Pushing Forward with Alycia | A Disability Podcast

Alycia Anderson

Pushing Forward with Alycia | A Disability Podcast Pushing Forward with Alycia is the weekly podcast that gives disability a voice and welcomes everyone—disabled people, allies, families, and inclusive employers—into a courageous, judgment‑free space to learn, ask questions, and advance access together. Launched June 29, 2023 and dropping new episodes every Thursday, host Alycia Anderson—disabled motivational speaker, DEI educator, entrepreneur, athlete, and storyteller—shares lived experience and amplifies voices across the global disability community. The show began as a safe, respectful space to talk honestly about difference, ableism, and belonging; that welcoming spirit remains its heartbeat today. What You’ll Hear From headline issues to everyday wins, we dig into DEI + disability, digital accessibility, workplace inclusion, disabling ableism, Disability Pride Month, intersectionality, airlines & disability discrimination, and so much more. If it shapes how disabled people live, learn, work, travel, play, create, love, and lead—we’re talking about it. Nearly 100 Episodes (and Counting!) In just two years we’ve published 98 full episodes (as of July 16, 2025) and are racing toward our 100th celebration. Recent conversations feature boundary‑breaking guests like Marsha Elle (bionic model, Billboard artist), Tiffany Yu (Diversability & The Anti‑Ableist Manifesto), Gigi Robinson (chronic illness creator & strategist), Kristen Anderson (global inclusive leadership champion), Isaac Harvey MBE (East London influencer & entrepreneur), and many more advocates, athletes, artists, policy shapers, siblings, caregivers, and allies you’ll love meeting. Who It’s For Whether you identify as disabled, are new to advocacy, support a disabled loved one, or lead teams striving to build a more inclusive workplace, you’ll leave each episode with insight, language, and actionable takeaways you can bring to classrooms, boardrooms, events, and everyday life. Our mission is to be a safe place to learn, share, ask “no wrong” questions, and transform awkwardness into connection. Listen & Support Follow, subscribe, share, rate, and review to help amplify disability inclusion. Sign up for release alerts, suggest a guest, and bring Alycia to speak or train your organization in disabling ableism. However you engage, you’re helping open hearts and clear paths for all of us. Open hearts, clear paths. Let’s go.

  1. 4d ago

    The World Is More Accessible Than You Think | Karen Morales on Disability and Travel

    What if the trip you thought was impossible was simply waiting for the right access? For many disabled travelers, dreaming about a destination comes with an immediate second thought: But can I actually go there? In Episode 154 of Pushing Forward with Alycia, Alycia Anderson sits down with Karen Morales, luxury travel advisor, speaker, wheelchair user, disability travel advocate, and leader within Fora Travel's accessibility initiative, for a conversation that may completely change the way you think about accessible travel. Karen lives with limb girdle muscular dystrophy and began using a wheelchair full time in 2020. But losing mobility did not mean losing her identity as a traveler. Instead, it pushed her to rethink what independence, adventure, and possibility could look like. And she went exploring. Japan. Morocco. Sicily. Costa Rica. France. Canada. Africa. Karen discovered that some of the destinations disabled travelers assume will be impossible can deliver extraordinary experiences when the right people, information, creativity, and hospitality come together. Her work is also proving something the travel industry cannot ignore. Fora's accessibility initiative has been associated with $75 million in accessible travel sales, showing that accessible hospitality is not merely about regulations or checking an ADA box. It represents a significant and underserved business opportunity. Karen's philosophy is refreshingly simple: Travel is travel. Hospitality is hospitality. Whether someone needs a roll in shower, a specific bed height, allergy accommodations, a medical refrigerator, sensory support, a service animal accommodation, or simply a different pillow, great hospitality begins by understanding what that traveler needs before they arrive. This conversation goes far beyond accessible hotel rooms. Alycia and Karen talk about accepting mobility devices, reclaiming independence, traveling with progressive disability, universal design, raising expectations, the power of lived experience, and why disabled people should not have to beg to participate in life's most beautiful experiences. And Karen leaves us with one invitation: Stop assuming the world is closed to you before you explore what might actually be possible. 🌎 Passport to Possibility: What We Explore ♿ Wheelchair Travel and Independence How Karen's wheelchair ultimately restored independence that declining mobility had taken away. 🌎 Accessible Travel Around the World Why destinations including Sicily, Morocco, Japan, and Canada may be far more possible than disabled travelers assume. 🏨 Accessibility as Hospitality Why access should be viewed as part of exceptional guest service rather than simply legal compliance. 💰 The Business Case for Accessibility How accessible travel became connected to $75 million in sales through Fora's initiative. ❤️ Leading With Heart How small acts of awareness can make disabled travelers feel genuinely welcomed. 🛏️ Accessible Hotel Design Roll in showers, reachable toiletries, mirrors, balconies, room configuration, bed heights, and the details hotels often overlook. 🧳 Planning Reduces Travel Anxiety Why photos, measurements, advance communication, and knowledgeable travel advisors can transform the experience. 🦽 Accepting a Mobility Device Karen's emotional journey from resisting wheelchair use to realizing the wheelchair gave her freedom back. 🧠 Lived Experience Matters Why advisors who understand disability firsthand can ask questions that technology alone cannot anticipate. 👨‍👩‍👧‍👦 Multigenerational Accessibility Disability access also benefits older adults, children, caregivers, people with allergies, chronic illness, sensory needs, and families. 🏖️ Adventure Without Assumptions Beach wheelchairs, adaptive zip lining, accessible safaris, glamping, hiking, and other experiences many disabled travelers may never have considered possible. 🤝 Assuming Best Intentions Karen's Pushing Forward Moment about meeting differences and barriers with curiosity, empathy, and an assumption of positive intent. ✈️ Your Accessible Travel Itinerary 00:00 Podcast Welcome 00:28 Meet Karen Morales 01:46 Why Travel Matters 02:57 Luxury Access Gap 04:37 Accessible Travel Market 05:53 Hospitality Not Compliance 07:26 Japan Hotel Done Right 10:55 Small Fixes Big Impact 14:00 Shower Design Reality 16:22 Culture of Inclusion Abroad 19:33 Sicily Beach Magic 21:20 Alycia Wants In 21:50 Accessible Transport Options 23:02 Morocco Accessibility Myths 24:49 Living With Progression 25:49 Wheelchairs And Independence 30:05 Fora Accessibility Initiative 34:26 Wheelchair Zip Lining 35:11 Accessible Canada Road Trip 37:54 How To Work With Karen 39:10 Assume Best Intentions 💬 Postcards Worth Keeping “I don't want people to feel like a burden. I don't want people to feel like they're begging for access.” ~ Karen Morales “Travel is travel, and travel should be inclusive of anyone.” ~ Karen Morales “We can usually find greater peace when we assume the best intentions.” ~ Karen Morales Key Takeaways Accessibility and luxury belong together. Disabled travelers should not have to sacrifice quality, beauty, service, or adventure to receive accommodations. Information itself is an accessibility feature. Photos, measurements, room details, shower configurations, and proactive communication reduce uncertainty before a traveler ever arrives. Mobility devices can expand freedom. Karen's wheelchair initially represented something she resisted, but eventually became the tool that restored independence. Accessible travel is a major market opportunity. Fora's initiative demonstrates meaningful consumer demand for better accessible travel planning and hospitality. Do not eliminate destinations based on assumptions. Karen's experiences in Morocco, Sicily, Japan, and elsewhere demonstrate that infrastructure tells only part of the accessibility story. Connect With Karen Morales Ready to stop wondering “Can I go?” and start asking “Where next?” Karen Morales combines extensive personal travel experience with the lived perspective of navigating the world as a wheelchair user. Through Joyward Travel and Fora Travel, she helps individuals and families plan trips around their actual needs, preferences, abilities, and dreams. Karen's Links Joyward Travel (https://www.gojoyward.com/)  Karen's Fora Travel Advisor Page (https://www.foratravel.com/advisor/karen-morales)  Instagram (https://www.instagram.com/gojoyward/)  LinkedIn (https://www.linkedin.com/in/karen-morales-157b412/z)  Fora Travel (https://www.foratravel.com/)  Connect with Alycia Anderson Visit ⁠⁠AlyciaAnderson.com⁠⁠ to learn more about Alycia’s keynotes, disability inclusion programs, accessibility resources, and consulting services. Explore more episodes of ⁠⁠Pushing Forward with Alycia⁠⁠. Pushing Forward is how we roll. Learn more about your ad choices. Visit megaphone.fm/adchoices

