Kirsten Grind, Sam Schechner, Robert McMillan and John West:

More than 100 interviews and the Journal’s own testing of Google’s search results reveal:

• Google made algorithmic changes to its search results that favor big businesses over smaller ones, and in at least one case made changes on behalf of a major advertiser, eBay Inc., contrary to its public position that it never takes that type of action. The company also boosts some major websites, such as Amazon.com Inc. and Facebook Inc., according to people familiar with the matter.
• Google engineers regularly make behind-the-scenes adjustments to other information the company is increasingly layering on top of its basic search results. These features include auto-complete suggestions, boxes called “knowledge panels” and “featured snippets,” and news results, which aren’t subject to the same company policies limiting what engineers can remove or change.
• Despite publicly denying doing so, Google keeps blacklists to remove certain sites or prevent others from surfacing in certain types of results. These moves are separate from those that block sites as required by U.S. or foreign law, such as those featuring child abuse or with copyright infringement, and from changes designed to demote spam sites, which attempt to game the system to appear higher in results.
• In auto-complete, the feature that predicts search terms as the user types a query, Google’s engineers have created algorithms and blacklists to weed out more-incendiary suggestions for controversial subjects, such as abortion or immigration, in effect filtering out inflammatory results on high-profile topics.
• Google employees and executives, including co-founders Larry Page and Sergey Brin, have disagreed on how much to intervene on search results and to what extent. Employees can push for revisions in specific search results, including on topics such as vaccinations and autism.
• To evaluate its search results, Google employs thousands of low-paid contractors whose purpose the company says is to assess the quality of the algorithms’ rankings. Even so, contractors said Google gave feedback to these workers to convey what it considered to be the correct ranking of results, and they revised their assessments accordingly, according to contractors interviewed by the Journal. The contractors’ collective evaluations are then used to adjust algorithms.

Ten years ago, ⁦@safiyanoble⁩ used a variety of similar methods to begin compiling evidence that became Algorithms of Oppression. I recall people telling her those methods were somehow not rigorous enough or, worse, that she was wrong or lying. https://t.co/CyBfOb303V

— Sarah T. Roberts (@ubiquity75) November 15, 2019

Many taxpayer supported K-12 school districts use Google services, including Madison.

Vanessa Blanch:

When Jayden was in Grade 5, Roberts said, she had no choice but to quit her job to stay home with her son. He was spending most of his school day in a seclusion room, or else the principal was calling her to pick him up because of his poor behaviour​​​​​​.

Roberts explained that while her son scored in the 98th percentile in testing for block design, which measures your ability to mentally manipulate both two and three-dimensional figures, his overall processing speed was so slow it couldn’t be measured.

David Z. Hambrick, Madeline Marquardt:

There are advantages to being smart. People who do well on standardized tests of intelligence—IQ tests—tend to be more successful in the classroom and the workplace. Although the reasons are not fully understood, they also tend to live longer, healthier lives, and are less likely to experience negative life events such as bankruptcy.
Now there’s some bad news for people in the right tail of the IQ bell curve. In a study just published in the journal Intelligence, Pitzer College researcher Ruth Karpinski and her colleagues emailed a survey with questions about psychological and physiological disorders to members of Mensa. A “high IQ society,” Mensa requires that its members have an IQ in the top 2 percent. For most intelligence tests, this corresponds to an IQ of about 132 or higher. (The average IQ of the general population is 100.) The survey of Mensa’s highly intelligent members found that they were more likely to suffer from a range of serious disorders.
The survey covered mood disorders (depression, dysthymia and bipolar), anxiety disorders (generalized, social and obsessive-compulsive), attention-deficit hyperactivity disorder and autism. It also covered environmental allergies, asthma and autoimmune disorders. Respondents were asked to report whether they had ever been formally diagnosed with each disorder or suspected they suffered from it. With a return rate of nearly 75 percent, Karpinski and her colleagues compared the percentage of the 3,715 respondents who reported each disorder to the national average.

Gabriela Borter:

The U.S. Centers for Disease Control and Prevention reported a 9.8% increase in measles cases as of May 10, a resurgence that public health officials have attributed to the spread of misinformation about the measles vaccine. Data are updated every Monday.

In New York, 66 cases were reported according to CDC spokesman Jason McDonald, with 41 in New York City and 25 in Rockland County, about 40 miles (64 km) north of New York city.

Health experts say the virus has spread mostly among school-age children whose parents declined to give them the vaccine, which confers immunity to the disease. A vocal fringe of U.S. parents, some in New York ultra-Orthodox Jewish communities, cite concerns that the vaccine may cause autism. Medical science has debunked those concerns.

While the 2019 outbreak has spread rapidly within New York, the virus has not spread to any additional states since the previous week, when Pennsylvania became the latest state to confirm at least one case.

BBC:

A county in New York state has declared a state of emergency following a severe outbreak of measles.

Rockland County, on the Hudson river north of New York City, has barred unvaccinated children from public spaces after 153 cases were confirmed.

Violating the order will be punishable by a fine of $500 (£378) and up to six months in prison.

The announcement follows other outbreaks of the disease in Washington, California, Texas and Illinois.

Vaccination rates have dropped steadily in the US with many parents objecting for philosophical or religious reasons, or because they believe misleading information that vaccines cause autism in children.

Ashley May:

People choosing not to vaccinate has emerged into a global health threat in 2019, the the World Health Organization recently reported. The CDC has also recognized that the number of children who aren’t being vaccinated by 24 months old has been gradually increasing.

Some parents opt not to vaccinate because of the discredited belief vaccines are linked to autism. The CDC says that there is no link and that there are no ingredients in vaccines that could cause autism.

Logan Wroge:

The Madison School Board on Monday backed a proposed contract that would keep police officers at Madison’s four main high schools.

Board members voted 4-2 in favor of the proposed contract, which would emphasize alternative disciplines instead of arresting or citing students, lay the groundwork for a new complaint procedure against the officers and require more training in areas such as autism, adolescent brain development and implicit bias.

The board, though, added contract language that would give the Madison School District the ability to require an officer be replaced for cause.

“The reality is things that we don’t control make having (police officers) in our schools absolutely the best decision,” said board president Mary Burke. “Unfortunately yes, there are downsides, unintended consequences.”

Members T.J. Mertz, James Howard, Dean Loumos and Burke supported the contract, Nicki Vander Meulen and Kate Toews voted against it, and Gloria Reyes was not present for the vote.

Earlier in the meeting, the school board approved by a vote of 5-2 a new specialized learning track for its Personalized Pathways program to go in effect at East, La Follette and Memorial high schools during the 2019-20 school year.

Ni Dandan:

Cheng Yanbin always knew his son, nicknamed Junjun, was different from other kids. Whenever his fellow kindergarteners played together in gleeful twos and threes, Junjun sat off to one side and didn’t join in the fun. “Other kids would laugh at a funny game or story, but his facial expression just stayed the same,” says Cheng.

The now 12-year-old Junjun — whose real name is not being used to protect his privacy — exhibited other strange behaviors, too. He obsessively pursued certain interests, compulsively repeated certain actions, and often struggled to contain his emotions. In 2011, when Junjun was 6 years old, Cheng took him to see a psychologist at a hospital in Beijing, where the family lives. The psychologist said Junjun had a condition that Cheng had never heard of: Asperger’s syndrome.

