Where The Ramp Ends

Dr. Bradley Mays - Oklahoma's Developmental Disabilities Council Advocacy Training Coordinator

Please rate and review to help us reach others. Most people underestimate the power of simply sharing your story—and the profound impact it can have. Dr. Brad Mays, a man living with cerebral palsy and passionate advocate, reveals how authenticity and vulnerability transformed his life and advocacy journey in Oklahoma. Growing up and navigating a world that often overlooked accessibility, Brad shares deeply personal lessons about resilience, the importance of community, and why representation matters beyond inspiration. From childhood playgrounds to passing legislation, his story proves that your voice can spark systemic change—even when the odds seem stacked against you.You'll discover: * How Brad's experiences with IEPs and overcoming societal expectations shaped his advocacy work * The vital role of authentic storytelling in creating impact and fostering understanding * Practical advice for parents raising children with disabilities and young advocates stepping into leadership roles * Why "dignity of risk" is crucial for empowering people with disabilities to live fully * The power of community and lifelong friendships built through shared struggles and triumphs This episode is perfect for anyone committed to disability rights, advocates seeking inspiration, or parents encouraging their children to dream big despite challenges. Brad's perspective reminds us that behind every disability is a person with purpose, passion, and the desire to make a difference. Brad Mays is the advocacy training coordinator for the Developmental Disabilities Council of Oklahoma. His work as a self-advocate and educator is transforming perceptions—and lives—every day. If you believe storytelling can change the world, this episode will deepen that conviction. It’s an honest, heartfelt conversation about overcoming obstacles, challenging stereotypes, and why living your truth is the most powerful form of advocacy. Hit play and get inspired to lift others—and yourself.To connect with Where The Ramp Ends on social media click here: https://linktr.ee/where.the.ramp.ends?utm_source=linktree_profile_share

From Dominating Ironman Races to Building a Movement—Kyle Pease’s Blueprint for Making a Difference

Please hit the follow button and rate and review to help others find this podcast. Most people view success as a straight line — but Kyle Pease's story proves it’s a vibrant, unpredictable journey filled with resilience, love, and breakthroughs. When you're told you're never supposed to achieve what you dream of, Kyle flips the script, showing that passion and grit rewrite expectations every single day. If you're ready to embrace your true potential despite the odds, this episode is your wake-up call.Kyle Pease, a lifelong wheelchair user and Ironman champion, shares how his relentless pursuit of inclusion has transformed not only his life but inspired thousands. From training with Skittles and potato chips to conquering Hawaii’s toughest race, his journey reveals the power of perseverance and community. Kyle dives into how he’s built a foundation that’s helped over 4,000 families—and why asking for help, investing in mental health, and embracing independence are pivotal lessons for us all.You'll discover: Kyle's groundbreaking approach to navigating daily life with cerebral palsy, including independent travel on Atlanta’s Marta system and turning societal misconceptions into opportunities for growth. He reveals the significance of caregivers as family, the emotional highs of crossing an Ironman finish line, and why every obstacle is an invitation to prove what’s possible. Plus, insights on fostering inclusion, the importance of role models, and how a mindset focused on love and hope sparks extraordinary achievements.Living with a disability doesn’t mean living on the sidelines — it means breaking barriers, rewriting success stories, and inspiring the next generation to dream bigger. Whether you're a caregiver, athlete, parent, or someone seeking to unlock your own potential, this episode offers radical optimism and actionable wisdom to challenge what you thought was possible.Perfectly suited for those ready to transform limitations into launchpads for greatness, Kyle’s story will stay with you long after the final seconds of the race. Hit play and get inspired to see your own life as a race worth running. Guest Credibility: Kyle Pease is an Ironman finisher, two-time World Champion, and founder of the Kyle Pease Foundation, dedicated to empowering people with disabilities through sports and community. To learn more about The Kyle Pease Foundation click here. [https://l.instagram.com/?u=https%3A%2F%2Flinktr.ee%2FTheKylePeaseFoundation%3Futm_source%3Dig%26utm_medium%3Dsocial%26utm_content%3Dlink_in_bio%26fbclid%3DPAZXh0bgNhZW0CMTEAc3J0YwZhcHBfaWQMMjU2MjgxMDQwNTU4AAGnNv6oOjgTPwRC2o0HUJNAHSJxHXvjnTfttr3ZONm30NGsjhoi_X5RWYi2HD4_aem_8079ntRyLq7FjLR6Nokepw&e=AUDoUC1H8psZ0aHdt5bvHDzXYgD21m7qjOTLOT_m-nzUktjj0PumuLVP95e4IxVkdtnDNTNnJc7N1WXiivcWuM4cGMWv38k7e_7J1yg_mg] To learn more about Where The Ramp Ends click here. [https://linktr.ee/where.the.ramp.ends?fbclid=IwY2xjawRoKoNleHRuA2FlbQIxMABicmlkETExWkJ3OVVxdnRWVkhCWW1Ec3J0YwZhcHBfaWQQMjIyMDM5MTc4ODIwMDg5MgABHilpnx6foGte-eUZ2nfjtcBU3FqcHnD_CmqC1nk8syZwY7lv1Ce14fCh6y1Y_aem_KtjGZDPq8k7Bc-K_3BRfCA]

