KLS Foundation is seeking volunteers

Dear KLS community, As you know, the Kleine-Levin Syndrome (KLS) Foundation is a volunteer-run patient advocacy group established 16 years ago to support patients, families and healthcare professionals dealing with KLS. The KLS Foundation Board is now seeking to expand our capabilities to better serve the KLS community and bolster research initiatives.  This is your opportunity to volunteer your skills and time, to a cause you care about. The KLS Foundation has begun a KLS related database of patient, community and professional contacts to...

read more