To improve the quality of life for individuals and families worldwide affected by GBS, CIDP and variants by 1) providing a network for ALL patients, their caregivers and families 2) providing public and professional education programs worldwide designed to heighten awareness and improve the understanding and treatment of GBS, CIDP and variants. 3) expanding the foundation's role in sponsoring research and engaging in patient advocacy.
This 501(c)(3) elected the 501(h) safe-harbor — lobbying expenditures are capped under a clear dollar formula instead of the "insubstantial part" standard.