We pro­du­ce the maga­zi­ne «lupus», which is also popu­lar among heal­th­ca­re pro­fes­sio­nals and is available in many hos­pi­tals and doc­tors’ offices. For over ten years, we have main­tai­ned the lupus suis­se web­site, which was new­ly revi­sed in 2025. A new offe­ring is our con­stant­ly updated news­let­ter, which is sent regu­lar­ly via email. 

In various regi­ons of Switz­er­land, we orga­ni­ze medi­cal lec­tures and work­shops. Through the­se, we inform our mem­bers and indi­vi­du­als affec­ted by lupus about Syste­mic Lupus Ery­the­ma­to­sus. At the same time, we rai­se public awa­re­ness of this rare dise­a­se. The regio­nal self-help groups and cont­act per­sons available by pho­ne are also important ser­vices for our members. 

We want to con­ti­n­ue doing this in the future! And imple­ment fur­ther projects! 

To be able to offer all of this to indi­vi­du­als affec­ted by lupus, their rela­ti­ves, and other inte­re­sted par­ties, we need spon­sors in addi­ti­on to members.