Quote by Chloé Hayden

“After receiving a diagnosis, the minimal resources that we may be linked to (if we're lucky) are for the benefit of parents, carers and those who are third-party viewers, rather than for neurodivergent people. We're given books that have been created by doctors and psychologists and neurologists who may have studied our brains for a number of years and can spit out information until the cows come home. But, assuming they are neurotypical, they have never and will never experience or understand what it feels like to have our minds. We're given clinical books and clinical videos, and are taught as soon as the new label is attached to us that it's a cold, medical, distant thing, like our brains are no longer ours. And, when we try to rid ourselves of these views and do our own research in an attempt to find things that feel closer to home and less analytical and impersonal, we are led to articles, sob stories, and posts that highlight the disappointment, fear and sorrow that surround all aspects of us, making us feel further invalidated, segregated and alienated.”

Quote by Chloé Hayden