Leading up to Rare Disease Day 2024, RPV President and Founder Wes Michael was interviewed on It Happened to Me: A Rare Disease & Medical Challenges Podcast, and the episode is now live. On the show, patient advocates Cathy Gildenhorn and Beth Glassman share their medical challenges living with rare diseases and are joined by fellow advocates and experts. Listen in here as Wes discusses the origins of Rare Patient Voice and our roots in rare, and how the company has connected patients and family caregivers with opportunities to share their voices for over ten years.
