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Tag: American Cancer Society

  • Missing the first mammogram linked to increased risk of breast cancer death, new study suggests

    (CNN) — Women who miss their first screening appointment for breast cancer could have a 40% higher long-term risk of dying from the disease, according to a new study.

    I wanted to understand more about the importance of screening and the results of this large study — especially since October is Breast Cancer Awareness Month. The research, published September 24 in the journal The BMJ, involved more than 400,000 women in Sweden who were monitored for up to 25 years.

    When should women begin screening for breast cancer, and why could delayed initial screening result in a higher longer-term risk of cancer death? In addition to mammograms, are there other tests that women should ask for? What about breast self-exams? And what are steps women can take to reduce their risk of developing breast cancer?

    To guide us through these questions, I spoke with CNN wellness expert Dr. Leana Wen. Wen is an emergency physician and adjunct associate professor at George Washington University. She previously served as Baltimore’s health commissioner.

    CNN: How common is breast cancer?

    Dr. Leana Wen: In the United States, breast cancer is the second most common cancer among women and the second leading cause of cancer death among women, according to the US Centers for Disease Control and Prevention. In 2022, more than 279,000 new breast cancer cases in female patients were reported in the US; in 2023, more than 42,000 women died from the disease.

    A report published in February found that globally, 1 in 20 women will be diagnosed with breast cancer in their lifetime. At this rate, researchers estimate that by 2050, there will be 3.2 million new breast cancer cases and 1.1 million breast cancer-related deaths per year.

    Early screening is crucial because the best prognosis is when breast cancer is diagnosed and treated in its earliest stages. When breast cancer is diagnosed in its localized stages — before it has spread — the five-year survival rate is more than 99%, according to the American Cancer Society. When the cancer is detected after it has spread to other organs, the survival rate drops to about 32%.

    CNN: When should women begin screening for breast cancer?

    Wen: Last year, the US Preventive Services Task Force lowered the recommended age for most women to start receiving mammograms to age 40. The guidance is that women should receive a mammogram every other year until age 74. For those 75 and above, the decision to continue screenings is a personal one to make with one’s primary care provider.

    This recommendation covers people with an average risk of breast cancer. Those with a higher risk are encouraged to speak with their health care provider to discuss whether they should begin screenings sooner and at a higher frequency than every other year. Elements that increase risk include a history of radiation to the chest, certain genetic mutations, and having a first-degree relative (like a mother or sister) with breast cancer.

    CNN: What does this new study show?

    Wen: This study tracked outcomes from 432,775 women in Sweden for up to 25 years. Among women invited to their first mammogram screening, nearly one-third did not participate. The nonparticipants continued to be less likely to participate in subsequent mammograms and more likely to have breast cancer diagnosed in advanced stages, the researchers found.

    Notably, the odds of these initial nonparticipants being diagnosed with stage 3 cancer was 1.5 times greater, and 3.6 times greater for stage 4 cancer, compared with those who did participate in a first screening. Breast cancer deaths after 25 years for this group were significantly higher compared with those who followed through on a first mammogram.

    These results are notable because of the large population that the study team monitored over a substantial period of time. Researchers point out that findings may not generalize to all populations that have different health care systems from Sweden’s, though I think that the concept of perpetually missed screenings leading to higher cancer rates probably is the case around the world. An accompanying editorial in the same journal highlighted that the decision to attend the first mammography screening is not just a short-term health check-up — it’s a long-term investment that has implications for future health and survival.

    CNN: Why does delayed initial screening result in a higher longer-term risk of cancer death in this study?

    Wen: I think the key is that the initial nonparticipants were also more likely to persistently miss subsequent follow-up screening exams. The reasons for this are likely complicated and could be a combination of factors, including lack of awareness, barriers to access and fear of finding out the result. Cultural factors may also be at play. The result is that these individuals were more likely to have their cancers diagnosed at a later stage, when survival rates are lower, and therefore tragically ended up having more deaths from their cancers.

    CNN: In addition to mammograms, are there other tests that women should ask for?

    Wen: Mammograms, which are essentially an X-ray of the breast, are the standard screening test for most women at average risk of breast cancer. Those with higher risk of breast cancer may be recommended for additional tests, such as genetic testing, breast MRI or ultrasound. Women with dense breast tissue may also wish to ask their provider if additional tests are recommended, since the mammogram is less sensitive in detecting breast cancer in these individuals.

    CNN: What about breast self-exams?

    Wen: Breast self-exams are not routinely recommended as a screening test and should not replace the mammogram. However, women should know how their breasts look and feel and be on the lookout for any concerning changes.

    It is important to separate out screening from diagnosis. The mammogram is a screening test that is done when someone has no symptoms. But if someone detects a new mass or lump, they need to get it evaluated to see whether it could be cancer.

    Other potentially concerning changes including nipple discharge, pain or swelling in their breast, changes in the color of the nipple or breast, the nipple turning inward, painful or enlarged lymph nodes in the armpits or near the collarbone, or redness or flaky skin on the breast. People who notice these changes should not wait to make an appointment to see their health care provider.

    CNN: For women who are concerned about their risk of breast cancer, are there steps they can take to reduce their risk?

    Wen: Yes. Risk factors for developing breast cancer include smoking, heavy alcohol use, overweight and obesity. Quitting smoking, reducing alcohol consumption and keeping a healthy weight will help to reduce the risk of breast cancer. Being physically active and eating a nutritious diet can also reduce cancer risk, as well as improve health overall.

