With the increase in realisation that many women with autism often receive late diagnosis (often after several misdiagnoses) it seems odd to see the result.ing effects which I worry are repeating the mistakes of the past.
We are reiterating the importance of gender as the determining factor of how the condition manifests.
My lived experience says otherwise. - indeed by ascribing "autistic gender norms" in reverse you can pretty much summarise my journey to diagnosis.
I would argue that there is a different way of interpreting the information that makes more sense to me based on my lived experience and the disparate expressions of gender (in fluidity, rejections of ascribed roles etc) within the community.
What is termed Female ASD categorised by Masking, observational assessment leading to trial and error (fake it till you make it approach) is more about extrovert personalities seeking to fit in and adapting seeking to pre-empt and avoid problems leading to internalising challenges where as the signs traditionally observed which led to the current gender imbalance are active external reactions to present internal challenges.
Active external reaction/Meltdown vs Inactive external Reaction/Shutdown if we continue to gender the two main presentation types we only see two out of four quadrants of the xy graph.
NT Societal understanding of gender roles and associated traits led us to where we are - by thinking about male and female autism we will continue to have late or no diagnoses for those like me who whilst male have the lived experience of "Female" ASD.
Is there any research being done on this?
Hope that makes sense and interested to hear thoughts.