About Our Scleroderma Research Programs
Focusing on Collaborative Research
The Scleroderma Research Foundation brings together researchers and unites them in a research community. We host our Science Workshop, the GRASP Project annual meeting, the CONQUER meeting, and the biannual International Scleroderma Workshop. Collectively, these programs promote the sharing of ideas and new discoveries that further progress toward a cure.
Leading Large-Scale Research Projects
The Scleroderma Research Foundation has led the formation of two projects aimed at accelerating scleroderma research. The first is the CONQUER Registry, the first nationwide registry for scleroderma patients in the U.S. The second is the GRASP Project, a collaboration aimed at discovering genetic variations found in African-Americans with scleroderma. Both projects will provide essential data to help identify potential treatments—and hopefully lead to a cure.
Sustaining Centers of Excellence
Another core feature of our research program is the Scleroderma Research Foundation’s leadership in providing funding to establish and support Scleroderma Centers. At these Centers, clinical research can be accelerated, the standard of care can be advanced, and new scleroderma doctors and specialists can be trained.
Nurturing the Next Generation of Investigators
Knowing that future discovery will come from the next generation of scientists, the Scleroderma Research Foundation provides grants to young researchers. Postdoctoral fellowship grants allow researchers to enter the field of scleroderma research and work alongside established researchers. Several recipients of our Early Career Grants are now dedicating themselves to scleroderma research.