    Katia Hetter and CNN

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  • EmpowHer and Him organization aims to increase visibility of male breast cancer 

    After being diagnosed with breast cancer in 2021, advocate Daphne Meyers decided to elevate her mission of creating safe spaces and encouraging early detection by launching EmpowHer and Him. The organization aims to empower those who have been diagnosed and increase the visibility of men in the breast cancer conversation.

    The Atlanta Voice talked with Meyers about the organization’s annual brunch, the importance of early detection, and what it means to be on the frontline of this fight. 

    Photo by Laura Nwogu/The Atlanta Voice

    The Atlanta Voice: EmpowHER and HIM recently held its annual breast cancer awareness brunch. What’s been the most important part of getting to see how much this organization and the people who support it have grown?

    Daphne Myers: “When we started, it was called the Tatas and Tutus. I was an advocate for breast cancer, but had never really thought much about the men. It wasn’t until the second year that I was like, ‘Well, men can get breast cancer, so why am I not getting men to come to this event?’ The first year, none. In the second year, we probably had four, and one of them was my son. So I said, ‘Okay, I’m getting interest. Men are buying the tickets, but they’re sending their wives or sisters or daughters; they’re not coming.’

    “I changed the name in the third year to Tatas, Tutus, and Ties. The most rewarding aspect of that is seeing how it has grown from year one to year five. We probably had at least 60 men this year, and that’s grown from having none, to a year of four, and then maybe double that the following year. And so now it seems as if we have just as many men in there.” 

    AV: “I love that. Let’s go back a little. EmpowHer and Him is about uplifting every fighter, men and women, going through this battle. Can you talk about how the organization began?

    DM: “I was diagnosed with breast cancer in 2021. Based on my diagnosis, I thought, ‘I’ve always been an advocate, so where do I go from here to raise more awareness among men and women?’ Being diagnosed with breast cancer, you’re all over the place. First, you have to accept it, and then second, you have to figure out how to navigate. You’ve got to decide whether to do treatment or not, and how it’s going to affect your livelihood. So the questions that were in my mind as someone with breast cancer at that particular time prompted me to say, ‘You know what? If I had those questions, there are millions of other people who have those same questions. And if I have the answer to it, then I need to open up my mouth and be able to give the gift of awareness. 

    “This is bigger than me. It’s bigger than the Tatas, Tutus, and Ties. It’s about bringing about awareness, not just for women, but also for men. In the past year, I found myself doing a lot of speaking engagements, and a lot of men, just like women, don’t know about breast cancer. That’s where EmpowHER and HIM came about. I had to use this mouthpiece to bring about awareness so that people know that early detection is key. If I tell one person, then that person tells someone else; it becomes a domino effect. Your work is not done, but it keeps going.” 

    AV: I think that’s so admirable that your fight became perspective, and it became this thing about you wanting to lend a helping hand and be a support system for other people who may be going through their own breast cancer journey or fight.

    When it comes to the aspect of men being diagnosed with breast cancer, why do you think there’s not a lot of visibility in their fight?

    DM: “There’s no talk about it. Even from the medical profession, there’s not a lot of talk about it. I did an interview, probably about two or three weeks ago, and I was talking to this man about breast cancer, and he said, ‘Yeah, you don’t think about men with breast cancer.’ I said, ‘But you have a chest.’ He says, ‘OK, well, let’s maybe say breast and chest cancer.’ 

    “People don’t understand that they have breast tissue; this is our breastplate. It’s not just prostate [cancer], and it’s not just colon. We have to come together and understand that yeah, it may be a small percentage, but it is there. When you see the Susan G. Komen’s or the American Cancer Society, you see women, and the men are in the background. With EmpowHer and Him, we’re both standing there side by side. So that’s why the ribbon is half pink and half blue. It’s about making it more relatable to them. Men don’t know that they can get a mammogram. When you go to fill out your paperwork, it says, when  was your last period? How many pregnancies? You’re putting on this pink robe to get your mammogram, all of that. Our medical society doesn’t even pay attention to it as much as we should.”

    AV: What do you think there needs to be more awareness about when it comes to breast cancer?

    DM: “Early detection. That’s the key to anything. I know it sounds cliché-ish, but we have to start with checking our breasts and our chest at an early age, and especially if you have a history of it in your family. Because I was diagnosed with breast cancer, it kind of moves the scale up for my children to be checked.

    “People of color, our breast tissue is more dense, so it goes undetected. On a regular mammogram mine was missed the first time. It wasn’t until I got the 3D that detected my breast cancer. Had I gone on and thought it was clear, I may not have been sitting here talking to you today.”

    AV: For those that are looking for resources or someone to talk to, what can EmpowHer and Him be for that person?

    DM: “I’m frontline, and what better person to be frontline than the person who’s actually going through it? I get calls every week of a new diagnosis, and I have to put a lot of hats on. I have to speak, because the one thing people want to know is, ‘What’s your suggestion?’ Do what’s gonna be best for you. Don’t just run with the first thing and then say, this is what I’m gonna do without checking deeper into it. The other thing is for resources. When you’re going through treatment, you’re not gonna feel good. I had to go through 18 rounds. You’re tired, you’re sad, you go into depression. So you have to battle with all of those things. There are several support groups that are out there, including with us. 

