Wednesday, October 26th: 1:00 pm to 2:00 pm EST
- Lymphedema Treatment Act:Patricia Egan, Interim Executive Director & CEO, National Lymphedema Network
- Newborn Screening in California: Vignesh Ganapathy, Manager of Advocacy and Government Relations, EveryLife Foundation
- Capitol Hill Update: Max Bronstein, Senior Director of Advocacy and Science Policy, EveryLife Foundation
Agenda is OPEN, please submit possible agenda items to email@example.com
Once a month RDLA convenes in person and/or over the phone to discuss legislation and developments that affect the rare disease community. The meeting/conference calls are essentially a clearing house for legislation and participation does not imply support for any of the policy proposals or legislation that are discussed or promoted.