Disclaimer: For those of you who are used to my edublogging, this is a brief respite. Every so often, I need to blog about myself as a person, without my “teacher hat” on. If you don’t care to continue, I won’t begrudge you that.
Ever since my elder son’s diagnosis in November of last year – almost a year now, which is unfathomable to me – the subject of autism has been on my mind frequently. Okay, it’s probably been on my mind longer than that, since the diagnosis was no real surprise to us: all the stereotypies were there, as well as the developmental delays. I had done a fair amount of research on autism and its symptoms, having done a presentation on the subject in college for my special education course, and the speech therapist working with him had talked to us about it, since she had worked with several children on the spectrum. Since the diagnosis, I have tried to stay apprised of happenings in the autism community, most specifically the crazy antivaccinationists that use autism as a vehicle for their crazy conspiracies about “Big Pharma” and the evils of vaccines (like those dreaded “toxins”). In my time on the Internet, I’ve run into more than a few people who have made wild claims, and I keep up with them so that I can be prepared to counter them when I encounter them, just like I do my research on crazy ideas like FEMA death camps. (That’s not a joke, either; I had a student seriously ask me about these, his only evidence proffered being a YouTube video.)
But autism for me is a bigger issue than nutjobs like this. It is something that I live with daily, and not just in my son.