    The World Is More Accessible Than You Think | Karen Morales on Disability and Travel
  2. Aug 6

    Turning Disability Stigma Into Love and Inclusion with Cynthia Bauer

    There are an estimated 580 million children with disabilities worldwide, and approximately 80 percent of people with disabilities live in developing nations. Too many children are still hidden, neglected, denied access to inclusive education and equitable healthcare, or excluded from community life because of fear, misinformation, and deeply rooted disability stigma. In this powerful episode of Pushing Forward with Alycia, disability inclusion advocate and host Alycia Anderson welcomes Cynthia Bauer, US CEO and cofounder of Kupenda for the Children, for a conversation about transforming harmful disability beliefs into dignity, opportunity, and lasting inclusion. Kupenda trains thousands of families, young people, faith leaders, educators, healthcare providers, and government leaders to become disability advocates. These community advocates help children with disabilities gain access to education, medical care, protection, and meaningful inclusion in family and community life. Cynthia shares how her unexpected journey into advocacy began while she was studying wildlife biology in Kenya. Born without her left hand, Cynthia learned that harmful cultural beliefs about disability could have placed her own life at risk had she been born in a different community. That realization changed the direction of her life and eventually led her and Kenyan special education teacher Leonard Mbonani to create Kupenda. Together, Alycia and Cynthia explore why societal perceptions and attitudinal barriers often create greater limitations than physical disabilities themselves. They discuss the damage caused by faith healing claims, misinformation, segregated education, inaccessible environments, and charitable approaches that treat disabled people as objects rather than leaders. Cynthia also explains why Kupenda does not enter communities by condemning local leaders or simply telling people they are wrong. Instead, its community led disability inclusion workshops encourage honest discussion, respectful questioning, lived experience, and practical education. Pastors, traditional healers, parents, disabled advocates, and government leaders are invited to examine the consequences of their beliefs and discover better ways to support disabled children and their families. At the center of the conversation is a simple but powerful message: people with disabilities are fully human. They deserve the same love, freedom, opportunity, dignity, equality, and full participation in community life as everyone else. The word Kupenda means “to love” in Swahili. Cynthia describes it not simply as an emotion, but as a constant action of loving. That meaning reflects the organization’s mission to replace fear and exclusion with understanding, advocacy, dignity, and belonging. Love in Action: What We Explore in This Episode 🌍 The global realities facing children with disabilities 💛 Why Kupenda means a constant action of loving ♿ How disability stigma can become more limiting than disability itself 🧠 The difference between physical barriers and societal perceptions 📖 Why lived experience and storytelling change minds 🙏 The role faith leaders can play in either reinforcing or dismantling stigma 🗣️ How respectful conversations can transform harmful beliefs 👧 Why inclusive childhood experiences create more accepting adults 🏫 The damage caused when adults separate disabled and nondisabled children 🤝 Why disability can unite people across cultural differences 🌱 How community led advocacy creates lasting change 💼 Why disability must be included in education, healthcare, gender equity, poverty reduction, and global development 💰 Why disability funding must move beyond charity and medical models ✨ How personal challenges can become tools for helping others Rolling Through the Conversation 00:00 Podcast Welcome 00:29 Disability By Numbers 01:03 Meet Cynthia Bauer 02:57 From Wildlife To Advocacy 06:57 Stigma And Faith Healing 08:56 Workshops Changing Minds 13:45 Disability Across Cultures 18:15 Kids Lead Inclusion 20:55 One Day Workshop Model 22:45 Defining Disability 25:53 Why Kupenda Means Love 27:28 How To Support Kupenda 31:59 Funding And Human Rights 33:53 Pushing Forward Moment 35:50 Closing Thanks Words That Keep Pushing Us Forward “The disability unites us more than the cultures divide us.” ~ Cynthia Bauer “At the end of the day, what does every person want but to be loved and included?” ~ Cynthia Bauer CONNECT WITH CYNTHIA BAUER AND KUPENDA Learn more about Cynthia Bauer and the work Kupenda is doing to transform disability stigma into dignity, opportunity, and inclusion. About Cynthia Bauer Cynthia Bauer is the US CEO and cofounder of Kupenda for the Children. Born without her left hand, Cynthia first traveled to Kenya as a wildlife biology student. Her encounters with disabled people who faced extreme stigma and exclusion inspired her to help create an organization focused on disability justice and community transformation. For more than 25 years, Cynthia has worked alongside local leaders, disabled advocates, families, educators, faith communities, and nonprofit organizations to reduce disability stigma and develop sustainable, locally led solutions. Kupenda’s workshop model is now being replicated by organizations in multiple communities around the world. Kupenda for the Children https://kupenda.org/ Cynthia Bauer and Kupenda Leadership https://kupenda.org/our-team/our-team/ The Story of Kupenda https://kupenda.org/our-story/ Donate or Support a Child https://give.kupenda.org/ Kupenda Resources https://kupenda.org/resources/ Unlikely Gifts Podcast https://kupenda.org/podcast/ Cynthia Bauer on LinkedIn https://www.linkedin.com/in/cynthia-bauer-5246463/ Email kupenda@kupenda.org Kupenda also offers opportunities to volunteer, host events, arrange documentary screenings, invite speakers, and access disability advocacy resources. Connect with Alycia Anderson Visit ⁠AlyciaAnderson.com⁠ to learn more about Alycia’s keynotes, disability inclusion programs, accessibility resources, and consulting services. Explore more episodes of ⁠Pushing Forward with Alycia⁠. Pushing Forward is how we roll. Learn more about your ad choices. Visit megaphone.fm/adchoices

