Village Times Herald

File photo by Raymond Janis

SBU visa revocations demand official action, not platitudes

As a proud Stony Brook University alumnus (M.S. 2005), I was deeply troubled by the recent report detailing the revocation of student visas for 11 international students at SBU. No explanation or evidence has been provided to justify these revocations. This lack of transparency leaves us to assume that these revocations — along with the roughly 1,500 others reported at over 250 institutions nationwide — are either arbitrary or motivated by an unconstitutional intent to suppress free speech. (Visiting students are entitled to the same free speech protections as U.S. citizens.) While the federal government does have the authority to revoke visas, exercising that power arbitrarily constitutes a clear abuse of power.

Some may disregard the educational value of a diverse student body or the fact that smart international students elevate academic standards in the classroom. But even skeptics should recognize that international students pay higher tuition than domestic students, effectively subsidizing SBU’s operating budget. Considering that SBU, Brookhaven National Lab and Cold Spring Harbor Lab are leading Long Island employers with globally diverse workforces, even pragmatic business leaders should be concerned. A climate of fear could prompt many of the approximately 3,800 international students at SBU to transfer, and discourage future applicants altogether.

Vague affirmations by university officials are welcome, but appear toothless. SBU is a public institution of New York State. What actions will the state take to protect its residents and universities from federal overreach? Has the university president sought support from the governor, or the New York Civil Liberties Union? Will SBU provide legal representation to the students or join wider lawsuits to contest these revocations in federal court? If not, why? And if this situation escalates, will university police intervene to prevent warrantless ICE arrests, or will they stand aside as masked, unidentified agents in unmarked vans seize students on campus?

Blame for all this must be placed squarely on Rep. Nick LaLota (R-NY1) and his fellow House Republicans. As majority members of a co-equal branch of government, they have failed in their constitutional duty to perform oversight. Their role is to ensure the executive branch faithfully enforces laws enacted by Congress — not to stand idle as policy is dictated by executive fiat. While LaLota may disregard the voices of his Democratic constituents, perhaps his Republican supporters and donors can impress upon him the long-term consequences of his inaction.

John Hover

East Setauket

Solar and wind power will not fulfill energy needs

In his letter of April 10 [The realty of renewable energy on Long Island] Peter Gollon recommended a document entitled “Long Island Solar Roadmap,” which is basically a sales brochure for solar panels. It would be a simple matter, we are told, to install 10 to 15 million solar panels on various locations, including flat roofs, carports, industrial land and brownfields.

The largest source, however, 49%, will be from offshore windmills. In addition, there will also be a network of lithium-ion battery installations, which will be charged when the solar arrays and windmills are generating power in excess of the user demands. Then, when the sunlight and offshore winds are absent or diminished, the required power will be provided from the energy stored in the batteries.

The problem with this scenario is that, for a given amount of solar, wind and battery installations, the required power can be guaranteed for only a limited period of time, if the sun and wind do not cooperate. In this unfortunate situation, a total blackout will occur, and it will not end until adequate sunlight and wind levels have returned.

With the technology of today, we have systems that use “fossil fuels” (oil and gas), nuclear fission and solar/wind technology. Of these, only solar/wind systems are likely to experience blackouts caused by a lack of fuel. For a known solar/wind/battery design, and known sunlight and wind profiles, based on recorded meteorological records, it should be possible to generate computer simulation software to calculate the probability of a blackout for given periods of time, such as 3 days, 4 days, 5 days, etc. Possibly Peter Gollon and his colleagues have already done this. If so, it would be most helpful for them to share their results with us. I am sure they are not simply trying to get as many solar panels and windmills as they can, and hope to get lucky.

In an interesting related development, Microsoft is in the process of reactivating the Three Mile Island nuclear energy plant in Pennsylvania, with a capacity of 800 MW, for the purpose of powering their upcoming artificial intelligence computers. Here on Long Island, in Shoreham, we have the sleeping Shoreham Nuclear Power Plant, and it has a capacity of 820 MW. If we activate the Shoreham facility, and build two or three modern copies of it, we can have all of the power we could ever use, with zero carbon emissions, no possibility of a blackout, no thermal runaway and plenty of extra power for Connecticut and New York City during times when their sun and wind resources are in short supply. What is wrong with that?

