Northeast
New NYC 'char broil' rule would force restaurants to cut emissions by 75%
New York officials are considering imposing emissions restrictions on a popular grilling appliance as their latest climate crackdown, claiming that such regulations could prevent premature deaths.
The blue state’s Department of Environmental Protection proposed a new rule to establish emissions standards for under-fire commercial char broilers, a commonly used method of cooking meat that gives it a smokey taste.
The proposed rule would force all New York City restaurants using under-fire char broilers installed after May 2016 to cut emissions from the appliance by 75%.
Additionally, under the rule, NYC restaurants that char-broil more than 875 pounds of meat per week would not be allowed to operate, with the exception that the business has an approved emissions control device.
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Chef David Guerrero prepares char-grilled octopus and beef heart at Alma Cebiche bar Monday, Dec. 17, 2012, in Houston. (Brett Coomer/Houston Chronicle)
In the proposed rule, reviewed by Fox News Digital, officials claimed that such regulations on meat cooking appliances could prevent hundreds of deaths.
The document cited a study by the Department of Health and Mental Hygiene on premature deaths attributed to particulate matter (PM) — solid particles like smoke or dust, released when cooking or burning fires.
“If all char broilers had control technology installed, the reduction in ambient PM concentrations could have prevented nearly 350 of these premature deaths each year,” the proposed rule reads.
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The study reportedly found that commercial char broilers released an estimated 1,400 tons of PM per year in New York’s five boroughs, which they concluded contributed to more than 12% of PM attributable premature deaths annually from 2005 to 2007.
But restaurant owners are fuming at the potential regulation.
Jeramie Robinson, chef of Zimm’s Little Deck, prepares char-grilled oysters Wednesday, Oct. 27, 2010, in Houston. (Nick de la Torre/Houston Chronicle )
“The fact that this is even an issue is a nothingburger,” Alan Rosen, who owns Juniors in NYC, a restaurant that uses the charred meat method, told the New York Post.
“People are getting knifed in the subway, and they’re worried about charbroilers? We’ve been doing this for almost 75 years. It’s absolutely ridiculous.”
In the proposed rule, the department acknowledges the difficulty in requiring New York City restaurants to undergo emissions tests.
“Demonstrating the 75% PM reduction presented a challenge for many restaurant owners who do not have an Environmental Protection Agency Method 5 certified emissions control device,” the proposal reads.
A public hearing on the proposed rule will be held on Jan. 29, 2025.
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A woman was rushed to the hospital after being seriously hurt in a fire Saturday in Rocky Hill.
This all unfolded during the late morning hours at a home on Main Street.
Fire officials say they had to rescue the woman from the home and her injuries are considered life threatening.
Hoarding conditions did a play a factor in the fire, according to the fire department.
No other injuries were reported. Further details pertaining to the fire weren’t immediately available.
The cause of the fire is under investigation.
Dressed in a fuzzy chicken costume, a then-2-year-old girl — accompanied by her parents dressed as farmers — walked around their new neighborhood ringing doorbells and asking for candy. It was July.
That is how the Westbrook community first met and fell in love with Lucy Hanson five years ago.
Everyone in Lucy’s neighborhood is close, Sue Salisbury, her neighbor, said, but it’s particularly hard not to love Lucy. She trick-or-treats year round. She jumps into her neighbors’ piles of leaves as they’re raking. She rides around the neighborhood on a seat on her dad’s bike with a speaker playing music attached in the back.
“She’s got the whole neighborhood wrapped around her finger,” Joe Salisbury, Sue’s husband, said.
So when Lucy was diagnosed with cancer at the end of October, the neighborhood decided to flood her with love as she spends the next nine months, holidays included, in the hospital for chemotherapy treatment.
Friends, neighbors, strangers and even people from other countries have sent Lucy a deluge of holiday cards, donations, gifts and meals.
Lucy’s aunt, Juna Ferguson, shared Lucy’s story on social media and asked for donations and meals to help. She also submitted Lucy’s name to The Angel Card Project, an online charity that requests greeting cards for people in need, so Lucy would feel as much love as possible during the holiday season.
In just a few weeks, Lucy has received hundreds and hundreds of cards, letters and packages, including some from as far as Germany and Australia. On Meal Train — a website that facilitates meal giving to families in hard times — people have donated almost $22,000 for the Hanson family and sent dozens of meals. Lucy’s wish list sold out within five minutes — three separate times.
The Hanson family
In many ways, Lucy is just like any other 7-year-old girl from Westbrook.
She loves Harry Potter (she’s in Gryffindor, of course). She’s reading “Harry Potter and the Order of Phoenix,” but it’s a little scary for her. She just became a Brownie in the Girl Scouts. She wants to be a music teacher when she grows up. She loves to draw and sing and dance and do gymnastics and musical theatre. She has a best friend named Mallory who she has known since she was 6 months old. She’ll cry if there’s a snow day and she can’t go to school and see Mallory.
