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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 will always...
     

Our Stories

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My name is Julie Anne Stansfield and this is my story of when and how CMV changed my life. On the 12th February 2010, I found out I was pregnant, it seemed like a natural progression... Read more
Hi everyone, meet chocolate faced Darcie. She is my beautiful 20 month old daughter. I was diagnosed CMV positive when I was 6 months pregnant. It is thought that I caught it when I was 4... Read more

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