Category: Brandpoint Health

2025-11-07T15:42:55

(BPT) – Diabetes is one of the most common chronic health conditions worldwide.¹ Daily management is tough, but one of the biggest challenges for those living with diabetes is confronting stigma, judgment and misconceptions from people who don’t share the experience.²

Hear from three people who live with diabetes as they seek to change the narrative of stigma associated with the chronic condition.

Shaming hurts

Tomeka Porter, 50, has managed her diabetes for over 40 years, and feels empowered to make her own decisions thanks to effective diabetes management technology.

However, when dining out, her well-meaning friends and family sometimes question her decision to order dessert.

What they haven’t seen is that she’s already calculated the carbs, adjusted her insulin dose and checked her glucose levels.

“For me, having excellent control over my diabetes means using the tools that can give me real-time information to make real-time decisions,” said Porter. “The best tool I have is my continuous glucose monitor. It keeps me on track, in control and completely accountable, so the people I’m with don’t have to do it for me.”

Sean Hughes, 64, also lives with diabetes and finds that people fixate on what caused his condition, assuming that it stems from poor lifestyle choices.

“There’s this idea that people with diabetes are to blame for their condition,” he said. “It’s not as simple as, ‘You didn’t eat right.‘”

Criticism of food and lifestyle decisions is a common challenge. People with both Type 1 and Type 2 diabetes are often unfairly judged, reinforcing the false belief that diabetes is only caused by “bad” choices. In truth, diabetes is a complex condition influenced by genetics, immune system responses, environment and other factors.³

Here’s what Porter and Hughes wish everyone knew about living with diabetes:

1. Every day means constant decision-making.
   People with diabetes can make up to 180 health decisions daily.⁴ From predicting how their glucose responds to what they eat to choosing what activities they do – all while managing the medications they take – staying healthy requires constant vigilance.
2. There’s no one-size-fits-all plan.
   Everyone’s journey with diabetes is personal. What works for one person may not work for another.
3. It’s not just about sugar.
   Diabetes is about how the body processes glucose, which can be affected by insulin resistance, stress, illness, sleep and activity levels – not just food.⁵
4. A continuous glucose monitor (CGM) can help inform lifestyle choices.
   CGMs are discreet biowearables that monitor a person’s glucose in real-time, helping them understand how food, activity and medications affect their levels. This insight helps support informed decisions.
5. Support matters.
   Helpful language helps create a more supportive environment. In a survey conducted by Abbott, 70% of respondents said supportive comments from others can significantly boost their motivation to manage their condition.⁶

Bethany Dingman, 32, has lived with diabetes for more than 20 years and shares Porter and Hughes’ experiences and advice. “Diabetes does not define who you are as a person,” she said. “Yes, it is a serious medical condition but when treated correctly, whether through diet and exercise, checking your glucose levels or medication, you can still enjoy life.”

The weight of stigma

Abbott, a global leader in diabetes biowearables, recently released research capturing the real-life experiences of people living with diabetes.⁶ It showed:

• Nearly 70% believe there is stigma associated with their condition.⁶
• Almost 25% have avoided sharing their diagnosis with family or friends out of embarrassment or concern.⁵
• 40% have skipped or missed a doctor’s appointment due to shame.⁶

These findings reveal that stigmatizing comments don’t just hurt, they isolate. They can make people with diabetes less likely to seek care, less willing to share their struggles and more vulnerable to shame.

How you can be supportive

Start with empathy. Instead of asking what a person with diabetes “can” or “can’t” do, ask how you can support them. Respect that people with diabetes are the most knowledgeable about their own condition and how to manage it.

“People think that having diabetes means that I can’t have sugar, but it’s much more complex than that. I have an excellent system in place to help me manage it,” Porter said.

“Diabetes is something I work at managing every single day,” added Hughes. “The ideal support is respecting that I know my body and my needs. I am in control.”

“I am living proof that diabetes is not stopping me from living my best life,” shares Dingman. “I have the tools to ensure my glucose levels stay at a safe level and it helps me worry less while doing my workouts and planning my meals.”

To raise awareness about the health impact of diabetes-related misconceptions, Abbott launched the Above the Bias initiative. If you or someone you know is living with diabetes and would like to learn more about what better support looks like, visit AboveBias.com.

The views expressed in this story should not be used for medical diagnosis or treatment or as a substitute for professional medical advice. Individual symptoms, situations and circumstances may vary.

2025-11-06T12:31:00

(BPT) – Anaphylaxis is a severe, life-threatening allergic reaction that can happen at any age. In infants and toddlers, symptoms can escalate quickly. Spotting the early warning signs of anaphylaxis and acting fast can help keep a child safe.

The challenge for parents and caregivers? Infants and toddlers are unable to tell you what’s wrong. They don’t yet have the words to describe what they’re feeling. It’s up to you to recognize that something serious may be happening.

