Beyond 6 Seconds: Neurodiversity stories from neurodivergent people

Kantu (they/he) is the founder and co-owner of the social media presence known as the Angry Autist. Indigenous to the Andes in Abya Yala, Kantu is Quechua and is racialized as a visibly Native person. Kantu is autistic, has dissociative identity disorder (DID) and has experienced psychotic depression. When founding the Angry Autist, it was their goal to bring awareness to their experience as a multiply and visibly disabled, racialized, and medium support needs autistic person. Since then, he has become further radicalized as explicitly anti-racist, anti-ableist, and anti-saneist, drawing inspiration from the ten principles of disability justice, the CripplePunk movement, Indigenous philosophy, mad liberation, and fat liberation. During this episode, you will hear Kantu talk about: How they discovered they have DID How DID stereotypes affect real-life perceptions of DID How their autism affected their own experience of DID Their experience with psychotic depression symptoms and treatments The meaning and significance of mad liberation To find out more about Kantu and his work, follow them on Threads @angry_autist and Instagram @angry_autist. They can also be reached by email at angryandautistic [at] gmail [dot] com. Other Beyond 6 Seconds episodes about dissociative identity disorder (DID): Amber Louise Ainsworth (episode 194):  beyond6seconds.net/194   Crystals Multifaceted (episode 215):  beyond6seconds.net/215  Support or sponsor this podcast: BuyMeACoffee.com/Beyond6Seconds Watch the video of this interview on YouTube: youtube.com/watch?v=JVP1yibrlXg Read the episode transcript: carolynkiel.com/podcast/mad-liberation Follow the Beyond 6 Seconds podcast in your favorite podcast player: pod.link/1336740192 Subscribe to the FREE Beyond 6 Seconds newsletter for early access to new episodes: mailchi.mp/f9f6e8356138/insider *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.*

Torina Gedler is a musician who is also known as DEĀ EX MACHINĀ, which means "Goddess from the machine" in Latin. With their lush synth-pop sound, DEĀ EX MACHINĀ promotes harmony and inclusion in society through authentic Disability representation in music.  DEĀ EX MACHINĀ advocates for the arts, LGBTQIA+ rights and Environmental and Disability Justice. Their debut EP, APO/THECARY, comes out on July 29, 2026. During this episode, DEĀ EX MACHINĀ discusses: Their work as a musician before and after being disabled by a brain injury Why it's important to have disability representation in music The main themes of their debut EP How joining RAMPD (Recording Artists and Music Professionals with Disabilities) influenced their work as a musician Their EP release party on July 29 in Des Moines, Iowa Learn more about DEĀ EX MACHINĀ at www.DeaExMachina.music and listen to their music on Subvert, Spotify, Apple Music and Bandcamp. Learn more about Recording Artists and Music Professionals with Disabilities (RAMPD) at RAMPD.org. Listen to other Beyond 6 Seconds episodes with neurodivergent musicians: Adin Boyer (episode 227):  https://www.beyond6seconds.net/227  Kaishawna (episode 187):  https://www.beyond6seconds.net/187   Support or sponsor this podcast: BuyMeACoffee.com/Beyond6Seconds Watch the video of this interview on YouTube: youtube.com/watch?v=IldZ1PQYP4E Read the episode transcript: carolynkiel.com/podcast/dea-ex-machina Follow the Beyond 6 Seconds podcast in your favorite podcast player: pod.link/1336740192 Subscribe to the FREE Beyond 6 Seconds newsletter for early access to new episodes: mailchi.mp/f9f6e8356138/insider  *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.*

