GBS CIDP FOUNDATION
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Mission Statement
The GBS/CIDP Foundation International is the preeminent global non-profit organization supporting individuals and their families affected by Guillain-Barre syndrome (GBS) chronic inflammatory demyelinating polyeuropathy (CIDP) and related syndromes such as multi-focal motor neuropathy (MMN) through a commitment to support, education, research and advocacy.
About This Cause
Our Mission is to improve the quality of life for individuals and families affected by GBS, CIDP, or related syndromes such as MMN by: • Creating and nurturing a global network of volunteers, healthcare professionals, researchers and industry partners to provide those affected with GBS, CIDP, or related syndromes such as MMN with support and the most current available information; • Designing and implementing public, medical and professional education programs to increase awareness and improve understanding; • Funding research through grants, establishing fellowships and using other appropriate avenues to identify the causes of and discover treatments for GBS, CIDP, and related syndromes such as MMN; • Structuring partnerships to engage in advocacy at the federal, state and grass roots levels to advance our vision and mission with legislators and government agencies.