GBS

A Rare & Life-Changing Disorder

If you—or someone in your life—has been recently diagnosed with GBS, you probably have a lot of questions. And there’s a lot of information out there on the web to sort through. That’s why we continually work to consolidate the best of that information here.

One of our goals is to help those touched by these disorders to have immediate and easy-to-process information that provides not only accurate answers, but hope. Below is a good place to start.


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    rdday

    Walk & Roll for GBS-CIDP - Greater Delaware Valley

    Saturday, June 8, 2013 - Wilson Farm Park

    The Walk and Roll for GBS-CIDP is the new signature walk fundraising campaign of the GBS-CIDP Foundation International. This national Walk is designed to support the thousands of families forced to face the challenges caused by CIDP, GBS and its variants. Register or sponsor a participant today.

    CIDP: Diagnosis and Treatment

    Richard J. Barohn, MD, Professor and Chair Department of Neurology at the University of Kansas Medical Center, and a member of the GBS/CIDP Foundation International Medical Advisory Board gave a presentation to the Harris County Neurological Society in November – "CIDP: Diagnosis and Treatment". Sit back and watch the video (an hour long) and hear from one of the leading experts on CIDP in the world. Share it with your neurologist.

    cslbehring

    The PATH Study – CIDP Treatment with Subcutaneous Immunoglobulin

    CSL Behring is currently recruiting CIDP patients for a clinical trial. Click above link for full access to view article.

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