I've got really upset by a thread started by a parent of a severely autistic child discussing their experiences. This is great, they deserve a place to discuss their struggles parenting a profoundly disabled child and I know my struggles are vastly different from somebody who is profoundly autistic.
What upsets me is the fact that so many want to describe my autism as mild. Of course my experiences are different, I live independently, have mostly successfully parented a NT child, I can talk, toilet myself etc.
This doesn't mean my life is not severely affected. Just because I was diagnosed in adulthood doesn't mean I have had a problem free life. Aspergers didn't exist as a diagnostic term when I was a child so of course it was missed. I was just labeled a weird, withdrawn kid so left to struggle, bullied all the way through school (including by the teachers sometimes) which has had lasting effects on my self esteem and self image.
What they don't see is the fact I started self harming aged 8, had my first suicide attempt aged 15, developed eating disorders aged 13 which led me to being hospitalised aged 17. I also made multiple suicide attempts around that age and self harmed frequently needing hospital treatment a lot of the time.
I'm still in the psychiatric system 25 years on, at the moment I have agoraphobic levels of anxiety and barely leave the house. I work a few hours online a week but most of my income is disability benefits, I'm frequently suicidal and wake up shaking with anxiety a lot of the time.
But, yeah, my autism is mild.