    Turning Disability Stigma Into Love and Inclusion with Cynthia Bauer
  3. Jul 30

    Breaking Free from Expectations with Spencer West

    What happens when you stop trying to become the person the world expects and finally begin choosing who you want to be? In Episode 152 of Pushing Forward with Alycia, host Alycia Anderson welcomes global speaker, bestselling author, disability advocate, activist, and content creator Spencer West for a powerful conversation about disability identity, autonomy, interdependence, and breaking free from expectations. Spencer is the author of Breaking Free: Stop Following Expectations and Start Following Yourself, a new book that invites readers to question the expectations shaping their lives and begin choosing a more authentic path. Born with a genetic condition that prevented the muscles in his legs from functioning, Spencer underwent surgeries that resulted in the amputation of both legs just below his pelvis. Growing up, he was repeatedly told that he was “just like everyone else” and that every child wanted to walk. But prosthetic legs were not the best mobility choice for Spencer. By sixth grade, his parents and therapist gave him the opportunity to decide for himself how he wanted to navigate the world. Choosing to stop using prosthetic legs became one of his earliest lessons in bodily autonomy. “The moment I realized I could choose how I wanted to navigate the world, everything started to change.” That decision did not eliminate the pressure to fit in. Spencer shares how he continued confronting internalized ableism, social expectations, and the confusing message that disability should be ignored rather than embraced as part of his identity. The Life Changing Power of Autonomy Spencer and Alycia discuss why disabled children deserve the opportunity to participate in decisions about their own bodies, mobility, healthcare, and lives. Spencer credits his parents with giving him choices instead of assuming they always knew what was best for him. Looking back, he recognizes that this early experience helped him understand that he could make other meaningful choices too. For parents, educators, medical professionals, and leaders, his story offers an important reminder: supporting disabled people does not mean controlling every decision. It means creating space for autonomy, self discovery, and informed choice. Climbing Kilimanjaro and Redefining Help Spencer also shares the story behind climbing Mount Kilimanjaro. He was not motivated by a desire to prove that “anything is possible.” In fact, Spencer openly admits that he does not like camping and had never dreamed of becoming a mountain climber. The climb became part of a larger campaign called Redefine Possible, which raised more than its original $500,000 goal for clean water initiatives in East Africa. Spencer trained for a year alongside two of his closest friends. Although the original plan was to use both his wheelchair and his hands to climb, the terrain required him to navigate much more of the mountain on his hands than expected. Throughout the expedition, Spencer relied on his friends for physical support. But on summit day, both friends became sick from the altitude. Suddenly, the person who assumed he would need the most assistance became the person helping them continue. Spencer could not physically carry his friends, but he could stay beside them, encourage them, and keep moving forward with them. That experience transformed how he viewed strength. “We all need help. We all need to ask for help, and we all need to offer help.” Rather than celebrating the myth of the self made person, Spencer encourages people to embrace interdependence, the understanding that every person depends on support, relationships, community, and collaboration. Moving Beyond Inspiration Porn Spencer and Alycia examine the harmful narratives that often surround disabled people who accomplish highly visible goals. Spencer never wanted his Kilimanjaro climb reduced to a message suggesting that if a disabled person can climb a mountain, everyone should be able to overcome every barrier. That framing ignores systemic ableism, access needs, privilege, support, and the reality that every disabled person has a different body and experience. Spencer shares how disability justice advocate Naomi Ortiz challenged him to reconsider the way he talked about the climb. The true story was not that he overcame disability alone. It was that he reached the summit through community and interdependence. That conversation led Spencer to study disability history, disability justice, and the advocates who have shaped the movement. Today, much of his content reflects what he continues to learn and unlearn in real time. What Does It Mean to Break Free? Spencer’s new book, Breaking Free: Stop Following Expectations and Start Following Yourself, examines the expectations people absorb from the moment they enter the world. For Spencer, those expectations included: Do not think of yourself as disabled Overcome your disability Use prosthetic legs Follow a traditional career path Marry a woman Measure success through productivity Live according to society’s definition of a successful life As a disabled gay man growing up in a conservative Wyoming community, Spencer gradually realized that many of those expectations did not reflect who he was or what he wanted. Breaking free became the process of identifying which expectations belonged to him and which ones had been placed upon him by others. “My value and success are not tied up in what my body can produce.” Spencer explains that breaking free does not always require climbing a mountain or completely changing your career. It can begin with one small decision, such as leaving an unhealthy relationship, exploring a new passion, moving to another city, or making room for something that brings joy. Disability as Identity During a volunteer trip to Kenya, Spencer spoke with students about his disability. A young girl told him she had not realized that the loss of limbs could happen to a white person too. Her observation sparked a major realization. Until that moment, Spencer had viewed disability primarily as something that happened to him. He had not yet embraced it as part of his identity. That experience helped him begin connecting disability with the other layers of who he is, including being queer, a speaker, a creator, and an advocate. Spencer and Alycia reflect on how long it can take to fully embrace disability identity after growing up in environments that treated disability as something negative, shameful, or separate from the self. A Book Designed to Become a Tool Breaking Free is more than a memoir. Spencer designed the book as a practical guide for readers who are questioning the expectations shaping their lives. Each chapter includes exercises, reflection questions, key concepts, and opportunities for readers to begin their own process of change. The book also gives Spencer an opportunity to share parts of his life that he had not discussed publicly before, including the pressure he experienced to hide his queer identity while working within an organization concerned about conservative donors and religious partners. After years of advocacy from Spencer, queer colleagues, and allies, he eventually shared his coming out story publicly on June 26, 2015, the day marriage equality became law across the United States. For Spencer, that moment represented years of persistence, truth telling, and breaking free. Spencer West’s North Star Today, Spencer continues speaking, creating digital content, and helping organizations understand the value of hiring disabled talent. His work challenges myths about disabled employees and highlights the unnecessary ableism many disabled people face while trying to find meaningful employment. His current North Star is clear: get Breaking Free into the hands of people who need permission to question expectations, embrace their identities, and begin choosing themselves. In This Episode Why bodily autonomy matters for disabled children and adults Spencer’s decision to stop using prosthetic legs Unlearning internalized ableism The deeper story behind climbing Mount Kilimanjaro Why no one is truly self made Interdependence and the courage to ask for help How inspiration porn harms disabled people Learning from disability justice advocates Disability and queer identity Breaking free from society’s expectations Separating personal value from productivity Why Spencer wrote Breaking Free Disability inclusion and employment Memorable Quotes from Spencer West “The moment I realized I could choose how I wanted to navigate the world, everything started to change.” “The story was not that I reached the top alone. The story was interdependence.” The Pushing Forward Moment “Maybe our job is not to become anything. Maybe our job is to unbecome all the things that do not belong to us so we can become the person we were meant to be.” Spencer explains that this idea, inspired by a passage associated with Paulo Coelho’s The Alchemist, became the guiding thesis behind Breaking Free. Connect with Spencer West Visit Spencer2TheWest.com to learn more about Spencer, book him to speak, and find his new book. Follow Spencer on Instagram, TikTok, and YouTube at @spencer2thewest. Book: Breaking Free: Stop Following Expectations and Start Following Yourself Available wherever books are sold. Connect with Alycia Anderson Visit AlyciaAnderson.com to learn more about Alycia’s keynotes, disability inclusion programs, accessibility resources, and consulting services. Explore more episodes of Pushing Forward with Alycia. Pushing Forward is how we roll. Learn more about your ad choices. Visit megaphone.fm/adchoices

