www.wissensplattform.kmsk.ch provides fast and free access to knowledge (without medical diagnoses) and key contacts on the topic of rare diseases. So quick and targeted answers can be provided to any questions from patients’ families and professionals.
Since 2014, the Support Association for Children with Rare Diseases has set itself the goal of continuously and sustainably promoting knowledge transfer on the topic of children and young people with rare diseases. The new digital knowledge platform pools knowledge for both professionals and patients’ families. Among other things, they receive information on entitlements, assistance and support services.
More information can be found here.