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Curiosities of brain science

What the Ancient Bog Bodies Knew

January 30, 2023 by www.nytimes.com Leave a Comment

When Roy van Beek was a teenager in the Netherlands in the early 1990s, he made a field trip to a local museum to see an exhibit of bog bodies: ancient human remains, both skeletal and naturally mummified, interred in the wetlands and spongy turf of northern Europe. He recalled one cadaver on display that was remarkably intact and oddly disorienting. The contorted body of a female about his age, roughly 4 feet 6 inches tall, who had lived in the first century A.D. “She had been left in a shallow mire south of the modern-day village of Yde,” said Dr. van Beek, now an archaeologist at Wageningen University & Research. Her skin had been tanned in the dark tea of the bog.

The Yde Girl, as she became known, was unearthed in 1897 by peat diggers so spooked by their gruesome discovery that they reportedly chorused “I hope the Devil gets the man that dug this hole” and fled the scene. The corpse was wearing a much-darned woolen cloak, which concealed a stab wound near her collarbone. A seven-foot-long strip of cloth, perhaps a waistband, was wound around her neck three times and its slipknot indented below her left ear. “The cloth was probably used to strangle her,” Dr. van Beek said. Most of the bog mummies that have turned up also show signs of multiple traumatic injuries and are presumed to be murder victims.

This month, Dr. van Beek was the lead author of the first comprehensive survey of bog bodies — a burial tradition believed to span 7,000 years. The multidisciplinary study, published in the journal Antiquity, created a database of more than 1,000 such bog people, some arrestingly lifelike, from 266 historical bog sites across a swath of northern Europe, from Ireland to the Baltic States.

Relying on recorded folklore, descriptions and depictions, newspaper reports and antiquarian records, a team of Dutch, Swedish and Estonian researchers focused on the rise of bog burials starting around 5200 B.C., in the Neolithic period and into the Bronze Age. The team took particular interest in the tradition’s efflorescence from 1000 B.C. to 1500 A.D., from the Iron Age to the medieval period.

“While a number of bog scholars have been arguing that we need to reconceptualize bog bodies to include the skeletonized remains from more alkaline bog lands and wetlands, this is the first major study to do it systematically,” Melanie Giles, a British archaeologist not involved in the study, said in an email. “The results are really quite important, showing a formal burial phase in the Bronze Age and a rise in violent deaths during the time in which these bogs, within certain hot spots, grow exponentially.”

Cases are divided into three main categories: bog mummies, whose skin, soft tissue and hair are preserved; bog skeletons, with only the bones surviving; and a third group composed of the partial remains of both. “Many finds have been lost in the distant past or are only known through published sources,” Dr. van Beek said. “These ‘paper’ bog bodies are documented with varying degrees of detail and reliability.” Before the 19th century, bodies pulled out of bogs were often given a Christian reburial.

The cadavers owe their state to the natural chemistry of bogs. Layers of sphagnum moss and peat help pickle bodies by saturating the tissue in a cold, immobilizing environment that is highly acidic and almost devoid of oxygen. The decaying mosses release humic acids and sphagnan, a complex sugar, that make life difficult for the microorganisms that would normally cause rotting and decay. Sphagnan also leaches calcium from bones, eventually softening, breaking and warping them.

‘A dark elderberry place’

Bog-mummified people are mainly found in raised bogs — discrete, dome-shaped masses of peat that typically form in lowland landscapes and reach depths of 30 feet or more. (Blanket bogs are generally shallower and spread out widely over wet or upland areas.)

Uncovering the Past, One Discovery at a Time

  • Extinct Elephants: A study of butchered bones from 125,000 years ago suggests that for at least two millenniums Neanderthals hunted in what would come to be east-central Germany for the now-extinct straight-tusked elephants .
  • Bog Bodies: The first comprehensive survey of a 7,000-year-old bog burial tradition reveals an often violent final ritual .
  • Appian Way: An archaeological dig that began last summer, searching for the long-elusive “first mile” of the ancient Roman thoroughfare, has been stymied by ground water .
  • Animal Mummies: The discovery of 10 mummified crocodiles in an Egyptian tomb shed light on ancient mummification practices and the many lives of a necropolis.

