Podcasts

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.

 

Meet Tammy Boyd from the Black Women’s Health Imperative

Learn more about the Rare Disease Diversity Coalition, fueled by the Black Women's Health Imperative, and their work to alleviate the disproportionate burden of rare diseases on communities of color. 

Meet Sharon Wood with CMV Action UK

CMV is a global public health issue. Learn more about one of our partners, Sharon Wood from CMV Action UK, and how she continues to push forward with their important work in the time of COVID-19. 

Meet Kayla Keenan from CMV Canada

Hear from CMV Canada's Executive Director to learn more about its history including the focal points of the organization and what they're doing to handle programming and activities in light of COVID-19.

Meet the National CMV Team!

Learn more about our rock star staff and their experiences in public health and specifically, maternal health! Khaliah and Amanda both are working diligently to expand programming, enhance partnerships, and ultimately, help improve outcomes for children born with congenital CMV.

Catching Up with Dr. Sallie Permar

Take two! Physician scientist focusing on the prevention and treatment of neonatal viral infections, Professor of Pediatrics at Duke University, member of the Duke Human Vaccine Institute, an affiliate of the Duke Global Health Institute, and Associate Dean of Physician-Scientist Development at Duke University Medical School - get to know more about National CMV Foundation Board Director, Dr. Sallie Permar.

 

CMV Vaccine Update feat. Dr. Lori Panther of Moderna

Khaliah and Shayne chat with Lori Panther, MD, MPH, and Director of Clinical Development, Infectious Diseases at Moderna Therapeutics based in Cambridge, MA. They discuss where Moderna is in its quest for a CMV vaccine, why a vaccine is critical in preventing congenital CMV, and much more. 

CMV Dads Take Action for CMV Awareness - Part 2

Khaliah and Shayne sit down with CMV dads, Nic Maes and Andy Jones, to discuss their personal CMV experiences, what they're doing to raise CMV awareness in their communities, what needs to change with CMV education, and much more!

Meet Dr. Sallie Permar

Physician scientist focusing on the prevention and treatment of neonatal viral infections, Professor of Pediatrics at Duke University, member of the Duke Human Vaccine Institute, an affiliate of the Duke Global Health Institute, and Associate Dean of Physician-Scientist Development at Duke University Medical School - get to know more about National CMV Foundation Board Director, Dr. Sallie Permar.

Follow Sallie on Twitter @SalliePermar

Read more about Sallie in the recent Board Member Spotlight blog post.

Meet Dr. Megan Pesch

Practicing pediatrician, researcher, mom of 3, cCMV awareness advocate - get to know more about National CMV Foundation Board Member, Dr. Megan Pesch.

Follow Megan on Instagram @hearwithdess and Twitter @peschmegan.

Read more about Megan in the recent Board Member Spotlight blog post.

CMV Dads Take Action for CMV awareness

Step into the shoes of three CMV Dads: Brandon, Matt and Shayne to learn about their lives as CMV parents, their amazing CMV kiddos, their successes in raising CMV awareness, and their future goals to help STOPCMV.

More info on how you can take action for CMV awareness, here.

This podcast is brought to you by Meridian Bioscience – working to create healthcare solutions that help save lives with each discovery, each diagnosis, every patient, every day.