That’s why it’s important to learn the unique symptoms of anaphylaxis in very young children — and know how to respond quickly.

Allergy & Asthma Network, the leading national nonprofit organization dedicated to improving the health of people with asthma, allergies and related conditions, recently launched a new Infant Anaphylaxis online guide. It includes practical information and resources for parents and caregivers.

What is anaphylaxis?

Anaphylaxis occurs when the body’s immune system reacts to a substance — such as food, medication, an insect sting or latex — as if it were dangerous. This triggers the release of histamine and other chemicals, leading to a chain reaction of severe symptoms.

The response can affect multiple body systems, including the skin, breathing, digestion, nervous system, and heart. Because babies can’t tell you how they feel, the signs are more subtle — and easy to miss.

Without prompt treatment, anaphylaxis can cause swelling of the airways, breathing difficulties, or even shock. Epinephrine is the first line of treatment for anaphylaxis.

What causes anaphylaxis in young children?

Food allergies are the most common cause of anaphylaxis in infants and toddlers. Foods that may cause a reaction include cow’s milk, infant formula, eggs or peanut products. Infants may also develop symptoms when a mother consumes a food allergen and it passes into her breast milk.

Certain medications such as penicillin-based antibiotics may cause allergic reactions. Insect venom from a sting and latex are other potential allergic triggers. Latex can be found in bottle nipples, pacifiers and other rubbery products.

Experts now recommended introducing common food allergens to babies at 4-6 months of age. Research shows that when babies eat these foods early and often, their immune systems can learn to accept them instead of reacting to them. This can reduce the risk of food allergies later in life.

If your baby has eczema or already has a food allergy, speak with a pediatrician or pediatric allergist before introducing common food allergens into your child’s diet.

What are the symptoms of anaphylaxis in infants and toddlers?

Anaphylaxis can look different in infants and toddlers than it does in older children and adults. Recognizing the early signs is critical. Symptoms can change quickly and may become life-threatening if not treated right away.

It’s important for parents and caregivers to watch closely for physical or behavioral changes. Here are some common signs of anaphylaxis in each body system, with additional signs to watch for in infants and toddlers:

Breathing

• Common signs in all ages: shortness of breath, cough, tight or hoarse throat, swelling of lips or tongue that impacts breathing
• Additional signs in infants and toddlers: belly breathing, rapid breathing, nasal flaring, tugging the chest or neck, hoarse cry

Heart

• Common signs in all ages: skin color is pale or has a bluish tint, weak pulse, dizziness or fainting
• Additional signs in infants and toddlers: blotchy discoloration of the skin, fast heartbeat, appearing limp or wobbly with poor head control

Skin

• Common signs in all ages: many hives across the body
• Additional signs in infants and toddlers: obvious swelling on the face

Stomach

• Common signs in all ages: severe vomiting or diarrhea (may be combined with other symptoms)
• Additional signs in infants and toddlers: vomiting more than once, vomiting or diarrhea combined with other symptoms

Behavior

• Common signs in all ages: feeling of “doom,” confusion, agitation, altered consciousness
• Additional signs in infants and toddlers: very tired, difficult to wake up, withdrawn, crankiness, inconsolable crying

Symptoms of anaphylaxis may vary among babies and can be different each time a baby has an allergic reaction.

Treating anaphylaxis

Infant anaphylaxis is a medical emergency needing immediate action. Epinephrine is the only medication that effectively treats anaphylaxis. It’s key to always have at least two doses on hand, as symptoms can sometimes come back after the first dose is given.

If you think your child has been exposed to a food allergen, or severe symptoms are occurring in one or more body system, give epinephrine right away. If symptoms are mild but occurring in more than one body system, you should also give epinephrine. Seek emergency medical help if your baby’s symptoms are severe, come back or worsen after the first dose, or don’t go away completely.

Ask your child’s pediatrician for an epinephrine prescription for your child. Make sure you feel comfortable giving it. Teach others who care for your child how to administer it.

Learn more at AllergyAsthmaNetwork.org.

2025-10-29T12:01:02

(BPT) – When most people think of eczema, they picture a dry, red, inflamed and itchy rash. But on darker skin tones, eczema can look very different, sometimes appearing purple, gray or dark brown. These differences can lead to a missed diagnosis and delayed treatment.

This not only worsens the symptoms of this common skin condition, but it can also increase the chances of developing additional allergic conditions. Delaying treatment for eczema can take a toll on mental health as well, causing frustration, anxiety, stigma and emotional stress.

With greater awareness and culturally informed care, eczema patients can find relief — for their body, mind and spirit.

Allergy & Asthma Network and the American College of Allergy, Asthma & Immunology (ACAAI) created the website EczemaInSkinofColor.org to help patients and healthcare providers better identify eczema symptoms on skin of color.

What are the unique signs and symptoms of eczema in skin of color?

