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October 28, 2026

Communicator, Fall 2026

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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

1,215

Lindsay’s journey with Guillain-Barré syndrome (GBS) began with rapidly progressing weakness that left her unable to walk. After countless appointments and the struggle to be heard, she finally received a diagnosis.

Today, Lindsay is sharing her story of uncertainty, resilience, the power of support, and the ongoing journey of recovery.

Read Lindsay’s story and discover why every patient’s voice matters: click the link in our bio.

55 1

Open post by gbscidpfoundation with ID 18110904488229196

Lindsay’s journey with Guillain-Barré syndrome (GBS) began with rapidly progressing weakness that left her unable to walk. After countless appointments and the struggle to be heard, she finally received a diagnosis.

Today, Lindsay is sharing her story of uncertainty, resilience, the power of support, and the ongoing journey of recovery.

Read Lindsay’s story and discover why every patient’s voice matters: click the link in our bio.

A little Halloween fun at the Foundation!

Our team traded their usual workday attire for some Halloween spirit! From creative costumes to plenty of laughs, we’re having a little fun while continuing to do what we love — supporting the GBS, CIDP, and MMN community.

Think you can guess who (or what!) everyone is dressed up as? Drop your guesses in the comments! 👀

41 0

Open post by gbscidpfoundation with ID 18415427476091502

A little Halloween fun at the Foundation!

Our team traded their usual workday attire for some Halloween spirit! From creative costumes to plenty of laughs, we’re having a little fun while continuing to do what we love — supporting the GBS, CIDP, and MMN community.

Think you can guess who (or what!) everyone is dressed up as? Drop your guesses in the comments! 👀

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.

35 0

Open post by gbscidpfoundation with ID 17953711365279890

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.

¿Eres paciente de GBS, CIDP o MMN y buscas apoyo? Acompáñanos en la Conferencia Regional de Latinoamérica el 14 de noviembre. ¿No puedes asistir en persona? No hay problema, habrá una opción virtual. Esta conferencia se presentará en español con opciones de traducción.

¡Regístrate ahora! Haz clic en el enlace de nuestra biografía para registrarte.

37 3

Open post by gbscidpfoundation with ID 18647836663026109

¿Eres paciente de GBS, CIDP o MMN y buscas apoyo? Acompáñanos en la Conferencia Regional de Latinoamérica el 14 de noviembre. ¿No puedes asistir en persona? No hay problema, habrá una opción virtual. Esta conferencia se presentará en español con opciones de traducción.

¡Regístrate ahora! Haz clic en el enlace de nuestra biografía para registrarte.

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PA, United States, Pennsylvania.

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