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 | 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 | Jun 8, 2015 | Fundraisers, KLS Events, News Articles
“Touched by 2015 Run for Ryan” by Gaylene Grossman I feel very fortunate to have attended the 2015 Run for Ryan in Lancaster, South Carolina along with my son Brian, who is a person with KLS. It was an experience I will never forget and one that touched...
