Neurominority
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The Feeble Minded
The term "feeble-minded" was commonly used in the United States and Europe in the late 19th and early 20th centuries to describe individuals who were perceived to have intellectual disabilities, developmental disabilities, or mental illnesses. The term was intended to be a catch-all phrase for a variety of conditions that were poorly understood at the time, and was often used to refer to people who were deemed socially or morally "undesirable".
The use of the term "feeble-minded" was deeply stigmatizing and contributed to the marginalization and oppression of disabled people. The term was often used to justify forced institutionalization, sterilization, and other forms of eugenic control over disabled people, as well as to deny them basic human rights such as education, employment, and the right to marry.
In the United States, the term "feeble-minded" was used in the landmark 1927 Supreme Court case Buck v. Bell, in which the Court upheld the constitutionality of forced sterilization of individuals deemed "feeble-minded" and "unfit" to reproduce. The decision gave legal justification for the widespread practice of eugenics, which resulted in the forced sterilization of tens of thousands of people in the US and Europe.
The consequences of the use of the term "feeble-minded" were devastating for disabled people and their families. Many were subjected to forced institutionalization, where they suffered from abuse, neglect, and social isolation. Others were sterilized against their will, which had lasting effects on their physical and mental health, as well as their ability to have children.
The term "feeble-minded" fell out of use in the early to mid-twentieth century as medical and psychological professionals began to adopt more standardized and scientific classifications for intellectual disabilities. However, the use of the term persisted in some legal and bureaucratic contexts until the 1970s, when the Rehabilitation Act of 1973 mandated the removal of discriminatory language from federal laws and policies related to individuals with disabilities. Today, the use of terms like "feeble-minded" is generally considered outdated and offensive.
The use of the term "feeble-minded" was deeply stigmatizing and contributed to the marginalization and oppression of disabled people. The term was often used to justify forced institutionalization, sterilization, and other forms of eugenic control over disabled people, as well as to deny them basic human rights such as education, employment, and the right to marry.
In the United States, the term "feeble-minded" was used in the landmark 1927 Supreme Court case Buck v. Bell, in which the Court upheld the constitutionality of forced sterilization of individuals deemed "feeble-minded" and "unfit" to reproduce. The decision gave legal justification for the widespread practice of eugenics, which resulted in the forced sterilization of tens of thousands of people in the US and Europe.
The consequences of the use of the term "feeble-minded" were devastating for disabled people and their families. Many were subjected to forced institutionalization, where they suffered from abuse, neglect, and social isolation. Others were sterilized against their will, which had lasting effects on their physical and mental health, as well as their ability to have children.
The term "feeble-minded" fell out of use in the early to mid-twentieth century as medical and psychological professionals began to adopt more standardized and scientific classifications for intellectual disabilities. However, the use of the term persisted in some legal and bureaucratic contexts until the 1970s, when the Rehabilitation Act of 1973 mandated the removal of discriminatory language from federal laws and policies related to individuals with disabilities. Today, the use of terms like "feeble-minded" is generally considered outdated and offensive.
Vagaries of English Phraseology: Journey of An Autistic through GrammarLand
https://www.dailycal.org/2019/04/07/vagaries-of-english-phraseology-a-personal-essay/
Vagaries of English Phraseology: Journey of An Autistic through GrammarLand
My introduction to the world of academics was rather late, since I learned to communicate via typing for the first time in my life only after I was a teenager. I was stuck in a silent, non-communicative world of autism until then.
My first attempts at typing were, at best, fragments. The focus was communication for this nonspeaking boy with autism. I’d never had conversations with the outside world before. I was as excited as a toddler just learning to speak. No one, least of all me, cared for the things called “punctuation,” “grammar” or “semantics.”
There would be odd spaces, words that ran together, an occasional comma or period, sentence fragments and all. Bursts of thought came gushing out and it was important to get the key words out rather than worry about a well-structured sentence. My impulsive and hyperactive body did not make for smooth typing either. My finger would accidentally hit the caps lock key and a few uppERcase letters would appear in the middle of the word as I slowly typed.
No one, least of all me, cared for the things called
“punctuation,” “grammar” or “semantics.”
But communication was opening up my world, so I didn’t quite care. And when I started typing short pieces and poems, it was all in lowercase.
You see, using uppercase involved the use of two fingers: one on the shift key and the other on the letter key. But I was a one finger typer — a lone index finger on my right hand roamed the QWERTY keyboard, searching for and hopping slowly from letter to letter.
I soared in the power the written words afforded me. My written word substituted the spoken word. People never said pause or comma when they spoke so I figured I need not worry.