  4. Jul 23

    Rare Disability, Powerful Sisterhood | Karen Tamley

    What happens when you finally meet someone who understands how your body works? For Alycia Anderson and Karen Tamley, a LinkedIn introduction became the beginning of a powerful disability sisterhood. Both women were born with sacral agenesis, a rare congenital disability affecting the lower spine. They grew up using wheelchairs during a time when disabled children were routinely underestimated, accessibility was rare, and doctors placed devastating limitations on their futures. Then they met and immediately began comparing notes: “Wait, your body does that? Mine does too.” In Episode 151 of Pushing Forward with Alycia, Karen Tamley, President and CEO of Access Living, joins Alycia for an honest conversation about rare disability, peer support, leadership, aging, Disability Pride, and the urgent fight to protect disability rights. Finding Someone Who Understands Karen did not meet another person with sacral agenesis until her twenties. Before social media, finding others with the same disability was incredibly difficult. Meeting Alycia gave both women a rare opportunity to talk openly about their bodies, mobility, health, childhoods, and aging without having to explain every detail first. Karen describes that connection as a security blanket and safety net. Their friendship reflects the importance of peer support within the independent living movement. Disabled people hold knowledge that cannot always be found in medical offices or textbooks, and that lived experience can help others navigate healthcare, access, identity, and everyday life. Growing Up Before Accessibility Alycia and Karen remember life before the Americans with Disabilities Act. They recall inaccessible buses, oversized wheelchairs, buildings with stairs, restaurants without accessible bathrooms, and being carried into spaces. Karen shares that her mother carried her up four stairs every morning to reach a summer job in an inaccessible building. She also remembers putting flip flops on her hands so she could crawl across public restroom floors. Alycia had done the same thing. Their stories reveal how exclusion becomes normalized when disabled people are not protected by enforceable civil rights. Community Living Is a Disability Right Karen explains the importance of the 1999 Olmstead decision, which affirmed that unnecessary institutionalization and segregation can be discrimination under the Americans with Disabilities Act. The decision helped establish that disabled people have the right to receive services and live within their communities. Through Access Living and partner organizations, disabled people are supported as they transition from nursing facilities and institutions into their own homes. Karen warns that Medicaid reductions, weakened enforcement, and renewed conversations about institutionalization threaten decades of progress. Disabled people are asking for the right to live in their own homes, make decisions about their lives, and participate fully in their communities. Advocacy Belongs to Everyone Karen reminds listeners that advocacy is not limited to policy experts. People can make a difference by learning from trusted disability led organizations, sharing accurate information, contacting elected officials, submitting public comments, telling personal stories, amplifying disabled advocates, and connecting with a local Center for Independent Living. Her message is clear: Do not assume your voice will not be heard. Speak up anyway. Leadership Begins in the Deep End Karen credits her parents and mentors with encouraging her to take risks. Her mother often said they were going to throw Karen into the deep end of the pool and let her figure out how to swim. That mindset followed her throughout her career. Mentors including Judy Heumann, Ed Roberts, Wade Blank, and Marca Bristo recognized Karen’s potential and placed her in leadership roles before she always felt ready. Karen later served as Commissioner of the Chicago Mayor’s Office for People with Disabilities, was appointed to the U.S. Access Board, and became President and CEO of Access Living. Her journey demonstrates the power of leaders who believe in someone before that person fully believes in themselves. Disability Pride and Aging For Karen, Disability Pride means community, visibility, self worth, and being okay with who we are. It does not mean loving every part of disability every day. Pride can exist alongside pain, fear, frustration, internalized ableism, and uncertainty. Alycia and Karen also discuss the realities of aging with a rare disability, including concerns about mobility, transfers, travel, health, and future independence. Both women were given frightening medical predictions as children. Decades later, they are still here, leading, traveling, advocating, creating community, and celebrating every year they were told they might never have. Aging with disability can be uncertain. It is also a privilege. You Deserve to Be in the Space Karen’s Pushing Forward moment is a challenge to step outside your comfort zone. Attend the event. Accept the opportunity. Enter the room, even when you do not know anyone. Leadership does not eliminate fear or imposter syndrome. You deserve to be there. You deserve to be in that space. Two Women, One Rare Disability, and a Movement to Protect 🧬 Rare disability connection: Discovering someone else who lives with sacral agenesis 🤝 Disability sisterhood: The emotional and practical value of finding someone who understands ♿ Peer support: Why lived experience is a core part of independent living 🚌 Life before the ADA: Growing up without accessible buses, bathrooms, buildings, and mobility equipment 🚻 Normalized inaccessibility: Crawling, being carried, and adapting to spaces that excluded disabled people ⚖️ Disability civil rights: Protecting the laws and legal decisions that support integration and access 🏠 Community living: The right of disabled people to live outside institutions 💰 Medicaid and support services: How funding decisions affect independence and personal choice 📣 Everyday advocacy: Public comments, storytelling, education, organizing, and contacting representatives 👩‍💼 Disabled women in leadership: Karen’s path from advocacy roles to executive leadership 🔥 Mentorship: Being encouraged to enter roles before feeling completely ready 🎉 Disability Pride: Visibility, community, self worth, and accepting the full reality of disability 🧓 Aging with disability: Facing uncertainty while celebrating the privilege of growing older 💡 Imposter syndrome: Claiming your place even when confidence has not caught up yet From Rare Disability Sisterhood to Disability Rights Action TIMESTAMPS Words That Demand Visibility, Action, and Pride “There’s an inherent value in people with disabilities connecting with individuals with disabilities and sharing those lived experiences.” Karen Tamley “We have seen life before we had any rights.” Karen Tamley “Institutionalization and segregation is a form of discrimination.” Karen Tamley CONNECT WITH KAREN TAMLEY Stay Informed. Get Involved. Protect Disability Rights. Karen Tamley is President and CEO of Access Living, a Chicago based Center for Independent Living led by and for people with disabilities. ♿ ⁠Learn more about Karen Tamley⁠ 🏠 ⁠Visit Access Living⁠ 📣 ⁠Subscribe to the Access Living Advocacy Newsletter⁠ 💗 ⁠Support Access Living’s work⁠ 🤝 ⁠Get involved with Access Living⁠ 📍 ⁠Find a Center for Independent Living near you⁠ Connect with Alycia 🌐 Website: ⁠⁠https://alyciaanderson.com/⁠⁠ 🎙️ Podcast: ⁠⁠https://alyciaanderson.com/podcast⁠⁠ 💼 LinkedIn: ⁠⁠https://www.linkedin.com/in/alyciaanderson/⁠⁠ 📸 Instagram: ⁠⁠https://www.instagram.com/alyciaanderson/⁠⁠ About Pushing Forward with Alycia Pushing Forward with Alycia gives disability a voice through conversations about accessibility, inclusion, ambition, resilience, leadership, advocacy, and creating a more inclusive world for all people. Subscribe, like, share, and send this episode to someone who needs the reminder that there is no finish line when it comes to possibility, purpose, and pushing forward. Learn more about your ad choices. Visit megaphone.fm/adchoices

