by KLS Foundation | Aug 12, 2018 | KLS Events, Videos
At our June 2018 KLS International Conference, we shared short inspirational videos about Kleine-levin syndrome. Thank you to all who participated and submitted a video. Below are the inspirational videos: ...
by KLS Foundation | Jul 13, 2018 | KLS Events, News Articles
On Sunday, June 24th, I was travelling back from the KLS Conference to the UK on WOW airlines via Iceland. I was wearing my KLS T Shirt, reflecting on the inspirational stories of KLS families and the work of the dedicated researchers from around the world including...
by KLS Foundation | Jun 26, 2018 | KLS Events, News Articles
Lindsay was a teenager suffering from KLS when she attended the first KLS conference in 2011. She was inspired to see KLS Board member Dani Farber in attendance with his wife and infant son, Brody. “Wow,” Lindsay thought when she heard Dani speak about life after KLS,...
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...
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