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Our guest this week is Rebekah Taussig of Shawnee, KS who is a mother, wife, author, podcast host, outspoken advocate for those with disability and who, herself is a paraplegic. Rebekah and her husband, Micah have been married for seven years and are the proud parents of Otto, who is typical five year old. Rebekah was diagnosed with spine cancer at age one and due to multiple surgeries lost her ability to walk at age four. She was the youngest of six children and despite her disability, still slept on the top bunk upstairs in her family home. She credits much of her success and resilience to her parents and siblings, who didn't treat her any differently. Prior to Otto's birth, Rebekah was a high school English and Literature teacher. Rebekah combined her PhD in Creative Non-Fiction & Disability Studies from University of Kansas, with her passion for writing to author Sitting Pretty: The View From My Ordinary, Resilient Disabled Body (2020). and more recently, a children's book entitled: We Are the Scrappy Ones (2025).More recently Rebekah has partnered with Caitlin Metz to host the Scratch That: Parenting & Re-Parenting Off Script Podcast, now with more than 50 episodes. It's an uplifting story about family and a woman's resilience all on this episode of the SFN Dad To Dad Podcast. Show Notes -Phone – (913) 940-1714Email – rebekahgracetaussig@gmail.comLinkedIn – https://www.linkedin.com/in/rebekah-g-taussig-458668139/Website - https://www.rebekahtaussig.com/Books - Sitting Pretty: The View From My Ordinary, Resilient Disabled Body - https://tinyurl.com/mv4nc9tkWe Are The Scrappy Ones - https://tinyurl.com/49h7rdb4Special Fathers Network -SFN is a dad to dad mentoring program for fathers raising children with special needs. Many of the 800+ SFN Mentor Fathers, who are raising kids with special needs, have said: "I wish there was something like this when we first received our child's diagnosis. I felt so isolated. There was no one within my family, at work, at church or within my friend group who understood or could relate to what I was going through."SFN Mentor Fathers share their experiences with younger dads closer to the beginning of their journey raising a child with the same or similar special needs. The SFN Mentor Fathers do NOT offer legal or medical advice, that is what lawyers and doctors do. They simply share their experiences and how they have made the most of challenging situations.Check out the 21CD YouTube Channel with dozens of videos on topics relevant to dads raising children with special needs - https://www.youtube.com/channel/UCzDFCvQimWNEb158ll6Q4cA/videosPlease support the SFN. Click here to donate: https://21stcenturydads.org/donate/Special Fathers Network: https://21stcenturydads.org/ SFN Mastermind Group - https://21stcenturydads.org/sfn-mastermind-group/
Vanessa Magula went from being a Hamilton superfan studying pre-health at UCLA to being cast as the standby for all three Schuyler sisters on the Philip tour. No, for real. Vanessa has always been a self-described theatre kid, evidenced by the fact that Deaf West's Spring Awakening is what inspired her to minor in Disability Studies, but it took her a while to take the leap and be a full time performer. After going to an open call for Hamilton in 2016 and being given a literal golden ticket for a callback, everything changed as Vanessa realized that - whether she booked Hamilton or not - this is what she wanted to do. In between yearly Hamilton auditions, Vanessa thrived in the New York City improv comedy scene and even ended up collecting Yondr pouches during Freestyle Love Supreme's Broadway run. Come join our instant bff vibes as we talk about our love of Hamilton (Vanessa saw it in September of 2015 hello!), Anessa Folds, Utkarsh Ambudkar (UTK), Lin's Warriors, and tons of other stuff. Vanessa on Instagram /// Gillian's Website The Hamilcast on Twitter The Hamilcast on Instagram Join the Patreon Peeps
Chris Davies is joined by Lis Vukelich. Vukelich, who has a BS in Human Services with an emphasis in Disability Studies, has over 20+ years supporting individuals who have disability barriers. Despite her critical car accident that resulted in a TBI in July 2017, Lis is more passionate about supporting people with disability barriers than ever. She is currently the Referral & Quality Assurance Specialist at Kaposia, Inc. A special thank you to guest co-host Dupree Edwards from the University of Minnesota Institute on Community Integration.
Dr. Lucy Barnhouse from Arkansas State University joins me in the Greenwood for a fascinating and joyful discussion about using disability studies to examine the middle ages and how it relates to Robin Hood adaptations.Further readings:Disability and Medieval (In)Justice in The Adventures of Robin Hood (1938) and Robin of Sherwood (1984)Good People, Poor Sick: The social identities of lepers in the late medieval RhinelandAzeem and the Witch: Race, Disability, and Medievalisms in Robin Hood: Prince of Thieves For more from Into the Greenwood:www.instagram.com/intogreenwood/www.threads.net/@intogreenwoodbsky.app/profile/intogreenwood.bsky.socialwww.facebook.com/intogreenwoodTo support the podcast go to:www.patreon.com/IntoGreenwoodorwww.buymeacoffee.com/intogreenwoodOur selected charity: Trees, Water & PeopleInto the Greenwood is produced by Thaddeus PapkeTheme music is by Plastic3intogreenwood@gmail.comSupport the show
How to Be Disabled in a Pandemic is the first book to document the experiences of those hardest hit by the COVID-19 pandemic in New York City—disabled people. Diverse disability communities across the five boroughs have been disproportionately impacted by city and national policies, work and housing conditions, stigma, racism, and violence—as much as by the virus itself. Disabled and chronically-ill activists have protested plans for medical rationing and refuted the eugenic logic of mainstream politicians and journalists who “reassure” audiences that only older people and those with disabilities continue to die from COVID-19. At the same time, as exemplified by the viral hashtag #DisabledPeopleToldYou, disability expertise has become widely recognized in practices such as accessible remote work and education, quarantine, and distributed networks of support and mutual aid. How to Be Disabled in a Pandemic (NYU Press, 2025) charts the legacies of this “mass disabling event” for uncertain viral futures, exploring the dialectic between disproportionate risk and the creativity of a disability justice response. How to Be Disabled in a Pandemic includes contributions by wide-ranging disability scholars, writers, and activists whose research and lived experiences chronicle the pandemic's impacts in prisons, migrant detention centers, Chinatown senior centers, hospitals in Queens and the Bronx, working from bed in Brooklyn, subways, schools, housing shelters, social media, and other locations of public and private life. By focusing on New York City over the course of three years, the book reveals key themes of the pandemic, including hierarchies of disability vulnerability, the deployment of disability as a tool of population management, and innovative crip pandemic cultural production. How to Be Disabled in a Pandemic honors those lost, as well as those who survived, by calling for just policies and caring infrastructures, not only in times of crisis but for the long haul. A full transcript of this interview is available at the link here Mara Mills is Associate Professor in the Department of Media, Culture, and Communication at New York University. Mills is cofounder of the NYU Center for Disability Studies and coeditor of Crip Authorship: Disability as Method. Harris Kornstein is Assistant Professor of Public and Applied Humanities at the University of Arizona. They have published research and essays in Surveillance & Society, Curriculum Inquiry, Wired, and others. Faye Ginsburg is Kriser Professor of Anthropology at New York University. Ginsburg is cofounder of the NYU Center for Disability Studies and author of Contested Lives: The Abortion Debate in an American Community and coauthor of Disability Worlds. Rayna Rapp is Professor Emerita in the Department of Anthropology at New York University, and the author of Testing Women, Testing the Fetus: The Social Impact of Amniocentesis in America and coauthor of Disability Worlds. Learn more about your ad choices. Visit megaphone.fm/adchoices Support our show by becoming a premium member! https://newbooksnetwork.supportingcast.fm/new-books-network
How to Be Disabled in a Pandemic is the first book to document the experiences of those hardest hit by the COVID-19 pandemic in New York City—disabled people. Diverse disability communities across the five boroughs have been disproportionately impacted by city and national policies, work and housing conditions, stigma, racism, and violence—as much as by the virus itself. Disabled and chronically-ill activists have protested plans for medical rationing and refuted the eugenic logic of mainstream politicians and journalists who “reassure” audiences that only older people and those with disabilities continue to die from COVID-19. At the same time, as exemplified by the viral hashtag #DisabledPeopleToldYou, disability expertise has become widely recognized in practices such as accessible remote work and education, quarantine, and distributed networks of support and mutual aid. How to Be Disabled in a Pandemic (NYU Press, 2025) charts the legacies of this “mass disabling event” for uncertain viral futures, exploring the dialectic between disproportionate risk and the creativity of a disability justice response. How to Be Disabled in a Pandemic includes contributions by wide-ranging disability scholars, writers, and activists whose research and lived experiences chronicle the pandemic's impacts in prisons, migrant detention centers, Chinatown senior centers, hospitals in Queens and the Bronx, working from bed in Brooklyn, subways, schools, housing shelters, social media, and other locations of public and private life. By focusing on New York City over the course of three years, the book reveals key themes of the pandemic, including hierarchies of disability vulnerability, the deployment of disability as a tool of population management, and innovative crip pandemic cultural production. How to Be Disabled in a Pandemic honors those lost, as well as those who survived, by calling for just policies and caring infrastructures, not only in times of crisis but for the long haul. A full transcript of this interview is available at the link here Mara Mills is Associate Professor in the Department of Media, Culture, and Communication at New York University. Mills is cofounder of the NYU Center for Disability Studies and coeditor of Crip Authorship: Disability as Method. Harris Kornstein is Assistant Professor of Public and Applied Humanities at the University of Arizona. They have published research and essays in Surveillance & Society, Curriculum Inquiry, Wired, and others. Faye Ginsburg is Kriser Professor of Anthropology at New York University. Ginsburg is cofounder of the NYU Center for Disability Studies and author of Contested Lives: The Abortion Debate in an American Community and coauthor of Disability Worlds. Rayna Rapp is Professor Emerita in the Department of Anthropology at New York University, and the author of Testing Women, Testing the Fetus: The Social Impact of Amniocentesis in America and coauthor of Disability Worlds. Learn more about your ad choices. Visit megaphone.fm/adchoices Support our show by becoming a premium member! https://newbooksnetwork.supportingcast.fm/public-policy
How to Be Disabled in a Pandemic is the first book to document the experiences of those hardest hit by the COVID-19 pandemic in New York City—disabled people. Diverse disability communities across the five boroughs have been disproportionately impacted by city and national policies, work and housing conditions, stigma, racism, and violence—as much as by the virus itself. Disabled and chronically-ill activists have protested plans for medical rationing and refuted the eugenic logic of mainstream politicians and journalists who “reassure” audiences that only older people and those with disabilities continue to die from COVID-19. At the same time, as exemplified by the viral hashtag #DisabledPeopleToldYou, disability expertise has become widely recognized in practices such as accessible remote work and education, quarantine, and distributed networks of support and mutual aid. How to Be Disabled in a Pandemic (NYU Press, 2025) charts the legacies of this “mass disabling event” for uncertain viral futures, exploring the dialectic between disproportionate risk and the creativity of a disability justice response. How to Be Disabled in a Pandemic includes contributions by wide-ranging disability scholars, writers, and activists whose research and lived experiences chronicle the pandemic's impacts in prisons, migrant detention centers, Chinatown senior centers, hospitals in Queens and the Bronx, working from bed in Brooklyn, subways, schools, housing shelters, social media, and other locations of public and private life. By focusing on New York City over the course of three years, the book reveals key themes of the pandemic, including hierarchies of disability vulnerability, the deployment of disability as a tool of population management, and innovative crip pandemic cultural production. How to Be Disabled in a Pandemic honors those lost, as well as those who survived, by calling for just policies and caring infrastructures, not only in times of crisis but for the long haul. A full transcript of this interview is available at the link here Mara Mills is Associate Professor in the Department of Media, Culture, and Communication at New York University. Mills is cofounder of the NYU Center for Disability Studies and coeditor of Crip Authorship: Disability as Method. Harris Kornstein is Assistant Professor of Public and Applied Humanities at the University of Arizona. They have published research and essays in Surveillance & Society, Curriculum Inquiry, Wired, and others. Faye Ginsburg is Kriser Professor of Anthropology at New York University. Ginsburg is cofounder of the NYU Center for Disability Studies and author of Contested Lives: The Abortion Debate in an American Community and coauthor of Disability Worlds. Rayna Rapp is Professor Emerita in the Department of Anthropology at New York University, and the author of Testing Women, Testing the Fetus: The Social Impact of Amniocentesis in America and coauthor of Disability Worlds. Learn more about your ad choices. Visit megaphone.fm/adchoices