    Rare Disability, Powerful Sisterhood | Karen Tamley
  5. Jul 16

    No Finish Line: IndyCar Champion Sam Schmidt on Life After Paralysis

    “If you do nothing, you will get nothing.” Former IndyCar champion Sam Schmidt joins host Alycia Anderson for a powerful conversation about spinal cord injury recovery, quadriplegia, adaptive technology, disability advocacy, neurorehabilitation, resilience, and life after paralysis. After a 180-mile-per-hour crash changed his life in an instant, Sam transformed an unimaginable diagnosis into a mission rooted in recovery, innovation, and purpose. “If you don’t try, you won’t know.” Sam shares how he went from winning his first IndyCar race in 1999 to surviving a devastating high-level spinal cord injury and waking up dependent on a ventilator. When doctors predicted a short life in a nursing home, his family refused to accept that prognosis. Their relentless advocacy connected Sam with intensive spinal cord injury rehabilitation that helped him breathe independently, rebuild his health, and begin creating a future with no finish line. Two important themes emerge from Sam’s story: never accept one person’s prognosis as the final answer, and learn how to advocate for the rehabilitation, equipment, and healthcare support you need. Sam and Alycia explore the realities of insurance advocacy, accessible healthcare, caregiver support, mental health, aging with disability, and long-term spinal cord injury rehabilitation. Sam explains how he negotiated for the equipment, therapy, and resources that supported his independence while challenging a healthcare system that too often limits recovery before it has truly begun. “Racing is my passion. DRIVEN Neuro is my purpose.” The conversation also explores Sam’s memoir, No Finish Line: A Racer’s Journey of Passion, Perseverance, and Purpose, his championship-winning racing career, and the growth of DRIVEN Neuro, a nonprofit expanding access to activity-based neurorecovery, adaptive fitness, neurological rehabilitation, wellness programs, and disability community support for people living with spinal cord injuries and other neurological conditions. Sam’s story is more than a comeback. It is a call to action about self-advocacy, perseverance, accessible innovation, teamwork, and finding purpose after a life-changing injury. As Sam reminds us, progress may look different for every person, but possibility begins when we choose to take action. Racing, Recovery, Advocacy, and Purpose: The Big Takeaways from Sam Schmidt 🏁 Growing up in a family built around racing and competition 🏆 Achieving a lifelong dream with an IndyCar victory ♿ Adjusting to life after a high-level spinal cord injury 🫁 Fighting to recover independent breathing after ventilator dependence ❤️ The power of family advocacy after a life-changing diagnosis 🏥 Challenging medical assumptions and seeking additional opinions 📣 Learning to advocate for more time, care, equipment, and rehabilitation 💵 Understanding the economics behind insurance decisions 🧠 Supporting mental health alongside physical neurorecovery 💪 Why activity-based rehabilitation can remain important long after discharge 👨‍👩‍👧‍👦 Recognizing how spinal cord injury affects the entire family 🤝 Relying on caregivers, colleagues, clinicians, and community 🏎️ Moving from professional driver to championship-winning team owner 📖 Finding meaning in Sam’s memoir, No Finish Line 🔥 Understanding the difference between passion and purpose 🧑‍🦽 Aging with quadriplegia and protecting long-term health 🚗 Using adaptive and semi-autonomous technology to drive again ⚙️ Creating customized solutions that help disabled people return to what they love 🌱 Expanding affordable access to neurorecovery and adaptive wellness ✨ Making the most of life without waiting for perfect circumstances Unforgettable Quotes from Sam Schmidt “It’s whatever it takes to get you out of bed. That’s what you’ve got to do.” ~ Sam Schmidt “I’ve accomplished so much more the last 26 years being paralyzed than the previous 35 because I learned to rely on other people.” ~ Sam Schmidt Where to Listen: Sam Schmidt’s Most Powerful Moments 00:00 Podcast Welcome 00:25 Meet Sam Schmidt 02:04 Racing Roots and Dreams 03:37 IndyCar Victory in Vegas 05:33 Crash and Diagnosis 07:16 Finding the Right Rehab 09:42 Advocacy and Insurance Hacks 15:34 Family Resilience Lessons 17:37 Disability Pride Invite 18:12 Work Ethic and Recovery 20:01 Aging With Disability 22:37 No Finish Line Book 24:07 Driven Neuro Mission 27:56 Purpose Over Passion 32:25 How to Get Involved 34:20 Future Tech and Mobility 35:12 Driving and Adventure Again 36:43 Make Schmidt Happen 37:31 Final Thanks and Wrap Connect with Sam Schmidt Sam’s official website shares more about his racing career, memoir, speaking, adaptive technology, and work with DRIVEN Neuro. DRIVEN Neuro serves people living with spinal cord injuries and other neurological conditions through neurorecovery, adaptive wellness, research, resources, and community support. 🌐 Sam Schmidt’s Website: https://www.samschmidt.com/ 📖 Buy No Finish Line: A Racer’s Journey of Passion, Perseverance, and Purpose: https://www.simonandschuster.com/books/No-Finish-Line/Sam-Schmidt/9798895151617 🧠 Learn More About DRIVEN Neuro: https://drivenneuro.org/ 💛 Support DRIVEN Neuro: https://drivenneuro.org/ Connect with Alycia 🌐 Website: https://alyciaanderson.com/ 🎙️ Podcast: https://alyciaanderson.com/podcast 💼 LinkedIn: https://www.linkedin.com/in/alyciaanderson/ 📸 Instagram: https://www.instagram.com/alyciaanderson/ About Pushing Forward with Alycia Pushing Forward with Alycia gives disability a voice through conversations about accessibility, inclusion, ambition, resilience, leadership, advocacy, and creating a more inclusive world for all people. Subscribe, like, share, and send this episode to someone who needs the reminder that there is no finish line when it comes to possibility, purpose, and pushing forward. Learn more about your ad choices. Visit megaphone.fm/adchoices