    “I found myself telling people to just start journaling. Do what makes you feel good to get you through that. Ask for help. It’s not a death sentence. Just because we’re diagnosed with breast cancer doesn’t mean that that’s our end. It’s actually a beginning. And it was a beginning for me, because I was on one side of the Richter scale as an advocate, to now I’m a surviving advocate, and my goal is to put this out there as much as possible and really  help bring about this awareness with me.”

    AV: What does it mean for you to be on the front line and to see what the organization has grown into?

    DM: “I’m proud of myself. And a lot of times people say, ‘Oh, you shouldn’t brag.’ No, I am. I’m proud of myself, I’m proud of my friends, I’m proud of my family, because while I was a survivor of the disease, they were survivors of me, because they were there with me. I’m proud when that person comes to me and says, ‘Man, that event that you had opened up some doors. I’m gonna get tested.’ ‘I didn’t know that, because I’m a male…’ or ‘I didn’t know that just by changing your diet to this, that and the third could help…’ ‘I didn’t know how to do an exam.’ 

    “My first scare, believe it or not, was when I was eight years old, so by the time I was diagnosed, that was my fifth surgery. So it’s here. Unfortunately they say that there’s no cure, but there are some things that we can change. We just have to take care of ourselves, love one another, keep down the stress, and survive this game.”

    Laura Nwogu

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  • Atlantic City Casinos Unite to Support Breast Cancer Awareness

    Posted on: October 3, 2025, 03:14h. 

    Last updated on: October 2, 2025, 01:15h.

    • October is Breast Cancer Awareness Month
    • Atlantic City casinos are recognizing the initiative in various ways

    October is Breast Cancer Awareness Month, and the nine casinos in Atlantic City are uniting in support of the annual initiative that supports research and the early detection of the disease.

    Atlantic City Breast Cancer Awareness Month
    Resorts Casino Hotel in Atlantic City is lit pink to recognize October being Breast Cancer Awareness Month. Most casinos in town are also recognizing the month that raises awareness and support for breast cancer. (Image: Casino Reinvestment Development Authority)

    Since its founding in 1985 through a partnership between the American Cancer Society and the pharmaceutical division of Imperial Chemical Industries, today AstraZeneca, October has served as the national month to raise awareness regarding breast cancer. Atlantic City casinos are once again recognizing the month through a series of initiatives.

    Breast cancer impacts families in every community, but thanks to advances in detection and treatment, survival rates continue to rise. Each October during Breast Cancer Awareness Month, Atlantic City casinos stand united with our employees, guests, and the greater community to raise awareness and shine a light on this important cause,” said Mark Giannantonio, president of the Casino Association of New Jersey (CANJ) and Resorts Casino Hotel.

    “Atlantic City casinos remain committed to supporting groundbreaking research, promoting early detection, and ensuring care for all those impacted by this disease,” Giannantonio added.

    Pink Lights

    Throughout the month, Atlantic City casinos will display pink lights atop their hotel towers and on their facades.

    The color pink is associated with breast cancer awareness. In 1991, the Susan G. Komen Race for the Cure began distributing pink ribbons to participants. Pink is also seen as a feminine and compassionate color.

    Borgata, Caesars Entertainment’s three properties (Caesars, Harrah’s, and Tropicana), Ocean, Hard Rock, and Resorts all plan to light up their properties pink. At Golden Nugget, male staffers will wear pink and compete with one another to raise the most money for breast cancer research.

    Hard Rock is selling a pink-colored cocktail all month long, with a portion of the drink’s proceeds supporting breast cancer. Caesars is running a similar pink cocktail special and has committed $1 of every drink sold to the American Cancer Society’s Men Wear Pink campaign. Resorts is also offering a pink cosmopolitan, with proceeds benefitting the American Cancer Society.

    Golden Nugget says donated gaming vouchers will be given to Making Strides Against Breast Cancer. Resorts is donating its voucher buckets to the Men Wear Pink initiative of Greater Philadelphia.

    Borgata and Caesars properties are additionally offering free on-site mammogram screenings for team members.

    For a complete list of all Atlantic City casino breast cancer awareness activities, click here.

    Breast Cancer Statistics

    Among the most funded cancers, breast cancer is the most common cancer in women in the United States, except for skin cancers. Breast cancer accounts for about 30% of all new female cancers each year, the American Cancer Society says.

    The organization says there are more than four million breast cancer survivors in the US, inclusive of current patients and those who have completed treatment.

    The five-year survival rate for localized breast cancer, the lowest grade on the SEER (Surveillance, Epidemiology, and End Results) scale, is better than 99%. However, the five-year survival rate for a Distant SEER diagnosis, meaning the cancer has spread to distant parts of the body such as the lungs, liver, or bones, is just 32%.

    Devin O’Connor

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  • Coming to a neighborhood near you: New Mobile Prostate Cancer Screenings made possible by Winship, AMBFF

    On Tuesday, Sept. 2, 2025, the mobile prostate cancer screening unit, which is 38 feet long and has an exam room and lab inside, took up some space inside Mercedes-Benz Stadium.

    There will be more than an estimated 313,000 new cases of prostate cancer in the United States this year, according to data from the American Cancer Society. Of that estimation, nearly 36,000 men will die from prostate cancer.

    With 1 in every 8 American men being diagnosed with prostate cancer, getting screened for prostate cancer early can save lives. Black men have even greater chances of having their lives saved if prostate cancer screenings are more available.

