by KLS Foundation | May 10, 2018 | Fundraisers, KLS Events
KLS Foundation Board Member, Alanna Wong, reached out to Courts For Life to see if they would select the KLS Foundation as a beneficiary for their tennis tournament which was held on May 5th-6th, 2018. Courts For Life and Tennis on Campus at UCR hosted the tennis...
by KLS Foundation | Mar 19, 2018 | Fundraisers
KLS makes its first Times Square debut! Together wearing their KLS t-shirts proudly, this past Sunday (3/18/18) Josh Fiske & Warren Greenberg ran in the United Airlines NYC Half Marathon. Both men ran to raise awareness and funds for KLS research. The sense of...
by KLS Foundation | Feb 28, 2018 | Announcements, News Articles
The Stanford Center for Sleep Sciences and Medicine recently sent the KLS Foundation president, Stephen Maier, a thank you letter for their generous gift. Read the following thank you letter by clicking on the following link: Stanford Thank You...
by KLS Foundation | Feb 14, 2018 | KLS Research
Report on visit to Dr. Mignot’s lab (Stanford University) to discuss KLS research I visited Stanford University on January 9, 2018 to discuss KLS research in the Mignot lab. I met with Dr. Ling Lin, Senior Research Scientist, and Dr. Aditya Ambatyi,...
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...
by KLS Foundation | Aug 23, 2017 | KLS in the Media, Videos
Watch this incredible, inspiring, and heart-wrenching segment of a patient living with KLS. Thank you to Michael Hamper and his family for raising awareness of KLS and being such great advocates for all those suffering with this rare disorder! Credit to WSVN News...
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