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 | Apr 29, 2019 | Fundraisers, KLS Events
Courts for Life and University California Riverside (UCR) Tennis on Campus are partnering up to host the 4th Annual Charity Doubles Tournament. Courts for Life is glad to be promoting Kleine-Levin Syndrome (KLS) awareness once again! All proceeds raised by this event...
by KLS Foundation | Oct 30, 2018 | KLS in the Media
KLS Patient, Sarah, was featured in “Kids First” hospital magazine. Read the following KLS article. We want to give a big thanks to Sarah and her family for spreading the word about Kleine-Levin Syndrome. Click here: Kids First KLS Article...
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...
