I was born in Indonesia, Jember a small city in the Island of Java. At the age of two I was diagnosed with SMA (Spinal Muscular Atrophy). SMA is a genetic disorder causing progressive motor neuron degeneration, leading to muscle weakness and atrophy. There was no treatment at the time, and so I lived my life as much as I could.
Growing up, I always felt different and physically weaker, often … open the full bio bullied for it at school. As a pastor’s family, we moved frequently all around Indonesia so the concept of home has always been foreign to me. In 2010, my family moved to the U.S. in order for my parents to pursue higher education. It was one of the loneliest times of my life—everything from the culture to the language and social cues felt unfamiliar. Around this time, I began using a walker, then a scooter, and eventually a power chair. Little did I know that a friend’s suggestion to attend an art high school for film would completely change the course of my life.
Most of my high school and college years were spent immersed in the media arts. I worked on projects ranging from short films and live shows to musicals, commercials, and various other media-related art forms. I then went on to intern at Amazon Studios, researching on production resources all over the world. Then soon after moving to work at Netflix with a team focusing all around scaling studio technology. More recently, my involvement with the Hollywood Professional Association has allowed me to contribute to industry conversations, including serving as a panelist at the HPA Tech Retreat, where I along other panelists discussed the importance in recognizing and developing untapped and underrepresented talent. On my weekend I also volunteer a lot of my time at Indonesian churches within the Los Angeles county.

Lily Fox is the Executive Director of Women’s World On Wheels (Women’s WOW), a nonprofit dedicated to empowering and advocating for women wheelchair users. Lily leads events like annual camps, monthly webinars, and local events that create a supportive community for women to connect.
A graduate of the University of Miami, Lily earned a Bachelor of Business Administration in Legal Studies and … open the full bio Entrepreneurship. During her time there, she cultivated a passion for corporate law and business management while holding leadership roles in Alpha Kappa Psi, a professional business fraternity. Her internships in consulting and finance further sharpened her skills, preparing her for her current leadership role.
Now based in Colorado, Lily has revitalized Women’s WOW, creating a nationwide platform that connects and uplifts women wheelchair users. Outside her professional life, she enjoys design thinking, staying active, and cherishing time with friends and family. Lily is deeply committed to enhancing the quality of life for women in the wheelchair community and inspiring positive change.

I’m a 20-year-old college sophomore and full-time wheelchair user, navigating life after being injured by the HPV vaccine. This left me unable to see, talk, or eat, and paralyzed from the shoulders down. After months of neuro rehab, I regained many abilities, and moved to California to continue my recovery. Today, I’m an independent wheelchair user, and I’ve rediscovered my passion for dance, now … open the full bio as a wheelchair dancer. My dream is to become a child life specialist and professional wheelchair dancer, with a goal to create a dance program for hospitalized children, using movement to help them heal.

Holly Johnston has been a dedicated advocate for children and youth with diverse needs for over 25 years. From her early experiences in Child and Family Services, being a foster parent, and to her role as a Life Skill Coach and mother of 5. Inspired by the unique challenges faced by those with increased barriers, Holly recognized the pressing need to address the gap in menstrual accessibility for … open the full bio marginalized individuals, and started the nonprofit Periods for All to help create a world where menstrual equity is a reality for all.
Carly Pistawka is a physically disabled individual that is passionate about advocating for access and equity. In 2020, Carly co-founded Moon Time Sisters BC, a non-profit group aimed to send menstrual products to remote Indigenous communities in Northern BC and the Territories. Currently, Carly is the Education and Advocacy Lead for Periods for All. She is hoping to pursue a medical degree, and has a Bachelors of Science in Biotechnology from UBC.
At Periods for All we are passionate about creating resources that accommodate the diverse needs of folks who menstruate, especially those who may feel marginalized or overlooked. Our mission is to provide these invaluable tools free of charge to anyone who requests them, because we believe that everyone deserves access to support and empowerment. Whether you’re looking for workshops tailored for all abilities in the vibrant Metro Vancouver area or engaging online sessions, we are here for you! If there’s something specific you need but don’t have, please don’t hesitate to reach out; we’re committed to doing our utmost to assist you on your menstrual health journey. Together, we can foster an inclusive community where everyone thrives!

Christina is a 40 year old adoptive mom of 3. Boy/girl twins (6) & her oldest daughter (11) has special needs predominately living in a wheelchair. Christina runs a very successful home-based business & you may even recognize her as Tamra Judge’s hairstylist from the RHOC. She has extensive experience in the beauty industry & has used social media to grow her multi-million dollar … open the full bio home based business. She utilizes her Sobriety, life-traumas, and true stories & coaches others with her proven systems. It’s her mission to spread the message that you can take serious charge of your life without taking life too seriously! Her biggest call to action is her hope to inspire you to BE yourself!! Prepare for some laughs & tears as you follow along her transparent journey.

Anthony Kennedy Shriver is the Founder, Chairman & CEO of Best Buddies International, which he created in 1989 to foster one-to-one friendships between people with and without intellectual and developmental disabilities (IDD). Recognizing the tremendous volunteer potential of university students, Shriver first inspired his college peers to personally collaborate in expanding the realm of … open the full bio opportunities that people with IDD should experience.
Today, through Shriver’s stewardship and entrepreneurial spirit, Best Buddies® has grown into a leading nonprofit entity with increasing international reach across six continents, establishing a global volunteer movement that creates opportunities for one-to-one friendships, integrated employment, leadership development, inclusive living, and family support for people with IDD.
A graduate of Georgetown University, Shriver has been recognized for his work on behalf of Best Buddies with diverse international accolades and honorary degrees. He is the father of five beautiful children and resides in Miami Beach, Florida.

Nevaeh Hearn is a 22 year old senior fashion industry and merchandising student at Drexel University, whose passion for fashion is deeply rooted in her love for people. She is driven to innovate within the industry, bringing the same energy and determination that once fueled her as a competitive gymnast. However, after an unexpected shift changed the course of her life, Nevaeh discovered a new … open the full bio dream—revolutionizing the fashion industry to be more inclusive, functional, and forward-thinking.
She has been recognized for her work through the Ronald McDonald House Charities of Baltimore, where she served as a Co-Chair Speaker at the 2019 GALA. There, Nevaeh shared her story, raised awareness for the experiences of others, and helped raise over $100,000.
Most recently, Nevaeh was recognized Top 5 in the country as a finalist for the NRF Foundation’s Next Generation Scholarship, where she proposed an adaptive fashion strategy for NRF’s Partner of the Year, Uniqlo.
As a senior at Drexel University, Nevaeh has been deeply immersed in developing her senior thesis, which, of course, focuses on adaptive fashion. However, she sees this as more than just a thesis—it is the foundation for a vision she intends to bring to market after graduation.
She is committed to merging creativity with analytical strategy to drive meaningful change. With a mission to make fashion more accessible and adaptive, Nevaeh is shaping a future where style meets inclusivity in ways the industry has yet to fully embrace.

Sepsis Survivor Week: Honoring Strength, Raising Awareness
Sepsis Survivor Week is an annual observance dedicated to recognizing the resilience of individuals who have survived sepsis, raising awareness about its long-term effects, and educating the public on the importance of early detection and prevention. Held during the second week of February, this week is an opportunity to amplify the voices … open the full bio of survivors, highlight their challenges, and advocate for better understanding of post-sepsis recovery.
What is Sepsis?
Sepsis is a life-threatening medical emergency that occurs when the body has an extreme response to an infection, leading to widespread inflammation, organ failure, and, in severe cases, death. It can develop from common infections like pneumonia, urinary tract infections, or even minor cuts and wounds if left untreated. While early medical intervention improves survival rates, the road to recovery can be long and complex.
Why Sepsis Survivor Week Matters
Surviving sepsis is just the beginning of a challenging journey. Many survivors experience long-term complications, collectively known as post-sepsis syndrome, which can include:
• Chronic fatigue and weakness
• Cognitive impairment, memory loss, or difficulty concentrating (often called “brain fog”)
• Post-traumatic stress disorder (PTSD), anxiety, or depression
• Increased risk of future infections and lingering organ dysfunction
Sepsis Survivor Week serves as a platform to bring attention to these struggles, providing education, support, and resources for those affected.
How to Participate and Support Sepsis Survivors
1. Share Survivor Stories
Personal testimonials from sepsis survivors help others recognize symptoms, understand the realities of recovery, and feel less alone in their journey. Whether through social media, community events, or support groups, sharing experiences can be empowering and educational.
2. Raise Awareness on Social Media
Using hashtags like #SepsisSurvivorWeek, #StopSepsis, and #SepsisAwareness, individuals and organizations can spread knowledge about sepsis prevention, early detection, and survivor challenges. Graphics, videos, and infographics from trusted organizations like the Sepsis Alliance can further amplify the message.
3. Advocate for Better Healthcare Policies
Many sepsis survivors struggle with medical debt, disability accommodations, and the lack of widespread knowledge about post-sepsis care. Advocacy efforts can push for improved medical guidelines, research funding, and better post-sepsis support systems in hospitals and communities.
4. Educate Yourself and Others
Learning the signs of sepsis—confusion, extreme weakness, fever, rapid breathing, and decreased urine output—can save lives. Promoting education in workplaces, schools, and healthcare settings can lead to earlier diagnoses and improved outcomes.
5. Support Organizations Helping Survivors
Nonprofits like the Sepsis Alliance and the UK Sepsis Trust provide valuable resources, survivor networks, and research funding. Donating or volunteering with these organizations can make a meaningful impact.
The Power of Awareness and Community
Sepsis Survivor Week is not just about acknowledging those who have lived through sepsis—it is about giving them a voice, raising awareness, and fostering a community that understands and supports their journey. By coming together to share information and advocate for change, we can work toward a future where sepsis is recognized and addressed promptly, saving more lives and improving post-sepsis care.

Leah Kaplan’s journey from an orphanage in China to becoming a prominent adaptive athlete and disability advocate is a testament to resilience, self-discovery, and the power of community. Born with a congenital limb difference, missing her left arm below the elbow, Leah faced societal challenges from an early age. Abandoned at birth due to her disability, she spent her early years in a Chinese … open the full bio orphanage before being adopted and brought to the United States.
Growing up, Leah grappled with feelings of rejection and the societal expectations placed upon her due to her disability. In high school, she was introduced to adaptive sports, particularly swimming, which became a transformative outlet. Competing alongside other amputees across the country, Leah gained confidence and began to view her limb difference not as a limitation but as a unique strength. She realized that the true barriers were not physical but mental, stemming from societal perceptions and self-doubt.
Leah’s passion for adaptive sports expanded beyond swimming. She ventured into triathlons, embracing the challenges of running, cycling, and swimming. Her dedication and perseverance led her to compete on international stages, aiming for the Paralympics. Throughout her athletic journey, Leah emphasized the importance of participating in sports out of love and passion, rather than solely for accolades. She often shares her belief that one doesn’t need to make the Paralympics their entire life to find worth; it’s about doing what you love.
Beyond her athletic pursuits, Leah is a fervent advocate for disability inclusion and representation. She utilizes her platform to challenge societal norms and inspire others with disabilities to embrace their identities. Through storytelling and sharing her experiences, Leah fosters a sense of community and understanding. Her social media presence, under the handle “nubbin2seehere,” serves as a space where she offers unique perspectives, blending humor with advocacy to connect with a broad audience.
Leah’s advocacy extends into education, where she has worked in special education, bringing laughter and light to her students. Her experiences in the classroom have provided her with insights into the diverse challenges faced by individuals with disabilities, further fueling her commitment to bridging gaps in diversity and promoting empowerment through advocacy.
Throughout her journey, Leah has emphasized the importance of community and the power of embracing one’s identity. She believes that while everyone faces challenges, it’s the way we adapt and respond that defines our success. Her story serves as a powerful reminder that our differences are not disabilities but unique strengths that empower us to rewrite our own narratives.
In summary, Leah Kaplan’s life is a compelling narrative of overcoming adversity, embracing one’s true self, and advocating for a more inclusive world. Her journey from an orphanage in China to becoming an empowered individual exemplifies the strength of the human spirit and the transformative power of resilience, humor, and community.

