Do people with autism diagnosed early in life get treated worse today ?
I find using disability services very complicated slow and they can feel like they lack direction.
People might be very caring within these services but it’s patchy I don’t know if I finally trust them however I’ve seen people diagnosed later in life having less problems than myself.
(Maybe this isn’t always the case)
Certain people are so kind and helpful others keep asking for information in which I either don’t have or mightn’t be comfortable sharing yet.
I’m happy to give information about my diagnosis however I feel this can lead to more and more questions.
So far I’ve been told these is a service however I will be on a waiting list I believe this to be honest information at the moment however I don’t have tons for money for psychologist etc to re-enter my situation today as I already know the answer.
I feel when people find out I was early in life they don’t want to know me this might not be true but I get this impression anyway.