Life with LEMS: Encouraging Your Partners to Keep Moving
LEMS Ambassadors are compensated by Catalyst Pharmaceuticals, Inc. for the time they spend discussing their experiences with LEMS. For LEMS Caregiver Ambassador Mark, one of the hardest parts of his wife Jamie’s Lambert-Eaton myasthenic syndrome…
How I Do Some of the Same Things I Used to Do Before My LEMS Diagnosis, Just Differently
There is no question that a Lambert-Eaton myasthenic syndrome (LEMS) diagnosis will alter how you do some of the things you normally did in your day-to-day life. But that doesn’t necessarily mean you can no…
Caring for the LEMS Caregiver
LEMS Ambassadors are compensated by Catalyst Pharmaceuticals, Inc. for the time they spend discussing their experiences with LEMS. When caring for a loved one living with Lambert-Eaton myasthenic syndrome (LEMS), it can be hard to…
LEMS, Exercise, and Me
When first coming to terms with a Lambert-Eaton myasthenic syndrome (LEMS) diagnosis, it’s easy to focus on the new limitations imposed on you. Concerns about exercise and physical activities come to mind. Although you may…
My Disease Doesn’t Define Me
Being diagnosed with Lambert-Eaton myasthenic syndrome (LEMS) can be overwhelming, especially as abilities need to be reassessed and new realities have to be absorbed. But a LEMS diagnosis does not define a person. One of…