In the NHS clinic where I work, adults who suspect they may have Asperger syndrome wait almost a year for a diagnosis. The clinic takes referrals from all over Cambridgeshire and Peterborough (a population of 860,000), but we have to see all of them in the hours of a single full-time doctor. And the clinic is not given funds to run a follow-up support service once someone has been diagnosed. These individuals struggle to socialise, are neurologically different, and are overlooked because their disability is invisible. Many have experienced bullying in childhood, underemployment in adulthood and exploitation because of their social naivety. Many are made to feel inferior despite their often considerable talents. No surprise that many develop depression. Our study in the Lancet Psychiatry showed that two thirds of the patients in our clinic had felt suicidal, and a third had attempted suicide. Parliament passed an Autism Act back in 2009 to legislate for more services but, despite much talk, no new funding means precious little has changed.
Simon Baron-Cohen
Diary – 16 March 2017
Also in Simon Baron-Cohen’s diary: the ghosts of Berlin, a hopeful research project, and thoughts on a prize contender
issue 18 March 2017
Comments
Join the debate for just $5 for 3 months
Be part of the conversation with other Spectator readers by getting your first three months for $5.
UNLOCK ACCESS Just $5 for 3 monthsAlready a subscriber? Log in