    No Finish Line: IndyCar Champion Sam Schmidt on Life After Paralysis
  6. Jul 9

    Disability Pride, Digital Accessibility & the Power of “Why Not Me?” with Jessica Lopez

    Host Alycia Anderson welcomes Jessica Lopez, a disability rights advocate, keynote speaker, marketing strategist, and digital accessibility consultant working at the intersection of inclusive marketing, brand strategy, disability inclusion, accessible technology, and corporate accessibility. A recent Arizona State University graduate and Obama-Chesky Voyager Scholar, Jessica brings lived experience, business insight, and bold advocacy to conversations about accessible education, disability pride, inclusive hiring, digital accessibility, SEO, workplace inclusion, and why building accessibility from the start creates stronger brands, better customer experiences, and measurable business impact.  Jessica shares her lived experience as a woman born without hands and feet, a hearing aid user, and someone who later developed a chronic illness that changed the course of her education. From growing up in performing arts school, riding horses through adaptive recreation, and learning confidence on stage, to navigating inaccessible education systems and eventually graduating after gaining access to online learning, Jessica’s story is a powerful reminder that disabled people are not limited by their bodies, but by systems that fail to adapt. In this episode, Alycia and Jessica explore disability pride, accessible education, corporate inclusion, digital accessibility, inclusive marketing, career confidence, the ROI of accessibility, and what happens when companies stop assuming and start asking disabled people what they need. Confidence, Access, Advocacy, and “Why Not Me?”: The Big Takeaways from Jessica Lopez ♿ Disability identity, pride, and being born without hands and feet 🎤 Performing arts, confidence, and learning to take up space 🐎 Adaptive horseback riding as freedom, movement, and possibility 🦻 Navigating hearing loss, hearing aids, and visible disability 🏫 Inclusive education, school accommodations, and the power of the right support 💻 Online learning as accessibility, not convenience ⚖️ Systemic barriers in education and why access changes life trajectories 🌎 Travel, fellowships, and expanding what disabled ambition can look like 💼 Disability rights advocacy as a career path 🏢 Corporate accessibility, inclusive hiring, and leadership representation📲 Digital accessibility, accessible websites, alt text, SEO, and ROI 📣 Inclusive marketing and why disability must be built into brand strategy 👗 Accessible fashion, style, independence, and showing up polished 💛 Confidence for young disabled women chasing big dreams ✨ “Why not me?” as a mindset for opportunities, scholarships, speaking, and leadership 📈 Accessibility as a business advantage, not an extra cost 🤝 The power of asking disabled people directly what works for them Unforgettable Quotes from Jessica Lopez “My body was not the reason why I wasn’t able to do the things that I was hoping to do. It was really a result of a systemic barrier.” ~ Jessica Lopez “I don’t feel like I’m missing anything. All of my limbs are the way they are.” ~ Jessica Lopez “Accessibility is a bunch of small practices and small little things, and they add up to a massive turnaround on a big scale.” ~ Jessica Lopez Where to Listen: Jessica Lopez’s Most Powerful Moments 00:00 Podcast Welcome 00:25 Meet Jessica Lopez 02:55 Horses And Freedom 06:44 Born Different Early Life 07:43 Performing Arts Confidence 13:00 Aides And Accommodations 14:16 Prosthetics And Identity 16:35 Chronic Illness School Barriers 19:53 Disability Pride Keynote Invite 21:34 Advocacy Career Path 23:31 How Corporations Can Partner 26:35 Accessibility ROI In Marketing 29:25 Style And Stage Presence 31:19 Advice Why Not Me 35:16 Accessibility In 2026 37:23 Pushing Forward Moment 38:27 Closing Thanks And Subscribe Connect with Jessica Lopez 🌐 Website: https://jessical.me 💼 LinkedIn: https://www.linkedin.com/in/realjessl 📸 Instagram: https://www.instagram.com/realjessl 𝕏  Twitter/X: https://x.com/RealJessL 📘 Facebook: https://www.facebook.com/RealJessL  Connect with Alycia 🌐 Website: https://alyciaanderson.com/ 🎙️ Podcast: https://alyciaanderson.com/podcast 💼 LinkedIn: https://www.linkedin.com/in/alyciaanderson/ 📸 Instagram: https://www.instagram.com/alyciaanderson/ About Pushing Forward with Alycia Pushing Forward with Alycia gives disability a voice through conversations about accessibility, inclusion, ambition, resilience, leadership, and creating a more inclusive world for all people. Subscribe, like, and share to help push the conversation forward. Learn more about your ad choices. Visit megaphone.fm/adchoices

