In today's world, context is clarity, our podcast series highlights advocacy, education, industry, and scientific advancements in the space bringing congenital cytomegalovirus (CMV) to the forefront of the conversation.


Megan Nix

Join the National CMV team as they speak with CMV parent advocate and author, Megan Nix.

Kadesha Thomas Smith

Join the National CMV team as they speak with CMV parent and CEO/Founder of CareContent, Inc., Kadesha Thomas Smith.

Alyson Ward and the CMV Public Health & Policy Conference

Join the National CMV team as they speak with CMV advocate and Director of Quality Improvement for the National Center for Hearing Assessment and Management (NCHAM), Alyson Ward. 

Tami Hoffman and LOHL

Join the National CMV Team as they speak with CMV parent, Tami Hoffman, LMSW, during Late Onset Hearing Loss (LOHL) Awareness Week.

Meet Kenya Simmons

The National CMV Team had the privilege of speaking with Kenya Simmons, a dedicated intern and student, working closely with the Foundation.

Dr. Megan Pesch & Navigating Care

Tune in to hear from our very own Dr. Megan Pesch as she discusses navigating care after a developmental disability diagnosis.

Meet Samantha Banerjee: PUSH for Empowered Pregnancy

Samantha catchs up with co-hosts Khaliah and Dr. Jennifer Jenks to share about PUSH's agenda and 2022 activities.

Meet Lisa Eickel: CMV Community Alliance Chair

Lisa shares her experiences as a Speech-Language Pathologist and active CMV advocate.

Meet Richard Hughes IV from Moderna

Moderna is now a household name. What is mRNA and how will CMV awareness and policy shape the future for a CMV vaccine?

Meet Ilene Miller from Rare Epilepsy Network (REN)

CMV outcomes may include one or some potential neurological disorders. Learn more about one of our partners, Rare Epilepsy Network (REN) from its Director, Ilene Penn Miller.