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Emotional Responses after your LEMS diagnosis
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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