
Our commitment is our story. It all began with eight people sitting around a dining table over 30 years ago.
Through the hard work and determination of our founder, Estelle Benson, the Foundation grew larger and has become able to support many patients, family members, friends and caregivers. The Foundation is committed to continuing to provide the experience of care and support so indicative of the original Foundation.
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Our commitment is to support those touched by the GBD/CIDP disorders so that every patient experiences an early diagnosis, proper treatment, & the opportunity for a full recovery. |
Meet the original Founders, Estelle & Bob Benson. Enjoy their interesting story of how the Foundation got its start and hasn’t looked back since. |
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Our Board of Directors are committed to evolving the Foundation through success. This new website is proof of that, and there’s more to come in 2012. |
Our organization is extremely fortunate to be associated with some of the top experts in the neurology field of medicine. This expertise extends to you in many ways, including the Centers of Excellence program which they helped create and maintain. |
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With chapters in 33 countries and over 30,000 members, the Foundation has grown to reach international patients & others touched by GBS & CIDP. Check your area to see if there’s a chapter close to you. |
What’s great about having such a diverse community just that: diversity. That even translates down to preferred methods of communication. Whether you’d like to contact us via phone, social media or our contact form, we’re happy to use whatever works best for you. |
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GBS/CIDP Foundation International is extremely concerned about protecting your privacy. Read the details about our privacy policy on information gathering and storage. |