Health awareness

Prostate cancer: stigma, early screening and support

A prostate cancer survivor and a caregiver and advocate want to inspire more people to talk about the disease

April 26, 2024

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Even after losing his father and grandfather to prostate cancer, Henry H. Washington III, Ph.D., was still shocked by his prostate cancer diagnosis after a routine screening. A retired Army Major and longtime athlete, Washington saw himself as the picture of health.

“After fighting for my country in the military and then to find out I have prostate cancer – how do I deal with that? It was a lot of emotions. I think as men we aren’t allowed to have emotions. We are taught that we need to be strong.”

  • Henry H. Washington III

Screening for prostate cancer is key in early detection

After skin cancer, prostate cancer is the second most common cancer for men in the U.S. Anyone who was born with a prostate can develop it. About 1 in 8 men will be diagnosed during their lifetime, and Black men are more likely to develop prostate cancer.

 In its early stages, prostate cancer can be difficult to identify because there are usually no symptoms.

Routine screening for those who are at risk can help detect prostate cancer early before it has spread. The greatest risk factor is age. Men over the age of 65 have the highest risk. Additional risk factors include inherited gene mutations and a family history of certain cancers.

Speaking out and supporting loved ones with prostate cancer

Courtney Bugler, president and CEO of ZERO Prostate Cancer who herself is a cancer survivor, said she was inspired to take on this role to support her father, who is living with the disease.

“There’s a stigma around prostate cancer and watching my dad made me want to shine a light on something that, quite honestly, I don’t think gets enough attention. After almost 20 years of him supporting me after my own diagnosis, it’s time for me to be there for him.”

  • Courtney Bugler
    CEO of ZERO Prostate Cancer

The stigma associated with prostate cancer can be attributed in part to the nature of the disease and its treatment disrupting normal urinary, bowel and sexual function, all of which can impact a patient’s body image and self-esteem. The thought of impaired sexual health, in particular, may even lead men to avoid screening for prostate cancer altogether.

Statistics show there’s still unease around prostate cancer diagnosis

A 2022 study of 200 metastatic prostate cancer patients, conducted by Merck and Cerner Enviza, found:

  • 58% of patients agree there’s a stigma around prostate cancer.
  • 39% didn’t share their feelings about having prostate cancer with loved ones because they felt they needed to “stay strong.”
  • More than a third felt uncomfortable, embarrassed or vulnerable talking to their loved ones (37%) or their doctor (38%) about emotional challenges.

Now cancer-free for a decade, Washington said he sees helping others as his purpose. He faces the potential unease head-on by educating others about prostate cancer, encouraging men to get checked early and working with men who have been diagnosed.

“Survivorship is not a linear experience; sometimes it’s two steps forward, five steps back,” said Washington. “The support I received from my friends, my support groups, my mother and my family is what gave me strength to educate others about prostate cancer.”

"Finding support and having people beside you who know what you're going through is what will help get you through.”

For more information about prostate cancer and access to helpful resources visit ZERO Prostate Cancer.

Health awareness

How we can strengthen vaccination programs and build vaccine confidence together

Two Merck leaders share how we’re working to help protect communities from vaccine-preventable illnesses

February 21, 2024

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How we can strengthen vaccination programs and build vaccine confidence together

Vaccines are one of the most significant public health achievements in modern history, playing a vital role in helping to prevent certain infectious diseases and protect communities across the globe.

Unfortunately, the COVID-19 pandemic brought forth a new set of challenges in sustaining vaccination efforts for other preventable diseases — highlighting existing disparities and inequalities in access to health care and underscoring the urgent need for action.

In two op-eds for Devex, an independent news organization covering global development, Drew Otoo, Pharm.D., president of global vaccines, and Alfred Saah, M.D., executive director of scientific affairs, highlighted some of the ways we’re working to address these challenges at the global, national and local levels.

Collaborating to help increase health equity

Otoo said collaboration across sectors is key to building trust, enabling equity and establishing stronger, more resilient vaccination programs.

Drew Otoo

“Now more than ever, we have an opportunity to evaluate and strengthen our approach… Together, we can help create a more equitable future where vaccines are available to and accepted by all who can benefit from them.”