George Altemose

Setauket

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We welcome your letters, especially those responding to our local coverage, replying to other letter writers’ comments and speaking mainly to local themes. Letters should be no longer than 400 words and may be edited for length, libel, style, good taste and uncivil language. They will also be published on our website. We do not publish anonymous letters. Please include an address and phone number for confirmation. Email letters to: [email protected] or mail them to TBR News Media, P.O. Box 707, Setauket, NY 11733

 

Pixabay photo

By Daniel Dunaief

Daniel Dunaief

Words pour out of our mouths like different kinds of liquids.

Sometimes, those words can offer necessary relief from white hot anger, agony or discomfort, serving as a cooling salve, bringing a smile to our miserable faces and turning, as the cliche would suggest, a frown upside down.

Other times, the words people choose to share can exacerbate an already inflamed state, serving as lighter fluid, threatening to turn us from a mild shade of pink into a deep red.

Words can also become an avalanche, forcing us to look elsewhere as a nonstop collection of words, phrase or ideas threatens to bury us beneath their verbal weight. Desperate to get away, we might hope the speaker gets distracted by a flying turtle.

A diatribe, lesson or self-aggrandizing soliloquy can be exhausting and irritating.

But, it’s not just the words and their effect that are so familiar in conversations.

No, you see, it’s the facial expressions. Many people have a remarkable ability to run the gamut of human emotions and thoughts without saying a word. A tightening of the skin around their eyes, a slight narrowing of the lids, a crooked smile, or a baring of teeth, which is probably the least subtle of the facial reactions, can reveal something about our inner state or disclose how we’re feeling about the world around us or, more precisely, the person in front of us.

To varying degrees, actors and actresses have mastered the art of using their often photogenic, compelling, or sympathetic faces to tell stories and, perhaps, to reveal the inner conflict we know they are feeling when, say, their sister asks them to be a bridesmaid when she’s planning to marry a person the actress has loved for years. Yes, that was a mildly amusing movie and yes, you probably know it.

The rest of us mere facial mortals, however, may not be as capable of altering our features to reflect the wide range of emotions we might reveal in response to the way we feel behind the masks we try to wear.

When I lived in Manhattan, I thoroughly enjoyed people watching. It’s a form of endless entertainment. Leaning on the railing at Rockefeller Center in mid December years ago, I watched an elderly couple gliding around the rink together, holding hands and glancing contentedly at each other, clearly enjoying the moment. With gloved fingers interlaced, they synchronized their legs as well as any pairs figure skaters might.

While I imagined that they had been together for decades and that they might have gone to an ice skating rink on an early date, they also could have been together for a couple of months or, perhaps, gotten married a year earlier.

Either way, their faces, which I can still picture decades later, revealed a keen and profound satisfaction.

Some people undoubtedly have mastered the art of the poker face, appearing interested or attentive when they are thinking about where to eat dinner later that night, what laundry they need to take to the dry cleaner, or when to sell a stock that’s been teetering with all the others amidst concerns about corporate profits and a potential slowdown in the economy.

Others, however, can reveal the equivalent of an SOS call, with a slight turn of their neck, widening eyes, and a faint but noticeable grimace around their pained mouths.

When we get to know family or friends well, we can read their expressions or hear the flat tone in their voices, knowing that the word “interesting,” or “you don’t say,” really means, “please stop talking. I’ll pay you to stop talking. In fact, here is a set of fake plastic ears that look like mine. Chew on them and, when you’re done, please recycle what’s left over.”

Sometimes, when I know someone well enough, I’ll watch their faces as they listen to a perspective that irritates them, a joke they don’t find remotely amusing, or a comment they don’t appreciate and I’ll recognize the unspoken but deeply held thoughts etched in their faces.

With all the finely tuned muscles in our faces and our ability to raise or lower our eyebrows, we can send signals that the attentive listener or others can read like a subtle or, perhaps more obvious, signal.

