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Lambert-Eaton Myasthenia is a very rare neuromuscular autoimmune

Posted by cgahl @cgahl, Dec 20, 2023

I was diagnosed with LEMS ~3 years ago. Similar to Myasthenia Gravis but much less common.
Would like to hear from anyone already diagnosed or suspicious of the disease.

Carol

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Mentor
John, Volunteer Mentor | @johnbishop | Dec 20, 2023

Hello Carol @cgahl, Welcome to Connect. There is an older discussion on LEMS that you might find helpful to read through the posts:
-- Any LEMS (Lambert-Eaton Myasthenic Syndrome) people out there?: https://connect.mayoclinic.org/discussion/lambert-eaton-mysathenic-syndrome/

@emonty, @kjaffee, @spider777, @taosmary and @shawnamarie posted in the discussion above and may have some suggestions or information on LEMS to share with you.

Are you able to share any more about your treatment for LEMS?

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