February 2017

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A Step Backward: HRSA’s Elimination of the ACHDNC Threatens Progress on Newborn Screening

Author: NCMVF Board of Directors
Posted: 4/25/2025
Category: Advocacy, Awareness
The National CMV Foundation is deeply concerned by HRSA’s recent decision to dissolve the Advisory Committee on Heritable Disorders in Newborns and Children (ACHDNC)—a cornerstone of equitable, evidence-based newborn screening for over 20 years. Without this federal oversight, there's now no national process to evaluate and recommend new conditions—including congenital cytomegalovirus (CMV), the most common infectious cause of birth defects and developmental disabilities in the U.S.

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2017 CMV Legislation Proposed in Four States

Posted: 2/28/2017
Category: Advocacy, Awareness

What do Idaho, Iowa, Oregon, and Maine have in common? These states have proposed state CMV legislation for 2017! Thanks to the hard work of sponsors, parents, physicians, and other advocates within these states, CMV legislation with proposed education and/or screening programs will be evaluated during this legislative session in each individual state. So what's in all of these bills? Check out our blog for summaries and links to bill text and updates. 


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​Microcephaly 101

Posted: 2/15/2017
Category: Clinical
Microcephaly has been making headlines over the last year as potential brain malformation connected to women diagnosed with Zika during pregnancy. However, kids are at risk of being born with microcephaly even in areas of the world not hit by the Zika virus. Many of these cases are caused by cytomegalovirus, or CMV. Unlike Zika, which is only being actively transmitted in a small area of the world, CMV exists virtually everywhere. To reduce these cases, we need to increase awareness of CMV: causes, detection, treatments, etc. 

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