CRPS is everyone's business - because anyone can get it
A project from CRPS Netzwerk gemeinsam stark e.V. in Köln, Germany
It is important to raise awareness of the rare disease CRPS in order to diagnose those affected and to prevent chronification and severe disability through intensive therapy. Informed doctors need to know the Budapest criteria.
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About this project
Marion Burk from CRPS Netzwerk gemeinsam stark e.V. is responsible for this project
Worldwide, millions of people are certainly affected by this terrible yet rare disease and the number of children affected is worrying. The exact number of people suffering from CRPS is unfortunately not known, but it is known that the number of unreported cases is much higher because many people are diagnosed very late or sometimes not at all. The fatal thing about it is that the consequences of no or incorrect treatment can lead to a loss of mobility of the affected limbs.
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