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Funny, it isn't hard to make a comedy show that autistic adults can enjoy too

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Funny, it isn't hard to make a comedy show that autistic adults can enjoy too

Joshua Meyrowitz stepped up to the stage at the Laugh Factory in Hollywood and announced himself to the crowd as “your fellow autistic,” spurring whoops and applause.

“One of the hardest things as an autistic person is being able to relate to people,” the comedian said, “and as a stand-up comic, you are required to relate to people.

“With an audience full of autistic people, I don’t have to relate to s— now!” Meyrowitz declared as laughter rippled through the room. “I’m in the zone, brother!”

It was a Wednesday night at the storied club on Sunset Boulevard, and in many ways, the show unspooling on its brightly lit stage sounded like any other comedic lineup in the Sunset Strip area, with punchlines about genitalia pics, politics, married life and the grosser side effects of Ozempic.

But its goal was a lofty one: Make the raucous world of stand-up comedy a welcoming place for people whose brains work differently. This show was playing out before a crowd full of autistic adults and other neurodivergent people, many joined by their neurotypical family and friends.

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The tweaks to a typical show were small ones: A “chill-out space” for anyone who needed to step out for a break. Lowering the volume on the music playing inside and avoiding any sudden, noisy changes in music between acts. Letting the comedians know to lay off if someone jumped up or blurted something out.

Comedian Jeremiah Watkins performs at the Laugh Factory.

(Michael Blackshire / Los Angeles Times)

Funnily enough, making a comedy show inclusive for neurodivergent people is “not a big adjustment at all — it’s just something that no one’s thought to do,” said Rob Kutner, a comedy writer and co-producer of the Wednesday show.

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“You need almost nothing, except a little bit of thoughtfulness.”

When Jeremiah Watkins heard someone in the audience interject, “What about trains?” the comedian welcomed the chance to riff.

“What about trains?” he replied enthusiastically. “Are you a fan of trains? Nice. What’s your favorite kind of train?” he asked before launching into his next bit.

At a smaller comedy show for an autistic crowd months earlier, Watkins recalled, he surprised an audience member who quoted a “Harry Potter” line at him by responding with an impression of Professor Severus Snape.

The show that Wednesday, dubbed “Let It Out,” can be a model for comedy performances around the world, Kutner and co-producer Mike Rotman said. The pair worked with advocates including Autism in Entertainment, which promotes the employment of people on the autism spectrum in the industry, to publicize and document the show.

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What they want people to know is that inclusion can be easy. “This should be normalized,” Rotman said. “This should be existing weekly.”

Willie Hunter laughs while hosting a comedy show at the Laugh Factory.

Willie Hunter laughs while hosting “Let It Out,” a comedy show that aimed to be inclusive for neurodivergent people.

(Michael Blackshire / Los Angeles Times)

As growing numbers of Americans are diagnosed with autism — a condition that can shape how people think, relate to others and experience the world — and generations have grown up with the protections of the Americans with Disabilities Act, there has been an ongoing push for inclusion in daily life.

Many public spaces have taken steps to better accommodate neurodivergent people and their sensory needs: Some movie theaters offer “sensory friendly” screenings where lights remain on and sound is softened. Museums may have designated days and times when fewer people are admitted to limit crowds.

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Even so, Maja Watkins, whose work focuses on teaching social and emotional skills, says there is still a dearth of fun, accessible options tailored for autistic adults.

“You’re in high school. You go to prom, and a lot of times the special ed department will make these fun opportunities for you. And then you graduate and slowly services and programs just start cutting away,” Watkins said.

Her husband is a comedian — the one who riffed on trains that Wednesday night — and she said that her 38-year-old brother, who has autism, loves comedy shows but has sometimes disliked the loud noise or late hours.

“How cool would it be if it was a comedy show that made everybody laugh … but maybe the seating is set up in a way where people aren’t so squished together?” Maja Watkins said. “Maybe it’s not crazy loud at the beginning? Maybe if somebody needs to take out a fidget … to be more calm, then that’s OK?”

Or being able to get up and take a break without facing a barb from someone onstage — “that’s what my brother would have needed to stay through the whole show,” she said.

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A young man is interviewed in the comics' lounge at the Laugh Factory before a comedy show.

Kole Spickler gives an interview backstage at the Laugh Factory.

(Michael Blackshire / Los Angeles Times)

The Wednesday crowd included young adults taking a class at the Miracle Project, an organization based in Los Angeles, that teaches social skills through improv. Teacher Sandy Abramson said for her students, “going to a place like this can be overwhelming because you have to adapt to the social norm, which is, ‘Don’t talk. You can’t take breaks.’ Things like that.”

At this show, she said, “they don’t have to feel nervous or anxious about how they will be perceived.”

