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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: [block:webform=client-block-366] We've put together Awareness Raising packs for you to...
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

July 2018 Our Story – Orla and Cytomegalovirus. On the 2nd July 2018 my wife Hannah went in to labour, it was unremarkable (at least as much as such a thing is) and Orla was born... Read more
December 2011 When I was pregnant my baby was measuring small and I had to go for weekly dopplers and fortnightly growth scans. A month before my due date, I was told there was no... Read more

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