Kleine Levin Syndrome Foundation
The Kleine Levin Syndrome (KLS) Bands are an easy and fun way to spread awareness and remember those who are suffering from KLS.
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...
continue readingFeaturing Dr. Emmanuel Mignot (Professor of Psychiatry and Behavioral Sciences and Director of the Center for Narcolepsy at Stanford Medical...
continue readingDonna White led the initiative to honor the memory of her son Ryan, who struggled with KLS and tragically died of unrelated health...
continue readingThe 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...
continue readingFrank Borgese, a teacher with the Placentia Yorba Linda Unified School District was honored for his voluntary assistance to educators...
continue readingNeal M. Farber, PhD, co-President of the KLS Foundation visited with Prof. Emmanuel Mignot and his research team at Stanford University on...
continue readingThe Stanford University Center for Narcolepsy and Hypersomnia Research has received funding from the National Institutes of Health to study...
continue readingStudies at the Center for Narcolepsy research (CNR) at Stanford University reveal that in 72% of the analyzed cases, the initial episode was...
continue readingA 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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