Get Support

     
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...
CMV_Action_Infographic_Panel1
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

December 1997 Lewis was born 3 weeks early on 23rd December 1997 following a normal healthy pregnancy. The labour was not easy, but relatively quick being 4 hours in total but he was... Read more
February 2014 Our family consists of my husband, Yoav, and our two daughters, Maya and Leila. Our youngest daughter, Leila, was born with congenital cytomegalovirus (cCMV) and has... Read more

Latest Events

Reg. charity no: 1171773