The information I have seen suggests that there may well a diagnostic ascertainment factor but that may reduce the ratio from 4 to 2 in favour of boys. Why would autism be massively under diagnosed in women and not in ME/CFS? We might just about claim that autism had a ratio nearer 1 but that is still in contrast to a 3:1 for women to men for ME/CFS.
Maybe the same underlying molecular abnomality tends to manifest differently depending on the gender (and age of onset) and some additional factors.
Frustrating that the research just isn't happening.
I don’t think this is necessarily a problem as I suspect it’s a bit of a “double whammy” situation for autistic women. You’d just be checking if ME is more common in autistic over neurotypical women, and more common in women than men with autism.The information I have seen suggests that there may well a diagnostic ascertainment factor but that may reduce the ratio from 4 to 2 in favour of boys. Why would autism be massively under diagnosed in women and not in ME/CFS? We might just about claim that autism had a ratio nearer 1 but that is still in contrast to a 3:1 for women to men for ME/CFS.
According to the Autism SubReddits, it's because women mask (Disguise their Autistic traits) more.Why would autism be massively under diagnosed in women and not in ME/CFS?
Yes, women face much steeper social consequences for not behaving as expected especially at a young age. I witnessed it first hand when I was a tutor.According to the Autism SubReddits, it's because women mask (Disguise their Autistic traits) more.
in the diagram showing putative overlap between ME/CFS and autism almost everything in the overlap zone looks dubious and a good part of it spurious.
Young girls who don’t behave correctly get all the same, plus they get subjected to what I can only describe as a constant collective psychological conditioning process. It feels like everyone in their life turns on them and constantly tries to modify all their behaviors through shame until they learn to just pretend that everything’s fine.
But the text may contain more of interest. I need to have a detailed look.
Yes, not to say that "constant conditioning" is absent in how autistic men are treated--just that there is a specific pattern stemming from societal misogyny that seems to result in the observed pattern of autistic women being more likely to evade diagnosis (or even recognize that their own experiences fit with autism).With respect, and not to minimise your experience at all, but I had very similar experiences of constant conditioning to perform 'masculinity' I was growing up (autistic man diagnosed late in life) with devastating consequences in terms of my mental health.
Yes, not to say that "constant conditioning" is absent in how autistic men are treated--just that there is a specific pattern stemming from societal misogyny that seems to result in the observed pattern of autistic women being more likely to evade diagnosis (or even recognize that their own experiences fit with autism).
The conditioning that I'm referring to is definitely tied into pressures to perform femininity as well (and specifically the dynamics in social interactions that entails). But it also has aspects of social enforcement that are unique simply because it's being enforced on girls.
It's an experience that exists at the intersection of what autistic men also experience by virtue of being autistic, and what women experience by virtue of being women, which gives rise to dynamics of interpersonal violence (physical, mental, and social) that may not necessarily be experienced by autistic men and allistic women respectively [edit: in that particular way].
Same thing happened to me. I was stuck un a noisy house between 2001 and 2013, the sleep deprivation got gradually worse and as my Deteriorative Sensory Overload got worse, I kept getting disturbed during my sleep more and more. My doctor refused to write a letter to the local housing association stating that the house I was living in was destroying my health. I didn't manage to find a new house until it was too late and now my sensory issues are permanently worse, I'm bed bound and have been peeing in to bottles since 2013. This is what I mean when I say the treatment for ME is considerationI experienced something like an extreme autistic burnout when I was 18/19 and had bad insomnia, dpdr and mental health issues ever since.
Same, I was misdiagnosed with CFS when really my fatigue, brain fog, and sensory issues were Autistic Burnout.Unfortunately I was diagnosed shortly after getting ME and confused my ME symptoms with sensory sensitivities and burnout for quite a while.