Resources

Resources
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.  

Blog

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

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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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Other Helpful Organizations

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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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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