Fundación Libellas was founded by Isabel Pastor, who is the mother of a child with a NALCN-related syndrome.
We believe that with adequately funded research, life-changing treatment options can be available to NALCN patients.
The Foundation's Board is responsible for determining the Foundation's mission, setting goals and priorities, implementing policies and planning for the Foundation's future.

FOUNDER AND PRESIDENT
Isabel Pastor Alfonso

VICE PRESIDENT
María Márquez Pastor. MD

BOARD MEMBER
Ricardo Mantecón