“It was a completely new concept to me,” says the middle-aged electronics engineer. “My wife was calmer about it, though. She said she did similar things when she was a kid, but gradually grew out of them.” Cheng adds that, during his wife’s childhood, her parents assumed that she was excessively disobedient, and never approached a doctor about her behavior.

No official data exists on how many children in China live with neurodevelopmental disorders, which include Asperger’s, autism spectrum disorder (ASD), and attention deficit hyperactivity disorder (ADHD). (Health care professionals generally categorize Asperger’s as a mild form of ASD.) A 2016 study by The Lancet concluded that China was home to the second-highest number of children under 5 who live with ASD, after India. The same study found that China had the highest number of children under 5 living with ADHD. (In the United States, around 1.1 percent of children between 3 and 17 years old have ASD, and around 6.8 percent have ADHD, according to the Centers for Disease Control and Prevention.)

A boy plays with his shadow at a school for children with autism in Taiyuan, Shanxi province, April 3, 2013. Hu Yuanjia/VCG

Julio Ochoa:

Children registering for school in Florida this year were asked to reveal some history about their mental health.

The new requirement is part of a law rushed through the state legislature after the February shooting at Marjory Stoneman Douglas High School in Parkland, Fla.

The state’s school districts now must ask whether a child has ever been referred for mental health services on registration forms for new students.

“If you do say, ‘Yes, my child has seen a counselor or a therapist or a psychologist,’ what does the school then do with that?” asks Laura Goodhue, who has a 9-year-old son on the autism spectrum and a 10-year-old son who has seen a psychologist. “I think that was my biggest flag. And I actually shared the story with a couple of mom friends of mine and said, ‘Can you believe this is actually a thing?’”

Travis Pillow, via a kind Deb Britt email:

Twenty-five years ago CRPE was founded on the idea of the school as the locus of change. Today we are reexamining our old assumptions in light of new technical possibilities, changes in the economy, and a recognition that even the most effective schools may need to develop new approaches to better serve students whose needs warrant more individualized learning pathways or supports. This post is part of a series on what the school or learning system of the next 25 years might look like.

Beginning in third grade, Brandon Berman got kicked out of school or pulled out by his mother almost every year. Autism, a rare form of muscular dystrophy, and a range of other complications that triggered seizures and required him to eat through a feeding tube made him a difficult fit for the public school system in Volusia County, Florida.

Ironically, each time another frustrated team of educators said their best efforts didn’t seem to be working, and his mother threw up her hands and pulled him out of school, he started making actual progress. Donna Berman took time away from her job as a nurse to teach him at home, full-time. The school district’s hospital/homebound program provided four hours of instruction per week with a certified teacher. With one-on-one attention, Donna started seeing signs of real progress. Brandon started learning to read. His instructor set up a mock grocery store in the family’s pantry where Brandon learned to compute change, making some headway in math.

The Economist:

ONE of the internet’s most odious conspiracy theorists has had his videos and podcasts removed from Apple, YouTube, Spotify and Facebook. Alex Jones (pictured), who has a radio show and runs a few websites, including Infowars, has raised doubts about the murders of 26 children and teachers in the Sandy Hook mass shooting, claiming the story was manufactured by gun-control advocates. He has suggested that America’s government was involved in the Oklahoma City bombing in 1993 and the September 11th terrorist attacks. He says that vaccinating children will give them autism. He repeatedly warns that America is on the brink of another civil war.

Mr Jones’s websites peddling this rubbish are still fully operational. But with the worlds’ biggest media platforms removing his pages and links over the past few days, he has lost direct access to millions of listeners and viewers. Mr Jones has, naturally, seen machinations in this too: the decisions by Apple, swiftly followed by others, to remove his material from their platforms feed with comic precision into his conspiracy theorising about mainstream media. “Apple, Spotify, Facebook and YouTube all banned Infowars within 12 hours of each other”, an Infowars writer wrote on August 6th. This is proof that the “purge was a co-ordinated effort” to meddle with the mid-term elections November rather than a good-faith effort to enforce the sites’ rules about hate speech.

Nicholette Zeliadt:

There are different views on whether ‘people with autism’ or ‘autistic people’ is the better way to refer to individuals on the spectrum. Some of the people quoted in this article prefer to say ‘autistic,’ but Spectrum’s style is to refer to ‘people with autism.’

It wasn’t until Anna Remington had nearly finished collecting data that she uncovered the flaw in her study.

A couple of years ago, Remington, then a lecturer at University College London, was investigating how people determine whether someone is trustworthy. She and her colleagues showed participants with the condition a series of images of unfamiliar faces, along with some hypothetical information about each person. They then asked the participants, “Would you approach this person — either in a social or financial context?”

Overwhelmingly, the participants with autism said “no,” even in response to characters who had been described as trustworthy. Eventually, one of them pulled her aside to explain: He wasn’t interested in “approaching” anyone.

Said Jilani:

Authors Jonathan Wai, a research fellow at Geisinger Health System at the Autism and Developmental Medicine Institute, and Kaja Perina, the editor-in-chief of Psychology Today, collected a sample of 1,979 employees working at two of America’s most prominent and influential newspapers, the New York Times and the Wall Street Journal, during 2016.

They set out with a simple question: How many of those employees attended elite schools for college (if they attended college)? The researchers sought to address the question of whether journalism, at the highest level, “is a profession only of the culturally elite,” or it is also “a profession of the cognitively elite.” They did not have access to individual employees’ SAT scores or academic performance, so, pulling information from staffers’ LinkedIn profiles, they looked at schools as a proxy for cognitive ability — with the assumption that highly selective schools mostly admit people with very high academic achievement.

There are, of course, problems with using SAT scores to define a “cognitive elite.” Factors such as race and class have been shown to affect performance on standardized tests, as well as admissions to elite schools.

Perina acknowledged that their study is not all-encompassing. “There are cognitively elite students at many schools; they just cluster in numbers in the ones we identified obviously,” she told The Intercept. “The fact is the combination of social networks plus high ability tends to get these people out of the Ivy Leagues and into these top papers with much more frequency.”

unit 9:

The Party is based on a concept by the author Lucy Hawking and is written by Sumita Majumdar, who drew on her own experiences as a person with autism in similar social situations. Throughout the film, viewers hear Layla’s thoughts, voiced by the autistic teenager Honey Jones. The storyline was developed after extensive focus groups and interviews with people on the autism spectrum as well as with input from the National Autistic Society, the Autism Research Trust and the University of Cambridge Autism Research Centre.

The visual and auditory effects in the film were based on scientific research about the kinds of symptoms seen in autistic individuals, such as difficulties with processing faces, and hypersensitivity to lights, loud noises and strong odours. Interviews conducted with autistic women also revealed they had issues with how things sound during a meltdown, including having difficulties distinguishing between sounds, hearing echoing voices and being unable to process the other information around them.

BBC:

About 700,000 people in the UK are on the autism spectrum, according to the National Autistic Society

Five times as many males as females are diagnosed

Autism is under-diagnosed in females

Gloria Orrigi:

The paradigm shift from the age of information to the age of reputation must be taken into account when we try to defend ourselves from ‘fake news’ and other misinformation and disinformation techniques that are proliferating through contemporary societies. What a mature citizen of the digital age should be competent at is not spotting and confirming the veracity of the news. Rather, she should be competent at reconstructing the reputational path of the piece of information in question, evaluating the intentions of those who circulated it, and figuring out the agendas of those authorities that leant it credibility.
 
