May 31, 2018
Member of Lupus Research Alliance Young Leaders group, lupus spokesperson, blogger and champion Shanelle Gabriel shares her experience living with lupus from diagnosis to day-to-day management. Her main message –people of color are under-represented in clinical trials and need to participate so that new treatments can be tested among the people who need them most.
This video is part of a collaboration between the Lupus Research Alliance and the digital health company Antidote to share patient perspectives on clinical research.
