To improve the quality of life for individuals and families worldwide affected by GBS, CIDP and variants by:

Providing a network for all patients, their caregivers and families so that GBS or CIDP patients can depend on the Foundation for support, and reliable up-to-date information.

Providing public and professional educational programs worldwide designed to heighten awareness and improve the understanding and treatment of GBS, CIDP and variants.

Expanding the Foundation’s role in sponsoring research and engaging in patient advocacy.