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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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Download and share all our publications and support materials: We provide printed copies of our resources free of charge to families and professionals....
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 will always...
     

Our Stories

Ours is a relatively simple story, so whilst it is great that the media portray worst case scenarios, it's good to realise that the number one effect is hearing loss, which is the only... Read more
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My pregnancy was fine up until 20 weeks when I went for my ultrasound.  They noticed there was no fluid around my baby and I had actually lost my waters at 18 weeks pregnant. Not... Read more

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