A statue of Balto in Central Park. Photo courtesy of Wikimedia Commons/Roman Eugeniusz

By Leah S. Dunaief

Leah Dunaief,
Publisher

While most of us know “of the famous ride of Paul Revere,” quoting Longfellow, there is another ride that happened 100 years ago that we can commemorate. It has to do with one of my favorite dogs. His name was Balto, an Alaskan husky and sled dog born in Nome, and he led a team of sled dogs, driven by Gunnar Kaasen and carrying vital diphtheria antitoxin through fierce Alaskan storms across the wilderness and into history. 

The serum was desperately needed to combat an outbreak of the disease. Planes such as they were in 1925, were grounded by the intense weather. The only hope for rescue was with the perilous trip by sled. Kaasen insisted that Balto was the true hero. A movie, a nationwide tour on the vaudeville circuit and a bronze statue in Central Park resulted.

Now I visited Central Park most Sundays, when the weather permitted, throughout my elementary school years, with my dad and younger sister. It was my dad’s way of giving my mother a few hours off and of having some time with us since he worked six days a week, left early in the morning, and only returned for a late dinner. He would cook us breakfast, and then we would walk through the Park, taking a different route each time until my mother would join us in the late afternoon with a picnic supper. 

Most often, he made sure our meanderings took us past the statue of Balto. I would climb up on the rock on which he stood, then sit astride his back, and listen as my dad read the words on the plaque adorning the site “dedicated to the indomitable spirit of the sled dogs that relayed antitoxin six hundred miles over rough ice, across treacherous waters, through Arctic blizzards from Nenana to the relief of stricken Nome in the winter of 1925: endurance, fidelity, intelligence” Visuals of the trip would run through my mind as I sat there, courtesy of Jack London, whose books I read. I loved Balto.

But there is quite a back story.

For starters, Balto was an underdog in a literal sense. He was owned by Leonhard Seppala, a native Norwegian, sled dog breeder, musher and competitive racer, and was named after an Arctic explorer. Balto had a black fur coat, a small, stocky build with two white stocking front feet and was considered “second rate” as a racer by Seppala, who had him neutered at six months and used him to haul freight for short runs and help pull railcars with miners over a disused railroad track. Gunnar Kaasen, another native Norwegian and a close family friend of Seppala, with 21 years of dog sledding experience who worked for the breeder, came to know Balto and believed Seppala had misjudged the dog because of his short stature.

Early in 1925, doctors realized a deadly diphtheria epidemic could affect the  people of Nome, Alaska, and putting the city under quarantine, transmitted with Morse code that the town desperately needed more serum, whose supply was almost depleted. Mushers were summoned to relay the precious cargo. Radio, a recent invention, picked up the story, as well as newspapers, and followed the more than 20 mushers as they took turns through storms and strong winds. Kaasen was appointed to drive a team of Seppala’s dogs, and although Seppala wanted a dog named Fox to lead the team, Kaasen picked Balto. They left the town of Bluff with the antitoxin at 10 p.m.

Shortly after they started, a blizzard caused them to become confused and lost. Kaasen yelled, “Go home, Balto,” and the dog, used to hauling heavy loads, navigated his team through the wild winds. At one point, Balto unexpectedly stopped before some ice on the Topkok River that broke in front of him, thereby saving Kaasen’s life and that of the entire team, according to the musher. The package was delivered in time, and the residents were saved.

There is more to the story. Especially as money entered the picture, lies and deception, jealousy and hatred all became part of the human saga. But Balto will always remain my 100-year-old dog. 

METRO photo

By Daniel Dunaief

Symptoms can range from dizziness and lightheadedness on standing to an inability to get out of bed.

These symptoms, which are characteristic of several medical conditions, are at the heart of a condition called Postural Orthostatic Tachycardia Syndrome, or POTS.

Affecting considerably more women than men, POTS, which is caused by a sudden and sometimes dramatic increase in heart rate when people stand, can be anything from a nuisance to a debilitating condition.

On Saturday, April 26, at 9 a.m. to 4 p.m., several doctors, working with Dysautnomia International, will present information at a continuing medical education course at the MART auditorium at Stony Brook University about POTS, which people can also attend virtually. Details and registration can be found below. This course is designed for medical professionals, but patients and caregivers are welcome to register too.