The first recorded body emerged from Schalkholz Fen in Holstein, Germany, in 1640. Since then, the cold-weather swamps of northern Europe have yielded such regional curiosities as Windeby Girl, Haraldskjaer Woman, Lindow Man, Clonycavan Man, Old Croghan Man and Koelbjerg Man. The bones of Koelbjerg Man, recovered in 1941 on the Danish island of Funen, date to 8000 B.C. Seamus Heaney’s melancholy “Bog Poems” include a lament for Grauballe Man, whose throat was slit in the third century B.C.:

The cured wound

opens inwards to a dark

elderberry place.

Of the 57 bog people whose cause of death could be determined in Dr. van Beek’s study, at least 45 met violent ends, and quite a few were bludgeoned or suffered mutilation and dismemberment before they died. Tollund Man, dating to the fifth century B.C. and dredged from a Danish peat bog in 1950, was hanged. Bone arrowheads were found embedded in the skull and sternum of Porsmose Man, recovered from peat elsewhere in Denmark. Seven victims appear to have been slain by several means, a practice that scholars call overkilling. Almost all of the overkills in Dr. van Beek’s study occurred from 400 B.C. to 400 A.D.

The bog of war

While most sites held just a single deceased person, some were used repeatedly, with one Danish bog, Alken Enge, estimated to hold the disarticulated remains of more than 380 ancient warriors killed in a brutal conflict and left in open water. The bones, exclusively male and predominantly adult, date to early in the first century A.D., when Germanic tribes engaged in intratribal warfare. Researchers believe that the dead were cleared from the battlefield and dumped into the bog with their weapons and personal ornaments.

This would have been one of the lesser indignities that befell bog people. Many were hastily extracted or improperly conserved; in the Netherlands of the late 18th century, four bog corpses were even ground into mumia — mummy powder — and sold as remedies.

A fundamental question about these Iron Age victims is why. Were they murdered? Executed? Sacrificed to the gods, perhaps as fertility offerings? Miranda Aldhouse-Green, emeritus professor of archaeology at Cardiff University and author of “Bog Bodies Uncovered,” has argued that ritual sacrifices may have been undertaken at times of crisis in a community: famine, extreme weather, war threats, the perceived need to kill foreign hostages.

Two features recur among Iron Age bog bodies: youth and disability. Many bodies were those of adolescents, at the cusp between childhood and adulthood. “In some traditional societies, such individuals were perceived to have shamanic powers, enabling them to segue between the material and spirit worlds, just as people at puberty contain elements of childhood and adulthood,” Dr. Aldhouse-Green said in an email.

The Yde girl had severe scoliosis, a twisting of the spine that meant her growth was stunted and she would have walked with a lurch. Dr. Aldhouse-Green has proposed that disabled people may have been perceived to be “touched” by divinity.

“Ceremony was key to keeping communities bound together, and ritual killing would provide spectacle similar to Roman gladiatorial shows,” she said. Recent findings from Denmark and north Germany suggest that the people chosen may sometimes have been of high status and had therefore undertaken long journeys in the months before their deaths.

Disease was the likely culprit in a few instances, and from 1100 A.D. on, there were six possible suicides and four accidental deaths. In 1674, a man and a woman died in a snowstorm on the upland peat bog of Hope Woodland in Derbyshire, England. Far to the north in Shetland, during a cold spell late in the same century, the so-called Gunnister Man is believed to have succumbed to exposure. In 1828, a German traveling salesman and falconer named Johann Spieker died in Lower Saxony, probably by drowning.

“His grave was marked with a wooden cross and a fence that remained visible for a long time,” Dr. van Beek said. “During the excavation, only his cloak, some coins and a prayer book apparently were found.”

Arguing against suicide theories, Dr. Aldouse-Green noted that many ancient bog bodies were naked, some found with clothes placed beside them. “Leather and linen survive in bogs due to the presence of sphagnum moss,” she said. Dr. van Beek countered that “nakedness is a very difficult factor to take into account” and that other fabrics can degrade without a trace even when a body is preserved.

