Are Transgender People at Risk of Breast Cancer?

Are Transgender People at Risk of Breast Cancer?
Are Transgender People at Risk of Breast Cancer?

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People of all genders can get breast cancer, so it’s important for trans men and trans women to consider that as part of their health care.

“Anyone who has breast tissue could potentially or theoretically develop breast cancer,” says Fan Liang, MD, medical director of the Center for Transgender Health at Johns Hopkins Medicine in Baltimore.

Many things influence your breast cancer risk, including your own medical history, any family history of breast cancer, whether you have certain genes that make breast cancer more likely, and whether you get gender-affirming treatment.

There aren’t yet official breast cancer screening guidelines that are specific to trans people. But experts do have general recommendations, detailed below.

You should talk with your doctor about what screening you need, when to start, and how often. Of course, if you notice a lump or other unusual breast change, see your doctor to get it checked out. (“Screening” refers to routine checking for possible signs of breast cancer, not diagnosing what a lump or other change may be.)

Breast Cancer Screening Recommendations for Trans Women

Each person is unique. In gauging trans women’s breast cancer risk, one of the factors that doctors consider include whether they are taking hormone therapy, their age, and for how long. That’s on top of all the other breast cancer risk factors a person might have.

Trans women who take estrogen as part of hormone therapy: If you’re older than 50, get a mammogram every 2 years after you’ve been taking hormones for at least 5 to 10 years.

Not all trans women take gender-affirming hormone therapy. Those who do will develop breast tissue. Any breast tissue can develop breast cancer. And estrogen, which is part of this therapy, does raise the risk for breast cancer.

If you start taking estrogen as an adult, it may not raise your risk as much as if you start taking it as a teen because over your lifetime, you’d have less exposure to estrogen. There hasn’t been a lot of research in this area yet, so it’s not clear how much taking estrogen raises risk for people of various ages.

Trans women with the BRCA1 or BRCA2 genes and/or a strong family history of breast cancer: These genes raise your risk of breast cancer. So it’s very important that you discuss with your doctor how to manage this risk, such as with screenings or other preventive care. You may need to start getting mammograms earlier – and get them more often.

“There are other health conditions, not just cancer, that might not make you a good candidate for estrogen,” says Gwendolyn Quinn, PhD, professor of obstetrics and gynecology at NYU Grossman School of Medicine in New York. “That’s why the decision to use hormones should be overseen by a health care provider, but many trans people don’t have access to a clinician and buy their hormones on the internet.”

If you aren’t taking gender-affirming therapy but are considering it, make sure your doctor knows that you are BRCA-positive.

“It’s not a formal recommendation, but there has been talk about testing trans women for BRCA before starting gender-affirming hormones,” Quinn says. “But a lot of people feel that gender-affirming hormones are lifesaving and that it’s unreasonable to ask that trans women get tested first.”

If you do have a doctor and want to get tested for the BRCA genes – and other genes linked to breast cancer – your doctor can help you find out about what’s involved.

Trans women who don’t take hormones: Although there’s no recommended screening timing, be sure to see your doctor if you notice any breast lumps or changes – and tell them about anyone in your family who’s had breast cancer.

Trans women who got breast augmentation: Some trans women choose to get breast augmentation surgery to create the look of breasts. This is done with implants, fat transferred from another place on the body, or a combination of those methods.

Fat transfer uses your own body fat from somewhere else on your body to create breasts, and studies don’t show that this raises breast cancer risk. Today’s breast implants don’t cause breast cancer, either. They have been linked to a low risk of a rare form of cancer called anaplastic large-cell lymphoma (ALCL). There hasn’t been a lot of research on implant-related ALCL specifically in trans women. But in one review, researchers called it a “rare but serious” complication and recommended being aware of the risk and keeping up with any follow-up care after getting the implants.

Breast Cancer Screening Recommendations for Trans Men

Among the many factors that can affect your risk are whether you’ve had “top surgery” to change the appearance of your chest, whether you take testosterone, and whether you have certain genes that make breast cancer more likely.

Trans men who have not had top surgery or who have only had breast reduction: Get a mammogram every year or two starting at age 40.

If you haven’t had top surgery, your breast cancer risk is the same as it was before you transitioned. That’s true whether or not you’ve had a hysterectomy (surgery to remove your uterus). Removal of the ovaries and uterus only somewhat lowers breast cancer risk. Removing the breasts makes the biggest impact on breast cancer risk.

Trans men who have had top surgery: You may not have enough breast tissue to put in a mammogram machine, so your doctor may recommend that you do self-exams and also get breast exams done by a doctor.

Not every trans man gets top surgery. But some do. Top surgery lowers breast cancer risk, but not as much as a mastectomy you’d get to prevent or treat breast cancer.

With a breast cancer mastectomy, the goal is to remove as much breast tissue as possible, including tissue under the arms and on the ribcage. With top surgery, the aim is different: to change the chest’s appearance to be flatter. “The breast mass is removed, but we don’t go after every single cell because it’s not necessary to do that in order to get the overall result that we want,” Liang says.

“How much surgery lowers [breast cancer] risk depends on how much tissue is left behind, including the nipple, where there’s also potential for cancer cells to develop,” Quinn says.

Trans men who have the BRCA1 or BRCA2 gene mutations and have had standard top surgery (but not a complete preventive mastectomy): You may need annual breast cancer screenings. Since you likely won’t have enough breast tissue to put into a mammogram machine, a breast cancer specialist may need to give you a chest exam. It’s important that your doctors know that you are BRCA+ so they can make a preventive screening plan for you based on how much breast tissue you have.

Trans men who take hormone therapy with testosterone: Testosterone suppresses estrogen. So if you take hormone therapy with testosterone consistently over time, your breast cancer risk is likely to be somewhat lower. But if you don’t take testosterone – or if you only take a low dose or take it intermittently – you won’t have that protective benefit.

Regardless of whether or not you take testosterone therapy, there is still at least some risk for breast cancer. Your doctor can advise you about what screening you need.

Finding Gender-Affirming Care

While experts can make recommendations about cancer screenings for trans people, finding a gender-affirming health care provider is easier said than done in some places.

