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The word "Crip" has traditionally or historically been understood as a derogatory term, but is now redefined and reclaimed by disabled people. Its modern terminology refers to the idea of the way(s) we experience disability together, despite the contrasts in our lived experiences. Some disabled folks may not necessarily agree if the term doesn't resonate with them. For others, especially disabled scholars and activists, we choose to use the verb. How has "Crip" shaped and redefined disability as a socio-political phenomenon? I am joined by Sean Lee (he/they), a disabled curator, artist and director of programming at Tangled Art + Disability. Sean and I explore this subject through conversations about disability arts as a site of political resistance. For instance, Sean articulates reimagining the future through crip horizons.

In the second episode of the book talk episode, I'm joined by Emily Ava Gillespie (they/she). Ava is a neurodivergent author who has published their latest book, Wait With Me, which follows a fictional character who challenges barriers in the healthcare system. The plot and supporting characters were based on her lived experience with mental health and the medical model of disability. Furthermore, Ava discusses the benefits and limitations of writing books with disability, privilege vs. oppression and the status quo. Her book is available to buy online http://www.amazon.ca/Wait-Me-Emily-Ava-Gillespie/dp/1069635103/ref=asc_df_1069635103?tag=bingshopdesk-20&linkCode=df0&hvadid=80195840416882&hvnetw=o&hvqmt=e&hvbmt=be&hvdev=c&hvlocint=&hvlocphy=5254&hvtargid=pla-4583795327954055&psc=1&msclkid=306634107a50145e8b3f5eca2181e3cf Sick Stories: Books, Zines, & Poetry | Sick Stories

Part 1 of the special two-part book author episode. I am joined by returning guest speaker Ghofran Alyass, a disabled writer and educator. Ghofran and I discuss her debut memoir, You Have 24 Hours to Live, by exploring emerging themes of perseverance, grievance, and her academic journey. Additional links below for more information about her work Welcome to my author website. This is a journey from staying alive to living the life I desireYou have 24 Hours to Live: A memoir: Alyass, Ghofran: 9781068916700: Books - Amazon.ca Fundraiser by Ghofran Alyass : Help me turn my memoir into an audiobook

The future looks brighter than ever for disabled youth in a program where you can just be yourself. Launched over a year ago, FUTURES is a leadership program for disabled youth who are passionate about making social change. The program offers a variety of programs for disabled youth. This includes a book club, social media internship, and a visual arts program. Prospective participants can choose to join an in-person or online cohort (Fall, winter, spring or summer). The question we'll be answering is: What are some ways FUTURES can help disabled youth become innovative leaders? For the Season 3 premiere, Kelly Johnston joins me in this exciting conversation. Kelly and I became close friends in the Fall 2025 cohort! We discussed our favourite moments from the program, such as the Map Mission and dance workshop activity. We discussed our journey in the program and offered advice to prospective participants. If you're disabled, D/deaf, hard-of-hearing, or neurodivergent and are passionate about building community, FUTURES is the right program for you. Additional information can be found on its website: Futures - The AccessStudioSeasons 1 and 2: The complete series is available to listen.

When non-disabled people hear the word "accessibility", they think about wheelchair ramps and automated doors with a push button. Let's consider accommodations in post-secondary education. Let's consider how we, as disabled people, have to pay extra money out of our pockets for psycho-educational assessments or medical equipment. We experience financial barriers in Ontario, and with the new school year, Doug Ford makes financial life harder for disabled students. In the season finale episode, Julie "Jules' Emeid and I discuss our lived experience with college and university accommodations. We discuss ways of making post-secondary life accessible and how to improve accessibility policies. This includes giving disabled students a seat at the table as consultants, compensating them for panel talks, and building relationships with professors. The complete episodes of seasons 1 and 2 are available to listen to on Spotify and Apple Podcasts. Season 3 will be premiering on October 2nd. Our Voices: Conversations of Disability is a podcast series. Distributed by Cafe Time Productions

Artist Talks is how we learn to explore and engage in conversations that involve politics and identity. Because Tangled Arts is Canada's first accessible gallery in downtown Toronto, the organization firmly believes in audience engagement. Disability arts challenges the traditional museum norms of visualizing art. This includes the tactile touch of an exhibit. It's important to emphasize that disability must be represented authentically. How have artist talks shaped nuanced perceptions of disability, D/deaf culture, and neurodiversity? In this episode, Sarah Sproule and I had a thorough conversation around our experience with artist talks and curating art exhibitions. Sarah introduces me to the intersections of disability and religion by explaining the ableist logic of the afterlife, arguing that a disabled body can be left behind. We both agreed that this belief is ableist. Disabled bodies and minds are, in fact, desirable. Furthermore, Sarah offered moral support for disabled artists by advising us to work on crip time; the ability to adapt our own pace and productivity level.

