By Haleemah Atobiloye, Program Manager
When we raise our collective voices, we create systemic change.
Recent updates: Wins!
In partnership with other patient advocates and the Lymphedema Advocacy Group, in December of 2022, we were successful in urging legislators to pass the Lymphedema Treatment Act (LTA) into law. The LTA is a bill that requires Medicare coverage for lymphedema compression garments and supplies.
On January 1, 2024, this new coverage came into effect.
Our allies in the Lymphedema Advocacy Group have put together an easy-to-understand one-pager outlining key information about the insurance coverage for lymphedema compression garments and supplies.
To help you better advocate for yourself or someone in your community, or if you’re a clinician or a lymphedema compression supplier, take a moment to review this resource, and share it with your network as appropriate.
In May 2023, alongside 100+ allied organizations, we signed on to support the Center for Biological Diversity’s letter to the United States Geological Survey (USGS) urging the agency to protect the National Pesticide Use Map database, which was undermined and vulnerable to termination from the previous administration.
The pesticide use map is a valuable tool used by scientists and advocates alike. The changes made to the Pesticide Use Mapping Project in 2019 resulted in a significant reduction in the number of pesticides tracked and reported, as the the scope of the project was reduced from tracking around 500 agricultural pesticides, to just 72 pesticides. This is unacceptable, and a potential harm to public health.
As of February 2024, our collective voice was heard and the USGS reversed its cuts to this important resource, and restored the scope of this Pesticide Use Mapping Project to its pre-2019 level.
Our critical lens, along with our collective action to protect people living with and at risk of breast cancer, made this happen!