For peat’s sake

The growth of boglands was stimulated more than 10,000 years ago by the collapse of the Eurasian Ice Sheet and release of freshwater, which abruptly raised sea levels and groundwater tables. Plant decomposition is slowed to such an extent in these areas that dead vegetation accumulates to form peat, effectively storing carbon dioxide. As a result, preserving bog lands is considered a powerful tool to help mitigate climate change.

“Many bogs across Europe are currently protected nature reserves, often with attempts to restore and expand them,” Dr. van Beek said. He added, with chagrin, that in the Irish Midlands, the Baltic States and parts of Germany, peat is still being cut.

“Never before have we needed to care as much about peatlands,” said Dr. Giles, whose book “Bog Bodies: Face to Face With the Past” explores what she calls “the black hole of the peat pool.” “Yet for hundreds of years we’ve told awful tales about these maligned landscapes, encouraging people to steer clear, to drain and damage those precious places.”

Yde Girl and Tollund Man are a reminder that humans once had very different and more respectful relationships with the bog, she said: “Bog bodies — and artifacts and eco-facts — become strange kinds of ambassadors from deep time. They re-enchant us with these landscapes through their stories.”

Filed Under: Science Peat, Mummies, Wetlands, Cadaver, Skeleton, Archaeology;Anthropology, Antiquity, England, Ireland, your-feed-science, internal-sub-only, Science, Mummies and..., bog bodies why, bogged bodies, peat bog body meaning, peat bog bodies ireland, peat bog bodies scotland, peat bog body preservation, peat bog body found, peat bog bodies uk, bog body where is, where bog bodies

Google launches AI chatbot Bard to rival wildly successful ChatGPT

February 6, 2023 by news.sky.com Leave a Comment

Google has launched its own artificial intelligence (AI) chatbot, in answer to the wildly successful ChatGPT.

The new conversational AI service will be named Bard and will be put out to “trusted users” before a public release in the coming weeks, Google’s parent firm Alphabet Inc announced on Monday.

It comes following the release of ChatGPT – an AI chatbot trained on a huge amount of text data, which it leverages to help generate answers and carry out realistic conversations.

Released by research firm OpenAI late last year, the chatbot threatened to upend how people prepare for job interviews , journalists write stories , and children do homework .

The chatbot has been such a success, that earlier this month it was revealed that the service had been used by more than 100 million users worldwide in under two months.

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Chat GPT explained 2:16

Will this chatbot replace humans?

The announcement was made in a blog post on Monday by Alphabet chief executive Sundar Pichai, who also announced more artificial intelligence for its search engine as well as developers.

He wrote: “It’s a really exciting time to be working on these technologies as we translate deep research and breakthroughs into products that truly help people.

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“That’s the journey we’ve been on with large language models.

“Bard can be an outlet for creativity, and a launchpad for curiosity, helping you to explain new discoveries from NASA’s James Webb Space Telescope to a nine-year-old, or learn more about the best strikers in football right now, and then get drills to build your skills.”

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Read more: We let an AI chatbot help write an article – here’s how it went Israel president uses ChatGPT artificial intelligence to write part of major speech

Google’s service Bard will be powered by LaMDA, the company’s AI that can generate prose so human-like that a company engineer last year called it sentient – a claim the technology giant and scientists widely dismissed.

Google has been cautious about chatbots until now, with LaMDA restricted to limited testing.

Explaining how Bard would be released, Pichai wrote: “We’re releasing it initially with our lightweight model version of LaMDA.

“This much smaller model requires significantly less computing power, enabling us to scale to more users, allowing for more feedback.

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Isaac Herzog 0:47

Israel’s president, Isaac Herzog, used artificial intelligence to write part of his major speech.

“We’ll combine external feedback with our own internal testing to make sure Bard’s responses meet a high bar for quality, safety, and groundedness in real-world information.

“We’re excited for this phase of testing to help us continue to learn and improve Bard’s quality and speed.”

Rival Microsoft is also set to shake up its own products with AI, including search engine Bing, after making a multibillion-dollar investment in OpenAI.

Microsoft has since announced plans to implement ChatGPT into its Teams software, where it will do things like summarise meetings, but the features will be restricted to a premium pricing plan.

