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ERNICA website goes live!

The European Network for Rare and Inherited Congenital Abnormalities (ERNICA) website has now gone live and we would like your feedback on it to ensure that it can continue to develop and improve for patients as well as Medics. You can read all about ERNICA and find out about CDH UK’s involvement as a founding  patient organisation and ePAG on the patient involvement page. You can email with your suggestions or comments on the website itself.