Kleine-Levin Syndrome Foundation Inc.

Recent scientific study published on sleep disorders and the subsequent news coverage

There have been several news stories in the popular press and circulating on the internet about the results of a recent scientific study about...

The programme will run on Wednesday 5th December when the morning session will be devoted to Narcolepsy and the afternoon session to Kleine...

The Kleine Levin Syndrome (KLS) Hats and T-Shirts are now available for $22.50 as seen at the First International KLS Conference and can be...

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

About 200 patients and their families are gathering in Burlingame August 12-14th, 2011 for the world’s first Kleine-Levin Syndrome conference...

The Conference got off to a great start on Friday afternoon with nearly 100 people arriving, checking in and being able to meet face to face...

For UK KLS patients and their families there is a new support group linked to the US based KLS Foundation to provide support and information...

It was an exciting day on Sunday, April 24, 2011 that was preceded by days of anticipation when two KLS families met face-to-face! The Wongs...

A new website for Kleine-Levin Syndrome has been launched. This website is in French and was started by Johnny Bienvenu who suffers from...

More than 4 years after their last episodes of KLS, the Farber siblings tackle the last of the physical and emotional hurdles in their journey...