Filed Under: Uncategorized google launches, Google Home AI, google ai, ai chatbot, google launches new app, google launch, ai chatbots

A Psychologist Offers 3 Reasons Why Love And Intelligence Always Go Together

February 6, 2023 by www.forbes.com Leave a Comment

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We all have a personalized list of qualities that we seek in an ideal partner — a list that seems to get longer and more specific with each passing year. These cover everything from sense of humor to hygiene to political values, and even pet-parenting skills.

There is one quality — more specifically, a compatibility metric — that can help us slash our checklist considerably. An intelligent partner with whom you can form an intellectual connection can be a boon when it comes to the quality of your relationship.

Mental health research gives us three reasons why finding an emotionally and cognitively intelligent partner might be the missing piece to our relationship puzzle.

#1. They are skilled communicators.

Couples’ therapists will be the first to tell you that most problems in relationships stem from a breakdown in communication. This means that relationship problems can often be resolved through open and effective communication — and this is more likely to occur in a bond with a strong intellectual component.

Finding an intellectual equal ensures that all cards are on the table and that misunderstandings are fewer and farther in between. This is probably why, according to research , intellectual connections tend to last longer and qualities like physical attractiveness are more relevant for both men and women for short-term relationships.

Relationship longevity isn’t just a result of effective conflict resolution, intellectually stimulating conversations also play a role. Two people who can keep up with each other emotionally and intellectually can turn even the most mundane chat into a satisfying and expansive experience.

#2. They complement your intelligence.

Different life experiences lead to distinct intellectual strengths and ways of thinking. Research published in Frontiers in Psychology has shown that wisdom, a quality associated closely with mental prowess, can present differently in men and women due to cultural and societal reasons.

While you may bring the strengths of decisiveness and practicality to the table in your relationship, your partner may show an incredible capacity for empathy, compassion, and other prosocial forms of wisdom.

This could push your collective capacity for growth farther than you could ever take it alone. Being exposed to distinct but complementary worldviews makes life exciting and enriching.

#3. They are always open to learning.

Any intellectual match worth its salt has an appetite for change. Perhaps the truest test of an ‘intelligent’ person is how well they understand the limits of their intelligence, according to research published in Personality and Individual Differences . A healthy long-term relationship is usually built on a foundation of intellectual humility — i.e., the flexibility to change your mind about things and being able to discern when you should.

A partner that is cognitively flexible, open to counter-opinions, averse to binary thinking, and genuinely open to the possibility of being wrong shows intellectual humility. A bond steeped in intellectual humility can ensure that both partners in the relationship feel seen and heard.

Conclusion

Finding or being an intelligent partner is not about having a high IQ or multiple degrees. In most cases, it is about developing your character and approaching your relationships with genuine curiosity and empathy.

Filed Under: Uncategorized how important is intelligence in finding love, is it okay to date someone smarter than me, how important is IQ in dating, mark travers...

Adults newly diagnosed as autistic quickly learn a key lesson about how they fit into society

February 5, 2023 by www.abc.net.au Leave a Comment

Being diagnosed as autistic as an adult made these people want to make a change. Now they’re flipping the switch on the negative perceptions of autism.

“I am a broken person, trying to put the pieces back together in the (perhaps vain) hope that maybe the repaired version will be more beautiful than the scars that pain left behind …”

I first wrote these words online in mid-2019.

I had just experienced a psychotic episode — not my first — and had suffered several years of “hell” as I struggled through an array of challenging and, at times, devastating mental health struggles.

By this point in my life, I’d almost completely lost any sense of who I was.

I used my camera to help me cope, exploring my home town on Wiradjuri country.

ABC News: Jessica Horner

I hid behind various social masks, which I subconsciously wore each day, as I tried to fit into a social world that so often felt foreign and difficult to comprehend.

My camera became an impenetrable barrier to stop anyone from getting too close to a version of myself that I considered too much for anyone else to love.

What I did not know as I wrote those words was that just a few months later, at the age of 27, I would walk out of a clinical psychologist’s office as one of the estimated one in 70 Australians diagnosed with autism spectrum disorder.

Being diagnosed autistic as an adult would change my life in an immeasurably positive way — but first, it would nearly destroy me.