The World Professional Association for Transgender Health has an online directory of providers of gender-affirming care. You may also simply call doctors in your area and ask about their experience with providing care to trans patients.

“If you can’t find a transgender health clinic near where you live, call the doctor beforehand,” Liang says. “Ask about the provider’s experience with transgender preventive care. See how they respond to the question – whether they have an understanding of what you need or whether the question seems to them to come out of left field.” Your health concerns – about breast cancer or anything else – should be taken seriously and treated with respect by your health care team.

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2022 Arnold Strongman Classic UK Roster Confirmed

2022 Arnold Strongman Classic UK Roster Confirmed
2022 Arnold Strongman Classic UK Roster Confirmed

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The 2022 Arnold Strongman Classic (ASC) UK will take place on Sept. 24, 2022, in Marston Green, England. It is a segment of the overall Arnold Sports Festival UK, which takes place over the course of the entire weekend. 

The one-day contest will see 14 different top-notch strongmen tackle respective events such as the Super Yoke and the traditional closing Atlas stones. Here’s the confirmed roster of competitors for the 2022 ASC:

2022 Arnold Strongman Classic UK Roster

[Related: How to Do the Push-Up — Benefits, Variations, and More]

Notably, the defending champion of the Arnold Strongman Classic UK, Evan Singleton, will not return to defend his title this year. Singleton toppled Oleksii Novikov (second place) and Trey Mitchell (third place) to win the inaugural edition in 2021. 

Here’s an overview of the competitive events in Marston Green.

Super Yoke

Each competitor will have to move a 500-kilogram (1,102.3-pound) yoke during this event as fast as they can. Athletes like Novikov and Hooper might be the favorites for this portion due to their unique combination of agility and strength. In particular, Hooper seemed to thrive with speed events during a 2022 World’s Strongest Man (WSM) early-round blitz. 

Deadlift

The 2022 ASC’s Deadlift event is for reps. Athletes will attempt to successfully lock out a 370-kilogram (815.7-pound) deadlift as many times as they can. While it’s different from a traditional deadlift with a barbell, Novikov could again be one of the favorites after pulling 15 reps of a Car Deadlift during the 2022 WSM

[Related: How to Do the Goblet Squat for Lower Body Size and Mobility]

Bag Over Bar

The Bar Over Bar event will also be predicated on speed. The athletes that can move their respective implements the fastest will be in a far more favorable position. 

Dumbbell Press

During the Dumbbell Press, the competitors will attempt to complete a 100-kilogram (220.5-pound) dumbbell press. With a dumbbell press of 153.2 kilograms (337.8 pounds) from an October 2021 training session, Novikov is once more in a quality spot. That mark would have surpassed Mateusz Kieliszkowski’s official record by 3.2 kilograms (7.1 pounds) if it occurred during a sanctioned competition. 

[Related: How to Do the Triceps Kickback for Arm Size]

Arnold Stone Carry

As one of the closing events of the 2022 ASC, the Arnold Stone Carry might be about the heavier athletes utilizing their power and who will still have energy after a grueling contest. Some of those competitors like Žydrūnas Savickas, for example, could elect to concede a degree of points on agility-related events so they can perform better during the carry.  

Atlas Stones

A strongman tradition continues to push ahead. The Atlas Stones, once more, close a strongman competition. Every athlete’s Atlas Stone run will be determined by their cumulative score from the previous five events. Those scores will have more weight and might determine who wins the final segment. With their agile builds, Hooper and Novikov could be the favorites here, but that will only be clear once most of the dust settles on the 2022 ASC.

Featured image: @mitchellhooper on Instagram

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Desperate Long COVID Patients Turn to Unproven Alternative Therapies

Desperate Long COVID Patients Turn to Unproven Alternative Therapies
Desperate Long COVID Patients Turn to Unproven Alternative Therapies

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Editor’s note: Find more information about long COVID in Medscape’s Long COVID Resource Center.

Sept. 22, 2022 – Entrepreneur Maya McNulty, 49, was one of the first victims of the COVID-19 pandemic. The Schenectady, NY, businesswoman spent 2 months in the hospital after catching the disease in March 2020. That September, she was diagnosed with long COVID.

“Even a simple task such as unloading the dishwasher became a major challenge,” she says.

Over the next several months, McNulty saw a range of specialists, including neurologists, pulmonologists, and cardiologists. She had months of physical therapy and respiratory therapy to help regain strength and lung function. While many of the doctors she saw were sympathetic to what she was going through, not all were.

“I saw one neurologist who told me to my face that she didn’t believe in long COVID,” she recalls. “It was particularly astonishing since the hospital they were affiliated with had a long COVID clinic.”

McNulty began to connect with other patients with long COVID through a support group she created at the end of 2020 on the social media app Clubhouse. They exchanged ideas and stories about what had helped one another, which led her to try, over the next year, a plant-based diet, Chinese medicine, and vitamin C supplements, among other treatments.

She also acted on unscientific reports she found online and did her own research, which led her to discover claims that some asthma patients with chronic coughing responded well to halotherapy, or dry salt therapy, during which patients inhale micro-particles of salt into their lungs to reduce inflammation, widen airways, and thin mucus. She’s been doing this procedure at a clinic near her home for over a year and credits it with helping with her chronic cough, especially as she recovers from her second bout of COVID-19.

It’s not cheap – a single half-hour session can cost up to $50 and isn’t covered by insurance. There’s also no good research to suggest that it can help with long COVID, according to the Cleveland Clinic.

McNulty understands that but says many people who live with long COVID turn to these treatments out of a sense of desperation.

“When it comes to this condition, we kind of have to be our own advocates. People are so desperate and feel so gaslit by doctors who don’t believe in their symptoms that they play Russian roulette with their body,” she says. “Most just want some hope and a way to relieve pain.”

Across the country, 16 million Americans have long COVID, according to the Brookings Institution’s analysis of a 2022 Census Bureau report. The report also estimated that up to a quarter of them have such debilitating symptoms that they are no longer able to work. While long COVID centers may offer therapies to help relieve symptoms, “there are no evidence-based established treatments for long COVID at this point,” says Andrew Schamess, MD, a professor of internal medicine at Ohio State Wexner Medical Center, who runs its Post-COVID Recovery Program. “You can’t blame patients for looking for alternative remedies to help them. Unfortunately, there are also a lot of people out to make a buck who are selling unproven and disproven therapies.”