How to Be Disabled in a Pandemic is the first book to document the experiences of those hardest hit by the COVID-19 pandemic in New York City—disabled people. Diverse disability communities across the five boroughs have been disproportionately impacted by city and national policies, work and housing conditions, stigma, racism, and violence—as much as by the virus itself. Disabled and chronically-ill activists have protested plans for medical rationing and refuted the eugenic logic of mainstream politicians and journalists who “reassure” audiences that only older people and those with disabilities continue to die from COVID-19. At the same time, as exemplified by the viral hashtag #DisabledPeopleToldYou, disability expertise has become widely recognized in practices such as accessible remote work and education, quarantine, and distributed networks of support and mutual aid. How to Be Disabled in a Pandemic (NYU Press, 2025) charts the legacies of this “mass disabling event” for uncertain viral futures, exploring the dialectic between disproportionate risk and the creativity of a disability justice response. How to Be Disabled in a Pandemic includes contributions by wide-ranging disability scholars, writers, and activists whose research and lived experiences chronicle the pandemic's impacts in prisons, migrant detention centers, Chinatown senior centers, hospitals in Queens and the Bronx, working from bed in Brooklyn, subways, schools, housing shelters, social media, and other locations of public and private life. By focusing on New York City over the course of three years, the book reveals key themes of the pandemic, including hierarchies of disability vulnerability, the deployment of disability as a tool of population management, and innovative crip pandemic cultural production. How to Be Disabled in a Pandemic honors those lost, as well as those who survived, by calling for just policies and caring infrastructures, not only in times of crisis but for the long haul. A full transcript of this interview is available at the link here Mara Mills is Associate Professor in the Department of Media, Culture, and Communication at New York University. Mills is cofounder of the NYU Center for Disability Studies and coeditor of Crip Authorship: Disability as Method. Harris Kornstein is Assistant Professor of Public and Applied Humanities at the University of Arizona. They have published research and essays in Surveillance & Society, Curriculum Inquiry, Wired, and others. Faye Ginsburg is Kriser Professor of Anthropology at New York University. Ginsburg is cofounder of the NYU Center for Disability Studies and author of Contested Lives: The Abortion Debate in an American Community and coauthor of Disability Worlds. Rayna Rapp is Professor Emerita in the Department of Anthropology at New York University, and the author of Testing Women, Testing the Fetus: The Social Impact of Amniocentesis in America and coauthor of Disability Worlds. Learn more about your ad choices. Visit megaphone.fm/adchoices
Five years ago, the World Health Organization declared COVID-19 a global pandemic. Since that time, the world has changed dramatically, from the way we think about public health to the way we socialize to the way we watch movies. But those changes haven't had the same impact on everyone. This hour, we’re talking about COVID-19’s impact on existing inequities. We talk about the diverse experiences of disabled people over the last five years, and take a broader look at the history of health and race. GUESTS: Mara Mills: Associate Professor and Ph.D. Director in the Department of Media, Culture, and Communication at New York University. She is Co-Founder and Director of the NYU Center for Disability Studies. She co-edited the recent book How to be Disabled in a Pandemic. Edna Bonhomme: Historian of science. Her new book is A History of the World in Six Plagues: How Contagion, Class and Captivity Shaped Us, from Cholera to COVID-19. To learn more about public health and COVID-19, you can listen to our episode reflecting on four years since the World Health Organization declared COVID-19 a pandemic.See omnystudio.com/listener for privacy information.
Through a thoughtful investigation, Disability in Ptolemaic Egypt and the Hellenistic World: Plato's Stepchildren (Routledge, 2024) reveals often-overlooked narratives of disability within Ptolemaic Egypt and the larger Hellenistic world (332 BCE to 30 BCE). Chapters explore evidence of physical and intellectual disability, ranging from named individuals; representations of people and mythological figures with dwarfism, blindness and vision impairments; cerebral palsy; mobility impairments; spinal disability; and medicine, healing, and prosthetics. Morris examines the historiographical ways in which disability has been approached, and how ancient disability histories are (mis)represented in various contemporary spaces. It uses terminology informed by the disability community and offers guidance for disability inclusivity in curatorial and pedagogical museum and university contexts, as well as prioritizing disability as an essential area of research in ancient world studies and assisting readers with the identification of ancient disability artefacts. The first-book length treatment of the subject, Disability in Ptolemaic Egypt and the Hellenistic World provides a much-needed resource for students and scholars of ancient Egypt, Egyptology, Classics, Classical Studies, and disability in the ancient world. It is also suitable for researchers in Disability Studies, practitioners in broader Ancient World Studies, and museum and heritage professionals. It is accessible to disabled people curious about their own history, as well as nondisabled people interested in disability history and those interested in a more accurate view of ancient Egyptian history. Learn more about your ad choices. Visit megaphone.fm/adchoices Support our show by becoming a premium member! https://newbooksnetwork.supportingcast.fm/new-books-network
Through a thoughtful investigation, Disability in Ptolemaic Egypt and the Hellenistic World: Plato's Stepchildren (Routledge, 2024) reveals often-overlooked narratives of disability within Ptolemaic Egypt and the larger Hellenistic world (332 BCE to 30 BCE). Chapters explore evidence of physical and intellectual disability, ranging from named individuals; representations of people and mythological figures with dwarfism, blindness and vision impairments; cerebral palsy; mobility impairments; spinal disability; and medicine, healing, and prosthetics. Morris examines the historiographical ways in which disability has been approached, and how ancient disability histories are (mis)represented in various contemporary spaces. It uses terminology informed by the disability community and offers guidance for disability inclusivity in curatorial and pedagogical museum and university contexts, as well as prioritizing disability as an essential area of research in ancient world studies and assisting readers with the identification of ancient disability artefacts. The first-book length treatment of the subject, Disability in Ptolemaic Egypt and the Hellenistic World provides a much-needed resource for students and scholars of ancient Egypt, Egyptology, Classics, Classical Studies, and disability in the ancient world. It is also suitable for researchers in Disability Studies, practitioners in broader Ancient World Studies, and museum and heritage professionals. It is accessible to disabled people curious about their own history, as well as nondisabled people interested in disability history and those interested in a more accurate view of ancient Egyptian history. Learn more about your ad choices. Visit megaphone.fm/adchoices
Through a thoughtful investigation, Disability in Ptolemaic Egypt and the Hellenistic World: Plato's Stepchildren (Routledge, 2024) reveals often-overlooked narratives of disability within Ptolemaic Egypt and the larger Hellenistic world (332 BCE to 30 BCE). Chapters explore evidence of physical and intellectual disability, ranging from named individuals; representations of people and mythological figures with dwarfism, blindness and vision impairments; cerebral palsy; mobility impairments; spinal disability; and medicine, healing, and prosthetics. Morris examines the historiographical ways in which disability has been approached, and how ancient disability histories are (mis)represented in various contemporary spaces. It uses terminology informed by the disability community and offers guidance for disability inclusivity in curatorial and pedagogical museum and university contexts, as well as prioritizing disability as an essential area of research in ancient world studies and assisting readers with the identification of ancient disability artefacts. The first-book length treatment of the subject, Disability in Ptolemaic Egypt and the Hellenistic World provides a much-needed resource for students and scholars of ancient Egypt, Egyptology, Classics, Classical Studies, and disability in the ancient world. It is also suitable for researchers in Disability Studies, practitioners in broader Ancient World Studies, and museum and heritage professionals. It is accessible to disabled people curious about their own history, as well as nondisabled people interested in disability history and those interested in a more accurate view of ancient Egyptian history. Learn more about your ad choices. Visit megaphone.fm/adchoices
About the Guest(s):Dr. Priya Lalvani is a professor of Disability Studies at Montclair State University, where she also coordinates inclusive education graduate programs. Holding a PhD in developmental psychology from CUNY and a Master of Arts in Special Education from Columbia University, Dr. Lalvani brings over 14 years of professional experience working with young adults with disabilities in New York City. Her academic focus is on ableism, the segregation of students with disabilities in educational settings, and she has authored over 20 research articles alongside the co-authored book, "Undoing Ableism."Episode Summary:In this thought-provoking episode of Think Inclusive, host Tim Villegas engages in a deep conversation with Dr. Priya Lalvani, an esteemed professor and advocate for the rights of children with disabilities. The episode kicks off with Dr. Lalvani's poignant thoughts on the paradox of segregating children to foster a sense of belonging, asking difficult questions about educational environments that fail these students. This podcast episode is an insightful dive into the history and ongoing challenges of parent advocacy in special education.Dr. Priya Lalvani shares her extensive research on ableism in education, uncovering systemic resistance parents face when fighting for inclusive educational practices. A significant part of the discussion revolves around Dr. Lalvani's recent study on "battle fatigue" experienced by parents advocating within the system, offering both a critique of current practices and practical solutions to overcome these barriers. This episode is a must-listen for educators, policymakers, and advocates passionate about genuine inclusion, as it delves deeply into the responsibilities and challenges of creating inclusive spaces for all learners.Complete show notes + transcript: https://mcie.org/think-inclusive/battle-fatigue-the-fight-for-inclusive-education-with-dr-priya-lalvani/Key Takeaways:Segregation vs. Inclusion: Dr. Lalvani questions the logic behind segregating students with disabilities to create spaces of belonging, advocating instead for transforming existing educational environments to become more inclusive.Parent Advocacy and Systemic Challenges: The history and current landscape of parent advocacy in special education reveal systemic barriers that make the fight for inclusion strenuous for families.Battle Fatigue in Advocacy: Dr. Lalvani introduces the concept of "battle fatigue," describing the emotional and physical toll on parents as they continuously advocate for their children's rights in a resistant educational system.Privilege Disparities: The discussion highlights how disparities in privilege affect the efficacy of advocacy efforts, with certain families able to leverage resources and knowledge to push for change more effectively than others.Policy Recommendations: Practical solutions, such as improving professional development for educators on IDEA and inclusive practices, could shift the current paradigm towards more effective inclusion.Resources:Undoing Ableism: https://bookshop.org/p/books/undoing-ableism-teaching-about-disability-in-k-12-classrooms-susan-baglieri/ Battle Fatigue: Parents, Institutionalized Ableism, and the “Fight” for Inclusive Education: https://journals.sagepub.com/doi/10.1177/15407969241259365Thank you to our sponsor, IXL: https://www.ixl.com/inclusive Hosted on Acast. See acast.com/privacy for more information.
