- Rationale for Treatment with LSD and UML
Our interest in these drugs was due in part to their psychotomimetic effect, hoping thereby that the autistic defenses of schizophrenic children might be broken down. Of equal interest, on a theoretical basis, is the serotonin inhibiting effect and of greater interest is their effect on the autonomic and central nervous system. Brodie has described the effects of LSD and other hallucinogenic agents as "arousal and increased responsiveness to sensory stimuli, preponderance of sympathetic activity and increased skeletal muscle tone and activity." Of particular interest is their tonic effect on the vascular bed especially of the brain, as has been shown with UML in vascular headaches. The known effects of these drugs on perception further increases¬ their interest in the treatment of schizophrenia.
Such drugs were of interest to us for the treatment of childhood schizophrenia since our definition of this condition is a disorder in maturation characterized by an embryonic primitive plasticity in all areas of integrative brain functioning from which behavior subsequently arises. This includes all autonomic functions, perception, emotion, intelligence. It was hoped that 'these drugs might prove some-what specific in modifying the basic process as well as the secondary symptoms. Autism is seen as a withdrawal or denial defense against disturbing sensations arising from disturbed autonomic function and perceptual function and anxiety in the young child with lagging and atypical maturation. It was hoped that this autism might be disrupted and that more normal autonomic functions in the vascular bed, brain, intestines, skin and other organs as well as in perception would permit more normal development.
- L. Bender, L. Cobrinik, G. Faretra, D.V. Siva Sankar, "The Treatment of Childhood Schizophrenia with LSD and UML", Biological Treatment of Mental Illness, Proceedings II of the International Conference of the Manfred Sakel Foundation, 10/31-11/3/1962, 1966; 2(4):463-91.
- Facial emotion perception is significantly affected in autism spectrum disorder, yet little is known about how individuals with autism spectrum disorder misinterpret facial expressions that result in their difficulty in accurately recognizing emotion in faces. This study examined facial emotion perception in 45 verbal adults with autism spectrum disorder and 30 age- and gender-matched volunteers without autism spectrum disorder to identify patterns of emotion misinterpretation during face processing that contribute to emotion recognition impairments in autism. Results revealed that difficulty distinguishing emotional from neutral facial expressions characterized much of the emotion perception impairments exhibited by participants with autism spectrum disorder. In particular, adults with autism spectrum disorder uniquely misinterpreted happy faces as neutral, and were significantly more likely than typical volunteers to attribute negative valence to nonemotional faces. The over-attribution of emotions to neutral faces was significantly related to greater communication and emotional intelligence impairments in individuals with autism spectrum disorder. These findings suggest a potential negative bias toward the interpretation of facial expressions and may have implications for interventions designed to remediate emotion perception in autism spectrum disorder.
- Shaun M Eack, Carla A Mazefsky, Nancy J Minshew, "Misinterpretation of facial expressions of emotion in verbal adults with autism spectrum disorder", The National Autistic Society, (February 17, 2014), Volume: 19 issue: 3, page(s): 308-315.
- Autistics are solitary people that need space from others in general. Public Housing does not provide this sort of housing as a general rule, and this has to change.
- Phil Gluyas, Inquiry into services for people with Autism Spectrum Disorder Final Report Family and Community Development Committee, Parliament of Victoria June 22, 2017
- If by some magic, autism had been eradicated from the face of the earth, then men would still be socializing in front of a wood fire at the entrance to a cave.
- Temple Grandin, Thinking in Pictures: My Life with Autism (2006).
- The effort to cure autism, [autism right advocates] say, is not like curing cancer, but like the efforts of a previous age to cure left-handedness.
- Thimerosal is a controversial mercury based (sic) vaccine preservative that research scientists and vaccine safety advocates have connected to the epidemic of brain disorders (Autism) in children.
- One of the things that I think affected me was in primary school when I got the diagnosis. In primary school I got bullied. The programs were all about how socially you have to be able to stand up for yourself or whatever. The implied thing with that, in my opinion, was that it was saying that if you do not behave in the right way, you are asking to be bullied... When I went out of primary school there was less bullying, because I was able to go to the library and I actually found other autistic people to hang out with, which was good. But there are still issues that arise from it, like anxiety.