Sniffing Out the Snake Oil

With few evidence-based treatments for long COVID, patients with debilitating symptoms can be tempted by unproven options. One that has gotten a lot of attention is hyperbaric oxygen. This therapy has traditionally been used to treat divers who have decompression sickness, or the bends. It’s also being touted by some clinics as an effective treatment for long COVID.

A very small trial of 73 patients with long COVID, published this July in the journal Scientific Reports, found that those treated in a high-pressure oxygen system 5 days a week for 2 months showed improvements in brain fog, pain, energy, sleep, anxiety, and depression, compared with similar patients who got sham treatments. But larger studies are needed to show how well it works, notes Schamess.

“It’s very expensive – roughly $120 per session – and there just isn’t the evidence there to support its use,” he says.

In addition, the therapy itself carries risks, such as ear and sinus pain, middle ear injury, temporary vision changes, and, very rarely, lung collapse, according to the FDA.

One “particularly troubling” treatment being offered, says Kathleen Bell, MD, chair of the Department of Physical Medicine and Rehabilitation at the University of Texas Southwestern Medical Center, is stem cell therapy. This therapy is still in its infancy, but it’s being marketed by some clinics as a way to prevent COVID-19 and also treat long-haul symptoms.

The FDA has issued advisories that there are no products approved to treat long COVID and recommends against their use, except in a clinical trial.

“There’s absolutely no regulation – you don’t know what you’re getting, and there’s no research to suggest this therapy even works,” says Bell. It’s also prohibitively expensive – one Cayman Islands-based company advertises its treatment for as much as $25,000.

Patients with long COVID are even traveling as far as Cyprus, Germany, and Switzerland for a procedure known as blood washing, in which large needles are inserted into veins to filter blood and remove lipids and inflammatory proteins, the British Medical Journal reported in July. Some patients are also prescribed blood thinners to remove microscopic blood clots that may contribute to long COVID. But this treatment is also expensive, with many people paying $10,000-$15,000 out of pocket, and there’s no published evidence to suggest it works, according to theBMJ.

It can be particularly hard to discern what may work and what’s unproven, since many primary care providers are themselves unfamiliar with even traditional long COVID treatments, Bell says. She recommends that patients ask the following questions:

  • What published research is there to support these claims?
  • How long should I expect to do this treatment before I see an improvement?
  • What are the potential side effects?
  • Will the medical provider recommending the treatment work with your current medical team to monitor progress?

“If you can’t get answers to these questions, take a step back,” says Bell.

Sorting Through Supplements

Yufang Lin, MD, an integrative specialist at the Cleveland Clinic, says many patients with long COVID enter her office with bags of supplements.

“There’s no data on them, and in large quantities, they may even be harmful,” she says.

Instead, she works closely with the Cleveland Clinic’s long COVID center to do a thorough workup of each patient, which often includes screening for certain nutritional deficiencies.

“Anecdotally, we do see many patients with long COVID who are deficient in these vitamins and minerals,” says Lin. “If someone is low, we will suggest the appropriate supplement. Otherwise, we work with them to institute some dietary changes.”

­This usually involves a plant-based, anti-inflammatory eating pattern such as the Mediterranean diet, which is rich in fruits, vegetables, whole grains, nuts, fatty fish, and healthy fats such as olive oil and avocados.

Other supplements some doctors recommend for patients with long COVID are meant to treat inflammation, Bell says, although there’s not good evidence they work. One is the antioxidant coenzyme Q10.

But a small preprint study published in The Lancet this past August of 121 patients with long COVID who took 500 milligrams a day of coenzyme Q10 for 6 weeks saw no differences in recovery than those who took a placebo. Because the study is still a preprint, it has not been peer-reviewed.

Another is probiotics. A small 2021 study published in the journal Infectious Diseases Diagnosis & Treatment found that a blend of five lactobacillus probiotics, along with a prebiotic called inulin, taken for 30 days, helped with long-term COVID symptoms such as coughing and fatigue. But larger studies need to be done to support their use.

One that may have more promise is omega-3 fatty acids. Like many other supplements, these may help with long COVID by easing inflammation, says Steven Flanagan, MD, a rehabilitation medicine specialist at NYU Langone in New York who works with long COVID patients. Researchers at the Mount Sinai School of Medicine in New York are studying whether a supplement can help patients who have lost their sense of taste or smell after an infection, but results aren’t yet available.

Among the few alternatives that have been shown to help patients are mindfulness-based therapies – in particular, mindfulness-based forms of exercise such as tai chi and qi gong may be helpful, as they combine a gentle workout with stress reduction.

“Both incorporate meditation, which helps not only to relieve some of the anxiety associated with long COVID but allows patients to redirect their thought process so that they can cope with symptoms better,” says Flanagan.

A 2022 study published in BMJ Open found that these two activities reduced inflammatory markers and improved respiratory muscle strength and function in patients recovering from COVID-19.

“I recommend these activities to all my long COVID patients, as it’s inexpensive and easy to find classes to do either at home or in their community,” he says. “Even if it doesn’t improve their long COVID symptoms, it has other benefits such as increased strength and flexibility that can boost their overall health.”

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Let’s Find This Reader A First-Day-of-School Outfit!

Let’s Find This Reader A First-Day-of-School Outfit!
Let’s Find This Reader A First-Day-of-School Outfit!

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Recently, a Cup of Jo reader reached out for help finding a first-day-of-school outfit…

“This year, I’m turning 40 and making a career shift,” wrote Anne. “I start law school in the fall, just as my oldest child starts kindergarten (we get to buy school supplies together!). I’m excited but nervous about being pegged as ‘the old lady,’ so on the first day, I want to appear confident and interesting to eat lunch with. Please share advice!”

