Kleine Levin Syndrome Foundation
If you are interested in obtaining a copy of the DVDs from the First International KLS Conference that was held in San Francisco on August 12-14th 2011, you can do so by making a donation to the Foundation of at least $120 and providing your mailing address along with that donation.
Please consider donating today! Contributions from individuals assist in maintaining the ongoing success of the KLS Foundation’s efforts to educate, support and find a cure for KLS.
Our goals are as follows:
• Fund medical research
• Increase physician awareness
• Provide information and support to patients and families
• Organize a Kleine-Levin Syndrome Conference
Kleine-Levin Syndrome Foundation, Inc. is a 501(3)c non-profit organization and all contributions are tax deductible. All funds go directly to support KLS Foundation projects.
To use your credit card to make a donation, please use the Donate Now button above. The Donate Now button will also allow you to make your donation in the name of a loved one and will send them a direct message if you wish.
If you would prefer to make a contribution by check, please make your check payable to Kleine-Levin Syndrome Foundation, Inc. and send it to:
Kleine-Levin Syndrome Foundation, Inc.
P.O. Box 5382
San Jose, CA 95150-5382
The Kleine-Levin Syndrome Foundation is grateful to all its supporters for their generosity. Your contributions have enabled the KLS Foundation to provide information and support to those suffering from KLS, as well as to provide vital funding for KLS research. With your help the KLS Foundation continues raising awareness about KLS and exchanging information with the medical community to determine the cause of KLS while working toward finding a cure to this life-altering disorder.