Advocating for Patients and Families Affected by Cold Agglutinin Disease
Episode 13, Nov 18, 2021, 03:35 PM
Larry Luxner, senior correspondent for Rare Disease Advisor, interviews Cori Forster, vice-president of the Cold Agglutinin Disease Foundation (CADF) — a nonprofit organization formed to advocate for patients and families affected by CAD. We also talk about research on new therapies for this extremely rare anemic disorder.