First, congratulations! We’re rooting for you. Second, 40 is young and cool! Remember this comment from a reader named Libby? “The most amazing woman I have ever known retired from a journalism career at 62 and promptly enrolled in law school. She practiced law until she was 94. It is NEVER too late.” For first-day-of-school outfits, here are eight great pieces (that would also work well for the office)…

first-day-of-school outfit

The oversized blazer: An academic setting begs for a blazer, so give the people what they want! This modern version is polished enough for visiting professor office hours, but casual enough for grabbing drinks with classmates.

dark washed denim shirt

The denim shirt: If you’re looking for a fresher take on the white-shirt-with-slacks uniform, swap in a fitted denim shirt. With a dark wash and crisp feel, this top is the cool cousin of button-down shirts. I’d tuck it into these drapey pants.

wide legged trousers

Wide-legged trousers: I wish everyone could own a pair of wide-legged trousers. They instantly elevate any outfit and have character without looking costume-y. (Plus, they create the ultimate weekend look with white sneakers.)

statement sweater

The statement sweater: When you’re heading to the law library (quiet, please!), add a pop of color to liven things up. This red polo sweater gives a cheery impression and would pair beautifully with a favorite pair of jeans. This other red sweater is just as fun and only $22.

slip midi skirt

The slip skirt: This midi is a closet staple. The sheen and subtle flip make it both elegant and playful, which are two attitudes we could all channel more of in our lives.

sweater dress

The sweater dress: To feel confident, comfort is key. This calf-skimming sweater dress strikes the perfect balance between flattering and cozy. It’s giving “look gorgeous while wearing a blanket” vibes. This size-inclusive line also has the dreamiest jewel tones.

fall booties

The low-heeled bootie: The last thing you need to deal with after a day of lectures, commuting and parenting are pinched feet. So, keep the feeling in your toes with low-heeled booties (they also come in warm brown).

black nylon tote

The sturdy tote: Law school requires walking from class to class with heavy books. To save yourself from a Home Alone situation, invest in a sturdy bag. These nylon totes have a cult following for a reason: they’re sleek, durable, and have enough room for a laptop, books and snacks.

Thoughts? What would you wear on your first-day-of law school? Or when returning to office?

P.S. Pants we wear to work and a criminal defense attorney’s week of outfits.

(Graphic layout by Miss Moss. Photo by Simone Anne/Stocksy.)

Note: If you buy something through our links, we may earn an affiliate commission, at no cost to you. We recommend only products we genuinely like. Thank you so much.

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How to Stay Safe in a Storm

How to Stay Safe in a Storm
How to Stay Safe in a Storm

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Sept. 22, 2022 — Sonia Chavez was on the balcony of her midrise Dallas apartment when the unthinkable happened: As she was filming a thunderstorm with her cellphone, lightning struck her in a flash of blinding light and searing heat that knocked her off her feet.

The thunderbolt, which Chavez captured on film, damaged her eyes and left her with some cognitive, speech, and mobility issues.

But somehow, she survived.

“When it hit, it sounded like a bomb going off,” says Chavez, 38. “I felt this intense electric force that hit me hard, like a gut punch or whiplash. It was the biggest pain you could imagine. I remember seeing the electricity coming off my hands and seeing different colors — blue, then red, and then white — and there was ringing in my ears.

“I don’t remember much after that, but the next thing I knew I was in the closet of my apartment, pinching and scratching myself to see if I was dead or alive.”

As traumatic as the experience was, Chavez is one of the lucky ones. While she is still recovering from injuries caused by the strike 18 months ago, she lived to tell her story.

Many others struck by lightning don’t. And lightning fatalities are on the rise in the U.S., possibly due to an increase in severe storms tied to global climate change.

So far, the U.S. has recorded 17 lightning fatalities this year, according to the National Weather Service (NWS). That’s more than the 11 that occurred by this time last year and as many as were seen in all of 2020.

“I do feel like I’ve been lucky,” says Chavez, who is receiving physical and speech therapy, as well as ongoing treatments to address her vision loss from the strike. “I’ve had teams of people helping me, including my husband, who found me in the closet a half-hour after it happened [and] got me to the hospital.”

Aaron Treadway, a lightning specialist with the National Weather Service, explains that lightning-strike survivors like Chavez are not as rare as you might think. Indeed: Nine in 10 people struck by lightning survive the incident.

“On average around 300 people are struck by lightning each year, with roughly 10 percent of those being fatal injuries,” says Treadway. “For those who are struck and do not die, many have serious injuries.”

While lightning fatalities have been rising in recent years, they are still well below what they were 20 years ago, he says. Between 1970 and 2000, the average annual lightning death tally was over 70, National Weather Service figures show.

“The reduction in fatalities [since 2000] is due to the success of the lightning safety campaign that many people and organizations have contributed to,” Treadway says. “These include NWS offices across the country and our many partners in the broadcast and print media, outdoor and sports organizations, emergency management officials, and other safety organizations.

“Sayings like ‘When Thunder Roars, Go Indoors’ or ‘See a Flash, Dash Inside’ for our deaf and hard-of-hearing community are easy to remember and apply, keeping people safe.”

Lightning Strikes: By the Numbers

The National Weather Service maintains a detailed website of facts on lightning strikes that provides a compelling overview of how, when, and where people die during thunderstorms.

It offers a glimpse into the kinds of activities individuals were engaged in at the time of fatal strikes, providing key clues to how best to avoid risky behaviors during a storm.

For instance, of the 17 lightning deaths so far this year:

  • Five people were struck during camping trips or visits to public parks.
  • Four were killed while engaging in water sports: boating, jet skiing, or swimming.
  • Four were hit as they were working around the house: doing yard work, loading tools into a van, standing on a roof, and replacing a window.
  • Four died while walking a dog, flying a remote-control plane in a field, fixing a truck on a highway, and during Army training exercises.

The National Weather Service has also compiled an extraordinary online database of lightning survivors, including detailed interviews, their stories, and the health impacts they suffered.

Beyond these personal stories, the National Weather Service has publicized a wealth of information on these giant sparks of electricity in the atmosphere that often strike the ground.

