European Cleft Gateway
Last update 03 November 2012
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Parents talk about their bitter experience in the Maternity Unit after giving birth to a child with facial anomaly.
The Story of I. D. We won’t be able to tell the names or show pictures to illustrate this story due to reasons that will very soon become clear but I believe that this story could help more people to understand what it means to have a cleft palate, which is corrected at a…
Over 500 participants attended the European Craniofacial Congress. The main topic of the Congress was clefts of the lip and/or the palate and other craniofacial anomalies connected with them […]
Many guests and families of children with clefts attended ALA’s Christmas Party. For the youngest it was organized a Carnival with costumes and presents […]
Plovdiv, Bulgaria – 4 September, 2013 – Up to 40% of parents of babies born with cleft lip/ palate in Bulgaria are told to place their child in institutions, through lack of understanding of the straightforward care (such as simple feeding techniques) required during the first months of life. Today, however, marks a triumphant milestone for these children and their families; representatives from several countries including Bulgaria are meeting in Vienna, Austria to produce the first-ever set of EU-wide guidelines for the early care of babies born with the condition.