 Whenever we are at the point of accepting or rejecting new information, we should ask ourselves: Where does it come from? Does the source have a good reputation? Who are the authorities who believe it? What are my reasons for deferring to these authorities? Such questions will help us to get a better grip on reality than trying to check directly the reliability of the information at issue. In a hyper-specialised system of the production of knowledge, it makes no sense to try to investigate on our own, for example, the possible correlation between vaccines and autism. It would be a waste of time, and probably our conclusions would not be accurate. In the reputation age, our critical appraisals should be directed not at the content of information but rather at the social network of relations that has shaped that content and given it a certain deserved or undeserved ‘rank’ in our system of knowledge.
 
 These new competences constitute a sort of second-order epistemology. They prepare us to question and assess the reputation of an information source, something that philosophers and teachers should be crafting for future generations.

Susan Du:

Over the past few months, Humboldt High teacher Rachel Wannarka started noticing a lot of kids being transferred to her special education math class after failing out of regular math.

While regular math takes place daily, special ed math is every other day, taught at a level several grades lower than what many of these students were used to. Wannarka knew the kids were smart enough to succeed in the mainstream class, so she started looking for an explanation why they couldn’t keep up.

Special ed students all have unique learning disabilities – autism, cognitive difficulties, emotional behavioral disorders. But federal law stresses students with disabilities are entitled to be taught alongside students without them. It’s the school’s job to provide the extra support to make that possible.

That’s why all special ed students have a custom Individualized Education Program (IEP), a legal document that spells out when an aide is needed at their side to help them focus, get their work done, and make it through the day without incident.

Suspecting that Humboldt wasn’t giving students the extra support they needed, Wannarka cross-referenced students’ IEPs with staff schedules. She found that dozens of kids weren’t getting the time with aides that the law requires.

As a result, they’re failing out of the less restrictive mainstream classes and squandering their potential in special ed classes, where they just keep falling further behind, says Wannarka.

Sandor Farkas:

One hour into the lecture, an audience member asked her whether she thinks Buchanan’s libertarian philosophy was motivated by “personal greed” or “malevolence,” to which she responded by speculating that support for individual liberty might actually be the result of a mental disorder.

“It’s striking to me how many of the architects of this cause seem to be on the autism spectrum—you know, people who don’t feel solidarity or empathy with others, and who have difficult human relationships sometimes,” she answered.”

Stuart Richie:

‘IQ tests just measure how good you are at doing IQ tests.’ This is the argument that is almost always made when intelligence-testing is mentioned. It’s often promoted by people who are, otherwise, highly scientifically literate. You wouldn’t catch them arguing that climate change is a myth or that vaccines might cause autism. But saying that IQ tests are useless is just as wrong as these notions: in fact, decades of well-replicated research point to IQ tests as some of the most reliable and valid instruments in all of psychological science.

So what does an IQ test – which might consist of, for example, shape-based puzzles, timings of how quickly you can check through lists of meaningless symbols, memory tests, and vocabulary measures – actually tell you? The strongest correlation is perhaps unsurprising: an IQ score is highly predictive of how people will do in school. One large study found that IQ scores at age 11 correlated 0.8 (on a scale of -1 to 1) with school grades at age 16. Surely this gives us some basis for calling these measures ‘intelligence tests’. But that’s just the beginning: higher IQ scores are predictive of more occupational success, higher income, and better physical and mental health. Perhaps the most arresting finding is that IQ scores taken in childhood are predictive of mortality. Smarter people live longer, and this association is still there after controlling for social class.

Lisa Speckhard Pasque:

Madison School Board members Anna Moffit and Mary Burke have announced they will be running for re-election in 2018.

In April, the terms will expire for seats 1 and 2 on the Madison Metropolitan School Board, currently occupied by Moffit and Burke. Burke has filed a declaration of candidacy with the Madison city clerk’s office and Moffit said she had done the same, although it’s not yet reflected on the city’s website.

Moffit ran unopposed for seat 1 in 2015, emphasizing advocacy for students with disabilities. Moffit has a son with autism and speaks out for people with disabilities outside her role as a school board member. She’s a former elementary school teacher and while on the board has been a proponent of Natural Circles of Support, a social and emotional support program for students of color.

All School Board seats are at-large, but the Seat 1 member oversees Allis, Glendale, Lindbergh, Schenk and Shorewood elementary schools, Sherman and Whitehorse middle schools and Memorial high school.

Madison has long tolerated disastrous reading results, despite spending far more than most.

2017 Madison School Board election notes and links.

More school board links

Madison spends far more than most, for average results.

David Z. Hambrick, Madeline Marquardt:

There are advantages to being smart. People who do well on standardized tests of intelligence—IQ tests—tend to be more successful in the classroom and the workplace. Although the reasons are not fully understood, they also tend to live longer, healthier lives, and are less likely to experience negative life events such as bankruptcy.

Now there’s some bad news for people in the right tail of the IQ bell curve. In a study just published in the journal Intelligence, Pitzer College researcher Ruth Karpinski and her colleagues emailed a survey with questions about psychological and physiological disorders to members of Mensa. A “high IQ society”, Mensa requires that its members have an IQ in the top two percent. For most intelligence tests, this corresponds to an IQ of about 132 or higher. (The average IQ of the general population is 100.) The survey of Mensa’s highly intelligent members found that they were more likely to suffer from a range of serious disorders.

The survey covered mood disorders (depression, dysthymia, and bipolar), anxiety disorders (generalized, social, and obsessive-compulsive), attention-deficit hyperactivity disorder, and autism. It also covered environmental allergies, asthma, and autoimmune disorders. Respondents were asked to report whether they had ever been formally diagnosed with each disorder, or suspected they suffered from it. With a return rate of nearly 75%, Karpinski and colleagues compared the percentage of the 3,715 respondents who reported each disorder to the national average.

Sarah Karp:

After Julie Rodriguez enrolled her 10-year-old autistic son at a public school on Chicago’s Southwest Side last year, she found herself navigating a maze of paperwork that she said seemed designed to prevent her son from getting the special education services he needed.

Rodriguez had just moved to the city from the suburbs, and she brought with her a legally binding special education plan for her son from his suburban public school. She also had a thick binder detailing his behavioral and academic problems, including a detailed analysis from some of the most highly respected doctors in Chicago.

In addition to autism, he suffers from attention deficit disorder, speech delays, and oppositional behavior disorder.

Kathryn Schulz:

I learned this fact about myself (and you) from one of the more unlikely books I lately committed to reading: “Teeth: A Very Short Introduction,” by Peter S. Ungar, a professor of anthropology at the University of Arkansas. Like its subject, “Teeth” is both a freestanding entity and part of a larger body: the Very Short Introduction series, a project of Oxford University Press. At present, that series consists of five hundred and twenty-six books; “Teeth” clocks in at No. 384. If you are so inclined, you can also read a Very Short Introduction to, among a great many other things, Rivers, Mountains, Metaphysics, the Mongols, Chaos, Cryptography, Forensic Psychology, Hinduism, Autism, Puritanism, Fascism, Free Will, Drugs, Nutrition, Crime Fiction, Madness, Malthus, Medical Ethics, Hieroglyphics, the Russian Revolution, the Reagan Revolution, Dinosaurs, Druids, Plague, Populism, and the Devil.

