Short Bio |
I was diagnosed with Lambert-Eaton Myasthenic Syndrome in August 2020. It took multiple doctors more than eight months to diagnose me, which I now understand, might be fairly quick. I am married to a wonderful man (my childhood crush) who is my caregiver and the love of my life. I continue to work full time from home as a Public Information Specialist for county government. I still enjoy life, even with LEMS. I spend time spoiling our two rescue dogs and am writing my first screenplay, a romantic-comedy featuring another love of mine: golf. I hope resume playing the game one day. I have benefitted so much from the Lambert-Eaton News digest. Having a good, factual resource of information and the experiences of my compatriots with LEMS is very comforting and uplifting. More to come…
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How long have you or the person that you are caring for had LEM? |
1 1/2 years
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