Chantelle Johnson, Founder & CEO of Talent4dCulture LLC, is a seasoned executive with over two decades of experience leading enterprise-wide strategies that empower leaders to build thriving cultures and nurture high-performing talent. With a deep commitment to inclusion, she has successfully developed and implemented transformative initiatives that shape positive organizational culture and … open the full bio drive sustainable growth. Chantelle’s expertise lies in her ability to work across diverse teams and industries, helping organizations cultivate inclusive environments that champion innovation, collaboration, and employee engagement. Her strategic insights and hands-on approach have consistently delivered impactful results, positioning her as a trusted advisor and change agent dedicated to fostering workplaces where every individual can succeed.
She has built an impressive portfolio of experience as a senior executive, leading strategic initiatives for some of the most respected names in industry. She has worked with Fortune 50 companies, and large integrated health systems, where she led dynamic teams and executed comprehensive programs focused on talent development, employee resource groups, and cultural transformation. Her expertise extends across industries and in her most recent role with as Enterprise Associate Vice President of Workforce & Culture, she successfully advised executives and cross-functional teams on aligning organizational goals with inclusive leadership principles. Chantelle’s impact is evident in the enhanced employee engagement, retention rates, and talent pipelines she has helped build, consistently elevating workplace cultures and reinforcing the value of diverse perspectives as engines for innovation and growth.
In addition to her corporate expertise, she serves as a Advisory Board Member with the Robinhood Family YMCA, DEI Committee Member with the Women Business Leaders of the U.S. Healthcare Industry Foundation, and inaugural member of ForbesBLK. She has also served as a speaker on workplace strategies with She’s Got Time, a community dedicated to creating thriving cultures for Women in Sports, the Certified Age-Friendly Institute, and previously served as a Member Lead for the Institute for Corporate Productivity – DEI Member Group.
Chantelle is a Certified Diversity Professional, Six Sigma Greenbelt and holds an MBA with a focus on Human Resources Management from Walden University, a BA from Strayer University and a professional Certificate in AI: Implications for Business Strategy from MIT Sloan School of Management. Known for her unique blend of maverick-like attributes and empathy to her leadership, enabling her to challenge conventional thinking while understanding and valuing diverse perspectives. This balanced approach allows her to drive impactful outcomes that resonate across teams, fostering an environment where bold, innovative strategies thrive alongside a deep respect for people and culture.

Marty and Alycia Anderson are a powerhouse couple united by their passion for advancing inclusion, accessibility, and representation. Together, they form a dynamic partnership that merges lived experience with professional expertise, delivering impactful solutions for businesses and individuals seeking to embrace diversity and create meaningful change.
Alycia Anderson
As the CEO and Founder of The … open the full bio Alycia Anderson Company, Alycia is a TEDx speaker, disability advocate, and sought-after consultant. Her work focuses on breaking barriers and enabling organizations to see the immense value of inclusion, particularly for people with disabilities. Born with sacral agenesis and a wheelchair user her entire life, Alycia has built a career on redefining perceptions of disability. She passionately shares her personal story to inspire audiences and ignite action, emphasizing the untapped potential of underrepresented communities. Her keynote speech, “Disabling Ableism: The Modern Pathway to Inclusion,” has become a cornerstone of her advocacy, blending storytelling, education, and practical strategies to drive lasting change.
Alycia’s influence extends beyond the stage. She collaborates with businesses across industries to implement accessibility practices, foster diverse hiring initiatives, and create environments where everyone can thrive. Her work has garnered accolades, and she’s recognized as one of the leading voices in disability inclusion and intersectionality. Her message is clear: diversity is not complete without disability, and inclusion benefits everyone.
Marty Anderson
Marty brings a unique perspective and invaluable support to their mission. With years of experience in leadership and operational strategy, Marty complements Alycia’s advocacy with a pragmatic approach to organizational change. He understands the challenges companies face when striving for inclusion and works tirelessly to ensure the implementation of sustainable practices that align with Alycia’s vision. Marty’s ability to connect with people and build meaningful relationships makes him a key figure in their shared mission to foster change.
As a partner in both life and business, Marty provides steadfast encouragement and logistical support, enabling Alycia to amplify her message and expand her reach. Together, they demonstrate the power of collaboration, showing that meaningful progress requires unity and shared purpose.
A Shared Mission
The Andersons’ work is rooted in the belief that embracing diversity—including disability—is essential for innovation and growth. They advocate for creating inclusive spaces that unlock human potential, where differences are celebrated as superpowers. By drawing from their personal experiences and professional insights, Marty and Alycia inspire others to view inclusion as an opportunity rather than a challenge.
From keynote addresses and workshops to consulting engagements, their efforts resonate with audiences and organizations worldwide. Whether speaking to students, corporate leaders, or government entities, Marty and Alycia’s message is always empowering and actionable. They remind us that inclusion is not just a moral imperative; it’s a strategic advantage that fosters resilience, creativity, and success.
To learn more about their work or to book Alycia as a speaker, visit alyciaanderson.com/request-a-booking.

Danny J. Gomez — A professional actor who was paralyzed from the waist down in a 2016 mountain bike accident that nearly killed him. He is best known for roles in such hit shows as NCIS: Hawai’i, New Amsterdam, All Rise, and feature film Martinez Margaritas and Murder . He is a two-time Easterseals Disability Film Challenge winner, for the films I/0 (2019) and Check Mate (2018), and has been a … open the full bio finalist in other years. He was awarded the Christopher Reeves Acting Scholarship in 2020. Most recently, Danny completed a successful Off-Broadway run in the play All of Me which garnered rave reviews.

Jason Tabansky is a decorated U.S. Army veteran and accomplished para-archer who has achieved significant milestones both in military service and sports. A former Ranger, Tabansky was seriously injured in combat, which led to his medical retirement. His resilience and determination saw him transition into a new chapter as a world-class para-athlete and advocate for veterans.
Jason is a member of … open the full bio Team USA’s Para Archery squad, competing at the international level, including the Paralympic Games. He secured a gold medal at the 2024 World Archery Para Championships, marking a pivotal moment in his career and showcasing his dedication to his craft. His journey to the Paralympics, marked by intense physical rehabilitation and training, underscores his grit and ability to overcome adversity.
In addition to his athletic endeavors, Jason has benefited from organizations such as the Gary Sinise Foundation, which provided him with a specially adapted smart home to accommodate his mobility needs. He has also received support from Wheelchairs for Warriors, highlighting his commitment to raising awareness and advocating for injured veterans and first responders​.
Jason’s inspiring story is a testament to his unwavering determination and his role as a champion for the veteran community.

Leslie is a double-certified Functional Nutritionist committed to empowering busy ambitious women to identify the root cause of their health challenges and heal using food and lifestyle as medicine. I guide my clients with an individualized, holistic approach that’s focused on elevating our food standards and creating an abundant relationship to nourishing our bodies rather than restricting.
Women … open the full bio deserve to feel balanced, energized, and in control of their health. Through stabilizing hormones, gut imbalance, nervous system dysregulation, and reducing excess fat storage, we can transform the way we experience life in our body. The LJW method is designed to empower women to identify and solve dysfunction, restore balance, and redesign body chemistry so we can experience our highest quality of life.

Tobias Forrest is a performer with a disability who has a background in accessible consulting and MS in psychology. He won the Christopher Reeve Acting Award for the film ”Daruma” and has credits including “The Academy Awards”, “Media Access Awards”, ”Law & Order: Organized Crime”, “How To Get Away With Murder”, “Queen Sugar” and many others. He has also done voiceover for animation as well as … open the full bio audio description for TV, narration for audiobooks and been the MC for nonprofit events.
John Lawson started playing piano at age three and began formal lessons by four, dedicating 18 years to studying classical piano. He majored in piano and theater in college, focusing more than half his life on music. At 30, an electrical accident led to the amputation of both his hands. After six months in the North Carolina Jaycee Burn Center in Chapel Hill, he began building a new path.
John is now the first double hand amputee certified as a private pilot in the United States and the first worldwide to qualify as a PADI Scuba Instructor. He has since logged over 500 flight hours and completed nearly 1,000 dives in oceans around the world.
For 35 years, he has worked as an advocate for people with disabilities, in front of and behind the camera. Today, he’s an actor and director with over 58 film and television credits, including his recent award-winning role in DARUMA at the Slamdance Film Festival.

Ali is a disability advocate and coach helping other disabled creators and entrepreneurs build their own brands. Originally from Argentina, she’s based in Vancouver, BC, where she lives with her two dogs and husband. On @seated.perspectives and beyond, she is fiercely committed to changing and expanding disability narratives by centering disabled joy.

Lizzy O is an influential and dynamic content creator celebrated for her engaging and diverse approach to digital storytelling. As a dedicated mother, wife, and lifestyle influencer, she skillfully balances her personal life with her professional endeavors, creating content that spans family life, fashion, beauty, fitness, and her experiences as a woman with a physical disability. Through her … open the full bio blog, (http://www.thelizzyo.com), and her strong presence on social media, Lizzy O shares insights into her journey, offering inspiration and relatability to a broad audience. Her thoughtful and authentic approach to content creation makes her a valuable partner for brands and a standout figure in the online community, where she serves as a role model and source of motivation, particularly for those navigating similar challenges.

Katie Davis, a renowned advocate and long-time friend of Alycia Anderson, joins this week’s episode of Pushing Forward with Alycia / Disability Podcast to reflect on their decades-long friendship and shared journey of disability advocacy. In an unforgettable moment at Runway of Dreams, Alycia took to the runway wearing Target’s adaptive clothing line, showcasing the growing commitment of major … open the full bio brands to inclusivity. From representing Target to partnering with corporations like Netflix and PBS, Alycia’s story highlights the importance of representation in the media and fashion industries.
Katie has stood by Alycia through every triumph and challenge, from working at a restaurant together in college to to their powerful trip to the Runway of Dreams event, where Alycia’s participation made waves in the world of disability representation.
Their deep connection has paved the way for an inclusive narrative that celebrates the importance of showing up—not just for oneself but for others in the disability community.
Discover the impact of inclusivity initiatives and how corporations like Target are supporting adaptive fashion through their clothing lines.

Chris Ruden is an amputee, Type 1 diabetic record-holding powerlifter, keynote speaker and disabled model who was featured on The Rock’s hit TV show “Titan Games”. From being humiliated and labeled broken because of his disability to struggling with mental health and living in a non disabled- inclusive world, Chris learned to turn his obstacles into opportunities, now using his badass bionic arm, … open the full bio diabetes technology, and message of “creating your world without limits” to impact people around the world.