Some of these books are concise introductions to topics you might later wish to pursue in greater depth: Modern India, say, or Shakespeare’s Tragedies. Others, like “Teeth,” contain pretty much everything the average layperson would ever want or need to know. All of them, however, take their Very Short commitment seriously. The length of each book is fixed at thirty-five thousand words, or roughly a hundred and twenty pages. (See Very Short Introduction No. 500, “Measurement.”) Never mind that the Roman Empire got some four thousand pages from Edward Gibbon, and that was just to chronicle its demise; here it gets the same space as Circadian Rhythms, Folk Music, and Fungi.

Tom Chivers:

It started simply enough – with suggestions that her child should follow an unremarkable-sounding special diet. “They did these tests: a stool test and a urine test,” Layla (not her real name) tells BuzzFeed News. “I can’t remember where they were from – not the NHS, obviously, but some lab. The results had all these red markers.” The tests, from an alternative medicine practitioner who was recommended by and paid for by a major charity, apparently showed that Layla’s son, an autistic boy who was 3 at the time, had various issues with his gut and his metabolism. “I was shocked,” says Layla. “I didn’t realise – my son had all these deficiencies, these toxins in his system.”

The tests recommended a gluten-, casein-, and dairy-free diet. “It didn’t seem like a really big deal,” says Layla. “I thought, gluten, it’s bread and pasta – it’s not a massive thing.” The practitioner told her to monitor her son’s sleep and behaviour, and to expect improvements in the symptoms of his autism if they followed the diet.

Glenn Howatt and Faiza Mahamud:

As Minnesota confronts its second measles outbreak in seven years, public health officials are battling to contain the disease while also trying to educate parents in the face of an organized opposition.

As happened in 2011, anti-vaccine activists are reaching out to Minnesota’s Somali community, where both outbreaks have been centered, with messages that reinforce the discredited belief that vaccines cause autism.

On Sunday afternoon, a coalition of anti-vaccine organizations plans a meeting at the Brian Coyle Community Center on Minneapolis’ West Bank in an effort to bring their message to Somali families, saying “The epidemic is autism, not measles.”

Travis M. Andrews:

Along with her twin sister, she was born 26 weeks early. At 1 pound 12 ounces, she weighed slightly less than the healthy Keeley. Then, 10 hours into life, Kara suffered a brain hemorrhage. Seventeen years later, she’s lucky to be alive. But she has cerebral palsy and severe autism, which in her case causes compulsive self-injurious behavior that began with she was 4 years old.

“It’s a terrible sight to see,” her father, Mark Zartler, told The Washington Post via telephone from his home in Richardson, Tex. “She hits herself in the face repeatedly. She gets into a loop, and she can’t really stop. Sometimes she can self-recover, but other times it just extends and extends and extends.”

Peter Hotez:

It’s looking as if 2017 could become the year when the anti-vaccination movement gains ascendancy in the United States and we begin to see a reversal of several decades in steady public health gains. The first blow will be measles outbreaks in America.

Measles is one of the most contagious and most lethal of all human diseases. A single person infected with the virus can infect more than a dozen unvaccinated people, typically infants too young to have received their first measles shot. Such high levels of transmissibility mean that when the percentage of children in a community who have received the measles vaccine falls below 90 percent to 95 percent, we can start to see major outbreaks, as in the 1950s when four million Americans a year were infected and 450 died. Worldwide, measles still kills around 100,000 children each year.

The myth that vaccines like the one that prevents measles are connected to autism has persisted despite rock-solid proof to the contrary. Donald Trump has given credence to such views in tweets and during a Republican debate, but as president he has said nothing to support vaccination opponents, so there is reason to hope that his views are changing.

Brian M. Rosenthal:

During the first week of school at Shadow Forest Elementary, a frail kindergartner named Roanin Walker had a meltdown at recess. Overwhelmed by the shrieking and giggling, he hid by the swings and then tried to escape the playground, hitting a classmate and biting a teacher before being restrained.

The principal called Roanin’s mother.

“There’s been an incident.”

Heidi Walker was frightened, but as she hurried to the Humble school that day in 2014, she felt strangely relieved.

She had warned school administrators months earlier that her 5-year-old had been diagnosed with a disability similar to autism. Now they would understand, she thought. Surely they would give him the therapy and counseling he needed.

Leif Reigstad:

The video was posted on Facebook as a trailer for Vaxxed, a documentary film directed by disgraced former doctor Andrew Wakefield, the author of a since-retracted study that linked vaccines with autism. The film, which doubled down on his research, drew so much criticism from actual doctors that it was pulled from the Tribeca Film Festival this spring. The trailer preceded a longer eleven-minute promotional video released on Tuesday featuring LaHood and his wife, who claim vaccinations are responsible for health problems that their two children have developed.

On Wednesday, LaHood continued his anti-vaccination campaign, posting a long rant on Facebook encouraging parents to “educate yourselves for the sake of your precious children,” and to “stay away from rhetoric and look at hard facts.” As of Thursday morning, the post had garnered nearly 1,500 comments. LaHood’s responses to some of the more critical commenters are politely defensive, though he does call one commenter a “fool with your head in the sand” and “the typical zealot without an open mind.”

BBC News:

Donald Grey Triplett was the first person to be diagnosed with autism. The fulfilling life he has led offers an important lesson for today, John Donvan and Caren Zucker write.

After Rain Man, and The Curious Incident of the Dog in the Night-time, the next great autism portrayal the stage or screen might want to consider taking on is the life of one Donald Grey Triplett, an 82-year-old man living today in a small town in the southern United States, who was there at the very beginning, when the story of autism began.

The scholarly paper which first put autism on the map as a recognisable diagnosis listed Donald as “Case 1” among 11 children who – studied by Baltimore psychiatrist Leo Kanner – crystallised for him the idea that he was seeing a kind of disorder not previously listed in the medical textbooks. He called it “infantile autism”, which was later shortened to just autism.

University of Cambridge:

Autistic traits are not the same as having a diagnosis of autism; instead, these are characteristics of personality and behaviour that are found throughout the general population and are linked to what is seen in the clinical condition of autism. Everyone has some autistic traits – such as difficulty in taking another person’s point of view, difficulty in switching attention flexibly, and excellent attention to detail – and there is a wide range in the population. 15 years ago a team of scientists at the University of Cambridge developed a way of measuring these, using a questionnaire called the Autism Spectrum Quotient, or AQ. This comprises 50 questions, each one representing one autistic trait.

The Economist:

Neurotribes: The Legacy of Autism and the Future of Neurodiversity. By Steve Silberman. Avery; 544 pages; $29.95. Allen & Unwin; £16.99.

EVERYTHING about autism, which is among the most common and the most slippery of mental conditions, is contested. The American Psychiatric Association, which determines what ailments American insurance companies will pay to treat, classifies it as a disorder. Many parents of autistic children are desperately searching for a cure, and find themselves easy prey for people who overpromise, selling remedies that have no scientific basis. Plenty of other people think that autism—which is characterised, among other things, by an inward focus that makes it hard to abide by the conventions of social behaviour—is not a disorder at all, and therefore has no need of a cure. America’s Centres for Disease Control and Prevention thinks that one in 68 children in the country have at least a touch of autism, which if true means there are more autistic Americans than Jewish ones. This too is contested.

