Amanda Greene became an engaged patient activist after living with Lupus (and other autoimmune conditions) for over 35 years. Amanda is using her passion to share her story to impact the healthcare community. She has represented the Lupus Research Alliance and the Lupus Foundation of America advocating on Capitol Hill. Amanda is the International Pain Foundation’s Director of Advocacy. Amanda is constantly working on new ways to engage and connect to the Lupus and global health community. Find her on Twitter at @LAlupusLady.