Kam Redlawsk is an award-winning disabled Industrial Designer, artist, writer, and advocate who intimately shares her story that spans from South Korea, as a Korean American adoptee, Michigan and California. Living with a rare and progressive form of Muscular Dystrophy (GNE Myopathy) that has shaped her life’s journey, Kam uses a creative platform to foster a greater understanding not just for … open the full bio rare diseases and disability, but also the human condition as she invites you into her world through her art, writing and wheelchair travels around the world. Kam’s progressive condition will one day leave her completely immobile, but she doesn’t let this stop her from living her life to the fullest and achieving visibility for disability through her talents and perspective. Kam has traveled the world and is up for adventuring from skydiving to parasailing, and seeks to elevate the disabled human experience through various creative projects like be a debut author & illustrator with a picture book inspired by her rare disease and disability, coming out next summer.

Jess Gregory (she/her) is a poet and patient advocate from Australia. Her debut chapbook “Burns Unit – Poetry to Heal the Wounds of Medical Gaslighting” was published in 2023 by Written Tales, and is based on her experiences growing up with undiagnosed Ehlers-Danlos Syndrome and several co-morbidities. From the dismissal of her and her parents’ concerns by doctors, to crucial mistakes that delayed … open the full bio her diagnosis, Jess came to realise that medical gaslighting and negligence were nothing short of an epidemic in the chronic illness and disability community. She now seeks to educate fellow patients about the flaws in the modern medical model so that they can not only better advocate for themselves, but also let go of the guilt and shame that she lived with for so long while struggling to find answers. She also seeks to increase awareness of the fact that illness and disability almost always begin before diagnosis, and broaden public perception of what it means to be a part of the disability community.

Cassidy Huff is a disabled disability rights activist, best-selling author, content creator, actress, and voice-over artist. With a powerful voice in advocacy, Cassidy has dedicated her life to championing the rights and inclusion of disabled individuals. Her multifaceted career spans writing, performing, and creating content that educates and empowers audiences worldwide.

Alycia Anderson, a passionate advocate for inclusion and empowerment, and her husband Marty recently embarked on a thrilling journey to Paris, France, for the 2024 Paralympics. After a long flight from Sacramento, California, they arrived just as the opening ceremonies had begun. Despite missing the start, the couple’s excitement was palpable as they made their way through the bustling streets of … open the full bio Paris to the iconic Roland Garros stadium, the world-renowned home of French tennis.
At Roland Garros, they were eager to catch some of the most exciting matches in the Wheelchair Tennis Event. Alycia and Marty cheered from the stands as they watched the Men’s Semi-finals unfold, their hearts racing with every point. The energy of the crowd was electric, and the anticipation only grew as the Women’s Gold Medal match and the Quad Singles Gold Medal match followed, each one a stunning display of athleticism, determination, and sportsmanship. The spirit of the Paralympics was alive and thriving in every serve, volley, and rally, and Alycia felt inspired by the athletes’ resilience and drive.
Beyond the courts of Roland Garros, the couple set out to explore the beauty and grandeur of Paris. They roamed the grounds of the magnificent Palace of Versailles, marveling at its sprawling gardens and stunning architecture. As passionate supporters of adaptive sports, they also attended a Para Equestrian competition, where they were moved by the grace and strength of both the riders and their horses. Later, they made their way to the historic Grand Palais to witness the intense competition of Para Fencing. The sounds of clashing swords and the sight of agile movements against the backdrop of the grand, glass-domed structure created a truly unforgettable experience.
Yet, no trip to Paris would be complete without indulging in the city’s timeless charm. Alycia and Marty took their time to savor the city’s delights, dining at street-side cafes where the aroma of freshly baked croissants and rich espresso filled the air. They wandered through the narrow, cobblestone streets, enjoying every moment of their Parisian adventure. The Eiffel Tower, standing tall against the Parisian sky, was a must-see, as were the Arc de Triomphe, the Louvre, and the historic Notre Dame Cathedral. They also hoped to discover more hidden gems and immerse themselves in the city’s unique culture.
After days of adventure and exploration, Alycia and Marty packed their bags for the next leg of their journey: New York City. They were headed to the Big Apple for the “Runway of Dreams” fashion extravaganza in Brooklyn. A night filled with fashion, fun, and forward-thinking design awaited them, celebrating inclusive fashion and the breaking of barriers in the fashion industry.
As they wrapped up their whirlwind trip, they couldn’t help but feel a deep sense of fulfillment and excitement for what lay ahead. Returning home, they knew they had just a short time to prepare for another action-packed October, celebrating National Disability Employment Awareness Month. Alycia, ever the advocate, was ready to continue her mission, inspired by the incredible experiences and people she met along the way.
Paris had left its mark on them both, a city of dreams, inspiration, and endless possibilities.

Dana Mathewson stands as one of the most prominent Paralympians in U.S. history, recently honored as the flag bearer for Team USA in the Santiago Para Pans 2023, where she also won two gold medals in Singles and Doubles wheelchair tennis, punching an early ticket to Paris 2024. A two-time Paralympian, Dana holds the title of the top-ranked American woman in wheelchair tennis and secured the … open the full bio Wimbledon Ladies’ Doubles championship in 2022, marking a historic milestone as the first American woman to claim a Grand Slam title in wheelchair tennis. Her journey culminates with the upcoming Paris 2024 Paralympic Games.
Diagnosed with the rare auto-immune condition transverse myelitis at the age of 11, Dana was left paralyzed from the waist down. Through her mother’s persistence and unyielding support, she was introduced to wheelchair tennis at 13. It was through wheelchair tennis that Dana discovered her passion, reclaiming her independence. Today, she holds the distinction of being the highest-ranked American in wheelchair tennis and boasts partnerships with iconic brands like Adidas Tennis, Wilson, Dobel Tequila, and Deloitte. She is also the only American woman to have played in all Grand Slam events as the top 8 ranking athlete. Dana has mentored countless up-and-coming tennis players and continues to coach in clinics across the country.
In December 2023, Dana tied the knot with her fiancé, Dristin Hughes, a medical resident in Gainesville, FL. Dana is a proud dog mom to Riley and holds a Doctorate degree in Audiology. She is looking forward to representing Team USA in her third and final Paralympic Games.

A passionate disability advocate, award-winning business leader, speaker, and podcast host, Julie Sowash is a true innovator in the DEIB and TA/HR field. As Co-Founder and Executive Director of Disability Solutions, she and her team have partnered with over 80 companies of every size and industry, including PepsiCo, Synchrony, and Bristol Myers Squibb, who value people with disabilities by helping … open the full bio them implement outcome-based programs and solutions throughout the engagement, hiring and retention process.   She is also a person who lives with multiple invisible disabilities.
She supports the building and deployment of strategic solutions by first assessing current structures, systems, policies, and processes to identify areas for improvement. Julie provides a real-world perspective to her work as both someone living with a disability and a professional having worked in public, private, and vendor environments.
Julie regularly speaks at state, national, and international conferences, including the United Nations Day of Persons with Disabilities Celebration and DisruptHR, focusing on topics such as compliance and disability inclusion. She is the host of the Changing Minds and Changing Lives Podcast, discussing diversity, equity, and inclusion in everyday life. She leads Ability, Stronger, the DEIB strategy for Ability Beyond. She was also recognized as one of the Top 100 in Talent Acquisition Technology by TA Tech in 2021 and one of the Top 100 DEIB professionals by Untapped in 2022. 

Jayne Mattingly
Jayne@JayneMattingly.com
@JayneMattingly
Bio:Jayne is a Leader, Author, and Advocate who speaks up for those that are disabled and in the Body Image and Eating Disorder community. She is the Co-Founder of Disabled Voters for Harris and her content, mission, and now debut Book, “This is Body Grief” provide a safe space and support for an unseen and unheard community.She holds a … open the full bio Master’s Degree in Clinical Mental Health Counseling
Jayne is disabled by her progressive and degenerative illnesses; Ehlers Danlos Syndrome, intracranial hypertension, Endometriosis, and now a severe allergy to the metal that has been implanted in her body and as a result has had more than 19 brain procedures and total hysterectomy. She relies on her rollator, wheel chair and her service dog Wheatie.

Lisa Cox is a TEDx speaker, author, globally published writer, internationally awarded thought leader and inclusive communications consultant. She has combined her professional background in advertising and media, with a personal experience of disability. Lisa is passionate about empowering professionals to navigate the nuances of disability inclusion with practical solutions and HOW-TO advice. … open the full bio She is working with business and industry to create content that better reflects our community, approximately 20% of whom have a disability but are rarely represented well, if at all. It’s through more consistent and authentic representation that some of the world’s largest and most powerful industries can impact social outcomes, like employment, for people with disability. Lisa is the inaugural Disability Affairs Officer at Media Diversity Australia, has worked with Advertising Council Australia’s Diversity & Inclusion Taskforce and currently sits on Griffith University Inclusive Futures Engagement Council.

Andraéa LaVant is a nationally and internationally sought-after disability inclusion expert. She is President and CEO of LaVant Consulting, an award-nominated disabled, black-queer woman led social impact-strategy and communications firm dedicated to shaping the way the world reaches, views and values disabled people.

Angelea is a Nashville-based photographer, specializing in fashion and portraiture. Her portfolio encompasses a diverse range of clients, from local brand campaigns and publications to international fashion editorials and key art for some of the most reputable artists in music and entertainment.
Angelea thrives with congenital scoliosis and VACTERL. Without the past 23 surgeries and medical … open the full bio experiences throughout the years, she wouldn’t have the perspective she has today.
Driven by her goal to make a positive difference in the world with photography, Angelea launched her project, “Let Them Stare,” which will evolve the fashion industry into a more inclusive light.

Lorraine Woodward is an industry leader dedicated to disability advocacy. Lorraine pulls no punches when talking about the reality of the lack of accessibility within the vacation rentals industry and how as a community we can (and need to!) make small but significant changes to create more accessible spaces for every kind of guests.
Adam Norko is an accomplished business development and marketing … open the full bio executive with extensive experience in the hospitality and real estate industries. Proven track record of driving growth and enhancing operational efficiencies across multiple roles. Demonstrates strong leadership skills with a focus on innovative strategies, customer satisfaction, and achieving significant revenue growth.

Having formerly managed a division at Apple for iPhone, Watch and Airpods – Dhaval Patel is an engineer, a keynote speaker and an Individual of Extraordinary Ability as accredited by the US government with over 37 patents in sensing & haptics. Dhaval is the Founder & CEO of Lotus – who’s mission is to build technology that is useful to everyone by optimizing for disability first. To that … open the full bio end, Lotus has built a wearable Ring that controls objects at home by pointing.

🎉🎙️ Celebrating One Year of “Pushing Forward with Alycia”! 🎙️🎉
🌟 Wow, what an incredible journey it has been! Today marks the first anniversary of “Pushing Forward with Alycia,” and we couldn’t be more grateful for this amazing community that has grown around our podcast. 🌟
From our very first episode to this moment, each conversation, story, and insight shared has been a testament to the power of … open the full bio resilience, courage, and determination. “Pushing Forward with Alycia” was born out of a simple yet profound idea: to inspire and empower our listeners by showcasing the stories of those who have overcome challenges and achieved remarkable feats.
Over the past year, we’ve had the privilege of hearing from extraordinary individuals who have faced adversity head-on and emerged stronger. Their stories have touched hearts, sparked conversations, and ignited hope. Whether it was exploring personal growth, navigating career milestones, or discussing societal change, each episode has been a beacon of inspiration.
To our incredible guests: thank you for sharing your journeys with us and for being the driving force behind our podcast’s success. Your authenticity and courage have resonated deeply with our audience, encouraging them to push forward in their own lives.
To our listeners: thank you for tuning in, for your support, and for being part of this uplifting community. Your feedback and enthusiasm continue to fuel our passion for creating meaningful content that makes a difference.
As we look ahead to the future, we are excited about the possibilities that lie ahead. We remain committed to bringing you more engaging conversations, insightful perspectives, and stories that inspire positive change. Together, we will continue pushing forward, learning, growing, and celebrating the triumphs of the human spirit.
Here’s to many more years of “Pushing Forward with Alycia” and to the limitless potential of what we can achieve together. Thank you for being part of this incredible journey!
With gratitude and excitement,
Alycia & Marty Anderson
“Pushing Forward with Alycia”
🎧 Listen to our anniversary episode and join the celebration on Apple Podcasts and wherever you get your podcasts! 🎧
#PushingForward #PodcastAnniversary #Inspiration

Kaylee Bays, 27, A dancer on wheels from The Bay Area. Kaylee was born with Ehlers Danlos Syndrome, a multi systemic connective tissue disorder, and was a medical mystery for the majority of her young life. Kaylee was the first visibly disabled dancer to ever work for Disney Live Entertainment when she was a part of the opening cast for “Rogers the Musical”. She would later go on to be the first … open the full bio wheelchair user to ever dance on the television hit “So You Think You Can Dance.” Kaylee’s mission is to expand dance spaces for the artists who, like her, didn’t fit the box. She currently works professionally as a dancer, performs with the LA dance team Rollettes, and runs her virtual dance studio “Studio Slay”.