Bigotry, ableism, discrimination. This is the reality we experience every day across the world. These issues occur when we are left vulnerable to discriminatory policies and right-wing politicians. Despite living in dark times, disabled and neurodivergent people in the LGBTQA+ communities continue to resist in a unified voice. This includes advocating trans rights and gender-affirming care, gay rights, and centring disability justice in social movements. How do we interpret community care? Why is it important to speak up? What does it mean to fight for your rights? In this episode, I'm joined by Derek Newman-Stille (they/them), a faculty member from the Gender and Social Justice Department at Trent University. We had an intimate conversation about the social constructions of disability and queerness, analyzing anti-trans rhetoric, and being intentionally vulnerable about authentic identity. We also emphasized the significance of community care through active listening and storytelling.

When non-disabled people think about the terms "disability" or "disabled", they recognize it as a physical appearance. What happens when they meet someone whose disability is non-apparent? The answer: frequent stigmatization. For instance, accusing a chronically ill person of faking their disability or an autistic person being told they don't look autistic. In this episode, Kat and I chatted about her lived experience as a neurodivergent Vietnamese woman in her education and workplace. Secondly, we uncovered the many reasons why non-visibly disabled people face stigmatization, one-sided tropes and stereotypes by society. We also discussed the wonderful social group we made on Instagram called NeuroAmigos.

Disabled people have been categorized as the most unemployed group not only in Ontario, but also in Canada (statistically). Issues can range from fear of disclosing accommodations to the influence of employer and policy attitudes in the workplace. What happens when accommodations are not met? What are your rights and responsibilities as a disabled employee? Mary Neilans, founder of AIM for Inclusion, joins me in this episode. With many years of experience as an aging consultant, Mary works closely with employers to make workplaces accessible through AODA training and consultation. We both discuss the contrasts between accommodations (individual requests), accessibility, and inclusivity. We then discuss disclosing one's accommodation to an employer, acquiring access needs, common misconceptions, and the hiring process. Should you require a transcript version of the episode, feel free to reach out: [email protected]

How have disability art events amplified disabled, D/deaf, and neurodivergent people? In this episode, I'm joined by a kind friend of mine, Emily Maxwell (She/they). Emily is a disabled, queer, and neurodivergent artistic director for The Disability Collective - an organization that coordinates arts-based events made for and by disabled people. Sunday, Dec. 7th, was our fourth year of the Disability Holiday Festival at Wychwood Barns in Toronto. Emily and I chatted about the significance of putting community care over profit (supporting disabled artists and their work), humble beginnings and the development of TDC, experiences with financial barriers for disabled people, and the importance of emphasizing access needs. We also shared some of our favourite moments from the TDC events, the day we first met three years ago, and our shared lived experiences as disabled people. If you would like to learn more about this organization, you can find them on social media! They post detailed information about events they host. This includes access and venue guides, visual descriptions, and "save your spoons" guide videos. This is the last production episode for this year and will return in 2026! Thank you so much, everyone, for all your support this year. Should you request a transcript, please don't hesitate to reach out. Email me at: [email protected]

Why Mad Studies? How have mad studies periodically shaped nuanced perceptions of psychiatry and madness? In this episode, I am joined by Max Ferguson (he/they) as we dive into a thorough understanding of the conception of mad studies, how it exposes oppressive attitudes in psychiatric institutions, and its relationality to disability studies. Although some people may disagree with the term "Mad," well-known scholars such as Geoffrey Reaume, Rachel Gorman, Danielle Landry, and Jenna Reid use it as reclaimed language to rationalize lived experience with the mental health system. This further extends to grassroots movements (mad pride, consumer/survivor/ex-patient movement) that reject societal prejudices from medical professionals and policies that dictate diagnoses or treatment. Max introduces us to the term "sanism," which is a prejudiced belief that favours able-minded, healthy brains and frowns upon psychiatric minds. Lastly, we both discussed learning to set boundaries on consuming news media in Canada and from the United States. *Content warning: Max briefly discusses suicidal ideation from a book he read and a family experience. Because this brief piece of content is subjectively heavy, I am giving a head of caution for those who may feel sensitive to this subject* Book recommendations: Mad Matters: A Critical Reader in Canadian Mad Studies (2013). Brenda A. LeFrancois, Robert Menzies, and Geoffrey Reaume.