Tailor-made healthcare

Jonathan Ho is a mental health GP who lives and works in Wagga Wagga in the NSW Riverina.

Dr Ho has been my GP since early 2019 so our clinical relationship is well established, but when we sit down to chat in late-2022 the nervous energy in the room is palpable.

This particular day we are sitting down to talk about being autistic adults, an identity that, like myself, Jonathan came to recognise later in life, at the age of 41.

Jonathan talks about “moving at the speed of trust” with his patients.

ABC News: Jessica Horner

Back in medical school, he had tried to seek help for what he thought was a learning difficulty.

“I went to see the right doctors and initially there was a lot of dismissal,” he says.

“That minimisation, that because … I have a job or I’m able to pass my examinations, I’m able to converse with people and have warm and friendly chats, that there was possibly nothing wrong with me and it’s just in my head.”

Now 43, he openly speaks about his diagnosis.

“It dawned on me that I’d had [autism] all my life, but it was never recognised,” he says.

Jonathan’s approach to clinical practice is as unique as his numerous colourful suits, each of which he bespoke tailors and sews by hand.

“A lot of my patients say that I’m very fashionable and stylish,” he says.

“I actually hand-make my tailoring, rather than using a machine. It is often very comfortable.

“It is an objective example of how I am comfortable with who I am; I would like to invite you to reciprocate and be comfortable with who you are.”

As we sit I listen with curiosity, contemplating various metaphors he has carefully woven throughout his practice.

The conversation soon turns to the topic of his fountain pens, which he uses daily to write his scripts in green ink.

I tentatively ask the meaning behind the pens, already knowing the answer.

“Each fountain pen is unique,” he says.

“I would buy a fountain pen really as a commemorative object to a patient who I have lost from suicide.

“When I use that fountain pen it is really an embodiment of how precious individuals are.”

My heart sinks.

In September 2019, nine months after we met, and within weeks of confirming I was autistic, I determined that I was irrevocably broken, and I attempted to take my own life.

I hesitantly push through the distinct tension hanging in the air and ask Dr Ho how it felt to interact with me back then.

He shows some hesitation before answering,

“My understanding was that you didn’t get the help that you needed. There wasn’t a system or approach to really listen to your needs and respond to them,” he says.

“There was this innate feeling in me of we have to do something. I don’t want to buy another pen.”

To say hearing this was unsettling is an understatement.

Moreover, I sit discomforted by the knowledge that my story is not unique.

Autistic individuals have a suicide rate nine times higher than the general population.

If you or anyone you know needs help:

  • Lifeline on 13 11 14
  • Kids Helpline on 1800 551 800
  • Beyond Blue on 1300 224 636
  • Suicide Call Back Service on 1300 659 467
  • headspace on 1800 650 890
  • MensLine Australia on 1300 789 978
  • Care Leavers Australasia Network (CLAN) on 1800 008 774
  • ReachOut
  • Head to Health

‘Every system in my life collapsed’

Jennifer Hankin, 29, was diagnosed autistic five years ago.

When I arrive at her home in Newcastle, she is in an NDIS phone meeting. Her concentration has an intensity to it, and she appears stressed and somewhat frustrated.

She asks many “why” questions about the way the system works, as she struggles to get the support she feels she needs to live life on her own terms.

After the meeting, her persona dramatically changes. She hurries to greet me with an enthusiastic hug.

We began corresponding via social media back in May last year, but this is the first time we have met in person.

When we sit down on her bright red couch to chat, Jennifer nestles under her rainbow-coloured weighted blanket, which matches her colourful, hand-sewn overalls.

“I’m cold all the time. The level of warmth a weighted blanket provides is the best level of warmth,” Jennifer says.

ABC News: Jessica Horner

It soon emerges that Jennifer has also struggled with her mental health for many years.

In 2017, she turned to the internet for help following more than a decade of unrelenting depression symptoms and it didn’t take long for her to realise she was probably autistic.

But when Jennifer approached her psychologist, she was initially taken aback by the idea.

“There is the traditional idea of what  autism looks like, and then there is what autism looks like in me,” Jennifer says.

Jac Den Houting, an autistic post-doctoral research fellow at Macquarie University, tells me this experience is particularly common among women and girls, as well as other socially marginalised groups.