  • Drew Otoo, Pharm.D.
    President of global vaccines, Merck

Otoo shared examples of our work with local and global stakeholders to develop tailored approaches to improve vaccine confidence and supply vaccines for communities that might otherwise be without them:

  • Local organizations and community leaders have a deep understanding of the issues contributing to inequities and low routine vaccination rates in their communities, and they’re essential to identifying and executing solutions. We know this to be the case from our efforts through ImmUNITY Chicago, an initiative we helped catalyze with local stakeholders to address lower vaccination rates among neighborhoods in the Southwest Side of Chicago, predominantly among communities of color.
  • Strategic global collaborations are also critical to enabling stronger, more sustainable vaccination programs. We work with Gavi, the Vaccine Alliance — a global alliance that has helped to vaccinate nearly half of the world’s children in low-income countries.

Combating vaccine hesitancy and building trust

Saah emphasized our commitment to addressing vaccine hesitancy (the reluctance or refusal to vaccinate despite the availability of vaccines) and building confidence at local, national and global levels.

“By understanding the knowledge gaps and prioritizing strategies that strengthen how we communicate…we can potentially combat vaccine hesitancy, improve vaccine confidence and make a difference in global public health.”

  • Alfred Saah, M.D.
    Executive director of scientific affairs, Merck

Despite the well-documented benefits of vaccines, hesitancy is a longstanding public health issue that can result in under-vaccination and global disease outbreaks. The reasons behind vaccine hesitancy are often connected to the 3Cs Model, defined by a World Health Organization strategic advisory group:

  • Complacency: The perception that vaccine-preventable diseases pose little risk to individuals.
  • Convenience: The degree to which vaccination services are accessible.
  • Confidence: The degree to which an individual believes vaccines work, are safe and effective and are part of a trustworthy public health and medical system.

Saah shared some of our efforts to improve vaccine confidence, which include:

  • Working with collaborators to reach the global population and engage communities through mediums that resonate, such as social media, and through messages that can be delivered by trusted community members.
  • Building capabilities for our colleagues in local markets to better understand the strengths and vulnerabilities of vaccination programs on a global and national scale.

Continuing our work to improve vaccine access

Despite the challenges ahead, both Saah and Otoo are optimistic about the future.

“Combating vaccine hesitancy is not an easy feat and has been a challenge our global society has faced for centuries,” wrote Saah. “However, these challenges bring new opportunities to improve our approach and be better advocates for ourselves, our families and our communities.”

“By going where the need exists and continuing to invest in innovative, strategic and diverse collaborations, I'm confident we'll find new ways to solve complex public health problems.”

— Drew Otoo

Learn more about how collaborations can help yield stronger vaccination programs.

Health awareness

‘Wonder Angie’ enlists her ‘super friends’ to fight oral cancer

After receiving an oral squamous cell carcinoma diagnosis, a head and neck cancer survivor finds hope by embracing science, prioritizing mental health and leaning on her work family

January 26, 2024

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Wonder Angie

In 2017, Maria Angelica Rosario Marquez — or Angie, as she likes to be called — joined Merck in Colombia as a clinical data specialist. She had lost her father the year before and was looking forward to starting a new chapter. The novelty of that first year, however, was short-lived, as her mother was diagnosed with cancer in 2018.

Angie spoke to her manager, and he encouraged her to put family first. She booked a ticket to Chile and was there to support her mother and sister during the illness and her mother’s passing.

Just five months later, 34-year-old Angie was diagnosed with head and neck cancer, specifically squamous cell carcinoma of the tongue.

Head and neck cancer includes cancer of the oral cavity, throat (pharynx), voice box (larynx), nose (nasal cavity), sinuses (paranasal sinuses), and salivary glands. In 2023, an estimated 66,920 people were diagnosed with a head and neck cancer in the U.S. Some risk factors that can contribute to the development of head and neck cancers include tobacco use and alcohol consumption — but Angie’s disease was not linked to these typical risk factors.

