The Centers for Disease Control and Prevention: Cytomegalovirus (CMV) and Congenital CMV Infection.
CMV information is provided for families and professionals about Signs and symptoms, Who is at risk, How it spreads, Prevention, Testing and diagnosis, and Treatment and recovery.
The National CMV Foundation – Cytomegalovirus (CMV)
The National CMV Foundation has a vision to eliminate congenital cytomegalovirus (CMV) in the United States for the next generation. It’s mission is to prevent pregnancy loss, childhood death, and disability due to congenital CMV. They provide valuable resources and support for families and professionals.
Educational Downloads for families and professionals are available from the National CMV Foundation. Print and share these materials to raise awareness.
Parent to Parent Support Network
”The National Congenital CMV Disease Registry assists nearly 600 families affected by CMV by providing a way to exchange information and by offering help and support to one another.”
Michigan Hands and Voices
Michigan Hands & Voices supports families of children who are deaf or hard of hearing, regardless of communication mode or language. They believe all children can reach their full potential. The non-profit offers free events, trainings, and family support programs.