Monday, September 29, 2025

NEWS RELEASE: 2025 PILOT MBC SCREENING FOR THE RESCUE COMMUNITY

PRESS RELEASE

FOR IMMEDIATE RELEASE


Male Breast Cancer Global Alliance and BardDiagnostics Launch 2025 Pilot Screening Program for Rescue Servicemen











New York, NY – September 29, 2025 – The Male Breast Cancer Global Alliance (MBCGA), in partnership with BardDiagnostics, today announced the official launch of its 2025 Pilot Screening Program for Early Detection of Male Breast Cancer designed specifically for the rescue service community. This initiative marks a historic step in addressing the heightened cancer risks faced by firefighters, EMTs, law enforcement, and other frontline rescue personnel due to occupational exposures.

Dr. Robert L. Bard, internationally recognized diagnostic imaging specialist and early detection advocate, first joined the MBCGA in 2018. Since then, he has delivered private screenings for hundreds of men through his Second Opinion Scan and Fight Recurrence programs. Building upon this foundation, the new partnership transforms years of individual services into the first coordinated screening program officially dedicated to the rescue service sector.

Addressing a Critical Need

Studies and firsthand reports from across the U.S. have confirmed that rescue servicemen are disproportionately affected by male breast cancer and other cancers. This elevated risk stems from chronic exposures to toxins such as smoke, soot, fuel byproducts, and chemical agents encountered in the line of duty. In recent years, the MBCGA has tracked a growing number of cases among firefighters and first responders, highlighting the urgent need for proactive health measures.

“The rescue community faces daily risks most of us cannot imagine,” said Cheri Ambrose, Co-Founder and President of MBCGA. “Our alliance has seen firsthand the rising number of breast cancer cases linked to these exposures. This program is more than a pilot – it is a promise to provide the tools of early detection to those who protect us.”

The Screening Program

The 2025 pilot will begin in New York City, offering state-of-the-art ultrasound screening and diagnostic imaging conducted by BardDiagnostics. The program will provide:

  • Free baseline screenings for eligible rescue service members.

  • Access to advanced 3D Doppler ultrasound imaging, a non-invasive tool proven effective in detecting early signs of tumors.

  • Educational outreach on occupational cancer risks and the importance of routine monitoring.

  • Confidential follow-up consultations for men flagged for further evaluation.

Screenings are supported by donors of the AngioInstitute’s educational initiatives, ensuring participants also receive guidance on next steps, prevention strategies, and available clinical care pathways.


Leadership Perspective: “Launching this program is the culmination of years of advocacy and science,” said Dr. Robert Bard, Diagnostic Director of BardDiagnostics. “We’ve learned that occupational exposures play a direct role in breast cancer cases among men in the rescue service. Early detection is our strongest weapon. By providing rescue workers with imaging access now, we can save lives before disease progresses.”

A Public Service Partnership: The program reflects the MBCGA’s mission to expand awareness, improve survivorship, and fight the stigma surrounding male breast cancer. By partnering with BardDiagnostics, the Alliance ensures that frontline heroes are not only recognized for their sacrifices but also given proactive access to life-saving care.

The 2025 pilot will serve as a model for future national rollouts, with plans to expand screenings to additional firehouses, EMS stations, and police departments across the country.

Call to Action: The Male Breast Cancer Global Alliance invites public and private partners, civic leaders, and healthcare organizations to join this groundbreaking initiative. Together, we can build a national framework of protection and prevention for those who risk their lives daily.

For more information, or to schedule a screening, visit www.mbcglobalalliance.org or contact cheri@mbcglobalalliance.org.



About the Male Breast Cancer Global Alliance (MBCGA):

The MBCGA is a worldwide advocacy organization dedicated to raising awareness, providing education, and advancing research into male breast cancer. The Alliance unites survivors, clinicians, researchers, and advocates to dismantle stigma, accelerate early detection, and support men and families affected by this rare but devastating disease.

About BardDiagnostics:
Founded by Dr. Robert L. Bard, BardDiagnostics is a New York-based clinical practice specializing in advanced diagnostic imaging for cancer detection and recurrence monitoring. Known as a leader in ultrasound, 3D Doppler, and image-guided diagnostics, BardDiagnostics has pioneered early detection programs for high-risk groups, including first responders and military veterans.




Thursday, September 4, 2025

Male Breast Cancer Awareness in Tanzania: Insights from Dr. Godwin Nnko

 In a landmark dialogue bridging continents, the Male Breast Cancer Global Alliance (MBCGA) met with Dr. Godwin Nnko, a clinical oncologist serving at Iman Christian Medical Center in northern Tanzania. This conversation offered a candid view into the realities of treating cancer in resource-limited settings and underscored the need for global collaboration to improve awareness, reduce stigma, and expand access to life-saving technologies.


Tanzania’s Northern Cancer Center

Dr. Nnko outlined the vast responsibility of his center, which serves nearly 10 million people across northern Tanzania. Until recently, the facility offered chemotherapy and surgery but lacked local radiotherapy. Patients requiring radiation were forced to travel to Dar es Salaam, a costly and logistically difficult journey. Encouragingly, a radiotherapy unit has now been installed, with services expected to launch by October—an important step toward becoming a comprehensive cancer center.