Kimberly Daya, a 45-year-old married mother to a 16 & 21 year old, is the host of the Humanity Unlocked podcast. In 2007 she faced a devastating blow to her health that left her unable to walk, drive, and independently care for her family. After being diagnosed with Multiple Sclerosis in 2008, it was determined after 5 years that she was actually battling Lyme disease. For over a decade she … open the full bio struggled to come to terms with the discrepancy that existed between the reality of her condition and the lack of understanding she encountered from the public. Kimberly understands that oftentimes the difference between empathy and judgment is knowing each person’s full story. With that in mind, she has taken to her podcast to unlock the humanity behind a wide range of topics that are often pre-judged and stigmatized, with a goal to foster a greater awareness of the diverse experiences that connect us all.

Get ready for a heartwarming and joyous reunion as Alycia’s beloved sisters make their grand return for a twin sister birthday celebration! This special episode promises to be a delightful mix of laughter, nostalgia, and sisterly love, as Regina, Alycia’s twin, and Corinna, her younger sister, come together to celebrate Alycia & Regina’s birthday in a way that only they can. Hosted by Corinna, … open the full bio the episode will take viewers on a trip down memory lane, revisiting unforgettable moments from previous appearances while creating new memories that will be cherished for years to come.
Regina, Alycia’s identical twin, first captured our hearts in Episode 12, where the twin sisters’ uncanny resemblance and deep bond shone through their hilarious banter and heartfelt conversations. Regina’s vivacious personality and infectious laughter complemented Alycia’s more reserved demeanor, creating a perfect balance that left fans yearning for more. Their sibling synergy brought a unique dynamic to the show, and this birthday celebration promises to reignite that same magic, with Regina bringing her characteristic warmth and humor to the festivities.
Corinna, the youngest of the Busciglio sisters, made a memorable entrance in Episode 15, where her exuberance and creative flair added a fresh and exciting twist to the show. As the host of this special birthday episode, Corinna’s organizational prowess and attention to detail will be on full display. Her ability to blend sentimental moments with spontaneous fun ensures that this celebration will be both emotionally touching and entertaining. Fans will recall her knack for surprising Alycia with thoughtful gestures, and we can expect nothing less this time around.
In this episode, viewers can look forward to a series of fun-filled segments and heartfelt surprises. The sisters will share cherished memories from their childhood, including hilarious anecdotes and touching moments that have shaped their unbreakable bond. Regina and Corinna have also planned a few surprises for Alycia, guaranteed to bring both tears of joy and peals of laughter. With their distinct personalities shining through, the sisters’ interactions will remind fans why the Busciglio family holds such a special place in their hearts.
As the episode unfolds, the love and camaraderie among the sisters will be palpable, making it a must-watch for longtime fans and new viewers alike. Whether it’s through Regina’s witty remarks, Corinna’s heartfelt hosting, or Alycia’s genuine reactions, this twin sister birthday celebration will be a testament to the enduring bond of sisterhood. So, mark your calendars and join us for an episode filled with laughter, love, and the irreplaceable joy.

Steph Aiello has “made her hands her brand.” She’s a super quadriplegic with an “I Can Attitude” living in Southern California. Steph is a makeup artist, content creator, and disability advocate. Over the years she’s had the honor of being the first wheelchair model for Ulta Beauty, Maybelline New York Ambassador & Product Testing, and brand partnerships with Revlon, Fenty Beauty, Estée … open the full bio Lauder, Buxom cosmetics, Amazon, Herbal Essences, Braun, Redken, Flip Beauty, and Tarte Cosmetics. She’s been featured in articles; by People Magazine, Bustle, Teen Vogue, Pop Sugar, and Daily Mail. Steph continues to glide through life and the future looks bright for this incredible trailblazer. You can follow Steph’s journey on TikTok & Instagram at @uwalk_iglide

Hi, my name is Samuel Benifield-Chivore, an almost 16 year old sophomore in high school. I was diagnosed with Arteriovenous Malformation of the brain, AVM at the age of 3. During my childhood and teenage years, I spent a lot of time in hospitals, underwent numerous surgeries, procedures, and Gamma Knife Radiation treatments. As a result of the AVM, I lost the use of my dominant right hand. I had … open the full bio to learn how to use my left hand to write, build strength with my right hand, work on my right side balance, and incorporate this into my day-to-day life. 
As a child it was difficult to be a child and still go to my appointments and hospital visits. Since I couldn’t do any contact sports I wasn’t allowed to participate in the larger gym classes with my friends. I had to find new hobbies that didn’t include physical sports and the freedom to use only one hand. So I tried building lego sets, chess, art, painting, drawing, video games, writing awards, and Lego competitions. As I grew older, people told me I couldn’t do things because I only had the use of one hand but I proved them wrong time after time. I learned to play the trumpet, learned to sew on a sewing machine, ceramics, drums, buddy ball soccer, buddy ball basketball and finally in HS I was able to take adaptive gym. 
One of my greatest accomplishments is that I have been an Honor Roll Student since before the Pandemic. Also, last year, I told my family I wanted a job and they encouraged me to open up an Etsy Store. So I started a store called Samuel’s Bricks which was just a hobby and is now a part time job. I build custom Lego scenes using one hand and people are very amazed when they watch me build. Recently, I tried out for the school play and was cast as the teen angel in Grease.  If someone would have told me 10 years ago that I would be in a play singing and dancing without falling and keeping up with the rest of the kids I would have laughed. Although some might see my disability as a disadvantage (in reality it is not). Now that I am older I never let my AVM limit my dreams.

I’m a father, husband, designer, disability advocate and international speaker who happens to have been born without hands. As an advocate and influencer I have worked with brands such as General Motors, Amazon, Lids, Rocket Mortgage, Zappos and many others.
My son, Noah and I started a consulting company called Equal Accessibility. Equal Accessibility is a consulting company dedicated to helping … open the full bio businesses create equal experiences for ALL. Our mission is to break free from the confines of standard compliance and, instead, collaborate with businesses to create environments that are not only inclusive but genuinely welcoming for disabled guests.

Alycia and I reminisce on our mothers to honor them this Mother’s Day. Marsha and Peggy both fought hard to pave the way for their disabled children in a time when that was not a thing to do. These mothers through their love and care would raise their disabled children to be confident, resourceful and resilient despite the hardships they would face throughout their lifetimes. There strength … open the full bio would be forged by the tragedies of their own lives but would also transcend these struggles to foster feelings of belonging, unity and family that have outlasted them and still provide true cornerstones for our outlooks today. Happy Mother’s Day to all the mothers out their facing these challenges today. May you find some inspiration from the stories we share, and may our mothers’ to inspire you to blaze the trails for your children.

Hi I’m mason! I am a content creator and T12 paraplegic. I show the world what is possible for wheelchair users as I push the limits and provide resources for my community along the way! Feel free to use my affiliate code “mason” on a firefly at riomobility.com for free shipping! Or “mason” at vapor wheels for 10% off an item!

Peggy Sellery lives in Boise, Idaho with her husband and three amazing kids. She is an MIT and Columbia graduate, an entrepreneur and founder of No Guesswork SAT/ACT Test Prep and Tutoring, and a nonfiction creative writer.
Recent surveys of youth reveal that the risk factors for depression, anxiety, and suicidality include a lack of authentic social connection. Understanding that this lack of … open the full bio authentic connection stems from a profound fear-based inability to feel like we can truly be ourselves and still be embraced in belonging, Peggy has started a mental wellness initiative called Let’s See Love Today. It encourages people to look at each other AND themselves through the lens of love, with the deeper perspective that true beauty comes from being who we really are.

The Be Like Josh foundation is a non profit organization dedicated to the study and advocacy of dogs with neurological disabilities. We are proud to celebrate all abilities on the canine neurological spectrum. It is an honor to rescue, rehabilitate and re-home these exceptional animals, to tell their stories, from rescue to adoption, and every adventure along the way. They serve as ambassadors of … open the full bio our mission, which pushes back against ableism in the veterinary community and promotes true inclusion, for animals and humans alike. Through our work, we share the message that all animals and people, wherever they are on the spectrum of abilities, are worthy of being seen, loved and appreciated.
Our rescue arm operates much like a traditional rescue organization, however we predominantly take in dogs with special needs. Because these types of animals can often require more attention and expense, we generally manage no more than 5 or 6 dogs in our rescue at any given time. Through donations, the Be Like Josh Foundation pays for all intake evaluations, vaccines, spay/neuter and any needed diagnostics, including MRI’s, which can be rather costly. Our rescue also pays for follow up medical exams, proper nutrition, supplements, medications, behavioral training (if needed) and any other remedies or therapies prescribed by attending veterinarians. Our financial support continues until the dog is officially adopted.
As part of our Community Outreach program, we visit schools across the country. We have a Be Like Josh curriculum based upon acceptance and inclusion. We inspire the children to be kind toward, and embrace all people, regardless of their differences. Our Special Abilities Program is focused on connecting with Josh through physical interaction, and asking questions. Your donations help to cover the expense of travel to schools across the country, allowing us to make a broader impact.
We believe that every dog is worthy of a quality life filled with exercise, enrichment, and a forever family to love them regardless of their physical abilities.
Due to the nature of the work we do, the dogs in our care stay with us longer than the typical rescue dog. Our vetting and diagnostic process is extremely thorough and we spend a lot of time with each case to understand the dog in his or her totality, taking into account all aspects of their mental and physical well-being. Dogs that enter the Be Like Josh Foundation serve as ambassadors of our message which is that regardless of where we sit on the spectrum of abilities, all animals (and people) are worthy of love, respect and belonging. Our goal is to challenge the ableist mindset that discriminates against neurological differences to create a more compassionate and deeper understanding for all beings who exist in the world. Learn more at belikejosh.org

As an entrepreneurial leader in User Experience (UX) mixed methods research, I identify problems, pitch solutions and get buy-in to make improvements in products. My passion lies in finding new ways to apply Artificial Intelligence (AI) to user research. My professional journey spans over a decade, during which I’ve led research and design for more than 100 software projects and products across … open the full bio diverse industries. My unique blend of experience, from spearheading a UX agency to contributing to Fortune 100s, has equipped me with a deep understanding of how user needs intersect with business objectives.

