An Autistic Patient Uprising Is Happening Now
How one autistic mother’s pursuit of truth is part of a broader shift toward patient-led accountability, ethics, and reform.
How one autistic mother’s pursuit of truth is part of a broader shift toward patient-led accountability, ethics, and reform.
Ember Green debunks “profound autism” and anti-neurodiversity, with its cherry-picked numbers and fear-mongering, as “This is about the future of autism care, the way we view our disabled community members, and importantly, who gets to speak.”
When parents of newly identified autistic kids ask me what they should know, the first thing I say is: “We get tired.” This is so important. We need rest, more frequently and in greater durations than non-autistic people.
That so much of the sex ed made for Autistic people emphasizes compliance with neurotypical expectations—as opposed to advocating for their own boundaries and needs—feels particularly painful in light of my experiences as a survivor.
If your child has recently been diagnosed with autism, as my son was in 2003, here’s what I want you to know: Learn from me, don’t be me.
T.C. Waisman, Monique Botha, and Wenn Lawson—three deeply compassionate autistic experts—talk about their experiences with, and insights for, navigating this planet and our societies.
Diane J. Wright is the founder of Autastic.com—a resource and community hub for thousands of autistic adults, including spaces specifically for autistic people of color. She talked with us about her advocacy, including shaping the stories of autistic PoC as told in popular media.
Many autistic people rely on multimodal communication for accessibility. Kaishawna Fleming discusses why showcasing different forms of communication is so important for disability representation.
People who tell you that colonoscopies are hard may not know how tough you are. Many autistic people have significant physical disabilities or diseases, and we are used to life being hard.
I would like a term to describe myself, as just one person among many many autistics, but the problem is ableds hear, “low support needs” and think, “OK then it’s fine to round down to zero.”