The condition is triggered by a problem with the autonomic nervous system, which controls heart rate, blood pressure, digestion and temperature regulation among other functions.

“I’ve had patients who were previously athletes who can’t exercise anymore,” said Dr. Jeffrey Boris, a pediatric cardiologist with a private practice, an expert in POTS, and one of the speakers at the course at Stony Brook. 

In a previous study Boris conducted, he found that two out of three of his POTS patients had at least 10 symptoms, while half of them had at least 14 symptoms and 30 percent had at least 26 symptoms.

“The degree of debility can vary from some exercise intolerance to pretty much unable to get out of bed,” said Boris, who sees patients exclusively through telehealth and who is licensed to practice medicine in 18 states, not including New York.

An estimated one to three million Americans had some form of POTS before Covid. That number has increased to as many as six million.

Often triggered by an infection like the Epstein Barr virus, which causes mononucleosis, by Lyme Disease or even by concussions, POTS has no specific standard of care, as doctors have used a variety of pharmacological and non pharmacological treatments to help people suffering with these symptoms.

Some studies suggest that genetics plays a role in contributing to the disease.

Several high profile women have shared their battles with POTS, including Olympic gold-medal swimmer Katie Ledecky and Tori Moore, the wife of Super Bowl winning quarterback Nick Foles. Some doctors recommend swimming to POTS patients.

Medical education

The health care field hasn’t focused as much on POTS as it does on other diseases or conditions.

Doctors don’t always recognize POTS because they never learned about it in school, don’t believe it exists or didn’t train for this in their specialty work, Boris said.

The combination of these factors makes it harder for patients to receive a diagnosis.

Additionally, several other conditions have similar symptoms, including thyroid disease, low vitamin D, low iron and Addison’s Disease, among others.

The average patient takes four years to get an accurate diagnosis, according to Lauren Stiles, founder and president of Dysautonomia International (DI) and Research Assistant Professor of Neurology at the Renaissance School of Medicine at Stony Brook University. Stiles is the course co-chair for the POTS.

Indeed, Jennifer Samghabadi, who works as a registered nurse for neurologist Dr. Mark Gudesblatt, had symptoms of POTS as early as 2004, but didn’t receive a diagnosis until after her symptoms worsened in 2012 following a bout with swine flu.

POTS “is often misdiagnosed,” said Samghabadi, who is a resident of Port Jefferson Station. “Symptoms mimic so many other things. Your autonomic nervous system is misfiring in every which way.”

Stiles, who founded DI in 2012 and has created support groups in over 80 countries for people who suffer from this condition, has been working with medical schools around the country to create more training for doctors.

Patients are typically treated through a combination of pharmacological and non pharmacological approaches. The medicines they have used, including ivabradine, have been approved for the treatment of other conditions and are used in an off-label basis.

Boris is planning to talk to doctors about various types of treatments he’s used that work.

“I can’t routinely predict what therapies are going to help,” Boris said. “It’s really variable from patient to patient. It can be a lot of trial and error.”

Non-pharmacological treatments include elevating the head of the bed frame about six to eight inches. That can cause the kidneys to hold onto salt and water, which can lesson symptoms, Boris explained.

Additionally, doctors recommend a high salt, high liquid diet, which can include three liters or more of water each day.

Boris has had some success working with abdominal binders, which he has found are more effective than compression stockings.

To be sure, some patients have gastrointestinal issues, including nausea, bloating and constipation. For those patients, as well as people who have autism spectrum disorder, abdominal pressure won’t likely provide any relief and may make some symptoms or discomfort worse.

In the talk Boris is giving, he would like doctors to recognize that the disease exists, it’s validated and it’s something that, if health care professionals are creative and thoughtful, they can find possible treatment options for patients who are often suffering through different levels of symptoms.

At this point, federal funding for research into POTS stands at about $4 million per year, which is up from $2 million per year before Covid, but is still short of what doctors and advocates would like to see for a potentially debilitating disease.

Boris hopes that further research will provide a better idea of what is leading to POTS, which may lead to a Food and Drug Administration-approved treatment.