With the ability to communicate came the expressed longing for education. When the transition from special education took place, I leapt into eighth grade mainstream academics with anticipation and glee — straight into the arms of Shakespeare, algebra and biology.
An unexpected side of pedantics then reared its head — there was demand for these things called “grammar” and “punctuation.” Grammar was hardly the thing to teach in my former special education world. In special education, I was thought capable of only learning C-A-T spells cat and D-O-G spells dog, and single digit addition like 8+2 = 10.
My mind wrapped around a whole host of new terminology that was part of mainstream academics. Bits of sentences linked to grammar terms, however, simply had no relevance for me.
Grrr! Gerunds were strangers that growled at me.
Modifiers dangled for some reason.
Mood was an imagined subjunctive
instead of happy every season.
Why were the verbs tensed?
I told them, don’t stress, just meditate.
“Is language not something to enjoy, rather than to be dissected like a frog?” I moaned. Did we have to reduce a sentence to a string of grammar terms?
Bursts of thoughts flow from the brain
Authority insists, must confine to rules
Macrocosm bound by microcosm chain
Drown in grammar phraseology
Lost in punctuation terminology
Essays needed punctuation and spell check; it was mandatory. I needed to bring my other index finger into play to hold down that shift key. Even punctuation like the lowercase comma had their issues.
Sometimes the Oxford comma was needed by the teacher and at other times, it was a no-show. I wondered if the poor comma made the journey from Oxford, England to the Bay Area each time it was needed.
Word processor spell checks somewhat came to my rescue. I enjoyed the composition, literature and vocabulary parts of English.
but grammar terminology —
— definitely, not in my list of graces.
In a strange new world I was navigating.
It was in an American literature class that I first met e e cummings. The first poem I read by him was “in Just-.”
His poetry confounded me. A first glance, I sat up and wondered, “IS THIS WRITTEN BY A BOY WITH AUTISM — with poor fine motor ability like me? He uncapitalized, words ran together, there were white spaces and a general lack of punctuation. I was baffled and nonplussed, absolutely fascinated. I gaped and stared at the poem on the page.
What was going on and who was this person?
How did such a poem by a person with fine motor challenges make its way into my school textbook?
I soon discovered that e e cummings was a famous poet who intentionally decried grammar convention and punctuation. Even his name was all lowercase. No one had liked him initially, so he had to self-publish. But his unconventional style ended up being much admired by generations of critics thereafter.
There was meaning in his very lack of punctuation
which gave me a lot of courage. Maybe I need not conform.
There was meaning in his very lack of punctuation which gave me a lot of courage. Maybe I need not conform. Perhaps my autism challenges could be transformed into strengths along the way. I just had to — had to — write in kind. I wrote the following poem in response to cummings’ assertions in his poem “since feeling is first“ and wrote it in the nonconformist style of his other poem “in Just-.”
noPeriods, Period
death’s no parenthesis
asserts e e cummings.
actually
death
is
a
comma
an
ellipsis
whitespace
aPause
as the soulRenewsBody
life’s no paragraph
avows e e cummings
just face it
life — is
a
smorgasbord
no grammar syntax
…just flows…..
noPeriods. Period.
says e e hari
I have to thank e e cummings for giving me additional perspectives on breaking the boundaries. “it takes courage to grow up and become who you really are,” he once said.
I can break free to just be me.
Contact Hari Srinivasan at hari@dailycal.org.
8th Annual Autism Walk at UC Berkeley
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| Giving an Intro Speech at the Autism Run |
Hi everyone. My name is Hari Srinivasan and I’m a student here at Cal. I also write for the Daily Cal.
Berkeley is the birthplace of the disability rights movement and autism is one of the fastest growing neurodevelopmental disabilities today. Autism in all its forms has a voice and we want to make it heard. Did you know my friend David and I are the first two non-verbal students with autism here at Cal. It goes to show that autism too is a diversity category with the wide range of neuro diverse minds that comes with it. Only with more exposure to individuals on the spectrum, will there be a change in mindsets and greater acceptance. Having students with autism can be a win win for all.
When I turned up for the autism walk last year, I did not even know that there was a spectrum organization here at Cal. Since then, I have been doing a wonderful walk with this student organization and learning about the other interesting activities being done in the community for the autism population. I started off on the autism acceptance committee where I did tabling and flyering for the first time in my life. This semester I am actually teaching a class on autism to 20 neurotypical students.
Autism is like a cocoon that morphs into all sorts of unexpected colorful butterflies. If you notice our new logo is a butterfly. The butterfly effect says a small local change can lead to profound and complex changes around the world. That is what you are all doing here today by participating. You are all part of the butterfly effect that will change the way autism is perceived, understood and accepted.