Kole Spickler, 23, was excited for the show to start. “I just like being out in public,” said Spickler, who is autistic and counts Jim Gaffigan and Brian Regan among his favorite comedians.

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Like many autistic people, he can be frank, sometimes humorously so. Asked about what he was learning in social skills class — a Miracle Project staffer at his side — he said, “I’m not sure if I really learned anything.”

Had he enjoyed it?

“Yes. Sort of,” he said. “Some of my peers can be really annoying.”

During the show, the crowd relished jokes about autism. “I was born with autism, but everything else is my parents’ fault,” Meyrowitz quipped. Kruger Dunn told the audience he had been diagnosed on the spectrum late in life.

A young man claps during a comedy show at the Laugh Factory.

Bryan Miguel attends a comedy show at the Laugh Factory.

(Michael Blackshire / Los Angeles Times)

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Doctors had told him, “You don’t lie. You like to memorize a lot of facts, and you won’t go for help even if there’s trouble,” Dunn said. “I’m like, ‘So what you’re saying is, I’m trustworthy, smart, and I ain’t no snitch?’”

“You use the word ‘disability’ a lot, but those sound like abilities to me, Doc,” Dunn said to laughter and applause.

But Maja Watkins and others involved in organizing the show at the Laugh Factory stressed that accommodating the crowd didn’t mean doing a comedy show all about autism, nor discarding their usual jokes. Rotman said some comics had asked him, “Are you looking for me to do neurodivergent material?”

“No, not at all,” he told them. “Do your set … Do your seven minutes.”

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Laugh Factory hostess Carmella Rogers said she insisted on working that Wednesday night after finding out about the show, because “I wouldn’t have to mask as I normally would” to appear neurotypical to showgoers.

In her line of work, you have to “show a lot of emotions, be really happy all the time,” which can sometimes be difficult for Rogers, who is autistic and has attention-deficit/hyperactivity disorder. In a break between shows that night, she said was gratified that the comedians hadn’t infantilized the neurodivergent crowd.

“People tend to think if you’re autistic, you need to be treated like a child,” she said. “I’m just like a regular adult — there’s just certain things about me that make me different from the average person.”

Comedian Laurie Kilmartin performs at the Laugh Factory.

Comedian Laurie Kilmartin performs during “Let It Out” at the Laugh Factory.

(Michael Blackshire / Los Angeles Times)

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Ahead of her set, comedian Laurie Kilmartin said she was “mostly just doing a regular show,” but not reacting the way she might otherwise if someone piped up in the crowd.

“I’ve done every hell gig possible in the world so I’m not easily thrown,” said Kilmartin, before hastening to add, “Not that I am implying this is a hell gig — I’m just saying!”

Stand-up might seem, at first glance, like an unexpected place for autistic people, who may miss social cues or communicate in ways that typical people struggle to understand. But it has often been a haven for people who don’t fit the norm.

Meyrowitz, who has been performing for more than a decade and a half, said his anxiety made it hard from him to work “normal jobs,” but in comedy, “we’re all a bunch of weirdos.” He once thought he would live with his parents his whole life. Now he shares an apartment with other comics.

Comedy, Meyrowitz said, “gives me a community of friends I never had before.”

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California confirms first measles case for 2026 in San Mateo County as vaccination debates continue

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California confirms first measles case for 2026 in San Mateo County as vaccination debates continue

Barely more than a week into the new year, the California Department of Public Health confirmed its first measles case of 2026.

The diagnosis came from San Mateo County, where an unvaccinated adult likely contracted the virus from recent international travel, according to Preston Merchant, a San Mateo County Health spokesperson.

Measles is one of the most infectious viruses in the world, and can remain in the air for two hours after an infected person leaves, according to the CDPH. Although the U.S. announced it had eliminated measles in 2000, meaning there had been no reported infections of the disease in 12 months, measles have since returned.

Last year, the U.S. reported about 2,000 cases, the highest reported count since 1992, according to CDC data.

“Right now, our best strategy to avoid spread is contact tracing, so reaching out to everybody that came in contact with this person,” Merchant said. “So far, they have no reported symptoms. We’re assuming that this is the first [California] measles case of the year.”

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San Mateo County also reported an unvaccinated child’s death from influenza this week.

Across the country, measles outbreaks are spreading. Today, the South Carolina State Department of Public Health confirmed the state’s outbreak had reached 310 cases. The number has been steadily rising since an initial infection in July spread across the state and is now reported to be connected with infections in North Carolina and Washington.

Similarly to San Mateo’s case, the first reported infection in South Carolina came from an unvaccinated person who was exposed to measles while traveling internationally.

At the border of Utah and Arizona, a separate measles outbreak has reached 390 cases, stemming from schools and pediatric centers, according to the Utah Department of Health and Human Services.

