The KLS Foundation, based in San Jose, CA, is a non-profit organization dedicated to raising awareness and providing support for individuals affected by Kleine-Levin Syndrome (KLS). They offer resources, educational materials, and a patient registry to help those with KLS and their families navigate the challenges of this rare neurological disorder.
With a focus on research and collaboration, the KLS Foundation strives to advance understanding of KLS through their medical advisory board, research program, and grants awarded to support scientific investigations. Through their outreach efforts and media presence, they aim to shed light on KLS and share stories of hope, while also advocating for the rights of KLS patients in terms of disability and education.
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