Cornell University research sponsored by the U.S. Department of Labor's Office of Disability Employment Policy has identified approaches to designing employer career webpages that can significantly heighten the likelihood of a company's success in attracting job seekers with disabilities and encouraging them to apply for open positions.Susanne Bruyère, a professor of Disability Studies and academic director of the Yang-Tan Institute on Employment and Disability at the Cornell ILR School, takes a close look at this research—and what it means for employers as well as people with disabilities—and offers insights for recruiting applicants with disabilities, finetuning hiring processes and understanding how a person with a disability may choose to self-identify to potential employers.What You'll LearnApproaches to disability-inclusive messaging on Fortune 500 company career webpagesHow job seekers with disabilities approach job searching onlineHow to tailor messaging to encourage job seekers with disabilities to apply and self-identifyThe Cornell Keynotes podcast is brought to you by eCornell, which offers more than 200 online certificate programs to help professionals advance their careers and organizations. Susanne Bruyère is an author of these programs:Neurodiversity at WorkWorkplace Disability InclusionResources mentioned in the episode:Checklist for Employers: Facilitating the Hiring of People with Disabilities through the use of eRecruiting Screening Systems, Including AIDisability Outreach and Inclusion Messaging: Assessment Checklist for Career PagesODEP websiteYang-Tan Institute on Employment and Disability Website Did you enjoy this episode of the Cornell Keynotes podcast? Watch the full Keynote. Follow eCornell on Facebook, Instagram, LinkedIn, TikTok, and X.
Whitney Dirks joins Jana Byars to talk about her new book, Monstrosity, Bodies, and Knowledge in Early Modern England: Curiosity to See and Behold (Amsterdam University Press, 2024). In 1680, the poor cottager Mary Herring gave birth to conjoined twins. At two weeks of age, they were kidnapped to be shown for money, and their deaths shortly thereafter gave rise to a four-year legal battle over ownership and income. The Herring twins' microhistory weaves throughout this book, as the chapter structure alternates between the family's ordeal and the broader cultural context of how so-called 'monstrous births' (a contemporary term for deformed humans and animals) were discussed in cheap print, exhibited in London's pubs and coffeehouses, examined by the Royal Society, portrayed in visual culture, and litigated in London's legal courts. This book ties together social and medical history, Disability Studies, and Monster Studies to argue that people discussed unusual bodies in early modern England because they provided newsworthy entertainment, revealed the will of God, and demonstrated the internal workings of Nature. Learn more about your ad choices. Visit megaphone.fm/adchoices Support our show by becoming a premium member! https://newbooksnetwork.supportingcast.fm/new-books-network
Whitney Dirks joins Jana Byars to talk about her new book, Monstrosity, Bodies, and Knowledge in Early Modern England: Curiosity to See and Behold (Amsterdam University Press, 2024). In 1680, the poor cottager Mary Herring gave birth to conjoined twins. At two weeks of age, they were kidnapped to be shown for money, and their deaths shortly thereafter gave rise to a four-year legal battle over ownership and income. The Herring twins' microhistory weaves throughout this book, as the chapter structure alternates between the family's ordeal and the broader cultural context of how so-called 'monstrous births' (a contemporary term for deformed humans and animals) were discussed in cheap print, exhibited in London's pubs and coffeehouses, examined by the Royal Society, portrayed in visual culture, and litigated in London's legal courts. This book ties together social and medical history, Disability Studies, and Monster Studies to argue that people discussed unusual bodies in early modern England because they provided newsworthy entertainment, revealed the will of God, and demonstrated the internal workings of Nature. Learn more about your ad choices. Visit megaphone.fm/adchoices Support our show by becoming a premium member! https://newbooksnetwork.supportingcast.fm/history
Whitney Dirks joins Jana Byars to talk about her new book, Monstrosity, Bodies, and Knowledge in Early Modern England: Curiosity to See and Behold (Amsterdam University Press, 2024). In 1680, the poor cottager Mary Herring gave birth to conjoined twins. At two weeks of age, they were kidnapped to be shown for money, and their deaths shortly thereafter gave rise to a four-year legal battle over ownership and income. The Herring twins' microhistory weaves throughout this book, as the chapter structure alternates between the family's ordeal and the broader cultural context of how so-called 'monstrous births' (a contemporary term for deformed humans and animals) were discussed in cheap print, exhibited in London's pubs and coffeehouses, examined by the Royal Society, portrayed in visual culture, and litigated in London's legal courts. This book ties together social and medical history, Disability Studies, and Monster Studies to argue that people discussed unusual bodies in early modern England because they provided newsworthy entertainment, revealed the will of God, and demonstrated the internal workings of Nature. Learn more about your ad choices. Visit megaphone.fm/adchoices
Whitney Dirks joins Jana Byars to talk about her new book, Monstrosity, Bodies, and Knowledge in Early Modern England: Curiosity to See and Behold (Amsterdam University Press, 2024). In 1680, the poor cottager Mary Herring gave birth to conjoined twins. At two weeks of age, they were kidnapped to be shown for money, and their deaths shortly thereafter gave rise to a four-year legal battle over ownership and income. The Herring twins' microhistory weaves throughout this book, as the chapter structure alternates between the family's ordeal and the broader cultural context of how so-called 'monstrous births' (a contemporary term for deformed humans and animals) were discussed in cheap print, exhibited in London's pubs and coffeehouses, examined by the Royal Society, portrayed in visual culture, and litigated in London's legal courts. This book ties together social and medical history, Disability Studies, and Monster Studies to argue that people discussed unusual bodies in early modern England because they provided newsworthy entertainment, revealed the will of God, and demonstrated the internal workings of Nature. Learn more about your ad choices. Visit megaphone.fm/adchoices Support our show by becoming a premium member! https://newbooksnetwork.supportingcast.fm/european-studies
Whitney Dirks joins Jana Byars to talk about her new book, Monstrosity, Bodies, and Knowledge in Early Modern England: Curiosity to See and Behold (Amsterdam University Press, 2024). In 1680, the poor cottager Mary Herring gave birth to conjoined twins. At two weeks of age, they were kidnapped to be shown for money, and their deaths shortly thereafter gave rise to a four-year legal battle over ownership and income. The Herring twins' microhistory weaves throughout this book, as the chapter structure alternates between the family's ordeal and the broader cultural context of how so-called 'monstrous births' (a contemporary term for deformed humans and animals) were discussed in cheap print, exhibited in London's pubs and coffeehouses, examined by the Royal Society, portrayed in visual culture, and litigated in London's legal courts. This book ties together social and medical history, Disability Studies, and Monster Studies to argue that people discussed unusual bodies in early modern England because they provided newsworthy entertainment, revealed the will of God, and demonstrated the internal workings of Nature. Learn more about your ad choices. Visit megaphone.fm/adchoices
Whitney Dirks joins Jana Byars to talk about her new book, Monstrosity, Bodies, and Knowledge in Early Modern England: Curiosity to See and Behold (Amsterdam University Press, 2024). In 1680, the poor cottager Mary Herring gave birth to conjoined twins. At two weeks of age, they were kidnapped to be shown for money, and their deaths shortly thereafter gave rise to a four-year legal battle over ownership and income. The Herring twins' microhistory weaves throughout this book, as the chapter structure alternates between the family's ordeal and the broader cultural context of how so-called 'monstrous births' (a contemporary term for deformed humans and animals) were discussed in cheap print, exhibited in London's pubs and coffeehouses, examined by the Royal Society, portrayed in visual culture, and litigated in London's legal courts. This book ties together social and medical history, Disability Studies, and Monster Studies to argue that people discussed unusual bodies in early modern England because they provided newsworthy entertainment, revealed the will of God, and demonstrated the internal workings of Nature. Learn more about your ad choices. Visit megaphone.fm/adchoices Support our show by becoming a premium member! https://newbooksnetwork.supportingcast.fm/british-studies
Welcome to the Back to Business Podcast, where we spotlight Calgary's industry leaders and delve into the heart of entrepreneurialism in our vibrant city!Matt Ashdown serves as the Director of Mission Impact at Goodwill Industries of Alberta, where he drives initiatives to build inclusive communities and create meaningful employment opportunities for individuals with disabilities and other barriers. With over 25 years of leadership experience in disability services and community development, Matt combines expertise with a deep passion for equity and empowerment. A graduate in Community Rehabilitation and Disability Studies, he is dedicated to fostering belonging and growth through purposeful work. Matt's leadership is grounded in collaboration, innovation, and a commitment to positive social impact.Get Connected With Matt:https://www.goodwill.ab.cahttps://www.linkedin.com/in/matt-ashdown-9188462b/Visit www.calpeteclub.com for information on our next networking and membership opportunities.https://calpeteclub.com/https://twitter.com/calpeteclubhttps://www.linkedin.com/in/calgary-petroleum-club-3a5868117/https://www.facebook.com/calpeteclubhttps://www.youtube.com/user/calpeteclub
This volume of Osiris places disability history and the history of science in conversation to foreground disability epistemologies, disabled scientists, and disability sciencing (engagement with scientific tools and processes). Looking beyond paradigms of medicalization and industrialization, the volume authors also examine knowledge production about disability from the ancient world to the present in fields ranging from mathematics to the social sciences, resulting in groundbreaking histories of taken-for-granted terms such as impairment, infirmity, epidemics, and shōgai. Some contributors trace the disabling impacts of scientific theories and practices in the contexts of war, factory labor, insurance, and colonialism; others excavate racial and settler ableism in the history of scientific facts, protocols, and collections; still others query the boundaries between scientific, lay, and disability expertise. Contending that disability alters method, authors bring new sources and interpretation techniques to the history of science, overturn familiar narratives, apply disability analyses to established terms and archives, and discuss accessibility issues for disabled historians. The resulting volume announces a disability history of science. Jaipreet Virdi is a historian of medicine, technology and disability. Her research and teaching interests include the history of medicine, the history of science, disability history, disability technologies and material/visual culture studies. She received her Ph.D. from the Institute for the History and Philosophy of Science and Technology at the University of Toronto (2014). Mara Mills is Associate Professor and Ph.D. Director in the Department of Media, Culture, and Communication at New York University. She is cofounder and Director of the NYU Center for Disability Studies; a founding editor of the award-winning journal Catalyst: Feminism, Theory, Technoscience; and a founding member of the steering committees for the NYU cross-school minors in Science and Society and Disability Studies. Sarah Rose is an associate professor of history at the University of Texas at Arlington, where she founded and directs the Minor in Disability Studies. There are more than 120 Disability Studies graduates from UTA now. She also co-founded and serves as faculty advisor for UTA Libraries' Texas Disability History Collection, for which she and Trevor Engel co-curated the Building a Barrier-Free Campus traveling and digitized exhibit. Her book, No Right to Be Idle: The Invention of Disability, 1840s-1930s, was published by University of North Carolina Press in 2017 and was awarded the 2018 Philip Taft Prize in Labor and Working Class History and the 2018 Disability History Association Outstanding Book Award, among other awards. She has also published with Dr. Joshua Salzmann in LABOR on how baseball players and teams have managed health and fitness and in the Journal of Policy History on disabled veterans' access to the GI bill and higher education after World War II. Learn more about your ad choices. Visit megaphone.fm/adchoices Support our show by becoming a premium member! https://newbooksnetwork.supportingcast.fm/new-books-network