Despite these advances, gaps remain. Tanzania, like much of East Africa, lacks access to advanced modalities such as CyberKnife radiosurgery or portable point-of-care ultrasound (POCUS) systems that could transform early detection and precision care.


Male Breast Cancer in Tanzania: A Hidden Burden

Though male breast cancer accounts for only 1% of cases globally, Dr. Nnko emphasized that it is far from absent in Tanzania. He personally diagnoses a new case approximately every three months, while managing several ongoing follow-ups monthly.

Unfortunately, late presentation is the rule rather than the exception. He shared the case of one man who, despite being diagnosed two years earlier, delayed treatment due to stigma and cultural myths. By the time he returned, the disease had spread to his lungs. Only after initiating tamoxifen did he experience significant tumor shrinkage.

This story reflects a larger pattern: deep-rooted beliefs that cancer is a curse or punishment often push patients toward faith healers, traditional remedies, or avoidance—resulting in advanced, less treatable disease.


The Role of Stigma and Cultural Beliefs

A recurring theme in Dr. Nnko’s account is the social stigma of male breast cancer. Patients often fear ridicule, denial, or misconceptions about masculinity. Cultural myths that cancer is “not a disease but a curse” reinforce delays in seeking medical help.

The MBCGA team noted parallels with stigma in the U.S., though in Tanzania the barriers are compounded by limited public education and healthcare access. For many, acceptance of medical treatment only comes after exhausting alternative routes, often when disease has already progressed.


Building Bridges: Research and Advocacy

Dr. Nnko’s interest in research and data collection led him to discover the MBCGA. His proposed study aims to analyze age distribution, geographic origins, and pathological profiles of male breast cancer patients in Tanzania. He stressed that data visibility is crucial: if male breast cancer is statistically reframed from “rare” to “more common than believed,” advocacy and funding will follow.

MBCGA leaders reinforced this by inviting Dr. Nnko to join their Medical Advisory Board, encouraging him to contribute both patient data and survivor stories. By connecting Tanzania’s cases with a global database, the Alliance hopes to amplify African voices in what has often been a Western-dominated conversation.


Technology and Access: A Shared Challenge

The discussion also explored innovative technologies:

  • CyberKnife – While not available anywhere in East or southern Sub-Saharan Africa, Dr. Nnko recognized its precision and reduced side effects. MBCGA suggested potential cross-border collaborations with centers in India.

  • POCUS (Portable Ultrasound) – Unlike large hospital machines, handheld ultrasound devices could bring screening into rural villages, where access to major hospitals is limited. Dr. Nnko was intrigued by the potential of such tools to democratize cancer detection.

Both sides acknowledged that regulatory approval remains a barrier, but advocacy for equitable access could make a long-term difference.


Education Tools: Self-Exam Cards

Another practical step discussed was the use of male breast self-examination cards developed by MBCGA. Dr. Nnko committed to translating these materials into Swahili, ensuring accessibility for patients and families across Tanzania. He envisioned distributing them in clinic waiting areas so both men and women could learn how to identify warning signs.

Such initiatives, he noted, could begin to chip away at stigma and cultural myths, encouraging earlier presentation.


Toward a Global Partnership

The meeting concluded with optimism. For Dr. Nnko, joining MBCGA represents both an opportunity and a responsibility: to elevate Tanzania’s hidden patient population onto the global stage and to draw attention to the needs of African oncology centers. For MBCGA, his inclusion strengthens their claim of being truly global and ensures that Africa is no longer absent from survivor databases and advocacy maps.


Conclusion

The conversation with Dr. Godwin Nnko highlighted a paradox: male breast cancer in Tanzania is not as rare as global statistics suggest, yet stigma, cultural barriers, and limited technology keep it in the shadows. By linking Tanzanian cases to global advocacy networks, translating educational materials, and exploring new technologies, MBCGA and Dr. Nnko have planted seeds for transformation.

Their collaboration affirms a vital truth: awareness is the first battlefield against cancer. When stories are told, data is collected, and survivors are counted, the invisible becomes visible—and the rare becomes urgent.

Wednesday, September 3, 2025

Psychiatry in the Cancer World: Dr. Barbara Bartlik’s Perspective

In nearly four decades of psychiatric practice, Dr. Barbara Bartlik has witnessed firsthand the profound emotional and psychological impact that cancer carries into her patients’ lives. Her long career has shown her the wide spectrum of human response: some individuals confront a diagnosis with resilience, adopting healthier lifestyles and even emerging stronger after treatment, while others become deeply burdened by anxiety, depression, or a pervasive sense of doom. For many, cancer is not just a physical illness but a transformative psychological challenge.

The Overlooked Emotional Dimension

Dr. Bartlik stresses that cancer care often remains narrowly focused on surgery, chemotherapy, and radiation, while patients’ emotional and mental health needs are sidelined. Yet psychiatric conditions are common in this population—ranging from depression and post-traumatic stress disorder to anxiety, anger, and profound sexual health concerns. “Someone needs to speak out for these patients,” she emphasizes, underscoring her commitment to ensuring that psychiatric support becomes an integral part of comprehensive oncology care.

