Nobody wanted long COVID on our collective pandemic Bingo card, but there it is. In her “The Daily Show” interview, OG disability rights badass Judy Heumann told Trevor Noah that the likelihood of his acquiring a disability, temporary or permanent, was statistically high. He took her statement as a threat in jest, but there’s truth in that for us.
It’s flying graduation caps season! We’re not post-pandemic, but graduates are embarking on a world stage that looks different from what it was two or three years ago. Some of those differences are alarming.
Bring out your flower bouquets and your brunch reservations! This Sunday is Mother’s Day, and we’re bringing the books to take you into the weekend and beyond. These books show how every kind of mother needs to be valued and supported in the catch-all societal stew we call the US. Mothers of color. Immigrant mothers. Mothers who become parents at a young age. Mothers separated from their families because of incarceration. Mothers challenging the medical establishment about misconceived notions of disability.
A Q&A with Terry Galloway | It’s a Hallmark film of a movie and, as such, has every Deaf cliché you can think of, including how hot Deaf people are in bed—although I’m inclined to perpetuate that myth. “CODA,” written by a hearing person and adapted by another hearing person, made the Deaf family the nominal villains: backwards, unthinking, unfeeling, selfish bumpkins. Until, of course, their hearing, singing savior of a child makes them see the error of their dumb ole Deaf ways.
By Lennard Davis | Like many Children of Deaf Adults [CODAs], I was heartened to see that the film “CODA” had won Best Picture at the Academy Awards. It is very exciting that Troy Kotsur, who plays the Deaf father of the hearing child in the film, was the first Deaf male actor won for Best Supporting Male Performance. It is also encouraging to see a movie in which all the roles of the Deaf characters were actually played by Deaf actors. Hurray! All a major step forward in the fight against audism. But as a CODA, I should step back from the cheering crowds of appreciative hearing and Deaf fans to express some serious regrets.
We did it! We made it to the finish line of another plague year! Just a few more weeks left. Even though it’s not New Year’s Eve yet, uncork some bubbly to celebrate. We earned it. Our big wish for the new year: no more COVID variants. Delta, Mu, Omicron . . . Worst. Upgrades. Ever. Before we slam the door on 2021, we need to applaud and thank our authors and staff for the blog posts they wrote for the Broadside.
By Ben Mattlin | On July 25, 2021, a day before the thirty-first anniversary of the Americans With Disabilities Act (ADA), the New York Times Magazine published a story about the proliferation of ADA litigation. “The Price of Access” was the headline of the print edition; the online version, which had appeared a few days earlier, was titled “The Man Who Filed More Than 180 Disability Lawsuits.”
By Marga Vicedo | A two-and-a-half year old girl sits on the floor. Her mother lays besides her, making random marks with a brush and paint on a piece of paper. She is hoping her little girl, Jessy, will imitate her. Unlike most children her age, Jessica has shown little interest in imitating her siblings or her parents. She seems content playing alone, placing some set of objects carefully in rows. Jessica did not start to use the brush and paint herself that day with her mom; but, remarkably, she did so three days later, on her own. From then on, her mother made sure Jessy always had paper, crayons, and paints. These tools would open up a new world of experiences and interests for Jessica.
By Marga Vicedo | “You are being emotional,” someone may tell you during a conversation. It is not a compliment. It usually means you are being irrational or at least unreasonable. The underlying assumption is that you are not thinking clearly because you are letting your emotions interfere with your reasoning. This belief is not only prevalent in daily interactions. The separation between cognition and affects has a long history in philosophical and scientific approaches in the Western world. The emotional and cognitive realms are often seen as separate, if not opposed to each other.
A Q&A with Emily Paige Ballou | I think I actually benefited more from being diagnosed as an adult than I would have as a child. It came as a huge vindication and a relief, to have confirmation that I wasn’t just imagining all the ways I was different. Things really were harder for me. I wasn’t making it up. I wasn’t being spoiled or dramatic, and I wasn’t just broken.