Eczema (also referred to as atopic dermatitis) affects people of every race and ethnicity. However, research shows that people with skin of color — especially children — are at higher risk of developing eczema and often experience more severe symptoms.

Eczema on black and brown skin often doesn’t appear as the typical red rash seen on lighter skin tones. Instead, it might look purplish, ashen gray or darker than the surrounding skin. As a result, many patients and healthcare providers may not identify the skin condition as eczema. They may diagnose it as something else or dismiss it as “just a rash.”

Without proper treatment, eczema can cause patches of lighter or darker skin in people with skin of color. (This is known as post-inflammatory hyperpigmentation or hypopigmentation.) It may also cause the skin to thicken over time. These visible changes can be especially distressing for people of color.

How does eczema affect mental health in people with skin of color?

If eczema makes you feel self-conscious, anxious or depressed, you’re not alone. The visible nature of the condition, along with the itching, discomfort and social stigma, can lead to feelings of embarrassment or isolation. Over time, this emotional strain can worsen depression, anxiety and stress.

Research presented at the ACAAI annual meeting in 2023 found that 72% of people with eczema reported they had poor mental health for 1-10 days of the previous month. Another study published in the May 2025 issue of Annals of Allergy, Asthma & Immunology found that adults with eczema are two to three times more likely to have depression and anxiety. Yet these mental health needs too often go unaddressed.

For people of color, the emotional burden of living with eczema can be even greater. Barriers such as limited access to affordable or culturally competent healthcare, greater exposure to environmental triggers, and social and economic factors make it harder for many to get effective treatment. These challenges can lead to worse mental health outcomes.

A lack of representation in healthcare, historical and ongoing mistrust of care, and limited medical training on how eczema appears on darker skin tones all contribute to delayed eczema and mental health treatment.

Addressing eczema in skin of color means not only treating the skin but also supporting the whole person.

How can I find support for mental health?

Many resources are available to help you recognize symptoms, access treatment and find support for the emotional challenges that often accompany eczema. When you visit your healthcare provider — ideally an eczema specialist such as an allergist — ask for a referral to a mental health specialist. Addressing both your skin and emotional well-being is an important part of managing eczema and improving your quality of life.

The EczemaInSkinofColor.org website is a comprehensive educational guide with advice on how to talk with your healthcare provider about stress, self-esteem, anxiety and depression related to your skin condition. It includes helpful tips for parents and caregivers of children with eczema, such as creating an “eczema kit” with creams, moisturizers and wipes to bring to school or activities.

You don’t have to manage the physical and mental burden of eczema alone. To learn more about how eczema presents on skin of color and find more resources for care and support, visit EczemaInSkinofColor.org.

2025-10-22T02:01:00

(BPT) – Open enrollment is here, which means it’s time to review your health coverage options for 2026 and make changes if you need to. With a little prep, choosing a plan through Medicare, your employer or the Affordable Care Act Marketplace doesn’t have to be stressful.

“Health insurance jargon can be confusing, but the details matter,” said Cindy George, MPH, senior personal finance editor at GoodRx. “Taking a little time to understand how premiums, deductibles, networks and medication coverage work for you can help you save money and land a plan that fits your needs.”

If you’re ready to shop smart, start with George’s five expert tips:

Keep your information current

If you use the ACA Marketplace or programs like Medicaid, CHIP or Medicare’s Extra Help, update your income and household details each year during open enrollment. This can change what you qualify for and how much you save.

If you have an employer plan, make sure your dependents and beneficiaries are correct and report life changes like marriage, a new baby or a move, so your coverage stays up to date.

Check your medication coverage

Don’t assume your prescription coverage will be the same as last year. Plans often update which medicines they cover and how much you’ll pay. If you have Medicare Advantage or a Part D plan, double-check that your prescriptions are still covered. A quick review now can prevent costly surprises.

“Put your most important prescriptions at the center of your plan search,” says George. “If a plan doesn’t cover medication you need or moves it to a higher price level, you can check the GoodRx cash price. In many cases, that price may be much lower than your insurance copay.”

Think beyond insurance

Insurance alone may not provide the medication coverage you need. GoodRx research shows that plans can exclude some medications entirely or add restrictions like prior authorization. It often helps to compare your copay with prices available outside of insurance. For example, resources like GoodRx let you compare cash prices and savings options for both brand name and generic medications. GoodRx is not insurance, but it can often beat your copay price, so it may be worth factoring that into your plan choice and overall budget.

Don’t auto-renew without reviewing

Insurance coverage shouldn’t be a set-it-and-forget-it process. Because costs and coverage shift every year, it pays to shop around. Letting your plan roll over without a second look could mean missing out on better coverage or lower costs.

“Even if you like your current plan, compare before you renew,” George says. “Check the deductible, out-of-pocket maximum and whether your regular doctors and medicines are covered to avoid surprises next year.”

