To improve the quality of life for individuals and families worldwide affected by GBS, CIDP, MMN, and their 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.
Our vision is that every person afflicted with Guillain-Barré Syndrome, CIDP or variants has convenient access to early and accurate diagnosis, appropriate and affordable treatments, and dependable support services.