Google
Trusted Resources: News & Events
Latest announcements and gatherings
Rare Across America 2021
Rare Disease Legislative Advocates (RDLA) staff organizes virtual meetings for rare disease advocates with their Members of Congress and/or the Member’s staff. The RDLA team also helps to prepare advocates for their meetings, providing legislative resource materials and hosting pre-meeting training webinars.
No prior advocacy experience is necessary.
Registration for this event and all RDLA events are free for rare disease advocates.
When:
February 22, 2021 – March 5, 2021
Where:
Virtual meetings with your Members of Congress and Virtual Advocacy Events
+myBinderRelated Content
-
Class of 2021-2023 Graduation BookOne of the most significant events of 10...
-
Sickle Cell Disease Association of Illinois Management of Sickle Cell Disease ConferenceThe Sickle Cell Disease Association of I...
-
Coronavirus Preparedness for People With Chronic Diseases – WebinarEvent Date: Mar. 13, 2020 Event...
-
UH Researcher Reports the Way Sickle Cells Form May Be Key to Stopping ThemUniversity of Houston associate professo...
-
Webinar Series: Sickle Cell Science: Path to Progress – Bone Marrow Transplants, Other Therapies, and Sickle C...To commemorate Sickle Cell Awareness Mon...
-
Sickle Cell: Call The Midwife Shines Spotlight on DiseaseViewers and people with sickle cell dise...
-
CDC Expands SCD Data Collection Program to 7 More US States in Effort to Improve ServicesThe Centers for Disease Control and Prev...
To improve your experience on this site, we use cookies. This includes cookies essential for the basic functioning of our website, cookies for analytics purposes, and cookies enabling us to personalize site content. By clicking on 'Accept' or any content on this site, you agree that cookies can be placed. You may adjust your browser's cookie settings to suit your preferences. More Information
The cookie settings on this website are set to "allow cookies" to give you the best browsing experience possible. If you continue to use this website without changing your cookie settings or you click "Accept" below then you are consenting to this.
Powered by
Support for this site is provided by
This platform is made possible through a partnership with the Sickle Cell Disease Association of America, Inc. (SCDAA) and its member organizations. SCDAA's mission is to advocate for people affected by sickle cell conditions and empower community-based organizations to maximize quality of life and raise public consciousness while advancing the search for a universal cure.