She’s witty and kind and bubbly and fun.
But in other ways, Lucy’s life doesn’t resemble that of other kids.
Last month, she spent more time in the hospital than at home. If she’s in the hospital, she has a robot she can drive around school to participate in her classes. (She dressed up the robot with a jacket, a hat and a sparkly backpack to make it look more like her).
Lucy is much smaller than most girls her age, as a genetic condition slows her growth. And she knows a lot more about cancer than most children.
She’s used to doctors and nurses and hospitals.
A few months after she was born in July 2018, she developed a rash on her face, which eventually spread to other parts of her body. After visiting three dermatologists and ruling out eczema, Lucy ultimately was diagnosed with Rothmund-Thomson syndrome type 2, a rare genetic condition that primarily affects her skin and bones and increases her chances of developing several types of cancer. Lucy is one of about 500 documented cases of RTS in the world.
For six years, Lucy was healthy. But in October, while she was attending a conference for families affected by RTS in Salt Lake City, she started to limp. She seemed to get better after a while, but a week and a half later, she couldn’t put any weight on her foot.
That’s when she was diagnosed with osteosarcoma in her right tibia. The doctors said Lucy will need nine months of chemotherapy and a below-the-knee amputation in February of 2026.
“How will we navigate the rest of Lucy’s life?” Staci Hanson, Lucy’s mom, thought.
Even though their lives had flipped upside down, Staci and her husband Jason decided to live as normally as possible.
They make sure Lucy does school work and takes walks. A school teacher checks in with her at the hospital and a child life specialist comes to play with her. Last week, they made slime together.
The nurses and doctors at MaineHealth Barbara Bush Children’s Hospital, where Lucy is receiving her chemotherapy treatments, have made magic in a very nonmagical situation, Staci said. In the hospital, Lucy got to pick out her own Christmas tree and ornaments for her room and even made a gingerbread house.
In the past month, the Hansons have spent just five days at home. Staci and Jason take shifts at the hospital. One night, mom stays with Lucy, the next it’s dad. They only live 15 minutes from the hospital, so it’s not a long drive to come home to get new things or do laundry, Jason said.
“It feels like a long time,” Lucy protested.
Her parents are honest with her about RTS, osteosarcoma and her approaching amputation in February.
“We try to lift her up and tell her, ‘Yeah, your world is going to look a little bit different, but you can still live a super normal life even with a prosthetic,’” Staci said. “So we’ve shown her lots of videos of people doing gymnastics and dance and just living fulfilling lives even though they have a prosthetic.”
Rallying around
Since Lucy met Joe and Sue Salisbury while trick-or-treating in the summer years ago, she has become part of their family.
“It’s like having a grandchild,” Joe said.
Lucy will often randomly call the Salisburys to invite them over for a movie night. No matter what they’re doing, even if they’re in the middle of dinner, they always accept.
“You don’t say no to her,” Sue said.
So they will stop what they’re doing, walk across the road in their slippers, and cuddle up with Lucy on the couch to watch whatever movie she wants.
Now, Sue and Joe hold on to those memories of her until they can resume that tradition.
In the meantime, the community is doing everything it can to help the family. The less the Hansons have to worry about, the more they can focus on Lucy and themselves.
Joe and Sue volunteered to receive the letters for Lucy, since the Hansons are rarely home to check their mail.
“This is Lucy’s fan following,” Joe said, pointing to two packages and a bag stuffed with letters.
The Salisburys collected at least 400 cards for her in three weeks. They go to the hospital about once a week to visit Lucy and give her the letters. They would like to see her more, but the visits are limited due to Lucy’s compromised immune system.
The Salisburys own the Daily Grind, a coffee shop in Westbrook. Customers come through all the time to drop off packages and cards for Lucy and ask about her.
Neighbors pick up the Hansons’ mail and plow their driveway.
Joe isn’t surprised by the response from the community. In Westbrook, people have always helped each other out.
“I think it’s just another example of how great the Westbrook community is that everybody is pulling together for Lucy,” Sue said.
The Hanson family has received so many letters and donations, it’s impossible to write enough thank you cards, Staci said. They are saving most of the cards to give to Lucy later, because she still has many more months in the hospital.
“I don’t know how we’ll ever repay our community for the love that we’ve received,” Staci said.
Lucy’s favorite card so far has a drawing of two ducks sitting in a yellow bowl of tomato soup with some crackers on the side.
“Thought some soup and quackers might make you feel better,” Lucy read from the card.
In another package, Lucy received fake snowballs. So Lucy did what any other kid would do —started a snowball fight in her hospital room with her doctors and nurses.
Those interested in sending gifts and cards or signing up to give a meal can visit mealtrain.com/trains/w4lwd0. The RTS Foundation accepts donations at rtsplace.org/. People can also join “The Lucy League” by buying merchandise at bonfire.com/store/bravelikelucy/. All profits go to the Hanson family.
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