What Is Count Me In?
Count Me In is a nonprofit research initiative that enables patients to accelerate cancer research by sharing their samples, their clinical information, and their voices. With patient consent, all data collected by and generated through Count Me In are shared regularly with the research community (after being stripped of identifying information) through freely available scientific databases, so researchers anywhere can help rapidly accelerate the pace of discovery, expand our understanding of cancer, and develop new treatment strategies – breaking down silos that exist in cancer research.