It all started with pain in Angie’s tongue 

When Angie developed bruxism (grinding, clenching, or gnashing of the teeth), she consulted her physician for evaluation. Angie also noticed that she was continuously biting the same spot on her tongue while she was sleeping. She assumed it was due to stress caused by the devastation of losing both of her parents and her move to a new country without her family by her side. When the pain on the right side of her tongue increased to a point that made it difficult to eat or brush her teeth, her doctor decided to take a biopsy, and in March 2019, he informed her of the diagnosis.

“It was the most frightening thing I’ve ever felt in my life,” she said.

A week later, Angie had surgery to remove the right portion of her tongue, which contained the cancerous tissue, as well as 21 lymph nodes on the right side of her neck. A further analysis of the lymph nodes showed evidence of cancer, so her oncologist followed up with a treatment plan that included three chemotherapy sessions and 30 days of radiation on her neck and tongue.

The toll of Angie’s treatment for oral cancer

Following her surgery and throughout treatment, Angie experienced a burning feeling in her mouth and throat, and it became extremely difficult for her to speak or eat — two of her favorite activities. Instead, she relied on a feeding tube for several months to receive her meals.

Though Angie was eventually able to resume eating normally, her sense of taste was impaired for a year after she finished treatment. The fact that chocolate, one of her favorite foods, tasted disgusting to her was heartbreaking.

“The doctor told me that he didn’t think I’d ever be able to speak well again. I told him that wasn’t an option because I love talking too much.”

— Angie Rosario

When Angie started to feel a deep depression, she prioritized her mental health and sought treatment from a psychologist, who taught her to focus on the present. Her psychologist encouraged her to visualize herself as a strong and healthy woman.

“I always say cancer was my teacher; it taught me how to live. If you have air in your lungs, you have everything you need,” Angie said.

Strong support and a welcome party from her work family

Angie is grateful for the science and research that helped play a part in her treatment. As of her last doctor’s visit, she remains healthy with no evidence of disease. Angie credits her work family at Merck for supporting her through much of her recovery. With the recent loss of her parents, her co-workers came to her aid with powerful emotional support that helped her through the toughest times. A lifelong collector of superhero toys, Angie came back to the office to find her desk covered in dolls, figurines and other gifts. Inspired by Angie’s courage, her colleagues even gave her a super-nickname: ‘Wonder Angie.’

desk decorated
colleagues standing behind large table with cake in the middle having a celebration

“I’m thankful for the science and medicine that helped save my life,” Angie said. “I can talk without pain, and that’s amazing. I can brush my teeth every day, and that’s amazing. I can eat, and that’s amazing.”

Angie’s sense of taste has returned for the most part, and she’s enjoying chocolate once again.

Health awareness

Empowering others to speak up about HPV-related cancers

The impact of Gina’s diagnosis inspired her to help others prioritize their health

January 5, 2024

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Empowering others to speak up about HPV-related cancers_ Photo 1

After 20 years of normal cervical screenings,* Gina Esposito was confident her next routine screening wouldn’t be any different. So, when she was diagnosed with human papillomavirus (HPV)-related cervical precancer at 47 years old, she was surprised.

“The sinking feeling I had when I received my diagnosis was intense because I wasn’t expecting it,” she said.

*A cervical screening, often referred to as a pap test or pap smear, looks for precancers or cell changes that might become cervical cancer if not treated appropriately.

The impact of HPV-related cancers and diseases

More than 80% of cervical cancers are associated with HPV. For most people, HPV clears on its own. But for those who don’t clear the virus, it could cause certain cancers and diseases.

After her diagnosis, Esposito underwent a procedure to remove the abnormal cells from her cervix. When a follow-up test showed that there were still some abnormal cells present, she consulted with a doctor and decided to get a hysterectomy.

At first, she felt embarrassed by her diagnosis. As she started to share her story, she noticed that others felt ashamed to speak about HPV-related cancers and diseases. She knew something had to change.

“I have a newfound responsibility to take the stigma away, to say ‘the shame has to go away,’ whether you’re a woman or a man,” Esposito said.

Throughout her experience, she says her daughter has been a source of strength.

