Maine
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.
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.
Many Maine municipalities will open cooling centers this week with the National Weather Service issuing a variety of heat advisories covering the next few days.
The Maine DEP also issued an air quality alert for Wednesday with ground-level ozone expected to reach levels that are unhealthy for sensitive groups.
All of York County, interior Cumberland and Androscoggin counties, and the southern half of Oxford County will fall under an extreme heat warning from 11 a.m. Wednesday to 8 p.m. Friday.
The warning calls for “dangerously hot conditions” that could feature heat index values of up to 110 degrees, with overnight lows only expected to fall into the 70s, according to the weather service’s office in Gray.
The rest of the state — save northern Aroostook, Piscataquis and Somerset counties — falls under a heat advisory from 11 a.m. to 8 p.m. on Wednesday. However, the weather service has also placed much of the state under an extreme heat watch for Thursday.
Heat index values, which measure how hot it feels to the human body when relative humidity is combined with the air temperature, are expected to reach up to 104 degrees during the heat advisory period, the weather service warns. They could reach 110 degrees Thursday, when the extreme heat watch is in effect.
Northern Oxford and Franklin counties, and central Somerset County, can expect a heat index value of up to 99 degrees Wednesday, according to the weather service.
The weather service advises people to drink plenty of fluids, stay in air-conditioned rooms when possible, avoid extended periods in the sun and check up on relatives and neighbors. It also warns not to leave young children and pets in unattended vehicles, as “car interiors will reach lethal temperatures in a matter of minutes.”
Cooling Centers
The Maine Department of Environmental Protection has also issued an air quality alert from 10 a.m. to 11 p.m. on Wednesday along the coast from Kittery to Acadia National Park. The agency warns that ground-level ozone concentrations are expected to reach levels that are unhealthy for sensitive groups.
Ozone levels may reach “moderate levels” further inland, according to the Maine DEP, including in all of Androscoggin and Kennebec counties, as well as parts of Cumberland, Knox, Lincoln, Penobscot, Sagadahoc, Waldo, Washington and York counties.
Elevated ozone levels can pose a risk to children, older adults and people suffering from respiratory or heart diseases, according to the Maine DEP. Anyone exerting themselves outdoors may also experience health effects, which could include coughing, shortness of breath, throat irritation and mild chest pain.
Ozone levels were already climbing in southern New England on Tuesday, according to the Maine DEP, and winds are expected to bring those conditions to Maine on Wednesday.
The Maine DEP recommends that vulnerable populations avoid strenuous outdoor activities, keep windows closed, and circulate indoor air with fans or air conditioners. Those with asthma are also advised to keep quick-relief medication handy.
Particle pollution levels are also expected to be moderate across the state on Wednesday due to wildfire smoke, the Maine DEP said in its announcement Tuesday. Wildfires in Colorado, which have claimed the lives of three firefighters, had burned nearly 90,000 acres as of Tuesday, according to the Denver Post.
Maine could face up to $50 million in penalties next year due to errors in its payments for federal food benefits under the Supplemental Nutrition Assistance Program.
Newly released data from the U.S. Department of Agriculture find that Maine’s error rate last year was nearly 11%, the bulk of which were overpayments. That’s in line with the U.S. average. But starting in October of next year, states with error rates above 6% must cover a portion of the SNAP benefits.
Anna Korsen, executive director of Full Plates, Full Potential, said the overpayments aren’t fraud — they’re human error. She said this new cost-shifting policy enacted last year under the Trump administration further complicates the SNAP application process.
“Instead, we could make this program more accessible and more efficient,” Korsen said. “And that would reduce the number of errors and also ensure that Mainers who are eligible for SNAP have access to it.”
She’s urging Congress to delay or reverse the policy under the farm bill that’s currently under consideration.
Maine’s Department of Health and Human Services said it’s taking steps to reduce the error rate, including modernizing its systems and hiring an additional 40 eligibility specialists.
This story appears through a media partnership with Maine Public.
PORTLAND (WGME) — The third annual Celebration of America 300 is set for Thursday night at Oxford Plains Speedway.
This race was a favorite of NASCAR star Kyle Busch, who tragically passed away back in May. He was just 41.
Now, a Maine-born driver who worked on Busch’s team is ready to take the 8 car into victory lane.
For the past five years, Windham native Derek Kneeland was Busch’s eye in the sky, working as a spotter for the cup star. Kneeland says his relationship with Busch was like a brotherhood.
“I was fortunate enough where I got to have a personal relationship with him,” Kneeland said. “He came up, and he ran several races with me in late models and stuff at Oxford and Lee Speedway, and we got to do a lot of cool things together.”
Kneeland says dealing with the sudden loss has been both painful and difficult.
“It’s still hard,” Kneeland said. “I’m having a hard time with it. The weekdays are the hardest. At the track is where I’m most comfortable.”
Kneeland will be at the track and behind the wheel Thursday night, competing in the Celebration of America 300, driving the number 8 car.
“You know, a few days after everything went down, his dad called me, and his dad is a man of very few words, and I said, ‘You know, I’m thinking about running the 8 or 51 as long as I have your guys’ blessing, I would like to do that.’ And he said, ‘Short track world knows him as 51, but the world knows him as 8,’” Kneeland said.
Kneeland says it will be an emotional race, but he’s confident he’ll have a special co-pilot leading the way.
“Hoping he’s going to be on my shoulder and give me the guiding way and but to win it for Kyle, I think that would put the stamp on it,” Kneeland said.
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