What is Lambert-Eaton Myasthenic Syndrome?

Lambert-Eaton myasthenic syndrome (LEMS) is an autoimmune disorder of the neuromuscular junction where nerve cells meet muscle cells and help activate the muscles. It is caused by a disruption of electrical impulses between these nerve and muscle cells.

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What is it like to have Lambert-Eaton Myasthenic?

Common symptoms How bad it is What people are taking for it
Severity
Severe
Moderate
Mild
None
Nothing reported yet
Nothing reported yet
Nothing reported yet
Nothing reported yet
Nothing reported yet

What do patients take to treat Lambert-Eaton Myasthenic and its symptoms?

Treatments reported by members Perceived effectiveness Overall rating of side effects # of Evaluations
(Mestinon, Kalymin 60N)
0
(Pulmison, Prednisone Intensol, Encorton, Deltasone)
0
(Azasan, Imurel, Imuran, Azapress)
0
(Octagam, Privigin, Gamunex, Gammagard)
0
0

These charts show data from Lambert-Eaton Myasthenic patients' latest treatment evaluations

Who has Lambert-Eaton Myasthenic at PatientsLikeMe?

<20 20s 30s 40s 50s 60s 70+
Current Age
Distribution of females vs. males
Gender
90% Females
10% Males
Age at first symptom
Age at first symptom # of patients Proportion
0-19 years 0
20-29 years 0
30-39 years 1
40-49 years 1
50-59 years 3
60-69 years 1
70+ years 0
Diagnosis status
Diagnosis status # of patients Proportion
Diagnosed 7

These charts show data from Lambert-Eaton Myasthenic patients who have completed their condition history