Donate to the KLS Foundation

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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

We can also accept donations of stock. Please email us at for details.

If you have any questions regarding your donation to the Foundation, please contact the Kleine-Levin Syndrome Foundation, Inc. at:

Hall of Fame

The Kleine-Levin Syndrome Foundation, Inc. is very grateful to its supporters for their generosity. With their contributions we have been able to provide information and support to those suffering from KLS as well as provide monetary support for KLS research. The KLS Foundation plans to continue exchanging information with the public and the medical community to determine the cause of KLS and find a cure to this life-altering disorder.

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About Us

What is Kleine-Levin Syndrome?

Kleine-Levin Syndrome (KLS) is a rare and complex neurological disorder characterized by periods of excessive amounts of sleep and altered behavior. The disorder strikes adolescents primarily. At the onset of an episode the patient becomes progressively drowsy and sleeps for most of the day and night (hypersomnolence), waking only to …  continue reading

STANFORD’S KLS RESEARCH PROGRAM SEEKING VOLUNTEERS FOR GENETIC AND VIRAL STUDIES

To reach the goal of the Stanford University KLS genetic and viral research studies, we need to continue recruiting as many KLS patients as possible.  Only patients with typical KLS symptoms are being sought, to reduce the possibility of a false diagnosis. These patients and their parents (if willing) are …  continue reading