European Cleft Gateway
Last update 03 November 2012
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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…
On 10th November, 2012, Contact parents from all over Bulgaria gathered in Plovdiv. The meeting was held at the Complex for social services for children and families […]
On the annual General Meeting of ALA Association on October 16, 2011 ALA members made a decision to introduce some changes in the Board Members […]
Specialists from Spain are interested in the Electronic Medical Record for Facial Anomalies (EMRFA) developed by ALA and are keen to implement it in their practice. At the invitation of Val d’Hebron Hospital, Barcelona and the Spanish Society for Facial Anomalies, and through the COST project CA16234 – Inequalities in the treatment of facial anomalies…
Since 2012 and for the next 2 years Association ALA offers to all families of children with clefts to take the opportunity and apply for financial support of speech therapy and/or orthodontic treatment for their children from 3 to 18 years […]
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The Second National Conference on Rare Diseases was held on September 2011 in Plovdiv. It took place at the Congress centre of the Novotel – Plovdiv. Dr. Youri Anastassov and Dr. Parvan Voynov attended the forum […]