When couples enter a new phase of their relationship, parenthood becomes a new responsibility. Many of them are either caregivers to a disabled child or a disabled parent. However, this comes at a price when non-disabled caregivers and disabled parents confront benevolent and/or internalized ableism that would become detrimental. How can parents of a disabled child change the way people perceive disability and parenthood? In what ways can disability literature books and guest talks become valuable resources? In this episode, Adelle Purdham (she/her) and I had a thoughtful conversation about her new book titled I Don't Do Disability and Other Lies I Told Myself. Adelle is a faculty member and professor at Trent University, where she teaches non-fiction creative writing. Adelle's book comprises a series of essays based on her lived experience with ableism in her early life, and how she learned to change the way she perceives disability as an adult. We also elaborated on the idea of building acceptance in our "big, beautiful life", the ability to unlearn what we think we know about disability, and to relearn our understanding with new knowledge by disabled people. Last year, Adelle gave guest talks at several book launch events to discuss what it means to care for a child with Down Syndrome. Her book can be purchased at your local bookstores, including the Another Story Bookshop in Toronto. Fun fact about Adelle: she was one of two guest speakers in my Disability Issues course at Sheridan College back in 2017. Should you need to request a transcript version of the episode, please don't hesitate to contact me: [email protected] or [email protected]

How have social movements and leadership shaped fresh, nuanced perceptions of disability? How can we transform ourselves into innovative leaders in our community? Join Kristina McMullin and me as we engage in a critical yet insightful conversation about disabled people as leaders in the social justice movement. Kristina is a disabled activist who currently works as a facilitator for FUTURES. It's a program that invites disabled and neurodivergent youth to learn to become prospective leaders. Kristina and I discuss the importance of honouring the legacies of disabled leaders, learning to be self-aware about our own vulnerabilities, and identifying leadership traits that we already value. Kristina sprinkles her great words of wisdom in this exciting episode! To learn more about FUTURES, visit Access Now's website, which provides information about the program enrollment. Website link below Futures - The AccessStudio If you would like to request a transcript version of the episode, please send me an email, and I will get back to you: [email protected]

There are primary and secondary factors that lead disabled people on paths to homelessness: inflation, barriers to healthcare services, addiction, substance abuse, prejudiced attitudes and stigma, and flawed housing policies. In Ontario, we have many organizations and advocacy groups that address poverty and homelessness from a disability justice and a mad studies perspective. Homelessness can happen to anyone at any point in their life; children, adolescents, families, and senior citizens. In this episode, I am joined by Jenn Byford (She/her) as she discusses her lived experience of navigating through homelessness as a neurodivergent woman. Jenn and I discuss ways to resist stigma and negative attitudes towards homeless people, her religious beliefs, pursuing a Child and Youth program at George Brown College, and aspiring to advocate for justice and support. We also talked about how empty words from politicians can lead to false hope and the importance of following through with action. Lastly, we emphasized pivoting community connections with disabled people, allies, friends, family, and educators. Jenn is also affiliated with the Toronto Underhoused and Homeless Union. To learn more, it has a website of its mission, values, and how it empowers and connects with homeless people across Toronto. Toronto Underhoused and Homeless Union — RP Community MinistryThe link to the transcript cannot be reached here. If you like to receive the transcript version of each episode, please send me your request via email: [email protected]

Welcome everyone to season 2 of Our Voices: Conversations of Disability! For the season premiere episode, I am joined by Megan Suggitt, business owner of Beautiful Minds. Join us as we conceptualize neurodiversity through discussions of lived experiences, social and medical model rhetoric, contrasts between autism and non-verbal learning disability, and Indigenous knowledge. We've also discussed Megan's advocacy business that helps to empower neurodivergent youth to see their potential and strengths. Episode 1 transcript: file:///C:/Users/aletc/Downloads/Our%20Voices%20Season%202%20transcript.pdf Season 1: All episodes are available to stream and listen