Joci Scott is an actress, singer, and dancer based in Los Angeles. She became paralyzed at 20 years old by sustaining a T12 spinal cord injury when her family survived a plane crash, and has adjusted to life with a disability. Noticing a lack of disability in entertainment, Joci is a passionate advocate for disability representation and portraying complex disabled stories. Joci has been a … open the full bio Rollettes dance team member since 2021, empowering women through dance and community. Her leading performance in “Smash or Pass” received a “Best Actor” nomination in the 2023 Easterseals Disability Film Challenge and the film went to the 2024 Slamdance Film Festival. Her latest film “Body Swap” made for the 2024 Disability Film Challenge explores what happens when a wheelchair user and a non-disabled person switch bodies for a day. Spoiler alert – hilarity ensues. Her ultimate goal is to be a working actor in the industry and show the world that disabled people have stories to tell too.

Joanne Lopez: Banking Leader Extraordinaire
Joanne’s journey to the United States started at the age of 13, when she and her family made the life-changing decision to immigrate to New Jersey. Right from the outset, Joanne showcased an exceptional talent for numbers and an unwavering passion for providing excellent customer service. Upon successfully completing her education, she wasted no time … open the full bio embarking on her professional voyage, taking her inaugural step into the realm of finance as a bank teller at National Westminster Bank.
Her career in banking was off to a promising start, and it was evident that Joanne possessed a unique blend of skills and competencies that would set her apart in the industry. She quickly ascended the ranks, and her journey through the financial industry was marked by a series of noteworthy achievements.
Joanne’s core skills and competencies read like a comprehensive toolkit for a banking professional. She demonstrated strong leadership abilities, a keen sense of financial planning, exceptional quantitative skills, and an ability to perform under pressure. Her knack for problem-solving and risk assessment was complemented by her unwavering commitment to customer service. Joanne’s attention to detail, analytical skills, and proficiency in various software, made her a force to be reckoned with in the banking sector.
Career Highlights
Joanne’s most recent role at Valley Bank in Montclair, NJ, sees her leading the charge in planning and executing strategies to drive the overall operations and profitability of multiple branches. She has demonstrated her ability to manage budgets, improve revenues, and create an environment that exceeds client expectations. Her leadership extends to team development, market intelligence, and ensuring operational functions meet compliance requirements. Joanne excels at building and expanding customer relationships while representing the bank in an excellent manner.
Throughout her distinguished 27-year banking career, Joanne consistently demonstrated her expertise in delivering exceptional results, leading high-performing teams, and nurturing robust customer relationships. Her constant dedication to her profession has garnered her a plethora of accolades, most notably the prestigious distinction of Business of the Year by the Montclair Chamber of Commerce in March 2019. Furthermore, she has taken on the role of a board member for the N.J. Latino Law Enforcement Coalition since June 2023. In addition to these commitments, Joanne currently serves as a board member for Out Montclair and proudly carries the title of Ambassador for NJ Reentry Corporation.
One of the proudest achievements of Joanne’s career materialized through her recent partnership with NJ Reentry, a pivotal turning point. As an Ambassador for NJ Reentry, Joanne had firsthand exposure to the organization’s profound impact on individuals who have previously been incarcerated. NJ Reentry provides critical support in areas such as housing, food, medical care, clothing, substance abuse treatment, mental health care, employment, and education. Yet, one essential element was absent, which was the opportunity for these individuals to establish a bank account.
Recognizing this gap, Joanne initiated a transformative collaboration with Valley Bank. Together, they created a tailored banking solution for NJ Reentry clients, affording them the crucial opportunity for a second chance to build a secure and healthy financial future. This initiative represents a crowning achievement in Joanne’s distinguished career, embodying her commitment to social impact and financial empowerment.
Today, Joanne is a dedicated mother to two lovely teenage daughters and a loving wife to her husband. Her most cherished moments are centered around creating precious family memories and crafting unforgettable experiences during vacations.
Joanne’s life story serves as a testament to the American dream, where the combination of hard work, innate talent, and reliable dedication has led to remarkable success. Her amazing journey from the tiny island of Trinidad and Tobago to the pinnacle of the U.S. banking sector stands as an inspirational example of what can be accomplished with unwavering determination and a firm commitment to excellence. Joanne is undeniably an accomplished and elite banker, leaving an enduring impact on the banking industry that resonates today.

Catarina is a dynamic public speaker, DEI consultant, and content creator. She works with companies to improve disability awareness, inclusion, and accessibility. As a disabled Latine woman, she is passionate about sharing her own unique story to help build a more inclusive world.

Lindsay Ulrey, is an active, busy mama of two young boys and enjoys being outside, family bike rides and adventures of all kind! Lindsay is a licensed clinical psychologist and certified perinatal mental health practitioner (PsyD, PMH-C) and runs a private practice in northern CA. She feels passionately about supporting individuals in the perinatal stages of life and creating safe spaces that … open the full bio facilitate growth and healing during a difficult transition. Lindsay is also a total foodie (and appeared on season 13 of Check Please, Bay Area!) and enjoys going out and trying new restaurants as well as getting crazy in the kitchen trying out new recipes.

Jillian is a writer, content creator, and advocate for dwarfism and disability awareness. She is the host of the podcast Always Looking Up where she speaks to little people, disabled people, those that are disability-adjacent and allies about living in a world that was not necessarily designed for them.

When she was just 18, Donna Walton’s dreams of being a dancer, a singer, and an actress were shattered when she was diagnosed with life-threatening bone cancer and had to have most of her left leg amputated to save her life.
Over the following decades, as she struggled to simply return to a “normal” life, she learned—despite disasters, setbacks, trials and tribulations—how to survive and even … open the full bio thrive with a disability.
“I know now that broken lives can be renewed, remade, rebuilt, recycled, reinvented and rebranded,” says Walton, who graduated with a doctorate in rehabilitation counseling in 2005 and is trained in cognitive behavioral therapy. “In fact, in many cases, our new lives can be even better than our old ones—if we know how to deal with the trauma.”
After reinventing her own life, Walton’s new dream was to help others. As a result, in 2012, she founded The Divas With Disabilities Project to support other black and brown girls and women with disabilities, and the organization has since grown into an international movement.
In addition to helping ensure that these women and girls don’t fall through the cracks of a world that wasn’t made for them, her earlier dreams of being a performer have also come full circle.
Since founding DWD, she has also modeled, done public speaking, and acted in several films, including the 2020 Black Oak TV series The Retreat and the 2023 Hulu series The Other Black Girl.
In 2024, she shows no signs of slowing down on creative projects, including co-producing a digital docuseries titled Divas in the City.
For more information about Walton and DWD, please visit divaswithdisabilities.org.

Jonathan Goodwin has been called “the closest thing we can boast to a real life superhero”, and “the worlds greatest theatrical stunt performer”. Jonathan has been hanged, buried alive, locked in a box while covered in 200,000 bees, attacked by sharks, bitten by rattlesnakes and hung from his toes from helicopters. Jonathan has performed on every continent except Antarctica and in every US State … open the full bio except Alaska. Goodwin has played Broadway, London’s West End, Sydney Opera House and Radio City Music Hall.
In 2021 Jonathan was involved in an accident while rehearsing a stunt for American tv. The accident left Jonathan with horrendous injuries and resulted in him being permanently paralyzed from the waist down. Now retired from stunt performing Jonathan has turned his attention to writing, presenting, Hypnotherapy and being a roll model (pun intended) for both disabled and able bodied people alike

Aiesha Robinson, a vibrant keynote speaker and self-love advocate, embarked on her empowering journey at 18 when diagnosed with vitiligo. Fueled by personal experiences, she founded Born To Rise, a nonprofit fostering resilience through shared stories. Aiesha’s impactful talks on self-love, resilience, grief, and bullying resonate globally, drawing from her authentic journey. As a speaking and … open the full bio self-coach, she guides others towards empowerment, embodying the strength found in embracing vulnerability. Aiesha Robinson is more than a speaker; she is a beacon of hope, inspiring individuals to rise above challenges and discover their inner resilience.

Valentine’s Day, celebrated annually on February 14th, is a day dedicated to love, affection, and romance. Its origins trace back to ancient Roman and Christian traditions, but today it is celebrated worldwide as a day to express love and appreciation for those close to us.
One interpretation of Valentine’s Day dates back to ancient Rome, where mid-February marked the celebration of Lupercalia, a … open the full bio fertility festival dedicated to Faunus, the Roman god of agriculture. During this festival, young men would draw names of young women from a jar, forming temporary romantic pairings. This tradition evolved over time to become associated with courtship and love.
The Christian association with Valentine’s Day is believed to stem from the commemoration of Saint Valentine, a third-century Roman priest who defied Emperor Claudius II’s ban on marriage for young men, believing that single men made better soldiers. Saint Valentine continued to perform marriages in secret, for which he was eventually martyred. The legend suggests that before his execution, he sent a letter to the jailer’s daughter signed “from your Valentine,” thus establishing the tradition of sending love letters.
Today, Valentine’s Day is celebrated with various customs and rituals. The exchange of greeting cards, flowers, chocolates, and gifts has become synonymous with the holiday, symbolizing affection and appreciation. Couples often go on romantic dates, share intimate moments, and express their love through gestures of kindness and thoughtfulness.
However, Valentine’s Day is not limited to romantic love. It also celebrates platonic love, friendship, and familial bonds. Many people use the occasion to show appreciation for their friends, family members, and even pets, spreading love and positivity to all those who hold significance in their lives.
Critics of Valentine’s Day argue that it has become overly commercialized, with the focus shifting towards consumerism rather than genuine expressions of love. However, proponents argue that the holiday serves as a reminder to cherish and celebrate the love we share with others, regardless of its commercial aspects.
In recent years, Valentine’s Day has also been reclaimed as a day of self-love and self-care. Individuals practice acts of self-love, such as pampering themselves, engaging in activities they enjoy, or simply taking time to appreciate their own worth and value.
Ultimately, the meaning of Valentine’s Day lies in the expression of love and appreciation for others. Whether it’s through grand gestures or simple acts of kindness, the holiday serves as a reminder to celebrate the bonds of love that connect us all. It is a day to cherish the relationships we hold dear and to spread love, joy, and positivity to those around us.

Regina and Shane Weinstein’s journey as parents of a congenital heart defect (CHD) warrior is a testament to the power of resilience and love in the face of adversity. Their story serves as an inspiration to many, especially during important awareness weeks dedicated to raising understanding and support for those affected by CHD.
Their unwavering commitment to their child’s well-being and their … open the full bio ability to navigate the challenges associated with CHD showcases the strength of the human spirit. By sharing their experiences, Regina and Shane not only raise awareness about CHD but also offer hope and encouragement to other families who may be going through similar struggles.
Their story reminds us all of the importance of empathy, support, and advocacy for individuals and families impacted by CHD. Through their resilience and love, Regina and Shane Weinstein exemplify the power of unity and compassion in overcoming life’s obstacles.

After being thrown out of a Las Vegas hotel in a drunken haze, jeopardizing his career and relationships, Nick Klingensmith had to make a change. A 4-time cancer survivor, type-1 diabetic, recovering alcoholic with herniated discs, nerve damage and sleep apnea, he defies it all when he finds Obstacle Course Racing. Refusing to accept his limitations, he’s completed over 100 Spartan Races, 6 Major … open the full bio Marathons, several Ultras and scores of other obstacle and endurance events.
As someone who has walked the path of a sales professional, Nick is an expert in propelling other achievement-driven professionals and leaders to overcome fear and rejection and push past self-limiting doubts, by inspiring them to take purposeful action towards their goals. Nick is a raw and passionate storyteller who holds nothing back when revealing who he used to be and the person he is now.