    The mobile screening units would help make a difference for thousands of men who might or don’t want to make the appointments necessary to schedule screenings. The Winship Cancer Institute of Emory University and the Arthur M. Blank Family Foundation are taking steps to help with that with a new mobile screening clinic.

    The PSA screenings can be done inside the mobile unit and can be completed in 30 minutes. Photo by Donnell Suggs/The Atlanta Voice

    The mobile prostate cancer screening unit took up some space inside Mercedes-Benz Stadium on Tuesday, Sept. 2, 2025. It was on display for a media tour that morning.

    Several physicians were scheduled to speak to the media about what was next in terms of where it was going to be in metro Atlanta. The 38-foot-long unit has an exam room and a lab inside. The screenings are free, do not require patients to have medical insurance, and take 30 minutes from start to finish. Patients get their prostate-specific antigen (PSA) blood test results in the afternoon.

    The mobile unit will make 15-20 scheduled stops around Atlanta, including in Piedmont Park and Emory University’s campus.

    Dr. Kennard Hood is a family physician with Emory University, is the medical director for the prostate cancer screening unit. Hood, like many of the physicians and healthcare specialists that The Atlanta Voice talked to on Tuesday, believes PSA screenings and early detection will help saves lives. The mobile screening unit can make those screenings much easier.

    “If you can detect prostate cancer early, there is a better chance of finding a cure,” Hood, who also works as a family physician at an Emory University clinic in Henry County, said.

    The mobile unit has an exam room inside. Photo by Donnell Suggs/The Atlanta Voice

    “With this mobile screening unit, we can actually take this unit to the community,” Hood said.

    Emory Healthcare and Winship Cancer Institute Lab Technician Andre Posey II said being ahead of the game and accessible to the Black community will make a big difference.

    “We have to be proactive, not reactive,” Posey, a Chicago native, said.

    Posey’s great-grandfather died from complications brought on by prostate cancer, and he believes that not getting screening and the misconceptions of prostate screenings with the Black community led to his great-grandfather being less prepared for the fight.

    “I want the numbers to change for everybody, because it’s just a screening and not invasive,” Posey II said.

    According to research done by the National Institute of Health, Black men are disproportionately affected by prostate cancer.

    “Bringing prostate cancer screening directly into neighborhoods helps break down the barriers that too often keep men from getting tested,” said Martin Sanda, MD, Louis McDonald Orr Distinguished Professor of Urology at Emory University School of Medicine and director of Winship’s Prostate Cancer Program.

    Sanda leads the team running the screening initiative and told The Atlanta Voice that making prostate cancer screenings more convenient and accessible, “We can find the disease earlier, when it’s most treatable, and ultimately save more lives.”

    Donnell Suggs

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  • Biden announces $150 million in research grants as part of his ‘moonshot’ push to fight cancer

    Biden announces $150 million in research grants as part of his ‘moonshot’ push to fight cancer

    NEW ORLEANS (AP) — President Joe Biden is zeroing in on the policy goals closest to his heart now that he’s no longer seeking a second term, visiting New Orleans on Tuesday to promote his administration’s “moonshot” initiative aiming to dramatically reduce cancer deaths.

    The president and first lady Jill Biden toured medical facilities that receive federal funding to investigate cancer treatments at Tulane University. Researchers used a piece of raw meat to demonstrate how they are working to improve scanning technology to quickly distinguish between healthy and cancerous cells during surgeries.

    The Bidens then championed the announcement of $150 million in awards from the Advanced Research Projects Agency for Health. Those will support eight teams of researchers around the country working on ways to help surgeons more successfully remove tumors from people with cancer. It brings the total amount awarded by the agency to develop breakthrough treatments for cancers to $400 million.

    Cancer surgery “takes the best surgeons and takes its toll on families,” Biden said. He said the demonstration of cutting-edge technology he witnessed would offer doctors a way to visualize tumors in real time, reducing the need for follow-on surgeries.

    “We’re moving quickly because we know that all families touched by cancer are in a race against time,” Biden said.

    The teams receiving awards include ones from Tulane, Dartmouth College, Johns Hopkins University, Rice University, the University of California, San Francisco, the University of Illinois Urbana-Champaign, the University of Washington and Cision Vision in Mountain View, California.

    Before he leaves office in January, Biden hopes to move the U.S. closer to the goal he set in 2022 to cut U.S. cancer fatalities by 50% over the next 25 years, and to improve the lives of caregivers and those suffering from cancer.

    “I’m a congenital optimist about what Americans can do,” Biden said. “There’s so much that we’re doing. It matters”

    Experts say the objective is attainable — with adequate investments.

    “We’re curing people of diseases that we previously thought were absolutely intractable and not survivable,” said Karen Knudsen, CEO of the American Cancer Society and the American Cancer Society Cancer Action Network.

    Cancer is the second-highest killer of people in the U.S. after heart disease. This year alone, the American Cancer Society estimates that 2 million new cases will be diagnosed and 611,720 people will die of cancer diseases.

    Still, “if all innovation ended today and we could just get people access to the innovations that we know about right now, we think we could reduce cancer mortality by another 20 to 30%,” Knudsen said.

    The issue is personal enough for Biden that, in his recent Oval Office address about bowing out of the 2024 campaign, the president promised to keep fighting for “my cancer moonshot so we can end cancer as we know it.”

    “Because we can do it,” Biden said then.

