Mary Ann, living with LEMS
You Are Part of a Larger Community
Living with a rare disease, such as Lambert-Eaton myasthenic syndrome (LEMS), can be isolating. But you’re really not alone. There are thousands of other people dealing with similar challenges. Many of those living with LEMS have found answers, fellowship, and a voice on the Catalyst Patient Facebook Community page. Check out some of the posts below—you may find a helpful tip you can use or the encouragement you’ve been looking for!