KLS is a very rare syndrome affecting roughly 1000 people worldwide.

As a result there is very little incentive for researchers and pharmaceutical companies to invest in KLS research.

Please consider donating today! Contributions from individuals are critical to the ongoing success of the KLS Foundation’s efforts to educate, support families and find a cure for KLS.

Thank you for your support!

2014 KLS Fundraising Calendar 2014 Kleine-Levin Syndrome Calendar

Order the Digital PDF Here

Your Donation Helps

• 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.

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.

Make a Donation

To use your credit card to make a donation, please use the form below.

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 contact us for details.

Make A Donation Now

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