Kleine-Levin Syndrome Foundation

Global Genes Global Advocacy Alliance member focused on rare disease support, education, advocacy, or research. The mission of the Kleine-Levin Syndrome Foundation is to (1) build awareness of KLS, (2) offer support for our community of KLS patients and caregivers, and (3) drive the search for a cause and a cure for KLS. Directory information only; not medical advice, legal advice, or endorsement. Services and eligibility should be confirmed with the organization.