People who wants to learn more about the condition can visit the web site CurePOTS.org. Dysautonomia International offers a list of doctors skilled in diagnosing and treating POTS as well as other autonomic disorders.

Samghabadi, who is on the board of DI, urged medical care professionals to attend the course.

“It’s going to teach you everything you need,” she said. “It’s practical, evidence-based strategies for diagnosing and treating dysautonomia and is immediately applicable to patients.”

Even doctors who don’t think they can treat these patients should be aware of it so they know where to send patients, she suggested.

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DETAILS AND REGISTRATION: 

Dysautonomia International and Stony Brook University School of Medicine invite you to join us for a Continuing Medical Education course, Updates in Postural Orthostatic Tachycardia Syndrome Clinical Care & Research, on Saturday, April 26, 2025, 9am-4pm ET, held at the Stony Brook University MART Auditorium.

A networking reception with light refreshments will be held from 4 to 5 p.m. after the course.
Advanced registration is required. Up to 5.50 AMA PRA Category 1 Credit(s)™ are available for online or in person CME registrants. Please see the event website for details on CME credits. The lectures will be recorded and made available to all registered guests after the live event. CME credit is only available by watching the live broadcast or attending in person.
In Person Registration Fees:
Stony Brook University Students, Faculty & Staff (with CME credit): FREE
Community Physicians (with CME credit): $100
RN, PT, OT, Allied Health: (with CME credit): $75
Patients & Caregivers/Public (no CME credit): $25
Livestream Registration Fees:
Stony Brook University Students, Faculty & Staff (with CME credit): FREE
Livestream with CME credit: $100
Livestream with no CME credit: $25
If you are unable to attend in person or watch the livestream, but would like access to the recorded lectures, you can register for the “Livestream with no CME credit” option.

Online and in person registration options are available at bit.ly/StonyBrookCME

 

One in 36 children aged eight in the U.S. were diagnosed with the Autism Spectrum Disorder (ASD), according to the Centers for Disease Control and Prevention. One in 36 means that around 32 students are affected by ASD in a high school of 1238 students–the number of students enrolled at Smithtown High School West from 2023-2024. It means that 76 students from kindergarten to sixth grade in the Three Village School District may have trouble socializing, communicating and learning.

The number of adults impacted is less defined, with some adults going undiagnosed, though the CDC estimates 1 in 45 adults in the U.S. have ASD. These individuals are artists. They are educators, technicians, writers, engineers and leaders. They helped make our community, but our community was not made for them. 

Often people with ASD have to “mask.” According to the National Autistic Society, people with ASD sometimes mask in order to appear non-autisitic. Autistic people have described masking as “tightly controlling and adjusting how you express yourself based on the real or anticipated reactions of others.” 

ASD causes the person to have trouble communicating in social situations. They may exhibit repetitive behaviors called “stimming” or strictly adhere to a fixed routine. They may get overstimulated by certain sensations or experiences. Autism is a spectrum, so it affects everyone in varying degrees. 

People with ASD have helped shaped our society in significant ways. Greta Thunberg, for example, is a 22-year old environmental activist who inspired thousands to advocate for environmental protections. She is also on the autistic spectrum. 

Renowned actor Anthony Hopkins is also reportedly on the autistic spectrum and was diagnosed late in his life. 

Most people have some connection to a person who has ASD. Expanding consideration to the different needs and preferences of autistic individuals does not take much work. Offering different resources and services, like Father Andrew Garnett is doing in holding a sensory-friendly church service, is a great way to show that people with different abilities are valued. We can ask questions–what can we do to help? Perhaps we can communicate differently and avoid sarcasm. We can be cognizant of sensory issues. Most importantly, we can listen. Let’s make an effort to be more considerate to those with ASD and to learn about how we can make our community more inclusive, not just this April during Autism Awareness Month  but always. 

‘The Lady of the Lake’ stars Seth Gilliam, Chris Roach, Taylor Red Fox, and Veronica Kelly come out to show support. 