Use comparison tools like a pro

Free tools can make plan shopping faster and clearer during open enrollment. Use Medicare Plan Finder to compare Medicare Advantage and Part D options, HealthCare.gov or your state marketplace to review ACA plans and see your estimated savings, and GoodRx to cross-check prescription prices so you can better estimate your total yearly costs.

“Don’t wait until the end of the open enrollment period,” George said. “Start now, understand your options and choose a plan with confidence.”

Ready to get started? Visit GoodRx.com to find resources to help you navigate open enrollment and explore savings on prescription medications.

2025-10-14T08:03:00

(BPT) – Is your neck stiff and tight? Are your wrists aching after hours of typing? Do your back and shoulders hurt from lifting and twisting? These are some common signs of repetitive stress disorder (RSD). RSD doesn’t happen out of the blue. The repetitive strain can cause microtears in your soft tissue, causing pain that comes and goes but never seems to lessen.

RSD can happen to anyone. While jobs that are physically demanding, like construction and trade professions, can increase your chance of RSD, any job that includes repetitive motion can lead to pain, stiffness and reduced range of motion, and swelling of your joints and muscles. That means office professionals, retail and food service workers, and health care providers can be affected, among others.

The good news is that RSD is treatable. Read on to learn about four ways you can take care of your body that may help ease your pain.

1. Lifestyle changes

Your daily habits can sometimes be the cause of your pain. From poor posture or lack of movement to too much movement, what you do and how you do it can create or worsen a repetitive stress injury.

Think about how you can make simple changes to your lifestyle habits. For example, take regular breaks during work to gently stretch, change positions often, drink plenty of water and alternate tasks to avoid overuse of the same muscles and joints.

2. Ergonomics

Your workspace should work for you, not the other way around. Consider your work environment and identify changes you can make to support your posture.

Sometimes all it takes is adjusting your chair height and repositioning your screens. However, if you spend hours at a desk, consider using a standing desk. A standing desk is a great tool that can help make you more aware of your posture, reduce strain and encourage movement throughout your workday.

3. Chiropractic care

Chiropractic care may be able to help your body recover from repetitive strain injuries. When you repeat the same movement, your joints can lose mobility, muscles become tight and nearby nerves become compressed. Because chiropractic adjustments may help improve joint motion, reduce muscle stiffness and relieve pressure on nerves, you may regain comfortable, confident movement.

Consider visiting a chiropractic clinic like The Joint Chiropractic, the nation’s largest provider of chiropractic care. Known for its retail setting and concierge-style services, you can visit a Joint location near you without making an appointment or dealing with insurance. Not sure you can fit a chiropractic visit into your busy schedule? Thanks to The Joint’s accommodating hours of operation, including evenings and weekends, you can find a time that works best for you.

4. Posture

Poor posture, whether sitting or standing, makes your body work harder and causes daily strain. Start to notice your posture and consider how you can improve it. Avoid slouching when sitting or standing. If you repeatedly lift objects throughout the day, make sure to squat with a straight back and lift with your legs. Retraining your posture may be difficult at first, but the time you take to correct it can pay off in the long term.

Maintaining better posture has the potential to reduce stress on muscles, tendons and joints, and may help prevent repetitive strain injuries. Keeping your body more aligned may allow tissues to work more evenly, support circulation and reduce nerve compression. Simple adjustments, like supporting your lower back, keeping wrists straight while typing or keeping elbows closer to your body may allow you to protect against strain and support recovery.

Bodies are adaptable, and with the right support, they can reset and reconnect with the strength and ease that movement is supposed to bring. Learning how to recognize pain at an early stage and how to move forward with more comfort, freedom and control is key to a healthier and better life.

Using these tips, you can address your RSD and get on the road to feeling better in your body. To learn more about RSD and how chiropractic care may help you manage your pain, visit TheJoint.com.

2025-10-14T06:01:01

(BPT) – Ovarian cancer in women remains one of the most difficult cancers to diagnose. This is partly because its symptoms are not always readily apparent. As a result, a diagnosis may be delayed or initially attributed to another condition, and a diagnosis often comes when the disease is already in later stages — meaning it has spread beyond the ovaries to other areas of the body.

Platinum-based chemotherapy has long been the standard of care for women diagnosed with ovarian cancer. It is often used after surgery, which is done first to remove as much cancerous tissue as possible. This type of chemotherapy works by attacking the cancer cells, damaging the cells’ genetic material and leading to cell death.

Even after successful initial treatment with surgery and chemotherapy, cancer cells can remain in the body. These cells may be resistant to the initial therapies, or they may simply be too small to detect. Over time, these cells can grow and form new tumors, causing cancer to return.

Patients whose cancer returns within six months of platinum-containing therapy are said to have “platinum-resistant” ovarian cancer. This means cancer has become resistant to these platinum-based treatments. However, new research may bring options for women with platinum-resistant ovarian cancer.

The Role of Cortisol and the Glucocorticoid Receptor in Ovarian Cancer

Scientists now believe that cortisol may play a role in how tumors respond to chemotherapy.

