
← Patient Advocacy Voices2 jul · 38 min
Leading Change in Rare Disease: What We Can Learn from the GBS-CIDP Foundation
Leading Change in Rare Disease: What We Can Learn from the GBS-CIDP Foundation
Patient advocacy leaders work every day to make sure patient voices do more than get heard. They want those voices to shape decisions, improve care, guide research, and advance policies that affect patients’ lives. In this episode of Patient Advocacy Voices, we hear from an organization doing exactly that. Host Eric Racine is joined by co-host Melissa Dupont, Global Public Affairs Lead, Neurology at Sanofi, for a conversation with Lisa Butler, President and CEO of the GBS-CIDP Foundatio...