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At CMV Action we understand just how difficult a diagnosis of CMV can be for your family. The early days following diagnosis can be bewildering and upsetting....
Joining the CMV group helps you to keep up to date with what we are doing at CMV Action . It also gives us vital information about the extent of CMV and allows...
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So sorry but at the moment we are unable to send out any awareness packs or resources. You can download and share all our publications and support materials...
Listed here a some of the support groups and social media pages available to help people affected by CMV. We are not responsible for the content of theses...
One of CMV Action's key objectives is to support the development and implementation of research into better testing, treatment and management of CMV...
At CMV Action we aim to provide information and support to families. We empower parents to work effectively with professionals and advocate on behalf of...
  CMV Action is a UK based charity and primarily support families living in the UK. We sometimes receive enquiries from families living abroad and we...
     

Our Stories

Siân was born on 11th March 1980, apparently normally after a normal pregnancy. She was small for birth-weight but this was not felt to be a problem – it runs in the family. The first few... Read more
Jamie-CMV
Hello, my son’s name is Jamie and he is 14 months old.  He was born with congenital CMV. Pregnancy wise, everything was normal, I had 5 scans, all fine... It was only 3 weeks... Read more

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