In this episode Erica & Stefan talk to Lauren Walrath about the Japanese concept of Wa (和) in patient access and care. Wa focuses on group harmony over individual expression, maintaining smooth relationships, consensus-based decision-making, emphasis on social order, and mutual obligation.

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In this episode of Patient to Purpose, Erica & Stefan tackle the alarming resurgence of measles and the declining vaccination rates threatening public health in the U.S., UK, and beyond. We explore how healthcare is inherently political and why wealthy nations are beginning to lose our long-held “measles elimination” status. Beyond the political debate, we discuss the severe, life-altering impacts of the disease, from deafness to blindness, and why collective herd immunity remains our strongest defense.

Post production edit: California, New York, and other states have joined the World Health Organization's Global Outbreak Alert & Response Network (GOARN)

Resources:

American Academy of Pediatrics

Pan American Health Organization

American Medical Association

World Health Organization

European Centre for Disease Prevention & Control

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On this episode Erica & Stefan hear from access and engagement expert Keri McDonough, MA to unpack what “access” really means beyond cost. Drawing on powerful patient stories and more than 20 years of experience, Keri explores the hidden barriers to clinical trials, the importance of peer connection, and why embedding patient insights across the healthcare lifecycle is essential. The conversation highlights how sustained relationships, better communication, and truly patient-centered design can transform healthcare from the inside out.

Resources:

Equitable Access to Clinical Trials Project

National Health Council: Capturing & Including the Patient Voice

Multi-Regional Clinical Trials Center Health Literacy in Clinical Research Glossary

Patient Focused Medicines Development

Society for Public Health Information-Health Literacy

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In our premiere episode, hosts Stefan Walzer, Ph.D. and Erica Bersin, BCPA dive into the frustrating, confusing, and often invisible barriers patients face when trying to access the treatments they need. Erica shares her personal journey with multiple sclerosis, from being diagnosed in Switzerland to managing care in the U.S. system, and reveals how drastically access can differ depending on where you live.

National MS Society (U.S.)

MS Views & News (U.S.)

European Multiple Sclerosis Program (Europe)

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#PatientEngagement #PatientAdvocacy #MedicalAdvocacy #Pharma #HealthcareInnovation #HealthcareDecisions