#N95s4UCSF: Call to Action
#N95s4UCSF: Call to Action I’m alive, bitches! My recent column in Teen Vogue about the surge and its impact on me as a high risk disabled person became … Continue Reading #N95s4UCSF: Call to Action
"Creating, sharing, and amplifying disability media and culture"
#N95s4UCSF: Call to Action I’m alive, bitches! My recent column in Teen Vogue about the surge and its impact on me as a high risk disabled person became … Continue Reading #N95s4UCSF: Call to Action
My ICU Summer: A Photo Essay Alice Wong Content notes: medical trauma, hospitalization, blood, systemic ableism, death, anxiety This is a semi-accurate account of what happened to … Continue Reading My ICU Summer: A Photo Essay
Two years into the pandemic, I’m not sure if I can trust nondisabled people anymore: It feels like I am seeing a guy stick his head into an alligator’s mouth … Continue Reading Two years into the pandemic, I’m not sure if I can trust nondisabled people anymore
How CBT Harmed Me: The Interview That the New York Times Erased Alana Saltz In August, I was contacted by a reporter writing an article for the New York … Continue Reading How CBT Harmed Me: The Interview That the New York Times Erased
Below is an open letter from a number of disabled people in the US impacted by a recall of 13 ventilators, CPAPs and BiPaps manufactured by Philips Respironics including signatures … Continue Reading Letter from Disabled Ventilator Users on Philips Respironics Recall
https://media.blubrry.com/disability_visibility/content.blubrry.com/disability_visibility/FINAL_Ep_81.mp3Podcast: Play in new window | Download | EmbedSubscribe: Apple Podcasts | Email | RSS We’re right in the middle of the summer and the coronavirus pandemic in the United … Continue Reading Ep 81: Bioethics
The following is a short adapted excerpt from Chapter 24 in a new memoir by Nadina LaSpina, Such a Pretty Girl: A Story of Struggle, Empowerment, and Disability Pride. Chapter … Continue Reading Book excerpt from Nadina LaSpina’s memoir “Such a Pretty Girl”
Hey there! I’m super excited to announce that I’ll be a monthly columnist for Healthline.com. Got a question about being disabled or specific issues such as healthcare advocacy, personal assistance … Continue Reading Disability Visibility: A Healthline.com Column
Indigenous Lives and Disability Justice Jen Deerinwater Content notes: genocide, colonization, suicide, death, medical neglect, discrimination, racism, settler colonialism, rape, sexual assault, murder, eugenics, forced sterilization, trauma, intergenerational trauma, historical … Continue Reading Indigenous Lives and Disability Justice
https://media.blubrry.com/disability_visibility/content.blubrry.com/disability_visibility/45_Ep_45_v2.mp3Podcast: Play in new window | Download | EmbedSubscribe: Apple Podcasts | Email | RSSToday’s episode is about mental health and people of color. My guest today is Dior Vargas, … Continue Reading Ep 45: Mental Health and People of Color
I am a lover all all types of media, including graphic novels and comic books. Here’s an interview with Nadia Shammas about her current project, CORPUS: A Comic Anthology of Bodily … Continue Reading CORPUS Comics Anthology: Interview with Nadia Shammas
The Disability Visibility Project® is thrilled to offer new swag recognizing the activism taking place right now as disabled people fight for everyone’s right to healthcare, especially Medicaid: OUR EXISTENCE IS RESISTANCE. … Continue Reading Our Existence Is Resistance: Summer fundraiser for @NationalADAPT
Disability and the Dilemma of Accessing Quality Women’s Healthcare: A Cautionary Tale By H. Lee I am a woman with muscular dystrophy in her late 30s who uses a power … Continue Reading Guest blog post: Disability and the Dilemma of Accessing Quality Women’s Healthcare
This is the second of a two-part interview with Emily Wolinsky and Laura Halvorson about Dear Julianna: Letters to Children from Adults with Neuromuscular Disabilities (NMD). They talk at length about their experiences … Continue Reading Dear Julianna: Interview with Emily Wolinsky and Laura Halvorson, Part 2
This is the first of two parts of an interview with Emily Wolinsky and Laura Halvorson about Dear Julianna: Letters to Children from Adults with Neuromuscular Disabilities (NMD). Read part two of … Continue Reading Dear Julianna: Interview with Emily Wolinsky and Laura Halvorson, Part One