    Disability Pride, Digital Accessibility & the Power of “Why Not Me?” with Jessica Lopez
  7. Jul 2

    Jay & Pamela: Disability Love, Reality TV & Becoming Unapologetically Seen on TLC

    Host Alycia welcomes Jay and Pamela, stars of TLC’s GLAAD nominated series Jay & Pamela, returning June 30 for season two, and discusses their dual disability relationship as full time wheelchair users with osteogenesis imperfecta type III. They reflect on Pamela’s quote about reaching dreams alongside the one you love, describe personal and relationship growth from being on TV, and explain how they set boundaries around sharing intimate topics like access, sex, marriage, and fears. Jay addresses misconceptions about two wheelchair users as partners and the dehumanization of disabled people, while both emphasize disability representation in fashion, travel, and everyday life, including a New York runway. Jay shares his work in music production, voice acting, modeling, and neurodivergence through autism and ADHD. They outline OI’s impacts and share Disability Pride mantras about self worth and not letting the world define you. Love, Access, Fashion, and Pride: The Big Takeaways from Jay & Pamela ⭐ Disability representation on reality TV ❤️ Disabled love, marriage, and partnership ♿ Dual disability relationships and shared lived experience 🎬 TLC’s role in expanding disability visibility 🌈 Disability Pride and unapologetic self acceptance 💬 Breaking assumptions about intimacy, dating, and disabled relationships 🏡 Independent living, accessibility, and building a life together 👗 Adaptive fashion, modeling, and body confidence 📺 Vulnerability, boundaries, and sharing real life on camera 🦴 Understanding osteogenesis imperfecta and rare disability experiences 🚗 Accessible transportation and the need for inclusive mobility options 🏢 Universal design, accessible housing, and beauty beyond ADA minimums ✨ Dreaming bigger than the world expects 🧠 Neurodivergence, confidence, and navigating life authentically 💛 Self worth beyond achievement or external validation Unforgettable Quotes from TLC’s Jay & Pamela  “Your value is not by the things that you do. You have value just because you are you.” ~ Jay Thomas Manuel “Don’t let the world identify you.”  ~ Pamela Chavez Manuel Where to Listen: Jay & Pamela’s Most Powerful Moments  00:00 Podcast Welcome 00:37 Meet Jay and Pamela 02:12 Dreams and Love Quote 04:31 Season Two Growth 06:53 Vulnerability and Impact 08:44 Sharing Boundaries 11:17 Dual Disability Bias 17:23 New York Runway Moment 20:09 Body Confidence Breakthroughs 21:39 Jay Creative Mission 23:24 Asking for Help 25:47 Overthinking And Neurodivergence 26:49 Explaining Osteogenesis Imperfecta 28:39 Surgeries Hearing And Health Risks 30:09 Season Two Highlights And Pride 32:12 Hopes For Unity And Accessibility 35:48 Future Dreams Modeling Acting Brands 40:40 Big Asks Vans And Accessible Housing 42:17 Disability Pride Mantras 46:51 Final Thanks And Where To Watch  Connect with Jay & Pamela  Jay & Pamela on TLC.com | Jay & Pamela Season 2 Official Trailer | Jay on Instagram | Pamela on Instagram | TLC on Instagram Connect with Alycia 🌐 Website: ⁠⁠https://alyciaanderson.com/⁠⁠ 🎙️ Podcast: ⁠⁠https://alyciaanderson.com/podcast⁠⁠ 💼 LinkedIn: ⁠⁠https://www.linkedin.com/in/alyciaanderson/⁠⁠ 📸 Instagram:⁠⁠ https://www.instagram.com/alyciaanderson/⁠⁠ Pushing Forward with Alycia gives disability a voice through conversations about accessibility, inclusion, ambition, resilience, leadership, and creating a more inclusive world for all people. Subscribe, like, and share to help push the conversation forward. About Pushing Forward with Alycia Learn more about your ad choices. Visit megaphone.fm/adchoices

    Jay & Pamela: Disability Love, Reality TV & Becoming Unapologetically Seen on TLC
  8. Jun 25

