The little girl Revan is the main protagonist of this blog. It was on 5 May 2009 Beylagan, a district near the Armenian and Iranian border with a cleft lip and palate born. Revan is the second child of a young Azerbaijani family living in very poor conditions and in confined space with many other relatives. Habiba and Ceyhun, the parents of Revan knew during the pregnancy that their child could cope with a congenital malformation of the world. Screening in the Western world may be in the area of Azerbaijan nobody afford. After Revanes'Geburt were therefore first of all shocked and alarmed at the first feelings that you held the child. Medical education has not yet taken place so far. In the next few days to get the girl in Baku an expensive initial investigation. Whether the provision of medical care can be financed in the amount of the estimated cost of the hospital depends.
Why this blog?
A few days ago I learned about our Azerbaijani interpreter and friend in Vienna, the fate of the newborn girl and his family. The economic misery and ignorance and concern about the malformation was to the parents Adoption, foster or residential care to think. After a sleepless night and endless musings, I've decided to launch a fundraising campaign to life. Economic crisis or not - there are certainly people who are helping to shoulder the medical and therapeutic care of Revan! To these people keep on Revanes'weiteres destiny and its development up to date, I would like to make this blog. In it I will report on all fund raising, which I will start with pictures and current articles.
