Our mission is to educate women of childbearing age about congenital CMV, so we may eliminate this devasating virus for the next generation of newborns.
We work to educate others on specific prevention measures to protect against the risk of CMV infection. Read about our mission, vision, and key objectives.
The passion, commitment, and motivation of our National CMV board members help shape our organization and cultivate our community.
All moms to CMV kiddos, these six women are incredible advocates for the cause. Meet our founders to understand their motivation for eliminating congenital CMV.
Read about our strategic plan, which rallies the organization around our interdependent goals and overarching objectives, which will further propel the mission of the National CMV Foundation through 2020.
We are thrilled to offer funding for various awareness and research awards specific to congenital CMV education, diagnosis, screening, treatment, or vaccine development.
We are grateful for the support of our donors, partners and volunteers. Your generosity allows for the growth and expansion of our programs focused on CMV awareness and prevention education for women of childbearing age.
We are actively recruiting volunteers and participants to join our rapidly expanding team! Learn about our committees and how you can play a role.
Not sure if you or your child has CMV? Are you struggling with a new or existing cytomegalovirus diagnosis? We welcome your questions, comments or suggestions.