This volume of Osiris places disability history and the history of science in conversation to foreground disability epistemologies, disabled scientists, and disability sciencing (engagement with scientific tools and processes). Looking beyond paradigms of medicalization and industrialization, the volume authors also examine knowledge production about disability from the ancient world to the present in fields ranging from mathematics to the social sciences, resulting in groundbreaking histories of taken-for-granted terms such as impairment, infirmity, epidemics, and shōgai. Some contributors trace the disabling impacts of scientific theories and practices in the contexts of war, factory labor, insurance, and colonialism; others excavate racial and settler ableism in the history of scientific facts, protocols, and collections; still others query the boundaries between scientific, lay, and disability expertise. Contending that disability alters method, authors bring new sources and interpretation techniques to the history of science, overturn familiar narratives, apply disability analyses to established terms and archives, and discuss accessibility issues for disabled historians. The resulting volume announces a disability history of science. Jaipreet Virdi is a historian of medicine, technology and disability. Her research and teaching interests include the history of medicine, the history of science, disability history, disability technologies and material/visual culture studies. She received her Ph.D. from the Institute for the History and Philosophy of Science and Technology at the University of Toronto (2014). Mara Mills is Associate Professor and Ph.D. Director in the Department of Media, Culture, and Communication at New York University. She is cofounder and Director of the NYU Center for Disability Studies; a founding editor of the award-winning journal Catalyst: Feminism, Theory, Technoscience; and a founding member of the steering committees for the NYU cross-school minors in Science and Society and Disability Studies. Sarah Rose is an associate professor of history at the University of Texas at Arlington, where she founded and directs the Minor in Disability Studies. There are more than 120 Disability Studies graduates from UTA now. She also co-founded and serves as faculty advisor for UTA Libraries' Texas Disability History Collection, for which she and Trevor Engel co-curated the Building a Barrier-Free Campus traveling and digitized exhibit. Her book, No Right to Be Idle: The Invention of Disability, 1840s-1930s, was published by University of North Carolina Press in 2017 and was awarded the 2018 Philip Taft Prize in Labor and Working Class History and the 2018 Disability History Association Outstanding Book Award, among other awards. She has also published with Dr. Joshua Salzmann in LABOR on how baseball players and teams have managed health and fitness and in the Journal of Policy History on disabled veterans' access to the GI bill and higher education after World War II. Learn more about your ad choices. Visit megaphone.fm/adchoices Support our show by becoming a premium member! https://newbooksnetwork.supportingcast.fm/history
This volume of Osiris places disability history and the history of science in conversation to foreground disability epistemologies, disabled scientists, and disability sciencing (engagement with scientific tools and processes). Looking beyond paradigms of medicalization and industrialization, the volume authors also examine knowledge production about disability from the ancient world to the present in fields ranging from mathematics to the social sciences, resulting in groundbreaking histories of taken-for-granted terms such as impairment, infirmity, epidemics, and shōgai. Some contributors trace the disabling impacts of scientific theories and practices in the contexts of war, factory labor, insurance, and colonialism; others excavate racial and settler ableism in the history of scientific facts, protocols, and collections; still others query the boundaries between scientific, lay, and disability expertise. Contending that disability alters method, authors bring new sources and interpretation techniques to the history of science, overturn familiar narratives, apply disability analyses to established terms and archives, and discuss accessibility issues for disabled historians. The resulting volume announces a disability history of science. Jaipreet Virdi is a historian of medicine, technology and disability. Her research and teaching interests include the history of medicine, the history of science, disability history, disability technologies and material/visual culture studies. She received her Ph.D. from the Institute for the History and Philosophy of Science and Technology at the University of Toronto (2014). Mara Mills is Associate Professor and Ph.D. Director in the Department of Media, Culture, and Communication at New York University. She is cofounder and Director of the NYU Center for Disability Studies; a founding editor of the award-winning journal Catalyst: Feminism, Theory, Technoscience; and a founding member of the steering committees for the NYU cross-school minors in Science and Society and Disability Studies. Sarah Rose is an associate professor of history at the University of Texas at Arlington, where she founded and directs the Minor in Disability Studies. There are more than 120 Disability Studies graduates from UTA now. She also co-founded and serves as faculty advisor for UTA Libraries' Texas Disability History Collection, for which she and Trevor Engel co-curated the Building a Barrier-Free Campus traveling and digitized exhibit. Her book, No Right to Be Idle: The Invention of Disability, 1840s-1930s, was published by University of North Carolina Press in 2017 and was awarded the 2018 Philip Taft Prize in Labor and Working Class History and the 2018 Disability History Association Outstanding Book Award, among other awards. She has also published with Dr. Joshua Salzmann in LABOR on how baseball players and teams have managed health and fitness and in the Journal of Policy History on disabled veterans' access to the GI bill and higher education after World War II. Learn more about your ad choices. Visit megaphone.fm/adchoices
This volume of Osiris places disability history and the history of science in conversation to foreground disability epistemologies, disabled scientists, and disability sciencing (engagement with scientific tools and processes). Looking beyond paradigms of medicalization and industrialization, the volume authors also examine knowledge production about disability from the ancient world to the present in fields ranging from mathematics to the social sciences, resulting in groundbreaking histories of taken-for-granted terms such as impairment, infirmity, epidemics, and shōgai. Some contributors trace the disabling impacts of scientific theories and practices in the contexts of war, factory labor, insurance, and colonialism; others excavate racial and settler ableism in the history of scientific facts, protocols, and collections; still others query the boundaries between scientific, lay, and disability expertise. Contending that disability alters method, authors bring new sources and interpretation techniques to the history of science, overturn familiar narratives, apply disability analyses to established terms and archives, and discuss accessibility issues for disabled historians. The resulting volume announces a disability history of science. Jaipreet Virdi is a historian of medicine, technology and disability. Her research and teaching interests include the history of medicine, the history of science, disability history, disability technologies and material/visual culture studies. She received her Ph.D. from the Institute for the History and Philosophy of Science and Technology at the University of Toronto (2014). Mara Mills is Associate Professor and Ph.D. Director in the Department of Media, Culture, and Communication at New York University. She is cofounder and Director of the NYU Center for Disability Studies; a founding editor of the award-winning journal Catalyst: Feminism, Theory, Technoscience; and a founding member of the steering committees for the NYU cross-school minors in Science and Society and Disability Studies. Sarah Rose is an associate professor of history at the University of Texas at Arlington, where she founded and directs the Minor in Disability Studies. There are more than 120 Disability Studies graduates from UTA now. She also co-founded and serves as faculty advisor for UTA Libraries' Texas Disability History Collection, for which she and Trevor Engel co-curated the Building a Barrier-Free Campus traveling and digitized exhibit. Her book, No Right to Be Idle: The Invention of Disability, 1840s-1930s, was published by University of North Carolina Press in 2017 and was awarded the 2018 Philip Taft Prize in Labor and Working Class History and the 2018 Disability History Association Outstanding Book Award, among other awards. She has also published with Dr. Joshua Salzmann in LABOR on how baseball players and teams have managed health and fitness and in the Journal of Policy History on disabled veterans' access to the GI bill and higher education after World War II. Learn more about your ad choices. Visit megaphone.fm/adchoices Support our show by becoming a premium member! https://newbooksnetwork.supportingcast.fm/science-technology-and-society