The Long Island Music and Entertainment Hall of Fame (LIMEHOF) honored director Maria Capp (originally from Ronkonkoma), and screened her latest film, The Lady of The Lake: The Legend of Lake Ronkonkoma, on Saturday, April 19 at the museum, located at 97 Main Street in Stony Brook. This event was the lead-off film of LIMEHOF’s recently announced Monthly Local Filmmakers Series, which turns the spotlight on Long Island-based directors and their films. 

Capp flew out from Los Angeles to participate in the event and was joined on stage by some of the film’s stars, including Seth Gilliam, Chris Roach, Taylor Red Fox, and Veronica Kelly for a Q&A after the screening. They all spoke about being part of the film. 

“I think it’s wonderful, and I’m really grateful to everybody who has opened their arms and provided this opportunity to be the first film in the film series,” said Capp. “It’s really important what’s being done—and that is to keep arts in the community and bring local artists to the forefront. It’s been really quite an enjoyable experience and a pleasure working with everybody here.”  

Seth Gilliam, perhaps best known for his roles in The Walking Dead and The Wire, plays Adam Schultz, the main character’s father, in Lady of the Lake. He says it was great to screen and watch it with a local Long Island audience.   

“The crowd was really attentive and seemed to really dig it, and that makes it all worth the price of admission to me,” Gilliam said. “I wanted to be part of a coming-of-age story, but I’ve long since ‘come of age’—so being the father was the only role that I could actually play. I was drawn to it [the film] because of Maria Capp’s passion for the project and need to tell the story, and I wanted to be a part of it.” 

Chris Roach is a comedian from Ronkonkoma. He says he was aware of the real legend of the lake and wanted to be part of the film when Maria told him about it.

“She sent me the script and I really liked the role,” Roach said. “He’s a guy who adds some comic relief to the movie, which is something I really love doing. Being a proud Long Islander, it’s important to come out and represent whenever you can. This was extra special because I had a little part in it—and I love Maria and her family.” 

 Taylor Red Fox is an actress who has recently appeared in the TV series Manifest, has acted in off-Broadway theater, and is also a member of The Shinnecock Nation. She plays Tahoma in Lady of the Lake. 

“I’m excited that we’re all here as Long Island community members and we can help add to the artists in the area,” Red Fox said. “We were able to portray a side of the story that wasn’t disrespectful or dishonoring the memories of anyone living in the area. It was great working with Maria and Seth and the other actors, and I love that we were able to include actors who are local from the area in ways they may already be involved in the community—like being a comedian.”  

The film series is sponsored by Rick Eberle of Magnetic Vine and G&R Events. LIMEHOF Vice Chairman Tom Needham organized the event and emceed the Q&A that followed the screening. 

“The LIMEHOF Monthly Local Filmmaker Series is a celebration of the incredible filmmaking talent emerging from our region,” said Needham. “Each month, we showcase the creativity, passion, and dedication of local filmmakers—providing them with a platform to share their work and connect with audiences who appreciate the power of storytelling. This series is an important part of our mission to support the arts and highlight Long Island’s impact on the entertainment industry.”

For over 20 years, Maria has worked in film and with the arts community on Long Island, NY and in Los Angeles, CA in a variety of roles as an award-winning writer, director, producer, and acting coach. In addition to The Lady of the Lake, she has been involved as a producer with many notable movie credits which include narrative features in the storytelling: Reach, DIVOS!, Four Cousins and a Christmas, and the Weekly World News Studios’ The Zombie Wedding.

The Lady of The Lake: The Legend of Lake Ronkonkoma is a Native American folklore thriller distributed by Vision Films Inc. This film was shot on location, in around filmmaker Maria Capp’s childhood hometown Ronkonkoma, and stars Seth Gilliam (The Walking Dead) and Nia Sioux (Dance Moms) as, respectively the father and daughter protagonists. Also featured are Larry Saperstein (High School Musical: The Musical [TV Series]), Emery Kelly (Netflix’s Alexa & Katie), Steven Thomas Capp (Fat Camp), and Julie Dove (Days of our Lives).

