Connect with the LEMS Community
The LEMS journey has its ups and downs, but you don’t have to ride it solo. At the LEMS Family Association, connection leads to confidence, understanding, and hope.
Ways to Connect
Connection doesn't just help. It heals.
Living with Lambert-Eaton Myasthenic Syndrome (LEMS) can feel isolating, especially given how rare the condition is. The LEMS Family Association offers several ways to connect with others who truly understand what you’re going through. Whether you’re newly diagnosed, years into your journey, or a caregiver, these programs are designed to foster connection, learning, and support.
Join the LEMS Community
Turn Your Experience into Impact
Volunteer to support patients, raise awareness, and help build a stronger future for the LEMS community.