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Today on #GivingTuesday, Chris, a CIDP patient, shared the moment he became empowered by our community, which ultimately changed his outlook on his condition. To continue to empower our patient community, we need you! Patients have come together to transform their personal battles into powerful missions of hope, encouragement, and change. And they need your support to make it happen. Donate today! https://p2p.onecause.com/givingtuesdaygbscidp/donate | GBS-CIDP Foundation International
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FacebookGBS-CIDP Foundation International
✨ 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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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
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