Redefining Possibilities in CIDP Care. I had the privilege of interviewing Dr. Jeffrey Allen, a neurologist and neuromuscular specialist at the University of Minnesota, to discuss the evolving landscape of chronic inflammatory demyelinating polyneuropathy (CIDP), and the important work led by the GBS|CIDP Foundation Leadership Collaborative to establish standardized definitions for key clinical terms used in both patient care and clinical research. Dr. Allen shared his insights on: - The value of clear definitions for terms such as relapse, response, refractory, and remission. - How patient voices helped reshape the meaning of “refractory” to reflect hope and treatment potential. - Emerging research into inflammation, the complement system, and biomarkers that may transform how we understand and track disease activity. 📺 Watch the full interview here: https://lnkd.in/eZfMNvZi #CIDP #Neurology #PatientCentricity #ClinicalResearch #GBSCIDPFoundation #MedicalInnovation #RefractoryCIDP #AutoimmuneNeuropathy
Interview with Dr. Allen on CIDP care and research
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1wAlex Seluzhytsky, MD, MBA this is such an important discussion. Standardizing definitions for terms like relapse, response, refractory, and remission is foundational not only for advancing clinical research but also for ensuring patients and providers share the same language of care. With an estimated 30,000–40,000 people living with CIDP in the U.S. (NINDS), clarity in diagnosis and treatment pathways is critical. I really appreciate how you highlighted the role of patient voices in reshaping the meaning of “refractory” toward hope and treatment potential—showing how science and patient experience must evolve together. The focus on biomarkers, inflammation, and the complement system is exciting for the future of neurology. These advances could transform how we track disease activity and ultimately deliver better outcomes for patients.