Canada, another long-standing “measles-free” nation, lost ground in its battle with measles in November. The Public Health Agency of Canada announced that the nation is battling a “large, multi-jurisdictional” measles outbreak that began in October 2024.

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If American measles cases follow last year’s pattern, the United States is facing losing its measles elimination status next.

For a country to lose measles-free status, reported outbreaks must be of the same locally spread strain, as was the case in Canada. As many cases in the United States were initially connected to international travel, the U.S. has been able to hold on to the status. However, as outbreaks with American-origin cases continue, this pattern could lead the Pan American Health Organization to change the country’s status.

In the first year of the Trump administration, officials led by Health Secretary Robert F. Kennedy Jr. have promoted lowering vaccine mandates and reducing funding for health research.

In December, Trump’s presidential memorandum led to this week’s reduced recommended childhood vaccines; in June, Kennedy fired an entire CDC vaccine advisory committee, replacing members with multiple vaccine skeptics.

Experts are concerned that recent debates over vaccine mandates in the White House will shake the public’s confidence in the effectiveness of vaccines.

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“Viruses and bacteria that were under control are being set free on our most vulnerable,” Dr. James Alwine, a virologist and member of the nonprofit advocacy group Defend Public Health, said to The Times.

According to the CDPH, the measles vaccine provides 97% protection against measles in two doses.

Common symptoms of measles include cough, runny nose, pink eye and rash. The virus is spread through breathing, coughing or talking, according to the CDPH.

Measles often leads to hospitalization and, for some, can be fatal.

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Trump administration declares ‘war on sugar’ in overhaul of food guidelines

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Trump administration declares ‘war on sugar’ in overhaul of food guidelines

The Trump administration announced a major overhaul of American nutrition guidelines Wednesday, replacing the old, carbohydrate-heavy food pyramid with one that prioritizes protein, healthy fats and whole grains.

“Our government declares war on added sugar,” Health and Human Services Secretary Robert F. Kennedy Jr. said in a White House press conference announcing the changes. “We are ending the war on saturated fats.”

“If a foreign adversary sought to destroy the health of our children, to cripple our economy, to weaken our national security, there would be no better strategy than to addict us to ultra-processed foods,” Kennedy said.

Improving U.S. eating habits and the availability of nutritious foods is an issue with broad bipartisan support, and has been a long-standing goal of Kennedy’s Make America Healthy Again movement.

During the press conference, he acknowledged both the American Medical Association and the American Assn. of Pediatrics for partnering on the new guidelines — two organizations that earlier this week condemned the administration’s decision to slash the number of diseases that U.S. children are vaccinated against.

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“The American Medical Association applauds the administration’s new Dietary Guidelines for spotlighting the highly processed foods, sugar-sweetened beverages, and excess sodium that fuel heart disease, diabetes, obesity, and other chronic illnesses,” AMA president Bobby Mukkamala said in a statement.

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Contributor: With high deductibles, even the insured are functionally uninsured

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Contributor: With high deductibles, even the insured are functionally uninsured

I recently saw a patient complaining of shortness of breath and a persistent cough. Worried he was developing pneumonia, I ordered a chest X-ray — a standard diagnostic tool. He refused. He hadn’t met his $3,000 deductible yet, and so his insurance would have required him to pay much or all of the cost for that scan. He assured me he would call if he got worse.

For him, the X-ray wasn’t a medical necessity, but it would have been a financial shock he couldn’t absorb. He chose to gamble on a cough, and five days later, he lost — ending up in the ICU with bilateral pneumonia. He survived, but the cost of his “savings” was a nearly fatal hospital stay and a bill that will quite likely bankrupt him. He is lucky he won’t be one of the 55,000 Americans to die from pneumonia each year.

As a physician associate in primary care, I serve as a frontline witness to this failure of the American approach to insurance. Medical professionals are taught that the barrier to health is biology: bacteria, viruses, genetics. But increasingly, the barrier is a policy framework that pressures insured Americans to gamble with their lives. High-deductible health plans seem affordable because their monthly premiums are lower than other plans’, but they create perverse incentives by discouraging patients from seeking and accepting diagnostics and treatments — sometimes turning minor, treatable issues into expensive, life-threatening emergencies. My patient’s gamble with his lungs is a microcosm of the much larger gamble we are taking with the American public.

The economic theory underpinning these high deductibles is known as “skin in the game.” The idea is that if patients are responsible for the first few thousand dollars of their care, they will become savvy consumers, shopping around for the best value and driving down healthcare costs.

But this logic collapses in the exam room. Healthcare is not a consumer good like a television or a used car. My patient was not in a position to “shop around” for a cheaper X-ray, nor was he qualified to determine if his cough was benign or deadly. The “skin in the game” theory assumes a level of medical literacy and market transparency that simply doesn’t exist in a moment of crisis. You can compare the specs of two SUVs; you cannot “shop around” for a life-saving diagnostic while gasping for air.

