The societies for MPS and related diseases are patientdriven organizations that were founded as early as the 1980s by parents ofaffected MPS patients. The main tasks of the MPS societies are to provide advice, guidance and support to patients and their relatives as well as networking, especially with physicians and scientists, and international cooperation. Representing the societies, the country representatives (photo from left to right) Michaela Weigl (
MPS Austria), Fredi Wiesbauer (
MPS Switzerland) und Carmen Kunkel (
MPS Germany) are organizing the MPS Congress 2024 in Würzburg in collaboration with
face to face event. The contact person for the face to face event is
Tanja Gutike.
The patron of the event, Eva Luise Köhler, wrote a
greeting.