Beyond 6 Seconds: Neurodiversity stories from neurodivergent people

Content warning: This episode discusses suicidality, paranoia, hallucinations and delusions, and mentions drug use and homelessness. Michelle Hammer is a schizophrenia activist who spends her time passionately fighting stigma. She is a New York City native who is featured in the WebMD documentary “Voices,” which was nominated for a Tribeca X Award at the Tribeca Film Festival.  Michelle was diagnosed with schizophrenia at 22 after a misdiagnosis of bipolar at age 18. At 27, Michelle decided to use her artistic talents and fearless personality to do something that could benefit the mental health community. In May 2015, she founded a mental health-focused clothing brand called Schizophrenic.NYC with the mission of reducing stigma by starting conversations about mental health.  Michelle has also been featured in many publications such as Mashable, The Daily Mail, Stylist, and Buzzfeed, and has also been featured on TV networks like ABC, NBC, and CBS. During this episode, you will hear Michelle talk about: Experiencing her first symptoms of schizophrenia in high school and college What it’s like for her to experience hallucinations and delusions What inspired her to start her clothing brand, Schizophrenic.NYC People’s reactions to her designs and pop-up events in New York City Challenging stereotypes and misconceptions about schizophrenia Find out more about Michelle on her clothing brand’s website Schizophrenic.NYC and on Instagram, TikTok and YouTube. Watch the video of this interview on YouTube. Read the episode transcript. Follow the Beyond 6 Seconds podcast in your favorite podcast player. Subscribe to the FREE Beyond 6 Seconds newsletter for early access to new episodes. Support or sponsor this podcast at BuyMeACoffee.com/Beyond6Seconds! *Disclaimer: The views, guidance, opinions, and thoughts expressed in Beyond 6 Seconds episodes are solely mine and/or those of my guests, and do not necessarily represent those of my employer or other organizations. These episodes are for informational purposes only and do not substitute for professional medical advice. Consult a medical professional or healthcare provider if you are seeking medical advice, diagnoses, or treatment.*

CW: Mentions of suicidality. In the third grade, LeDerick Horne was labeled as “neurologically impaired” – a label that followed him through his schooling until he was eventually diagnosed with dyslexia. Today, LeDerick is a dynamic spoken-word poet, a respected author, and a passionate advocate for people with disabilities. He has performed at prestigious venues such as the White House and the United Nations. His workshops, speeches and poetry open doors to discussions on inclusive education, equal opportunity, systemic change, and hope for individuals with disabilities. During this episode, LeDerick talks about: The challenges he faced in K-12 special education, before being diagnosed as dyslexic What inspired him to go to college – and how the meaningful support and inclusive education he got there helped him thrive as a student  Discovering his passion for poetry, which led to his career as a spoken-word poet and author His work as a speaker and trainer on the topics of inclusive education and the intersections of education, disability and race Co-hosting the Black and Dyslexic podcast Stay tuned to the end of this episode to hear LeDerick read two of his poems! Find out more about LeDerick at his website LeDerick.com, find his social media and more on his LinkTree, and learn about his new video course "6 Steps to Empowering Young People with Disabilities." Watch the video of this interview on YouTube. Read the episode transcript. Follow the Beyond 6 Seconds podcast in your favorite podcast player. Subscribe to the FREE Beyond 6 Seconds newsletter for early access to new episodes. Support or sponsor this podcast at BuyMeACoffee.com/Beyond6Seconds! *Disclaimer: The views, guidance, opinions, and thoughts expressed in Beyond 6 Seconds episodes are solely mine and/or those of my guests, and do not necessarily represent those of my employer or other organizations. These episodes are for informational purposes only and do not substitute for professional medical advice. Consult a medical professional or healthcare provider if you are seeking medical advice, diagnoses, or treatment.*