According to the National Weather Service and other federal agencies:

  • A typical lightning flash carries about 300 million volts. By comparison, a household current is 120 volts.
  • Lightning can heat the air it passes through to 50,000 degrees Fahrenheit. That’s five times hotter than the surface of the sun.
  • Lightning strikes somewhere in the U.S. 25 million times each year on average.
  • Florida is the nation’s lightning capital, with the highest average number of cloud-to-ground strikes, ranked by flashes per square mile. The Sunshine State also has the most fatalities of any state due to the frequency of lightning and because most people are outdoors during the peak lightning season (June to August).
  • Florida sees 1.2 million strikes in a typical year, covering 20 square miles. Next in line: Louisiana (875,136, 18.9 miles); Mississippi (768,126, 16.1 miles); Oklahoma (1.1 million-plus, 15.8 miles); and Arkansas (837,978, 15.7 miles).
  • Worldwide, the U.S. had the second most lightning strikes in 2021. Brazil was first.
  • Certain occupations carry a higher risk for lightning strikes, including those in the logging, construction, utility, lawn services, and recreational industries, according to the U.S. Occupational Safety and Health Administration.

National Weather Service officials have also collected a surprising list of lightning myths and facts. They are:

  • Crouching down or lying flat on the ground in a thunderstorm won’t reduce your risk of being struck. You can still be vulnerable to ground current from bolts that strike the earth nearby. It’s better to run to a building or vehicle for shelter.
  • Lightning can strike twice in the same place and often does. The Empire State Building is hit 23 times every year, on average.
  • Even if it’s not raining outside you can still be struck by a “bolt from the blue” — literally — because lightning can strike 10 to 15 miles from the center of a storm.
  • Metal watches, jewelry, and personal electronic devices such as cellphones and portable music players do NOT attract lightning.
  • Your mother was right: Don’t stand under a tree during a storm. Being beneath a tree during a storm is the second-leading cause of lightning fatalities.

Why Are Fatalities Up and What Can You Do?

What’s behind the recent increase in fatal lightning strikes? Treadway says global climate change might be a factor. But he notes scientists aren’t entirely certain, in part because they have not been tracking the weather phenomenon for very long.

“While a warming climate will produce more ingredients that are conducive to the development of thunderstorms, quantitatively, the period of record of ground-based lightning detection is fairly short,” he explains. “In order to say that there is a substantial increase in lightning coverage, scientists need to have a longer period of data to make those types of conclusions.”

But that research has shown that education and awareness or risks can help reduce lightning fatalities overall.

“Lightning doesn’t follow rules; it strikes where it wants to,” he says. “It is up to the public to take those safety precautions and reduce their risk of getting struck overall.”

With that in mind, National Weather Service officials recommend keeping the following safety tips and information in mind to reduce your risk during an electrical storm:

  • If you can hear thunder, lightning is close enough to strike you, so you should seek shelter in a building or hard-topped vehicle with the windows rolled up.
  • Wait 30 minutes after you hear the last crack of thunder before going outside.
  • Stay off landline phones, computers, and other electrical equipment that put you in direct contact with electricity during a storm.
  • Avoid plumbing, including sinks, baths, and faucets.
  • Stay away from windows and doors, and don’t venture onto porches or balconies.
  • Don’t lie on or lean against concrete walls.
  • Avoid elevated areas such as hills, mountain ridges, and peaks if you’re caught outdoors and can’t seek shelter.
  • Don’t lie flat on the ground, and keep away from trees or objects that can conduct electricity (like metal or wire fences, power lines, and windmills).
  • Don’t swim or go near ponds, lakes, or other bodies of water.

Treadway also recommends checking weather forecasts before engaging in outdoor summer activities and adjusting your plans accordingly.

“About two thirds of the victims were enjoying outdoor leisure activities before being struck, with water-related activities topping the list,” he notes. “Of the water-related activities, fishing ranked highest, with boating and beach activities also contributing significantly to the water-related deaths.

“Camping, ranching/farming, and riding an exposed vehicle (bike/motorcycle) also ranked highly in activities people were doing when fatally struck. Among the sports activities, soccer ranked highest, followed by golf and running. … Interestingly, about 80% of lightning fatalities are men.”

Looking back on her experiences, Chavez says she knew she was taking a risk standing on her balcony, filming the electrical storm on the day she was struck by lightning. She acknowledges that she didn’t believe she was at risk because it was not raining outside, which she now knows is a dangerous falsehood.

She is still in recovery.

“I’m a work in progress,” she says, noting that she struggles with vision problems and mobility. She speaks slowly and deliberately, but articulately, about her experiences.

But Chavez says she is regaining her abilities little by little every day. She recently returned to work as a project manager and even started jogging again — something she had to give up after the strike.

There is one surprising development she attributes to the lightning strike, she says: The experience gave her a new outlook on life and that her mind is calmer, with less “brain chatter” than before.

“Through this journey, I actually feel very blessed,” she says. “Having had a near-death experience completely changes your outlook on life. And even though this created such havoc on my mind and body, it actually helped my soul.

“The brain chatter I used to experience is gone because I can only concentrate on the current moment. And to me that is just so peaceful. You just hit this different space, and a few other survivors will tell you that they have felt similar things.”

Chavez also says she feels compelled to share her story, believing it may help others avoid what happened to her as well as those who’ve survived lightning strikes.

“There needs to definitely be more education around what happens to people who have been impacted by a lightning incident [and] who have experienced electrical shock in general,” she says. “A lot of us experience the same things, they do rattle our brains and nervous systems, and it’s not as rare as you think.

“I want to help as much as possible to spread awareness in hopes that it helps someone else.”

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How to Invite a Disabled Friend Over

How to Invite a Disabled Friend Over
How to Invite a Disabled Friend Over

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Kelly Dawson

The first time my friend Ann invited me over to her house, I had to pretend I was a spy. As I spotted her front door, up a staircase partially without rails, I knew I couldn’t get to it without a little ingenuity.

I took a deep breath and looked around. Were there any sticks I could lean on for balance? I once found a sturdy one at the edge of a yard that I used to climb up a sloping lawn, arriving at an entryway as if I were sticking a flag into a peak. There was the time I took off my cardigan to cover my hand so I could gingerly fling myself from the side of a cactus toward the landing of another address. And in the “great greenery incident of 2007,” I leaned on a line of cascading potted plants to get me down to the street.

