by KLS Foundation | Apr 26, 2022 | KLS in the Media
“This too shall pass:” This is the simple phrase that stuck with me as I endured fifteen KLS episodes. As I approach my decade milestone since my last episode, I feel reflective and so fortunate to have come through to the other side. During my adolescence, KLS...
by vcc | Mar 2, 2022 | KLS in the Media
NEWS RELEASE: Kleine-Levin Syndrome Foundation Urges Lawmakers to Bring National Awareness to KLS research Foundation Honors KLS community on Rare Disease Day by lobbying for inclusion in NIH Sleep Research Plan Feb. 28, 2022 – WASHINGTON: The Kleine-Levin Syndrome...
by KLS Foundation | Feb 3, 2022 | KLS in the Media
I am 33, I live in Toronto, I have been married for five years and I have two beautiful daughters, ages 4 and 1.5, a fulfilling career and wonderful friendships. My last episode was in January 2015. I have reached the point in my life that I no longer think about KLS...
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 | 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 | 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...