“You don’t want your child to be without you or to experience the loss of a parent. You want to be around for all of their milestones and they want you around,” Esposito said. “So, she keeps me motivated because there’s an expectation that mom’s going to be around.”

Gina Esposito HPV Story Image 2

“I try to be a positive disruptor in this space and normalize it so that people go for early screenings and routine screenings and that they get treatment if they need it.”

— Gina Esposito

The importance of routine care

In some ways, Esposito considers herself lucky. Her commitment to prioritizing routine care helped her catch her disease early.

“I’m so glad I took the time to go to my screening – it helped catch my disease early,” she said.

Esposito is working to ensure her daughter also prioritizes getting routine care and understands the value of prioritizing her health, especially as she approaches adulthood.

“She knows you need to own your own health because no one else is going to do it for you,” she said. Esposito encourages colleagues across our company to prioritize their health, too.

Esposito plans to continue helping men and women feel comfortable discussing HPV-related disease and get the preventative care they need.

“When I talk with others, I focus on what happened to me so they can use it as an example,” Esposito said. “I get people emailing me, texting me, going, ‘I’m going to make my appointment today.’ And if we can have one person that we get early, then my job is done.”

Health awareness

Biomarker testing may help inform treatment decisions in certain cancers

An oncologist explains why cancer biomarkers may provide more precise information about a person's cancer

December 5, 2023

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Scientist at Merck

Over the past 20+ years, there’s been an evolution in how we think about cancer. Cancer biomarkers — substances produced by tumor cells that reflect unique features of a tumor — can change the approach to certain cancers.

Advances in biomarker testing may help inform treatment decisions

It wasn’t long ago when conversations were about simply “breast cancer” or “lung cancer.” Now, physicians can get a lot more precise.

Merck's Scott Pruitt

“We’ve come to understand that two people with the same type of cancer may have differences in the specific changes in the genes, proteins and other substances that may allow cancer cells to grow and spread.”

  • Dr. Scott Pruitt
    Associate vice president, early-stage development, clinical oncology, Merck Research Laboratories

“The field of breast cancer research was arguably the first to realize that there are multiple cancer subtypes and that biomarker testing could help inform therapy,” said Pruitt.

In the treatment of breast cancer, understanding various tumor biomarkers and pairing that understanding to help guide selection of relevant medicines has helped physicians evaluate potential treatment approaches. And the same is true in lung cancer where understanding tumor biomarkers has been used to help guide therapy aimed at targeting certain genetic mutations.

Biomarkers may help us understand a cancer better and how to approach it. That’s why biomarker testing may be an important next step after a cancer diagnosis.

Key terms to know:

  • Biomarker: a measurable indicator of a biological state or condition found in blood or tissues.
  • Biomarker testing: medical tests to look for measurable indicators (genes, proteins and other substances) that may provide information about a biological state or condition.
  • Biopsy: the removal of cells or tissue for examination.
  • Genetic testing: medical tests to look for certain mutations in a person’s genes that may be a sign of a disease or condition.

Biomarker testing after a cancer diagnosis

blood test vial

Blood test

microscope

Biopsy of the tumor

Testing for proteins and/or genes to look for known biomarkers

Testing for proteins and/or genes to look for known biomarkers

Biomarker testing and genetic testing may enable detailed characterization of some cancers

Some biomarker tests can find inherited genetic changes that you may have been born with that may increase your risk of cancer or other diseases. Genetic testing might help determine if you have certain mutations (for example, the BRCA gene) which could help inform treatment options.

Merck has been at the forefront of research to advance the understanding of biomarkers for certain cancers.

"We're fully invested in leveraging biomarker data to help inform cancer care."

— Dr. Scott Pruitt

“Across our oncology studies in every phase of development, we continue to incorporate multiple biomarker approaches to more fully understand biology as well as identify new targets of interest,” Pruitt said.

Discussing biomarker testing with a health care provider

If you’ve been diagnosed with cancer, it’s important to ask your doctor about biomarker testing. Start with these questions which may help you prepare for conversations with your doctor:

  • Is biomarker testing appropriate for the type of cancer that I have?
  • If there’s a chance my cancer was caused by an inherited risk factor, should I undergo further testing?
Health awareness

The new generation making an impact on HIV

Meet these young advocates helping to lead the response to HIV around the world

November 10, 2023

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HIV young leaders collage

HIV remains a global pandemic. In 2022 alone, an estimated 1.3 million people worldwide were newly diagnosed with HIV.

