Want to explore? See helpful travel tips and stories from people who live with CIDP. ​ CIDP=chronic inflammatory demyelinating polyneuropathy.​ ​ ©2025 argenx. All rights reserved. | Shining Through CIDP
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GBS|CIDP Foundation International | LinkedIn
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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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CIPD | Foundation Certificate in People Practice
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Have you visited the Foundation's advocacy pages lately? We recently gave them a little refresh so that information about our advocacy program and our advocacy-related resources are even easier to access. If you're new to the world of advocacy, this video will give you an overview of what we do at the Foundation and how you can learn more. All of the information above can be found at gbs-cidp.org/advocacy/. | GBS-CIDP Foundation International
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✨ The Foundation staff is ready to greet you in Denver! Here’s to a weekend of connection, learning, and community at the 2025 International Symposium. | GBS-CIDP Foundation International
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