You are here: Home / Rare Disease Information / Patient Organizations Database

Search Patient Organizations

Enter organization name or disease name to search for organizations that help people with rare diseases.

0-9 - A - B - C - D - E - F - G - H - I - J - K - L - M - N - O - P - Q - R - S - T - U - V - W - X - Y - Z

**IMPORTANT**

The information contained in the Organizational Database (ODB) is provided for informational purposes only. There is no implied endorsement by NORD. NORD does not promote or endorse participation in any specific organization. The information is subject to change without notice. Every effort is made to ensure that the details for each entry are as current as possible.

Kleine-Levin Syndrome Foundation

a/k/a: KLSF

Address

PO Box 5382
San Jose, CA 95150-5382

Phone

408-265-1099

Fax

408-269-2131

Email Address

facts@klsfoundation.org

Website

http://www.klsfoundation.org

The Kleine-Levin Syndrome Foundation (KLS Foundation) provides information and support to patients and families affected by Kleine-Levin syndrome (KLS); a rare disorder characterized by episodes of excessive need for sleep, excessive food intake, and altered behavior. The KLS Foundation exchanges information among patients, their families, and the medical community to help in the diagnosis and care of those affected by KLS. The goals of the KLS foundation are to raise awareness, support research, and find effective treatment and a cure for KLS. The foundation offers patient networking, education, and referrals to KLS patients and their families.

0-9 - A - B - C - D - E - F - G - H - I - J - K - L - M - N - O - P - Q - R - S - T - U - V - W - X - Y - Z

NORD's Rare Disease Information Database is copyrighted and may not be published without the written consent of NORD.

 
Copyright ©2014 NORD - National Organization for Rare Disorders, Inc. All rights reserved.