Cortisol, often referred to as the stress hormone, is a natural hormone that plays a vital role in many processes within the body. Cortisol regulates these processes by binding to a protein called the glucocorticoid receptor. This binding acts like a light switch, turning on a series of cellular signals that impact bodily functions such as regulating metabolism, blood pressure, and cell growth.

The interaction between the glucocorticoid receptor and cortisol has also been found to play a role in cancer cells, including ovarian cancer. Turning on that light switch may cause ovarian cancer cells to become resistant to chemotherapy and may impact how well certain chemotherapy treatments work. This can happen even with normal levels of cortisol in the body.

Navigating Recurrence: Your Role and Resources

Because treatment options are limited, especially after disease recurrence, it’s important for women diagnosed with ovarian cancer to partner with their care team to better understand their disease and treatment options. This partnership helps them get the best care.

“Not every treatment has the same outcome or response for everyone,” explains Rachel, a patient first diagnosed with ovarian cancer in 2018. “It’s okay and advisable to ask a lot of questions and get second and even third opinions. This gives you information and a fuller picture to inform your personalized, targeted plan. It also helps you know that people are listening to you. This is a journey — people need to support you where you are on this journey.”

For women who have faced an ovarian cancer diagnosis, understanding recurrence is a vital part of their ongoing health journey. Here are three things women need to know about recurrence:

Recurrence Is Common. Ovarian cancer can have a high recurrence rate — you are not alone. And new science continues to bring new potential options for women with platinum-resistant ovarian cancer.

Maintain the Right Mindset. When faced with platinum-resistant ovarian cancer, focusing on what you can control is a good way to stay positive when dealing with the challenges of this disease. While it can be intimidating to ask questions or offer your perspective in the moment, it’s important to advocate for yourself and speak up at appointments. This way, you and your care team can work together to find the best way forward.

A Strong Support System Is Critical. Living with recurrent ovarian cancer can be emotionally and physically challenging. Building a strong support system is crucial. Lean on family and friends for emotional and practical support. Consider connecting with other women through support groups to share experiences and find helpful resources. You can also seek help from mental health professionals like therapists or counselors who can help you navigate the emotional toll of recurrence.

For women with ovarian cancer whose disease becomes platinum resistant, it’s important to understand this chapter in their journey. Patients can visit IlluminateRecurrence.com to learn more. They can also download resources, such as a discussion guide they can use to ask their doctor about managing recurrence, how to work with their care team and other important topics during their appointments.

2025-10-09T07:45:00

(BPT) – It’s that time of year again: fantasy football season! Whether it’s your first time joining in on the fun or you’re a regular league member, playing fantasy football allows you to feel like you’re part of the action on the field. However, it’s critical that you work on your defense plan against a real-life threat: stress-induced teeth grinding.

The grind behind the game

Fantasy football sparks 1.2 billion hours of rivalries yearly, fueling stress that hits your oral health hard. In fact, more than 70% of dentists see a rise in teeth grinding from stressful situations like intense rivalries from playing in a fantasy football league.

To shed a little light on the subject, DenTek^®, the #1 over-the-counter dental guard brand, surveyed fantasy football participants and found that 65% of players were extremely, very or somewhat stressed about their fantasy football team. More than half of high-stress fans said that they experienced physical symptoms, including teeth clenching and jaw pain related to their team’s performance. Stress can impact more than just your mental health — it can take a toll on your smile.

So, how can you continue to challenge your friends, cheer on your team and protect your teeth? You’ll need to draft an expert defensive lineman.

Your #1 draft pick to defend against teeth grinding

DenTek^® is kicking off the season with “Fantasy Guards” to crush teeth-grinding stress from fantasy football. These BPA-free Professional-Fit, Ultimate and Comfort-Fit nighttime mouth guards are custom-fit champs with a six-month guarantee and unbeatable comfort — your top pick for stress-busting oral care.

DenTek^® mouthguards are so effective that even professional football players are getting in on the action.

“Defending against stress is like leaping into the end zone,” said Hall of Fame safety LeRoy Butler. “DenTek^® mouth guards give you that winning edge to protect against nighttime teeth grinding.”

Turn losses into unforgettable wins

Almost 20% of football fantasy players said that one aspect of the game that contributes the most stress is a last-place punishment. To fight back against the grind and turn losses into laughs, DenTek^® has launched the “Ultimate Fantasy Football Punishment” contest. Backed by NFL stars like LeRoy Butler, Tiki Barber, Austin Ekeler, Dwight Freeney, Ted Ginn Jr., Ronde Barber, NFL veteran and dentist Joe Holland and University of Connecticut quarterback and X-League star Dave Pindell, this contest lets you up the stakes for the league loser while also snagging a deal on smile-saving night guards.

