by KLS Foundation | Aug 31, 2019 | Uncategorized
Attend in person or on a “virtual” mat if you can’t be with us. Registration is free! Description Outdoor open donation yoga class to support Kleine-Levin Syndrome research. This gentle, slow flow Spa yoga class will be led by teachers from The Yoga Exchange in...
by KLS Foundation | Oct 13, 2017 | Uncategorized
Yoga in the Park benefit for the Kleine Levin Foundation On a sunny afternoon on Sunday, September 10th, 2017, the first annual Yoga in the Park with The YOGA Exchange fundraising event to benefit Kleine-Levin Syndrome (KLS) research was held at Goodwill Park in...
by KLS Foundation | Oct 13, 2017 | Uncategorized
KLS Foundation funds new study of potential biomarkers of KLS led by Dr. Emmanuel Mignot at Stanford University The cause of KLS is unknown but recent results have suggested a genetic marker. The KLS Foundation has recently funded Dr. Emmanuel Mignot’s lab at...
by vcc | Jan 12, 2015 | Uncategorized, Videos
Great video from our friend Mat Sherman, what a great attitude and a powerful reminder for all of us! For more videos from Mat and his experiences with KLS, check out his YouTube page, and don’t forget to subscribe. Thanks for letting us share the video Mat!...
by KLS Foundation | Aug 15, 2014 | Uncategorized
Alanna Wong wrote an article about tips for Living With Kleine-Levin Syndrome (KLS). You can read the 12 Tips she writes about here: 12 KLS Tips by Alanna
by Varda | Feb 18, 2014 | Announcements, News Articles, Uncategorized
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...