The next director to be recognized in the series is Sean King from Huntington on Saturday, May 17 at 1 p.m. Sean will be screening his latest film ScreamWalkers and be accompanied by Glenn McBride Jr. (Actor), Celia Spero (Actor), and Peter Bune Jr. (Producer). LIMEHOF welcomes nominations of local film directors and movies for consideration to feature in the series. For more information, visit the LIMEHOF website at https://www.limusichalloffame.org/

 

METRO photo

As of April 21, all local gasoline prices are a penny to three cents lower than a week ago, except Long Island which held steady, according to a report from AAA Northeast. The national average fell three cents.

The AAA Fuel Prices website shows today’s New York City average at $3.09 per gallon, a penny less than last week. Connecticut is also down one cent at $3.04. Long Island remains flat at $2.99. New Jersey is down three cents to $2.97.

Prices continue lower on weak demand. Last week, according to the Energy Information Administration (EIA), Americans consumed just 8.46 million barrels of gasoline per day—a slight uptick of 37,000 barrels a day over the prior week, but still trailing 2024’s pace by roughly 200,000 barrels a day. Next week’s figures, which will include data encompassing the Easter holiday, will be closely watched by market analysts to see if demand breaks out of the spring doldrums.

“As demand has continued to stay soft, refiners have dialed back gasoline production to keep a floor beneath pump prices, which are the lowest for this time of year since 2021,” said Robert Sinclair of AAA Northeast. “Across the country, drivers are spending between 50 and 60 cents less per gallon than this time last year.”

On April 21, Mississippi and Tennessee have the lowest prices in the nation, at $2.68 and $2.70, respectively. California and Hawaii hold the highest prices in the nation this week at $4.84 and $4.50, respectively.

AAA Northeast is a not-for-profit auto club with offices in Rhode Island, Massachusetts, Connecticut, New Jersey, New Hampshire and New York, providing more than 6.5 million local AAA members with travel, insurance, financial and auto-related services.

Ward Melville High School. File photo by Greg Catalano

By William Stieglitz

Students and parents spoke out at the April 9 Three Village Central School District BOE meeting, arguing for the programs and staff they did not want to see cut. The board had previously announced that in order to balance the proposed budget with later start times for high school students, it would need to remove 14 elementary teachers as well as the fourth-grade Intellectually Gifted (IG) program.

Students who once participated in the IG program, as well as parents of such students, voiced their support for it, saying it provided them with an academic challenge and motivation they were not able to experience before. “Once I joined the IG program, I was toward the bottom of the pack, so it was wonderful to finally get that experience,” said Althea Grubbs Albrecht, who joined as a sixth grader in the program’s last year. “It really prepared me for academic struggles in junior high and now in high school.”

“The teachers I had there, they encouraged my love for reading, they encouraged my ability to think about and consider different ideas,” said new valedictorian Oliver Wu. “Eliminating the IG program without putting anything else in its place, without initiating a new program to give enrichment to students who would benefit from it, is very harmful.” He, along with others, expressed concern that the IG program could be phased out, though  Superintendent Kevin Scanlon said this would not happen.

Simultaneously, many parents stressed the importance of later high school start time levels for students’ health. “We all want our children to be academically excelled, but they need health first,” said Jade Zheng, a mother of two kids in the district. “If I have to make a choice, health first.” Others stressed the long timeline of the effort to make the change, citing a petition from 2019 that garnered 1,700 votes.

The proposed cuts to elementary teachers were a concern too, not just for the sake of the teachers, but for the elementary students who would then be forced into larger-sized classes. Oliver Wu said he has been “one of the biggest supporters of start time changes,” but if the board “had to choose between cuts to dozens of staffs and educational programs or the start time, I would support delaying the start time.”

Board members responded that all three concerns were priorities to them, and they did not want students and parents to have to argue for one program over another. “We’re at a point this year, unfortunately,” said Vice President Karen Roughley, “where we need to put the education of our elementary students against start times for the older students and I don’t think that’s a good place to be.” Trustee Stanley Bak also expressed concern that the board could have better communicated the planned cuts beforehand so they came as less of a surprise. “Programs cost money,” he said. “Communication does not.”

