Skip to Main Content
Skip to Main Navigation
Skip to Footer

Walk & Roll
Community Forum
Ask the Health Navigator
Contact Us

Donate

GBS | CIDP Foundation International, home page

- About Us
- Partners & Committees
- News
- 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.
- Ask the Health Navigator
  Get personalized support from our Health Navigator for insurance questions, resources, and care planning tailored to your unique patient journey.
- 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.
- Patient Stories
  Hear lived experiences from patients, caregivers, and advocates living with GBS, CIDP, and MMN. Stories of strength, recovery, and resilience.
- Treatments & Access
  Explore the access portal, and learn about treatment options, medication support, and patient assistance programs available through our pharmaceutical partners.
- Life After Diagnosis
- Centers of Excellence
- Volunteer
- Advocacy
- 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

Home
CIDP Research and Clinical Trials: What Patients Should Know

October 21, 2026

CIDP Research and Clinical Trials: What Patients Should Know

Share:

Categories:

Webinars

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

Toll-Free: (866) 224-3301
Direct: (610) 667-0131

We’d like to thank Grifols for their support in bringing education and support to patients worldwide.

gbscidpfoundation

1,209

¡La Conferencia de la Ciudad de México te espera!

14 de noviembre de 2026

¡Participa en persona o virtualmente desde cualquier lugar del mundo!

Conéctate con especialistas, aprende y comparte con la comunidad GBS|CIDP y MMN.

🎟️ ¡El registro es GRATIS!

👉 ¡Regístrate hoy! Haz clic en el enlace de nuestra biografía para reservar tu lugar.

34 3

Open post by gbscidpfoundation with ID 18113062892626379

¡La Conferencia de la Ciudad de México te espera!

14 de noviembre de 2026

¡Participa en persona o virtualmente desde cualquier lugar del mundo!

Conéctate con especialistas, aprende y comparte con la comunidad GBS|CIDP y MMN.

🎟️ ¡El registro es GRATIS!

👉 ¡Regístrate hoy! Haz clic en el enlace de nuestra biografía para reservar tu lugar.

Research is helping us learn more about CIDP—and patients play an important role in moving that research forward.

Join us for CIDP Research & Clinical Trials: What Patients Should Know to learn what clinical trials are, what participation looks like, and what to consider before saying yes.

October 20th | 12PM ET

👉 Click the link in our bio to visit our events page on the website.

https://www.gbs-cidp.org/event/cidp-research-and-clinical-trials-what-patients-should-know/

15 0

Open post by gbscidpfoundation with ID 18090876428682430

Research is helping us learn more about CIDP—and patients play an important role in moving that research forward.

Join us for CIDP Research & Clinical Trials: What Patients Should Know to learn what clinical trials are, what participation looks like, and what to consider before saying yes.

October 20th | 12PM ET

👉 Click the link in our bio to visit our events page on the website.

https://www.gbs-cidp.org/event/cidp-research-and-clinical-trials-what-patients-should-know/

What does it mean to move forward with confidence?

Join Rare in Motion on October 18 in New York City or via livestream for a one-day exercise and wellness experience created for people living with—or facing—mobility loss from rare neuromuscular diseases.

The event will bring together patients, caregivers, families, clinicians, and advocates for:
✨ Adaptive exercise and practical mobility strategies
💬 Honest conversations about emotional wellbeing
🔬 Expert insights on symptoms, diagnosis, treatment, and the latest research
🤝 Community connection and shared experiences

Featuring voices from across the rare disease community, including MMN patient and Health Haven founder Edward Gent and CIDP advocate Amanda Coronado.

Click the link in our bio to learn more!

23 2

Open post by gbscidpfoundation with ID 17968587993190508

What does it mean to move forward with confidence?

Join Rare in Motion on October 18 in New York City or via livestream for a one-day exercise and wellness experience created for people living with—or facing—mobility loss from rare neuromuscular diseases.

The event will bring together patients, caregivers, families, clinicians, and advocates for:
✨ Adaptive exercise and practical mobility strategies
💬 Honest conversations about emotional wellbeing
🔬 Expert insights on symptoms, diagnosis, treatment, and the latest research
🤝 Community connection and shared experiences

Featuring voices from across the rare disease community, including MMN patient and Health Haven founder Edward Gent and CIDP advocate Amanda Coronado.

Click the link in our bio to learn more!

A story worth seeing.

No One Rides Alone follows Clive Phillips, who lives with MMN, and four fellow veterans as they take on the Tour de MMN—tackling mountains, challenges, and the realities of Clive’s journey with MMN. 🚲

A story of resilience, friendship, and community.

📍 Boston • New York • Philadelphia • San Francisco • Los Angeles
🎟️ Screenings + tickets: https://makingthemostofnow.co.nz/no-one-rides-alone/

A portion of proceeds supports MMN research.

26 1

Open post by gbscidpfoundation with ID 18136707703639824

A story worth seeing.

No One Rides Alone follows Clive Phillips, who lives with MMN, and four fellow veterans as they take on the Tour de MMN—tackling mountains, challenges, and the realities of Clive’s journey with MMN. 🚲

A story of resilience, friendship, and community.

📍 Boston • New York • Philadelphia • San Francisco • Los Angeles
🎟️ Screenings + tickets: https://makingthemostofnow.co.nz/no-one-rides-alone/

A portion of proceeds supports MMN research.

Follow on Instagram

Copyright Information

375 East Elm Street Suite 101, Conshohocken,
PA, United States, Pennsylvania.

GBS | CIDP Foundation International |

Sitemap

Social Media

LinkedIn
Youtube
Facebook
Instagram
Tiktok

✕

Search for:

CIDP Research and Clinical Trials: ​ What Patients Should Know

Other Articles You May Like

CIDP Clinical Trial Awareness: Helping Patients and Care Partners Understand Opportunities in CIDP Research

The Power Behind the Treatment: Plasma and Immunoglobulins​ in CIDP Care

Dr. Luis Querol, MD, PhD, Appointed Vice Chairman of GMAB and Chairman of Center of Excellence Committee

gbscidpfoundation

CIDP Research and Clinical Trials: What Patients Should Know

The Power Behind the Treatment: Plasma and Immunoglobulins in CIDP Care