When you enter the Ultimate Punishment, you’ll have a chance to win a DenTek-sponsored twist on your league’s lowest scorer. And just for signing up, you’ll receive $5 off a DenTek Professional Fit Dental Guard, available on Amazon and major retailers, to protect against this season’s stress grinding!

Head to Dentek.com/UltimatePunishment. See the full rules and submit your league names and a short video online by Dec. 8, 2025.

“DenTek’s nighttime dental guards are your MVP for a tough season,” said Barber. “And the Ultimate Punishment? That’s a touchdown for fun.”

2025-10-08T16:17:01

(BPT) – As we head into fall and colder months approach, it’s important to stay vigilant of the increased risk of respiratory viruses, especially COVID-19. Over the past four years, data has shown that COVID-19 cases, hospitalizations and deaths consistently rise during the fall and winter seasons.¹

This seasonal trend is reflected in recent data, underscoring the ongoing impact of COVID-19 across the country. Recent estimates from the Centers for Disease Control and Prevention (CDC) show that between October 1, 2024, and August 9, 2025, COVID-19 led to approximately 320,000 to 480,000 hospitalizations and 37,000 to 56,000 deaths in the United States.² Older adults remain especially vulnerable. Those aged 65 and older accounted for two-thirds of COVID-19-related hospitalizations between March 2020 and September 2024.³

In August, the U.S. Food and Drug Administration approved updated COVID-19 vaccines for the 2025-2026 season targeting the LP.8.1 variant of SARS-CoV-2. The CDC’s Advisory Committee on Immunization Practices (ACIP) recommends that individuals consult with their health care providers to determine if the COVID-19 vaccine is right for you, especially for those under the age of 65 who have health conditions that put them at higher risk for severe illness.⁴

“Many people view COVID-19 as a thing of the past, but the reality is, it’s still making people sick,” said Dr. Donald Middleton, Professor of Family Medicine at the University of Pittsburgh School of Medicine and Vice President of Family Practice Education at UPMC St. Margaret. “While many have stopped testing when they feel ill, they could still have COVID-19 and unknowingly spread it. That’s why it’s so important to reduce your risk of serious illness by getting vaccinated. COVID-19 frequently changes, so an updated vaccine can help keep you protected, even if you have been vaccinated previously.”

Here are three reasons to get the updated COVID-19 vaccine this fall:

1. Your immunity to COVID-19 wanes over time

The SARS-CoV-2 virus is constantly changing, and immunity from previous vaccinations or infections decreases over time.^5,6 The updated vaccines are designed to provide better protection as the virus mutates, prevent serious COVID-19 outcomes, and even help prevent Long COVID.^5,7

Per the CDC, if you have recently recovered from a COVID-19 infection, you may consider delaying your vaccine dose by three months.⁸ For example, if you had COVID-19 in July, you could wait until October to get your vaccine. Speaking to your healthcare provider remains one of the best ways to learn more about staying up to date with your vaccinations.

2. Many people have a high risk for complications

Approximately three in four adults in the U.S. have at least one underlying health condition that can increase their risk for developing severe illness from a COVID-19 infection.⁹ These underlying conditions include but are not limited to diabetes, obesity, heart conditions, lung disease and possibly high blood pressure (hypertension).¹⁰

In addition to underlying medical conditions, additional factors that can elevate a person’s risk of developing severe COVID-19, include:¹⁰

• Older adults are at highest risk of getting very sick from COVID-19.
• Your risk of severe illness from COVID-19 increases as the number of your underlying medical conditions increases.
• Some people are at increased risk of getting very sick or dying from COVID-19 because of where they live or work, or because they can’t get health care.

The risk of severe illness increases with the number of underlying conditions a person has.¹⁰ Older adults, especially those aged 65 and older, are particularly vulnerable due to age-related weakening of the immune system.¹¹ This group, made up of roughly one in six Americans, accounts for the majority of COVID-19–related hospitalizations and deaths.^3,12

Given these risks, it’s important for all adults, especially those with underlying conditions or who are older, to take appropriate precautions to protect themselves and others.

3. Long COVID still poses a threat

Healthcare professionals estimate that nearly one in three Americans who have had COVID-19 experience Long COVID, regardless of age or prior health status.¹³ This means that anyone who contracts COVID-19 is potentially at risk.

Long COVID is a chronic condition that persists for at least three months after initial infection with SARS-CoV-2.⁷ It can involve a wide range of symptoms, including difficulty concentrating, fatigue and chest pain. These symptoms may improve, worsen or persist over time, lasting for several months or even years.^7,14 In addition to these symptoms, individuals who experienced severe acute COVID-19 are at an increased risk for long-term complications such as cardiovascular disease, diabetes, kidney issues and gastrointestinal disorders.¹⁵

Certain groups are more likely to develop Long COVID, including those who are unvaccinated, aged 65 and older, or have underlying health conditions. For these individuals, the risk of both severe illness and long-term effects is significantly higher.⁷

Protect yourself and your loved ones this fall

Vaccination remains one of the most effective tools in defending yourself against COVID-19.¹⁶ If you’re unsure about when to get vaccinated, what your personal risk factors are, or how best to protect yourself during respiratory illness season, talk to your healthcare provider to make informed decisions.

