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Since we encountered a few inconsistencies in the diagnosis and non-treatment of Fabry disease, we had to investigate the correlations more intensively than we thought as non-professionals. We noticed that there are still many unanswered questions.

It annoyed us that patients are not treated despite a proven genetic defect and massive complaints. Therefore we would like to contribute to the clarification with our side, so that some of the rare ones again are categorized as psychosomatic and are only treated symptomatically, although a causal therapy is available.

All information can be verified with sources!