Merck has been committed to advancing science for the treatment and prevention of HIV for more than 35 years, but we know it takes all of us to make a difference for the HIV community.

And that’s just what these International AIDS Society (IAS) Young Leaders are doing. In 2022, our company was proud to be one of the groups to support 11 Young Leaders to co-create the Youth Hub — a youth-led networking platform that empowers young change-makers living with and affected by HIV to lead in the HIV response. They’re an inspiring group of advocates with different backgrounds and experiences in the response to HIV, each striving to empower and educate others from their respective corners of the globe.

Let’s meet some of these young change-makers.

Norman Chong | Malaysia

Norman Chong is using their gift of storytelling to encourage young people across the world to ask “Why?” Chong has been working to develop a solution-oriented platform to help address gaps in the HIV response for young people in Malaysia.

With their platform, called “We Ask the Y (WAY)”, Chong aims to provide tools for young people living with and affected by HIV to learn and network in support of social health, as well as economic and political justice. Chong also trains young researchers to translate and communicate findings into evidence-informed policies and practices to address barriers to health care for young people.

“If I have anything at all, it’s anchored on moving the dial with the question, “Why?”, and advocating for health care to be accessible to all, for policies designed to protect and empower, and never to divide and conquer.”

  • Norman Chong

Linda Joseph Robert | Uganda

Dismantling HIV stigma to support young people is the motivation for everything Linda Joseph Robert does. As a youth advocate, he helps to promote increased access to quality adolescent sexual and reproductive health services for young people through peer support interventions, community engagements and strategic partnerships. His passion for youth advocacy, activism and HIV-related programming came to life when he led a campaign to help reduce HIV stigma and discrimination during the COVID-19 pandemic.

As a young person living with HIV, Robert is driven to help increase access to HIV prevention, treatment and care services. Robert has held leadership positions including the role of youth advocate at AIDS Healthcare Foundation-Uganda Cares, and serves as a U=U Africa Forum Ambassador in Uganda.

“I’m motivated by the progress that has been made in the HIV field and excited to be part of the next generation of HIV professionals who will continue the journey toward ending the AIDS pandemic, where no one is left behind.”

  • Linda Joseph Robert

Elizabeth Onyango | Kenya

UKIMWI UNAUA is a term Elizabeth Onyango and others in Kenya know too well. Translated to “HIV kills,” this phrase influenced Onyango’s perception of HIV at a young age — as the messaging around HIV in her country was mostly about death and fear. Growing up, she lost close family and friends to HIV and saw how cultural beliefs and practices exposed young women and girls to HIV. It wasn’t until she went to high school that Onyango learned about ways to protect against HIV, which helped reduce the fear she grew up with — and sparked an interest in HIV prevention.

After high school, she volunteered at a female sex worker-led organization that champions human and health rights of sex workers. Today, Onyango continues to encourage young women to take action to ensure they have a say in decisions about their health.

“My goal is to champion meaningful engagement of women and girls in HIV prevention and advocate for structural changes to improve the quality of life of women living with HIV.”

  • Elizabeth Onyango

Isaac Ogunkola | Nigeria

A background in public health has given Isaac Ogunkola deep insight into the world of infectious diseases, especially HIV. His passion for HIV advocacy became clear after volunteering to encourage harm reduction for people who use drugs and promote sexual and reproductive health and rights programming for homeless children, refugees and young people.

Having witnessed young people in his community die as a result of drug overdose and HIV, Ogunkola is committed to unifying public health, harm reduction and human rights. Through his peer education project, he engages young refugees in West Africa to lead HIV prevention programs in their communities.

“I don’t want to see death in any age group or population caused by HIV or drug overdose again.”

