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.Disease Support Organization Last Updated: 30 Jan 2019
Our mission is to ensure that everyone in the world with a rare disease has a safe place to go and connect with others like them.Disease Support Organization Last Updated: 13 Nov 2018
Contact a Family improves the lives of all families with disabled children. With them, we transform their lives, break down barriers and tackle disadvantage through ambitious, collaborative and innovative work. We make a real and lasting impact and are a force for positive change.General Support Organization Last Updated: 13 Nov 2018
To provide free information, advice and advocacy services to patients with chronic illnesses, in areas including health and disability insurance, Social Security disability, employment discrimination, school-based accommodations, and resource location.General Support Organization Last Updated: 13 Nov 2018
Any Baby Can serves families that have a child under the age of 13 with a chronic illnes, developmental delay or health risk, through case management and other support services.General Support Organization Last Updated: 13 Nov 2018