    He said in that speech that the initiative would be a priority of his final months in office, along with working to strengthen the economy and defend abortion rights, protecting children from gun violence and making changes to the Supreme Court, which he called “extreme” in its current makeup during a recent event.

    Both the president and first lady have had lesions removed from their skin in the past that were determined to be basal cell carcinoma, a common and easily treated form of cancer. In 2015, their eldest son, Beau, died of an aggressive brain cancer at age 46.

    “It’s not just personal,” Biden said Tuesday. “It’s about what’s possible.”

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    The president’s public schedule has been much quieter since he left the race and endorsed Vice President Kamala Harris, making Tuesday’s trip stand out.

    Advocates have praised Biden for keeping the spotlight on cancer, bringing stakeholders together and gathering commitments from private companies, nonprofit organizations and patient groups.

    They say that the extra attention the administration has paid has put the nation on track to cut cancer death rates by at least half, preventing more than 4 million deaths from the disease, by 2047. It has done so by bolstering access to cancer treatments and reminding people of the importance of screening, which hit a setback during the coronavirus pandemic.

    “President Biden’s passion and commitment to this effort has made monumental differences for the entire cancer community, including those who are suffering from cancer,” said Jon Retzlaff, the chief policy officer at the American Association for Cancer Research.

    Looking ahead, Retzlaff said, “The No. 1 thing is for us to see robust, sustained and predictable annual funding support for the National Institutes of Health. And, if we see that through NIH and through the National Cancer Institute, the programs that have been created through the cancer moonshot will be allowed to continue.”

    Initiatives under Biden include changes that make screening and cancer care more accessible to more people, said Knudsen, with the American Cancer Society.

    For instance, Medicare has started to pay for follow-up colonoscopies if a stool-based test suggests cancer, she said, and Medicare will now pay for navigation services to guide patients through the maze of their cancer care.

    “You’ve already paid for the cancer research. You’ve already paid for the innovation. Now let’s get it to people,” Knudsen said.

    She also said she’d like to see the next administration pursue a ban on menthol-flavored cigarettes, which she said could save 654,000 lives over the next 40 years.

    Scientists now understand that cancer is not a single disease, but hundreds of diseases that respond differently to different treatments. Some cancers have biomarkers that can be targeted by existing drugs that will slow a tumor’s growth. Many more targets await discovery.

    “We hope that the next administration, whoever it may be, will continue to keep the focus and emphasis on our national commitment to end cancer as we know it,” said Dr. Crystal Denlinger, CEO of the National Comprehensive Cancer Network, a group of elite cancer centers.

    Will Weissert, Carla K. Johnson and Associated Press

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  • Daffodils donated to Albany Med cancer patients

    Daffodils donated to Albany Med cancer patients

    ALBANY, N.Y. (NEWS10) — The American Cancer Society delivered daffodils to cancer patients at Albany Medical Center on Thursday. Daffodils are known as the first flower of spring, and to many, they are a symbol of hope.

    The delivery was through the annual Daffodil Days of the Capital Region campaign. It raised $20,000 this year and donated hundreds of daffodils to cancer patients in the Albany area.

    Lizzie Hunter, the director of the American Cancer Society Albany Region, said it’s a great way to bring the community together to raise funds for those with cancer.

    “To be able to bring a little bit of sunshine, light to cancer patients,” she said. “Daffodils are a sign of spring and happiness, so to be able to brighten up someone’s day that, you know, may need it.”

    All money raised through Daffodil Days goes to research, services and programs for cancer patients.

    Courtney Ward

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  • Daffodil Days presented by American Cancer Society

    Daffodil Days presented by American Cancer Society

    ALBANY, N.Y. (NEWS10) — The American Cancer Society is presenting Daffodil Days. According to the American Cancer Society’s website, participants can order daffodils and tulips by Sunday, February 18 online to help save lives, celebrate lives, and share hope for a world without cancer.

    According to the American Cancer Society, the daffodil is a symbol of hope, being the first flower of spring. A bunch of tulips for $15, potted mini daffodils for $15, and a gift of hope donation for $25 are all available, as well as additional donations anyone would like to make.

    All daffodils and tulips will be available for pickup from 1 Penny Lane in Latham the week of March 18. For more information, you can email Brendan Egan at brendan.egan@cancer.org, or call (518) 504-3931.

    Michael Mahar

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  • The Moral Case Against Euphemism

    The Moral Case Against Euphemism

    The Sierra Club’s Equity Language Guide discourages using the words stand, Americans, blind, and crazy. The first two fail at inclusion, because not everyone can stand and not everyone living in this country is a citizen. The third and fourth, even as figures of speech (“Legislators are blind to climate change”), are insulting to the disabled. The guide also rejects the disabled in favor of people living with disabilities, for the same reason that enslaved person has generally replaced slave : to affirm, by the tenets of what’s called “people-first language,” that “everyone is first and foremost a person, not their disability or other identity.”

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    The guide’s purpose is not just to make sure that the Sierra Club avoids obviously derogatory terms, such as welfare queen. It seeks to cleanse language of any trace of privilege, hierarchy, bias, or exclusion. In its zeal, the Sierra Club has clear-cut a whole national park of words. Urban, vibrant, hardworking, and brown bag all crash to earth for subtle racism. Y’all supplants the patriarchal you guys, and elevate voices replaces empower, which used to be uplifting but is now condescending. The poor is classist; battle and minefield disrespect veterans; depressing appropriates a disability; migrant—no explanation, it just has to go.

