Steven is half a year old now. Meanwhile we moved back to Germany again and we are living in Oldenburg. I hope to learn more about the chri-du-chat-syndrome here.

I`m very disappointed. In Germany, there also is no more literature or information about the CDC syndrome than in the USA. Our hopes on a more positive report are wrecked.

Steven gets physiotherapy and early support now. I go with him for swimming and in child groups so that he gets contact to other children. But Steven hardly gets in contact to the outside world.