From Awareness to Action — Together, We Can Stop Congenital CMV

Your voice can help stop the most common preventable cause of birth defects and pregnancy loss

Who We Are

Meet the families, advocates, and experts leading the movement

Key Issues

Learn what’s at stake — and why congenital CMV advocacy matters

Our Work

Discover how we are advocating to end congenital CMV

Take Action

Join the fight! Lend your voice, share your story & help further CMV advocacy

KEY ISSUES

Protecting every baby. Empowering every family. Driving policy for a cCMV-free future.

Universal Newborn
Screening

Universal Newborn Screening.

Innovation starts with early detection -- which saves lives. We advocate for CMV testing in every state so all babies can access care and intervention.
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Comprehensive Prenatal
Education

Comprehensive Prenatal Education

Knowledge is prevention. Every pregnant person deserves to know how to reduce cCMV risk - education should be part of the standard prenatal care.
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Increased Research
Funding

Increased Research Funding

Innovation states with investment. We push for stronger federal and state funding to advance research on CMV detection, outcomes and treatments.
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Support for Vaccine
Development

Support for Vaccine Development

A vaccine can end CMV for good. We champion policies that accelerate vaccine resarch and bring prevention within reach.
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Never heard of congenital CMV?



Most people have never heard of congenital CMV, despite it being the most common congenital infection in North America. Learn more about congenital CMV and why increasing awareness is critical!

What is CMV?

Learn the basics about the most common virus you've never heard of

Why newborn CMV screening?

Without screening most babies with CMV aren’t tested or diagnosed early

How prenatal education helps

Empowering families and changing
lives through risk reduction

Meet the faces of congenital CMV

Frequently Asked Questions

What is congenital CMV and why does it matter?

Congenital cytomegalovirus (CMV) is the most common congenital infection in the US and Canada, affecting over 30,000 babies each year. It is a leading cause of hearing loss and developmental delay, yet most infants go undiagosed without newborn screening.

Why not focus on prevention?

Increasing education about ways to reduce the risk of catching CMV in pregnancy is important and one of our key issues. However, CMV is a virus that stays in your system for a lifetime, so even if a pregnant person is very vigilant about hygiene, there is still the chance that an old infection could reactivate.

Isn't there limited data on screening feasibility?

That's no longer true. Since 2021, Minnesota has implemented universal newborn screening, with Connecticut following suit in 2025. Canadian provinces have been screening since 2019. Many use dried blood spot testing that fits directly into existing newborn screening services. Results show that universal screening is feasible, scalable and cost-effective.

There is a lot of controversy about vaccines - why support them?

Scientists have been trying to find a way to stop CMV for 50 years because it is a common cause of miscarriage, stillbirth and disability. Recent mRNA vaccine technology has been a breakthrough in how a vaccine might be able to stop a person from catching CMV, and reduce the occurrence of miscarriage, stillbirth and disabilities. There are no medications to prevent CMV, and even the best hand hygiene in pregnancy does not completely reduce one's risk. CMV has taken the lives of far to many precious children - this new science gives us hope that in our lifetime we will see an end to CMV.

Does early detection really change outcomes?

Yes. Early antiviral treatment improves hearing and neurodevelopmental outcomes in babies with symptoms and those with hearing loss. Even for babies who appear healthy at birth, early detection enables hearing surveillance and early-intervention services that improve language and learning outcomes. Families report feeling relieved and empowered to have an explaination and access to early supports.

My child/grandchild has congenital CMV - how can I help?

If you would like to share your child's story, help us reach out to lawmakers please visit our Take Action page or reach out to us at advocacy@nationalcmv.org

Contact Us