Skip to Main Content
Skip to Main Navigation
Skip to Footer

Walk & Roll
Community Forum
Ask the Health Navigator
Contact Us

GBS | CIDP Foundation International, home page

<img src="https://www.gbs-cidp.org/wp-content/uploads/2025/10/Foundation-Logo-2025.png" class="custom-logo" alt="Logo - GBS | CIDP Foundation International" decoding="async" fetchpriority="high" width="707" height="172" data-default-src="https://www.gbs-cidp.org/wp-content/uploads/2025/10/Foundation-Logo-2025.png" data-sticky-src="https://www.gbs-cidp.org/wp-content/uploads/2025/10/Foundation-Logo-2025.png" srcset="https://www.gbs-cidp.org/wp-content/uploads/2025/10/Foundation-Logo-2025.png 707w, https://www.gbs-cidp.org/wp-content/uploads/2025/10/Foundation-Logo-2025-570x139.png 570w" sizes="(max-width: 707px) 100vw, 707px" />

- About Us
- Partners & Committees
- News
  - Research News
  - Newsletters
- GBS
  - Intro to Guillain-Barré Syndrome
- CIDP
  - Intro to Chronic Inflammatory Demyelinating Polyneuropathy
- MMN
  - Intro to Multifocal Motor Neuropathy (MMN)
- Related Conditions
  - Intro to Related Conditions
- Looking for resources tailored for you? Get started here:
- Education Center
  Explore trusted tools and resources to help patients, caregivers, and medical professionals better understand and manage GBS, CIDP, and MMN.
  
  Share:
- Ask the Health Navigator
  Get personalized support from our Health Navigator for insurance questions, resources, and care planning tailored to your unique patient journey.
  
  Share:
- Events Calendar
  Join us to connect, inform, and inspire. From local chapter meetings to educational programs and awareness initiatives, we love coming together as a community.
  
  Share:
- Patient Stories
  Hear lived experiences from patients, caregivers, and advocates living with GBS, CIDP, and MMN. Stories of strength, recovery, and resilience.
  
  Share:
- Treatments & Access
  Explore the access portal, and learn about treatment options, medication support, and patient assistance programs available through our pharmaceutical partners.
  
  Share:
- Life After Diagnosis
- Volunteer
- Advocacy
  - Overview
  - Advocacy Resources
- Fundraise
  - DIY Fundraise
  - Find a Walk & Roll
- Give
- Connect
  - Community Forum
  - Care Partner Community
- Events

GBS | CIDP Foundation International, home page

Search this Site

When autocomplete results are available use up and down arrows to review and enter to go to the desired page. Touch device users, explore by touch or with swipe gestures.

Walk & Roll
Community Forum
Ask the Health Navigator
Contact Us

Donate

Search this Site

Symptoms, diagnosis, and treatment of CIDP

Share:

A patient’s life with Chronic Inflammatory Demyelinating Polyneuropathy.

Footer

The GBS | CIDP Foundation brings patients, caregivers, and medical professionals together with trusted care, helpful tools, and support.

Sign up for our newsletter and never miss a resource, research update, event, or opportunity to make a difference.

Enter your email address(Required)

Δ

Menu

Policies
Medical Disclaimer
Volunteer Portal
Board Portal
Contact Us

Follow us on Instagram

gbscidpfoundation

1,156

GBS|CIDP Foundation International is excited to share the first edition of the GBS|CIDP Global Update, our new bi-annual newsletter that highlights the incredible work happening around the world. Inside, you’ll discover stories of impact, regional initiatives, global partnerships, and the inspiring individuals helping ensure that no one walks this journey alone.

Check out the first edition of the GBS|CIDP Global Update below and see the impact our global community is making around the world!

https://www.gbs-cidp.org/wp-content/uploads/2026/06/Summer-Global-Newsletter.pdf

17 0

Open post by gbscidpfoundation with ID 18092432606022713

GBS|CIDP Foundation International is excited to share the first edition of the GBS|CIDP Global Update, our new bi-annual newsletter that highlights the incredible work happening around the world. Inside, you’ll discover stories of impact, regional initiatives, global partnerships, and the inspiring individuals helping ensure that no one walks this journey alone.

Check out the first edition of the GBS|CIDP Global Update below and see the impact our global community is making around the world!

https://www.gbs-cidp.org/wp-content/uploads/2026/06/Summer-Global-Newsletter.pdf

Highlights from the Peripheral Nerve Society (PNS) meeting in Maastricht, Netherlands.