  • Isaac Ogunkola

Ashley Rose Murphy | Canada

Ashley Murphy was 7 years old when her adoptive parents told her she was living with HIV. By age 10, Murphy began to speak publicly about living with HIV, talking to young people around the world about the stigma around HIV and how to protect and advocate for themselves. She’s been a key voice for youth activists engaged in the HIV response in Canada ever since presenting at the U.N. General Assembly and the Global Fund, and even hosting a TED Talk.

Today, Murphy is an ambassador for several foundations committed to ending the AIDS epidemic through research, government-funded programs, global advocacy, prevention, testing and treatment options. Murphy remains an inspiration for young Canadians living with or affected by HIV.

Ashley Rose Murphy

“I want everyone to know that an HIV diagnosis does not have to be the end of the world. We can continue to live healthy and fulfilling lives, but it starts with educating yourself about your diagnosis and, most importantly, being your own advocate.”

  • Ashley Rose Murphy

Paul Mavesere Ndhlovu | Zimbabwe

Paul Ndhlovu has been using his voice to help young people living with and vulnerable to HIV in his native Zimbabwe for years. He’s produced a peer-led radio show as the creative radio champion for Zvandiri, an organization that “connects children and young people living with HIV with peer counselors to help assure health, happiness and hope.”

In his role, Ndhlovu — together with other adolescents and young people — has created a youth-friendly environment for people living with HIV to freely discuss challenges and issues in their own lives. The show explains to young people the importance of HIV prevention behaviors, the need for increased HIV testing, their sexual and reproductive rights, and available resources to help with mental health and well-being needs.

Paul Mavesere Ndhlovu

“The Zvandiri Radio Show is such an important platform. We’re providing an open forum for people living with HIV to freely come as themselves and talk about any challenges they may face.”

  • Paul Mavesere Ndhlovu

Stefano Regner | Philippines

Stefano Regner’s schedule is always busy, and as a physiotherapist and sexual health advocate, his work revolves around helping others.

As a trained HIV screener, counselor, and speaker, Regner is constantly on the move — traveling across the Philippines to help link people living with HIV to immediate care and empowering people when it comes to understanding safer sex. He’s also been a research assistant for one of the Philippines’ largest grassroots HIV test-and-treat centers.

And today, as both a medical student and a social media influencer, Regner provides educational resources for people living with HIV, using health campaigns and videos.

Stefano Regner

“Social media provides a new platform and method to translate and communicate important topics about health and increasing health literacy. I enjoy sharing key information with my followers, especially as it relates to sexual and reproductive health among at-risk populations in the Philippines.”

  • Stefano Regner

Kalisito Biaukula | Fiji

Kalisito Biaukula’s motivation to give a voice to the voiceless and speak up for those in need is evidenced by their work across their island nation of Fiji and surrounding regions. 

As an intersectional, queer, feminist activist and human rights defender, Biaukula has worked with various civil society organizations addressing intersecting human rights issues for people with diverse sexual orientations, gender identities and expressions, and sex characteristics, in Asia and the Pacific.

Biaukula is a major advocate for people living with and impacted by HIV, fighting to ensure they receive the proper care and government assistance, and calling for comprehensive sexuality education at all levels.

Kalisito Biaukula

“It’s important for young people, especially those living in the Asia-Pacific region, to take a leading role in decisions that affect our bodies. We must all use our voices to stand up for human rights and ensure all populations are receiving equal opportunities to access care.”

  • Kalisito Biaukula

Sara Thapa Magar | Nepal

From a young age, Sara Magar developed an interest in social issues related to women and children living with HIV. This passion eventually led her to advocate for the needs and rights of affected populations living in the Asia-Pacific region.

Magar has been a board member of the International Community of Women Living with HIV Asia & Pacific (ICWAP) and has also spoken publicly about the need to support women-led organizations. In her current role as president of the National Federation of Women Living with HIV and AIDS (NFWLHA) in Nepal, Magar works to tackle gender inequalities and end gender-based violence.

Sara Thapa Magar

“As youth leaders, we need to continue bringing these issues to the forefront and work to partner with the government and advocacy groups to address the challenges of women and children living with HIV.”

