You have the power to fuel research discoveries when you join the FSR Patient Registry. Create your online profile, answer survey questions, and update your information over time to tell the story of how this disease has affected your life. When added to the information shared by other patients around the world, your survey answers will help us better understand this disease and stand up to false beliefs about sarcoidosis. The Registry also allows FSR to show doctors and researchers the strength of this community and interest of patients like Jackie in speeding up research.