Mission
To improve the quality of life for individuals and families worldwide affected by GBS, CIDP and variants by:
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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
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.
Expert diagnosis & management of inflammatory neuropathies is critical to our patients. This is what our medical advisory board members had in mind when setting up the new Centers of Excellence program. A year later, we continue to add healthcare facilities providing exactly that.
