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Nature Reviews publishes an article on Guillain–Barré syndrome

January 13, 2025

Nature Reviews publishes an article on Guillain–Barré syndrome

To read the Nature Reviews article on Guillain–Barré syndrome, please click here.

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¡Una Conferencia, Una Comunidad, Estés Donde Estés! 💙💚

¡Acompáñanos en la Conferencia Regional de GBS, CIDP y MMN en Ciudad de México el sábado 14 de noviembre!

📍 Participa de manera presencial o virtual desde cualquier parte del mundo. La conferencia será en español, brindándote la oportunidad de aprender, conectar y encontrar apoyo sin importar dónde te encuentres.

📅 14 de noviembre de 2026, a las 9:00 a. m.

🔗 Más información e inscripciones: https://www.gbs-cidp.org/event/2026-conferencia-regional-de-america-latina-2/

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¡Una Conferencia, Una Comunidad, Estés Donde Estés! 💙💚

¡Acompáñanos en la Conferencia Regional de GBS, CIDP y MMN en Ciudad de México el sábado 14 de noviembre!

📍 Participa de manera presencial o virtual desde cualquier parte del mundo. La conferencia será en español, brindándote la oportunidad de aprender, conectar y encontrar apoyo sin importar dónde te encuentres.

📅 14 de noviembre de 2026, a las 9:00 a. m.

🔗 Más información e inscripciones: https://www.gbs-cidp.org/event/2026-conferencia-regional-de-america-latina-2/

The GBS|CIDP Foundation and Annexon are teaming up to collect 110 GBS stories in honor of the 110th anniversary of Guillain-Barré Syndrome! 💙💚

Take a moment this weekend to share your experience and help raise awareness. Not sure where to start? Watch stories shared by fellow patients for inspiration and see the power of our community coming together.

Every story matters. Will yours be one of the 110?

🔗 Watch stories and share your own: click the link in our bio.

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The GBS|CIDP Foundation and Annexon are teaming up to collect 110 GBS stories in honor of the 110th anniversary of Guillain-Barré Syndrome! 💙💚

Take a moment this weekend to share your experience and help raise awareness. Not sure where to start? Watch stories shared by fellow patients for inspiration and see the power of our community coming together.

Every story matters. Will yours be one of the 110?

🔗 Watch stories and share your own: click the link in our bio.

Rare disease progress moves faster when we share what we know and look beyond one condition at a time. Join Lisa Butler, CEO and President of the Foundation, at the 2026 #NORDSummit for three days of learning and collaboration across the rare disease community, Oct. 25–27 in Washington, DC.

Register:https://nordsummit.org/

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Rare disease progress moves faster when we share what we know and look beyond one condition at a time. Join Lisa Butler, CEO and President of the Foundation, at the 2026 #NORDSummit for three days of learning and collaboration across the rare disease community, Oct. 25–27 in Washington, DC.

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Lights, Camera, Walk & Roll!

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Join us for the Los Angeles Walk & Roll as we celebrate the strength, resilience, and spirit of our incredible patients and families. Let’s roll out the red carpet, come together, and make this a day to remember!

🌟 Learn more and join us by clickin the link in our bio.

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