Nonprofit
Kleine Levin Syndrome Foundation
About Us
The Kleine-Levin Syndrome Foundation is a non-profit patient advocacy organization whose mission is to build awareness of KLS, help doctors understand the complexities of KLS, support the community of KLS patients and caregivers, promote patient and caregiver advocacy, and drive the search for a cause and a cure for KLS.
We are an all-volunteer organization founded in 1999. The first Executive Director of the Foundation will play a crucial role in shaping the strategic direction of the organization, managing day-to-day operations, and representing the interests of patients and their families. This part-time position offers the opportunity to make a significant impact on the lives of those affected by Kleine-Levin Syndrome.
The Kleine-Levin Syndrome Foundation is a non-profit patient advocacy organization whose mission is to build awareness of KLS, help doctors understand the complexities of KLS, support the community of KLS patients and caregivers, promote patient and caregiver advocacy, and drive the search for a cause and a cure for KLS.
We are an all-volunteer organization founded in 1999. The first Executive Director of the Foundation will play a crucial role in shaping the strategic direction of the organization, managing day-to-day operations, and representing the interests of patients and their families. This part-time position offers the opportunity to make a significant impact on the lives of those affected by Kleine-Levin Syndrome.
Issue Areas Include
- Health & Medicine
Location & Contact
- 2026433055
- info@klsfoundation.org
- San Jose, CA, USA
