If you are a scientist researching some aspects of Wagner syndrome you are most welcome here. You provide the information essential for better understanding and better care. We hope you will leave information about your research here, so everybody knows what can be expected.

But that is true for yourself also. It must be interesting to know what fellow-researchers are doing, but also remarks from patients and doctors can help you getting new ideas. There are so few -patients, doctors and researchers- that a community website will be advantageous for everyone. We hope you agree.