The KLS Foundation is a great source to find informative and valuable information. They are the first non-profit foundation set up for Kleine-Levin Syndrome. There are endless resources on this website! Below is the link:
KLS Foundation
KLS Support UK was founded by three KLS moms. They understand how painful and devastating KLS is. Their goal is to create awareness and support families afflicted with KLS. Below is the link:
KLS Support UK
The France KLS website was created by Johnny Bienvenu, a KLS sufferer. Below is the link:
France KLS Website
