Your voice matters and makes a difference.
Join More Than Lupus and their efforts to be a voice and influencer to increase lupus awareness and funding on a national scale.
March is Advocacy Month!
Don't miss your opportunity to join Kelli & The Lupus Research Alliance
March 16-19th. Click here for more information.
"We know that without government funding there is no lupus research, and without research, there will be no cure."
A Mission on a National Scale
In a Nation where 2/3rd's of its people know little to nothing about a disease that affects more people than muscular dystrophy, multiple sclerosis, and cystic fibrosis - combined, it is detrimental to our cause to amplify the lupus patient's voice! Every person has the right and responsibility to lift their concerns to their local and national representatives. At MTL, we take that call very seriously. We know that without government funding there is no lupus research, and without research, there will be no cure. That is why we have joined the efforts advocating for more federal funding to be allocated to the National Institute of Health and the CDMRP's Lupus Research Program. Additionally, any legislation that may affect access to care, or research initiatives that may limit quality of care, are carefully analyzed and advocated for (or against) through our patient lense. It is our mission to continue to collaborate with National and Grassroots organizations and "fight the good fight" as we represent the collective "Lupus Patient Voice" for those who feel unheard and unrepresented in the community
Click on image below to view additional media interviews and an update from the work on Capital Hill.