To learn more about the COVID-19 vaccine, visit the CDC website. To find a vaccine near you, visit your local pharmacy’s website.

Content sponsored by Moderna.

2025-10-08T07:01:00

(BPT) – Could you be experiencing chronic hand eczema (CHE)? It’s different from atopic dermatitis (eczema)¹ and is one of the most common skin disorders that affects approximately one in ten adults worldwide.^2,3

Some CHE symptoms, like itching, redness and dry, flaky skin may seem relatively minor, although irritating.¹ However, the condition is also characterized by pain, thickening of the skin, blisters, swelling and cracking skin on hands and wrists.¹ Often, people diagnosed with CHE face functional and emotional challenges that can impact career, self-confidence, relationships and more^4,5 — a reality that Monique T. knows all too well.

Monique’s journey with CHE

Monique — a resident of Shelby Township, Michigan — has lived with CHE since she was a child but experienced more intense symptoms starting in her 40s. At first, her hands became red and itchy, but she soon developed dry, flaky skin, lesions and blisters. Her CHE symptoms not only make her feel embarrassed about her hands, but she also struggles with everyday function, a common effect among CHE patients.

According to a recent survey conducted by Ipsos for LEO Pharma, Inc. — a medical dermatology company — 95% of U.S. dermatology providers surveyed agreed that moderate-to-severe CHE has a strong impact on patients’ work and home lives.⁶

For Monique, CHE makes it difficult to hold things, even the steering wheel of her car, a brush or a bottle of shampoo.

“Living with chronic hand eczema is a daily challenge,” Monique said. “The constant itching and pain make even simple tasks like driving to the store or washing my hair in the shower feel impossible because my hands are so sensitive and cracked that it hurts to touch anything.”

These physical symptoms can also make it difficult for patients with CHE to hold down a job. For example, 86% of health care providers surveyed said moderate-to-severe CHE has caused their patients to struggle at work.⁶ Also, 54% said CHE impacts their patients’ financial situation and 51% agreed that CHE has caused their patients to stall in their careers.⁶

“The hardest thing about having chronic hand eczema is its impact on my financial security,” Monique said. “It’s difficult to work full time when I’m having a flare and needing to call in sick or having to mask my pain while interacting with customers or co-workers.”

Beyond the physical and financial realms, CHE can make emotional and social aspects of life very difficult.⁶ Dermatology providers reported that CHE impacts their patients’ emotional health (93%) and self-consciousness (92%).⁶ These emotional challenges can have a strong impact on patients’ dating life (72%), relationships with family and friends (72%) and desire for intimacy with their partner (68%).⁶

For Monique, she struggles to participate in social activities because she is constantly thinking about her hands and her CHE.

“Chronic hand eczema has a big impact on my self-esteem and my social life,” Monique said. “I don’t like to make plans because I’m self-conscious about my hands and live in fear of having a flare and needing to cancel.”

How to manage CHE

If you’re experiencing CHE symptoms, start by removing products that may exacerbate the condition.¹ When performing cleaning tasks, consider using gloves to keep your skin from contacting harsh chemicals.¹ It’s also important to keep the skin moisturized frequently throughout the day to enhance the barrier function of the skin, even when CHE is not flaring.¹

When it comes to emotional challenges, it’s important to create a routine and have plans in place for how to manage the anxiety that can come from living with CHE.¹ To keep her mind occupied and her emotions under control, Monique turns to nature and her dogs. She also incorporates regular exercise into her routine, goes on long walks through the park, and uses a stress ball when she’s feeling anxious. It’s also important to build a support system. Monique has relied on her boyfriend for encouragement and understanding, but he’s also helped her when it was too painful for her to do certain tasks herself, like shower during a severe CHE flare.

Talk with your doctor

If you are living with CHE or suspect you’ve developed this skin disorder, it’s important to talk with your doctor about your condition and possible treatment plans. To learn more about a treatment option for adults with moderate-to-severe CHE, visit www.learnaboutche.com.

References

1. Thyssen JP, Schuttelaar MLA, Alfonso JH, et al. Guidelines for diagnosis, prevention, and treatment of hand eczema. Contact Dermatitis. 2022;86(5):357-378.

2. Lee GR, Maarouf M, Hendricks AK, Lee DE, Shi VY. Current and emerging therapies for hand eczema. Dermatol Ther. 2019;32(3):e12840.

3. Quaade AS, Simonsen AB, Halling A-S, Thyssen JP, Johansen JD. Prevalence, incidence, and severity of hand eczema in the general population – A systematic review and meta-analysis. Contact Dermatitis. 2021;84:361–374.Voorberg AN, Loman L, Schuttelaar MLA. Prevalence and Severity of Hand Eczema in the Dutch General Population: A Cross-sectional, Questionnaire Study within the Lifelines Cohort Study. Acta Derm Venereol. 2022;102:adv00626.