Shannon Pinkerton with The Pinkerton Boys Discusses Adoption, Foster Care and Disability

Please rate and review to help others find this podcast. Thank you for your support! Most people view Down syndrome and children with disabilities through a narrow, often negative lens — but Shannon Pinkerton flips that perspective on its head. Shannon and her husband adopted six boys, five with Down syndrome, Shannon shares her inspiring, unfiltered journey of adopting, fostering, and loving children who often fall through the cracks of the system — and proving that these kids are capable of more than society expects.In this heartfelt episode, Shannon challenges the stereotypes that shroud disabilities. You’ll discover how her family’s unwavering approach fosters independence, respect, and dignity for her boys, even in moments that seem like setbacks. From navigating foster care and adoption to breaking down misconceptions and confronting societal ableism, her story is a testament to the power of love and advocacy. She shares practical advice on how to treat children with Down syndrome as “normal,” emphasizing that expectations and community support make all the difference.We break down: * How to shift your mindset from pity to empowerment * The importance of exposing children with disabilities to mainstream settings * Why nurturing biological family connections enriches a child's identity * The impact of community and social media in fighting stigma * Real stories of resilience, including Cameron’s quest to find his biological family and Tracy’s unexpected adoption journey Every parent, educator, or caregiver who wants to see beyond labels and unlock the full potential of children with disabilities will find inspiration and actionable strategies here. Shannon’s experience illustrates that when society treats kids with Down syndrome as capable individuals, everyone wins.This episode isn’t just a story — it’s a rallying cry for inclusion, dignity, and love. Perfect for anyone involved in special needs advocacy, fostering, or simply looking to broaden their understanding. Tune in and discover why these kids aren’t just surviving — they’re thriving, with the right support, expectations, and community.Join Shannon and her family in redefining what’s possible — because everyone deserves to be seen, loved, and celebrated. You can follow The Pinkerton Boys on TikTok [https://www.tiktok.com/@pinkertonboysadventures] and on Facebook [https://www.facebook.com/Pinkerton.Joey]. You can follow all of Where Ramp Ends socials and stay informed on our projects here [https://linktr.ee/where.the.ramp.ends?utm_source=linktree_profile_share<sid=83fd486e-3327-43ed-b7cb-e78af657c7d2].

