Autism is treated differently than other developmental disabilities. It goes directly to why Autism Acceptance Month—a critical step up from Autism Awareness Month—is so valuable and important a distinction and change. Awareness historically has been more about something being wrong and a cry for help and donations. Awareness has been more about the “plight” of…
Autism and disability pride movements assert unique cultures and identities. Can intellectually disabled people be more openly and equitably represented in them—and also better develop intellectual disability as a unique, empowered movement all its own? When I tell my intellectually disabled and autistic 19-year-old son, Nicholas, that I love him, he often responds with…
I opened my talk at the 2019 HANd Autism & Neurodiversity Conference, themed as “My Autism Journey—Various Perspectives,” in this way, less for the little allegory itself, which is obvious and unremarkable, and more for my own realization with it, which comes near the end and then led into the substance of my talk. I also…
I told this story in my keynote address at the HANd Autism & Neurodiversity Conference in fall 2019 at Appalachian State University in North Carolina. Some of my son Nicholas’ hardest years were between when he experienced that early regression in his communication and connection through about third grade. His frustrations around expressive communication, his…
I was invited again this year to give a short talk as part of the Disability Day of Mourning vigil held in Western North Carolina on the campus of the University of North Carolina Asheville on March 1, 2019. The Disability Day of Mourning is an annual event to honor and remember disabled…
I think we widely recognize the silos of information and perspective we now live in, as a society and as individuals. Hopefully, even given the benefits it sometimes has of fostering identity and a certain kind of community, we also recognize and acknowledge the injury this siloing causes—the disconnection between communities and people, the lack…
Earlier this week I recorded a podcast with Melanie Vann for Springbrook’s Converge Autism Radio. It posted today. The podcast title is taken from my recent blog post, Autism Adulthood: Caring for the Future and the Present Moment, which the generous interviewer, Melanie, had just read when we had the conversation. However lovely that title…
Part of this piece was written for a recent conference panel talk—that actually instead turned into pure Q&A—so the beginning, at least, starts off pretty formally with background. Like all my work involving him, my son Nicholas has read and approved this article, because he hopes his journey—and ours together—will help others. My son, Nicholas,…
We’re in Charlotte waiting for my son Nicholas’ Remicade infusion right now. We both got up early this morning and Nicholas asked, “Are we going to Charlotte today, Poppa?” I said, “Yes, because I want you to be healthy. That’s the second most important thing I want for you. What do you think is the…
I have served on the organizing committee for Zipping for Autism for three years. The annual event raises money—now about $230,000 in seven years—for autism programs in North Carolina. It takes place in Asheville, N.C., on the first Sunday in June. My son, Nicholas, has been one of the top fundraisers each of the past two…