Jack Pabich is a Quality Assurance Support Analyst who found his current job through an autism employment program run by CAI Neurodiverse Solutions. He is responsible for processing requests of potential conflicts of interest, ensuring parties are correctly assigned to the location within the database, and rearranging information to improve database efficiency. Jack’s attention to detail is his biggest strength and he uses it to proactively streamline tasks. In his free time, he enjoys being active with various sporting activities and spending time with friends. During this episode, you will hear Jack talk about: How the autism employment program helped him find work after college The work he does at his current employer, and how it leverages his strengths and helps him learn new things and grow as a leader His working relationships with his coworkers and managers  The type of work he wants to do in the future Watch the video of this interview on YouTube. Read the episode transcript. Follow the Beyond 6 Seconds podcast in your favorite podcast player. Subscribe to the FREE Beyond 6 Seconds newsletter for early access to new episodes. Support or sponsor this podcast at BuyMeACoffee.com/Beyond6Seconds! *Disclaimer: The views, guidance, opinions, and thoughts expressed in Beyond 6 Seconds episodes are solely mine and/or those of my guests, and do not necessarily represent those of my employer or other organizations. These episodes are for informational purposes only and do not substitute for professional medical advice. Consult a medical professional or healthcare provider if you are seeking medical advice, diagnoses, or treatment.*

Amee is a dedicated health care provider known for her expertise and compassionate care. Beyond her professional achievements, she is a passionate mental health advocate and openly shares her personal journey living with epilepsy on her Instagram @behindthebindis. She is a powerful voice for those who feel they cannot speak up for themselves, working to raise awareness and foster understanding about mental health and invisible illnesses in the South Asian community and beyond.   During this episode, you will hear Amee talk about: What was it like growing up with epilepsy, but not really talking about it How her experience with epilepsy changed from childhood to adulthood The hospital stay that prompted her to disclose her epilepsy to her closest friends  What inspired her to discuss her epilepsy publicly on her social media – and the meaning of “behind the bindis” Follow Amee on Instagram @behindthebindis to learn more about her epilepsy advocacy. Watch the video of this interview on YouTube. Read the episode transcript. Follow the Beyond 6 Seconds podcast in your favorite podcast player. Subscribe to the FREE Beyond 6 Seconds newsletter for early access to new episodes. Support or sponsor this podcast at BuyMeACoffee.com/Beyond6Seconds! *Disclaimer: The views, guidance, opinions, and thoughts expressed in Beyond 6 Seconds episodes are solely mine and/or those of my guests, and do not necessarily represent those of my employer or other organizations. These episodes are for informational purposes only and do not substitute for professional medical advice. Consult a medical professional or healthcare provider if you are seeking medical advice, diagnoses, or treatment.*

Dr. Kana Grace is a research psychologist, advocate, Specialist Mentor, and educator, specializing in the mental and physical health of neurodivergent people. Currently, Kana is an Honorary Research Fellow at the Centre for Research in Autism and Education (CRAE) at the Institute of Education, University College London (UCL), where she completed her PhD. Kana has lived experiences with autism, ADHD, dyslexia, Tourette syndrome, dyspraxia, hypermobility Ehlers-Danlos syndrome (hEDS), Postural Orthostatic Tachycardia Syndrome (POTS), and Mast Cell Activation Syndrome (MCAS).  She founded Valtameri (which means ocean in Finnish) to advocate for and support neurodivergent people and their families, based in Okinawa, Japan. Through Valtameri, she offers one-to-one support for neurodivergent people of all ages. She also gives talks and public lectures to deepen the understanding of neurodivergence in Okinawa Japan, and all over the world. Fluent in both English and Japanese, Kana bridges cultures in her extensive work.  During this episode, you will hear Kana talk about: How she discovered she is neurodivergent while at University What her life was like before she was diagnosed  Why she decided to focus her PhD on the study of loneliness in autistic adults The importance of involving autistic researchers in autism research  Her experience working in academia  Her observations about how autism and neurodivergence is viewed in Japan The goals she wants to achieve with her research Find out more about Kana and her work on her Linktree. Watch the video of this interview on YouTube. Read the episode transcript. Follow the Beyond 6 Seconds podcast in your favorite podcast player. Subscribe to the FREE Beyond 6 Seconds newsletter for early access to new episodes. Support or sponsor this podcast at BuyMeACoffee.com/Beyond6Seconds! *Disclaimer: The views, guidance, opinions, and thoughts expressed in Beyond 6 Seconds episodes are solely mine and/or those of my guests, and do not necessarily represent those of my employer or other organizations. These episodes are for informational purposes only and do not substitute for professional medical advice. Consult a medical professional or healthcare provider if you are seeking medical advice, diagnoses, or treatment.*