“The vast majority of what we know about autism, and even how we define autism, is based on research that was conducted with boys: white, middle-class boys in Western countries,” they say.

“We have started to recognise that autism is a lot more heterogenous than that.

“There is not just one way of being autistic.”

Dr Den Houting explains this acknowledgement of the broad ways autism can present has only started to emerge in the past decade or so.

As a result, many psychologists’ clinical training is not up to date with recent research.

“If you’re smiling, nobody will judge your feelings, even if you tell them how you are feeling,” Jennifer says.

ABC News: Jessica Horner

Jennifer tells me her hard-to-recognise autism is actually a presentation that is “highly masked”.

Masking within the autistic community is the experience of camouflaging behaviour or acting a particular way, sometimes subconsciously, to hide in plain sight, in a society where autists often don’t feel socially accepted.

It’s a reality I am far too familiar with.

“Wearing a mask for me means I am presenting as socially and societally acceptable, no matter what my internal experience may be,” Jennifer says.

“Nobody thinks you’re sad if you show up wearing a rainbow.”

Jennifer tells me she lives a “double work life” where teaching flute provides financial stability, and sits alongside her work as a professional flautist.

She describes being a flute player as “the only career that I’ve ever wanted”.

Despite the common idea that autistic people only excel in science and technology, creativity can be an innate part of the autistic experience.

But regardless of the field, sustaining a meaningful career as an autistic person isn’t without its challenges and compromises.

About 31.6 per cent of autistic adults in Australia are unemployed and many more are underemployed.

For Jennifer, sustaining her career has been challenging due to long-term autistic burnout — which feels intense, unrelenting, and permanent.

“From what I understand, in regular society, burnout doesn’t necessarily mean a collapse of every system in your life. It might just be one or two,” she says.

“Every system in my life collapsed. I’ve been referring to this as a burnout/complete system breakdown lately. But I think we need to find a better word.”

Jennifer may live in a dual world as a creative professional and an autistic adult, but I have a sense that she’s starting to lean into this existence.

One thing she clearly values is the empathetic and nurturing relationships she forged with other autistic adults along the way.

“Neurotypical folks are attracted to other neurotypical folks because their brains function in a neurotypical way. And they socialise really well,” she says.

“On the flip side, neurodivergent folks are attracted to other neurodivergent folks.

“And the social difficulties that are recorded in the various diagnostic and statistical manuals, they melt away.”

What she’s just described is better known as the double empathy problem, first suggested by an autistic researcher, Dr Damian Milton, in 2012.

The theory asserts that autists don’t lack empathy, but rather we have different ways of expressing ourselves and communicating, which often leads to a social disconnect that is erroneously perceived by non-autistic people as a lack of empathy.

Jennifer elaborates.

“Being around other neurodivergent individuals doesn’t cost me anything,” she says.

‘It’s really a heavy thing’

“I only ever thought of it as a negative thing, to be autistic,” says 55-year-old Kathy Halbsch.

Kathy and I met in an online support group for autistic women, which I was co-facilitating. That was almost a year ago, but this is our first meeting face-to-face.

Her one-bedroom social housing unit in Wagga Wagga is sparsely furnished, so much so that her TV is balanced upon a pair of cardboard boxes.

As I take in my surrounds, I realise that throughout the room are meaningfully placed ornamental pieces and artwork, which lend small bursts of vibrancy and personality to the space.

The most compelling object in the room is a life-sized mask made of concrete that, once spotted, is hard to ignore.

“The mask I made, it’s made of concrete and that’s to show just the weight of it, it’s really a heavy thing,” she explains.

“Flat, featureless, with the eyes looking out, like the person you are looking out onto the world through this heavy mask.”

Through the safety and support of engaging with other autistic adults her perspective on what autism is has profoundly changed.

“Autism is not like a disease,” she asserts.

“Neurodiversity … doesn’t make you stupid, it doesn’t make you not deserve dignity, it doesn’t make your goals something to be belittled.

“The truth is that you’re completely valid the way you are.”

I glance towards the bench near the windowsill, where the mask is placed.

The midday sun filters through the eyes revealing an inner layer of gold that hides behind the flat facade. I ask her about the meaning.