This volume of Osiris places disability history and the history of science in conversation to foreground disability epistemologies, disabled scientists, and disability sciencing (engagement with scientific tools and processes). Looking beyond paradigms of medicalization and industrialization, the volume authors also examine knowledge production about disability from the ancient world to the present in fields ranging from mathematics to the social sciences, resulting in groundbreaking histories of taken-for-granted terms such as impairment, infirmity, epidemics, and shōgai. Some contributors trace the disabling impacts of scientific theories and practices in the contexts of war, factory labor, insurance, and colonialism; others excavate racial and settler ableism in the history of scientific facts, protocols, and collections; still others query the boundaries between scientific, lay, and disability expertise. Contending that disability alters method, authors bring new sources and interpretation techniques to the history of science, overturn familiar narratives, apply disability analyses to established terms and archives, and discuss accessibility issues for disabled historians. The resulting volume announces a disability history of science. Jaipreet Virdi is a historian of medicine, technology and disability. Her research and teaching interests include the history of medicine, the history of science, disability history, disability technologies and material/visual culture studies. She received her Ph.D. from the Institute for the History and Philosophy of Science and Technology at the University of Toronto (2014). Mara Mills is Associate Professor and Ph.D. Director in the Department of Media, Culture, and Communication at New York University. She is cofounder and Director of the NYU Center for Disability Studies; a founding editor of the award-winning journal Catalyst: Feminism, Theory, Technoscience; and a founding member of the steering committees for the NYU cross-school minors in Science and Society and Disability Studies. Sarah Rose is an associate professor of history at the University of Texas at Arlington, where she founded and directs the Minor in Disability Studies. There are more than 120 Disability Studies graduates from UTA now. She also co-founded and serves as faculty advisor for UTA Libraries' Texas Disability History Collection, for which she and Trevor Engel co-curated the Building a Barrier-Free Campus traveling and digitized exhibit. Her book, No Right to Be Idle: The Invention of Disability, 1840s-1930s, was published by University of North Carolina Press in 2017 and was awarded the 2018 Philip Taft Prize in Labor and Working Class History and the 2018 Disability History Association Outstanding Book Award, among other awards. She has also published with Dr. Joshua Salzmann in LABOR on how baseball players and teams have managed health and fitness and in the Journal of Policy History on disabled veterans' access to the GI bill and higher education after World War II. Learn more about your ad choices. Visit megaphone.fm/adchoices
An episode that breaks the mold!Here's what's to come in this episode: * We kick off this episode by discussing Courtney Love and her candid acknowledgment of her autism in a 1994 Rolling Stone interview. While she's open about her experiences, some of her language is problematic—for instance, referring to non-speaking autism as "introverted."* However, we delve into how many of the judgments and perceptions surrounding Courtney Love may be rooted in ableism, influenced by her autism diagnosis.* We explore the inherent connection between musical subcultures and autism, highlighting how these spaces can become a refuge for those who feel ostracized elsewhere.* Next, we dive into the powerful intersection between punk ethos and neurodivergence, unpacking how these two worlds resonate deeply with shared values and traits. Punk celebrates nonconformity, rejecting the rigid societal expectations and hierarchies that often marginalize neurodivergent individuals. It embraces the idea that standing up for what you believe in—no matter how unconventional—is a strength, not a flaw.* This ethos aligns with the autistic experience of navigating a world that frequently misunderstands or undervalues difference. Punk fosters a sense of belonging by creating a community for misfits—a safe haven for those who've been excluded or overlooked in more traditional spaces. In this way, punk and neurodivergence together challenge norms, celebrate authenticity, and amplify the voices of those too often silenced.* Realizing you are neurodivergent doesn't erase your punk identity—it deepens it. Subculture isn't just about aligning with a particular music scene or fashion; it's a gateway to discovering and embracing your most authentic self.* We also discuss how loud music, often a hallmark of punk, can be soothing and sensory-stimulating for many of us on the autism spectrum.* Punk and punk-era band names are often defined by connotations of violence, aggression, sex, fetishism, turmoil, and eruption, with many even referencing disability. This rebellious language reflects the feelings of being "othered"—a sensation that resonates deeply with the autistic experience. Just as punk challenges societal norms and embraces marginalization, the association with disability within punk culture highlights how both the neurodivergent community and the subculture at large confront rejection, discrimination, and the struggle to be understood.* Punk intertwines with the refusal to be seen through the neurotypical lens, rejecting the pressure to conform to societal expectations. It's about resisting the influence of outside forces and voices that seek to define who you are, instead embracing self-expression and authenticity on your own terms.* We also discuss how body modifications, like tattoos and piercings, play into this idea of reclaiming autonomy and defying societal norms. For many in the punk and neurodivergent communities, these mods serve as a powerful way to express individuality, resist outside judgment, and celebrate personal identity on their own terms.* We discuss how autism is often framed through neurotypical-centric lenses, such as infantilization, pity, and the "superhero" trope, which limit our agency and self-expression. Punk, however, challenges these narratives by reclaiming our power and refusing to let society define or diminish us.* Punk embraces an anti-aesthetic that celebrates imperfections, rejecting the need for polished or conventional beauty standards. This ties directly to autism, as both challenge societal expectations of "perfection" and instead embrace authenticity, quirks, and individuality.* The culture of punk is, at its core, authenticity without apology—and that's exactly what autistic people desire: spaces and cultures where they can be their true selves without the need to mask or conform.“When I talk about being introverted, I was diagnosed autistic. At an early age, I would not speak. Then I simply bloomed. My first visit to a psychiatrist was when I was like three. Observational therapy, TM for Tots, you name it, I've been there.” - Courtney Love (the one and only!!)“You [an autistic person] can't just go into a space and say, ‘yes, I am perfectly at home here.'” No, you have to change it to fit your needs. And that's fairly punk, because punk doesn't show up and say, ‘yes, this is acceptable.' No, we are going to rage against the machine.” - Matt“Yes, we want you, you misfit toys, to fit in perfectly here. You are a part of our merry band of autistics and you are perfect just the way you are.” - Angela“Yes, punk is saying we are different and that's enough, like we are enough and this f*****g sucks at the same time. It's not saying, like, ‘fix me', necessarily. It's saying, ‘this is my identity.'” - Angela Did you notice the connection between punk, subculture, and the autistic experience? In today's episode, we explore how punk's defiance and authenticity reflect the autistic spirit. Thanks for tuning in! Share your thoughts on the conversation in the comments, and use #AutisticCultureCatch to connect with fellow listeners on social media. Which parts of the punk ethos resonated most with you?Resources:Rolling Stone article where Courtney comes out - https://www.rollingstone.com/music/music-news/courtney-love-life-without-kurt-81520/Interview with Courtney where she talks about her diagnosis Autisticasfxxk - Raise your middle finger to neuronormativity!
In today's deep dive, we’ll learn about some issues at the University of Illinois that continue to create barriers for disabled students.
Series: Medical “Finding Hope in the Midst of Medical Complexity” with Andrea Bourne Foster Welcome to the podcast. This episode is full of heart and hope. Today we begin our Medical series with author, speaker, educator and advocate Andrea Bourne Foster. Andrea is the mom of 2 beautiful daughters diagnosed with tuberous sclerosis and epilepsy. She is no stranger to hospital stays and ongoing procedures and we are blessed to have this most amazing mom and advocate on with us today. Let's listen in as she shares her families story. Bio: Andrea Foster is a speaker, writer, disability advocate/educator, wife and mom. Andrea has been married to Kirk since 1998 and they are parents to four young adults. Their youngest, Audrey and Annie are identical twins who were diagnosed with Tuberous Sclerosis Complex at age five months. This resulted in further diagnoses of epilepsy, autism, intellectual disability and other medical complexities. Andrea and Kirk experienced grief at the loss of dreams and face daily challenges as they fulfill the role of parent-caregivers for their twin daughters. They live in Brampton, Ontario, Canada where Kirk is a professional Firefighter and have been part of Bramalea Alliance Church since 2001. Andrea holds a Master of Science in Education (Disability Studies), Bachelor of Theology and Early Childhood Education Diploma. She shares her experiences through speaking and writing. Her articles are published in Testimony Magazine (PAOC), Alliance.ca magazine, ChristianWeek online magazine and in Women Together online magazine. She has also been a guest writer for Key Ministry and guest blogger for the Huffington Post. She has been interviewed on 100 Huntley St., The Drew Marshall Show and by other podcast hosts. Andrea guest lectures at Bible Colleges and Seminaries, and is working to make Disability Studies part of all such curriculums. Andrea longs to help families not only cope, but also thrive and truly know the joy of the Lord, in spite of disability, disappointment and ongoing seasons of trial. She believes all people belong in the Church but understands that not all leaders are well prepared for ministry with people affected by disability. Her passion is to equip everyone for better interaction so the Body of Christ will become a place of belonging for everybody. One of her favourite things is encouraging other families affected by disability to press into Jesus through Bible study, Church connection and Corporate Worship. Connect with Us: If you enjoy this podcast please share us with others and be sure to follow us so won't miss an episode. We'd love to hear from you so please leave us a comment or rating and connect with us on social media or on our website. Email us Website: Instagram Facebook: Facebook Group Free Youtube Resource Library
This Saturday, the longest running disability film festival in the world begins. Whether online or in person, you're sure to see diverse, unabashed and engaging cinema. In the two decades of Pushing Limits, we've watched the ethos of disability organizing from the 1970s be embraced by a new generation of disabled cultural workers and organizations. Superfest's parent, the Longmore Institute at S.F. State, with its new disability cultural center is one keeper of these flames. Our guest this week, Dr. Emily Beitiks, interim director for the Longmore Institute, has seen these happy developments close and personal. Eddie Ytuarte hosts. SUPERFEST Superfest Disability Film Festival is coming October 17-20, and whether you are joining in person in the Bay Area or online anywhere in the world, you need to be a part of it! Superfest is the longest running disability film festival in the world. Since 1970, it has celebrated cinema that portrays disability through a diverse, unabashed and engaging lens, and we can't wait to come together as a community to take in this much-loved disability cultural event for its 38th festival, hybrid for the second year, with new levels of access. EMILY BEITIKS: Emily Beitiks received a Ph.D. in American Studies with a focus in Disability Studies at the University of Minnesota. She has served as adjunct faculty at five universities, centering disability studies in her curriculum. Dr. Emily Beitiks From 2012 to the present, she has worked at the Longmore Institute on Disability at San Francisco State University, serving as Interim Director for three years. While there, she developed her praxis as a scholar-activist of disability to promote creative forms of access for the arts and generate spaces that promote disability culture, serving as project director for a touring exhibition “Patient No More,” and serving as co-director of Superfest Disability Film Festival. She exists in this world because her mother's sudden disability diagnosis prompted her to have a child, and her first-hand experiences of disability have grown throughout her 20 years of experience working in the disability community. 2024 Superfest Disability Film Festival Flyer The post Superfest & The Longmore Institute – Pushing Limits – October 18, 2024 appeared first on KPFA.