The board debated withdrawing from their emergency reserves, a possibility touched on by parents, but according to Scanlon, spending those funds would only cover costs to next year, and would put them at risk in case of an unexpected emergency. “When COVID-19 hit, we spent $7.3 million out of our reserves,” said Scanlon. “If another COVID-like event occurred… we will not be able to do [what we did] in 2020.”

The board also discussed removing start time changes for this year, as it would save over $1 million to fund other programs. With how long parents had been pushing for the change, some members, such as Bak, were hesitant to delay this another year. Referring to the 2019 petition, he said “Here we are in 2025, and I think about those parents… Is 2025 different?” However, others like board President Susan Rosenzweig, felt elementary classes were the higher priority. In a 4-3 vote, the measure passed.

Afterward, the board voted 6-1 to adopt the proposed budget at just over $238 million. This would be an increase of approximately $2 million from last year and mean a $336 increase in tax per household. The proposed budget offers a line-item budget for how the funds would be distributed, though these can still be changed over the next month. The next budget meeting is set for April 30, with the budget hearing on May 13 to discuss final details and the vote on May 20.

“This has been an impossible budget cycle,” said Rosenzweig before the end of the meeting. “It is not pretty, it is not perfect, people will lose, everybody’s going to lose a little bit, but it is the best that we can do.”

File photo

Suffolk County Police Sixth Squad detectives are investigating a crash that killed a motorcyclist in
Stony Brook on April 20..

Airton Santos-Alexandre was operating a 2015 Suzuki GSX-R750 on Southbound Nicolls Road, when
he lost control, and struck a guardrail on the right shoulder at approximately 11:10 a.m. The impact
ejected Santos-Alexandre.

Santos-Alexandre, 26, of Medford, was pronounced dead at the scene. The motorcycle was impounded for a safety check.

It is said that all good things come in threes and the The Ward Melville Heritage Organization (WMHO)’s  event on April 11 was no exception as it hosted ribbon cuttings for Stony Brook Village Center establishments Georgio’s Coffee Roasters; North Shore Injury Lawyer Mark Freeley, Esq.; and The Little Cheese Shop.

For over 20 years, Georgio’s Coffee Roasters has been perfecting the art of roasting coffee in Farmingdale. Now they are thrilled to expand their legacy with a new location at 131 Main Street in Stony Brook. Founded by Lydia and Georgio Testani, the coffee shop offers Georgio’s signature roasted coffee beans and freshly ground coffee, available in 21 varieties. Their extensive drink menu features specialty lattes, cappuccinos, and rich hot chocolate, featuring house-made syrups. For those on the go, Georgio’s also serves delicious to-go items, such as bacon, egg, and cheese tacos and challah peanut butter and jelly sandwiches. They are open every day from 9 a.m. to 6 p.m. For more information, call 631-841-1700 or visit georgioscoffee.com.

North Shore Injury Lawyer, Mark Freeley, Esq., brings over 30 years of personal injury litigation experience to his new office at 111 Main Street in Stony Brook. A longtime local resident and Senior Partner at a respected law firm in Woodbury, Freeley offers clients in the Three Village area personalized legal services backed by the strength of a full legal team. He is available by appointment in Stony Brook with a flexible schedule. In addition to handling injury cases, Freeley provides free reviews of auto insurance policies to help ensure proper coverage. Known for his daily walks with his rescue dogs and his volunteer work with Last Chance Animal Rescue, he is a familiar face in the community he proudly serves. By appointment only, call 631-495-9435 or visit northshoreinjurylawyer.com.

Little Cheese Shop at 127 Main Street in Stony Brook is run by Chris and Krystal Abate—industry professionals with over 20 years of experience in the food world. The charming boutique cheese shop offers an impressive selection of over 30 international and artisanal cheeses, many of which are rare finds on Long Island. In addition to cheese, the shop is stocked with gourmet pantry staples including jams, spreads, crackers, and mustards, as well as a curated selection of charcuterie. Perfect for entertaining or gifting, they also offer custom cheese platters, grazing tables, and beautifully packaged gift baskets. Cheese lovers can enjoy their full sandwich and grilled cheese menu, featuring over 20 delicious options made fresh to order. To learn more or place an order, call 631-223-0245 or visit littlecheese.shop.