A Q&A with Sharon daVanport | AWN finds our history deeply rooted in the need to find community and shared-lived experiences. At the time AWN entered the autism community, the narrative centered mostly around young white boys and men. In those early days, we discovered quickly that AWN was an initiative that was desperately needed.
A Q&A with Morénike Giwa Onaiwu | It’s interesting, because it kind of makes me think about certain medications. Some do not have any adverse reaction when taken together. Neither is there a positive reaction. They just coexist simultaneously but aren’t necessarily interrelated in any meaningful way. Another medication might help enhance the efficacy of another—maybe by increasing its metabolism rate or boosting its effect in some other way so they interact in a helpful way.
By Emily Paige Ballou | My guess is that if you have a child or family member on the autism spectrum or have been involved with the special education system or disability services as a professional, you have most likely been taught, at some point, that the correct way of referring to people with disabilities is to use “person-first language,” or to “put the person first.”
By Gustavus Stadler | I knew that when my book came out, I would inevitably be asked questions like, “What would Woody Guthrie do today? Where would he stand on this issue? What would he think of this candidate or that elected official?” I’m mostly accustomed to writing about topics at least several decades distant from the present, and I try hard to honor the otherness of the past, rather than portray it as a simpler version of the now. Plus, responses to such questions so often depend more on the projections of the answerer than on historical evidence.
A little over half a century ago, zero federal laws made it illegal to discriminate against disabled people. Today’s accessibility accommodations in buildings and services were nonexistent. We have disability rights activist and supreme badass Judy Heumann to thank for sparking a national movement for the protection of disabled peoples’ rights that led to the creation of the Americans with Disabilities Act. And it benefits everyone.
This year, the Americans with Disabilities Act has a thirtieth candle to blow out on its birthday cake. The ADA is the widest-ranging and most comprehensive piece of civil rights legislation ever passed in the United States, and it has become the model for disability-based laws around the world. We reached out to some of our authors to reflect on the impact of this landmark in disability history and on the ongoing fight for disability rights. We share their statements with you below.
We’re going two for two—our second author to appear this year on The Daily Show! On March 4, Trevor Noah interviewed disability rights activist Judith Heumann on The Daily Show in honor of Women’s History Month. And we’re squeeing again like the book groupies we are! “Reading this book, I expected to be impressed by it, but I wasn’t quite expecting how much of a badass you would be,” Noah told Heumann. And he’s right: she’s a total badass!
By Kristen Joiner | Judy Heumann isn’t nice. Let me be clear. Judy Heumann, one of the most transformative disability rights leaders of our time, is very friendly. Just take a walk around her Washington, DC, block. You’ll see that she’s on a first-name basis with everyone, from the doorman to the bus driver. But she is not nice. For the past three years, I’ve had the privilege of waking up and imagining myself into Judy Heumann’s shoes.
By Chris Gabbard | August’s blithe pterodactyl shrieks mingled with the sounds I heard when dropping him off at the Mt. Herman Exceptional Student Center. each morning, I would drive six miles northwest on I-95, crossing the fuller-Warren bridge spanning the St. Johns river and skirting the western edge of downtown. Just off eighth Street, it sat on the opposite side of I-95 from UF Health Shands Hospital. once parked, I would wheel him in the front door and sign him in with Miss Beverly, the front-desk secretary. It was a short walk from there to his classroom.
By Ben Mattlin | In early March, an angry, dysfunctional couple spewed their venom on the Dr. Phil show. That’s not unusual. What was, however, was that the young man—Bailey—was quadriplegic and the young woman—Harley—was not. She was the principal provider of his personal care.“You can be his caregiver or you can be his lover. You can’t be both,” declared the host, whose full name is Phillip Calvin McGraw and who holds a PhD in clinical psychology from the University of North Texas but is not actually a medical doctor. “This won’t work,” he concluded. “One hundred out of one hundred times, this won’t work.”