    Equity-language guides are proliferating among some of the country’s leading institutions, particularly nonprofits. The American Cancer Society has one. So do the American Heart Association, the American Psychological Association, the American Medical Association, the National Recreation and Park Association, the Columbia University School of Professional Studies, and the University of Washington. The words these guides recommend or reject are sometimes exactly the same, justified in nearly identical language. This is because most of the guides draw on the same sources from activist organizations: A Progressive’s Style Guide, the Racial Equity Tools glossary, and a couple of others. The guides also cite one another. The total number of people behind this project of linguistic purification is relatively small, but their power is potentially immense. The new language might not stick in broad swaths of American society, but it already influences highly educated precincts, spreading from the authorities that establish it and the organizations that adopt it to mainstream publications, such as this one.

    Although the guides refer to language “evolving,” these changes are a revolution from above. They haven’t emerged organically from the shifting linguistic habits of large numbers of people. They are handed down in communiqués written by obscure “experts” who purport to speak for vaguely defined “communities,” remaining unanswerable to a public that’s being morally coerced. A new term wins an argument without having to debate. When the San Francisco Board of Supervisors replaces felon with justice-involved person, it is making an ideological claim—that there is something illegitimate about laws, courts, and prisons. If you accept the change—as, in certain contexts, you’ll surely feel you must—then you also acquiesce in the argument.

    In a few cases, the gap between equity language and ordinary speech has produced a populist backlash. When Latinx began to be used in advanced milieus, a poll found that a large majority of Latinos and Hispanics continued to go by the familiar terms and hadn’t heard of the newly coined, nearly unpronounceable one. Latinx wobbled and took a step back. The American Cancer Society advises that Latinx, along with the equally gender-neutral Latine, Latin@, and Latinu, “may or may not be fully embraced by older generations and may need additional explanation.” Public criticism led Stanford to abolish outright its Elimination of Harmful Language Initiative—not for being ridiculous, but, the university announced, for being “broadly viewed as counter to inclusivity.”

    In general, though, equity language invites no response, and condemned words are almost never redeemed. Once a new rule takes hold—once a day in history can no longer be dark, or a waitress has to be a server, or underserved and vulnerable suddenly acquire red warning labels—there’s no going back. Continuing to use a word that’s been declared harmful is evidence of ignorance at best or, at worst, a determination to offend.

    Like any prescribed usage, equity language has a willed, unnatural quality. The guides use scientific-sounding concepts to lend an impression of objectivity to subjective judgments: structural racialization, diversity value proposition, arbitrary status hierarchies. The concepts themselves create status hierarchies—they assert intellectual and moral authority by piling abstract nouns into unfamiliar shapes that immediately let you know you have work to do. Though the guides recommend the use of words that are available to everyone (one suggests a sixth-to-eighth-grade reading level), their glossaries read like technical manuals, put together by highly specialized teams of insiders, whose purpose is to warn off the uninitiated. This language confers the power to establish orthodoxy.

    Mastering equity language is a discipline that requires effort and reflection, like learning a sacred foreign tongue—ancient Hebrew or Sanskrit. The Sierra Club urges its staff “to take the space and time you need to implement these recommendations in your own work thoughtfully.” “Sometimes, you will get it wrong or forget and that’s OK,” the National Recreation and Park Association guide tells readers. “Take a moment, acknowledge it, and commit to doing better next time.”

    The liturgy changes without public discussion, and with a suddenness and frequency that keep the novitiate off-balance, forever trying to catch up, and feeling vaguely impious. A ban that seemed ludicrous yesterday will be unquestionable by tomorrow. The guides themselves can’t always stay current. People of color becomes standard usage until the day it is demoted, by the American Heart Association and others, for being too general. The American Cancer Society prefers marginalized to the more “victimizing” underresourced or underserved—but in the National Recreation and Park Association’s guide, marginalized now acquires “negative connotations when used in a broad way. However, it may be necessary and appropriate in context. If you do use it, avoid ‘the marginalized,’ and don’t use marginalized as an adjective.” Historically marginalized is sometimes okay; marginalized people is not. The most devoted student of the National Recreation and Park Association guide can’t possibly know when and when not to say marginalized; the instructions seem designed to make users so anxious that they can barely speak. But this confused guidance is inevitable, because with repeated use, the taint of negative meaning rubs off on even the most anodyne language, until it has to be scrubbed clean. The erasures will continue indefinitely, because the thing itself—injustice—will always exist.

    In the spirit of Strunk and White, the guides call for using specific rather than general terms, plain speech instead of euphemisms, active not passive voice. Yet they continually violate their own guidance, and the crusade to eliminate harmful language could hardly do otherwise. A division of the University of Southern California’s School of Social Work has abandoned field, as in fieldwork (which could be associated with slavery or immigrant labor) in favor of the obscure Latinism practicum. The Sierra Club offers refuse to take action instead of paralyzed by fear, replacing a concrete image with a phrase that evokes no mental picture. It suggests the mushy protect our rights over the more active stand up for our rights. Which is more euphemistic, mentally ill or person living with a mental-health condition? Which is more vague, ballsy or risk-taker? What are diversity, equity, and inclusion but abstractions with uncertain meanings whose repetition creates an artificial consensus and muddies clear thought? When a university administrator refers to an individual student as “diverse,” the word has lost contact with anything tangible—which is the point.

