by KLS Foundation | Jan 30, 2018 | KLS in the Media, News Articles
Cooper Grossman receives the 2017 New Jersey Youth Soccer Comeback Player of the Year Award! The award ceremony will take place on Friday February 2nd. “After being diagnosed with Kleine-Levin Syndrome, a disease that most of us never even knew existed, Cooper...
by KLS Foundation | Dec 4, 2017 | Fundraisers, KLS Events
The first annual Coop-A-Thon took place on October 21, 2017, at YB Fitness in Short Hills, N.J. The event came to be after very close family friends felt the need to help Coop & the rest of the KLS sufferers. Feeling helpless, they reached out to a local gym...
by KLS Foundation | Nov 11, 2017 | Fundraisers
Did you know that amazon donates 0.5% of every purchase made to the charity of your choice? As soon as we learned about this fantastic benefit, we signed up. To date we have received $685.02 from amazon smile. Our goals are to raise awareness, support scientific...
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...
