I want to start out by saying that I’m not trying to lay blame on anyone, especially my parents, with these posts. The purpose of this blog is twofold: 1. to explore my newly diagnosed autism, and 2. to help neurotypical parents of autistic children understand how some people experience autism. I say “some” because autism is a spectrum and, thus, differs from person to person. The only way I know how to do either of those things is to look back at my own experiences and how I interpret them now. I grew up in the 1970s and ’80s, when autism was not as well known as it is now. I’m not sure my parents had even heard the term autism, so forget about sensory processing disorder. Even if my parents had known I was autistic, they wouldn’t have known what to do about it or had access to therapies to help. And there was no internet to turn to. They were good parents who did their best. Love you, Mom.
That said, I want to continue the food discussion from the last post. Specifically, I want to address the fact that most of the effects of sensory issues are invisible to the person not experiencing them beyond the protestations of the person having the experiences. And fear. I think fear plays a big part in it, but I’ll get to that later. Even if the effect is visible, the cause and effect relationship isn’t always easy to make.