1 in 200 children is born with congenital CMV. NPO raising awareness of the leading viral, preventable cause of birth defects, developmental disabilities.

Worldwide
Joined February 2009
Please join us TOMORROW for a New to the Journey support group for families within the first 12 months of their cCMV journey. Register at: ow.ly/Y9CY50Zn3Gk
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Please join us for a New to the Journey support group for families within the first 12 months of their cCMV journey. Register at: ow.ly/eCoH50Zn3Gn
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Please join us for a New to the Journey support group for families within the first 12 months of their cCMV journey. Register at: ow.ly/eCoH50Zn3Gn
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CMV mom, Pamela Jessup Runner, joins the National CMV Foundation for an introduction to her story and new book Grief, Grit, Glory. Haven't read the book yet? No problem ! Get your copy now using promo code MAJ25 for 25% off. Register at us06web.zoom.us/meeting/regi…
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Happy Fourth of July from all of us at the National CMV Foundation! ❤️🤍💙 Wishing you a safe, joyful, and inclusive day filled with special moments with those you love.
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Read Hayley’s story and learn how lived experiences can fuel advocacy, awareness, and hope. nationalcmv.org/cmv-research… #CMVAwarenessMonth #StopCMV #CongenitalCMV #CMVAwareness #CMVCommunityAlliance
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No local Strides for CMV event near you? Join the Worldwide Walk for CMV on June 27, 2026 and walk, run, roll, or move your way through a 5K from wherever you are. Will you be joining us on June 27? #CMVAwarenessMonth #WorldwideWalkForCMV #StopCMV #CongenitalCMV #CMVAwareness
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📍 Geography Shouldn’t Decide. That’s the theme of Congenital CMV Awareness Month 2026. Our newest blog explores why geography shouldn’t decide outcomes for children affected by congenital CMV. Read the full blog at nationalcmv.org/cmv-research… #CMVAwarenessMonth
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Congenital CMV outcomes should not depend on geography. Across the world, inequities in awareness, screening, diagnosis, and access to care continue to shape what happens next for too many families. Every baby deserves the same start. #CMVAwarenessMonth2026 #CongenitalCMV
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It’s common. It’s often silent. And it can have a lasting impact when passed during pregnancy. The more we talk about it, the more families we can reach before it’s too late. Save this to come back to Share with someone who’s pregnant or TTC #StopCMV #CMVAwareness #CMV
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We are looking to form a team for the #Medtronic Twin Cities Marathon. Join us for any distance 5k to the Full marathon. Please reach out if you’re interested in joining team Stop CMV! Dm or [email protected]
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Please join us to learn about current recommendations and best practices for identifying and managing cCMV and to discover what’s new in Wisconsin!
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Interested in getting more involved with the National CMV Foundation? We are looking for highly motivated volunteers to serve on our Board of Directors. Email [email protected] to learn more!
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Team national CMV is looking for runners to participate in the 2026 Philadelphia Marathon! We are looking to form a team of 15 people to compete over marathon weekend. The foundation will pay your entry fees! email at [email protected] or send us a DM #stopcmv
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Interested in getting more involved with the National CMV Foundation? We are looking for highly motivated volunteers to serve on our Board of Directors. Email [email protected] to learn more!
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✨ Fun Friday check-in ✨ If you’re here, thank you for being part of a community that believes kids with congenital CMV deserve visibility, support, and understanding. Awareness doesn’t always have to be heavy — it just has to be shared. 💗
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Behind every CMV diagnosis is a family learning, adapting, and advocating. By sharing these stories, we create understanding, inclusion, and change. No family should feel alone. #CMVAwareness #CongenitalCMV #CMVFoundation #StopCMV #FamilySupport
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Simple habits like hand washing and not sharing food or drinks can make a difference — especially during pregnancy. Small changes. Big impact. Awareness saves futures. #CMVAwareness #CongenitalCMV #CMVFoundation #MaternalHealth #StopCMV
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