Severe, chronic vertigo associated with migraines like mine is a “silent” disability, one people can’t see. Many people are compassionate. But others lack sensitivity, assume you’re faking it or just have a headache and will get over it.
We’re wrapping up Autism on the Page, and announcing our next exciting event—a week of posts focusing on representation of mental illness.
Here is a key insight to creating realistic autistic characters: We do not do the visibly autistic things we do because of “autism,” full stop. Like non-autistic people, we are responding to our experiences of the world. Those experiences simply differ from those of non-autistic people.
As much as I crave representation in fiction, it bothers me that some people seem to see autism as a way to create conflict or add a unique viewpoint to a narrative. It is even more disturbing when so many of these portrayals are inaccurate or incomplete.
An estimated 1 in 7 women suffer from chronic pelvic pain; it’s bizarre and disappointing that despite these statistics, there are distinctly zero characters with this condition.
Thanks for keeping up with us, and we hope you enjoy the series. One more day!
Here’s the thing no one tells you about people with a medical condition: The disease is always on their mind, but they don’t always want to think about it.
When I received my diagnosis of Asperger’s syndrome seven years ago, I thought of all the young people today who face the social challenges and bullying that I faced decades earlier. I wanted to create a character like me, but one who fights back against the way others treat her in a way that I never did.
It wasn’t until I was an adult that I could finally understand that from the time of my diagnosis, my education was not going to be “complete,” because I did not have the full access I needed. It was as if intensive speech therapy and itinerant teachers were more important than having a sign language interpreter in my classes.