The Economist:

THE REBECCA SCHOOL for autistic children occupies all five floors of a building in midtown Manhattan. Its rooftop playground has a fine view of the Empire State Building. It features colourful classrooms and lots of places for children to lie down and recover from the sensory overload often suffered by autistic people. “My body doesn’t feel safe,” says one boy curled up in a corridor, asking to be left alone.

Kayleb Moon-Robinson is a 12-year-old boy who lives in Virginia. One day at school, he kicked a trash can and was charged with disorderly conduct in juvenile court. A few weeks later, he disobeyed a new rule (made just for him) that he stay behind in the classroom while his peers left. When the school resource officer (SRO) arrived to take him to the principal’s office for disobedience, Kayleb reportedly struggled and swore. The officer allegedly slammed the boy down on a desk and handcuffed him. Kayleb is now being charged with felony assault on a police officer, and his future is very much in doubt.

Kayleb is autistic and African-American. The state of Virginia wants to brand him a criminal. The Center for Public Integrity names it as the state most likely to send students to jail. Virginia was also home to the Reginald “Neil” Latson case, in which a young man with autism encountered a police officer, didn’t comply with orders, started walking away and ended up in a brutal fight. He spent years in solitary confinement as a result before finally being pardoned.

Daniela Hernandez:

Lee and her husband, who was getting his doctorate in computer science at the University of California, Berkeley, discovered their son’s condition was serious enough that they wouldn’t be able to go back to the life they had as game developers in South Korea. The family decided to stay in the U.S. Lee started toying with the idea of creating iPhone apps for children with special needs.

“Maybe I can develop something for my child to help him learn and help him explore the world,” Lee remembers thinking. But kids with autism sometimes have trouble with coordination and Lee found the iPhone screen was too small to support apps with which her son could interact. But when Apple launched the iPad with its bigger screen in April 2010, Lee and her husband saw an opening. They started a company, LocoMotive Labs, to develop a suite of iPad apps designed especially for children with autism. When he was about five, their son had been diagnosed with autism.

Hank Long:

Public schools are required by state and federal law to accept students with disabilities and to make appropriate accommodations for their learning.
So when a district – despite its best of intentions – fails to meet the individual educational needs of such students, where are the students and their families to turn?

That’s an issue Amy Christensen-Bruce grappled with for years before she discovered Academy of Whole Learning. The private school located in St. Louis Park primarily serves students with Autism Spectrum Disorder. Christensen-Bruce said it was the first school that was able gain her confidence that the unique needs of her now fourth-grade son – who has autism – were being met.
Whether he was enrolled at a local public school or a charter school, Christensen-Bruce said her child struggled to learn at the rate she knew he was capable of.

Philip Ball:

We’re surely now in the Age of the Brain. In the United States, the BRAIN Initiative, announced in 2013 and with a projected cost of $3bn, aims to map the activity of every neuron in the brain—first, those of mice and other animals, then of humans. The European Union has assigned €1bn to the ten-year Human Brain Project, which intends to deduce the brain’s wiring circuit in order to build a complete computer simulation of it. And now Japan has launched its own ten-year initiative, called Brain/MINDS, with a focus on understanding brain diseases and malfunctions such as Parkinson’s, schizophrenia and autism.

Of all these projects, the Japanese effort is the most modest, and likely to be the most useful. It will use a combination of brain imaging and genetics to try to figure out what goes wrong and why, in particular using marmosets as a model for humans. The European project, meanwhile, has already run into serious problems. Many neuroscientists are concerned that its ambitions are premature, and last July 130 researchers from labs around the world signed an open letter complaining of the “overly narrow approach, leading to a significant risk that it would fail to meet its goals.” The signatories say that the project could prove to be a huge waste of money, and criticize what they see as the opaque and unaccountable way the project is being run.

Some of those complaints are about infrastructure and management. But some go to the heart of what modern brain science is attempting to do, and what its realistic limits are. Those issues are searchingly explored in a new book, The Future of the Brain, edited by cognitive scientist Gary Marcus and neuroscientist Jeremy Freeman, which I have recently reviewed for Prospect.

The Economist:

DR BOB SEARS, a paediatrician from Orange County, California, does not like to call his patients “free-riders”. True, he specialises in treating vaccine-sceptics, those families who resent being told to immunise their children against nasty diseases, from measles to whooping cough. It is also the case that, as a trained doctor, he believes that immunisation works. He agrees that some scary illnesses have almost vanished in America because more than 90% of children are inoculated against them, creating a herd immunity that leaves diseases with few places to lurk. Yet he differs from many doctors in the conclusion that he draws from that success.

Precisely because most children are immunised, he tells parents that it is probably safe to skip or delay jabs for their offspring. This strategy amounts to “hiding in the herd”, he says delicately, as he sips a late-afternoon coffee near his surgery. Put another way, his patients worry more than most about possible side-effects from vaccinations, above all the (thoroughly discredited) claim that vaccines cause autism. Dr Bob—as he is known to fans of “The Vaccine Book”, his best-selling guide to “selective” immunisation—does not say that worried parents are right. He just thinks that, on balance, they can safely indulge their anxieties by “taking advantage of the herd all around them.” When pushed, he makes “no claim” that the alternative vaccine plans that he offers (involving fewer jabs, or jabs administered over a longer period than most doctors recommend) are safer. He concedes that if everyone refused vaccinations, some diseases would roar back.

Wisconsin Reading Coalition, via a kind email:

IDA Dyslexia Handbook: What Every Family Should Know is now available online

Free Open LETRS Training An overview of the professional development program Language Essentials for Teachers of Reading and Spelling. This session is especially for district administrators: superintendents, curriculum directors, special education directors, reading specialists, principals, etc. Let your district know you would like a few key people to attend!

Presented by Pati Montgomery, former executive director of the Colorado Office Of Literacy

Aimed at principals and other administrators responsible for raising reading achievement
Monday, December 8: WCTC Pewaukee
Wednesday, December 10: Madison College Truax Campus
8:00 – 3:30, lunch provided
Limit: two people per district
RSVP by November 15 to Kevin Kuckkan, 866-340-3692, kevin.kuckkan@voyagersopris.com

Lindamood-Bell Informational Session for Professionals and Parents

Learn about the Lindamood-Bell School Year Glendale Learning Clinic opening December 1st for 8 weeks: addressing dyslexia, hyperlexia, ADD/HD, and autism spectrum disorders
Thursday, November 20, 5:00 pm
Logemann Community Center, Ivy Room, 6100 W. Mequon Road, Mequon WI
Reserve your space by calling 888-414-1720 or email info@lindamoodbell.com

December repeat of Dyslexia 101 at WILDD

December 13, 9:00 – 12:00
636 Grand Canyon Drive, Madison 53719
$10
Call 608-824-8980 or email madison@wildd.org to register

Spotlight on Dyslexia: Interactive Virtual Conference from Learning Ally

Keynote speaker Dana Buchman (fashion designer and founding chair of the Promise Project); panel members Barbara Wilson (Wilson Language Corporation), Kelli Sandman-Hurley (Dyslexia Training Institute), Davis Flink (Eye to Eye), Ben Foss (Headstrong Nation), Susan Barton (Bright Solutions for Dyslexia), and Jamie Martin (Assistive Technology)
Friday, December 5, 8:30 am – 3:30 pm CST
Learning Ally members $59 ($89 after 11/15); non-members $89 ($119 after 11/15)
Discounted Early Bird registration until November 15

Ed Week Webinar Every Child Reading with Margie Gillis now available on demand; Powerpoint available at http://www.edweek.org/media/102814presentation.pdf

Radiolab:

3 months later a specialist sat Ron and Cornelia down and said the word that changed everything for them: Autism.

