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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.

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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

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¡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.

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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/

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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!

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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.

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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.

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