Thank you for making it here today.
When I turned up for the autism walk last year, I did not even know that there was a spectrum organization here at Cal. Since then, I have been doing a wonderful walk with this student organization and learning about the other interesting activities being done in the community for the autism population. I started off on the autism acceptance committee where I did tabling and flyering for the first time in my life. This semester I am actually teaching a class on autism to 20 neurotypical students.
Autism is like a cocoon that morphs into all sorts of unexpected colorful butterflies. If you notice our new logo is a butterfly. The butterfly effect says a small local change can lead to profound and complex changes around the world. That is what you are all doing here today by participating. You are all part of the butterfly effect that will change the way autism is perceived, understood and accepted.
Thank you for making it here today.
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| THE AUTISM BOARD AT UC BERKELEY |
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| Autism Run Participants |
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| Prepping Label for runners before the run. Opening safety pins is tough work. |
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| Jordan, my fellow DeCal student teacher |
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| The Autism Board |
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Crip Time
Crip Time
"Crip time" refers to the concept and practice of disability culture and community, which challenges the ableist notion that time is fixed and linear, and recognizes that different bodies and minds experience time differently.It acknowledges that disabled people, including autistics, often need more time to accomplish tasks and may have to adapt their schedules and routines to their own unique abilities and limitations. Crip time also challenges the notion that productivity and efficiency should be prioritized over rest and self-care.
"Rather than bend disabled bodies and minds to meet the clock, crip time bends the clock to meet disabled bodies and minds." Alison Kafer
Essentially, Crip Time is a shift towards valuing and centering the needs and experiences of disabled individuals, rather than expecting them to conform to ableist norms and standards.
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Plain Language Version
What is "Crip Time"?
"Crip time" is an idea from disability culture that says not everyone experiences time the same way. It challenges the usual way of thinking that time is strict and always the same for everyone.
Crip time recognizes that disabled people, including those with autism, often need more time to do things. They might need to change their schedules and routines to fit their own abilities and limitations. It also says that it's okay to prioritize rest and self-care over always being productive and efficient.
As Alison Kafer says, "Rather than bend disabled bodies and minds to meet the clock, crip time bends the clock to meet disabled bodies and minds."
In simple terms, Crip Time means valuing and focusing on the needs and experiences of disabled people, instead of expecting them to fit into strict, ableist time schedules and standards.
Delays in Diagnosis
Delays in Diagnosis
Girls, BIPOC, lower SES
- Delays in Dx → Impacts access to early intervention services (up to age 5)
- Girls: Traditionally thought to affect only males.
- BIPOC & lower SES - Access to Healthcare
- Blacks - mis dx as “Conduct Disorder” instead of ASD
- Access to state services only if dx before age 22
- Later years - dx is a relief, an explanation of “not fitting in”, provides a sense of community.
Camouflaging and Masking
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What is it.
Camouflaging or masking refers to the process by autistics learn to hide or suppress their autistic traits or behaviors in order to fit in and appear more neurotypical Essentially, it is the mimicking of NT behaviors. This can include things like suppressing stims (repetitive movements or sounds), forcing eye contact, or learning and mimicking social scripts or body language in order to appear more socially adept.
Why?
Masking or camouflaging is often a coping strategy used by autistics to navigate social situations that can be overwhelming or challenging. It is a means to fit-in and also a question of safety, as the display of atypical behaviors can lead to negative reactions from others.
Consequences.
It can also be exhausting and can lead to feelings of anxiety, depression, and burnout.
Do only certain "type" of autistics engage in masking/camouflaging?
No. Masking and Camouflaging is engaged in by autistics across spectrum. Do only certain "type" of autistics engage in masking/camouflaging?
People with higher support needs just may be less adept at pulling it off, but everyone has the desire to be safe from potential negative consequences.
Does sex play a difference.
Recent research has also suggested that females are able to camouflage better which results in late-diagnosis.
Recent research has also suggested that females are able to camouflage better which results in late-diagnosis.
Related Posts
- Masking & Camouflaging.https://uniquelyhari.blogspot.com/2021/09/cm.html
- Triple Bind and Masking in Autistic Femaleshttps://uniquelyhari.blogspot.com/2021/04/triple-bind-masking.html
- Masking as an evolutionary advantage https://uniquelyhari.blogspot.com/2020/04/masking-as-evolutionary-advantage.html
- CAT-Q measure to measure camouflaging in autistic females. https://uniquelyhari.blogspot.com/2021/04/cat-q-measure-to-measure-camouflaging.html
- Dont Cant Wont - Masking Camouflaging https://uniquelyhari.blogspot.com/2021/05/dcw.html
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