4. Koskelo M, Sinikumpu SP, Jokelainen J, Huilaja L. Anxiety and depression in patients with hand eczema: A population-based study among 853 middle-aged subjects. Contact Dermatitis. 2023;89(6):464-470.

5. LEO Pharma Inc. LEO Pharma Survey: Dermatology Providers Agree Chronic Hand Eczema Impacts Patients’ Emotional, Social, and Occupational Well-Being. Business Wire. Published April 22, 2025. Accessed May 8, 2025. Available at: https://www.businesswire.com/news/home/20250422320493/en/LEO-Pharma-Survey-Dermatology-Providers-Agree-Chronic-Hand-Eczema-Impacts-Patients-Emotional-Social-and-Occupational-Well-Being.

MAT-83866 September 2025

2025-10-07T08:01:00

(BPT) – Sponsored by Sanofi

By: Adam Schefter, Senior Football Insider and paid Sanofi spokesperson

Early information is my “currency” — I’ve built my career as a Senior Football Insider on the power and value of knowledge. From building strong relationships in the industry to moving fast on insights, getting the news before it breaks has always given me an edge in this space. Although advance notice has been the foundation of my career, I never considered how important it would be for my wife, Sharri, who was diagnosed unexpectedly with type 1 diabetes (T1D).

When my wife first found out she had T1D, it came as a complete shock. In fact, because T1D is often asymptomatic in its early stages, she didn’t have time to prepare for life with the disease and was instead immediately thrown into the realities of 24/7 disease management. Hearing her talk about her experience is a reminder that even the best laid plans can change, and we always have to be ready to pivot.

Every day, I watch Sharri navigate her disease — the ups, the downs, and everything in between. But just like players on a football field, I hate sitting and watching from the sidelines. I always have my head in the game. That’s why I feel incredibly strongly about the importance of early risk detection and spreading the word about the power of T1D autoantibody screening. Here’s three things you should know about T1D so you can put together an early detection playbook for yourself and your families.

T1D progresses in stages

It’s a common misconception that if someone is at risk of developing T1D, there’s nothing to do except wait and watch for symptoms. As part of this journey, I’ve learned that just one blood test can spot T1D before symptoms arise and insulin dependence begins. That means you can have the inside scoop on what’s going on in your body through T1D screening.

How is this possible? Well, the progression of T1D occurs in three stages. So, while my wife was diagnosed in Stage 3, it is possible to discover T1D in Stages 1 or 2. It’s during these early stages that a “silent” attack on beta cells (i.e., the cells responsible for keeping glucose levels in a healthy range) begins inside the body. By the time T1D progresses to Stage 3, the body’s ability to produce insulin becomes severely compromised, and therefore requires daily insulin injections.

Screening could be the difference between getting ahead of the game and discovering T1D in Stages 1 or 2 versus being caught off guard by a Stage 3 diagnosis. If my career has taught me anything, I’d say that being caught off guard is not a position you want to be in!

Certain risk factors can put you at an increased risk

There are certain risk factors — like certain autoimmune conditions — that may put you or your loved ones at an increased risk for developing T1D. Notably, family history is also a risk factor, and if even one family member has T1D, then the risk increases up to 15 times. For my family, that means my children are at an increased risk, which is something Sharri and I always keep in mind.

There’s no need to wait for symptoms to act

If I asked right now, how many of us could describe the signs and symptoms of T1D? Years ago, I certainly wouldn’t have been able to. Symptoms of T1D can include frequent urination, excessive thirst, unexpected weight loss, and more; but if you don’t know what you’re looking for, these symptoms can be easy to confuse (with other sicknesses) or explain away. But just like getting a break on an exclusive story, these symptoms are time-sensitive; if you don’t see a doctor in time, you could find yourself in an emergency due to complications of T1D. When screening is available, there’s no need to wait until symptoms arise.

Final thoughts

The unfortunate truth is that a staggering ~64,000 individuals are newly diagnosed in the U.S. every year — many who find out about their diagnosis in an emergency setting. However, T1D screening can give you and your loved ones time to plan and stay ahead of the game. Like breaking the news, the sooner you know, the better, so don’t wait because if you wait, it might be too late.

My wife Sharri was caught off guard by her T1D diagnosis, but with screening and subsequent monitoring, you and your loved ones might not have to be. Make a plan and talk to your doctor about T1D screening.

Visit ScreenForType1.com to learn more.

Sanofi does not provide medical advice, diagnosis, or treatment — information is provided for educational purposes only. Your doctor is the best source of health information. Talk to your doctor if you have any questions about your health or treatment.

Adam Schefter is a paid spokesperson for Sanofi.