Resources | National CMV Foundation

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

For Healthcare Professionals

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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Online Resources

Learning about congenital CMV, or any of its wide-ranging developmental diagnoses, often presents a range of challenges for both the child and his or her family members. There are resources available to help.

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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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Blog

Visit our blog to read up on timely insight around CMV. From industry news to thoughts from experts in the field, we have everything you need to keep yourself informed.

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Parent Stories

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

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Glossary

Education is critical in understanding CMV, raising awareness and speaking to your doctor about this virus. Here is a list of terms or words that are often associated with CMV.

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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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