    The Book Every Disabled Child Deserves: Angelea Yoder on Let Them Stare

    Alycia Anderson welcomes back Nashville photographer, disability advocate, and Let Them Stare creator Angelea Yoder to discuss her advocacy, her VACTERL Association diagnosis, and the liberation of moving from hiding invisible medical differences to sharing them publicly, including a Good Morning America segment that shifted her fears into feelings of acceptance. Angelea explains VACTERL and how it has impacted her life through multiple anomalies and more than 20 surgeries, and Alycia shares they have the same VACTERL-related experiences. They focus on Angelea’s first Let Them Stare phase, the photography-based children’s book Look at Me: Look What I Can Do, now on Kickstarter to raise $40,000 for self-publishing and printing, with tiers for preorders and donating books to schools and hospitals. They also discuss consent and privacy for disabled kids on social media, and Angelea previews future plans including an adult coffee-table book, a disability-focused modeling agency, and a community hub. The episode’s mantra is simple and powerful: “Let them stare.”  The Big Ideas Behind the Brave Moments  📸 Disability representation through real photography and storytelling 👀 Let Them Stare as a movement for visibility and pride 🧒 Helping disabled kids feel seen, celebrated, and less alone 💬 Moving from hidden medical differences to public advocacy 🧬 Understanding VACTERL Association and invisible disability ❤️ Finding liberation through vulnerability and shared lived experience 📚 Creating children’s books that reflect real disabled kids 🛡️ Consent, privacy, and dignity in disability storytelling 🏥 Navigating medical complexity, childhood surgeries, and self advocacy 🌎 Changing how the world sees disability, difference, and possibility 👗 Expanding disability representation in fashion, media, and modeling ✨ Building community around visibility, belonging, and the mantra “Let them stare” The Quotes We’re Carrying Forward  “I want to start doing something that can help people and change the world.” ~ Angelea Yoder “Even if it changes one child’s perspective of, ‘Oh, I’m not alone anymore,’ then this whole thing was worth it.” ~ Angelea Yoder “I would love to see disfigurement and disabilities in so many more media campaigns and PR campaigns.” ~ Angelea Yoder “Let them stare.” ~ Angelea Yoder From Hidden to Seen, One Moment at a Time  00:00 Podcast Welcome 00:25 Meet Angelea Yoder 02:39 From Radio to Purpose 04:44 Hidden to Heard 06:34 Understanding VACTERL 09:52 Shared Diagnosis Bond 13:19 Kids Book Let Them Stare 16:48 Kickstarter Funding Goals 17:35 Kids Privacy Online 22:09 How to Support and Tiers 23:54 Whats Next for Project 26:56 Final Links and Farewell 28:16 Pushing Forward Mantra  Connect with Angelea Yoder Keep up with Angelea Yoder, photographer, storyteller, disability advocate, and creator of LET THEM STARE, as she works to change the way the world sees disability, visible and invisible differences, and childhood representation. Her upcoming children’s photo book, Look At Me, Look What I Can Do!, celebrates the strength, joy, and ability of every child. Back the Book on Kickstarter: Look At Me, Look What I Can Do! Children’s Book Website:letthemstare.org LinkedIn:Angelea Yoder Instagram:@angeleaphoto Facebook:Angelea Photo Connect with Alycia 🌐 Website: ⁠https://alyciaanderson.com/⁠ 🎙️ Podcast: ⁠https://alyciaanderson.com/podcast⁠ 💼 LinkedIn: ⁠https://www.linkedin.com/in/alyciaanderson/⁠ 📸 Instagram:⁠ https://www.instagram.com/alyciaanderson/⁠ Pushing Forward with Alycia gives disability a voice through conversations about accessibility, inclusion, ambition, resilience, leadership, and creating a more inclusive world for all people. Subscribe, like, and share to help push the conversation forward. About Pushing Forward with Alycia Learn more about your ad choices. Visit megaphone.fm/adchoices

    The Book Every Disabled Child Deserves: Angelea Yoder on Let Them Stare
5
out of 5
43 Ratings

About

Pushing Forward with Alycia | A Disability Podcast Pushing Forward with Alycia is the weekly podcast that gives disability a voice and welcomes everyone—disabled people, allies, families, and inclusive employers—into a courageous, judgment‑free space to learn, ask questions, and advance access together. Launched June 29, 2023 and dropping new episodes every Thursday, host Alycia Anderson—disabled motivational speaker, DEI educator, entrepreneur, athlete, and storyteller—shares lived experience and amplifies voices across the global disability community. The show began as a safe, respectful space to talk honestly about difference, ableism, and belonging; that welcoming spirit remains its heartbeat today. What You’ll Hear From headline issues to everyday wins, we dig into DEI + disability, digital accessibility, workplace inclusion, disabling ableism, Disability Pride Month, intersectionality, airlines & disability discrimination, and so much more. If it shapes how disabled people live, learn, work, travel, play, create, love, and lead—we’re talking about it. Nearly 100 Episodes (and Counting!) In just two years we’ve published 98 full episodes (as of July 16, 2025) and are racing toward our 100th celebration. Recent conversations feature boundary‑breaking guests like Marsha Elle (bionic model, Billboard artist), Tiffany Yu (Diversability & The Anti‑Ableist Manifesto), Gigi Robinson (chronic illness creator & strategist), Kristen Anderson (global inclusive leadership champion), Isaac Harvey MBE (East London influencer & entrepreneur), and many more advocates, athletes, artists, policy shapers, siblings, caregivers, and allies you’ll love meeting. Who It’s For Whether you identify as disabled, are new to advocacy, support a disabled loved one, or lead teams striving to build a more inclusive workplace, you’ll leave each episode with insight, language, and actionable takeaways you can bring to classrooms, boardrooms, events, and everyday life. Our mission is to be a safe place to learn, share, ask “no wrong” questions, and transform awkwardness into connection. Listen & Support Follow, subscribe, share, rate, and review to help amplify disability inclusion. Sign up for release alerts, suggest a guest, and bring Alycia to speak or train your organization in disabling ableism. However you engage, you’re helping open hearts and clear paths for all of us. Open hearts, clear paths. Let’s go.

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