According to her bio, she recently got the PhD, but has been in the field for 15 years --
https://theconversation.com/profiles/jennifer-sarrett-181531
From what I see in her bio and the article, she strikes me more as an "Autism parents advocate." IE - she's an NT, with an NT's perspective, who has an NT's idea of what is "really Autism." Her bio does put her as more on the neurodiversity side of things, though her comments about whether "higher functioning" Autistics are "really Autistic" or "Autistic enough" and whether the diagnosis is too broad in the article suggest to me that she sits somewhere more in the middle between us and the more typical A$ types of people who seem to think that if you can talk and you don't have a meltdown on a daily basis, then you're not "really" Autistic. She's at least not
that bad, but I'm still a bit wary of her commentary. And...like most NTs (especially those in medicine), it seems to me that she's still kind of ignoring what we're saying about how we perceive the world and how we would like to see these issues solved.
*shrug* That kind of thinking always strikes me as odd. Does someone with a broken leg still have a broken leg and need some amount of help regardless of whether it's a hairline fracture or a compound break? Why is Autism treated in such a way that if we were to apply it to a broken bone, then hairline fracture wouldn't "really" be broken, and the person would have to make do without so much as a splint, simply because it's not a compound break?