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 | Jun 8, 2015 | Fundraisers, KLS Events, News Articles
“Touched by 2015 Run for Ryan” by Gaylene Grossman I feel very fortunate to have attended the 2015 Run for Ryan in Lancaster, South Carolina along with my son Brian, who is a person with KLS. It was an experience I will never forget and one that touched...
by KLS Foundation | Jun 27, 2014 | Fundraisers
Kleine-Levin Syndrome Foundation Fundraiser Benefiting: Nick Smith and all adolescents living with KLS All Proceeds go to Awareness and Research for the Kleine Levin Syndrome Foundation When: Saturday, July 19, 2014 Where: Indian Lake Country Club 10502 E 75th Street,...
by KLS Foundation | May 10, 2014 | Fundraisers
Kleine Levin Syndrome 10K Run “For many young people with Kleine Levin Syndrome it feels like time travelling – their last clear memory is being at a certain place doing whatever normal people do and suddenly they wake up somewhere else, they have no idea...
by KLS Foundation | Apr 7, 2014 | Fundraisers, KLS in the Media
The Running for Ryan KLS Fundraiser was held on April 5th, 2014! The event is held in memory of Ryan McKinney, who died of cardiac arrhythmia, which was caused by a missed diagnosis and over medication of KLS. Read the following article here: Running for Ryan Article...
by KLS Foundation | Apr 3, 2012 | Announcements, Fundraisers
Spring is here and so is the 6th annual Run for Ryan, a Kleine – Levin Syndrome Fundraiser. On Saturday April 14, a committee of dedicated volunteers headed by Donna White will sponsor the 6th annual Run for Ryan. This is a special day in Lancaster, South...
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