In this episode, the Suskind family finds an unlikely way to access their silent son’s world. We set off to figure out what their story can tell us about Autism, a disorder with a wide spectrum of symptoms and severity. Along the way, we speak to specialists, therapists, and advocates including Simon Baron-Cohen, Barry and Raun Kaufmann, Dave Royko, Geraldine Dawson, Temple Grandin, and Gil Tippy.

Heather Vogell:

Carson Luke, a young boy with autism, shattered bones in his hand and foot after educators grabbed him and tried to shut him into a “scream room.” Kids across the country risked similar harm at least 267,000 times in just one school year.

he room where they locked up Heather Luke’s 10-year-old son had cinder block walls, a dim light and a fan in the ceiling that rattled so insistently her son would beg them to silence it.

Sometimes, Carson later told his mother, workers would run the fan to make him stop yelling. A thick metal door with locks—which they threw, clank-clank-clank—separated the autistic boy from the rest of the decrepit building in Chesapeake, Virginia, just south of Norfolk.

The room that officials benignly called the “quiet area” so agitated the tall and lanky blond boy that one day in March 2011, his mother said, Carson flew into a panic at the mere suggestion of being confined there after an outburst. He had lashed out, hitting, scratching and hurling his shoes. Staff members held him down, then muscled him through the hallway and attempted to lock him in, yet again.

Gail Robinson :

Eleven-year-old Matthew Votto sits at an iPad, his teacher at his elbow. She holds up a small laminated picture of a $20 bill.

“What money is this?” she asks. Matthew looks at the iPad, touches a square marked “Money Identification,” and then presses “$20.” “Twenty,” the tablet intones, while the teacher, Edwina Rogers, puts another sticker on a pad, bringing Matthew closer to a reward.

They race through more questions. “What day of the week is it?” “What is the weather outside?” “What money is this?” In most cases Matthew, who has autism, answers verbally, but he is quicker and seems more comfortable on the device.

Jennifer Richler:

A few days ago, an old friend sent me a panicked email. She had just finished reading Ron Suskind’s beautiful essay in the New York Times Magazine about raising a son with autism: “Reaching My Autistic Son Through Disney.” Suskind describes how, at almost 3 years of age, his son Owen “disappeared.” The child was once “engaged, chatty, full of typical speech,” but then he stopped talking, lost eye contact, even struggled to use a sippy cup.

Owen was eventually diagnosed with a regressive form of autism, which Suskind says affects about a third of children with the disorder. “Unlike the kids born with it,” he continues, “this group seems typical until somewhere between 18 and 36 months—then they vanish.”

That was the line that alarmed my friend, whose son is nearing his third birthday. “What is this ‘regressive autism?’ ” she asked me, the resident autism expert in her peer group. (I conducted research on autism and regression in autism before becoming a freelance writer.) “I thought we were out of the woods!”

The Economist:

AUTISM is a strange condition. Sometimes its symptoms of “social blindness” (an inability to read or comprehend the emotions of others) occur alone. This is dubbed high-functioning autism, or Asperger’s syndrome. Though their fellow men and women may regard them as a bit odd, high-functioning autists are often successful (sometimes very successful) members of society. On other occasions, though, autism manifests as part of a range of cognitive problems. Then, the condition is debilitating. What is common to those on all parts of the so-called autistic spectrum is that they are more often men than women—so much more often that one school of thought suggests autism is an extreme manifestation of what it means, mentally, to be male. Boys are four times more likely to be diagnosed with autism than girls are. For high-functioning autism, the ratio is seven to one.

Moreover, what is true of autism is true, to a lesser extent, of a lot of other neurological and cognitive disorders. Attention deficit hyperactivity disorder (ADHD) is diagnosed around three times more often in boys than in girls. “Intellectual disability”, a catch-all term for congenital low IQ, is 30-50% more common in boys, as is epilepsy. In fact, these disorders frequently show up in combination. For instance, children diagnosed with an autistic-spectrum disorder often also receive a diagnosis of ADHD.

David Dobbs:

If you want a look at a high-profile field dealing with a lot of humbling snags, peer into #ASHG2013, the Twitter hashtag for last week’s meeting of the American Society of Human Genetics, held in Boston. You will see successes, to be sure: Geneticists are sequencing and analyzing genomes ever faster and more precisely. In the last year alone, the field has quintupled the rate at which it identifies genes for rare diseases. These advances are leading to treatments and cures for obscure illnesses that doctors could do nothing about only a few years ago, as well as genetic tests that allow prospective parents to bear healthy children instead of suffering miscarriage after miscarriage.
But many of the tweets–or any frank geneticist–will also tell you stories of struggle and confusion: The current list of cancer-risk genes, the detection of which leads some people to have “real organs removed,” likely contains many false positives, even as standard diagnostic sequencing techniques are missing many disease-causing mutations. There’s a real possibility that the “majority of cancer predisposition genes in databases are wrong.” And a sharp team of geneticists just last week cleanly dismantled a hyped study from last year that claimed to find a genetic signature of autism clear enough to diagnose the risk of it in unborn children.

Amanda Winkler:

We felt like our family was totally violated by the sheriff’s department and the school district,” says Doug and Catherine Snodgrass of Temecula, California. Last December their 17-year-old autistic high school son was arrested after twice buying marijuana for an undercover Riverside county police officer.
The undercover operation, titled “Operation Glass House,” spanned a few months and included undercover officers in three area high schools: Chaparral, Temecula Valley, and Rancho Vista Continuation. The officers posed as regular high school students and would ask other students for drugs. Twenty-two students were arrested – the majority of them are reported to be special needs students like the Snodgrass’ son.
Their son, who wished to remain unnamed, is noticeably handicapped and has been diagnosed with autism as well as bipolar disorder, Tourettes, and several anxiety disorders.
“Everyday is a challenge for him,” says his father.
Their son’s list of disabilities have many in the community wondering why he was targeted in this undercover drug operation.

David Mitchell:

