy, have helped raise over $10 million for the cause. Together, the Pease brothers continue to inspire through their racing, public speaking, and book, Beyond the Finish, which tells the story of their journey, their mission, and the power of relentless determination.   What You'll Learn in this Episode: How a single question sparked a life-changing partnership What it takes to complete an Ironman as a team when a wheelchair is involved, why inclusion in sport must go beyond labels and accommodations The moment Kyle realized his story could empower others How the Kyle Pease Foundation is creating jobs, purpose, and possibility The surprising power of “just five more feet” Why your struggles are not in the way—they are the way How real leadership is about showing up—for yourself and for others What Kona and Boston taught them about grace, grit, and growth   Resources & Links Kyle & Brent Pease Book: Beyond the Finish: A Story of Passion, Brotherhood and Relentless Determination Get a signed copy: Order through their site to receive Kyle's signature! Website: https://kylepeasefoundation.org/ Instagram: https://www.instagram.com/thekylepeasefoundation/ Facebook:https://www.facebook.com/TheKylePeaseFoundation LinkedIn: https://www.linkedin.com/company/kyle-pease-foundation Join the community, donate, or sign up to race: kylepeasefoundation.org   Ed Molitor LinkedIn: https://www.linkedin.com/in/themolitorgroup/ Website: https://www.themolitorgroup.com/

If you were hoping I wouldn't do another episode about the language surrounding disability, I have bad news for you. But, hope springs eternal!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 special episode of Right to Life Radio, John Gerardi and Jonathan Keller are joined by the insightful Kathryn Jean Lopez, senior fellow at the National Review Institute. The trio dives into the contentious legalization of physician-assisted suicide in New York, comparing it with similar legislation in California and discussing the chilling implications for vulnerable groups like the disabled. They also unpack the downsizing of Planned Parenthood, the ins and outs of the "One Big, Beautiful Bill" (OBBB), and what the future holds for pro-life legislation. Plus, Kathryn shares details about her must-read pro-life newsletter, The Lifeline.

In recognition of Disability Pride Month and the 35th Anniversary of the Americans with Disabilities Act, two CSD professionals share personal stories of disability advocacy.Angela Evenich—who has previously written about the influence of cerebral palsy on her career as a speech-language pathologist—discusses the people and ideas that have changed her perspective on disability.Then, audiologist Jasmine Simmons tells us about her book series on Usher syndrome. Simmons herself has Usher syndrome. And like Simmons, the protagonist of her first book, “Extraordinary Jordyn and Her Bionic Ears,” has a cochlear implant.Learn More:ASHA Voices: Creating ‘Ramps' to Communication Access in Health CareImagine True Inclusion: Defining the Social Model of DisabilityAn SLP Starts a Nonprofit to Provide Disability Support InternationallyFrom My Perspective/Opinion: SLP Views Ableism and Accessibility, Not Her Cerebral Palsy, as Real Career BarriersTranscript

Newsflash: Just because someone does something a disabled person doesn't like doesn't mean they're ableist.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

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!

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   —--------------------