- Ryan Kennedy, Inquiry into services for people with Autism Spectrum Disorder Final Report Family and Community Development Committee, Parliament of Victoria June 22, 2017
- The reason why the medical community doesn't support is because us moms aren't treating autism, we are treating a vaccine injury.
- It's [Autism has] prevented me from making a living or ever having a girlfriend. It's given me bad fine motor coordination problems where I can hardly write. I have an impaired ability to relate to people. I can't concentrate or get things done.
- But [not accomplishing] that does not stop me from wishing for a cure for future generations of children so they will not have to live like I have.
- Hopefully on my tombstone they will write, ‘We don't need no stinkin’ neurodiversity'.
- In America we've spent over a billion dollars on autism research. What have we got for that? We've not seen anything that's appreciably impacted the quality of life of autistic people, regardless of their place on the spectrum. Quite frankly, we've spent $1bn figuring out how to make mice autistic and we'll spend another $1bn figuring out how to make them not autistic. And that's not what the average person wakes up in the morning aspiring to. They think: am I going to be able to find a job, to communicate, to live independently, either on my own or with support? Those are the real priorities.
- Diversity in the workplace is way more than different races and religions disability affects people of different races and religious beliefs too. Employers need to realise this and think outside the box when considering employing people. Australia is one of the worst in the OECD for disability employment 21 out of 25 countries. We put more effort to being the best in sports in than [sic]looking after people with disability if only the effort put on that instead the benefits across the board would be massive.
- Meaghan O'Brien, Inquiry into services for people with Autism Spectrum Disorder Final Report Family and Community Development Committee, Parliament of Victoria June 22, 2017
- While autism is a developmental disorder, sometimes a devastating one, there is always within the autism a unique and sometimes strangely gifted individual. The great psychoanalyst Winicott used to feel that there was something like a tulip in every person and this was their essence and that this internal part of them was inaccessible to the person themselves and should not be meddled with or touched by psychoanalysis or anything else and one wonders if there is not some autistic essence like this tulip which needs to be respected and not meddled with.
- Oliver Sacks, "Rage For Order," episode of Oliver Sacks: The Mind Traveller
- When parents say,
- I wish my child did not have autism,
- what they're really saying is,
- I wish the autistic child I have did not exist, and I had a different (non-autistic) child instead. ...
- This is what we hear when you mourn over our existence. This is what we hear when you pray for a cure. This is what we know, when you tell us of your fondest hopes and dreams for us: that your greatest wish is that one day we will cease to be, and strangers you can love will move in behind our faces.
- You didn't lose a child to autism. You lost a child because the child you waited for never came into existence. That isn't the fault of the autistic child who does exist, and it shouldn't be our burden. We need and deserve families who can see us and value us for ourselves, not families whose vision of us is obscured by the ghosts of children who never lived. Grieve if you must, for your own lost dreams. But don't mourn for us. We are alive. We are real. And we're here waiting for you.
- I really hate any functioning labels whatsoever, because they do not represent individuals. High functioning just means without an intellectual disability. There is nothing more to it. If you want to talk about yourself or your child and your strengths and weaknesses, you focus on your strengths and weaknesses because that is going to tell the person more about you than the words ‘high’ or ‘low’ functioning. So I encourage every school and everybody I meet to not use that, because it does not give you any information. Does ‘high’ or ‘low’ tell you how to help the child or the adult? No, it does not.
- Stacey Smith, Inquiry into services for people with Autism Spectrum Disorder Final Report Family and Community Development Committee, Parliament of Victoria June 22, 2017
- Thirty years ago it seemed right that there be no stigma in education and that everyone should get the same start in life, but there are problems in mixing everyone together. I was never happy about the inclusion of children with severe autistic problems in schools, for example, and I certainly don't think it is working today.
- …realizing how my co-morbids are just damned hard for me and confusing to others has helped me chill out about their frustration…in real-time processing I had no idea other people were being so effected by my chaos. I do feel I unreasonably expected people to work from my ‘normality’ without having to explain it to them or help them adapt.