    The whole tendency of equity language is to blur the contours of hard, often unpleasant facts. This aversion to reality is its main appeal. Once you acquire the vocabulary, it’s actually easier to say people with limited financial resources than the poor. The first rolls off your tongue without interruption, leaves no aftertaste, arouses no emotion. The second is rudely blunt and bitter, and it might make someone angry or sad. Imprecise language is less likely to offend. Good writing—vivid imagery, strong statements—will hurt, because it’s bound to convey painful truths.

    Katherine Boo’s Behind the Beautiful Forevers is a nonfiction masterpiece that tells the story of Mumbai slum dwellers with the intimacy of a novel. The book was published in 2012, before the new language emerged:

    The One Leg’s given name was Sita. She had fair skin, usually an asset, but the runt leg had smacked down her bride price. Her Hindu parents had taken the single offer they got: poor, unattractive, hard-working, Muslim, old—“half-dead, but who else wanted her,” as her mother had once said with a frown.

    Translated into equity language, this passage might read:

    Sita was a person living with a disability. Because she lived in a system that centered whiteness while producing inequities among racial and ethnic groups, her physical appearance conferred an unearned set of privileges and benefits, but her disability lowered her status to potential partners. Her parents, who were Hindu persons, accepted a marriage proposal from a member of a community with limited financial resources, a person whose physical appearance was defined as being different from the traits of the dominant group and resulted in his being set apart for unequal treatment, a person who was considered in the dominant discourse to be “hardworking,” a Muslim person, an older person. In referring to him, Sita’s mother used language that is considered harmful by representatives of historically marginalized communities.

    Equity language fails at what it claims to do. This translation doesn’t create more empathy for Sita and her struggles. Just the opposite—it alienates Sita from the reader, placing her at a great distance. A heavy fog of jargon rolls in and hides all that Boo’s short burst of prose makes clear with true understanding, true empathy.

    The battle against euphemism and cliché is long-standing and, mostly, a losing one. What’s new and perhaps more threatening about equity language is the special kind of pressure it brings to bear. The conformity it demands isn’t just bureaucratic; it’s moral. But assembling preapproved phrases from a handbook into sentences that sound like an algorithmic catechism has no moral value. Moral language comes from the struggle of an individual mind to absorb and convey the truth as faithfully as possible. Because the effort is hard and the result unsparing, it isn’t obvious that writing like Boo’s has a future. Her book is too real for us. The very project of a white American journalist spending three years in an Indian slum to tell the story of families who live there could be considered a gross act of cultural exploitation. By the new rules, shelf upon shelf of great writing might go the way of blind and urban. Open Light in August or Invisible Man to any page and see how little would survive.

    The rationale for equity-language guides is hard to fault. They seek a world without oppression and injustice. Because achieving this goal is beyond anyone’s power, they turn to what can be controlled and try to purge language until it leaves no one out and can’t harm those who already suffer. Avoiding slurs, calling attention to inadvertent insults, and speaking to people with dignity are essential things in any decent society. It’s polite to address people as they request, and context always matters: A therapist is unlikely to use terms with a patient that she would with a colleague. But it isn’t the job of writers to present people as they want to be presented; writers owe allegiance to their readers, and the truth.

    The universal mission of equity language is a quest for salvation, not political reform or personal courtesy—a Protestant quest and, despite the guides’ aversion to any reference to U.S. citizenship, an American one, for we do nothing by half measures. The guides follow the grammar of Puritan preaching to the last clause. Once you have embarked on this expedition, you can’t stop at Oriental or thug, because that would leave far too much evil at large. So you take off in hot pursuit of gentrification and legal resident, food stamps and gun control, until the last sin is hunted down and made right—which can never happen in a fallen world.

    This huge expense of energy to purify language reveals a weakened belief in more material forms of progress. If we don’t know how to end racism, we can at least call it structural. The guides want to make the ugliness of our society disappear by linguistic fiat. Even by their own lights, they do more ill than good—not because of their absurd bans on ordinary words like congresswoman and expat, or the self-torture they require of conscientious users, but because they make it impossible to face squarely the wrongs they want to right, which is the starting point for any change. Prison does not become a less brutal place by calling someone locked up in one a person experiencing the criminal-justice system. Obesity isn’t any healthier for people with high weight. It’s hard to know who is likely to be harmed by a phrase like native New Yorker or under fire; I doubt that even the writers of the guides are truly offended. But the people in Behind the Beautiful Forevers know they’re poor; they can’t afford to wrap themselves in soft sheets of euphemism. Equity language doesn’t fool anyone who lives with real afflictions. It’s meant to spare only the feelings of those who use it.

    The project of the guides is utopian, but they’re a symptom of deep pessimism. They belong to a fractured culture in which symbolic gestures are preferable to concrete actions, argument is no longer desirable, each viewpoint has its own impenetrable dialect, and only the most fluent insiders possess the power to say what is real. What I’ve described is not just a problem of the progressive left. The far right has a different vocabulary, but it, too, relies on authoritarian shibboleths to enforce orthodoxy. It will be a sign of political renewal if Americans can say maddening things to one another in a common language that doesn’t require any guide.


    This article appears in the April 2023 print edition with the headline “The Moral Case Against Euphemism.” When you buy a book using a link on this page, we receive a commission. Thank you for supporting The Atlantic.