CW: Mentions of suicide and experiences with the criminal justice system as it relates to FASD. Patti Kasper is a Neurobehavioral Coach and Trainer who provides staff development training and coaching services to support people affected by Fetal Alcohol Spectrum Disorders (FASD). With over thirty years of experience in the fields of addiction, mental health, and child welfare, Patti draws on her personal experience with FASD, her degrees in social work and psychology, and her training as a Certified Facilitator of FASCETS Neurobehavioral Model.   Patti hosts a weekly podcast called Living with FASD. The second edition of her book, “Sip by Sip: Candid Conversations with People Diagnosed as Adults with Fetal Alcohol Spectrum Disorders (FASD),” was recently released with additional interviews and updated research. During this episode, Patti talks about: ●    What FASD is, and why it’s more common than most people realize ●    How she discovered in her 50s that she has FASD  ●    Some of the struggles that people with FASD may experience ●    How she supports families and individuals impacted by FASD Find links to Patti’s website, book, podcast and more. Watch the video of this interview on YouTube. Read the episode transcript. Follow the Beyond 6 Seconds podcast in your favorite podcast player. Subscribe to the FREE Beyond 6 Seconds newsletter for early access to new episodes. Support or sponsor this podcast at BuyMeACoffee.com/Beyond6Seconds! *Disclaimer: The views, guidance, opinions, and thoughts expressed in Beyond 6 Seconds episodes are solely mine and/or those of my guests, and do not necessarily represent those of my employer or other organizations. These episodes are for informational purposes only and do not substitute for professional medical advice. Consult a medical professional or healthcare provider if you are seeking medical advice, diagnoses, or treatment.*

In this episode, I'm sharing an interview from the podcast Art Heals All Wounds, where host Pam Uzzell talks with her daughter Allegra about Celebrating Neurodiversity, Beauty, and Belonging. I also added a short intro to this episode where I share some thoughts on belonging and how I've been looking for and finding community.  Check out the Art Heals All Wounds podcast for other stories about how art is a catalyst for healing and change.  Read the episode transcript. Follow the Beyond 6 Seconds podcast in your favorite podcast player. Subscribe to the FREE Beyond 6 Seconds newsletter for early access to new episodes. Support or sponsor this podcast at BuyMeACoffee.com/Beyond6Seconds! *Disclaimer: The views, guidance, opinions, and thoughts expressed in Beyond 6 Seconds episodes are solely mine and/or those of my guests, and do not necessarily represent those of my employer or other organizations. These episodes are for informational purposes only and do not substitute for professional medical advice. Consult a medical professional or healthcare provider if you are seeking medical advice, diagnoses, or treatment.*

Ian Otto is a Senior Producer with experience in animation, motion design, immersive, visual effects (VFX) and post production. After working in Berlin for many years, Ian now lives in Copenhagen, Denmark, where he is Senior Producer with WOODBLOCK, an animation studio for Design, Film and Immersive content. Recently, Ian began writing and speaking publicly about his experience as a person with Tourette syndrome who works in the creative industry. During this episode, you will hear Ian talk about: Growing up with Tourette’s in the 1990s What led him to work in the creative industry Working in a client-facing job as someone who has Tourette’s How he built his confidence at work   What has (and hasn’t) helped him manage his tics Connect with Ian on Instagram or through email: ian [at] woodblock [dot] tv Read Ian's article on Medium about working in the creative industry with Tourette’s Watch the video of this interview on YouTube. Read the episode transcript. Follow the Beyond 6 Seconds podcast in your favorite podcast player. Subscribe to the FREE Beyond 6 Seconds newsletter for early access to new episodes. Support or sponsor this podcast at BuyMeACoffee.com/Beyond6Seconds! *Disclaimer: The views, guidance, opinions, and thoughts expressed in Beyond 6 Seconds episodes are solely mine and/or those of my guests, and do not necessarily represent those of my employer or other organizations. These episodes are for informational purposes only and do not substitute for professional medical advice. Consult a medical professional or healthcare provider if you are seeking medical advice, diagnoses, or treatment.*

