by KLS Foundation | Oct 31, 2019 | Fundraisers, KLS Events
Excited to let you all know, the link is live!!!!!! PLEASE sign up to spin in person, virtually or to be a sponsor for the 3rd Annual Coop-A-Thon! Your constant support gives me HOPE, that the cause and cure for KLS will be found!!! It takes a village. Please click...
by KLS Foundation | Aug 31, 2019 | Uncategorized
Attend in person or on a “virtual” mat if you can’t be with us. Registration is free! Description Outdoor open donation yoga class to support Kleine-Levin Syndrome research. This gentle, slow flow Spa yoga class will be led by teachers from The Yoga Exchange in...
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 | Oct 10, 2018 | Fundraisers
The 2nd annual Coop-A-Thon, which took place on December 2, 2018, at YB Fitness in Short Hills, N.J., was a HUGE success. The generosity of family, friends, teachers, teammates, local businesses, and complete strangers was beyond our wildest expectations. The KLSF...
by KLS Foundation | Sep 26, 2018 | Fundraisers, KLS Events
We hope this email finds you well. The KLS Foundation has exciting news to share. KLS Fundraising at the Chicago Marathon KLS Board member, Dani Farber, is running the Chicago marathon on October 7 to support the KLS research efforts. Following the successful 2nd...
by KLS Foundation | Sep 20, 2018 | Fundraisers, KLS Events
It truly was an amazing day on Sunday, September 9th as we joined together with friends and family–in person and on virtual mats–to practice yoga, to practice compassion and to help raise funds for and awareness of KLS. My sister Andrea Goldstein and...
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...
by KLS Foundation | Jun 26, 2018 | KLS Events, News Articles
Lindsay was a teenager suffering from KLS when she attended the first KLS conference in 2011. She was inspired to see KLS Board member Dani Farber in attendance with his wife and infant son, Brody. “Wow,” Lindsay thought when she heard Dani speak about life after KLS,...