In the case of Ann’s home, I climbed the flight as if I were scaling a boulder, humming the Mission Impossible theme song to make myself smile and hoping that no one was around to watch.

For as long as I can remember, I’ve let my imagination shield me from the challenges of living with a disability. I was born with cerebral palsy three years before the Americans With Disabilities Act was passed, so I had to learn to walk on rolling ankles and inward-facing knees around the same time public spaces were required to become accessible to me. But the law is spotty in practice, and it’s not unusual for ramps to jut into back alleys or elevators to open down long corridors. As soon as it’s clear that my body isn’t as welcome in a place I’d like it to be, I picture myself putting on a black men’s suit, smirking, and saying, “We’ll just see about that.” (I should probably mention here that my dad raised me on James Bond movies.)

As a child, I interpreted these workarounds as an operation into a non-disabled world, a task that was best accomplished if I remained calm and focused, constantly looking for clear pathways into a subway station, sports stadium, or high-rise building without causing too much of a disturbance. The fact that I could walk for about 30 minutes before needing to rest only gave me a countdown of adrenaline-pumping proportions. Eventually, to blend in even further, I learned how to move without any aides at all.

Homes, on the other hand, are an entirely separate obstacle. There aren’t federal regulations for bungalows or brownstones to follow for accommodations, and wide-set doorways and textured flooring haven’t had quite the same design impact as, say, shiplap and fiddle leaf figs. So, every home I visit is unpredictable — from the hardscapes leading to the front door, to the amount of stairs separating rooms, to the presence of a high-edge bathtub rather than a walk-in shower. And unlike public spaces, where I can feel more anonymous, creating access in private is often done in front of a select audience.

Family members and childhood friends already know that I appreciate their carrying my plate to the table or offering an arm up the steps from a sunken living room, but acquaintances usually have to be asked. In college and into my twenties, I struggled with how to disclose that I might need help. What’s the best way to find out if a third-floor apartment is a walk-up? How should I say that it’s impossible for me to stand for hours on end? I was routinely stressed about the closest available parking, the nearest open seat, and how much to fill my glass so I could still carry it on my own. I tried not to let these considerations show, as I laughed at a joke or told a story, scared that the intricacies of my disability would cast an intimidating shadow on budding friendships and meet-cutes. So, most of the time, I said nothing.

My understanding of my disability in public was also how I learned to internalize it in private. All of those out-of-the-way elevators and ramps, all of the sideways glances and detached formalities that come with finding a way in, was only the outsized version of what I can encounter within the intimacy of a home. When I called myself a secret agent, it was because I felt my disability was something to shroud.

After I met Ann for the first time, she introduced me to a group of women who’ve become a support system for careers, relationships, and where to find the best pizza. As we got to know each other, and I became more comfortable in my skin, I began to talk about my disability over our monthly restaurant dinners — and with their encouragement, publicly with strangers. That’s when Laura sent me a text I had never received before. “Hey! I wanted to let you know before coming to my apartment that there’s one flight of stairs, with rails, leading up to it. Do you need help getting upstairs from your car?”

I know it sounds silly, but I looked at those words for a long time. I was used to solving the puzzle of access on my own, diminishing it into the background of a gathering. This text was Laura telling me to retire from my work as a secret spy, because the act was up: She was on to me. As a friend and host, she wanted to make sure that I would have as much fun as the next guest, whether they had dietary restrictions, pet allergies, or a reluctance to hear spoilers about a new show.

When I told her how much that check-in meant to me, she shrugged and said, “I just wanted to make sure you could be here.” Since then, Ann and others have sent similar texts letting me know where to park, how many stairs I might expect, and to call them if I need backup.

My disability was never something to be ashamed of, even though it took time for me to recognize that. It’s the part of my life that fosters creativity, builds empathy, and allows me to experience the world through a hard-won lens of unfair truths and casual inclusivity. I’m grateful for my cerebral palsy, as complicated as that gratitude may be. When someone invites me into their home with a kind acknowledgement of my disability, including any potential hazards and how they might be able to assist, it’s clear that they want me to show up as my full self once I get through the door. And as soon as I’m there, I can exhale.


Kelly Dawson is a writer, editor, and media consultant. Follow her on Instagram and Twitter. She has also written about making friends and disabled motherhood.

P.S. “Four things I wish people knew about disability,” and what’s the nicest thing anyone’s ever said to you?

(Photo from Kelly’s Instagram.)

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High hospital bills continue to plague parents of dying newborns : Shots

High hospital bills continue to plague parents of dying newborns : Shots
High hospital bills continue to plague parents of dying newborns : Shots

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Bennett Markow looks to his big brother, Eli (right), during a family visit at UC Davis Children’s Hospital in Sacramento. Bennett was born four months early, in November 2020.

Crissa Markow


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Crissa Markow

Bennett Markow looks to his big brother, Eli (right), during a family visit at UC Davis Children’s Hospital in Sacramento. Bennett was born four months early, in November 2020.

Crissa Markow

The day after his 8-month-old baby died, Kingsley Raspe opened the mail and found he had been sent to collections for her care.

That notice from the collections agency involved a paltry sum, $26.50 — absurd really, given he’d previously been told he owed $2.5 million for treatment of his newborn’s congenital heart defect and other disorders.

Raspe and his wife, Maddie, had endured watching doctors crack open the chest of their pigtailed daughter, Sterling, whom they called “sweet Sterly gurl.” The health team performed so many procedures. But they couldn’t keep her — or her parents’ dreams for her — alive.

The bills lived on for the Raspes, as they do for many other families of premature and very sick infants who don’t survive.

“What a lasting tribute to the entire experience,” Kingsley said angrily. “The process was just so heartless.”

More than 300,000 U.S. families have infants who require advanced medical attention in the newborn intensive care units every year. Some babies stay for months, quickly generating astronomical fees for highly specialized surgeries and round-the-clock care. The services are delivered, and in U.S. health care, billing follows. But for the smaller fraction of families whose children die, the burden can be too much to bear.

A patchwork of convoluted Medicaid-qualification rules seek to defray these kinds of bills for very sick children. But policies differ in each state, and many parents — especially those, like the Raspes, who have commercial insurance — don’t know to apply or think they won’t qualify.

