Lisa Salberg and Dr. Marty Maron break down new research reshaping how HCM is treated, from long-standing beta blockers to emerging targeted therapies. They also walk through arrhythmia risks, monitoring, and prevention—giving patients a clearer roadmap for managing symptoms and long-term outcomes in a rapidly changing care landscape.

Lisa Salberg sits down with Senator Anthony Bucco to discuss why Heart Month and knowing your family heart health history can save lives. They explore New Jersey’s leadership in cardiac screening laws, the importance of early detection for HCM, and ongoing efforts to improve insurance access and patient protections.

This conversation was recorded Feb. 20, 2026.

Lisa Salberg and Dr. Marty Maron reflect on Heart Month, HCM Awareness Day, and the rapid evolution of treatment options. They discuss new therapies, clinical trials, patient empowerment, and why clarity and lifelong care remain essential in the journey with hypertrophic cardiomyopathy.

This conversation was recorded Feb. 20, 2026.

Lisa Salberg and Dr. Marty Maron reflect on Heart Month, HCM Awareness Day, and the rapid evolution of treatment options. They discuss new therapies, clinical trials, patient empowerment, and why clarity and lifelong care remain essential in the journey with hypertrophic cardiomyopathy.

This conversation was recorded Feb. 13, 2026

Host Lisa Salberg talks with author Dr. Matt Martinez about living with hypertrophic cardiomyopathy while balancing family, career, and advocacy. The conversation explores personal perspective, patient empowerment, and how sharing lived experience can help others better understand and navigate an HCM diagnosis.

This conversation was recorded Feb. 6, 2026.

Host Lisa Salberg talks with author and educator Dr. Mary Massey about the loss of her son to sudden cardiac arrest and the book she wrote to honor his life and help other families understand hypertrophic cardiomyopathy. Their conversation explores grief, genetic risk, ongoing screening, and how sharing one story can help protect others.

This conversation was recorded Feb. 2, 2026.

Host Lisa Salberg is joined by Minnesota State Senator Carla Nelson to discuss her personal journey with hypertrophic cardiomyopathy and how that experience shaped her advocacy for cardiac screening and education. They explore the role of legislation, family heart health history, and public awareness in helping identify HCM earlier and protecting future generations.

This conversation was recorded Feb. 2, 2026

Host Lisa Salberg is joined by Dr. Milind Desai of Cleveland Clinic to discuss new research challenging how hypertrophic cardiomyopathy patients define “asymptomatic.” They break down what long-term data and stress testing reveal about hidden symptoms, why follow-up matters even when you feel well, and how new therapies are reshaping care during a rapidly evolving era in HCM treatment.

This conversation was recorded Jan. 30, 2026.

In this expert conversation, Tales From the Heart Host Lisa Salberg is joined by Dr. Alex de Feria to help patients think clearly about managing hypertrophic cardiomyopathy year by year. They break down testing, symptoms that hide in plain sight, new therapies, and how patients can advocate for consistent, proactive care. Practical, timely guidance as Heart Month approaches.

This conversation was recorded Jan. 22, 2026

In this special edition of Tales From the Heart, guest Debra Rafson takes the host seat and turns the tables on Lisa Salberg. The conversation pulls back the curtain on Lisa’s personal journey, the moments that shaped her advocacy, and how lived experience continues to drive the mission and direction of the HCMA.

This conversation was recorded Jan. 16, 2026.