by KLS Foundation | Feb 26, 2021 | KLS Research
How my story began… It all started years ago, February 2013 to be exact. I was in 8th grade and was studying hard for the my state standardized test, the FCAT. In addition, I was admitted into the incoming class of Pre-Medical Magnet students at my high school. Things...
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 | 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 | 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...
