I recently had the opportunity to chat with Patty Weltin from the Rare Disease United Foundation (RDUF). In our conversation, I learned more about the mission of her organization and the big impact she’s already making on the East Coast rare disease community after starting RDUF in 2011. I was so impressed by her commitment to the rare disease community that I wanted to share her story with our readers. In her interview with us, she tells us about RDUF, how she started, and an upcoming local event in Boston, Mass. Read on to hear more about the exciting things happening at RDUF.
Topics: Patient Advocacy