The 13-year-old author of The Reason I Jump invites you, his reader, to imagine a daily life in which your faculty of speech is taken away. Explaining that you’re hungry, or tired, or in pain, is now as beyond your powers as a chat with a friend. I’d like to push the thought-experiment a little further. Now imagine that after you lose your ability to communicate, the editor-in-residence who orders your thoughts walks out without notice. The chances are that you never knew this mind-editor existed, but now that he or she has gone, you realize too late how the editor allowed your mind to function for all these years. A dam-burst of ideas, memories, impulses, and thoughts is cascading over you, unstoppably. Your editor controlled this flow, diverting the vast majority away, and recommending just a tiny number for your conscious consideration. But now you’re on your own.
Now your mind is a room where 20 radios, all tuned to different stations, are blaring out voices and music. The radios have no off-switches or volume controls, the room you’re in has no door or window, and relief will come only when you’re too exhausted to stay awake. To make matters worse, another hitherto unrecognized editor has just quit without notice–your editor of the senses. Suddenly, sensory input from your environment is flooding in, too, unfiltered in quality and overwhelming in quantity. Colors and patterns swim and clamor for your attention. The fabric softener in your sweater smells as strong as air freshener fired up your nostrils. Your comfy jeans are now as scratchy as steel wool. Your vestibular and proprioceptive senses are also out of kilter, so the floor keeps tilting like a ferry in heavy seas, and you’re no longer sure where your hands and feet are in relation to the rest of you. You can feel the plates of your skull, plus your facial muscles and your jaw; your head feels trapped inside a motorcycle helmet three sizes too small which may or may not explain why the air conditioner is as deafening as an electric drill, but your father–who’s right here in front of you–sounds as if he’s speaking to you from a cellphone, on a train going through lots of short tunnels, in fluent Cantonese. You are no longer able to comprehend your mother tongue, or any tongue: From now on, all languages will be foreign languages. Even your sense of time has gone, rendering you unable to distinguish between a minute and an hour, as if you’ve been entombed in an Emily Dickinson poem about eternity, or locked into a time-bending sci-fi film. Poems and films, however, come to an end, whereas this is your new ongoing reality. Autism is a lifelong condition. But even the word autism makes no more sense to you now than the word 自閉症 or αυτισµός or .

Tom Cutterham:

Christopher Boone loves prime numbers and hates being touched. Oskar Schell has a hyperactive imagination. He won’t swear, but he will say, “Succotash my Balzac, dipshiitake.” The behavioral problems of Christopher and Oskar, the respective narrators and protagonists of The Curious Incident of the Dog in the Night Time and Extremely Loud and Incredibly Close, are never explicitly labeled as autistic spectrum disorders, In a brief statement, worth reading, Mark Haddon has written that “Curious Incident is not a novel about Asperger’s… If anything, it’s a novel about difference, about being an outsider.”but it has been easy for readers to identify them in these terms. As much as both novels have relied on an existing public understanding of autism, they have each — supported by stage and screen adaptations — also helped to construct it. More than any other two books, these have encoded the autistic perspective into a literary trope with its own set of mechanisms and effects.
While both the novels have male protagonists, and males are about four times more likely to have autistic spectrum disorders than females, the most prominent autobiographies of autism have been by women: See Temple Grandin’s Emergence and Donna Williams’ Nobody Nowhere.What distinguishes the autistic person is a difficulty gaining access to other people’s minds. TNI Vol. 18: Family Planning is out now. Subscribe for $2 and get it today. He lacks the ability to reconstruct and predict thoughts, feelings, desires, and reactions. The neurologist Simon Baron-Cohen has called this “mindblindness.” Those who don’t suffer from this problem, on the other hand, unconsciously translate myriad physical and symbolic cues — subtext, allusion, tone, and all the elements of body language. In Baron-Cohen’s terms, we can read minds.

Emily Le Coz:

The last word Watson Dollar spoke before autism erased his ability to do so was “lights.”
The chubby cheeked toddler lay in his father’s arms as anesthesia, administered for an ear-tube surgery, dimmed his consciousness. Head lolling back, body going limp, Watson gazed at the fluorescent lamps above him, uttering the one-syllable noun.
Then he closed his eyes and never spoke again. That was 20 years ago.
In the two months between Halloween and Christmas of 1992, Watson had lost almost of all of his 150-word vocabulary along with an interest in the world.
His parents initially failed to notice the change, chalking up the subtle signs to stubbornness or fatigue or the ever-changing nature of a developing child.
By New Year’s, though, the difference was both inescapable and worrisome.

K Jackson:

Some people see computers as little more than gaming consoles and shopping tools. Recently developed electronics, however, have revolutionized education for children with disabilities. If you know a child with disabilities who is struggling, you might want to explore some of these devices.
Technology for Kids With Autism
Children with autism often don’t develop typical communication skills. It takes years and years of therapy for some of these children to start using simple language. Just because a child cannot speak does not mean that he or she doesn’t have something to say.
That’s where revolutionary electronics come in. For years, counselors have used picture cards to communicate with non-verbal children. Now, they can use some of these apps that let autistic kids express practically any thought or feeling. They just load the app on a laptop of your choice so the kids can point and click their way to expression.

Colin Macilwain:

The United States spent more than US$3 billion last year across 209 federal programmes intended to lure young people into careers in science, technology, engineering and mathematics (STEM). The money goes on a plethora of schemes at school, undergraduate and postgraduate levels, all aimed at promoting science and technology, and raising standards of science education.
In a report published on 10 April, Congress’s Government Accountability Office (GAO) asked a few pointed questions about why so many potentially overlapping programmes coexist. The same day, the 2014 budget proposal of President Barack Obama’s administration suggested consolidating the programmes, but increasing funding.
What no one asked was whether these many activities actually benefit science and engineering, or society as a whole. My answer to both questions is an emphatic ‘no’.
Students with autism gravitate toward STEM majors
Taken individually, of course, these programmes are all very cuddly and wonderful. They are keenly pursued by governments around the world — particularly in countries that fret about their economic competitiveness, such as the United Kingdom and the United States.
But taken together, these schemes — which allocate perhaps $600 to each child passing through the US education system — constitute bad public policy. Government promotion of science careers ultimately damages science and engineering, by inflating supply and depressing demand for scientists and engineers in the employment market.

Aleks Eror:

It’s not exactly news that China is setting itself up as a new global superpower, is it? While Western civilization chokes on its own gluttony like a latter-day Marlon Brando, China continues to buy up American debt and lock away the world’s natural resources. But now, not content to simply laugh and make jerk-off signs as they pass us on the geopolitical highway, they’ve also developed a state-endorsed genetic-engineering project.
At BGI Shenzhen, scientists have collected DNA samples from 2,000 of the world’s smartest people and are sequencing their entire genomes in an attempt to identify the alleles which determine human intelligence. Apparently they’re not far from finding them, and when they do, embryo screening will allow parents to pick their brightest zygote and potentially bump up every generation’s intelligence by five to 15 IQ points. Within a couple of generations, competing with the Chinese on an intellectual level will be like challenging Lena Dunham to a getting-naked-on-TV contest.
Geoffrey Miller, an evolutionary psychologist and lecturer at NYU, is one of the 2,000 braniacs who contributed their DNA. I spoke to him about what this creepy-ass program might mean for the future of Chinese kids.

Related: New data reveal scale of China abortions and Eugenics.
Many links here.
Technology Review:

In its scientific work, BGI often acts as the enabler of other people’s ideas. That is the case in a major project conceived by Steve Hsu, vice president for research at Michigan State University, to search for genes that influence intelligence. Under the guidance of Zhao Bowen, BGI is now sequencing the DNA of more than 2,000 people–mostly Americans–who have IQ scores of at least 160, or four standard deviations above the mean.
The DNA comes primarily from a collection of blood ­samples amassed by Robert Plomin, a psychologist at King’s College, London. The plan, to compare the genomes of geniuses and people of ordinary intelligence, is scientifically risky (it’s likely that thousands of genes are involved) and somewhat controversial. For those reasons it would be very hard to find the $15 or $20 million needed to carry out the project in the West. “Maybe it will work, maybe it won’t,” Plomin says. “But BGI is doing it basically for free.”
From Plomin’s perspective, BGI is so large that it appears to have more DNA sequencing capacity than it knows what to do with. It has “all those machines and people that have to be fed” with projects, he says. The IQ study isn’t the only mega-project under way. With a U.S. nonprofit, Autism Speaks, BGI is being paid to sequence the DNA of up to 10,000 people from families with autistic children. For researchers in Denmark, BGI is decoding the genomes of 3,000 obese people and 3,000 lean ones.