Here are some areas to look for significant developments throughout the New Year of 2024 in Accessibility, Diversity Equity & Disability Inclusion:

Policy Changes: Let’s hope for and expect potential updates or changes in disability-related policies and regulations globally that will help national and global disabled populations in all countries all around the globe to live finding richer, … open the full bio fuller, and more inclusive opportunities within our society.
Technology Advancements: Anticipate new technologies and innovations aimed at improving accessibility and inclusion for individuals with disabilities. AI playing a major role in this conversation moving into 2024.
Corporate Inclusion Initiatives: Look for major companies implementing or expanding diversity, equity, and inclusion programs with a focus on disability inclusion. The word is getting out that the disabled community represents one of the world’s largest consumer bases, and leading companies want to know how they buy in.
International Disability Awareness Events: Events like the International Day of Persons with Disabilities (December 3rd) may see increased global awareness initiatives, and major milestone moments throughout the year like National Disability Employment Awareness Month (NDEAM), Global Accessibility Awareness Day(GAAD), Disability Pride Month and the nearly other 240 special disability related days listed on this calendar.
Advocacy Campaigns: Let’s hope that we will see catchy, mainstream impactful advocacy campaigns addressing disability rights, inclusion, and awareness.
Education Initiatives: Campaigns throughout the upcoming cycle should be focusing even more than ever on the development of inclusive education practices and initiatives supporting accessibility in educational institutions and the learning to move beyond compliance and bridge and connect the human elements of inclusion.
Accessible Infrastructure Projects: From Federal to State and even at County and City levels every step in the chain of command in our government should be seriously considering and be actively in the discovery phase of advancements in creating more accessible public spaces, transportation, and infrastructure as a way to fill the need of their growing numbers in populations.
Media Representation: There should be continued efforts to improve the representation of individuals with disabilities in media and entertainment. Where real people living with disabilities find work in sharing and developing the themes, topics and instances that reflect a life of living with a disability portrayed in these representations.
Inclusive Employment Practices: Lets encourage and find more companies adopting and promoting more inclusive hiring and workplace practices for individuals with disabilities by bringing a real stake in the game to the entrepreneurs, innovators and advocators building the foundations of for the benefits of disability inclusion in the workforce.
Global Conferences: Participation and discussions at major international conferences focusing on disability inclusion and accessibility should include more people with disabilities outlining pathways to pushing forward the disability empowerment movement.
Inclusive Design Trends: Keep an eye on the integration of inclusive design principles in various products, services, and environments, as the full gamut of the world’s industries realize the new frontier of universal barrier free designs and truly all inclusive environments.
Collaborations and Partnerships: Watch for collaborations between organizations, governments, and advocacy groups to enhance disability inclusion on a broader scale. And, for the allyship of even the members within our tight knit community of people with disabilities learn to lift up and work with each other to usher in the new era of opportunities that await.

Meet Josh Basile a C4-5 quadriplegic, power wheelchair user, disability rights advocate, trial attorney, inventor, and proud father. In 2004 at the age of 18, Josh was paralyzed below the shoulders in a beach accident. Soon after he formed the Determined2Heal Foundation, a 501(c)3 nonprofit, to empower newly injured families. Josh created the world’s largest paralysis video mentoring network … open the full bio through SPINALpedia.com with 30,000 videos searchable by physical functionality. As a medical malpractice lawyer and disabilities rights advocate, Josh serves persons with disabilities both in the courtroom and through policy initiatives. As a community leader and changemaker, Josh works tirelessly to improve the quality of life the people with disabilities and to continuously break down existing barriers to access and inclusion, independent living, transportation, employment, and web accessibility.

Meredith Sadoulet is the Founder and CEO of ProFound, a startup building a powerful professional network among disability-inclusive leaders. She launched ProFound after a 20+ year corporate career as a Finance, Strategy, and HR executive across multiple iconic Fortune 100 companies. With personal connection to disability, Meredith is passionate about amplifying disability leadership in the … open the full bio workforce and positively impacting global employment outcomes.

Chelsie Hill is professional dancer, community leader, content creator, and Founder/CEO of Rollettes, a Los Angeles based wheelchair dance team that’s committed to education, disability representation, and female empowerment.
As an entrepreneur, Chelsie created the very first women and kids empowerment event called the Rollettes Experience with seminars to empower, educate and connect the hundreds … open the full bio and hundreds of attendees who have traveled from across the country and 17 countries to attend every year on dance, fitness, yoga, makeup, special guest speakers and panels, pj party, pool party, talent showcase, and the Boundless Babe Awards.
The goal as a company and team is to empower women with disabilities to live boundlessly and shift perspectives through dance. Chelsie and the Rollettes are creating a global movement of Boundless Babes by helping them become community leaders and live independent lives.
The Rollettes dance team were featured on Adam Levine’s series “Sugar” on YouTube Premium, Vanderpump Dogs on Peacock and performed in numerous special events such as Garden of Dreams Talent Show with the Radio City Rockettes, 86th Annual Hollywood Christmas Parade, Redbull’s Wings for Life World Run, Disneyland, Festival Internazionale delle Abilità Differenti in Italy, and Gold meets Golden for the Golden Globes.
As a content creator, community leader, and personal brand, Chelsie and the Rollettes are highly sought out by production companies, producers and brands to create, produce and consult on projects for TV, Film, Commercials, YouTube and Social Media.

In 2023, Alycia and Marty reflected on their pivotal moments. They discussed the launch of their podcast, remarkable interviews, and professional milestones. Besides, they recounted impactful experiences such as advocacy work, historical trips, and personal growth. The couple aims to continue inspiring others and overcoming fear in their journey.

Lisa Zibelli Tetzloff, a retired paralegal, boasts an extensive 40-year tenure within the legal field. Her professional journey was marked by aiding numerous individuals in advocating the complexities of securing social security and disability benefits.
Beyond her professional achievements, she revels in a joyous marriage, embracing roles as a devoted wife, nurturing mother, and loving … open the full bio grandmother.

Bill Krebs grew up in Philadelphia and was labeled with a developmental disability at an early age. In first grade, it was hard for him to keep up with the regular kids, so he was left back the next few years until he was finally tested. It was revealed that Bill had a developmental disability. He was placed in special education classes where he was self-contained, meaning everything took place in … open the full bio the class and you didn’t get to see the other kids. After he graduated, Bill felt fortunate to find a group called “Speaking for Ourselves.” He now utilizes his lived experiences to teach individuals how to speak up for themselves and know their rights.
Bill now works for Liberty Resources supporting others with developmental disabilities and autism. He facilitates a monthly group in which he provides support and resources. Bill is also an advocate coordinator for individuals with developmental disabilities at Keystone Services, an organization that has offices all over the world. Bill Krebs is a leader of a self-advocate movement and sits on several committees throughout the state. He is a proud recipient of the Brighter Futures Award, Justin Dart Award, and the Mental Health Association Award, among others. He brings an IDS perspective to the PCTAB, and we are excited to have him on board.

Before starting the Runway of Dreams Foundation in 2014, Mindy Scheier spent 20 years working in fashion on the design team for the INC collection and as a stylist for Saks Fifth Avenue. Mindy was inspired to start Runway of Dreams after her son Oliver, who has Muscular Dystrophy, dreamed of wearing jeans like everyone else. After using her design skills to adapt a pair that met his needs and … open the full bio increased his confidence, she went on to conduct extensive research to develop modifications that would meet the needs of the largest minority in our world- people with disabilities. Following its launch, Runway of Dreams partnered with Tommy Hilfiger on the first mainstream adaptive clothing line for kids and continues to work with many mainstream brands such as Kohl’s, Target, JCPenney and Zappos.com. Founded on the basis that clothing is a basic human need, Runway of Dreams develops, delivers and supports initiatives to broaden the reach of mainstream adaptive clothing and promote people with disabilities in the fashion industry.
Due to the overwhelming amount of requests Mindy received at Runway of Dreams from a multitude of brands and industries for connection to PWDs, in 2019, Mindy created Gamut Talent Management to represent people with disabilities and create a marketplace where businesses and industries can connect to this target audience. Gamut is rebranding the way PWDs are viewed, marketed to and represented in the mainstream world. The continued support of the mission of Runway of Dreams will always be a component of Gamut, as the company’s 501c3 partner.
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Mindy has been featured in ​Newsweek’s ​ “The Creative Class of 2019: Innovators,” ​People magazine’s “Heroes Among Us” and Pix 11’s “Changemaker: Making the Fashion Industry More Inclusive.” She has also been featured in USA Today, Parents, The New York Times, The Washington Post, Vogue Business, WWD, NBC’s Today, ABC’s Good Morning America, Access, CNBC, Fox News Channel and more. An inspiring ​TED ​speaker, Mindy has received numerous awards including the Catalyst Award for “Marketing Influencer of the Year,” Citrin Cooperman’s “Women at the Wheel Leadership Excellence Award, the Association of Image Consultants International Bravo Award and Enable Inc.’s Michael Graves Award for Creativity and Persistence.
Mindy studied Fashion Design with a dual program at the University of Vermont and Fashion Institute of Technology.

Mike Box is the mind behind the magic at BOX Wheelchairs. Mike began building wheelchairs after his brother was involved in a tragic motorcycle accident at the age of 17. When his brother couldn’t get cooperation from the manufacturer of his tennis wheelchair regarding adjustments, they decided to do it themselves. In 1992 after being in the aerospace industry, he left his job and they formed … open the full bio their own wheelchair company.
Mike designed and built the chairs for that company until 2010 after the company had been sold. At that point the industry was going in a direction that was not in Mike’s heart. His philosophy is and always has been helping others and for him, there is no better way to make a comfortable, durable wheelchair that fits the individual, than one you build from scratch! At Box Wheelchairs, ALL chairs are custom made to order and fitted with only the best parts and components on the market today.
Mike’s heart and soul goes into each one… Success is defined with team work, love, and LISTENING to a person’s concerns and challenges, before overcoming them. Most of all what makes BOX Wheelchairs different from the rest, is the bespoke feel and custom touches exclusive to each and every chair… You don’t have to just “settle”, as there is no such thing as a standard BOX Wheelchair!

Dez Del Barba was a 21-year-old Sonoma State University college student when he took a leave of absence from his last semester of college in order to pursue and complete Basic Training for the U.S. Army at Fort Benning, Georgia. After basic training Dez was going to complete his degree and attend the Officer Candidate School (OCS) for the Army. Unfortunately, while in week 6 of basic training, he … open the full bio developed Streptococcus A was seen by several military medical providers for several days, but was not treated properly. Due to this he contracted a rare flesh-eating disease, known as Necrotizing Fasciitis.
Dez was sent to the ICU at Piedmont Hospital in Columbus, Georgia on February 11th, 2019. The medical team began the first of many surgeries removing infected flesh, skin and muscle from his legs and body. On February 13th, Dez was flown out on an air ambulance to the University of Alabama (UAB) medical burn unit. There, Dez was under the care of surgeons from UAB and surgeons from the United States Military.
On February 14th, his sister’s birthday, a lifesaving surgery was performed and his left leg was amputated. Dez would go through yet another surgery the following day removing even more muscle and flesh. At this point Dez’s right leg was in danger of being amputated. However, the surgeons were confident that they could save his leg if he was moved to a different facility.
On February 16th, Dez was flown on an air ambulance to the Institute of Surgical Research (ISR), a state-of-the-art military Burn Unit at Brooke Army Medical Center (BAMC) in Ft. Sam Houston, Texas. Here, Dez would spend 100 days in the ISR hospital ward and underwent weekly surgeries, skin grafts, reconstruction surgery, physical therapy, and wound care that was performed daily. A total of 43 surgeries were performed on Dez.
Once Dez recovered enough to be released from the ISR hospital ward, he was transferred to a Wounded Warrior Transition unit at Joint Base San Antonio/Ft. Sam Houston military base. During this time, he began intensive physical therapy, rehabilitation training, and learned to use his prosthetic leg and other devices at the Center for the Intrepid (CFI).
On March 15, 2020, Dez returned home to California where he continued his rehabilitation at the University of California San Francisco (UCSF). Dez remained in the Army and was medically retired on August 17, 2021. Today Dez is becoming stronger physically and emotionally every day. He is very active in weight training and works out every day. He continues to go to physical therapy weekly. Dez and his college sweetheart, Julia, live happily together. On December 15, 2021, Dez completed his Business degree from Sonoma State University and will be starting a new career with a large software company in January 2022.
Dez has endured a physical, emotional and spiritual battle since this tragedy started. However, Dez is a WARRIOR and his faith in God has shown what an amazing and inspirational and strong young man he is. The support of his family, friends and the medical professionals who helped save his life since February 11, 2019, were imperative to his recovery and survival.