From connecting with attendees at the GBS|CIDP Foundation booth, to bringing together past, current, and new GMAB members, to Nancy and Richard presenting priorities on the main stage as part of the Inflammatory Neuropathy Consortium—it was a valuable time spent advancing collaboration and elevating the patient voice.

#peripheralnervesociety #PNS #cidpwarrior #cidpawareness #guillainbarresurvivor #guillainbarresyndrome #multifocalmotorneuropathy #guillainbarré

50 0

Open post by gbscidpfoundation with ID 18013723178900746

Highlights from the Peripheral Nerve Society (PNS) meeting in Maastricht, Netherlands.

From connecting with attendees at the GBS|CIDP Foundation booth, to bringing together past, current, and new GMAB members, to Nancy and Richard presenting priorities on the main stage as part of the Inflammatory Neuropathy Consortium—it was a valuable time spent advancing collaboration and elevating the patient voice.

#peripheralnervesociety #PNS #cidpwarrior #cidpawareness #guillainbarresurvivor #guillainbarresyndrome #multifocalmotorneuropathy #guillainbarré

At eight years old, Ashley was diagnosed with Guillain-Barré syndrome and spent nearly a year in the hospital after losing the ability to walk. Despite doctors believing she would never walk again, her mother helped her slowly regain my mobility through years of dedication and recovery. Today, Ashley is a licensed professional counselor, using her experience to help others find resilience, healing, and hope.

▶ Learn more about Ashley and her journey with GBS by visiting our story portal.

#guillainbarre #rarediseasewarrior #gbssurvivor #nonprofitorganization #RareDiseases #PatientCommunity #Neurology #disabilitiesawareness #GBSAwareness

54 2

Open post by gbscidpfoundation with ID 18068417537394831

At eight years old, Ashley was diagnosed with Guillain-Barré syndrome and spent nearly a year in the hospital after losing the ability to walk. Despite doctors believing she would never walk again, her mother helped her slowly regain my mobility through years of dedication and recovery. Today, Ashley is a licensed professional counselor, using her experience to help others find resilience, healing, and hope.

▶ Learn more about Ashley and her journey with GBS by visiting our story portal.

#guillainbarre #rarediseasewarrior #gbssurvivor #nonprofitorganization #RareDiseases #PatientCommunity #Neurology #disabilitiesawareness #GBSAwareness

Did you know it’s been 110 years since Guillain-Barré Syndrome was first identified?

To honor this milestone, the GBS|CIDP Foundation created the GBS110 patient story archive to help share real experiences from our community around the world.
Whether you are a GBS patient or care partner, your voice can help raise awareness, inspire others, and ensure no one faces GBS alone.

We want to hear from YOU! Share your story today: https://thegbs110.com/

Learn more about the GBS|CIDP Foundation International: www.gbs-cidp.org

#StrongerTogether #PatientEducation #HealthEducation #RareDiseases #PatientVoices #Neurology #PatientCommunity #CIDPWarrior #GlobalImpact #nonprofitorganization #disabilitiesawareness #rarediseasewarrior #guillainbarre #SupportAndAwareness #AwarenessMonth #gbssurvivor #cidpawareness #cidpwarrior #guillainbarresurvivor #guillainbarresyndrome #guillainbarrésyndrome #cidp #guillainbarré

72 0

Open post by gbscidpfoundation with ID 18116862799884332

Did you know it’s been 110 years since Guillain-Barré Syndrome was first identified?

To honor this milestone, the GBS|CIDP Foundation created the GBS110 patient story archive to help share real experiences from our community around the world.
Whether you are a GBS patient or care partner, your voice can help raise awareness, inspire others, and ensure no one faces GBS alone.

We want to hear from YOU! Share your story today: https://thegbs110.com/

Learn more about the GBS|CIDP Foundation International: www.gbs-cidp.org

#StrongerTogether #PatientEducation #HealthEducation #RareDiseases #PatientVoices #Neurology #PatientCommunity #CIDPWarrior #GlobalImpact #nonprofitorganization #disabilitiesawareness #rarediseasewarrior #guillainbarre #SupportAndAwareness #AwarenessMonth #gbssurvivor #cidpawareness #cidpwarrior #guillainbarresurvivor #guillainbarresyndrome #guillainbarrésyndrome #cidp #guillainbarré

Follow on Instagram

Copyright Information

Copyright © 2026 | All Right Reserved
GBS | CIDP Foundation International |

Share:

Social Media

LinkedIn
Youtube
Facebook
Instagram
Tiktok

✕

Search for: