Welcome to the
Care-for-Rare Foundation
for children with rare diseases!

Children with rare diseases, orphans of medicine, are disadvantaged in many respects: endless odyssees from doctor to doctor, wrong diagnoses and clinical mismanagement determine their lives. Many rare diseases remain incurable up to date. Only through enhanced research activities and international cooperation can we change the fortune of many children.

The Care-for-Rare Foundation is the first and only foundation of its kind, it supports children cross-borders in order to give them hope for treatment – no matter what nationality, ethnic origins and financial background they present.

Prof. Dr. med Christoph Klein

President, Care-for-Rare Foundation

 

    

25.04.2017
3rd International Primary Immunodeficiencies Congress, 8-10 Nov 2017 in Dubai
06.03.2017
3rd International Klaus Betke Symposium on rare inflammatory bowel disease
28.02.2017
Application Science Award 2017