“Gold’s precious, who you are is precious,” Kathy passionately declares.

I’m struck with a sense of irony that among autists who are so often typecast as literal and uncreative thinkers, I continue to encounter such profound metaphors that challenge the pervasive stereotypes that we don’t feel or understand nuanced emotions.

But more importantly, I’m glad that Kathy appears to have reached a place of self-acceptance after several years of personal struggles where she didn’t get the support she needed.

Despite the validation of her autistic identity by clinical professionals and peers, Kathy still craves further supports, which she can only access with a formal diagnosis.

It’s something that remains unobtainable for her, as assessment for autism in adults can cost upwards of $2,500 in regional Australia.

Dr Den Houting tells me within the autistic community, self-diagnosis is valid and generally accepted.

They acknowledge that other autistic people are more likely to recognise factors such as the exorbitant cost, stigmatisation, and the medical model that underlies a diagnosis of autism in which autistic people are characterised by deficits.

Cumulatively these lead to formalised diagnosis being inaccessible for many adults.

Nevertheless, it’s clear that for Kathy a weight has been lifted.

Reconciling her autistic identity has come with a new-found sense of empowerment.

‘Us not-broken humans’

Megan Spindler-Smith is the chair of ABC Inclusive, the disability employee network at the ABC. We met when I joined the committee in 2022.

Megan was diagnosed autistic two years ago, at the age of 41.

When I arrive at their home in Richmond, in north-west Sydney, I immediately notice the letterbox covered with LGBTQIA+ and Aboriginal flags, nestled among the tree-lined streets .

Megan relaxes at home with their wife Kel.

ABC News: Jessica Horner

The letterbox is just one example of how Megan’s life involves embracing the world from an intersectional perspective.

“I’m non-binary and I am queer … I have a wife; my wife is Aboriginal. My younger sister is Korean, so I have grown up in multiple cultures,” they say.

There is a saying in the autistic community that if you know one autistic person, you know one autistic person.

“My experience as an autistic person will never be the same as your experience,” Megan says.

They are right, we are very different people, with very different life stories.

Despite our differences, Megan and I effortlessly hit our stride in conversation.

We certainly don’t sound like the stereotyped “expressionless” social expectation of autism — we can both be described as talkative and opinionated.

However, it’s important to acknowledge that ways of communicating vary, even for autistic individuals, and there is no singular correct way.

“Blame society for disability, not the human, because the fact is I’m a person with disability because society disables me,” Megan says.

ABC News: Jessica Horner

Megan and I have a few other traits in common, one of which is a strong sense of social justice with a particular fervour for changing the disability space.

“I do absolutely see autistic people as marginalised,” they say.

“Society is not set up to allow for me, or for other autistic people, to be 100 per cent themselves, which is why we have to do things like masking.”

Perhaps the most compelling commonality between us is that we both embrace the notion that autism is actually not a form of disorder.

We reject the medical model of autism, which defines people by so-called deficits.

Instead, we see autistic as simply a description of a particular type of brain, or neurotype.

The more we talk about our shared experiences the more passionate Megan becomes.

“We need to change the narrative of autism,” they say.

“We need to stop treating it as a bunch of broken people that need to be fixed.

“We need to fix society to allow us not-broken humans to function in the way that we add the value that we know we already add, but with lots of barriers.”

For Jonathan, Jennifer, Kathy, Megan, and myself, a common sentiment emerges from our largely divergent life stories. As Megan says:

“I’m not as broken as I thought … there’s nothing wrong with me; I’m just autistic.”

Each of us has expressed a similar mindset as we come to terms with our autistic identity as adults.

Slowly realising our worthiness and value as individuals and as part of the autistic community is an important understanding we all share.

Not hoping in vain

On August 30, 2019, I was diagnosed autistic.

At first it felt like a tragedy, and it very nearly was when I tried to end my life.

But being recognised as autistic later in life meant finding an identity and acknowledging that autism is so much more than a medically defined “diagnosis”.

Being autistic also means belonging and being part of a vibrant and intersectional community with shared cultural experiences.

Realising I was autistic was not a missing puzzle piece, but rather a rich new lens through which to understand my life more fully, both now and in retrospect.

