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    • #18177
      Ashley Gregory
      Moderator

      Good morning all!

      I know many of us had an extremely long period of time between when we first started experiencing LEMS symptoms and when we were actually diagnosed with LEMS.

      Lambert-Eaton News posted an article back in January about the possible emotional responses to a LEMS diagnosis.

      I found this article helpful to know that we all feel different emotions but also have a few similar ones.

      What were your feelings after you were diagnosed with LEMS?

      For me, I felt a sense of relief at finally having a source for all of the symptoms I was experiencing. I was relieved to know that I had treatment options that could decrease my symptoms and allow me to get back to a somewhat normal life.

      If your family member was diagnosed with LEMS, how do you think they felt and how did you feel after hearing about their diagnosis?

       

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