Mrinal Gokhale is an author, speaker and creative consultant based in Wisconsin. She has collaborated with organizations and media outlets such as Brown Girl Magazine, ADDitude Magazine, Medical College of Wisconsin, and more. Her most recent book is titled “Taboo: South Asian Mental Health Stories.” During this episode, Mrinal talks about: What inspired her to write about mental health in South Asian communities How she found people to interview for her book Common mental health themes that she noticed in her interviews How her own mental health journey inspired her writing and advocacy Find out more about Mrinal and her writing on her LinkTree page. Watch the video of this interview on YouTube. Read the episode transcript. Follow the Beyond 6 Seconds podcast in your favorite podcast player. Subscribe to the FREE Beyond 6 Seconds newsletter for early access to new episodes. Support or sponsor this podcast at BuyMeACoffee.com/Beyond6Seconds! *Disclaimer: The views, guidance, opinions, and thoughts expressed in Beyond 6 Seconds episodes are solely mine and/or those of my guests, and do not necessarily represent those of my employer or other organizations.*

CW: Mentions of suicidality Crystals Multifaceted is the founder of Multifaceted Journeys, where they use their lived experience of Dissociative Identity Disorder (DID) / plurality and healing with complex trauma and dissociation, to bring education to providers and facilitate groups for plurals. Crystals has a Master’s degree in Counseling Psychology. They serve as a moderator on The Refractory, a think tank for clinicians, researchers, peer support workers and coaches with lived experience of Dissociative Identity Disorder (DID), Other Specified Dissociative Disorder (OSDD), and Plurality. They have been a keynote speaker for the Plural Positivity World Conference.  Crystals’ podcast and Substack blog, both titled “Therapist Interrupted,” highlight stories related to getting through life’s interruptions, living with trauma and dissociation, and other topics related to multiplicity. During this episode, you will hear Crystals talk about: How they discovered they have DID  What it feels like for them to interact with the world as a DID system Where they have found support for their healing journey  What inspired them to start Multifaceted Journeys, and the types of services they’ve created for the Plural community The biggest misconceptions about DID  Connect with Crystals on their website, Substack, Patreon or through email at crystalsmultifaceted [at] protonmail [dot] com . Watch the video of this interview on YouTube. Read the episode transcript. Follow the Beyond 6 Seconds podcast in your favorite podcast player. Subscribe to the FREE Beyond 6 Seconds newsletter for early access to new episodes. Support or sponsor this podcast at BuyMeACoffee.com/Beyond6Seconds! *Disclaimer: The views, guidance, opinions, and thoughts expressed in Beyond 6 Seconds episodes are solely mine and/or those of my guests, and do not necessarily represent those of my employer or other organizations.*

Kala Allen Omeiza is a prolific author at the intersection of race, culture, and autism. Her latest book, "Autistic and Black: Our Experiences of Growth, Progress, and Empowerment," has received widespread acclaim for its in-depth exploration of the unique challenges and triumphs faced by autistic individuals of minority backgrounds. She has also worked on various research projects on neurodiversity and mental health at Harvard, Duke, Harvard Medical, and as a US Fulbright scholar in Nigeria. She is a graduate of Miami University and a masters graduate of Psychological Research from the University of Oxford. During this episode, Kala discusses: What inspired her to write “Autistic and Black” and share the experiences of Black autistic people across the African diaspora How she uses the Kwanzaa principle of Ujima to bring the stories in the book together Her experience interviewing nonspeaking autistic individuals  Writing about her own life experiences as a Black autistic woman To find out more about Kala and her work, you can visit her website, subscribe to her newsletter, and buy her book "Autistic and Black: Our Experiences of Growth, Progress, and Empowerment". Watch the video of this interview on YouTube. Read the episode transcript. Follow the Beyond 6 Seconds podcast in your favorite podcast player. Subscribe to the FREE Beyond 6 Seconds newsletter for early access to new episodes. Support or sponsor this podcast at BuyMeACoffee.com/Beyond6Seconds! *Disclaimer: The views, guidance, opinions, and thoughts expressed in Beyond 6 Seconds episodes are solely mine and/or those of my guests, and do not necessarily represent those of my employer or other organizations.*

Aashna Parikh is a Diversity, Equity, and Inclusion (DEI) consultant and inclusive marketing specialist based in India. Living with cerebral palsy and learning disabilities, she has consulted and collaborated with Forbes-listed and Fortune 500 companies across diverse sectors such as Fintech, Sustainability, Agriculture, and Technology. A strong advocate for neurodiversity, disability, and gender, she examines these issues through an intersectional lens.   During this episode, you will hear Aashna talk about: What was it like growing up and going to school with cerebral palsy and learning disabilities Living with disabilities in a world where people tell her she “doesn’t look disabled” The type of work that she does as a DEI consultant Her thoughts on DEI through an intersectional lens How DEI is addressed in different countries Her advice for requesting accommodations at work and in job interviews Connect with Aashna on LinkedIn or via email at aashnacparikh at gmail.com . Watch the video of this interview on YouTube. Read the episode transcript. Follow the Beyond 6 Seconds podcast in your favorite podcast player. Subscribe to the FREE Beyond 6 Seconds newsletter for early access to new episodes. Support or sponsor this podcast at BuyMeACoffee.com/Beyond6Seconds! *Disclaimer: The views, guidance, opinions, and thoughts expressed in Beyond 6 Seconds episodes are solely mine and/or those of my guests, and do not necessarily represent those of my employer or other organizations.*

Martina Kuzenski is a late-diagnosed autistic woman who received her autism diagnosis at age 28 near the end of her Master’s degree program. She is an IT Specialist for the U.S. federal government. She shares her experiences as a Black autistic woman in tech as a mentor for the Pathways in Technology Early College High School (P-TECH) program and as a co-author of the best-selling book “Ladies in Tech: Sharing Expertise for a Successful Career”.  During this episode, Martina talks about: Discovering that she is autistic in her late twenties, and what her life was like growing up How she got into a tech career  Her experience of not being “seen” in the tech industry as a Black autistic woman The importance of mentorship, and why she decided to become a P-TECH program mentor The challenges she has faced when trying to find leadership programs for neurodivergent people Why she doesn’t feel “autistic enough” in autistic spaces, and the flaws she sees in the neurodiversity movement Connect with Martina on LinkedIn and read her writing on  Diary of Self (Martina's blog posts about neurodiversity) and her book "Ladies in Tech: Sharing Expertise for a Successful Career."  Watch the video of this interview on YouTube. Read the episode transcript. Follow the Beyond 6 Seconds podcast in your favorite podcast player. Subscribe to the FREE Beyond 6 Seconds newsletter for early access to new episodes. Support or sponsor this podcast at BuyMeACoffee.com/Beyond6Seconds! *Disclaimer: The views, guidance, opinions, and thoughts expressed in Beyond 6 Seconds episodes are solely mine and/or those of my guests, and do not necessarily represent those of my employer or other organizations.*

Joshua Hoskins is a 25 year old man with Down syndrome who lives in Tamworth, England with his parents. He loves his family and friends, and his hobbies are horse riding, boxing, musicals, supporting Newcastle United Football team, going out on trips and going on holiday. Josh has two jobs: he loves them both and has great buddies at each place. Josh’s Mum Debbie helps him create posts on LinkedIn every week, because Josh wants to help other people with Down syndrome to get a job if they want to.   During this episode, you will hear Josh and Debbie talk about: How he had found his job at Marshall Fleet Services with WorkFit, and how the Down's Syndrome Association in the UK prepared him for the role What he does in his role with Marshall Fleet Solutions, and what he likes the most about it How LinkedIn helped him find his second job at Movianto  What inspired him to write about his life and work on LinkedIn How work has helped him grow as a person, build positive relationships with his coworkers, and support his local community Why employers should consider hiring people with Down syndrome, and how employers can include them in their companies  Follow Joshua Hoskins on LinkedIn to read his weekly posts. Watch the video of this interview on YouTube. Read the episode transcript. Follow the Beyond 6 Seconds podcast in your favorite podcast player. Subscribe to the FREE Beyond 6 Seconds newsletter for early access to new episodes. Support or sponsor this podcast at BuyMeACoffee.com/Beyond6Seconds! *Disclaimer: The views, guidance, opinions, and thoughts expressed in Beyond 6 Seconds episodes are solely mine and/or those of my guests, and do not necessarily represent those of my employer or other organizations.*

Grace Liu is an autistic author, blogger, speaker and pet portrait artist based in the Midlands of England. Grace's book, “Approaching Autistic Adulthood: The Road Less Travelled,” was published in October 2021. She blogs about autism, neurodiversity, diversity and inclusion, as well as her life as a biracial (British/Taiwanese) autistic gay woman, and has delivered multiple talks about autism and diversity. Grace has received many commissions for her pet portrait drawings, especially over the past year. She is a dedicated owner to four cats, having had an autistic interest in cats from a very young age!  During this episode, you will hear Grace talk about: Her early life after moving from Taiwan to the UK at the age of four, and how she and her family discovered that she is autistic  How she got started with her long-running blog back in 2013 Her experiences with racism, and with “coming out” as gay and autistic  Becoming an author and public speaker Find out more about Grace and her work at the links below: Book: artistic-autistic.co.uk/approaching-autistic-adulthood Blog: unwrittengrace.wordpress.com Art: artistic-autistic.co.uk/pet-portraits  Watch the video of this interview on YouTube. Read the episode transcript. Follow the Beyond 6 Seconds podcast in your favorite podcast player. Subscribe to the FREE Beyond 6 Seconds newsletter for early access to new episodes. Support or sponsor this podcast at BuyMeACoffee.com/Beyond6Seconds! *Disclaimer: The views, guidance, opinions, and thoughts expressed in Beyond 6 Seconds episodes are solely mine and/or those of my guests, and do not necessarily represent those of my employer or other organizations.*

Content note: This episode mentions thoughts about suicide and self harm.  Shayonee Dasgupta is a Mumbai-based freelance writer and editor who initially pursued a career in law, working with corporate law firms in India. She found out she's autistic and has ADHD in her 30s, prompting a transformative journey of self-discovery and learning to navigate life anew. During this episode, you will hear Shayonee talk about: What it was like growing up before her diagnosis  How the challenges she faced working as a lawyer led to her burnout The struggle she faced to get the right mental healthcare and support after her burnout  How she received her autism and ADHD diagnosis  Her decision to start a new career as a freelance writer Handling expectations from both her extended family and Indian society How she defines success in her own way To find out more about Shayonee and her work, you can connect with her on LinkedIn. Watch the video of this interview on YouTube. Read the episode transcript. Follow the Beyond 6 Seconds podcast in your favorite podcast player. Subscribe to the FREE Beyond 6 Seconds newsletter for early access to new episodes. Support or sponsor this podcast at BuyMeACoffee.com/Beyond6Seconds! *Disclaimer: The views, guidance, opinions, and thoughts expressed in Beyond 6 Seconds episodes are solely mine and/or those of my guests, and do not necessarily represent those of my employer or other organizations.*

Nick Heaney is a resident artist and co-founder of Artnova Gallery in Chatham, Massachusetts. Nick has always found art to be his most authentic way of connecting with the world around him. He was diagnosed with dyslexia during elementary school. He struggled with written language, but found a connection through art. Nick went on to study graphic design and fine art, earning a BFA in graphic design from the University of Massachusetts Dartmouth.  At the age of 26, Nick came out as gay to his friends and family. However, he still felt a sense of disconnect with the people around him, which led to a deeper struggle with his mental health. At the age of 28, Nick sought an autism evaluation which resulted in diagnoses of both autism and ADHD. During this episode, you will hear Nick talk about: What was it like growing up with dyslexia His early artistic talents at a young age What inspires his artwork today His experience of coming out as gay to his family, discovering his autism and ADHD, and finding supportive communities The story behind how he co-founded his art gallery Find out more about Nick and his work on his Instagram @nickheaneyart and on Artnova Gallery's website and Instagram. Watch the video of this interview on YouTube. Read the episode transcript. Follow the Beyond 6 Seconds podcast in your favorite podcast player. Subscribe to the FREE Beyond 6 Seconds newsletter for early access to new episodes. Support or sponsor this podcast at BuyMeACoffee.com/Beyond6Seconds! *Disclaimer: The views, guidance, opinions, and thoughts expressed in Beyond 6 Seconds episodes are solely mine and/or those of my guests, and do not necessarily represent those of my employer or other organizations.*

