May is GBS|CIDP Awareness Month
Building, Growing, and Expanding our community like never before! This awareness month we celebrate the expansion and inclusivity of our worldwide community! As our global network grows wider, our community…
Building, Growing, and Expanding our community like never before! This awareness month we celebrate the expansion and inclusivity of our worldwide community! As our global network grows wider, our community…
In the news today, the European Commission approves Takeda’s HYQVIA, a new maintenance therapy for patients with CIDP. The Foundation advocates for access to all products at all points of…
TAKEDA receives positive CHMP opinion for HYQVIA® as maintenance therapy in patients with Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) The European Medicines Agency’s (EMA) Committee for Medicinal Products for Human Use…
On 12 September 2023, the European Parliament adopted the report on new rules governing the use of so-called substances of human origin (SoHO) intended for human application. The Council still needs to…
As part of the GBS|CIDP Foundation International’s mission to provide education and support research, we offer research grants to qualified applicants. Through the generosity of these many individual contributors, to…
European Parliament adopts substances of human origin (SoHO) On 12 September 2023, the European Parliament adopted the report on new rules governing the use of so-called substances of human origin…
Statement regarding GBS alert in Peru July 10, 2023 July 10, 2023 The Foundation and its Global Medical Advisory Board are aware that Peru has issued a statement of emergency…
2023 Virtual Summit, Life After Diagnosis Back by popular demand, our 2023 Virtual Summit will feature a wide range of educational panels and presentations, as recorded at the 2022 Ponte Vedras, FL Patient Symposium &…
EIGHT GREATS….FOR GBS CIDP AWARENESS MONTH THIS MAY! There are plenty of ways to raise awareness! The most important thing to remember is that most successful awareness raising activities begin…
Ways to Get Involved in Awareness Month! If you have MMN, or know someone who does, you are not alone. MMN (Multifocal Motor Neuropathy) is a rare disorder in which focal areas…