In part two of the conversation, Elizabeth Kleinfeld and Julie Prebel discuss 'activist editing', the method that they and Sohui Lee used to edit the collection Disruptive stories: Amplifying voices from the writing center margins. About the authors Elizabeth Kleinfeld teaches rhetoric and writing theory and practice courses in the English department, coordinates the new Disability Studies minor, and directs the Writing Center at Metropolitan State University of Denver. She is writing a memoir about being her husband's caregiver and working on a scholarly project studying how the sex lives of disabled people are represented in memoirs. She is also a coach for the National Center for Faculty Development and Diversity, an end-of-life doula, and a hospice volunteer. Julie Prebel teaches courses in rhetorical theory, critical theory, and American cultural studies, and directs the Writing Center at Occidental College. Along with ongoing research in rhet-comp, she is currently working on a manuscript focused on the racialization of sentiment in (seemingly) feminist representations of rights discourse in literature and popular media. She presents her work regularly at national conferences such as IWCA, CCCCs, and the American Studies Association.
More and more people turn to quantified health, achievement, and ability measures, such as fitness apps and economic measures of well-being every single day. As part of this trend, medicalized approaches to human health often describe people in terms of statistics and data, sometimes failing to capture more important details. In particular, the quantified approach falls short in describing the needs and rights of disabled people, as seen in lawsuits and case studies involving algorithmic decision-making about disability benefits. Here to talk about algorithmic decision-making and quantification in disability benefits in the United States and India are Vandana Chaudhry, Associate Professor in the Department of Social Work and Disability Studies at the City University of New York who focuses on disability and digital justice in the Global South, and Lydia X.Z. Brown, activist for disability justice, Director of Public Policy at the National Disability Institute, and CDT's very own former policy counsel.
Susanne Bruyère, a professor of Disability Studies and academic director of the K. Lisa Yang and Hock E. Tan Institute on Employment and Disability at the Cornell ILR School, traces the opportunities and challenges encountered across the employment process in designing and implementing neurodiversity-affirmative hiring initiatives. Bruyère addresses the importance of creating a workplace culture that embraces a diverse workforce, including those who are neurodivergent.The Cornell Keynotes podcast is brought to you by eCornell, which offers more than 200 online certificate programs to help professionals advance their careers and organizations. Susanne Bruyère is an author of the Diversity, Equity, and Inclusion: Building a Diverse Workforce certificate program. Other relevant Cornell online courses include Workplace Disability Inclusion and Autism at Work.Reading List and Resources“Neurodiversity in the Workplace: Interests, Issues, and Opportunities” by Susanne Bruyère and Adrienne Colella (available at a 20% discount with the code FLA22)Employer Assistance and Resource Network on Disability Inclusion – Neurodiversity in the WorkplaceAutism Transition to Adulthood InitiativeDisability:IN Neurodiversity @ Work RoundtableCollege Autism NetworkNeurodiversity Hub (Australia)Autistic Self Advocacy Network – Identity-first LanguageDisabled World – What Is: Neurodiversity, Neurodivergent, NeurotypicalDid you enjoy this episode of the Cornell Keynotes podcast? Watch the Keynote. Follow eCornell on Facebook, Instagram, LinkedIn, TikTok, and X.
Season Two erupts in our ears with a film-noir soundscape—an eerie voice utters strange and disjointed phrases and echoing footsteps lead to sirens and gunshots. What on Earth are we listening to? We unravel the mystery with NYU media professor Mara Mills who studies the historical relationship between disability and media technologies. In Episode 8, “Test Subjects,” we examine the strange and obscure history of sound's use as a psychological diagnostic tool. In the late 20th century, while many disabilities were eliminated through medical interventions, a host of new disabilities were invented, especially within the realm of psychology. Mills's historical work in the audio archives of American Foundation for the Blind reveals how auditory projective testing was used to diagnose blind people with additional psychological disabilities. As we listen to these strange archival sounds, we learn how culture and technology shape the history of human ability and disability. Read Mara Mill's article on auditory projective tests, “Evocative Object: Auditory Inkblot” and visit NYU's Center for Disability Studies, which she co-directs with Faye Ginsburg. Thanks to archivist Helen Selsdon and the American Foundation for the Blind for the use of the auditory projective tests. This episode's theme music is by Mack Hagood with additional music by Graeme Gibson, Blue Dot Sessions, Claude Debussy, and Duke Ellington. The show was edited by Craig Eley and Mack Hagood. Learn more about your ad choices. Visit megaphone.fm/adchoices Support our show by becoming a premium member! https://newbooksnetwork.supportingcast.fm/new-books-network
Season Two erupts in our ears with a film-noir soundscape—an eerie voice utters strange and disjointed phrases and echoing footsteps lead to sirens and gunshots. What on Earth are we listening to? We unravel the mystery with NYU media professor Mara Mills who studies the historical relationship between disability and media technologies. In Episode 8, “Test Subjects,” we examine the strange and obscure history of sound's use as a psychological diagnostic tool. In the late 20th century, while many disabilities were eliminated through medical interventions, a host of new disabilities were invented, especially within the realm of psychology. Mills's historical work in the audio archives of American Foundation for the Blind reveals how auditory projective testing was used to diagnose blind people with additional psychological disabilities. As we listen to these strange archival sounds, we learn how culture and technology shape the history of human ability and disability. Read Mara Mill's article on auditory projective tests, “Evocative Object: Auditory Inkblot” and visit NYU's Center for Disability Studies, which she co-directs with Faye Ginsburg. Thanks to archivist Helen Selsdon and the American Foundation for the Blind for the use of the auditory projective tests. This episode's theme music is by Mack Hagood with additional music by Graeme Gibson, Blue Dot Sessions, Claude Debussy, and Duke Ellington. The show was edited by Craig Eley and Mack Hagood. Learn more about your ad choices. Visit megaphone.fm/adchoices Support our show by becoming a premium member! https://newbooksnetwork.supportingcast.fm/psychology
Season Two erupts in our ears with a film-noir soundscape—an eerie voice utters strange and disjointed phrases and echoing footsteps lead to sirens and gunshots. What on Earth are we listening to? We unravel the mystery with NYU media professor Mara Mills who studies the historical relationship between disability and media technologies. In Episode 8, “Test Subjects,” we examine the strange and obscure history of sound's use as a psychological diagnostic tool. In the late 20th century, while many disabilities were eliminated through medical interventions, a host of new disabilities were invented, especially within the realm of psychology. Mills's historical work in the audio archives of American Foundation for the Blind reveals how auditory projective testing was used to diagnose blind people with additional psychological disabilities. As we listen to these strange archival sounds, we learn how culture and technology shape the history of human ability and disability. Read Mara Mill's article on auditory projective tests, “Evocative Object: Auditory Inkblot” and visit NYU's Center for Disability Studies, which she co-directs with Faye Ginsburg. Thanks to archivist Helen Selsdon and the American Foundation for the Blind for the use of the auditory projective tests. This episode's theme music is by Mack Hagood with additional music by Graeme Gibson, Blue Dot Sessions, Claude Debussy, and Duke Ellington. The show was edited by Craig Eley and Mack Hagood. Learn more about your ad choices. Visit megaphone.fm/adchoices
Keywords: Memoir, Disability Studies, Writing Pedagogy, Non-Fiction, Non-Tenure Track. Dr. Jessie Male is a nonfiction writer and teacher-scholar with specializations in Disability Studies and Memoir. She is currently the Postdoctoral Associate in Disability Studies at the University of Pittsburgh, where she teaches, develops programs to support disabled studies and faculty, and curates a speaker series, "Creating a Culture of Access". She has an MFA in Memoir from Hunter College and an MA and PhD in English from The Ohio State University. Her current book project, Disability Memoir: A Study in Pedagogy and Practice, explores the writing and teaching of Disability Memoir by merging personal narrative with literary, rhetorical, and pedagogical analysis. For more information visit thebigrhetoricalpodcast.weebly.com and @thebigrhet across social media platforms.