Also, because many crises that befall premature or very sick babies are in-the-moment emergencies, there may not be time for the preapprovals that insurers often require for expensive interventions. That leaves parents in crisis — or in mourning — tasked with fighting with insurers to have treatment covered.

Three families detailed for KHN how medical bills compounded their suffering during a time when they were just trying to process their loss.

Bennett Markow needed a $71,000 ‘out-of-network’ emergency flight

As the hospital in Reno, Nev., was converting a parking garage into a COVID-19 unit in November 2020, Bennett Markow came into the world four months early. He weighed less than a pound. His care team loved to sing “Bennie and the Jets” to him as a nod to the jet ventilator keeping his tiny lungs working.

On Jan. 20, 2021, when he was 2 months old, Bennett’s parents were told he needed to go to UC Davis Children’s Hospital in Sacramento, Calif., for specialized care that could keep him from going blind. The transfer team would be there in an hour. And the Nevada care team said that because it was an emergency, the family needn’t worry about their insurance or the method of transportation.

Bennett’s eye problem ended up being less severe than the doctors had feared. And Crissa Markow and her husband, A.J., were billed for the plane ride from REACH Air Medical Services, which turned out to be out-of-network. Jason Sorrick, vice president of government relations for REACH’s parent company, Global Medical Response, said the ride happened during a “lapse” in Bennett’s Medicaid coverage.

The Markows said there was no lapse. They hadn’t applied for Medicaid yet because they thought they wouldn’t qualify — the family is middle-class, and Bennett was on Crissa’s insurance. They did not know they should apply until a social worker at UC Davis gave them more information — after the flight.

Bennett Markow cuddles with his dad, A.J., hours before the baby died in July 2021 at UC Davis Children’s Hospital in Sacramento, Calif.

Crissa Markow


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Crissa Markow

Bennett Markow cuddles with his dad, A.J., hours before the baby died in July 2021 at UC Davis Children’s Hospital in Sacramento, Calif.

Crissa Markow

Crissa Markow said her heart dropped to her toes when she realized she was being billed more than $71,000 — that’s more than she makes in a year as a social worker. (The federal No Surprises Act, which aims to eliminate surprise billing, could have prevented some of the family’s headaches — but Bennett was born before the law went into effect this year.)

Although Crissa was used to working toward solutions, the billing quagmires she found herself in were overwhelming as she juggled her job, caring for Bennett and her other son and the travel logistics required to stay with Bennett, who was now getting care about 2½ hours away from her home. Crissa estimates she spent six to eight hours a week dealing with medical bills to keep them from being sent to collections — which still happened.

Bennett died that July after doctors said his lungs could not fight anymore. The Markows spent their bereavement leave battling with insurers and other billing agencies.

Finally, Crissa called REACH, the air transport company, and said: “Look, my son died. I just want to be able to grieve, I want to focus on that. Dealing with this bill is traumatic. It’s a reminder every day I shouldn’t have to be fighting this.”

By October, the Markows had settled the bill with REACH on the condition that they not disclose the terms. Sorrick said that the company reaches agreements based on the financial and personal situations of each patient and their family and that the company’s patient advocates had talked to Crissa Markow 17 times.

“If every settlement amount was disclosed publicly, then those rates become the expectation of all patients and insurance providers,” Sorrick said. “Ultimately, that would lead to all patients wanting to pay below-cost, making our services unsustainable.”

Crissa Markow’s employer-provided insurance paid $6.5 million for Bennett’s care, not including what was covered by Medicaid. The Markows paid roughly $6,500 out-of-pocket to hospitals and doctors on top of their REACH settlement. But it was not those amounts — which the couple would have happily paid to save their son — but the endless harassment and the hours spent on the phone that haunt them.

“I just wanted to be with Bennett; that’s all I wanted to do,” Crissa Markow said. “And I just spent hours on these phone calls.”

Jack Shickel lived 35 days. His medical bill was $3.4 million

Jack Shickel was born with stunning silver hair and hypoplastic left heart syndrome. Even though he was surrounded by wires and tubes, the nurses at UVA Children’s Hospital would whisper to Jessica and her husband, Isaac, that they had a truly “cute” baby.

But his congenital disorder meant the left side of his heart never fully developed. Each year in the U.S., over a thousand babies are born with the syndrome.

After two surgeries, Jack’s heart could not pump enough blood on its own. He made it 35 days.

Weeks after his death, when the Shickels were trying to muddle through life without him in Harrisonburg, Va., they called the hospital billing department about two confusing bills. They were then told the full cost of his care was $3.4 million.

“I laughed and then cried,” Jessica said. “He was worth every penny to us, but that’s basically $100,000 a day.”

The Shickels with baby Jack at UVA Children’s Hospital in Charlottesville, Va. Jack was born with hypoplastic left heart syndrome — which means the left side of his heart never fully developed.

Jessica Shickel


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Jessica Shickel

The Shickels with baby Jack at UVA Children’s Hospital in Charlottesville, Va. Jack was born with hypoplastic left heart syndrome — which means the left side of his heart never fully developed.

Jessica Shickel

Bills from out-of-network labs and other prior approval notifications continued to overwhelm their mailbox. Eventually, they figured out how to get Medicaid. The Shickels ended up paying only $470.26.

Jessica got the final bills in March, seven months after Jack’s death.

She noted that all of this was happening as the University of Virginia Health System said it was rolling back its aggressive billing practices — after a KHN investigation found the prestigious university hospital was putting liens on people’s homes to recoup medical debt.

When KHN reached out to UVA Health for comment on the Shickel case, a spokesperson, Eric Swensen, expressed condolences to the Shickel family, and added that the health system works to help patients navigate the “complex process” of evaluating financial assistance, including Medicaid coverage.

The Shickels also got a call from UVA after that, saying that the hospital was refunding their payment.

The hospital care team had given the family a pamphlet about what to do when grieving, but a more useful one, Jessica said, would have been titled “How Do You Deal With Medical Bills After Your Child Has Died?”