Nikki Walsh was raised outside of Philadelphia, Pennsylvania. She went to Penn State University where she graduated with a bachelors in Kinesiology and exercise science. She is a NASM Personal Trainer and Nutrition coach, content creator, and a mentor for women with disabilities. She has been featured in Women’s Health magazine Online, and Love What Matters. She strives to show all wheelchair … open the full bio users that despite their disabilities, they can do anything they want to in life.

Brian McComak is the CEO & Founder of Hummingbird Humanity. He is a consultant, speaker, author, and facilitator with over 25 years of experience in DEI, HR, culture, change management, internal communications, and employee experience. He is an openly gay man and a person with a disability who shares his lived experiences in service of fostering workplaces where humans thrive.

In honoring the contributions that people with disabilities have made to our workforce and celebrating National Disability Awareness Month (NDEAM), this weeks episode highlights the many layers of Alycia’s climb from waitress in a wheelchair to founder and CEO of her own business and how she went from serving margaritas and fajitas to propelling herself through college. We dive into how Alycia’s … open the full bio early experiences laid the foundation for her unwavering commitment to inclusion in the workforce, and how in spite of the challenges and discrimination she faced, how she found the courage to share her story as a testament to the power of self-advocacy and overcoming insecurities. Her transition from waitress to businesswoman is a small peek into to her adaptability and determination that has propelled her to her life’s dreams.

Dani Izzie is a digital marketing professional uniquely positioned in the growing disability consumer marketplace. As the founder of Access Social, Dani’s mission is to help companies meet the 3rd largest market segment in the U.S. Living with a disability herself has also immersed her into the world of grassroots advocacy where she has worked with organizations on local and national levels. Most … open the full bio recently, she co-produced and starred in a documentary film and spearheaded an impact campaign amplifying issues faced by disabled parents. She is a multinational wheelchair-using mother to twins and resides outside of DC near Shenandoah National Park.

“Airline passengers with disabilities deserve to travel safely and with dignity,” said U.S. Transportation Secretary Pete Buttigieg. “DOT is proud to partner with the aviation industry and members of the disability community to ensure that all travelers with disabilities know their rights.” The Airline Passengers with Disabilities Bill of Rights, describes the fundamental rights of air travelers … open the full bio with disabilities under the Air Carrier Access Act and its implementing regulation, 14 Code of Federal Regulations (CFR) Part 382.
The Bill of Rights consists of:
1. The Right to Be Treated with Dignity and Respect.
2. The Right to Receive Information About Services and Aircraft Capabilities and Limitations.
3. The Right to Receive Information in an Accessible Format.
4. The Right to Accessible Airport Facilities.
5. The Right to Assistance at Airports.
6. The Right to Assistance on the Aircraft.
7. The Right to Travel with an Assistive Device or Service Animal.
8. The Right to Receive Seating Accommodations.
9. The Right to Accessible Aircraft Features.
10. The Right to Resolution of a Disability-Related Issue.
In preparation for the busy holiday travel season, and in celebration of the 37th anniversary of the Air Carrier Access Act (ACAA), the U.S. Department of Transportation (DOT) announced that it has launched a campaign, #AccessibleAirTravel, to raise awareness about the right of air travelers with disabilities to safe, dignified, and accessible air travel. An estimated 5.5 million Americans use a wheelchair, and many encounter barriers when it comes to air travel.
The #AccessibleAirTravel campaign will promote DOT’s Airline Passengers with Disabilities Bill of Rights through a quick and informative video that empowers individuals with disabilities to understand and assert their right to safe, dignified, and accessible air travel. DOT is partnering with airlines, airports, ticket agents, and disability organizations in this campaign and these partners are sharing the video on their respective websites and social media channels in October.
Last month, DOT announced that United Airlines will implement industry-leading actions that go above and beyond Federal requirements to improve the air travel experience for passengers who use wheelchairs. This action is part of an agreement with DOT that follows a lengthy investigation by the Department into a disability complaint filed against United by the late Engracia Figueroa.
DOT is committed to ensuring that air travel is safe and accessible and to improving the travel experience for individuals with disabilities. Air travelers who experience disability-related problems may file a complaint with the Department. The Department’s Office of Aviation Consumer Protection investigates every disability complaint that it receives.

Dustin Giannelli is the CEO & Founder of HearsDustin LLC based in Boston, MA. As a DEIA public speaker who happens to be profoundly deaf, Dustin shares his lived experiences to help bring more awareness to the importance of DEI best practices, accessibility and communication.
Dustin was diagnosed with a profound bilateral hearing loss at the age of five. However, to this day, being deaf has … open the full bio never defined him. Instead, it has allowed him to consistently overcome life’s challenges and spread positivity in a powerful way.
HearsDustin was born to share stories, motivate others and collaborate with brands and organizations that are focused on providing accessible and inclusive experiences for all.
As one of 48 million Deaf and hard of hearing Americans and over 430 million Deaf and hard of hearing people globally, Dustin’s mission is to bring awareness to the solutions that give those with (and without) hearing loss the equitable access they need to succeed.

Corinna Busciglio Kamilli is a seasoned strategic communication leader and entrepreneur, boasting almost a decade of experience in the dynamic realm of technology.
A proud alumna of the University of Arizona, Corinna completed her undergraduate studies in 2009, graduating with a degree in Communication and Business. This formative period laid the foundation for her deep-rooted passion for … open the full bio effective communication and the limitless possibilities it holds within the business world.
In her pursuit of continuous self-improvement and professional advancement, Corinna is currently pursuing her Master of Arts degree in Communication at Arizona State University, further refining her skills and expanding her knowledge.
In her personal life, Corinna relishes her most important roles as wife, mother, daughter, and sister. These roles highlight her warm, vibrant, and nurturing personality, which complements her dynamic and strategic leadership in the professional sphere.

Amy Wang-Hiller, a Shanghai-born virtuoso violinist, a violin educator, and a doctoral student at the University of North Texas in violin performance. She is the creator of the Thrive x Strive Musician Podcast which discusses mental health and inclusivity in the music industry. Despite her ongoing medical journey and progressive quadriparesis from the genetic disorder Ehlers-Danlos Syndrome, she … open the full bio keeps performing and teaching actively in the Dallas area and building her online presence by talking about her medical journey.
Starting violin at three, Amy’s talent grew through local competition and orchestras. She debuted at the Shanghai Oriental Art Center with Tchaikovsky Violin Concerto with orchestra at the age of 18. Coming to the U.S., she won the third prize in the ENKOR International Violin Competition and was a finalist in the Lewisville Concerto competition among other competitions. Amy’s musical range spans Baroque to contemporary, collaborating with esteemed musicians and ensembles. She also currently maintains a private studio and offers virtual lessons.
Over the past two years, spine complications stemming from cervical instability to tethered cord syndrome challenged her motor functions and flared up many other comorbidities. Amy adapts her performances with her unique understanding of the body’s anatomy and function.
Beyond music, she advocates for her own illness and encourages others with disabilities to empower and raise awareness for rare diseases and spinal cord injuries.

Kerri A. Vanderbom, Ph.D., was born with Spina Bifida. For over 15 years, Kerri competed in water skiing at a regional, national, international, and collegiate level. She was on the 1999, 2001, 2003, 2005, and 2017 US Disabled Water Ski Teams. She has held the overall national champion title in the sit-ski category many times and in 2001 won the Overall World Champion title. She was on her … open the full bio collegiate team, the Chico State Wildcats, competing in the tricks event against her peers without disabilities at tournaments, including at All-Stars and Nationals.
Kerri graduated from Oregon State University with a Ph.D. in Exercise Sport Science and conducted research to improve inclusion and access to recreation and health promotion programs in schools and communities for youth and adults with disabilities. She was an NIH research scholar for the Programs to Increase Diversity among Individuals Engaged in Health-Related Research, Research in Implementation Science for Equity at UCSF. Kerri completed a Postdoctoral Fellowship at the University of Alabama at Birmingham in the School of Health Professions. She was the project coordinator of the Obesity Prevalence, Adaptations, and Knowledge Translation in Youth and Young Adults with Disabilities study. In 2015 she became faculty and continued her research trajectory, developed and adapted inclusive health promotion strategies and recommendations, and put them into practice in communities across the U.S. through a CDC-funded grant. The most life-changing accomplishment was getting to study at the University of Queensland in Australia as a Rotary Ambassadorial Scholar.
Currently, Kerri is a Program Manager of an Injury Prevention Program for Butte County Public Health. She and her team work hard to conduct truly inclusive education, events, and activities for communities.
Kerri’s favorite things in life are being with family, friends, and dog, spending time outdoors with her husband, traveling, kayaking, and eating good food.

Regina is a highly motivated business, leader, with Over 18 years experience in technology and construction. Currently working for Trip Hazard and focusing on accessibility in her day to day professionally. Accessibility has always been in Regina’s DNA due to growing up in an inclusive environment being raised alongside her twin sister, Alycia. Family means everything to Regina who currently has … open the full bio the staring role as her daughter Ella’s mom.

Michael is the Founder, and CEO of Curiosity Lab, a purpose-driven venture studio and consultancy that builds products and experiences that teach empathy, and the author of The Power of Empathy coming October 24th and available for pre-order now. In his role as CEO, Michael creates and incubates businesses to help values-aligned individuals and organizations use empathy to live happier and … open the full bio healthier lives and to nurture productive and inclusive environments. In 2022, Curiosity Lab received an investment from Pharrell and the Black Ambition Prize.
Michael Tennant is an entrepreneur, keynote speaker, and author of The Power of Empathy coming October 24th and available for pre-order now, and the creator of Actually Curious™ the empathy conversation game, Values Exercise™, and the Five Phases of Empathy™. His work has been featured by the New York Times, Oprah and the TODAY Show for teaching empathy and fostering a thriving ecosystem of advocacy for diversity, mental health, and well-being through products, content, workshops, and technology. In 2022, Curiosity Lab received an investment from Pharrell and the Black Ambition Prize.

