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Hochul spearheads plan to pay NYers to switch to green appliances amid state money woes

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Hochul spearheads plan to pay NYers to switch to green appliances amid state money woes

New York is rolling out a new incentive for residents who switch to green alternatives for their household appliances. 

In an announcement Thursday, Gov. Kathy Hochul revealed that her state will be the first to offer a rebate under a new Appliance Upgrade Program.

The rebate, funded by the Inflation Reduction Act (IRA), offers low- and moderate-income households up to $840 if they switch out their fossil fuel-powered clothes dryers with heat pump-powered alternatives.

“New York is demonstrating its continued commitment to ensuring an equitable energy transition by leveraging all federal funds available to incentivize consumers to make energy-efficient appliance purchases a priority,” Hochul said in a statement. 

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New York Gov. Kathy Hochul speaks during an announcement on the inclusion of money for the Mental Health and Public Safety Budget for fiscal year 2025 at Midtown Community Justice Center in New York City on April 24. (Lev Radin/Pacific Press/LightRocket)

“As a result of these new rebates, low- and moderate-income New Yorkers will save energy and money while doing their laundry with modern technology that will reduce emissions,” she added.

5 INSANE BIDEN-HARRIS APPLIANCE REGULATIONS HEADING YOUR WAY

The New York State Energy Research and Development Authority (NYSERDA) also praised the new initiative.

“NYSERDA is pleased to start distributing this IRA funding for home appliance rebates through a customer-centric approach that ensures low-and moderate-income New Yorkers can easily upgrade inefficient clothes drying equipment or purchase a dryer for the first time,” NYSERDA said.

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The handout comes as New York ranks as having the second-highest debt burden in the nation in 2021, according to the New York State Comptroller.

New York Gov. Kathy Hochul revealed that her state will be the first to offer a rebate under a new Appliance Upgrade Program. (George Frey)

The comptroller’s office released a report on the state’s financing plan, which projected New York would issue over 3.4 times more debt than it will retire over the next five years.

New York has been pushing to phase out fossil fuels in the state but has been previously criticized for its initiatives.

Officials announced in May 2023 that beginning in 2026, New York will prohibit gas stoves and heating systems for new construction of buildings seven stories or fewer, according to reports.

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“I think it’s ridiculous, and I think the danger is that it almost seems comedic and so people can take it, you know, maybe not as seriously as they should,” New York Senate Minority Leader Rob Ortt told Fox News Digital in an interview before the ban. “It is going to increase people’s utility rates in the state of New York, it is going to decrease energy reliability in the state of New York, and it will do nothing to fight climate change.” 

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Connecticut

Woman suffers life threatening injuries in Rocky Hill house fire

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Woman suffers life threatening injuries in Rocky Hill house fire


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.

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No other injuries were reported. Further details pertaining to the fire weren’t immediately available.

The cause of the fire is under investigation.



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Maine

Christmas wishes flow in for 7-year-old Maine girl fighting cancer

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Christmas wishes flow in for 7-year-old Maine girl fighting cancer


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. 

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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. 

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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.

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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.

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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. 

Staci and Jason Hanson pose with their daughter, Lucy. (Courtesy of the Hanson family)

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. 

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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. 

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“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. 

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A box is filled with cards for Lucy Hanson to cheer her up while she spends the holidays in the hospital. (Courtesy of the Hanson family)

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. 

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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.

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“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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Massachusetts

After lawsuits, Mass. drops gender ideology mandate for foster parents

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After lawsuits, Mass. drops gender ideology mandate for foster parents


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Massachusetts will no longer require prospective foster parents to affirm foster children’s gender identity.

Massachusetts will no longer require prospective foster parents to affirm the sexual orientation and gender identity of the children they foster, following legal challenges and criticism from religious groups.

The change comes after the conservative legal group Alliance Defending Freedom (ADF) filed a federal lawsuit in September on behalf of two Massachusetts families, who claimed the requirement conflicted with their religious beliefs, according to a Fox News report. One couple had its foster care license revoked, while the other was threatened with revocation.

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That same month, federal regulators with the Administration for Children and Families (ACF) sent a letter to Massachusetts criticizing the mandate as discriminatory and a violation of the First Amendment. The agency said it would open an investigation into the matter.

On Dec. 12, the Massachusetts Department of Children and Families (DCF) updated its regulations, replacing language that required foster parents to affirm a child’s “sexual orientation and gender identity” with a requirement that they support a child’s “individual identity and needs.”

The shift comes amid a broader national debate, as states grapple with whether foster parents should be required to support children’s gender identity even when it conflicts with their personal or religious beliefs.

In a statement to GBH News, DCF Commissioner Staverne Miller said the agency’s top priority is ensuring children in foster care are placed in safe and supportive homes.

“We are also committed to ensuring that no one is prevented from applying or reapplying to be a foster parent because of their religious beliefs,” Miller said.

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ADF lauded the change in a statement released Wednesday. 

“Massachusetts has told us that this new regulation will no longer exclude Christian and other religious families from foster care because of their commonly held beliefs that boys are boys and girls are girls,” said ADF Senior Counsel Johannes Widmalm-Delphonse. 

“Our clients—loving, caring foster families who have welcomed vulnerable children into their homes—as well as many other families affected by this policy, are eager to reapply for their licenses,” Widmalm-Delphonse continued. “This amendment is a step in the right direction and we commend Massachusetts officials for changing course. But this case will not end until we are positive that Massachusetts is committed to respecting religious persons and ideological diversity among foster parents.”

Morgan Rousseau is a freelance writer for Boston.com, where she reports on a variety of local and regional news.





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