Amy SF Lutz:

Earlier this year, I was out to dinner with a friend and our combined eight kids. My 14-year-old son, Jonah, who has autism, was very excited about the imminent arrival of his hamburger and french fries, so he was acting as he does when he’s happy: bouncing in his seat, clapping his hands, and vocalizing a mishmash of squawks and catchphrases from his favorite Sesame Street videos. He wasn’t exceedingly loud, but the oddness of his behavior had clearly caught the attention of an older gentleman at the one other table occupied at that early hour.
“Shhhhhhh,” he hissed from across the room.
Everyone at the table instantly froze–except, of course, for Jonah. “I’m sorry,” I explained, rising from my seat and taking a few steps toward him so I wouldn’t have to holler. “My son is autistic … ”
“Oh, sorry,” he said.
“He’s not trying to disturb you intentionally … “

Katherine Beals:

Children have long been graded not just for academics, but also for elements of “character” — particularly behavior and emotional maturity. However, in the last few decades, socially eccentric children have seen their awkwardness or aloofness factored into their grades in math, language arts, and social studies. Ironically, this trend has coincided with a rise in diagnoses of autistic spectrum disorders.
For children on the autism spectrum, new social studies curricula pose a particular challenge. Once restricted to readings, worksheets, and essays on history, government, and politics, the subject increasingly requires students to reflect on their connections within their local communities. They are asked to present projects to their classmates (even in primary school), spend much of class time working in groups, and evaluate scenarios such as this one, from a worksheet for 3rd graders:

Erin Richards:

When Miriam Oakleaf was 10 months old, her parents noticed something was wrong.
By 2 1/2 she had been formally diagnosed with autism, epilepsy and a rare skin and central nervous system condition called linear nevus sebaceous syndrome.
Now 8 and in second grade at Crestwood Elementary School in Madison, Miriam’s schooling requires extensive support and planning from a variety of education professionals – administrators, therapists, teachers and aides – in addition to her parents.
The story of Miriam and children like her is at the heart of a $21 million proposal in Gov. Scott Walker’s state budget that would allow 5% of kids with disabilities in Wisconsin to attend private or public schools outside their home districts on a taxpayer-funded voucher.
The proposal has driven a wedge through the state’s network of special-needs parents. Some believe it would open up more schooling options for their children while others contend it will drain more resources from their local public schools.

Katie Rophie:

As the writer Andrew Solomon, his husband, John Habich, and their three-year-old son George descend the stone steps, they bring a burst of colour to the dark grey underworld of the New York Transit Museum: John in brilliant red corduroys, George in an orange-striped shirt, Andrew in a bright-blue striped shirt and scarlet socks.
I have brought along my son, Leo. Being three, the boys don’t really talk to each other, they run. There are antique buses to drive, models of the third rail to electrify, subways to bounce around.
Solomon has just published his spectacularly successful book Far from the Tree: A Dozen Kinds of Love, which chronicles the stories of children who, for various reasons, are extremely different from their parents. The book took 11 years to write and its 702 pages include autism, schizophrenia, Down’s syndrome, child prodigies, transgendered children, deafness, dwarfism, and crime. Each chapter tackles a different subject, seen through interviews with numerous families.

Nature:

Mutations generate sequence diversity and provide a substrate for selection. The rate of de novo mutations is therefore of major importance to evolution. Here we conduct a study of genome-wide mutation rates by sequencing the entire genomes of 78 Icelandic parent-offspring trios at high coverage. We show that in our samples, with an average father’s age of 29.7, the average de novo mutation rate is 1.20 × 10−8 per nucleotide per generation. Most notably, the diversity in mutation rate of single nucleotide polymorphisms is dominated by the age of the father at conception of the child. The effect is an increase of about two mutations per year. An exponential model estimates paternal mutations doubling every 16.5 years. After accounting for random Poisson variation, father’s age is estimated to explain nearly all of the remaining variation in the de novo mutation counts. These observations shed light on the importance of the father’s age on the risk of diseases such as schizophrenia and autism.

Allison Hertog:

Mississippi recently became the first state in the nation to adopt a public and private school choice program in which state and federal monies are provided directly to schools which parents choose. Aimed at students with dyslexia, it’s also the second special needs school choice program in the country designed for children with a single type of disability. (Ohio’s Autism Scholarship Program enacted in 2003 was the first.)
What makes this new program interesting is that it may be a starting point for other state legislatures where special needs voucher bills have failed due to concerns about parent accountability – Wisconsin comes to mind – or where special needs voucher laws have come under increased scrutiny due to reports of private school abuse of public money – Florida comes to mind.
Mississippi’s program morphed from a dyslexia screening and treatment bill (supported by a governor who struggled with the learning disorder) into a school choice measure during the proverbial sausage-making legislative process. It’s not as carefully or as broadly designed as it could have been. It also appears there’s currently only one school in the state which is specialized enough to meet the exceedingly specific criteria to participate. But nonetheless, it succeeds in incentivizing the growth of more highly-accountable school options for parents.

Alan Borsuk:

The 10-year flight of Wings Academy will end Tuesday. The closing of the small school on the south side where the vast majority of students qualify for special education leaves me thinking that nationwide we haven’t worked hard enough on figuring out what to aim for with special ed kids and how to figure out if we’re achieving it.
To what degree should we set the same goals for at least a large portion of special ed kids as for other kids, largely measured by test scores? Is success on less measurable fronts – personal development and preparation for adulthood – good enough? Better? Settling for too little?
Wings was an independent charter school, authorized to operate by the Milwaukee School Board. It had the atmosphere of a friendly, energetic, but, as one staff member put it, squirrelly family. Its program included phonics-oriented reading instruction, individualized and project-based work in many classes, tae kwon as its physical education focus, and a lot of relationship building among staff, students and families.
Test scores at Wings were, as Nicola Ciurro, co-founder and head of the school, put it, terrible. “We always knew that,” she said. Among 10th-graders in last fall’s testing, 34% were proficient in reading, 6% in math.
About 80% of the 150 students, who ranged from first- to 12th-graders, had attention deficit hyperactivity disorder, learning disorders, autism, Asperger’s syndrome, dyslexia or other special circumstances. Many of the other 20% were “gray area” kids when it came to special needs, Ciurro said.

Associated Press:

One in 3 young adults with autism have no paid job experience, college or technical schooling nearly seven years after high school graduation, a study finds. That’s a poorer showing than those with other disabilities including those who are mentally disabled, the researchers said.
With roughly half a million autistic kids reaching adulthood in the next decade, experts say it’s an issue policymakers urgently need to address.
The study was done well before unemployment peaked from the recession. The situation today is tough even for young adults who don’t have such limitations.

Oliver Chou:

Global public health crisis and a fast-growing epidemic: these were the stark terms used by experts at an international summit held here last weekend to describe the cost of autism. The descriptions are backed up by grim figures. In South Korea, as many as one in 38 children are diagnosed as having autism spectrum disorders.
The US Centres for Disease Control and Prevention reports prevalence at about one in 88 youngsters in the country. Hong Kong doesn’t have an official estimate, but groups say the number ranges from 70,000 to 200,000, depending on the screening criteria.