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Our Mission Statement

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.

Vision Statement

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.

 

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