This field-defining volume of queer anthropology foregrounds both the brilliance of anthropological approaches to queer and trans life and the ways queer critique can reorient and transform anthropology. Consisting of fourteen original essays by both distinguished and new voices, Unsettling Queer Anthropology: Foundations, Reorientations, and Departures (Duke UP, 2024) advances a vision of queer anthropology grounded in decolonial, abolitionist, Black feminist, transnational, postcolonial, Indigenous, and queer of color approaches. Critically assessing both anthropology's queer innovations and its colonialist legacies, contributors highlight decades of work in queer anthropology; challenge the boundaries of anthropology's traditional methodologies, forms, and objects of study; and forge a critical, queer of color, decolonizing queer anthropology that unsettles anthropology's normative epistemologies. At a moment of revitalized calls to reckon with the white supremacist and settler colonial logics that continue to shape anthropology, this volume advances an anthropology accountable to the vitality of queer and trans life. Contributors. Jafari Sinclair Allen, Tom Boellstorff, Erin L. Durban, Elijah Adiv Edelman, Lyndon K. Gill, K. Marshall Green, Brian A. Horton, Nikki Lane, Martin F. Manalansan IV, Shaka McGlotten, Scott L. Morgensen, Kwame Otu, Juno Salazar Parreñas, Lucinda Ramberg, Sima Shakhsari, Savannah Shange, Anne Spice, Margot Weiss, Ara Wilson Margot Weiss is Associate Professor of American Studies and Anthropology at Wesleyan University, where she directs the cluster in Queer Studies. Her research, teaching, and writing move between queer theory and anthropology. She is the author of the award-winning Techniques of Pleasure: BDSM and the Circuits of Sexuality and editor of Queer Then and Now and Unsettling Queer Anthropology: Foundations, Reorientations, and Departures. Past president of the Association for Queer Anthropology (AQA), she serves on the board of CLAGS: The Center for LGBT/Queer Studies and the Society for Cultural Anthropology (SCA). She is a founding member of the Wesleyan University Chapter of the AAUP. Clayton Jarrard is an incoming graduate student at NYU's XE: Experimental Humanities & Social Engagement program and a Research Project Coordinator at the University of Kansas Center for Research. His scholarly engagement spans the subject areas of Cultural Anthropology, Queer Studies, Disability Studies, Mad Studies, and Religious Studies. Clayton is also a host for the Un/Livable Cultures podcast. Learn more about your ad choices. Visit megaphone.fm/adchoices Support our show by becoming a premium member! https://newbooksnetwork.supportingcast.fm/new-books-network
This field-defining volume of queer anthropology foregrounds both the brilliance of anthropological approaches to queer and trans life and the ways queer critique can reorient and transform anthropology. Consisting of fourteen original essays by both distinguished and new voices, Unsettling Queer Anthropology: Foundations, Reorientations, and Departures (Duke UP, 2024) advances a vision of queer anthropology grounded in decolonial, abolitionist, Black feminist, transnational, postcolonial, Indigenous, and queer of color approaches. Critically assessing both anthropology's queer innovations and its colonialist legacies, contributors highlight decades of work in queer anthropology; challenge the boundaries of anthropology's traditional methodologies, forms, and objects of study; and forge a critical, queer of color, decolonizing queer anthropology that unsettles anthropology's normative epistemologies. At a moment of revitalized calls to reckon with the white supremacist and settler colonial logics that continue to shape anthropology, this volume advances an anthropology accountable to the vitality of queer and trans life. Contributors. Jafari Sinclair Allen, Tom Boellstorff, Erin L. Durban, Elijah Adiv Edelman, Lyndon K. Gill, K. Marshall Green, Brian A. Horton, Nikki Lane, Martin F. Manalansan IV, Shaka McGlotten, Scott L. Morgensen, Kwame Otu, Juno Salazar Parreñas, Lucinda Ramberg, Sima Shakhsari, Savannah Shange, Anne Spice, Margot Weiss, Ara Wilson Margot Weiss is Associate Professor of American Studies and Anthropology at Wesleyan University, where she directs the cluster in Queer Studies. Her research, teaching, and writing move between queer theory and anthropology. She is the author of the award-winning Techniques of Pleasure: BDSM and the Circuits of Sexuality and editor of Queer Then and Now and Unsettling Queer Anthropology: Foundations, Reorientations, and Departures. Past president of the Association for Queer Anthropology (AQA), she serves on the board of CLAGS: The Center for LGBT/Queer Studies and the Society for Cultural Anthropology (SCA). She is a founding member of the Wesleyan University Chapter of the AAUP. Clayton Jarrard is an incoming graduate student at NYU's XE: Experimental Humanities & Social Engagement program and a Research Project Coordinator at the University of Kansas Center for Research. His scholarly engagement spans the subject areas of Cultural Anthropology, Queer Studies, Disability Studies, Mad Studies, and Religious Studies. Clayton is also a host for the Un/Livable Cultures podcast. Learn more about your ad choices. Visit megaphone.fm/adchoices Support our show by becoming a premium member! https://newbooksnetwork.supportingcast.fm/critical-theory
This field-defining volume of queer anthropology foregrounds both the brilliance of anthropological approaches to queer and trans life and the ways queer critique can reorient and transform anthropology. Consisting of fourteen original essays by both distinguished and new voices, Unsettling Queer Anthropology: Foundations, Reorientations, and Departures (Duke UP, 2024) advances a vision of queer anthropology grounded in decolonial, abolitionist, Black feminist, transnational, postcolonial, Indigenous, and queer of color approaches. Critically assessing both anthropology's queer innovations and its colonialist legacies, contributors highlight decades of work in queer anthropology; challenge the boundaries of anthropology's traditional methodologies, forms, and objects of study; and forge a critical, queer of color, decolonizing queer anthropology that unsettles anthropology's normative epistemologies. At a moment of revitalized calls to reckon with the white supremacist and settler colonial logics that continue to shape anthropology, this volume advances an anthropology accountable to the vitality of queer and trans life. Contributors. Jafari Sinclair Allen, Tom Boellstorff, Erin L. Durban, Elijah Adiv Edelman, Lyndon K. Gill, K. Marshall Green, Brian A. Horton, Nikki Lane, Martin F. Manalansan IV, Shaka McGlotten, Scott L. Morgensen, Kwame Otu, Juno Salazar Parreñas, Lucinda Ramberg, Sima Shakhsari, Savannah Shange, Anne Spice, Margot Weiss, Ara Wilson Margot Weiss is Associate Professor of American Studies and Anthropology at Wesleyan University, where she directs the cluster in Queer Studies. Her research, teaching, and writing move between queer theory and anthropology. She is the author of the award-winning Techniques of Pleasure: BDSM and the Circuits of Sexuality and editor of Queer Then and Now and Unsettling Queer Anthropology: Foundations, Reorientations, and Departures. Past president of the Association for Queer Anthropology (AQA), she serves on the board of CLAGS: The Center for LGBT/Queer Studies and the Society for Cultural Anthropology (SCA). She is a founding member of the Wesleyan University Chapter of the AAUP. Clayton Jarrard is an incoming graduate student at NYU's XE: Experimental Humanities & Social Engagement program and a Research Project Coordinator at the University of Kansas Center for Research. His scholarly engagement spans the subject areas of Cultural Anthropology, Queer Studies, Disability Studies, Mad Studies, and Religious Studies. Clayton is also a host for the Un/Livable Cultures podcast. Learn more about your ad choices. Visit megaphone.fm/adchoices Support our show by becoming a premium member! https://newbooksnetwork.supportingcast.fm/anthropology
This field-defining volume of queer anthropology foregrounds both the brilliance of anthropological approaches to queer and trans life and the ways queer critique can reorient and transform anthropology. Consisting of fourteen original essays by both distinguished and new voices, Unsettling Queer Anthropology: Foundations, Reorientations, and Departures (Duke UP, 2024) advances a vision of queer anthropology grounded in decolonial, abolitionist, Black feminist, transnational, postcolonial, Indigenous, and queer of color approaches. Critically assessing both anthropology's queer innovations and its colonialist legacies, contributors highlight decades of work in queer anthropology; challenge the boundaries of anthropology's traditional methodologies, forms, and objects of study; and forge a critical, queer of color, decolonizing queer anthropology that unsettles anthropology's normative epistemologies. At a moment of revitalized calls to reckon with the white supremacist and settler colonial logics that continue to shape anthropology, this volume advances an anthropology accountable to the vitality of queer and trans life. Contributors. Jafari Sinclair Allen, Tom Boellstorff, Erin L. Durban, Elijah Adiv Edelman, Lyndon K. Gill, K. Marshall Green, Brian A. Horton, Nikki Lane, Martin F. Manalansan IV, Shaka McGlotten, Scott L. Morgensen, Kwame Otu, Juno Salazar Parreñas, Lucinda Ramberg, Sima Shakhsari, Savannah Shange, Anne Spice, Margot Weiss, Ara Wilson Margot Weiss is Associate Professor of American Studies and Anthropology at Wesleyan University, where she directs the cluster in Queer Studies. Her research, teaching, and writing move between queer theory and anthropology. She is the author of the award-winning Techniques of Pleasure: BDSM and the Circuits of Sexuality and editor of Queer Then and Now and Unsettling Queer Anthropology: Foundations, Reorientations, and Departures. Past president of the Association for Queer Anthropology (AQA), she serves on the board of CLAGS: The Center for LGBT/Queer Studies and the Society for Cultural Anthropology (SCA). She is a founding member of the Wesleyan University Chapter of the AAUP. Clayton Jarrard is an incoming graduate student at NYU's XE: Experimental Humanities & Social Engagement program and a Research Project Coordinator at the University of Kansas Center for Research. His scholarly engagement spans the subject areas of Cultural Anthropology, Queer Studies, Disability Studies, Mad Studies, and Religious Studies. Clayton is also a host for the Un/Livable Cultures podcast. Learn more about your ad choices. Visit megaphone.fm/adchoices Support our show by becoming a premium member! https://newbooksnetwork.supportingcast.fm/lgbtq-studies
For Dear Science this week, Professor Allan Blackman chatted to us about Beethoven's deafness, the first ever vaccination, and researchers mapping a small part of the human brain. Wire host Castor spoke to the National Party's Katie Nimon about nursing shortages in light of rallies last week and how the disestablishment of Te Aka Whai Ora could affect the health sector. He also spoke to New Zealand Nurses Organisation president Anne Daniels about these health issues from a frontline worker perspective. Producer Sofia spoke to Public Service Association Assistant Secretary Fleur Fitzsimons about the 325 job cuts to the Accident Compensation Corporation. She also spoke to Professor of Disability Studies and Inclusive Education Missy Morton at the University of Auckland about a new report from the Education Hub about how schools and early childhood centres are failing neurodivergent children.
Dr Miro Griffiths is a Disability Studies scholar, based in the School of Sociology and Social Policy, at the University of Leeds. His research is associated – primarily – with understanding disabled people's experiences of resistance, activism, social movement participation, and advocacy. His contribution to existing bodies of literature has progressed ideas and theories about power, resistance practices, and disabled people's pursuit for liberation. Dr Miro Griffiths is also a policy adviser to governments, civil society organisations, research networks, and private enterprises.
