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We recently held our first Annual General Meeting in Derbyshire, which was a great opportunity to discuss the outcomes of 2011, as well as the many things we have in the pipeline for 2012! Firstly, we are delighted to welcome two new trustees, Sarah Beadell and Liz Estall, to the board. Sarah will take on the role of Head of Fundraising, and Liz...
On Saturday 22nd October Emma & Andy Trim held a...

Just 3 weeks left to get your tickets which cost £75 and include

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CMV Action (formerly the UK Congenital CMV Association), has been supporting families and raising awareness since 1986, meaning that  in 2011, we are 25 years old! To celebrate, we have relaunched the website with a new look, a new name and a new logo.

One thing that will not change however, is our commitment to raising much-needed...

European Congenital Cytomegalovirus Initiative:
The European Congenital CMV Initiative (E.C.C.I.) is a network of professionals based throughout Europe with a united interest in congenital cytomegalovirus (CMV) infection. The group is composed of virologists, epidemiologists,...

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Our Stories

I found out I had CMV in pregnancy and thought I would share my experience in the hope that it might help (sorry if this is a bit lengthy!) All had been well at my 12 week scan and I had... Read more
Chloe
On the 20th January 1999 our lives changed forever. Our second daughter Chloe was born after a very difficult pregnancy and poor intrauterine growth. She was imediately taken to the SCBU... Read more

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