  • Sara Thapa Magar

The future is in good hands with these young leaders, advocates and activists, and we’re excited to continue to watch the impact they make on their local and global communities. To learn more about this youth-led collaboration, visit the IAS Youth Hub.

Health awareness

How you can help slow the threat of antimicrobial resistance

The growing burden of AMR is threatening the return to a world without effective antibiotics

October 30, 2023

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Mother and daughter washing hands

Before antibiotics were discovered in the 20th century, contracting an infection could be fatal. Their discovery was a turning point in human history, revolutionizing medicine and saving countless lives. However, the growing burden of antimicrobial resistance (AMR) is threatening the return to a world without effective antibiotics.

We all have a responsibility to address this threat, and it will take dedicated efforts from all sectors across health care, including patients, to make a difference.

Here are four groups that can play a role in helping slow the threat of AMR:

01.

Patients

Be vigilant in infection prevention efforts and always use antibiotics correctly

We each play an important role in slowing the threat of AMR— starting with preventing infections that require antibiotics in the first place. Washing hands, preparing food hygienically and keeping up to date with vaccinations are all measures to help avoid infections.

Another important action patients can take is using antibiotics only when they’re needed. Always follow health care providers’ (HCPs) directions and never share or take leftover antibiotics, which may not be needed and may cause resistance. If your HCP believes antibiotics are not the correct treatment to help your condition, ask about other options. Taking antibiotics when they’re not needed may advance AMR. Bottom line: It is important to follow the guidance that your medical team gives you for treatment.

Antimicrobial resistance pill

02.

Health care professionals

Be a source of antibiotic guidance

HCPs and medical systems need to preserve the effectiveness of antibiotics. It’s up to the health care providers to help ensure that the right treatment is given based on an accurate diagnosis. Hospitals should have a plan in place, with principles customized to their local needs, to guide the appropriate use of these medicines.

Nurse consulting patient

03.

Policymakers

Encourage antimicrobial innovation

We need new antibiotic options to stay ahead of the evolving bacteria. Governments can help. Incentive packages can provide a sustainable return on investment for the development of new antimicrobials. Encouraging innovation would allow companies to invest in the research and development needed. As a result, this would help provide health care professionals around the world with the tools they need to help patients fighting infections.

Signature

04.

Industry leaders

Invest in new developments

Finally, the participation of leading biopharmaceutical companies is crucial to addressing the growing threat of AMR.

For more than 100 years, Merck has played a significant role in the discovery and development of novel medicines and vaccines to combat infectious diseases. And, in an effort to affect widespread change, we’ve supported efforts around the world that aim to address AMR through surveillance initiatives, collaborating with hospitals to fund education and implement stewardship programs, and advocating for substantial policy changes.

Researcher in the lab

There is no single solution to the complex problem of AMR; it’s up to all of us to take collective action. We hope you’ll join our efforts and play your individual part to help ensure that patients have access to the antibiotics they need, now and in the future.

Health awareness

Understanding adult pneumonia: causes, symptoms and risk factors

Pneumonia is an infection of the lungs that can cause serious complications

October 27, 2023

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What is pneumonia?

Pneumonia is an infection of one or both lungs that can make it difficult to breathe and limit your ability to get sufficient oxygen. In 2019, pneumonia was the second leading cause of hospital admissions for U.S. adults.

What are the signs and symptoms of pneumonia?

Pneumonia can present differently in people based on a variety of factors, but common symptoms include:

Fever

Wheezing / difficulty breathing

Cough

Chills

Rapid breathing

Chest pains

Confusion

Loss of appetite

Which adults are most at risk?

Anyone can get pneumonia, but older adults are particularly at risk.

Medical conditions such as diabetes, chronic heart disease, COPD and HIV can also increase risks of pneumonia — even in younger adults.

illustration woman coughing

What can cause pneumonia?

There are two main types of pneumonia — viral pneumonia and bacterial pneumonia.

Bacterial pneumonia is often caused by the bacteria Streptococcus pneumoniae.

Pneumococcal pneumonia is one of the most common infections caused by this bacteria.

How does pneumonia spread?

