Rare Disease Legislative Advocates (RDLA) organizes meetings for rare disease advocates with their Legislators. Meetings with House Representatives will be in-person and meeting with Senators will be virtual. The RDLA team also helps to prepare advocates for their meetings, provides legislative resource materials, and hosts pre-meeting training webinars. No prior advocacy experience is necessary.
Learn More: HERE
Para Español: AQUÍ
Registration closes July 8, 2022. Register: HERE
August 08, 2022 - August 19, 2022