Her affiliations with organizations such as the Male Breast Cancer Global Alliance and the American Breast Cancer Foundation reflect this mission. Through these partnerships, Dr. Bartlik works to spotlight the importance of emotional well-being, advocating for routine screening of psychiatric symptoms at every clinical encounter. She believes in embedding psychiatric services directly into cancer treatment programs—whether through in-person visits, support groups, or increasingly accessible virtual consultations.

The Hidden Burden of Cancer Therapies

One of Dr. Bartlik’s most urgent concerns involves the psychiatric and sexual side effects of cancer drugs and chemotherapies. These medications, while often lifesaving, can disrupt hormone balance, alter brain chemistry, and trigger an array of psychiatric symptoms. Patients may experience depression, fatigue, anxiety, insomnia, or mood instability. Chemotherapy regimens and hormone-blocking drugs can also profoundly impact sexual health, causing vaginal dryness and fragility in women or erectile dysfunction and diminished desire in men.

Beyond physical symptoms, these treatments frequently contribute to feelings of isolation, loss of intimacy, and strained relationships. In some cases, the psychiatric toll becomes so severe that patients consider discontinuing essential therapies. Dr. Bartlik stresses the importance of providing strategies, coping skills, and clinical interventions to help patients endure the challenges of long-term treatment while maintaining quality of life.

Beyond symptom management, Dr. Bartlik emphasizes the critical importance of addressing suicidality, which occurs at nearly twice the rate in cancer patients compared to the general population. By embedding psychiatric professionals into oncology settings, patients gain access not only to medical treatments but also to vital emotional lifelines—whether through therapeutic interventions, crisis hotlines, or support groups.

As a psychiatrist and sex therapist, Dr. Bartlik guides patients toward flexibility, coping strategies, and alternative approaches to intimacy, while also offering evidence-based tools such as natural lubricants, moisturizers, and structured therapy. Her dual focus on mental health and sexual well-being provides a holistic approach that many cancer survivors find indispensable.

A Call for Integration

Dr. Bartlik’s message is clear: psychiatric care must be recognized as a core component of cancer treatment. By systematically identifying and addressing emotional distress, the medical community can ensure that patients not only survive cancer but also retain dignity, quality of life, and hope. Her work stands as a reminder that the cancer journey is never solely medical—it is deeply human, requiring attention to mind, body, and spirit.

Championing Equity in Cancer Care: Spotlight on Erling Donnelly of Pfizer at the 2025 MBCGA Summit

Introduction

When the Male Breast Cancer Global Alliance (MBCGA) convenes its international medical summit this October 24–25, one of the most anticipated speakers will be Erling Donnelly, PhD, Vice President, US Breast Cancer Franchise & Portfolio Marketing Lead at Pfizer. Donnelly brings with him more than two decades of leadership in oncology, a career that has straddled research, development, and commercialization. His presence marks a milestone: for the first time, a senior voice from the pharmaceutical industry will address the MBCGA summit directly, underscoring both Pfizer’s and Donnelly’s commitment to advancing care for often-overlooked patient populations.





 

A Career Shaped by Innovation

Donnelly’s career at Pfizer began on the development side, where he led the creation of two lung cancer medicines before moving into the breast cancer space. There, he guided the landmark development of Ibrance (palbociclib), shepherding it from early clinical findings through U.S. approval and global adoption. That achievement alone would cement his reputation, but his contributions went further: Donnelly became a pioneer in leveraging real-world evidence (RWE) to expand drug indications.

He recalls how, in the mid-2010s, patient advocacy groups began raising urgent concerns: men with breast cancer were struggling to secure insurance coverage for Ibrance. Listening to those voices, Donnelly and his team mined existing claims data and built an evidence base showing the drug’s benefits for male patients. Working closely with the U.S. Food and Drug Administration, Pfizer secured regulatory approval to include men in Ibrance’s official indication—an outcome that has since become a new standard across Pfizer’s clinical trials.

Breaking the Barrier: Male Inclusion in Breast Cancer Trials

At this year’s summit, Donnelly will spotlight that breakthrough: how Pfizer shifted its own policies to ensure that all future breast cancer studies include men. “We didn’t see any biological nor equitable reason why males should be excluded from breast cancer studies,” he explained. Today, Pfizer’s trials also routinely include pre- and perimenopausal women—populations that were once neglected in research but whose inclusion is now the norm.

For Donnelly, this is not just a scientific correction but a matter of principle. Equity, he stresses, is fundamental to advancing oncology. By widening the scope of who participates in trials, companies like Pfizer can ensure that new therapies reflect the needs of the diverse patient populations living with cancer.

Global Partnerships and Real-World Impact

Donnelly emphasizes that progress in oncology depends on partnerships—across borders, institutions, and sectors. Pfizer collaborates with patient advocacy organizations to drive clinical trial participation, address real-world access challenges, and gather the data necessary to influence regulatory bodies and insurers.

