Recent News

Cool KLS Wrist Bands Now Available

The Kleine Levin Syndrome (KLS) Bands are an easy and fun way to spread awareness and remember those who are suffering from KLS.

We are pleased to invite you to attend the KLS Foundation’s First International Conference

Please note the program begins with a Welcome Reception on Friday evening, 12 August, at 17:00, followed by an open Board of Directors meeting...

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KLS Foundation’s First International Conference

Featuring Dr. Emmanuel Mignot (Professor of Psychiatry and Behavioral Sciences and Director of the Center for Narcolepsy at Stanford Medical...

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KLS Fundraiser: Walk for Ryan

Donna White led the initiative to honor the memory of her son Ryan, who struggled with KLS and tragically died of unrelated health...

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ANNUAL RUN FOR RYAN SCHEDULED FOR APRIL 17

The annual Run for Ryan is planned this year for April 17 at the Lancaster High School T-track from 10 am until 1 pm.  The Lancaster High...

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SOUTHERN CA TEACHER AWARDED FOR WORK WITH KLS

Frank Borgese, a teacher with the Placentia Yorba Linda Unified School District was honored for his voluntary assistance to educators...

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KLS Foundation visits Stanford University KLS research group

Neal M. Farber, PhD, co-President of the KLS Foundation visited with Prof. Emmanuel Mignot and his research team at Stanford University on...

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

The Stanford University Center for Narcolepsy and Hypersomnia Research has received funding from the National Institutes of Health to study...

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Stanford’s KLS Research Program Seeking Volunteers For A Viral Study

Studies at the Center for Narcolepsy research (CNR) at Stanford University reveal that in 72% of the analyzed cases, the initial episode was...

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Videos – KLS Segments on Television

A selection of videos from past television shows has been added to our website. The videos showcase several of our KLS members and give...

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