The Lambert-Eaton LEMS Family Association
May 9, 2025 |
The Lambert-Eaton LEMS Family Association is a 501c3 non-profit organization founded in 2022 to support the Lambert-Eaton Myasthenic Syndrome (LEMS) community of patients. We work to increase awareness of LEMS in the medical and research communities. We promote research with a dedicated, LEMS Patient Registry, hosted by Sanford Research (CoRDS). In addition, we strengthen community within our patient population with webinars and on-line meetings.