“We know we need to partner again with advocacy groups, investigators in Europe, Asia, and Africa, and academic centers worldwide,” Donnelly said, reflecting on how new collaborations are uncovering unmet needs in previously undercounted regions such as Zambia, Uganda, and India.

This approach has already paid dividends. Pfizer’s strategy of pairing rigorous science with grassroots advocacy has enabled equitable access to breast cancer therapies and set a precedent for how pharmaceutical giants can work hand-in-hand with patient communities.


A Commitment to Screening and Early Diagnosis

While treatment innovation is at the heart of Donnelly’s portfolio, he is equally vocal about the need for early detection and screening. Pfizer has sponsored outreach initiatives across the U.S.—for example, in Texas, where they partnered with MD Anderson and local advocacy groups to counteract a post-COVID drop in cancer screenings. The company is now scaling such efforts to rural America, where disparities in access are especially stark.

But Donnelly stresses that screening is not enough. Patients must also undergo biomarker testing, which enables oncologists to match them with targeted therapies or clinical trials. “If patients know the oncogenic profile of their tumor, we can hopefully get them onto precision medicines that improve their chances of survival,” he said.

This vision aligns closely with the diagnostic community, and Donnelly has expressed enthusiasm for closer collaboration with radiologists and cancer imaging specialists such as Dr. Robert Bard, whose pioneering work in point-of-care ultrasound is already transforming detection of male breast cancer.


Engaging Rare and Underrepresented Cancers

The inclusion of men in breast cancer trials is part of a broader push by Pfizer to address rare and underrepresented cancers. Donnelly acknowledges that Pfizer has four main oncology pillars—breast, thoracic, genitourinary, and hematology—but he insists the company “follows the science.” That means exploring pediatric uses, partnering with academic institutions to run small but impactful studies, and expanding drugs into rare tumor types when evidence supports it.

Examples abound: drugs initially developed for large populations, such as lung cancer patients, have subsequently proven effective in rare pediatric tumors. Through investigator-sponsored research and collaboration with regulatory bodies, Pfizer ensures these niche populations are not left behind.

 

Reaching High-Risk Communities: Firefighters and Beyond

In the interview leading up to the summit, Donnelly was asked about cancer risks faced by firefighters—a community disproportionately affected by carcinogen exposure. While not yet tied to a specific Pfizer program, Donnelly acknowledged the importance of such partnerships and pointed to Pfizer’s extensive network of more than 300 advocacy group collaborations as a natural entry point. The company, he suggested, is open to aligning with occupational health advocates to ensure specialized populations receive the research attention and therapeutic access they deserve.

 

Why the Summit Matters

The MBCGA Summit is more than an academic gathering. It is a platform where survivors, clinicians, advocates, and industry leaders converge to reshape the landscape of male breast cancer. Donnelly’s participation is especially significant: for years, advocates have called for pharmaceutical companies to step forward and speak directly to both the medical community and patients. By doing so, Donnelly not only underscores Pfizer’s commitment but also validates the tireless work of advocates who pushed for male inclusion in research.

His talk will cover:

·        The story of Ibrance and how real-world evidence changed regulatory history.

·        Pfizer’s new standard of including men and underrepresented groups in all breast cancer studies.

·        The company’s outreach in screening, biomarker testing, and equitable access.

·        The expanding role of partnerships with diagnostics, advocacy, and global researchers.

·        How rare cancers and high-risk groups fit into Pfizer’s broader oncology vision.


Conclusion

As the MBCGA Medical Summit approaches, Erling Donnelly embodies the bridge between science, industry, and advocacy. His career illustrates how one leader within a pharmaceutical giant can drive systemic change—ensuring that men with breast cancer are no longer invisible in research, that underrepresented patients have a seat at the table, and that real-world data can reshape policy and access.

In spotlighting Donnelly, the summit also highlights the evolving role of pharmaceutical companies in the fight against cancer. No longer confined to laboratories and boardrooms, leaders like Donnelly are engaging directly with advocacy groups, diagnostic pioneers, and global communities. This October, his voice will remind the world that equity in cancer care is not an aspiration but a responsibility—and one that requires collaboration across every corner of the medical ecosystem.

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SPOTLIGHT REVIEW

By Dr. Robert L. Bard

As a cancer imaging specialist who has spent over four decades navigating the evolving landscape of oncology, I find Erling Donnelly’s presentation and Pfizer’s leadership both timely and inspiring. His reflections on the journey of Ibrance, and particularly the bold use of real-world evidence to secure male breast cancer inclusion, mark a historic step forward. For far too long, men with breast cancer were written off as statistical anomalies, denied equitable access to treatments simply because they did not fit the traditional mold of a clinical trial participant. Pfizer’s willingness to challenge that precedent is nothing short of groundbreaking.

What I applaud most is Donnelly’s insistence on equity—ensuring that all patients, from men with breast cancer to pre- and perimenopausal women, are represented in trials and have a fair chance at life-saving therapies. This reflects the same ethos that drives my own work in diagnostic imaging: uncovering what is hidden, shining a light on underserved populations, and ensuring no patient is left behind.

Equally vital is Pfizer’s recognition of the role that diagnostics, screening, and biomarker testing play in the cancer pathway. Treatment and detection must move hand in hand if we are to defeat cancer in all its forms.

