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...
by KLS Foundation | Aug 17, 2017 | KLS Research
The following articles, from the Broad Institute at Harvard, provide a respectable explanation for KLS research being done by Dr. Mignot and collaborators at Stanford University. The articles give a general account of the Genome-wide Association studies (GWAS). These...
by KLS Foundation | Aug 3, 2017 | Fundraisers
We have come a long way in research over the past few decades due to the generosity of others putting on fundraising events and donating to the KLS Foundation research fund. We are happy to share that the Grossman family is hosting a Fundraising event for the KLS...
by KLS Foundation | Jan 5, 2016 | KLS Research
KLS Foundation Awards Grant to Emmanuel Mignot of Stanford University for Genetic Research January 6, 2016 – The Kleine-Levin Syndrome (KLS) Foundation, a patient advocacy group promoting research and supporting families dealing with KLS, today announced that the KLS...
by KLS Foundation | Dec 2, 2015 | 2015 KLS Conference
Steve Maier, President of the KLS Foundation, kicks off the 2015 International Conference. See the PDF link and video below. PDF Link: KLS Foundation 2015 International Conference – Kickoff – Steve Maier KLSF President
by KLS Foundation | Dec 2, 2015 | 2015 KLS Conference
Professor Isabelle Arnulf PhD MD, Keynote Speaker, provides a very comprehensive 2015 update on Kleine-Levin Syndrome to include: KLS diagnosis criteria, long episodes, brain functional imaging, long term cognitive functioning and treatments. See the PDF link and...
by KLS Foundation | Dec 2, 2015 | 2015 KLS Conference
Dr. David Rye, MD, special guest speaker, gives a talk about his research concerning Hypersomnia Conditions. Subjects include Kleine-Levin Syndrome, Idiopathic Hypersomnia, and Narcolepsy. See video below.
by KLS Foundation | Dec 2, 2015 | 2015 KLS Conference
Ann Blackmon, special guest speaker, presents a check to the KLS Foundation in memory of Ryan McKinney and shares about the Running For Ryan Fundraiser. See video below.
by KLS Foundation | Dec 2, 2015 | 2015 KLS Conference
Dani Farber, KLS Foundation Board Member, presents a global research update on KLS. See the PDF link and video below. PDF Link: KLS Research Update – Dani Farber & Neil Farber PhD
by KLS Foundation | Dec 2, 2015 | 2015 KLS Conference
Caron Krieger, KLS Foundation Board Member and Co-Founder of KLS Support UK, shares about how KLS Support UK came to be and it’s attained success. See the PDF link and video below. PDF Link: KLS Support UK – Caron Krieger KLSF BOD
