I mean damn, my entire twitter account and blog weren't things that I actively wanted to do.
I was already writing stuff just to be able to process being autistic and navigating my life.
I saw how it helped others so I kept doing it..
and now it feels like I have an obligation to the community.
Don't get me wrong, I don't hate it.
But I don't really have the opportunity to think "hm this might reduce my future career opportunities so I guess I shouldn't speak up when researchers are calling me a disease.."
It's such a f*cking privilege to not have to care. That's true for any marginalized identity (I have tons of privilege in other identities).
I guess I see non-autistic people trying and all,
but non-autistic researchers will never understand just how horrific this is to us.
It will never be as important as it is to us. I used to think science was this amazing thing and I still do sometimes,
but I've learned that it's certainly not objective & can certainly be used for harm (just read Ann Memmott's research twitter threads..).
It's so disheartening.
Every autistic person I know who has been helping with #StopSpectrum10K is constantly apologizing for being burnt out, for extraneous circumstances, for not being able to do so much. We're all apologizing to each other.
Where are the non-autistic people in this?
Where are you?
If you're out there and you want to help, consider sharing, reading, and signing this -
And thank you to any and every autistic person who has been helping with #StopSpectrum10K
There have been so many autistic people reaching out & helping. Thank you.
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I would like to find the genes for neurotypicalism so they can get better supports early in life.
Finding out this information will help neurotypical well-being and quality of life, and help with co-occurring conditions.
Please ask your neurotypical children to spit in a tube.
We have 3 neurotypical ambassadors, 4 neurotypical people on our annual advisory panel, and we're willing to consult with neurotypical people and their families after starting to recruit.
We can't disclose researcher's diagnoses so we can't answer about the researchers.
We are not looking for a cure for neurotypicalism but this research may in the future lead to a genetic test for neurotypicalism.
CAN ANY SINGLE NON-AUTISTIC PERSON READ THIS PAPER AND GIVE A GODDAMN SUMMARY OF IT SO THAT AUTISTIC PEOPLE CAN UNDERSTAND THIS AND I DON'T HAVE TO DO EXTRA RESEARCH + BE ANXIOUS ABOUT MY PHD WORK ON THE WEEKEND?