The MBCGA Summit thrives when industry, clinicians, and advocates unite to share the latest solutions. By stepping into this space, Pfizer affirms what many of us have long believed: that progress in cancer care depends on collaboration at every level.

Tuesday, September 2, 2025

Dr. Fatima Cardoso: Advancing Global Collaboration in Breast Cancer Research

Dr. Fatima Cardoso, MD, MSc, FESMO is a senior consultant in medical oncology, internationally recognized for her leadership in breast cancer research, care, and advocacy. Board certified in medical oncology and internal medicine, she earned her medical degree at the University of Porto, with fellowships at the Jules Bordet Institute in Brussels and MD Anderson Cancer Center in Houston. She served as Assistant Professor at the Jules Bordet Institute and Scientific Director of the TRANSBIG research network before returning to Portugal in 2010 to establish and direct the first certified Breast Unit in the country at the Champalimaud Clinical Center.

Dr. Cardoso is founder and President of the Advanced Breast Cancer (ABC) Global Alliance and chair of the ABC International Consensus Guidelines Conference. Her research spans breast cancer biology, biomarkers, novel therapies, and clinical trials across phases I–IV. She is also Editor-in-Chief of The Breast Journal, associate editor of the European Journal of Cancer, and active in leading professional societies including ESMO, ASCO, AACR, and EORTC.

Honored with numerous international awards—including the Order of Santiago da Espada for Scientific Merit—she has authored over 400 publications and remains a driving force for innovation, equity, and global collaboration in oncology.

Dr. Fatima Cardoso has long stood at the forefront of international oncology, dedicating her career to addressing the challenges of both female and male breast cancer. As an oncologist and global advocate, she balances clinical leadership with a deep commitment to collaborative research, ensuring that even the rarest cancers receive the scientific attention and resources they deserve.


A GLOBAL PERSPECTIVE ON ACCESS TO CARE

Early in the conversation, Dr. Cardoso highlighted the work that the ABC Global Alliance is doing with the Max Foundation (Humanitarian PACT for Advanced Breast Cancer) and other partners such as WHO and the ATOM coalition (Access to Oncology Medicines). This project aims at providing low income countries with access to crucial treatments for advanced breast cancer and, simultaneously, contributes to capacity building and resource strengthening to improve cancer care. ATOM’s mission is straightforward yet vital: to improve access to cancer medicines in low- and middle-income countries at a fraction of the standard cost. She explained that while ATOM focuses on lowering the price barriers to treatment, it does not yet address other essential aspects of care, such as access to radiation therapy. This gap underscores the broader reality that oncology requires comprehensive solutions—drugs alone are not enough to save lives when infrastructure for diagnostics and radiation is lacking.

Her remarks reflected her internationalist vision: partnerships across organizations, industries, and borders are essential. For Cardoso, cancer care equity is a pressing humanitarian issue, and her work consistently seeks to bridge divides between high-resource and under-resourced nations.

DIAGNOSTICS AND THE MALE BREAST CANCER DEBATEDr. Cardoso also spoke about the diagnostic standards for male breast cancer, a rare disease that has historically been underserved in both awareness and research. She emphasized that current ASCO guidelines recommend using the same diagnostic protocols applied to female patients—principally mammography and ultrasound, with MRI reserved for specific cases. However, she also acknowledged the limitations of population-based screening for such a rare condition, noting that education and awareness remain far more impactful for early detection.

Her perspective struck a note of caution: while innovation is essential, the medical community must remain vigilant against overdiagnosis. Drawing lessons from decades of breast cancer screening in women, she warned that detecting cancers too early—or diagnosing in situ carcinomas unlikely to become life-threatening—can lead to unnecessary treatment and harm. She urged researchers and clinicians working on male breast cancer not to repeat these missteps, stressing the importance of balancing vigilance with restraint.

One of Dr. Cardoso’s major commitments has been the International Male Breast Cancer Program, a research initiative developed through unprecedented global collaboration. Run under the umbrella of  the Breast International Group (BIG) in Europe and the National Clinical Trials Network (NCTN) in the US North American intergroup and coordinated by  European Organisation for Research and Treatment of Cancer (EORTC) and the Translational Breast Cancer Research Consortium (TBCRC), the program has produced the largest body of research ever assembled on male breast cancer.

The program’s structure included three pillars:

  1. Retrospective studies and publications that laid a foundation of clinical knowledge.
  2. An international registry that successfully enrolled over 500 men—far surpassing the initial target of 200 patients in two years—demonstrating the feasibility of large-scale research in this rare cancer.
  3. A prospective clinical trial, intended to test targeted therapies, particularly drugs addressing the androgen receptor pathway.

Unfortunately, funding constraints have placed the program at risk. Cardoso noted that pharmaceutical companies, ultimately withdrew support from the most advanced therapeutic trial. Despite the proven ability to gather sufficient patient numbers, industry reluctance to invest in rare diseases has left the program struggling for survival.

She described the funding crisis faced by international collaborations, pointing to the restrictive legal environment in the United States that increasingly limits the flow of donations to non-U.S. research partners. Such restrictions, she warned, could jeopardize multinational studies that depend on pooling data across borders to achieve meaningful results.