Brad Parks is the pioneering founder of wheelchair tennis. During an amateur freestyle skiing competition, he suffered a disabling injury when he was 18. He began experimenting with tennis as a method of therapy, and in 1976, wheelchair tennis was born. The first wheelchair tennis tournaments were held in 1977 and were a major success. This success motivated Parks to found the National Foundation … open the full bio of Wheelchair Tennis (NFWT) as the organizing body for the sport. The purpose of the NFWT was to promote physical and psychological well being among the disabled regardless of age, sex, creed, or disability extent. This was accomplished through the presentation of instructional clinics, exhibitions and competitive tournaments and sports camps. As more athletes became involved, the Wheelchair Tennis Players Association (WTPA) was formed, giving players more of a say in the governance of tournaments, clinics and expansion of the game.
Parks started the first international wheelchair tennis event, the US Open, held in Irvine, California. He was the Tournament Chairman for 18 years, setting the standard for others to follow. Today the NEC Wheelchair Tennis Tour is comprised of 157 tournaments in 41 countries, exceeding a total of $1,500,000 in prize money. In 1985, as a result
of increased international presence at the US Open, the World Team Cup was started. Today this prestigious Fed Cup/Davis Cup-style team event has been contested by 52 different nations in its 25- year history, and boasts men, women, quads and junior competitions.
As a player from 1980 – 1989, Parks was ranked number one in singles in the world in the sport. He is a three time U.S. Open Singles Champion (1980, 1985, 1987) and a ten time U.S. Open Doubles Champion. Parks retired from competitive play in 1995. His competitive accomplishments include a gold medal in tennis doubles at the 1992
Paralympics in Barcelona, gold medals in Singles and Doubles at the 1987 Olympic Sports Festival, and he won two gold medals and one silver medal in wheelchair track at the 1980 Paralympics. He has also won over twelve National Wheelchair Tennis Singles titles.
Parks is also credited with spreading the sport internationally by holding clinics throughout Europe, Asia and the Pacific. In 1988, the International Wheelchair Tennis Federation (IWTF) was formed to govern this growing international sport with Parks as the inaugural president. He served on the Management Committee for many years and was the driving force behind international wheelchair tennis. In 1998, the IWTF was fully integrated into the International Tennis Federation, making it the first disabled sport to achieve such a union on the international level.
Today almost 100 countries offer wheelchair tennis programs, and the sport is played at all four Grand Slams.

In 2009 my life changed in the blink of an eye when I incurred a spinal cord injury. I quickly learned that if I could even find a home that would fit my physical needs, it was not in line with my personal style. With so much change in my life, I was holding on to the idea that my home could reflect who I am outside of my disability. Combining my perspective of disability with my life-long passion … open the full bio for interior design fueled me to advocate for others in their accessible home journey. In 2018 I founded Blue Copper Design with the mission to combine barrier free designs with beautiful interiors and the vision to create a world where everybody can participate.

Carli Ross is a dynamic leader and educator in the field of Kinesiology and Adapted Physical Education, International APE project coordinator, founder of Carli B Yoga, and certified Yoga Instructor. She leads the Adapted Physical Education service learning programs at California State University, Chico as well as running her own successful small business. Carli’s methodology focuses on helping … open the full bio connect mind with body. She incorporates a variety of traditional practices in movement, breath, and meditation to help each of her students practice their own unique form. Carli’s greatest passion is introducing people to the world of adaptive physical activity. She has shared her passion globally through connecting her students with communities around the world.

Christina V. Rodriguez is a first-generation Latina, born and raised in the San Francisco Bay Area. Her family is from Nicaragua and is proud to represent her Nicaraguan culture and heritage in spaces where there is lack of Central American representation. She is an wife, mother of 2, dogmom, edu-creator, inspirational speaker, podcaster, advocate, entrepreneur, storyteller and scholar who … open the full bio embraces a multi-cultural and equity mindset with a strong commitment in creating equitable opportunities for Women of Color in Business, Housing & Academia.
Rodriguez received her Bachelor’s degree in Latino/a Studies from San Francisco State University and went on to receive her Master’s degree (MBA) with an emphasis in Marketing at Notre Dame de Namur University. She is currently pursing her doctorate in Education from Mills College and provides 15+ years of marketing and housing experience in the San Francisco Bay Area.

Joze Piranian is a lifelong stutterer turned Forbes and TED featured Keynote Speaker and Stand-up Comedian in 3 continents and 4 languages. He has delivered keynotes about disability inclusion and conquering fears at the United Nations, Boeing, Google, Meta, TikTok, Starbucks, Pinterest, Tesla, IBM,Dell, BCG, Deloitte, as well as at major conferences and educational institutions worldwide.
Joze is … open the full bio a lifelong stutterer turned International Motivational Speaker helping people who hold back turn fear into action so that they overcome their “inner stutter” and unlock their true potential in life. By empowering others to own their uniqueness and conquer their obstacles, Joze delivers transformational experiences allowing his keynote audience members and coaching clients to access the hidden powers of fear and become champions of inclusion.
After avoiding speaking almost entirely for more than 25 years due to a debilitating stutter, Joze uncovered groundbreaking insights for personal transformation that turned his obstacle into triumphant public speaking and stand-up comedy performances in 3 continents and 3 languages. Joze is now on a mission to change people’s relationships with fear and discomfort so that they start taking action and unleash their inner greatness at work, school and in life.
Winner of the Inspirational Speaker of the Year award in 2017, Joze has shared the stage with Drake music video producer Director X, Disney’s CIO, Brendon Bouchard, Jim Kwik, Dragon Den’s Arlene Dickinson and comedians Hannibel Buress & Whitney Cummings.
Joze holds a Bachelors of Commerce and Psychology from McGill University, a Master of International Business from Queen’s University and a Certificate in Diversity and Inclusion from Cornell University. He has delivered his keynotes on Inclusion and Resilience at organizations such as Tesla, Dell, Diageo and Amgen as well as conferences such as the HR Leaders Summit and the Hollywood Innovation & Technology Summit.
With more than 3 000 000 views on his Goalcast featured speech about overcoming adversity and a growing social media following of 30 000, Joze has also been featured on TEDx, Forbes, NowThis (about Joe Biden’s stutter), CBC and Global News Canada.

Ryann “Ry” Mason, BS RN (she/they) is a 31 year old disability advocate, multi-specialty registered nurse, proud member of the LGBTQIA+ community, keynote speaker, model, adaptive athlete, sexuality educator, and self-proclaimed loudmouth southern belle. Ryann was born with a genetic collagen disorder called Ehlers-Danlos Syndrome (EDS) which caused them to begin utilizing a wheelchair for the … open the full bio majority of their mobility needs at the age of 26. Instead of allowing their disability to get them down, they decided to turn towards what they knew best, helping others. Ryann created an Instagram account called Chronically Ry, where they post photos, videos, and write ups showing her life and experiences living and working as a registered nurse with a chronic illness and degenerative disability. Over the past few years they have accomplished quite a bit including:wearing the crown for Ms. Wheelchair Virginia through both 2020 and 2021, having their story featured in numerous platforms including Woman’s Day, Scrubs , Frisson, Teen Vogue, and Forbes magazines, expanding their online presence to include Facebook, Twitter, TikTok, and LinkedIn, as well as amassing a following of over 19,000 people on their original Instagram page. Along with her disability advocacy work, Ryann has continued practicing as a registered nurse in the hospital setting throughout her disability journey and hopes to increase disability visibility and employment in the field of healthcare.
Ry could have let everything they’ve been through bring their life to a screeching halt, but instead they continue to share their story, educate, advocate, and inform others about the needs, rights, and experiences of the disability community.

26% of Americans identify with having some kind of disability – and as a double-amputee, I am one of them. I’m a lot of other things, too; I’m a woman. I’m progressive. I’m a community builder and organizer and activist. But, for the world at large, my disability is my defining characteristic.
When you’re disabled (much like when you’re a woman, Black, Latinx, Indigenous, Asian, LGBTQ+, or … open the full bio anything that isn’t a straight, cisgender white male) advocacy is not a choice. Our very existence is political. When the entire world has been constructed in ways that actively harm you – just being visible is an act of rebellion. Be it age, gender, ethnicity, orientation, religion or ability – we have to work harder to prove we can exist in spaces that never intended to include us.
I want to change that. My mission is to ensure more of us are seen and heard and advocated for. To leverage the resources I have access to and create access for those who don’t. To create opportunities, tear down the cultural and systemic barriers, and foster community, knowledge, and success.
Most importantly, I’m here to listen, learn, and grow.

Since 1990, Disability Pride Month has celebrated people with disabilities, their identities and culture, and their contributions to society. It also seeks to change the way people think about and define disability, to end the stigma of disability, and to promote the belief that disability is a natural part of human diversity in which people living with disabilities can celebrate and take pride. … open the full bio People with disabilities make up 15% of the world’s population and are the largest and most diverse minority in the United States making up approximately 26% of the population representing all ages, races, ethnicities, genders, sexual orientations, religions, and socio-economic backgrounds.
The concept of Disability Pride was born out of the Disability Rights movement and based on intersectional identity politics and social justice. The core concept of Disability Pride is based on a tenet of reworking the negative narratives and biases that frequently surround the concept of disability. Disability Pride is a response and counteraction against ableism and social stigma. The concept has roots in the same social theory that backs LGBT Pride and Black Pride. Disability Pride is a movement intended to celebrate the history of the Disability Rights movement and people with disabilities as positive contributors to society. It marks a break from traditional concepts of disabilities as shameful conditions, which were often hidden from public spaces and mainstream awareness. Disability Pride is built upon the social model of disability and is described as moving away from the medical model of disability.

In May 2021, one of Alycia’s longtime dreams came true when she was invited to speak at TEDx in South Lake Tahoe. Her talk, “Disabling Ableism: The Modern Pathway to Inclusion,” is a love letter to herself, others with disabilities, and society at large that brings light to the empowerment of having a disability. It’s also a call to action to examine — and dismantle — the ways that ableist … open the full bio thinking exists in our day-to-day lives.
Ableism is everywhere you turn. It’s ingrained in society so much so, it’s overlooked or goes unnoticed, but without recognizing ableism and its effects we will never fully understand what inclusion really means. I share the perspective that is missing from American TV, politics and generally any conversation, what does it look like when you put yourselves in another’s wheels not shoes. This talk focuses on shifting perceptions of what is perceived possible by disabling ableism, a social prejudice against people with disabilities based on the belief that typical abilities are superior. I explore the topic through my own personal journey over my lifetime, its cause and effects, and how we are taught from the time we are born to favor one over the other and because of this we don’t see the beauty of difference, no matter what shape it comes in. When we disable ableism we truly begin to value our differences bringing a broader outlook to our world, expanding possibilities for all!

Alycia Anderson is a TEDx motivational speaker, corporate Diversity, Equity, Inclusion & Accessibility consultant, advocate, and the founder & CEO of The Alycia Anderson Company, LLC. She studied Adapted Physical Education at California State University, Chico earning a bachelors degree and continued on to receive her Master’s Degree from KU Leuven, Belgium in Adapted Physical Activity … open the full bio emphasizing the benefits, practices, and principles of inclusion. Alycia’s authenticity and charisma draws others to her and she naturally connects them to inspire, mentor, champion and support.
Alycia Anderson started speaking because she is a bridge for all to see how to care about, practice and learn to be inclusive and this is her biggest life work. Alycia hopes to share with people that don’t know and are curious about how it is to live a lifetime with a disability. She naturally spans the gap from how to overcome, adapt and believe in what we think to be impossible… to be possible. She believes it’s all about the past, present and future and all of the collective progress along the way.
Alycia Anderson is a tennis player, cyclist, identical twin and a wheelchair user since birth. Alycia shares her journey globally to help communities and companies understand the true benefits inherent to building a diverse, inclusive and accessible workplace and society. She shines light on how our diversities are core to the qualities that make each of us uniquely qualified and able in life. Alycia right sizes everyday obstacles to open your mind to a world of possibility, and that’s how she rolls!