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

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

Event Date

Date: Event Date: Monday, October 19, 2026

Event Time

Time: Event Time: 12:00 AM

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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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¡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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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!

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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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