Cardoso also underscored the heavy reliance on industry funding in oncology research, acknowledging the conflicts and limitations that arise when commercial interests dictate which studies receive support. For diseases with little market potential, such as male breast cancer, the result is often stagnation. Her appeal is clear: the research community must diversify funding sources, cultivate individual donors, and build coalitions to ensure that scientific progress is not stifled by market forces

ADVOCACY BEYOND THE LABORATORYBeyond her scientific work, Dr. Cardoso is also President of the Advanced Breast Cancer (ABC) Global Alliance, which focuses on metastatic breast cancer worldwide. This role reflects her capacity to lead not only clinical trials and registries but also advocacy and policy-oriented initiatives.

A Personal World Tied to Her Work: Amid discussions of policy, data, and funding, Dr. Cardoso shared glimpses of her personal roots. Though born in Africa, she regards Porto, Portugal, as her true home—the city where she trained and became a physician. Today, she is based in Lisbon, but her heart remains closely tied to Porto. This grounding in both international and local contexts reflects her identity as a physician who thinks globally while remaining deeply connected to her origins.

A Champion for Patients Often Overlooked: Dr. Fatima Cardoso’s professional life embodies the tension between rare disease advocacy and the practicalities of modern oncology. Her efforts reveal a doctor’s dual role as both healer and activist: ensuring that patients receive the best evidence-based care today while also fighting to secure the research and funding needed to transform treatment tomorrow.

Whether advancing metastatic breast cancer advocacy through the ABC Global Alliance, or sustaining the fragile yet groundbreaking International Male Breast Cancer Program, Dr. Cardoso continues to challenge the systemic barriers that leave vulnerable patients underserved.

Her message is both sobering and inspiring. The world has the tools, knowledge, and networks to make meaningful progress. What remains is the collective will—across governments, industries, and advocacy groups—to ensure that no patient, whether a woman with metastatic disease or a man with breast cancer, is left behind.

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A Tireless Heart for Change

In the fight against breast cancer—whether in women or men—few leaders embody the courage, vision, and unwavering heart for advocacy as profoundly as Dr. Fatima Cardoso. From the first time I met her, it was clear that she carried more than the weight of scientific knowledge; she carried the voices of patients, families, and underserved communities who too often remain unheard.

Dr. Cardoso has never been content to limit her work to the laboratory or the lecture hall. She understands that science without advocacy is only half the battle. With courage and clarity, she has repeatedly stepped into arenas where policies are written, funding is debated, and inequities threaten to silence progress. She has spoken for patients in low- and middle-income countries who lack access to medicines. She has fought for international collaboration in rare diseases like male breast cancer, even when industry and politics put obstacles in her path. And she has done it all with grace, persistence, and the quiet but undeniable power of conviction.

What sets Dr. Cardoso apart is not only her brilliance as a clinician and researcher, but her tireless heart. She has built bridges across continents, uniting networks of physicians and advocates to pursue solutions that one country alone could never achieve. She has reminded us, time and again, that behind every statistic is a life worth saving—and that our responsibility is to push forward until better treatments, fairer access, and greater awareness are realities for all.

As President of the ABC Global Alliance and as a leader of the International Male Breast Cancer Program, she has given form to hope in spaces where many once felt forgotten. She has proven that advocacy from the clinical stage is not only possible, but essential.

To me, and to the countless others inspired by her, Dr. Cardoso represents the rare blend of scientific excellence and human compassion that defines true leadership. Her courage fuels our mission. Her vision lights our path. And her heart ensures that no patient—woman or man—will be left behind.

Cheri Ambrose, Male Breast Cancer Global Alliance

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Elevating Oncology Through Vision

By Dr. Robert L. Bard (Oncoradiology, NYC)

In more than forty years of work in cancer diagnostics, I have witnessed an extraordinary evolution in our field. From the early days of limited imaging options to today’s sophisticated landscape of precision diagnostics and targeted therapies, progress has always depended on those rare individuals who combine clinical excellence with visionary leadership. Dr. Fatima Cardoso is one of those rare leaders.

What distinguishes Dr. Cardoso is her ability to stand at the intersection of science, patient care, and international collaboration. She understands that breast cancer—whether in men or women—cannot be addressed in silos. It requires a network of minds, data, and resources spanning across borders. Her work with the Advanced Breast Cancer (ABC) Global Alliance and the International Male Breast Cancer Program exemplifies this truth. These initiatives have provided the kind of global infrastructure that oncology desperately needs if we are to make meaningful advances against rare and neglected cancers.

As a diagnostician, I know that every patient represents both an individual battle and a piece of a larger puzzle. Dr. Cardoso has repeatedly reminded the medical community that research must serve both ends: it must offer better solutions to the patient in front of us, while also building the evidence and systems that will guide the care of thousands more. Her insistence on equity and accessibility speaks directly to the ethical responsibilities we face as physicians.

I have also seen the challenges: funding gaps, industry hesitation to invest in rare cancers, and policy frameworks that too often slow innovation rather than enable it. Yet Dr. Cardoso continues to push forward. Her persistence reflects the kind of resilience our profession requires if we are to move beyond incremental progress and toward transformative change.

