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What we do

 

Our mission is to limit the devastating impact of CMV for those currently affected and for future generations.

We offer advice and support to anyone affected by congenital CMV.  

We work with medical professionals, support research and raise awareness of the virus.

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Our Stories

Lewis
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 in distress and... Read more
Natalie
Everything had been going fine with my pregnancy until the 18-week scan. Then I was told I had my dates wrong and they put me back by 5 weeks, originally it was August 15th, now it was... Read more

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2019 02 Congenital CMV Conference in...
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Thursday 28 February

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Counting the Costs of CMV

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