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The practice of medicine has never been easy. Years of demanding education. Long hours. Weekend call duty. Stress-laden procedures. Burgeoning regulatory requirements. Even a worldwide healthcare crisis. How is a physician to cope? This indispensable anthology of essential essays offers practical solutions. 'Physician Well-Being During Sustained Crisis' features over twenty authors, including active physician executives, counselors, and healthcare chaplains, addressing three core concepts related to the well-being of physicians.

Eugene A. Woods, CEO of Advocate Health, one of the largest non-profit health systems in the nation, provides a riveting behind-the-scenes look at healthcare in the United States. By sharing his insights from three decades in healthcare administration, as well as his personal journey, listeners gain a deeper understanding of the challenges facing healthcare systems and the impact on all of us. Woods sheds light on the inequities our communities face and presents actionable prescriptions to create a more equitable, just and accessible healthcare system.

This timely book offers a balanced and thoughtful review of the current mental health emergency and its impact upon and among medical professionals, supported by the best available evidence and illustrated through real-life cases. Recognizing the increasing stressors in the role including the impact of the environment in which doctors work, the book examines some of the key emotional drivers for this unhappiness among doctors at work—shame, stigma, suffering, and sacrifice—and offers practical steps to emotional and physical recovery.

Addressing nurse burnout is essential to enhance the nursing workforce's overall well-being and provide patients with the highest level of care possible. Having a reliable resource to provide assistance, guidance, and support can go a long way in mitigating burnout and ensuring that nurses feel supported in their roles. So, let's prioritize nurse burnout and strive to make nursing a profession that nurtures the mind, body, and soul of all those who dedicate their lives to helping others.

Wenn Metin nach Feierabend mal wieder an seine Kühlschranktür klopft, weiß er, dass an diesem Tag sehr viele Patient*innen nach ihm gerufen haben – Er ist Krankenpfleger durch und durch, und ohne diese Leidenschaft geht das in seinen Augen auch gar nicht. Denn das kaputtgesparte Gesundheitssystem, der stressige Klinikalltag und die mangelnde Wertschätzung machen seinen Job zu einer Herausforderung. Doch die Patient*innen stehen immer an erster Stelle und das Team hält zusammen.

La historia de cómo el trabajo de un pequeño grupo de personas creció hasta alcanzar el tamaño de su vocación: garantizar que el cuidado de la salud sea un derecho, no un privilegio.

Understanding the inevitable changes that technology has brought—and will continue to bring—to the healthcare industry will help all of us take more control over our well-being, prevent chronic diseases, and pursue care at the right time, at the right place, in the right way, from the right people.

Psychische Gesundheit ist politisch. In Ländern wie Deutschland und Österreich können wir uns auf eine medizinische Notversorgung verlassen. Gibt es einen Unfall, wird ein Rettungswagen gerufen, Patient*innen werden in ein Krankenhaus gebracht und schnellstmöglich versorgt. Selbstverständlich, oder? Immerhin wäre es für uns unvorstellbar, mit einem Knochenbruch wieder nach Hause geschickt zu werden, einschließlich einer Wartefrist von sechs Wochen. Bis ein Behandlungsplatz zur Verfügung steht. In etwa so gestaltet sich jedoch die Situation im Bereich der psychischen Erkrankungen.

Filled with firsthand insights and stories from the frontlines of healthcare, as well as innovative solutions, Care After Covid shows all stakeholders in the healthcare ecosystem exactly what needs to change and, more importantly, how to do it.

Myth: People from marginalized backgrounds have poorer health outcomes because of poor decision-making. Through extensive research and interviews, Health Care of a Thousand Slights: Connecting Legacy to Access to Healthcare debunks this myth, demonstrating that the historical legacy of discriminatory policies and culture has had an enduring impact on healthcare access and outcomes among marginalized communities.

There's an unspoken assumption when we go to see a doctor: the doctor knows our medical story and is making decisions based on that story. But reality often falls short. Medical records vanish when we switch doctors. Critical details of life-saving treatment plans get lost in muddled electronic charts. The doctors we see change according to specialty, hospital shifts, or an insurer's whims. In this gripping narrative from medicine's front lines, Ilana Yurkiewicz reveals how a system that doesn't talk to itself puts insupportable burdens on physicians, patients, and caregivers.

The American health-care system is failing us. It is a frustratingly complex, opaque, and unaffordable system that results in suboptimal care and a deterioration of the welfare of the majority of American families. The experience of the past few decades and the recent ravaging pandemic has shown us that doing more of the same is not going to deliver us from this dilemma. But there is hope. There is a way to create a more accessible, consumer-friendly, safer, and affordable system of care for all of us.

In an era defined by rapid technological advancements, Artificial Intelligence (AI) has emerged as a groundbreaking force with the potential to reshape every facet of human existence. Among its most promising applications, the integration of AI in the medical field stands out as a transformative and revolutionary endeavor. AI's ability to process vast amounts of data, learn from patterns, and make intelligent decisions has opened up unprecedented possibilities in the domain of healthcare.

Dr. Caleb Slater has a revolutionarily new approach to treating patients. With a slightly different view of the human body, he has been able to achieve groundbreaking results for a wide variety of symptoms, including pain, nausea, dizziness, abdominal discomfort, headaches, and breathing difficulties to name a few. If you have found the current treatments lacking and only managing your symptoms rather than providing a cure, then this book is for you.

Operating an ALF can be rewarding. The services you provide for people aged 62+ and their families help people live their best lives. You also contribute to the community and society at large by maintaining the health and well-being of a contributing member.

A Healthy Society offers a new approach to politics–and a new approach to building a healthier world. Dr. Meili argues that health delivery too often focuses on treatment of immediate causes and ignores fundamental conditions that lead to poor health such as income, education, employment, housing, and environment.

Health care as it stands today needs to be re-imagined. Redefining the Boundaries of Medicine by Paul Cerrato and Dr. John Halamka challenges the profession to renegotiate its priorities and address the fact that it’s become timid and reluctant to explore new care delivery models. The guiding premise of this book is that rethinking and reimagining the way medicine is practiced in the 21st century will improve health outcomes, and that technology is central to this transformation.

Dr. Peter Patterson understands that using antibiotics “just in case” is ingrained in our culture. Everyone, from health care professionals to patients and their advocates, shares the blame—but we cannot afford to let the practice continue. Becoming Good Stewards of Antibiotics is a call to action to restore and preserve antibiotic effectiveness.

This essential book helps demystify Medicare, offering listeners practical advice on how to optimize coverage and minimize costs. It offers a comprehensive comparison of Medicare Parts A & B, as well as alternative options, such as Medicare Advantage and Prescription Drug Plans. The book also offers common and uncommon questions, answered in an easy-to-follow FAQ format, practical checklists, cheat sheets, and templates to help organize and plan your Medicare journey. In addition, the book includes an exclusive Medicare Decoder that breaks down complex terminology into plain language.

Then one day at clinic, she noticed patients trading stories in the waiting room, sharing not just valuable advice, but empathy and encouragement. That was the genesis of the support group, a safe place where people dealing with cancer and its aftermath could talk openly about what they were going through. It was a lightbulb experience for Dr. Blackmon. Once she saw the difference a committed ally could make in a patient’s long-term survivorship, Dr. Blackmon sought to extend the principles of support to her colleagues.