Ricki Sabia -Senior Education Policy Advisor, National Down Syndrome Congress

Please rate and review! Hit the follow button and share! Help us grow our audience! Most parents of children with Down syndrome—and even advocates—would agree: understanding and navigating education policy can feel overwhelming and inaccessible. But what if your voice could shape real change, starting today? Ricki Sabia, Senior Education Policy Advisor at the National Down Syndrome Congress, shares the powerful story of how she shifted from a concerned parent to a fierce advocate influencing federal and state policies that impact millions of children like hers—and yours. Her journey proves that even small actions can spark systemic transformation.In this heartfelt and insightful episode, Ricki recounts her initial moments of advocacy sparked at the beach, observing her son’s uncertain future, and how she turned that worry into a call for systemic change. You'll discover concrete strategies for effective advocacy—whether you're confronting IEP meetings for the first time or advocating for inclusive education policies at the national level. Ricki breaks down complex topics like IDEA, federal funding, and the importance of community-based services, making these essential issues accessible and actionable for families everywhere.We break down the evolution of educational inclusion, highlighting how attitudes, policies, and community support have shifted—and why there’s still work to do. You'll learn: how to advocate assertively but collaboratively in school meetings, ways to build lasting relationships with educators, and why your personal story holds transformative power. Ricki shares practical tips for parents feeling intimidated at IEP meetings, and reveals the importance of setting future-focused goals—like independent living and employment—that can dramatically change your child's life trajectory. This episode isn’t just about policy—it's about empowering you to be a catalyst for change. Whether you’re new to advocacy or seasoned in activism, Ricki’s insights remind us that every voice matters. Her inspiring perspective prioritizes inclusion, respect, and the belief that every child can reach their full potential when we work together to dismantle barriers. Perfect for parents, educators, and advocates committed to creating a future of opportunity and respect for all children with disabilities.Join us as Ricki Sabia models how lived experience, persistence, and a passion for justice can turn personal challenges into powerful advocacy tools. Discover how your voice, big or small, can help shape a more inclusive, equitable future—one policy change at a time. All the resources Ricki mentioned in the podcast are here: NDSC website https://ndsccenter.org/ [https://ndsccenter.org/] NDSC Policy Pulse https://ndsccenter.org/policy/action-center/the-policy-pulse.html [https://ndsccenter.org/policy/action-center/the-policy-pulse.html] National Down Syndrome, Advocacy Coalition (NDAC) information and free application https://ndsccenter.org/policy/national-down-syndrome-advocacy-coalition-ndac/ [https://ndsccenter.org/policy/national-down-syndrome-advocacy-coalition-ndac/] Sign up for NDSC action alerts https://www.votervoice.net/mobile/NDSCCenter/Home [https://www.votervoice.net/mobile/NDSCCenter/Home]NDSC policy and advocacy resources. Find policy briefs for families on education here https://ndsccenter.org/policy/advocacy-training-resources/briefs.html [https://ndsccenter.org/policy/advocacy-training-resources/briefs.html] NDSC DC Policy Summit September 29-30 2026. Registration opens May 14. https://ndsccenter.org/policy/ndsc-down-syndrome-policy-summit/ [https://ndsccenter.org/policy/ndsc-down-syndrome-policy-summit/] TIES Center on Inclusive Policies and Practices for Students with Significant  Cognitive Disabilities https://tiescenter.org/ [https://tiescenter.org/] One pager with clickable links for TIES briefs https://ndsccenter.org/file_download/fd5f32f2-7e8d-405f-a0ce-a4c81cb4db10 [https://ndsccenter.org/file_download/fd5f32f2-7e8d-405f-a0ce-a4c81cb4db10] Find all the ways to connect with Where The Ramp Ends here: Where The Ramp Ends [https://linktr.ee/where.the.ramp.ends?fbclid=IwY2xjawRScXxleHRuA2FlbQIxMABicmlkETFMT2NSU0JOSjdrWXNNelkzc3J0YwZhcHBfaWQQMjIyMDM5MTc4ODIwMDg5MgABHtPeWv3zzsdmcU2z2cdhSzPq2Vvnra6efHcBtkkreKx-6O1Bq6KZn1gzfCwR_aem_2gdOw1ykVKVX1guRPQ6aJA]

Empowering Disability Advocacy: A Conversation with Morgan Davis

Please rate and review this podcast to help us reach more listeners. In this episode of Where the Ramp Ends, Bryce Wooten sits down with Morgan Davis, a passionate disability advocate living with cerebral palsy. They explore Morgan's journey through advocacy, the importance of representation, accessibility, and how societal perceptions shape experiences for people with disabilities. Main Topics: Morgan Davis’s advocacy journey and leadership programs like YLF and Partners in Policymaking The social model of disability and the importance of representation in media and education Practical and simple accommodations for accessibility in daily life and work The concept of dignity of risk and independence for people with disabilities The intersection of disability with race, identity, and DEI efforts Challenges in transportation, healthcare, and the financial burdens faced by the disability community Timestamps: (00:00) - Introduction to Morgan Davis and her advocacy background (02:04) - How leadership programs like YLF and LEND shaped Morgan’s advocacy skills (08:05) - Key lessons Morgan wishes she could tell her younger self (09:32) - Advice for parents of children with disabilities starting their advocacy journey (10:11) - The analogy of moving leaves on the road as advocacy in action (13:32) - The high cost of transportation when attending college with a disability (15:30) - Financial burdens and employment barriers faced by people with disabilities (18:49) - Simple accommodations such as glasses and voice-to-text technology (22:45) - The importance of proper resources and awareness of assistive technology providers like AbleTech (35:21) - Challenging misconceptions: disability as part of DEI and social inclusion (43:01) - Morgan’s reflections on her journey from disinterest to empowerment through knowledge (47:01) - The importance of mentorship and representation in media and society (49:27) - The need for accurate media portrayals of disability and social model understanding (50:04) - Addressing the stigma around dating and relationships with disability (54:26) - Personal story of taking Julia to the bowling alley and advocating for her independence (58:23) - Dignity of risk: empowering people with disabilities to make their own choices (61:13) - Morgan’s legacy and her hopes for future advocacy impact (63:38) - Final thoughts from Morgan on her journey and encouragement for others Resources & Links: Morgan Davis Instagram Oklahoma AbleTech Disability Rights Movement history Partners in Policymaking Connect with Morgan Davis: LinkedIn Twitter Additional Notes: Morgan emphasizes that disability rights and understanding must be integrated into education at all levels, advocating for universal design and early representation. She also highlights the personal and societal benefits of viewing disability through the social model lens—a view that society's barriers, not individual impairments, create disability. Her inspiring journey encourages ongoing advocacy, representation, and compassion to foster inclusion and dignity for all. You can find all of Where The Ramp Ends links including contact information here: https://www.fixfinderusa.com/other-services/where-the-ramp-ends [https://www.fixfinderusa.com/other-services/where-the-ramp-ends]