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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...
When parents first find out that their child was born with CMV they often ask why more isn't done to test for CMV and why isn't there a vaccine.  For a...
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

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July 2014 My name is Alex and this is the story of how I came to learn about CMV. January 13th 2014, I was stood staring at the positive pregnancy test in my hand. After 5 months of... Read more
March 2011 Clemmie was born 3 weeks early while my husband was serving with the British Army in Afghanistan. Up to that point, I’d had a normal pregnancy with no adverse scans or... Read more

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