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KLS patients and their families brought together by the KLS Foundation

Walking For Ryan KLS fundraiser March 29, 2008

Second Annual Montvale Plaza KLS Fundraise a Huge Success

SC Governor Declares March 29, 2008 as KLS Awareness Day

Major Kleine-Levin Syndrome genetic research funding awarded to Stanford University

Presentation on the Comparison of Narcolepsy and KLS to be presented at Annual Ped. Sleep Conference

STANFORD’S KLS RESEARCH PROGRAM SEEKING VOLUNTEERS FOR A VIRAL STUDY



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STANFORD’S KLS RESEARCH PROGRAM SEEKING VOLUNTEERS FOR A VIRAL STUDY

Over the past two years, the Center for Narcolepsy research (CNR) at Stanford University has invested a great deal of time and energy into investigating the nature of Kleine-Levin Syndrome (KLS).  In this research, the CNR works very closely with the KLS Foundation.  Below is a brief synopsis of that …  continue reading

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If you or someone you know is going to be on a television show or featured in an article in the newspaper about Kleine Levin Syndrome, please notify the KLS Foundation so we can place an announcement on the website. Our contact information is or 408-265-1099. Thanks.

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What is Kleine-Levin Syndrome?

Kleine-Levin Syndrome (KLS) is a rare and complex neurological disorder characterized by periods of excessive amounts of sleep and altered behavior. The disorder strikes adolescents primarily. At the onset of an episode the patient becomes progressively drowsy and sleeps for most of the day and night (hypersomnolence), waking only to …  continue reading

STANFORD’S KLS RESEARCH PROGRAM SEEKING VOLUNTEERS FOR GENETIC AND VIRAL STUDIES

To reach the goal of the Stanford University KLS genetic and viral research studies, we need to continue recruiting as many KLS patients as possible.  Only patients with typical KLS symptoms are being sought, to reduce the possibility of a false diagnosis. These patients and their parents (if willing) are …  continue reading