The KLS Foundation is pleased to invite anyone impacted by or interested in learning more about Kleine Levin Syndrome (KLS) to attend the KLS Foundation’s First International Conference for KLS in San Francisco, CA, USA on August 12-14, 2011. The three-day program is designed for medical professionals, people with KLS, their families and friends and will include an update on KLS research, discussions on dealing with KLS from various perspectives and the opportunity meet other families living with KLS. We hope that this meeting will bring together people living with KLS to be able to share their experiences.

See the KLS Foundation Home page for a link to more information and registration