David Egan is a leader and advocate who promotes the causes of people with disabilities. He is the first person with Down Syndrome to serve as a Joseph P. Kennedy Jr. Public Policy fellow on Capitol Hill and with the National Down Syndrome Society (NDSS). As a Special Olympics athlete and International Global Messenger, David has traveled extensively and speaks to diverse audiences, including the U.S. Senate, United Nations, and various universities, nonprofit and for-profit companies.  David has also received many awards throughout his career. He was honored by NDSS for his legacy, presented with the American Association for Intellectual Disabilities Media Award, and received the Global Down Syndrome Foundation’s highest honor: the Quincy Jones Exceptional Advocacy Award. As the author of the book “More Alike Than Different: My Life with Down Syndrome,” he inspires his audiences to see our shared humanity and focus on abilities and possibilities rather than limitations.   During this episode, you will hear David talk about: Growing up with Down Syndrome, and his biggest dreams as a child How he learned to accept his disability What he enjoyed about working at Booz Allen Hamilton, CBRE, and SourceAmerica  His experience as a Joseph P. Kennedy Jr. Public Policy fellow How he became a disability advocate The impact of Special Olympics on his life  To learn more about David and his work, visit his website at DavidEganAdvocacy.com and buy his book, “More Alike Than Different: My Life with Down Syndrome.” Watch the video of this interview on YouTube. Read the episode transcript. Follow the Beyond 6 Seconds podcast in your favorite podcast player. Subscribe to the FREE Beyond 6 Seconds newsletter for early access to new episodes. Support or sponsor this podcast at BuyMeACoffee.com/Beyond6Seconds! *Disclaimer: The views, guidance, opinions, and thoughts expressed in Beyond 6 Seconds episodes are solely mine and/or those of my guests, and do not necessarily represent those of my employer or other organizations.*

Katie York (aka The Distracted Autistic) is a late-diagnosed Autistic who also has ADHD. They are currently program coordinator at the Community College of Baltimore County in Baltimore, Maryland. Katie is also an advocate and community organizer. In 2022, they founded Harford County Neurodivergents to build a network for neurodivergent adults & provide neurodiversity-affirming resources and education. Katie is a member of Harford County Public Schools Special Education Citizens Advisory Committee and a proud board member of Upper Chesapeake Bay Pride. During this episode, you will hear Katie talk about: How they discovered their neurodivergence later in life   Creating the Harford County Neurodivergents group, and the local peer support and community it provides What it means to be “neurodiversity-affirming,” and how that can be important for neurodivergent people The impact that Harford County Neurodivergents has had on their members so far What inspired them to get into local politics and advocacy, and their advice for people who want to become more involved in their communities Learn more about Katie on their website at TheDistractedAutistic.com and on Facebook. If you want to join the Neurodivergent Podcasters Discord group, email beyond6seconds at gmail.com to receive an invite. Join the Autistic Corporate Professionals group on LinkedIn. Watch the video of this interview on YouTube. Read the episode transcript. Follow the Beyond 6 Seconds podcast in your favorite podcast player. Subscribe to the FREE Beyond 6 Seconds newsletter for early access to new episodes. Support or sponsor this podcast at BuyMeACoffee.com/Beyond6Seconds! *Disclaimer: The views, guidance, opinions, and thoughts expressed in Beyond 6 Seconds episodes are solely mine and/or those of my guests, and do not necessarily represent those of my employer or other organizations.*

Born and raised in Costa Rica, Claudia Scott was diagnosed with Tourette syndrome in her early teens. Now she lives in the U.S., where she is the Capital Access Manager for Kiva Northwest Arkansas (NWA) at Startup Junkie and an advocate for Tourette's education and support. Claudia uses her experiences to support people with Tourette's, especially in Spanish-speaking communities. During this episode, Claudia talks about: How she discovered she had Tourette’s when she was growing up in Costa Rica Her experience of how Tourette’s is viewed by the general public in Costa Rica and the United States How her Tourette’s has changed over the course of her life, and how she managed through those changes The support she provides to the Hispanic Tourette’s community, including a Tourette’s support group for Spanish speakers Learn more about Claudia at her travel blog The Tourette Traveler and follow her on Instagram and Facebook. Watch the video of this interview on YouTube. Read the episode transcript. Follow the Beyond 6 Seconds podcast in your favorite podcast player. Subscribe to the FREE Beyond 6 Seconds newsletter for early access to new episodes. Support or sponsor this podcast at BuyMeACoffee.com/Beyond6Seconds! *Disclaimer: The views, guidance, opinions, and thoughts expressed in Beyond 6 Seconds episodes are solely mine and/or those of my guests, and do not necessarily represent those of my employer or other organizations.*