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

BOARD MEMBER

Ricardo Mantecón

SECRETARY

Álvaro Márquez Rodríguez