Swedish CIDP – GBS | CIDP Foundation International

GBS|CIDP Foundation International is excited to share the first edition of the GBS|CIDP Global Update, our new bi-annual newsletter that highlights the incredible work happening around the world. Inside, you’ll discover stories of impact, regional initiatives, global partnerships, and the inspiring individuals helping ensure that no one walks this journey alone.

Check out the first edition of the GBS|CIDP Global Update below and see the impact our global community is making around the world!

https://www.gbs-cidp.org/wp-content/uploads/2026/06/Summer-Global-Newsletter.pdf

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Highlights from the Peripheral Nerve Society (PNS) meeting in Maastricht, Netherlands.

From connecting with attendees at the GBS|CIDP Foundation booth, to bringing together past, current, and new GMAB members, to Nancy and Richard presenting priorities on the main stage as part of the Inflammatory Neuropathy Consortium—it was a valuable time spent advancing collaboration and elevating the patient voice.

#peripheralnervesociety #PNS #cidpwarrior #cidpawareness #guillainbarresurvivor #guillainbarresyndrome #multifocalmotorneuropathy #guillainbarré

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Highlights from the Peripheral Nerve Society (PNS) meeting in Maastricht, Netherlands.

From connecting with attendees at the GBS|CIDP Foundation booth, to bringing together past, current, and new GMAB members, to Nancy and Richard presenting priorities on the main stage as part of the Inflammatory Neuropathy Consortium—it was a valuable time spent advancing collaboration and elevating the patient voice.

#peripheralnervesociety #PNS #cidpwarrior #cidpawareness #guillainbarresurvivor #guillainbarresyndrome #multifocalmotorneuropathy #guillainbarré

At eight years old, Ashley was diagnosed with Guillain-Barré syndrome and spent nearly a year in the hospital after losing the ability to walk. Despite doctors believing she would never walk again, her mother helped her slowly regain my mobility through years of dedication and recovery. Today, Ashley is a licensed professional counselor, using her experience to help others find resilience, healing, and hope.

▶ Learn more about Ashley and her journey with GBS by visiting our story portal.

#guillainbarre #rarediseasewarrior #gbssurvivor #nonprofitorganization #RareDiseases #PatientCommunity #Neurology #disabilitiesawareness #GBSAwareness

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At eight years old, Ashley was diagnosed with Guillain-Barré syndrome and spent nearly a year in the hospital after losing the ability to walk. Despite doctors believing she would never walk again, her mother helped her slowly regain my mobility through years of dedication and recovery. Today, Ashley is a licensed professional counselor, using her experience to help others find resilience, healing, and hope.

▶ Learn more about Ashley and her journey with GBS by visiting our story portal.

#guillainbarre #rarediseasewarrior #gbssurvivor #nonprofitorganization #RareDiseases #PatientCommunity #Neurology #disabilitiesawareness #GBSAwareness

Did you know it’s been 110 years since Guillain-Barré Syndrome was first identified?

To honor this milestone, the GBS|CIDP Foundation created the GBS110 patient story archive to help share real experiences from our community around the world.
Whether you are a GBS patient or care partner, your voice can help raise awareness, inspire others, and ensure no one faces GBS alone.

We want to hear from YOU! Share your story today: https://thegbs110.com/

Learn more about the GBS|CIDP Foundation International: www.gbs-cidp.org

#StrongerTogether #PatientEducation #HealthEducation #RareDiseases #PatientVoices #Neurology #PatientCommunity #CIDPWarrior #GlobalImpact #nonprofitorganization #disabilitiesawareness #rarediseasewarrior #guillainbarre #SupportAndAwareness #AwarenessMonth #gbssurvivor #cidpawareness #cidpwarrior #guillainbarresurvivor #guillainbarresyndrome #guillainbarrésyndrome #cidp #guillainbarré

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