    George Packer

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  • Lady M New York Announces Breast Cancer Awareness Month Campaign

    Lady M New York Announces Breast Cancer Awareness Month Campaign

    Lady M New York donates 100% of proceeds from Pink Éclair sales and joins The American Cancer Society’s Making Strides Against Breast Cancer Walk for Breast Cancer Awareness Month.

    Press Release



    updated: Oct 2, 2019

    Breast Cancer Awareness is a cause Lady M New York holds near and dear. Lady M has been a strong supporter of breast cancer research and is raising even more awareness and involvement for 2019. 

    For the month of October, Lady M will bring back the beloved Pink Éclairs ($6 each). One-hundred percent of proceeds from Pink Éclair sales go directly to The American Cancer Society’s Making Strides Against Breast Cancer Walk. Lady M has raised nearly $25,000 from Pink Éclair sales in the past two years and aims to raise even more this October. Pink Éclairs are handmade by Lady M pastry chefs, featuring golden choux pastry, strawberry custard cream, and baby pink chocolate glaze. Pink Éclairs are available exclusively at Lady M’s New York, California, and Boston boutiques for October. Boutiques will be outfitted with pink flowers and Lady M employees will wear pink pins. Lady M aims to bring breast cancer awareness to all boutique guests

    On Oct. 20, 2019, Lady M partners with American Cancer Society for the Making Strides of Central Park walk. Check-in for the walk begins at 7:30 a.m. at West 66th Street and Central Park West (Tavern on the Green). The walk is a leisurely four miles, and participants are encouraged to sign up for the Lady M New York team. There is no cost to participate, though donations to Making Strides are welcome. Lady M will also host a tent at the Survivor Village to serve bite-size Mille Crepes cakes. Support an important cause and enjoy cake!

    How can Lady M fans participate? Visit Lady M’s Pink for A Cause page to learn more and 1) Purchase Pink Éclairs (available at all Lady M U.S. boutiques from Oct. 1-31, 2019). 2) Join our Lady M New York team for the Making Strides of Central Park Walk on Oct. 20, 2019. 3) Donate directly online. 

    About Lady M New York:
    Lady M New York is an NYC cake brand with 40 boutiques worldwide. Created in 2001 and helmed by CEO Ken Romaniszyn, Lady M is known as the original creator of Mille Crepes. Lady M marries classic French techniques with Japanese sensibilities to develop creations that are a touch sweet and perfect for all occasions. Indulge in a world of cakes and confections at ​www.ladym.com

    ### MEDIA ONLY CONTACT:
    Kaiyi Chu | Head of Growth
    press@ladym.com

    Source: Lady M New York

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  • HalloweenCostumes.com Partners With the American Cancer Society for Hope is the Best Halloween Treat

    HalloweenCostumes.com Partners With the American Cancer Society for Hope is the Best Halloween Treat

    Press Release



    updated: Oct 2, 2019

    ​HalloweenCostumes.com creates and inspires unforgettable Halloween memories, year after year. That’s why this October, HalloweenCostumes.com is partnering with the American Cancer Society to help change lives across the country.

    “October is such an important month for cancer awareness,” said, Blaine Mauldin, Community Development Manager, American Cancer Society. “And this year with our new partnership, we are especially looking forward to launching this initiative with HalloweenCostumes.com and having an even greater impact in the fight against cancer.”

    From September 30 through October 30, HalloweenCostumes.com will donate 20% of their proceeds from shoppers who visit HalloweenCostumes.com/hope, to the America Cancer Society. With roughly 70% of Americans planning to celebrate Halloween this year, the online Halloween retailer hopes this campaign will make a large impact.

    “Nearly one-in-three lives are affected by cancer, which makes this hit home for many of our team members,” Mark Bietz, Chief Marketing Officer, said. “Our campaign, Hope is the Best Halloween Treat, is an opportunity for us to remember the lives we’ve lost, help those affected today, and come together in the fight against cancer.”

    The American Cancer Society is also partnering with Twitch streamers for their Gamers vs. Cancer initiative. During the month of October, HalloweenCostumes.com will donate costumes to 25 individual streamers involved in the initiative, who raise over $5,000 in donations.

    John Gillick, Twitch gamer and acute lymphocytic leukemia survivor, attributes gaming to be an activity that helped him get through his cancer which made his involvement in this initiative seamless.

    “During my weekly game, I could put cancer out of my head as much as possible and enjoy myself,” Gillick said. “That helped me as much as medication. Gaming was one of the things I attribute to helping me get through cancer, so why not use it to help others get through cancer?”

    For more info on Hope is the Best Halloween Treat, visit: HalloweenCostumes.com/hope

    For more info on Gamers vs Cancer, contact: gamersvscancer@cancer.org

    The American Cancer Society does not endorse any product or service.

    About HalloweenCostumes.com:

    Located in North Mankato, MN, HalloweenCostumes.com is a family-owned and operated business. What began as a small business operating out of a garage a couple of months a year, has turned into a globally-recognized online retailer with over 175 year-round employees and thousands of seasonal employees in less than a decade. The company ships to over 150 countries in the world year-round and is the largest costume producer in the world. For more information, please contact ross.smith@halloweencostumes.com

    Media Contact:
    Ross Hewett-Smith
    Phone: 507-386-0207
    Email: ross.smith@halloweencostumes.com

    Source: HalloweenCostumes.com

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