Resources | National CMV Foundation

If you, or someone you know, has been touched by congenital CMV, know that you are not alone. The National CMV Foundation offers parents, families, and professionals valuable information about congenital CMV. Read our blog, download informative literature, share your story, and get your frequently asked questions answered.

Podcasts

Casual conversations with congenital CMV parent advocates, healthcare providers, scientists and researchers regarding special interest topics to remind our audience why we do what we do.

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Family Stories

Every person touched by cCMV has a story. Read personal accounts of families living with this virus, and the efforts people are undertaking to raise awareness for cCMV.

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Educational Downloads

Help us raise awareness of CMV—share, post, and print our awareness flyers and help educate pregnant women, practitioners, and the public about CMV.

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For Childcare Providers

Parents with young children, or who work with young children, may be at greater risk for contracting cytomegalovirus, or CMV, during pregnancy. Studies in child-care settings suggest that as many as 75% of toddler-aged children have CMV in their urine or saliva.

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For Healthcare Providers

CMV can be a serious problem for babies who are infected before birth. This is referred to as congenital CMV and it occurs when a pregnant woman passes the virus to her unborn child.

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FAQs

We have compiled a list of frequently asked questions about CMV and pregnancy in order to educate and provide answers for expecting mothers and women of childbearing age.

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