My autistic identity informs and reframes how I think, feel about, interact with, and understand my world.

It has led to paradigm shifts I never imagined, relationships with new depth and meaning, and opportunities I will cherish forever.

Will the hard parts of being an autistic adult disappear in my lifetime? Maybe not.

But I am reassured that hoping the scars and painful parts will continue to fade, and something more beautiful will emerge, was not hoping in vain after all.

Credits:

  • Reporting and photography: Jessica Horner
  • Additional photography: Graham Horner
  • Digital production: Nicole Mills

Posted 20h ago 20 hours ago Sun 5 Feb 2023 at 6:52pm
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Filed Under: Uncategorized Autism, Autism spectrum disorder, adults, diagnosis, stereotypes, mental health, suicide, depression, identity, ..., lesson learned alicia keys, lesson 5.1 learning the key terms, lesson 5.2 learning the key terms, lesson 5.3 learning the key terms, lesson learned lyrics alicia keys, lesson 9.1 learning the key terms

Scientists Made a Startling Discovery After Dosing People with LSD

March 19, 2018 by www.livescience.com Leave a Comment

Scientists in Switzerland dosed test subjects with LSD to investigate how patients with severe mental disorders lose track of where they end and other people begin.

Both LSD and certain mental disorders, most notably schizophrenia , can make it difficult for people to distinguish between themselves and others. And that can impair everyday mental tasks and social interactions, said Katrin Preller, one of the lead authors of the study and a psychologist at the University Hospital of Psychiatry in Zurich. By studying how LSD breaks down people’s senses of self , the researchers aimed to find targets for future experimental drugs to treat schizophrenia.

“Healthy people take having this coherent ‘self’ experience for granted,” Preller told Live Science, “which makes it difficult to explain why it’s so important.”

Depression , she said, also relates to the sense of self. Whereas people with schizophrenia can lose track of themselves entirely, people with depression tend to “ruminate” on themselves, unable to break obsessive, self-oriented patterns of thought. [ 7 Ways to Recognize Depression in 20-Somethings ]

But this kind of phenomenon is challenging to study, Preller said.

“If you want to investigate self-experience, you have to manipulate it,” Preller said. “And there are very few substances that can actually manipulate sense of self while patients are lying in our MRI scanner .”

One of the substances that can, however, is LSD. And that’s why this experiment happened in Zurich, Preller said. Switzerland is one of the few countries where it’s possible to use LSD on human beings for scientific research. (Doing so is still quite difficult, though, requiring lots of oversight.)

The experiment itself didn’t sound like the most exciting use of the drug for the test subjects, all of whom were physically healthy and did not have schizophrenia or other illnesses After taking the drug, the subjects lay inside MRI machines with video goggles strapped to their faces, trying to make eye contact with a computer-generated avatar. Once they accomplished this, the subjects then tried to look off at another point in space that the avatar was also looking at. This is the kind of social task, Preller said, that’s very difficult if your sense of self has broken down.

Previous studies on animals had suggested that 5-HT2 played a key role in LSD’s ability to mess with sense of self. The researchers suspected that blocking the receptor in humans might somewhat reduce the effect of LSD.

But it turned out to more than “somewhat” block the effect: There was no difference between the performance of subjects who took ketanserin and the placebo group. [ Why LSD’s Effects Last So Long ]

“This was surprising to us, because LSD interacts with a lot of receptors [in the brain], not just 5-HT2,” Preller said.

But LSD’s most dramatic measurable effects entirely abated when subjects first took ketanserin.

That tentatively indicates that 5-HT2 plays an important role in regulating sense of self in the brain, Preller said. The next step, she added, is to work on drugs that target that receptor and see if they might alleviate some of the symptoms of severe psychiatric illnesses that affect the sense of self.

The paper detailing the study’s results was published today (March 19) at The Journal of Neuroscience.

Originally published on Live Science .

Filed Under: Uncategorized scientist and their discoveries, scientist discoveries, scientist discovery, scientist inventions and discoveries, scientist and their discoveries list, scientists and their discoveries, scientists new discovery, scientist new discovery, scientists & their discoveries, scientist latest discovery

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