Sterling Raspe’s parents considered bankruptcy to pay their bills

Kingsley Raspe likes to say his daughter Sterling was “one special little lady” — not only did she have the same congenital heart defect as Jack Shickel, but she was also diagnosed with Kabuki syndrome, a rare disorder that can severely affect development. Sterling also had hearing loss, spinal cord issues and a compromised immune system.

An explanation of benefits from the Raspes’ commercial insurance indicated the couple would need to pay $2.5 million for Sterling’s care — an amount so large the numbers didn’t all fit in the column. Even Kingsley’s suspicion that the $2.5 million charge was likely erroneous — in large part or in whole — didn’t erase the sheer panic he felt when he saw the number.

(Left) To fend off medical debt, the Raspes were once advised to get divorced. (They declined.) Their daughter Sterling (right) was 8 months old when she died, and had spent most of her life in the hospital.

Kingsley Raspe


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Kingsley Raspe

(Left) To fend off medical debt, the Raspes were once advised to get divorced. (They declined.) Their daughter Sterling (right) was 8 months old when she died, and had spent most of her life in the hospital.

Kingsley Raspe

As a computer programmer making $90,000 a year, Kingsley had decent insurance. He frantically Googled “medical bankruptcy.”

Sterling had been denied Medicaid, which is available to children with complex medical problems in some states. In rejecting the application, Indiana cited an income threshold and other technical reasons.

Everyone kept telling Kingsley and Maddie to get divorced — just so Sterling would qualify for Medicaid. But that wasn’t an option for Kingsley, a British citizen who is in the U.S. on a green card tied to his marriage.

Ultimately, Kingsley’s health insurer revised the faulty notice that he owed $2.5 million. The family was told the mistake had occurred because Sterling’s initial hospital stay and surgeries had not been preapproved, although Kingsley said the heart defect was discovered halfway through the pregnancy, making surgery inevitable.

Throughout Sterling’s eight months of life, Kingsley did his programming job remotely — usually from his daughter’s bedside in her hospital room. Using his web-developer skills, he created visualizations that break down Sterling’s expensive care — it helped him make sense of it all. Then, and in the months afterward, he and his wife compiled advice for other families navigating long NICU stays with their babies.

Kingsley cries when he remembers those days.


Kaiser Health News
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He hates that Sterling’s life has been reduced to a 2-inch stack of printed-out medical bills and the still-frequent phone calls he endures from errant billers.

Despite receiving a plethora of other bills in the tens of thousands of dollars, he and his wife eventually only had to pay their $4,000 deductible, and a smattering of smaller charges and fees for equipment rentals that weren’t covered. In April, Maddie gave birth to a son, Wren. Kingsley said he knows Sterling served as her brother’s guardian angel.

“My daughter passed away. I’m not unscathed, but I’m not in financial ruin. The same can’t be said for every family,” he said. “How lucky am I? I went through the worst thing imaginable, and I consider myself lucky — what kind of weird, messed-up logic is that?”

KHN (Kaiser Health News) is a nonprofit, editorially independent program of the Kaiser Family Foundation that produces in-depth journalism about health issues.

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Watch This 80-Year-Old Deadlift 150 Kilograms (330.7 Pounds) On His Birthday

Watch This 80-Year-Old Deadlift 150 Kilograms (330.7 Pounds) On His Birthday
Watch This 80-Year-Old Deadlift 150 Kilograms (330.7 Pounds) On His Birthday

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Most people will probably celebrate their birthday with a big, festive cake. They might even get some candles, presents, and confetti. And maybe Norwegian athlete Magne did all that for his 80th birthday, but he also deadlifted 150 kilograms (30.7 pounds).

On Sept. 19, 2022, an Instagram post from SATS Norge in Oslo, Norway, featured Magne — whose last name and body weight wasn’t publicized — completing the pull. Per the caption of the post, it’s a new personal record (PR) for the athlete. Magne managed the eye-opening feat by using an overhand grip and a conventional stance while wearing a lifting belt

[Related: How to Do the Standing Calf Raise for Complete Leg Development]

After completing a successful lockout, Magne walked his loaded barbell back into his rack instead of dropping the weight. He notably took several steps while fully locked out before finally releasing his pull. Magne’s accomplishment seemed to be met with universal praise by onlookers who uproariously congratulated him for reaching the impressive milestone as he started another decade on Earth. 

According to the translated caption of the post, this deadlift benchmark was a long-standing ambition of the athlete’s. Magne and his physical therapist had previously wanted to time out this massive pull so that he would notch it when he turned 80. That’s because, the considerable strength aside, this deadlift had additional sentimental meaning to it for the athlete. 

His wife is physically handicapped. Magne is training to be strong enough to help her so that she can continue to live at home.

Magne is an official member of SATS Norge, a Norwegian gym that emphasizes full-body workouts. According to the organization’s website, the gym offers different extensive programs ranging from indoor running and cycling to strength training and demanding HIIT routines. Members can work out on their own, with a certified personal trainer, or even sign up for collaborative group sessions in the confines of the gym’s complex. 

[Related: How to Do the Push-Up — Benefits, Variations, and More]

At the time of this writing, it is unclear how long Magne has been training with SATS Norge. Judging by these noteworthy results, it seems apparent he’s getting precisely what he wants out of his commitment. If this is the high standard the newly-minted 80-year-old establishes with his deadlift, it might only be a matter of time before he reaches even greater heights. 

Featured image: @satsnorge on Instagram

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Stay Safe From Harmful Plants and Insects This Summer

Stay Safe From Harmful Plants and Insects This Summer
Stay Safe From Harmful Plants and Insects This Summer

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Summer is here and so are our favorite outdoor activities. When spending time in the great outdoors, it’s important to take all the necessary precautions, including protecting oneself from harmful plants and insects. Below, Nikki Pham, MD, a Family Medicine physician with Dignity Health Mercy Medical Group, shares tips on how to safely enjoy the outdoors this summer.Continue reading

Congratulations to Our Acts of humankindness Award Winners

Congratulations to Our Acts of humankindness Award Winners
Congratulations to Our Acts of humankindness Award Winners

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Dignity Health Medical Groups is honoring our people whose extraordinary kindness has made a life-changing difference in the life of a patient, coworker, or member of our community. Our award winners were nominated by their colleagues for going above and beyond. Congratulations to our award winners!



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