(Personally, I’ve always wanted to be tested but the 12 month plus waiting list and the $5k not covered by insurance means that I’ll probably continue going through the rest of my life without any form of work accommodation…)
Not unusual for kids to be picked out in grade school and referred for further diagnosis. But yeah, I can definitely get not wanting to bother going out of pocket on something like that as an adult. Not unless there’s a pressing need.
True facts. Unlike things like Fragile X Syndrome that have clear sex-based biological mechanisms behind prevalence rate differences (see below for example), I think the gender discrepancies don’t actually exist for most Disabilities. Raise all kiddos without racialized and gendered societal expectations, and prevalence rates will mostly come out in the wash (this is a broad sweeping statement that completely lacks nuance, but work with me).
(Example: people with 1 X chromosome present Fragile X Syndrome more frequently because there is only 1 X chromosome to carry the genetic load of the X chromosome, typically people with 2+ X Chromosomes present less (unless multiple copies carry it) because the non-affected X chromosomes can pick up the slack).
Certainly moreso than a generation ago.
Not unusual for kids to be picked out in grade school and referred for further diagnosis. But yeah, I can definitely get not wanting to bother going out of pocket on something like that as an adult. Not unless there’s a pressing need.
Primarily children of one gender presentation, to this day. Which again, makes me very curious as to the validity of the “autism” construct.
True facts. Unlike things like Fragile X Syndrome that have clear sex-based biological mechanisms behind prevalence rate differences (see below for example), I think the gender discrepancies don’t actually exist for most Disabilities. Raise all kiddos without racialized and gendered societal expectations, and prevalence rates will mostly come out in the wash (this is a broad sweeping statement that completely lacks nuance, but work with me).
(Example: people with 1 X chromosome present Fragile X Syndrome more frequently because there is only 1 X chromosome to carry the genetic load of the X chromosome, typically people with 2+ X Chromosomes present less (unless multiple copies carry it) because the non-affected X chromosomes can pick up the slack).