This year, together with advocates like you, we convinced Congress to restore millions in funding for lupus research. We made it clear that investing in lupus research – and all medical research – is one of the wisest investments we can make. Now it is time to build on that massive win!
We are inviting YOU to join us for our Virtual Advocacy Day from March 23-25 and speak directly with lawmakers or their staff as research funding levels for next year are being considered.
The Lupus Research Alliance and our partners in Washington, D.C. will help you set up virtual meetings with your legislators, providing you with talking points and resources to powerfully convey the importance of lupus research.
Your voice is so important! Congress needs to hear how funding innovative research could lead to better diagnostics, new treatments, and even a cure — significantly improving the lives of millions of people living with lupus.
Tags: virtual advocacy, washington d.c., lupus research funding, D.C., congressional leaders, congress, advocate, advocacy, Lupus Research Program