Julie Neale is a life and leadership coach, mom to two neurodivergent boys, and creator of Mother's Quest, the Mother's Quest Podcast, and the Live Your EPIC Year Planner. Started in 2016, Mother's Quest provides inspiration, coaching, and community for mothers who want to live their version of an E.P.I.C. life while raising their children. At the age of 50, Julie received a diagnosis of ADHD, realizing that she is also neurodivergent. The diagnosis explained a lot and has provided a window for her to understand better what it's like for her children to embrace their differences while finding strategies to address the challenges. This year, Julie is serving on the UCLA Parents' Council. She looks forward to working alongside her son Ryan, from a parent perspective, to support neurodivergent students and their families at UCLA. Ryan Neale is a neurodivergent sophomore at UCLA, planning to double major in Communication and Disability Studies with a minor in Film Studies. He is part of the College Scholars Program at UCLA and recently was selected as part of the 2023 Chancellor's Leadership Program cohort. He is passionate about neurodiversity advocacy and sharing his own experiences to pave the way for others. He is currently a staff member at the Bruin Resource Center, where he is a student lead on a new campus-wide neurodiversity initiative to make UCLA more inclusive for students like him. This summer, he served on staff for the Stanford Neurodiversity Project - Research, Education, and Advocacy Camp for high schoolers wanting to create neurodiversity advocacy projects. He was also a speaker at the 2021 Stanford Neurodiversity Summit and has been a guest host on the Mother's Quest Podcast. Ryan was diagnosed with autism at the age of 18 months old and also identifies with ADHD and anxiety. April is Autism Awareness Month. April 2nd is Autism Awareness Day. I was so honored to have Ryan and Julie here to talk about neurodiversity, including autism, and all that Ryan is doing to build inclusive spaces for kids like him on college campuses. Listen in to hear Ryan and Julie share: Ryan's optimism around the neurodiversity movement, esp in collegiate environments Ryan's autism diagnosis at 18 months and his experience of learning of his diagnosis at age 13 Ryan's disconnection from his diagnosis given his propensity for rich connections How Julie was diagnosed with ADHD when going through menopause The difference in the ways Ryan and Julie accepted and integrated their respective diagnoses What Ryan's transition into college life has been like How Ryan has leaped into neurodivergence advocacy at UCLA Links mentioned: Connect with Julie: https://mothersquest.com Connect with Ryan: www.ryanjneale.com Mother's Quest on IG: www.instagram.com/mothersquestpod Ryan on IG: www.instagram.com/ryan.neale04 Ryan on LinkedIn: https://www.linkedin.com/in/ryan-neale-031112176/ Autism Story Telling Project in San Fransisco: https://www.autismstorytellingproject.com/ Spark Course about Ryan's college experience Mother's Quest Podcasts with Ryan related to neurodiversity: https://mothersquest.com/ep-93-learning-outside-the-lines-in-college-with-neurodivergent-advocates-ryan-neale-jonathan-mooney/ https://mothersquest.com/embracing-neurodiversity-and-being-an-adult-with-julie-lythcott-haims-and-ryan-neale/ https://mothersquest.com/ep-18-yolo-you-only-live-once-and-other-milestone-reflections-with-ryan-neale/ Learn more about your ad choices. Visit megaphone.fm/adchoices
I am a proud voting American. From local, national, primary, or general, I never miss my opportunity to participate in my civic duty and cherished right to vote. I love the process of going to my polling precinct and casting my ballot. I slap that sticker on my chest and walk around all day with pride, knowing that instead of choosing to do nothing, I chose to vote. And I believe, that my vote is counted. It may not win, but it is always counted.But I am aware that I may be in the minority who believes that my vote is counted.In January 2024, Data for Progress found that 43% of likely voters are either not confident at all or only a little confident in the security of elections. That percentage rises to 50% if you only look at registered Independents and rises to 69% if you only look at registered Republicans.That is a lot of Americans who do not trust the security of our elections! I wanted to learn more about the election process. To see if there is a reason to not trust the system, or to see if this growing mistrust is fueled by misinformation. My guest this week is Tate Fall, Director of Elections for Cobb County Georgia. She guides me through the history and process of administering elections, shares how much elections have changed through the years, and dispels some of the most common myths about voter fraud. This is a conversation you are not going to want to miss.Tate Fall currently serves as the Director of Elections for Cobb County. She has previously served as the Deputy Director of Elections for Arlington County, VA, a Communications Specialist for the United States Election Assistance Commission (EAC), and as a Voting Rights Advocate for Alabama Disabilities Advocacy Program. Tate has her B.S. in Rehabilitation and Disability Studies, a Master of Public Administration and a Graduate Certificate in Election Administration all from Auburn University. Support the showKeep up with all things WeSTAT on any (or ALL) of the social feeds:InstagramThreads : westatpodFacebookLinkedInTwitterHave a topic or want to stay in touch via e-mail on all upcoming news?https://www.westatpod.com/Help monetarily support the podcast by subscribing to the show! This is an easy way to help keep the conversations going:https://www.buzzsprout.com/768062/supporters/new
Emma Farley is a Disability Studies student and disability activist based in Brooklyn, New York. Emma has both visible and invisible disabilities - a rare form of muscular dystrophy, ADHD, and dyscalculia. Emma's involvement within the disability community stretches back to early childhood, when she began public speaking about her lived experience with muscular dystrophy, and she continues to do this as a Diversability Leadership Collective Member, hosting several discussions with the Diversability group about various disability-related topics. Passionate about creating connections with the disability community and taking an intersectional approach to activism, Emma is launching a new podcast called Unsilent: Disability On Our Terms in Spring 2024.
Disgust, often seen as a primal and universal emotion, can reveal a lot about our values, boundaries, and cultural norms. In this week's episode, both of our storytellers are confronted with something that grosses them out. Part 1: While on a school trip in Russia, Cassandra Hartblay's vegetarian dietary restrictions keep getting tested. Part 2: As a meat lover, Jenny Kleeman has high hopes for the world's first lab-grown chicken nugget. Dr. Cassandra Hartblay is an Assistant Professor at the University of Toronto, where she works with graduate students in Anthropology, European, Russian, and Eurasian Studies, Disability Studies and Sexual Diversity Studies, as well as undergraduates in Health Humanities. She is author of the 2020 book "I Was Never Alone or Oporniki" (University of Toronto Press 2020) and numerous articles, a documentary play, and co-curator of the #CripRitual art exhibition. If you can't find her, she's probably our running or swimming with her dog, an Aussie-Retriever mix named Arlo. Jenny Kleeman is a journalist, broadcaster and author. She writes for the Guardian, the Sunday Times and The New Statesman and makes radio and podcasts for the BBC and the Times. Her latest series for BBC Radio 4 and BBC Sounds, The Gift, tells the story of the remarkable truths that emerge when people take at-home DNA tests. On television, Jenny has reported for BBC One's Panorama, Channel 4's Dispatches and VICE News Tonight on HBO, as well as making 13 films from across the globe for Channel 4's Unreported World. Her first book, Sex Robots & Vegan Meat, was published in 2020 and has been translated into ten languages. Her second book The Price of Life, was published in March 2024. Learn more about your ad choices. Visit podcastchoices.com/adchoices
Mimi Khúc is a PhD, writer, scholar, and teacher of things unwell. She is currently the Co-Editor of The Asian American Literary Review and an adjunct lecturer in Disability Studies at Georgetown University. Her work includes Open in Emergency, a hybrid book-arts project decolonizing Asian American mental health; the Asian American Tarot, a reimagined deck of tarot cards; and the Open in Emergency Initiative, an ongoing national project developing mental health arts programming with universities and community spaces. Her new creative-critical, genre-bending book on mental health and a pedagogy of unwellness, dear elia: Letters from the Asian American Abyss (Duke University Press, 2024), is a journey into the depths of Asian American unwellness at the intersections of ableism, model minoritization, and the university, and an exploration of new approaches to building collective care. Julia H. Lee is professor of Asian American Studies at the University of California, Irvine. She is the author of three books: Interracial Encounters: Reciprocal Representations in African and Asian American Literatures, 1896-1937 (New York University Press, 2011), Understanding Maxine Hong Kingston (University of South Carolina Press, 2018), and The Racial Railroad (New York University Press, 2022). With Professor Josephine Lee, she is co-editor of Asian American Literature in Transition, 1850-1930 (Cambridge University Press, 2021), a Choice Outstanding Academic Title for 2022. You can find her on Instagram @julia.x.lee. Learn more about your ad choices. Visit megaphone.fm/adchoices Support our show by becoming a premium member! https://newbooksnetwork.supportingcast.fm/new-books-network
The use of disability as a metaphor is ubiquitous in popular culture – nowhere more so than in the myths, stereotypes and tropes around blindness. To be 'blind' has never referred solely to the inability to see. Instead blindness has been used as shorthand for, among other things, a lack of understanding, immorality, closeness to death, special insight or second sight. Although these 'meanings' attached to blindness were established as early as antiquity, readers, receivers and spectators into the present have been implicated in the stereotypes, which persist because audiences can be relied on to perpetuate them. Marchella Ward's book Blindness and Spectatorship in Ancient and Modern Theatres: Towards New Ways of Looking and Looking Back (Cambridge UP, 2023) argues for a new way of seeing – and of understanding classical reception - by offering assemblage-thinking as an alternative to the presumed passivity of classical influence. And the theatre, which has been (incorrectly) assumed to be principally a visual medium, is the ideal space in which to investigate new ways of seeing. Corinne Doria is a historian specializing in the social history of medicine. She is a lecturer at the Chinese University of Hong Kong in Shenzhen and teaches Disability Studies at Sciences-Po (Paris). Her work focuses on the history of ophthalmology and visual impairment in the West. Learn more about your ad choices. Visit megaphone.fm/adchoices Support our show by becoming a premium member! https://newbooksnetwork.supportingcast.fm/new-books-network
The New Discourses Podcast with James Lindsay, Episode 135 We all know that equity is a form of socialism now, almost. We're also entering a new phase of the societal debate about the topic, so it's worth clarifying the issue. As it turns out, we do embrace and want to embrace certain forms of "equity" programs as it is actually defined, but only under certain conditions. Those limits to equity are most comprehensible by the many approaches to disability discussed in both the sane and the Woke-insane literature that might broadly be classified as "disability studies" or the philosophy of the phenomenon of disability in society. In this episode of the New Discourses Podcast, host James Lindsay walks through four distinct models of interpreting disability and uses them to draw out the true limits to equity programs. Join him to learn how to discuss this topic with greater clarity and compassion so we can leave the Marxist versions behind forever. Get James Lindsay's book, The Marxification of Education: https://amzn.to/3RYZ0tY Support New Discourses: https://newdiscourses.com/support Follow New Discourses on other platforms: https://newdiscourses.com/subscribe Follow James Lindsay: https://linktr.ee/conceptualjames © 2024 New Discourses. All rights reserved. #NewDiscourses #JamesLindsay #Equity
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