Luke hosts the Howdy Beans Podcast, where he reviews movies, TV shows, video games, books, and all things pop culture. He is dyslexic with an overlap of dyspraxia and dyscalculia, and he's currently on the waiting list for an autism assessment. Luke is an avid reader who writes short stories and poems, and he's currently writing a dark fantasy novel. During this episode, you will hear Luke talk about: ●    How he discovered that he was neurodivergent at a young age ●    Why he doesn't take reading and writing for granted ●    His passion for writing stories ●    What led him to start the Howdy Beans Podcast and how he's kept it going for five years Listen to the Howdy Beans Podcast on Spotify: open.spotify.com/show/74Pe9IWfTxxbVgEcTt47SG?si=af480bede172486c&nd=1&dlsi=0d644bd85ad24e46  Follow the Howdy Beans Podcast on Instagram and YouTube @thehowdybeanspodcast and on TikTok @the_howdybeans_podcast. Support or sponsor Beyond 6 Seconds: BuyMeACoffee.com/Beyond6Seconds Watch the video of this interview on YouTube: youtu.be/3RGlfliUoIQ Read the episode transcript: carolynkiel.com/podcast/luke-howdy-beans-podcast Follow the Beyond 6 Seconds podcast in your favorite podcast player: pod.link/1336740192  Subscribe to the FREE Beyond 6 Seconds newsletter for early access to new episodes: mailchi.mp/f9f6e8356138/insider 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. Eugene Manley Jr. is a cancer scientist, health equity leader, and longtime patient advocate working at the intersection of biomedical sciences, cancer care, AI ethics, and leadership. As a Black healthcare advocate and founder of SCHEQ (STEMM* & Cancer Health Equity), a nonprofit focused on cancer health equity, Eugene runs an annual lung cancer summit that brings together patients, clinicians, researchers, and industry to co-create solutions to disparities in screening, diagnosis, and treatment. Eugene has ADHD, which didn't get diagnosed until he was in graduate school.  *STEMM stands for Science, Technology, Engineering, Mathematics, and Medicine. Content note: This episode discusses medical/healthcare trauma and physical injuries. During this episode, you will hear Eugene talk about: Discovering his ADHD later in life, and how ADHD shaped him as a person  How his academic interests, education and career experiences led him to start his nonprofit The impact of a recent traumatic experience he had as a patient in the healthcare system How SCHEQ helps people understand their rights and options in healthcare settings Learn more about Eugene's work at SCHEQ.org. Support or sponsor this podcast: BuyMeACoffee.com/Beyond6Seconds Watch the video of this interview on YouTube: https://www.youtube.com/watch?v=H13-WoQuP9o Read the episode transcript: carolynkiel.com/podcast/eugene-manley-scheq Follow the Beyond 6 Seconds podcast in your favorite podcast player: pod.link/1336740192 Subscribe to the FREE Beyond 6 Seconds newsletter for early access to new episodes: mailchi.mp/f9f6e8356138/insider  *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.*

As the hosts of the Othering Podcast, Mike and Dory advocate for marginalized communities. Their podcast provides a platform where neurodivergent, disabled and LGBTQ+ people can share their stories.  During this episode, you will hear Dory and Mike talk about: Why they started the Othering Podcast, and how they came up with the name of the show Sharing their own lived experiences of neurodivergence and disability on their podcast How they select their podcast guests and topics Why is it important to amplify the stories of disabled and LGBTQ+ people Learning from the feedback they have received about their podcast  The long-term impact they want their podcast to have Listen to the Othering Podcast interviews mentioned in this episode: Joseph Kibler: otheringpodcast.com/podcast/episode/6e011856/joseph-kibler-talks-about-disability-hiv-and-lgbtq-representation-in-hollywood  Mychal Threets: otheringpodcast.com/podcast/episode/7810e147/mychal-threets-reading-rainbow-adhd  You can find all episodes of the Othering Podcast at OtheringPodcast.com. Support or sponsor Beyond 6 Seconds: BuyMeACoffee.com/Beyond6Seconds Read the episode transcript: carolynkiel.com/podcast/othering-podcast Follow the Beyond 6 Seconds podcast in your favorite podcast player: pod.link/1336740192  Subscribe to the FREE Beyond 6 Seconds newsletter for early access to new episodes: mailchi.mp/f9f6e8356138/insider 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.