Press & Media


We welcome journalists, bloggers or social influencers and other media professionals to learn more about CMV Action and CMV (Cytomegalovirus).   

Quotes and stories

We can provide you with family stories and quotes from experts involved in CMV research.  We can arrange interviews with families who have experienced the impact of CMV in a variety of different conditions and disabilities, as well as relevant spokespeople and researchers working in the field. 

We welcome calls from print, broadcast and online journalists, as well as freelance journalists, with an interest in this area. We can also provide help and advice for documentary makers.

For all media inquires, please contact: 

Kat Foster:

Head of Awareness

Caroline Star: 

Chair of CMV Action

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Our Stories

We found out in January 2017 just after Gabe’s first birthday that he had Congenital CMV.  I had a great pregnancy and a delivery with no problems. However he was born with tiny purple... Read more
In November 2011 we found out we were expecting our second child. We were so happy and excited to be completing our family. I had a dream, trouble free pregnancy just like I had had with... Read more

Registered charity no: 1171773