Amanda Greene
Patient Advocate

Amanda is a dedicated healthcare advocate; She lives with Lupus and other autoimmune conditions. Recently she spoke on a patient experience panel at the American College of Rheumatology “s (or ACR’s) 2023 Convergence where Amanda presented her patient perspective poster “Lupus and slime” which shared how slime can improve ROM and QOL in patients with Lupus. She is excited to share how the advances in Virtual Medicine are impacting the patient community.

This May, Amanda is raising Lupus Awareness and supporting Lupus Research from Los Angeles to New York City. She embraces alternative treatments to manage pain and longs for the day when any patient who needs one can be given a headset to help reduce their severe pain and improve their overall health. Reach out to her at LAlupusLady@gmail.com