The medical community benefits immeasurably from her leadership. Her vision demonstrates what oncology should strive to be: rigorous in science, uncompromising in compassion, and committed to international cooperation. As someone who has spent decades in this field, I can say without hesitation that we need more voices like Dr. Cardoso’s—and more of her kind of care—on the global stage.

Robert L. Bard, MD, Diagnostic Imaging Specialist

Monday, September 1, 2025

Charlotte Bayala: The Voice of Caregivers and Champion of Cancer Awareness


Charlotte Bayala has become a powerful advocate in the cancer community, not through professional obligation, but through lived experience and relentless compassion. As the wife of a thyroid cancer survivor, she understands the unrelenting weight of caregiving—the fear, uncertainty, and exhaustion—and she has transformed that journey into a mission that now reaches thousands through her work, her podcast, and her advocacy with the Male Breast Cancer Global Alliance.

A Personal Journey into Caregiving


Charlotte’s story begins over a decade ago, when her husband was diagnosed with thyroid cancer. At the time, she was a yoga and meditation teacher who believed she had mastered balance and calm. That illusion shattered the moment she heard the words that changed their lives. “Everything fell apart,” she recalled. The diagnosis threw her into a storm of emotions—fear, anger, resentment, and exhaustion. Even with the tools of mindfulness at her disposal, she struggled to cope. That realization haunted her: if I fell apart, what about caregivers who don’t have these tools?

That question became the foundation of her life’s work. She would not only walk alongside her husband as his caregiver, but she would also dedicate herself to equipping other caregivers with the skills, support, and community they desperately need.

 

Bari Fleischer (artist) - Brushes with Cancer

The Cancer Caregiver Podcast: From this personal crucible, Charlotte launched The Cancer Caregiver Podcast. Over five years and nearly 300 episodes later, it has become a unique resource for families and patients alike. The podcast is intimate and practical, blending storytelling with actionable coping strategies drawn from her background in yoga, meditation, and mindfulness.

Each episode delivers what caregivers need most: validation and tools. Charlotte normalizes the often unspoken struggles—resentment, burnout, fear of the unknown—and provides simple practices to help restore balance. Importantly, she has designed her show to fit the realities of caregiving. Recognizing that caregivers rarely have an hour to spare, she condensed episodes into short, 15-minute segments. That decision increased her subscribers by 300%, underscoring how deeply her work resonates.

Listeners describe the podcast as “free therapy.” For many, Charlotte’s voice is the reminder they are not alone. As she explains: “I always hope that my voice and my existence in the caregiving world helps at least one person think, it’s not just me. I’m not alone. I matter.


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Connection with the Male Breast Cancer Global Alliance: Charlotte’s advocacy has extended beyond her own podcast. Her commitment to amplifying unheard voices brought her into partnership with the Male Breast Cancer Global Alliance (MBCGA). She first connected with the organization after producing episodes featuring male breast cancer survivors—a group whose experiences are often overlooked due to the rarity and stigma surrounding their diagnosis.

Through those interviews, Charlotte recognized the isolation men face when navigating a disease largely perceived as female. She also saw parallels with the invisibility of caregivers. In reaching out to MBCGA founder Cheri Ambrose, she found kindred spirits who shared her passion for equity, visibility, and support.

Today, Charlotte is not just a collaborator but an advocate within the Alliance’s global mission. She will be a featured speaker at the 2025 Fall Medical Summit, where her session, Before the Results: How to Stay Grounded When You Can’t Know What’s Coming, will help patients and families navigate the paralyzing anxiety of scan results and follow-up visits.

Her message is simple but profound: while no one can control outcomes, everyone can learn to pause, reconnect with loved ones, and reclaim small moments of joy even in uncertainty.

 


Advocacy through Human Connection:
 
At the heart of Charlotte’s work is her belief in human connection. Technology and online groups have value, she notes, but nothing replaces hearing another person’s voice or looking into the eyes of someone who understands.

“Being a caregiver is lonely in itself,” she says. “Having a role in life that automatically makes you feel alone makes it harder to enjoy life when you don’t have a community.” Her work strives to dissolve that isolation by creating spaces where caregivers can share, vent, and validate one another without judgment. That conviction fuels not only her podcast but her willingness to collaborate with organizations like MBCGA, where she is seen as both a mentor and a change-maker.

 

A Reluctant Advocate, a Relentless Voice: Despite her clarity of purpose, Charlotte remains strikingly humble. She jokes about struggling with self-promotion, cringing at the idea of asking for donations or “sustainability.” Yet her peers insist she is exactly the kind of leader the cancer community needs.

Her colleagues encouraged her to embrace her role as a change-maker, reminding her that her voice saves lives. Without sustainability, her platform—and the lifeline it provides—could disappear. Charlotte has begun to explore creative ways to keep her podcast thriving, from digital caregiver handbooks to corporate wellness programs.

What sets her apart is not just her authenticity but her refusal to commercialize suffering. She wants her resources to remain accessible for all caregivers, particularly because so few supports exist for them. That balance—valuing her work without compromising accessibility—reflects her integrity.