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A 2025 poll from the Kaiser Family Foundation points to this reality, finding that up to 38% of insured American adults say they skipped or postponed necessary healthcare or medications in the past 12 months because of cost. In the same poll, 42% of those who skipped care admitted their health problem worsened as a result.

This self-inflicted public health crisis is set to deteriorate further. The Congressional Budget Office estimates roughly 15 million people will lose health coverage and become uninsured by 2034 because of Medicaid and Affordable Care Act marketplace cuts. That is without mentioning the millions more who will see their monthly premiums more than double if premium tax credits are allowed to expire. If that happens, not only will millions become uninsured but also millions more will downgrade to “bronze” plans with huge deductibles just to keep their premiums affordable. We are about to flood the system with “insured but functionally uninsured” patients.

I see the human cost of this “functional uninsurance” every week. These are patients who technically have coverage but are terrified to use it because their deductibles are so large they may exceed the individuals’ available cash or credit — or even their net worth. This creates a dangerous paradox: Americans are paying hundreds of dollars a month for a card in their wallet they cannot afford to use. They skip the annual physical, ignore the suspicious mole and ration their insulin — all while technically insured. By the time they arrive at my clinic, their disease has often progressed to a catastrophic event, from what could have been a cheap fix.

Federal spending on healthcare should not be considered charity; it is an investment in our collective future. We cannot expect our children to reach their full potential or our workforce to remain productive if basic healthcare needs are treated as a luxury. Inaction by Congress and the current administration to solve this crisis is legislative malpractice.

In medicine, we are trained to treat the underlying disease, not just the symptoms. The skipped visits and ignored prescriptions are merely symptoms; the disease is a policy framework that views healthcare as a commodity rather than a fundamental necessity. If we allow these cuts to proceed, we are ensuring that the American workforce becomes sicker, our hospitals more overwhelmed and our economy less resilient. We are walking willingly into a public health crisis that is entirely preventable.

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Joseph Pollino is a primary care physician associate in Nevada.

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L.A. Times Insights delivers AI-generated analysis on Voices content to offer all points of view. Insights does not appear on any news articles.

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Ideas expressed in the piece

  • High-deductible health plans create a barrier to necessary medical care, with patients avoiding diagnostics and treatments due to out-of-pocket cost concerns[1]. Research shows that 38% of insured American adults skipped or postponed necessary healthcare or medications in the past 12 months because of cost, with 42% reporting their health worsened as a result[1].

  • The economic theory of “skin in the game”—which assumes patients will shop around for better healthcare values if they have financial responsibility—fails in medical practice because patients lack the medical literacy to make informed decisions in moments of crisis and cannot realistically compare pricing for emergency or diagnostic services[1].

  • Rising deductibles are pushing enrollees toward bronze plans with deductibles averaging $7,476 in 2026, up from the average silver plan deductible of $5,304[1][4]. In California’s Covered California program, bronze plan enrollment has surged to more than one-third of new enrollees in 2026, compared to typically one in five[1].

  • Expiring federal premium tax credits will more than double out-of-pocket premiums for ACA marketplace enrollees in 2026, creating an expected 75% increase in average out-of-pocket premium payments[5]. This will force millions to either drop coverage or downgrade to bronze plans with massive deductibles, creating a population of “insured but functionally uninsured” people[1].

  • High-deductible plans pose particular dangers for patients with chronic conditions, with studies showing adults with diabetes involuntarily switched to high-deductible plans face 11% higher risk of hospitalization for heart attacks, 15% higher risk for strokes, and more than double the likelihood of blindness or end-stage kidney disease[4].

Different views on the topic

  • Expanding access to health savings accounts paired with bronze and catastrophic plans offers tax advantages that allow higher-income individuals to set aside tax-deductible contributions for qualified medical expenses, potentially offsetting higher out-of-pocket costs through strategic planning[3].

  • Employers and insurers emphasize that offering multiple plan options with varying deductibles and premiums enables employees to select plans matching their individual needs and healthcare usage patterns, allowing those who rarely use healthcare to save money through lower premiums[2]. Large employers increasingly offer three or more medical plan choices, with the expectation that employees choosing the right plan can unlock savings[2].

  • The expansion of catastrophic plans with streamlined enrollment processes and automatic display on HealthCare.gov is intended to make affordable coverage more accessible for certain income groups, particularly those above 400% of federal poverty level who lose subsidies[3].

  • Rising healthcare costs, including specialty drugs and new high-cost cell and gene therapies, are significant drivers requiring premium increases regardless of plan design[5]. Some insurers are managing affordability by discontinuing costly coverage—such as GLP-1 weight-loss medications—to reduce premium rate increases for broader plan members[5].

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