Viral and bacterial pneumonias are contagious. People who are infected can spread the virus or the bacteria with respiratory droplets in the air when they cough, sneeze or talk. People can occasionally catch pneumonia by touching something that has the virus or bacteria on it and then touching their noses or mouths.

Ask your health care provider for more information.

Health awareness

Staying positive with pulmonary arterial hypertension

From struggling to breathe to advocating for others, one woman with PAH shares her story

October 24, 2023

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A decade ago, Nola Martin was having trouble breathing, and she was gaining weight. She assumed it was simple: She started to focus on improving her diet and getting more exercise, but she wasn’t seeing results.

“Little did I know the situation was a lot more serious than that,” she said.

Martin was diagnosed with pulmonary arterial hypertension (PAH) and scleroderma. PAH is a disease of high blood pressure in the lungs. Her PAH was associated with scleroderma, a connective tissue disease that can affect the skin, blood vessels and organs and can cause PAH.

“I had two illnesses, and I had no idea what they were from. How did I get them? I was hearing all these terms I’d never heard of before.”

  • Nola Martin

Finding the right care

Martin said that the confusion and complexity of having two chronic diseases made the beginning of her journey the most challenging. Through her experience with PAH, she said she learned that “you must find a facility that is familiar with your disease.” She recommends the Pulmonary Hypertension Association as a great place to start learning about PAH.

While she knows her PAH is progressive, she chooses to stay positive.

“What I learned about advocating for myself with PAH is that no one is going to fight as hard for me as I will,” said Martin. “I know my body. I know when something is different, but I also know that my doctors are not mind readers. If I don’t share with them what is going on, including the smallest details, they can’t give me the proper treatment I need.”

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Staying hopeful through connection

It’s important to Martin to connect with other PAH patients and educate people about the disease.

Since her diagnosis, she’s educated numerous people about PAH and scleroderma. She believes in the importance of raising awareness and telling her story. It’s sometimes hard for her to explain to people that even if she doesn’t appear sick, she may still be dealing with difficult symptoms.

“PAH has affected so much of my daily life — simple things like vacuuming, doing the laundry, taking a shower and going to the grocery store,” Martin said. “I encourage others to be understanding and avoid making assumptions about a person with PAH based on their outward appearance.”

She urges people to be supportive and listen when someone shares their story.

Health awareness

Acting early in cancer detection

Diagnosing cancer early, before it has spread, may potentially lead to better outcomes

October 12, 2023

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Time is important with a cancer diagnosis. People with cancer may have the opportunity for better outcomes when the disease is detected early. And with increases in routine cancer screening, more cancer cases can be diagnosed before the disease has spread to other parts of the body.

“We’ve seen incredible progress in the fight against cancer in recent decades, driven by advances in early detection and the availability of new treatment options,” said Dr. Gregory Lubiniecki, vice president, oncology clinical research. “This progress makes me optimistic for a future where cancer is detected and treated as early as possible, giving patients the greatest chance to live cancer-free. We can’t rest now — I’m hopeful that we will continue to build on what we’ve learned about helping people with earlier stages of disease.”

But important work remains to continue to improve care and diagnose cancer early.

What is early-stage cancer?

After someone is diagnosed with cancer, doctors will try to figure out how much cancer is in the body and if their disease has spread — this process is called staging, which can help guide treatment decisions. Different cancer stages have different treatments and possible outcomes, and they’re associated with different odds of recurrence. 

Early-stage is a term that can be used to describe cancer that’s early in its growth, before it has spread to other parts of the body. However, each person’s experience with cancer is unique, and what doctors may define as early-stage can vary by the type of cancer.

When cancer is diagnosed, the goals of treatments are to slow, stop and possibly eliminate tumor growth.

Treatment may be more likely to be successful if it’s started before the cancer has spread, when surgery is a potential option. However, even after surgery, there is a risk that the cancer may spread to other parts of the body. Additional treatment may help lower that risk. In certain instances, other treatment options can be used before surgery (neoadjuvant) to help to reduce the size of the tumor, and/or after surgery (adjuvant) to lower the chance of the cancer from potentially coming back.

Detecting and treating cancer early may help reduce the risk of recurrence and increase the potential for survival.

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