Advocacy in Action: The October Summit - Charlotte’s upcoming presentation at the 2025 Fall Medical Summit is a natural extension of her advocacy. The virtual event, hosted by MBCGA and founder Cheri Ambrose, will convene global leaders, clinicians, and advocates to advance cancer awareness and solutions.

For Charlotte, the conference is another opportunity to bridge the gap between clinical care and the lived realities of patients and families. She will speak not as a researcher or physician, but as a wife, caregiver, and advocate who knows the terrain of uncertainty firsthand.

Her voice brings balance to the scientific discussions, reminding all participants that cancer care is not only about protocols and treatments—it is also about humanity, presence, and love.

Carrying the Stress with Grace: When asked about her husband today, Charlotte acknowledges the ongoing challenges. He is on targeted therapy, which carries side effects, but he is alive and living—a reality they both treasure. Her caregiving continues, now informed by years of reflection and community-building.

Her perspective is one of resilience, not denial. “We can’t lose sight of the why,” she says. “We are in this journey together with people. It’s about being able to enjoy the time we have instead of being consumed by the what-ifs.”

 

Conclusion: A Change-Maker in Caregiving

Charlotte Bayala embodies the power of turning pain into purpose. Her work as a caregiver, podcaster, and advocate demonstrates how personal struggle can blossom into collective strength. Through nearly 300 podcast episodes, her voice has reached caregivers who might otherwise feel invisible. Through her alliance with the Male Breast Cancer Global Alliance, she amplifies awareness and fights for greater equity in cancer care.

 She does this not for recognition, but because she knows what it feels like to sit in the quiet after a diagnosis, to wonder how to hold everything together, and to long for someone who understands.

In giving caregivers that understanding, Charlotte has become more than a supporter—she has become a symbol of resilience, advocacy, and hope. Her story reminds us that behind every patient is a caregiver, and behind every caregiver is a need for community. In lifting that truth into the light, Charlotte Bayala is not just speaking—she is changing the conversation on what it means to fight cancer together.

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A Voice That Heals Beyond Medicine

By Dr. Leslie Valle Montoya

In every episode of Charlotte Bayala's podcast, what strikes me most is her deep authenticity. She does not speak as someone removed from the struggle of cancer care—she speaks as a wife, a caregiver, and a relentless advocate who has lived it. That authenticity is powerful medicine in itself.

As a physician working in integrative and biological medicine, I often emphasize that healing extends beyond the physical body. It includes emotional resilience, spiritual grounding, and the ability to feel connected in the midst of hardship. Charlotte embodies this truth. Through her podcast, The Cancer Caregiver, she has created a sanctuary where caregivers can find validation, strategies, and above all, the reassurance that they are not alone. Nearly 300 episodes later, her voice has become a lifeline for thousands.

What inspires me most is her vision of caregiving as both a personal responsibility and a collective mission. She reminds us that the weight of cancer is carried not just by the patient, but by the entire family. By teaching practical mindfulness tools and fostering honest conversations, Charlotte helps transform fear and isolation into moments of presence, love, and even joy.

Her alignment with the Male Breast Cancer Global Alliance highlights another dimension of her leadership: the courage to advocate for those whose voices are too often overlooked. She has helped bring forward the stories of male survivors, challenging stigma while supporting the families who walk alongside them.

Charlotte Bayala is more than a caregiver—she is a connector, a guide, and a change-maker. Her work reinforces what we in integrative medicine know well: true healing requires human connection, compassion, and the courage to share our stories. She gives that gift daily, and the cancer community is stronger for it.

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From Caregiver to Global Advocate

By Dr. Robert L. Bard

In my decades of clinical practice, I have met countless families whose lives were upended by cancer. What distinguishes Charlotte Bayala’s journey is not only her role as a devoted wife and caregiver, but her decision to transform that experience into a public mission. She took the private hardships of caregiving and converted them into a platform of education, advocacy, and support. That transformation—from wife and caregiver to outspoken advocate and podcaster—is what moves the needle in awareness.

Her story demonstrates the vital importance of publishing and outreach. Each podcast episode, social media post, and public talk represents more than just content—it is testimony, knowledge, and hope offered to a community that desperately needs it. Caregivers often suffer in silence, feeling invisible. Charlotte gives them a voice, and by doing so, she strengthens the entire cancer ecosystem.

In today’s world, social media is the new town square. It is where people connect, share, and learn. Charlotte has harnessed these tools to bring forward the real conversations about caregiving, male breast cancer, and family resilience. By publishing her stories consistently, she has built a bridge between clinical professionals and everyday families, ensuring that information and empathy reach far beyond hospital walls.

For organizations like the Male Breast Cancer Global Alliance, her work is indispensable. Outreach is not optional—it is survival. Every caregiver who feels seen, every family who learns they are not alone, is another step toward reducing the stigma, isolation, and fear that surround cancer.

Charlotte reminds us that advocacy is not reserved for institutions; it begins with one voice willing to speak. By publishing her truth and leveraging the connective power of media, she has turned personal struggle into global impact.

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