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Submission: On June 13 via api from US — Scanned from DE
Submission: On June 13 via api from US — Scanned from DE
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Skip to Main Content * Search * How Can We Help * Find a Walk & Roll Near You * Donate Now Czech Danish Dutch English French German Hungarian Italian Portuguese Romanian Russian Spanish English MAIN NAVIGATION * About Us * WHO ARE WE? * Our Mission & Vision * Our Global Medical Advisory Board * Our Leadership Team * Our Staff * Meet our Founder, Estelle Benson * Academic Research Partners * MULTILINGUAL RESOURCES * International Support Groups * Multilingual Website * OUR POLICIES * Financial * Privacy * Medical Disclaimer * CONTACT US GBS|CIDP Foundation International 375 East Elm Street, Suite 101 Conshohocken, PA 19428 Phone: 866-224-3301 How can we help? * Understanding Our Conditions * GBS, CIDP & RELATED CONDITIONS * What is GBS? * What is CIDP? * What is Multifocal Motor Neuropathy (MMN)? * What is Miller Fisher? * What is Anti-MAG Peripheral Neuropathy? * EDUCATIONAL PUBLICATIONS * News and Blog * Overview Booklets * The Communicator, Quarterly Newsletter * It’s Only Rare Until it’s You * EDUCATIONAL VIDEOS * GBS * CIDP * Multifocal Motor Neuropathy (MMN) * Ask the Experts * Support & Resources * FIND A MEDICAL PRO * Centers of Excellence, Worldwide * Physical and Occupational Therapy * Doctor-to-Doctor Consultation * RESOURCES & WAYS TO CONNECT * Community Connections * Join our Community Forums * Connect with a Volunteer Near You * Local Chapter Meetings (virtual and in-person) * Youth, Teen and Young Adults * Monthly ZOOM Coffee Chats * Patient Story Portal * Liaison Portal * Get Social * Communication Cards * EDUCATIONAL CONFERENCES & WEBINARS * International Symposium * Ask the Experts Webinar * Regional Conferences * Virtual Summit * TREATMENT RESOURCES & INFORMATION * Financial Support for Treatments * Healthy Lifestyle Tips & Education * Insurance Information * Treatment Education * Participate in Research * Diagnosis and Manage GBS – Ten Step Guide * Americans with Disabilities Act (ADA) * All About Vaccines * Support for After the Hospital * Adaptive Devices * COVID-19 Resources * Research * FOR RESEARCHERS & HEALTHCARE PROFESSIONALS * Learn More About Research Grant Program * Free Resources for Healthcare Professionals (Be the Bridge) * WAYS TO GET INVOLVED IN RESEARCH * Participate in Research * Join Our Patient Registry * Christopher Cross Research Fund * Voice of the Patient Meetings * RESEARCH WE SUPPORT * International Guillain-Barre Study (IGOS) * International CIDP Study INCbase * Updates from Foundation Grant Recipients * Take Action * VOLUNTEER * Volunteer Opportunities * Greeting Card Alert Program * Healthcare Awareness Campaign (Be the Bridge) * College Students Campaigning for Plasma * ADVOCACY * All About Advocacy * Home Infusion for All * Join our Advocacy Team * Plasma Please * FUNDRAISING * Ways to Give * Find a Walk & Roll Near You * DIY Fundraising * DONATE * Make a Donation * Search * How Can We Help * Find a Walk & Roll Near You * Donate Now OUR MISSION AND VISION * Home / * About / * Our Mission and Vision SUPPORT EDUCATION RESEARCH ADVOCACY > The GBS | CIDP Foundation International is a global nonprofit organization > supporting individuals and their families affected by Guillain-Barre’ syndrome > (GBS), chronic inflammatory demyelinating polyneuropathy (CIDP), and related > conditions through a commitment to support, education, research and advocacy. OUR VISION Every person affected by GBS, CIDP, or related syndromes will have access to early and accurate diagnosis, appropriate treatment, and knowledgeable support services. OUR MISSION We improve the quality of life for individuals and families affected by GBS, CIDP, and related conditions. Our unwavering commitment to the patients we serve is built on four pillars: support, education, research and advocacy. * We support patients by nurturing a global network of volunteers, healthcare professionals, researchers and industry partners to provide them with critical, timely, and accurate information; * We educate doctors, clinicians, patients and caregivers to increase awareness and understanding; * We fund research through grants, establishing fellowships and other appropriate avenues to identify the causes of and discover treatments; * We advocate at the federal, state, and grassroots levels to educate policymakers and help them make informed decisions that benefit our patient community. * About Us * Mission * History * Financials and Policies * Privacy Policy * Medical Disclaimer * Global Medical Advisory Board * Leadership Team * Our Staff * Contact Us RECENT NEWS * Dr. Jeffrey Allen, New Global Medical Board Chairman * A one-year Research Update from the 2022 Benson Fellowship Awardee * May Awareness Proclamation * Understanding the Patient Experience with CIDP * Validation of Skin Biopsy to Detect Nerve Demyelination in the Diagnosis and Treatment of CIDP at Vanderbilt University Medical Center UPCOMING EVENTS * Different Ways to Volunteer with the Foundation Coffee Chat Tuesday, June 13 1:00 PM -to 12:00 AM * Communicating for Success at the Doctor’s Office Wednesday, June 14 2:00 PM -to 12:00 AM * Hizentra Patient Program Thursday, June 15 8:00 PM -to 12:00 AM * Philadelphia Walk & Roll Saturday, June 17 9:00 AM -to 12:00 AM * June 2023 Los Angeles VIRTUAL Chapter Meeting Tuesday, June 20 10:00 AM -to 10:40 AM $7.3 MILLION IN RESEARCH GRANTS AWARDED 71 RESEARCHERS FUNDED SINCE 2004 Learn More Learn More About Our National Walk & Roll Fundraising Program Learn More FOOTER © 2021 GBS/CIDP Foundation International Use of this Web site constitutes acceptance of our Terms of Use and Privacy Policy. GBS|CIDP Foundation International is a 501(c)3 tax-exempt organization. Mailing Address: 375 East Elm Street, Suite 101, Conshohocken, PA 19428 | Phone: 866-224-3301 ✕ Search for: