by KLS Foundation | Nov 18, 2022 | KLS in the Media
Just like everyone who suffers from KLS, my journey was a trying one, but I was fortunate to emerge stronger than ever. I was 16 and planning my first trip to Israel. My grandma took me to Target to shop for last minute essentials and immediately, we knew something...
by KLS Foundation | Aug 15, 2022 | KLS in the Media
I am 26 years old and have suffered from KLS for more than 10 years. I experienced multiple episodes a year at the age of 15, then an episode every two years, and recently had a lighter episode: I feel that there is light at the end of the tunnel. I’m making a...
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...
