1.8K views · 41 reactions | Nancy Di Salvo, Director of International Affairs and a CIDP patient, shares her journey of living with a rare condition on Rare Disease Day. We encourage all GBS, CIDP, MMN, and variant condition patients to step forward and share their stories to raise awareness and inspire others. Your voice matters! #RareDiseaseDay2025 For more information on Rare Disease Day: https://www.gbs-cidp.org/2025/02/rare-disease-day/ | GBS-CIDP Foundation International | Facebook
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FacebookGBS-CIDP Foundation International
Give your CIDP treatment plan a regular check-in. ✅ Work with your doctor to meet your personal goals: https://bit.ly/3VHy07y CIDP=chronic inflammatory demyelinating polyneuropathy. ©2025 argenx. All rights reserved. | Shining Through CIDP | Facebook
Give your CIDP treatment plan a regular check-in. ✅ Work with you…
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A special edition of the CIDP reality series—”Rare, Well Done”—will air on national TV for the first time. 🎉 Tag two friends in the comments to join your watch party! Tune in to Cozi TV on these dates and times: - Sat, Sept 13th: 9:30 PM EDT - Sun, Sept 14th: 11 AM EDT - Sat, Sept 20th: 9:30 PM EDT - Sun, Sept 21st: 11 AM EDT CIDP=chronic inflammatory demyelinating polyneuropathy. ©2025 argenx. All rights reserved. | Shining Through CIDP
A special edition of the CIDP reality series—”Rare, Well Done”—will ai…
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